-
1
-
-
0030848527
-
Cancer incidence after retinoblastoma: Radiation dose and sarcoma risk
-
Wong FL, Boice JD, Jr., Abramson DH, et al. Cancer incidence after retinoblastoma. Radiation dose and sarcoma risk. JAMA. 1997;278:1262-1267. (Pubitemid 27435614)
-
(1997)
Journal of the American Medical Association
, vol.278
, Issue.15
, pp. 1262-1267
-
-
Wong, F.L.1
Boice Jr., J.D.2
Abramson, D.H.3
Tarone, R.E.4
Kleinerman, R.A.5
Stovall, M.6
Goldman, M.B.7
Seddon, J.M.8
Tarbell, N.9
Fraumeni Jr., J.F.10
Li, F.P.11
-
2
-
-
0015043748
-
Mutation and cancer: Statistical study of retinoblastoma
-
USA.
-
Knudson AG, Jr. Mutation and cancer: statistical study of retinoblastoma. Proc Natl Acad Sci USA. 1971;68:820-823.
-
(1971)
Proc. Natl. Acad. Sci.
, vol.68
, pp. 820-823
-
-
Knudson Jr., A.G.1
-
3
-
-
0029787775
-
Second primary tumors in patients with hereditary retinoblastoma: A register-based follow-up study, 1945-1994
-
DOI 10.1002/(SICI)1097-0215(19960807)67:4<515::AID-IJC9>3.0.CO;2-V
-
Moll AC, Imhof SM, Bouter LM, et al. Second primary tumors in patients with hereditary retinoblastoma: a register-based follow-up study, 1945-1994. Int J Cancer. 1996;67:515-519. (Pubitemid 26274108)
-
(1996)
International Journal of Cancer
, vol.67
, Issue.4
, pp. 515-519
-
-
Moll, A.C.1
Imhof, S.M.2
Bouter, L.M.3
Joop Kuik, D.4
Den Otter, W.5
Dick Bezemer, P.6
Koten, J.W.7
Tan, K.E.W.P.8
-
4
-
-
33846960194
-
Retinoblastoma survivors: Sarcomas and surveillance
-
Meadows AT. Retinoblastoma survivors: sarcomas and surveillance. J Natl Cancer Inst. 2007;99:3-5.
-
(2007)
J. Natl. Cancer Inst.
, vol.99
, pp. 3-5
-
-
Meadows, A.T.1
-
7
-
-
0030806921
-
Germ-line mutations of TP53 in li-fraumeni families: An extended study of 39 families
-
Varley JM,McGownG, ThorncroftM, et al. Germ-linemutations of TP53 in Li-Fraumeni families: an extended study of 39 families. Cancer Res. 1997;57:3245-3252. (Pubitemid 27351742)
-
(1997)
Cancer Research
, vol.57
, Issue.15
, pp. 3245-3252
-
-
Varley, J.M.1
McGown, G.2
Thorncroft, M.3
Santibanez-Koref, M.F.4
Kelsey, A.M.5
Tricker, K.J.6
Evans, D.G.R.7
Birch, J.M.8
-
8
-
-
34249678301
-
Update on the management of familial central nervous system tumor syndromes
-
DOI 10.1007/s11910-007-0031-5
-
Hottinger AF, Khakoo Y. Update on the management of familial central nervous system tumor syndromes. Curr Neurol Neurosci Rep. 2007;7:200-207. (Pubitemid 46831513)
-
(2007)
Current Neurology and Neuroscience Reports
, vol.7
, Issue.3
, pp. 200-207
-
-
Hottinger, A.F.1
Khakoo, Y.2
-
9
-
-
35648976977
-
Does the evidence matter in medicine? The retinoblastoma paradigm
-
DOI 10.1002/ijc.22944
-
Mastrangelo D, De Francesco S, Di Leonardo A, et al. Does the evidence matter in medicine? The retinoblastoma paradigm. Int J Cancer. 2007;121:2501-2505. (Pubitemid 350022420)
-
(2007)
International Journal of Cancer
, vol.121
, Issue.11
, pp. 2501-2505
-
-
Mastrangelo, D.1
De Francesco, S.2
Di Leonardo, A.3
Lentini, L.4
Hadjistilianou, T.5
-
10
-
-
2342644064
-
Second Neoplasms in Pediatric Patients with Primary Central Nervous System Tumors: The St. Jude Children's Research Hospital Experience
-
DOI 10.1002/cncr.20253
-
Broniscer A, Ke W, Fuller CE, et al. Second neoplasms in pediatric patients with primary central nervous system tumors: the St. Jude Children's Research Hospital experience. Cancer. 2004;100:2246-2252. (Pubitemid 38580347)
-
(2004)
Cancer
, vol.100
, Issue.10
, pp. 2246-2252
-
-
Broniscer, A.1
Ke, W.2
Fuller, C.E.3
Wu, J.4
Gajjar, A.5
Kun, L.E.6
-
11
-
-
0034761908
-
Prognostic factors and secondary malignancies in childhood medulloblastoma
-
DOI 10.1097/00043426-200110000-00008
-
Stavrou T, BromleyCM,NicholsonHS, et al. Prognostic factors and secondarymalignancies in childhood medulloblastoma. J Pediatr Hematol Oncol. 2001;23:431-436. (Pubitemid 33031771)
-
(2001)
Journal of Pediatric Hematology/Oncology
, vol.23
, Issue.7
, pp. 431-436
-
-
Stavrou, T.1
Bromley, C.M.2
Nicholson, H.S.3
Byrne, J.4
Packer, R.J.5
Goldstein, A.M.6
Reaman, G.H.7
-
12
-
-
0025893028
-
An estimate of the heritable fraction of childhood cancer
-
Narod SA, Stiller C, Lenoir GM. An estimate of the heritable fraction of childhood cancer. Br J Cancer. 1991;63:993-999.
-
(1991)
Br. J. Cancer
, vol.63
, pp. 993-999
-
-
Narod, S.A.1
Stiller, C.2
Lenoir, G.M.3
-
13
-
-
0023627134
-
Patterns of multiple primary tumours in patients treated for cancer during childhood
-
Kingston JE, Hawkins MM, Draper GJ, et al. Patterns of multiple primary tumours in patients treated for cancer during childhood. Br J Cancer. 1987;56:331-338. (Pubitemid 17161768)
-
(1987)
British Journal of Cancer
, vol.56
, Issue.3
, pp. 331-338
-
-
Kingston, J.E.1
Hawkins, M.M.2
Draper, G.J.3
Marsden, H.B.4
Kinnier Wilson, L.M.5
-
14
-
-
0021953831
-
Second malignant neoplasms in children: An update from the Late Effects Study Group
-
Meadows AT, Baum E, Fossati-Bellani F, et al. Second malignant neoplasms in children: an update from the Late Effects Study Group. J Clin Oncol. 1985;3:532-538. (Pubitemid 15111401)
-
(1985)
Journal of Clinical Oncology
, vol.3
, Issue.4
, pp. 532-538
-
-
Meadows, A.T.1
Baum, E.2
Fossati-Bellani, F.3
-
15
-
-
0032578714
-
Risks of brain tumour following treatment for cancer in childhood: Modification by genetic factors, radiotherapy and chemotherapy
-
DOI 10.1002/(SICI)1097-0215(19981029)78:3<269::AID-IJC1>3.0.CO;2-T
-
Little MP, de Vathaire F, Shamsaldin A, et al. Risks of brain tumour following treatment for cancer in childhood: modification by genetic factors, radiotherapy and chemotherapy. Int J Cancer. 1998;78:269-275. (Pubitemid 28445359)
-
(1998)
International Journal of Cancer
, vol.78
, Issue.3
, pp. 269-275
-
-
Little, M.P.1
De Vathaire, F.2
Shamsaldin, A.3
Oberlin, O.4
Campbell, S.5
Grimaud, E.6
Chavaudra, J.7
Haylock, R.G.E.8
Muirhead, C.R.9
-
16
-
-
0033756283
-
Second malignant neoplasms after cancer in childhood and adolescence: A population-based case-control study in the 5 nordic countries the nordic society for pediatric hematology and oncology the association of the nordic cancer registries
-
Garwicz S, Anderson H, Olsen JH, et al. Second malignant neoplasms after cancer in childhood and adolescence: a population-based case-control study in the 5 Nordic countries. The Nordic Society for Pediatric Hematology and Oncology. The Association of the Nordic Cancer Registries. Int J Cancer. 2000;88:672-678.
-
(2000)
Int. J. Cancer
, vol.88
, pp. 672-678
-
-
Garwicz, S.1
Anderson, H.2
Olsen, J.H.3
-
17
-
-
34147123158
-
Inherited cancer susceptibility syndromes in paediatric practice
-
DOI 10.1111/j.1440-1754.2007.01027.x
-
Field M, Shanley S, Kirk J. Inherited cancer susceptibility syndromes in paediatric practice. J Paediatr Child Health. 2007;43:219-229. (Pubitemid 46570079)
-
(2007)
Journal of Paediatrics and Child Health
, vol.43
, Issue.4
, pp. 219-229
-
-
Field, M.1
Shanley, S.2
Kirk, J.3
-
18
-
-
0042855876
-
Ethical, legal, and social implications of genomic medicine
-
DOI 10.1056/NEJMra012577
-
Clayton EW. Ethical, legal, and social implications of genomic medicine. N Engl J Med. 2003;349:562-569. (Pubitemid 36951369)
-
(2003)
New England Journal of Medicine
, vol.349
, Issue.6
, pp. 562-569
-
-
Clayton, E.W.1
-
19
-
-
0031572583
-
Prenatal genetic carrier testing using triple disease screening
-
Eng CM, Schechter C, Robinowitz J, et al. Prenatal genetic carrier testing using triple disease screening. JAMA. 1997;278:1268-1272.
-
(1997)
JAMA
, vol.278
, pp. 1268-1272
-
-
Eng, C.M.1
Schechter, C.2
Robinowitz, J.3
-
20
-
-
0025340369
-
The cystic fibrosis gene: Medical and social implications for heterozygote detection
-
DOI 10.1001/jama.263.20.2777
-
WilfondBS, Fost N.The cystic fibrosis gene: medical and social implications for heterozygote detection. JAMA. 1990;263:2777-2783. (Pubitemid 20181572)
-
(1990)
Journal of the American Medical Association
, vol.263
, Issue.20
, pp. 2777-2783
-
-
Wilfond, B.S.1
Fost, N.2
-
21
-
-
0030828891
-
Family history and genetic risk factors: Forward to the future
-
Pyeritz RE. Family history and genetic risk factors: forward to the future. JAMA. 1997;278:1284-1285. (Pubitemid 27435619)
-
(1997)
Journal of the American Medical Association
, vol.278
, Issue.15
, pp. 1284-1285
-
-
Pyeritz, R.E.1
-
22
-
-
0029864134
-
Statement of the american society of clinical oncology: Genetic testing for cancer susceptibility adopted on
-
February 20 1996 1730-1736; discussion
-
Statement of the American Society of Clinical Oncology: genetic testing for cancer susceptibility, Adopted on February 20, 1996. J Clin Oncol. 1996;14:1730-1736; discussion 7-40.
-
(1996)
J. Clin. Oncol.
, Issue.14
, pp. 7-40
-
-
-
23
-
-
0038501057
-
American society of clinical oncology policy statement update: Genetic testing for cancer susceptibility
-
American Society of Clinical Oncology policy statement update: genetic testing for cancer susceptibility. J Clin Oncol. 2003;21:2397-2406.
-
(2003)
J. Clin. Oncol.
, vol.21
, pp. 2397-2406
-
-
-
24
-
-
33847680538
-
Neurofibromatosis 1 and neurofibromatosis 2: A twenty first century perspective
-
DOI 10.1016/S1474-4422(07)70075-3, PII S1474442207700753
-
Ferner RE. Neurofibromatosis 1 and neurofibromatosis 2: a twenty first century perspective. Lancet Neurol. 2007;6:340-351. (Pubitemid 46367948)
-
(2007)
Lancet Neurology
, vol.6
, Issue.4
, pp. 340-351
-
-
Ferner, R.E.1
-
25
-
-
0033674591
-
Malignancy in neurofibromatosis type 1
-
Korf BR. Malignancy in neurofibromatosis type 1. Oncologist. 2000;5:477-485.
-
(2000)
Oncologist
, vol.5
, pp. 477-485
-
-
Korf, B.R.1
-
27
-
-
0023885121
-
Neurofibromatosis conference statement national institutes of health consensus development conference
-
Neurofibromatosis. Conference statement. National Institutes of Health Consensus Development Conference. Arc Neurol. 1988;45:575-578.
-
(1988)
Arc. Neurol.
, vol.45
, pp. 575-578
-
-
-
28
-
-
0028799029
-
Deletion of the entire NF1 gene detected by the FISH: Four deletion patients associated with severe manifestations
-
Wu BL, Austin MA, Schneider GH, et al. Deletion of the entire NF1 gene detected by the FISH: four deletion patients associated with severe manifestations. Am J Med Genet. 1995;59:528-535.
-
(1995)
Am. J. Med. Genet.
, vol.59
, pp. 528-535
-
-
Wu, B.L.1
Austin, M.A.2
Schneider, G.H.3
-
29
-
-
0030783781
-
Familial neurofibromatosis 1 microdeletions: Cosegregation with distinct facial phenotype and early onset of cutaneous neurofibromata
-
DOI 10.1002/(SICI)1096-8628(1997)73:2<197::AID-AJMG17>3.0.CO;2-P
-
Leppig KA, Kaplan P, Viskochil D, et al. Familial neurofibromatosis 1 microdeletions: cosegregation with distinct facial phenotype and early onset of cutaneous neurofibromata. Am J Med Genet. 1997;73:197-204.7 (Pubitemid 27514732)
-
(1997)
American Journal of Medical Genetics
, vol.73
, Issue.2
, pp. 197-204
-
-
Leppig, K.A.1
Kaplan, P.2
Viskochil, D.3
Weaver, M.4
Ortenberg, J.5
Stephens, K.6
-
30
-
-
0018604894
-
Penetrance and variability in neurofibromatosis: A genetic study of 60 families
-
Carey JC, Laub JM, Hall BD. Penetrance and variability in neurofibromatosis: a genetic study of 60 families. Birth Defects Original Article Series. 1979;15:271-281. (Pubitemid 10183921)
-
(1979)
Birth Defects: Original Article Series
, vol.15
, Issue.5 B
, pp. 271-281
-
-
Carey, J.C.1
Laub, J.M.2
Hall, B.D.3
-
31
-
-
0030966414
-
Type 1 neurofibromatosis: A descriptive analysis of the disorder in 1,728 patients
-
DOI 10.1002/(SICI)1096-8628(19970516)70:2<138::AID-AJMG7>3.0.CO;2-U
-
Friedman JM, Birch PH. Type 1 neurofibromatosis: a descriptive analysis of the disorder in 1,728 patients. Am J Med Genet. 1997;70:138-143. (Pubitemid 27184570)
-
(1997)
American Journal of Medical Genetics
, vol.70
, Issue.2
, pp. 138-143
-
-
Friedman, J.M.1
Birch, P.H.2
-
32
-
-
0024154605
-
-
Bethesda, Md., USA, July 13-15, Neurofibromatosis. 1988;
-
National Institutes of Health Consensus Development Conference Statement: neurofibromatosis. Bethesda, Md., USA, July 13-15, 1987. Neurofibromatosis. 1988;1:172-178.
-
(1987)
National Institutes of Health Consensus Development Conference Statement: Neurofibromatosis
, vol.1
, pp. 172-178
-
-
-
33
-
-
33847112447
-
Molecular diagnosis of neurofibromatosis type 1: 2 Years experience
-
DOI 10.1007/s10689-006-9001-3
-
Griffiths S, Thompson P, Frayling I, et al. Molecular diagnosis of neurofibromatosis type 1: 2 years experience. Familial Cancer. 2007;6:21-34. (Pubitemid 46295293)
-
(2007)
Familial Cancer
, vol.6
, Issue.1
, pp. 21-34
-
-
Griffiths, S.1
Thompson, P.2
Frayling, I.3
Upadhyaya, M.4
-
34
-
-
0031060683
-
Mutational and functional analysis of the neurofibromatosis type 1 (NF1) gene
-
DOI 10.1007/s004390050317
-
Upadhyaya M, Osborn MJ, Maynard J, et al. Mutational and functional analysis of the neurofibromatosis type 1 (NF1) gene. Human Genet. 1997;99:88-92. (Pubitemid 26419862)
-
(1997)
Human Genetics
, vol.99
, Issue.1
, pp. 88-92
-
-
Upadhyaya, M.1
Osborn, M.J.2
Maynard, J.3
Kim, M.R.4
Tamanoi, F.5
Cooper, D.N.6
-
35
-
-
0033924917
-
Minor lesion mutational spectrum of the entire NF1 gene does not explain its high mutability but points to a functional domain upstream of the GAP- related domain
-
DOI 10.1086/302809
-
Fahsold R, Hoffmeyer S, Mischung C, et al. Minor lesion mutational spectrum of the entire NF1 gene does not explain its high mutability but points to a functional domain upstream of the GAP-related domain. Am J Human Genet. 2000;66:790-818. (Pubitemid 30470484)
-
(2000)
American Journal of Human Genetics
, vol.66
, Issue.3
, pp. 790-818
-
-
Fahsold, R.1
Hoffmeyer, S.2
Mischung, C.3
Gille, C.4
Ehlers, C.5
Kucukceylan, N.6
Abdel-Nour, M.7
Gewies, A.8
Peters, H.9
Kaufmann, D.10
Buske, A.11
Tinschert, S.12
Nurnberg, P.13
-
36
-
-
0031044804
-
Optic pathway gliomas in children with neurofibromatosis 1: Consensus statement from the NF1 optic pathway glioma task force
-
DOI 10.1002/ana.410410204
-
Listernick R, Louis DN, Packer RJ, et al. Optic pathway gliomas in children with neurofibromatosis 1: consensus statement from the NF1 optic pathway glioma task force. Ann Neurol. 1997;41:143-149. (Pubitemid 27082094)
-
(1997)
Annals of Neurology
, vol.41
, Issue.2
, pp. 143-149
-
-
Listernick, R.1
Louis, D.N.2
Packer, R.J.3
Gutmann, D.H.4
-
37
-
-
0028304193
-
Natural history of optic pathway tumors in children with neurofibromatosis type 1: A longitudinal study
-
DOI 10.1016/S0022-3476(94)70122-9
-
Listernick R, Charrow J, Greenwald M, et al. Natural history of optic pathway tumors in children with neurofibromatosis type 1: a longitudinal study. J Pediatr. 1994;125:63-66. (Pubitemid 24225179)
-
(1994)
Journal of Pediatrics
, vol.125
, Issue.1
, pp. 63-66
-
-
Listernick, R.1
Charrow, J.2
Greenwald, M.3
Mets, M.4
-
38
-
-
0028885150
-
Optic pathway tumors in children: The effect of neurofibromatosis type 1 on clinical manifestations and natural history
-
Listernick R, Darling C, Greenwald M, et al. Optic pathway tumors in children: the effect of neurofibromatosis type 1 on clinical manifestations and natural history. J Pediatr. 1995;127:718-722.
-
(1995)
J. Pediatr.
, vol.127
, pp. 718-722
-
-
Listernick, R.1
Darling, C.2
Greenwald, M.3
-
39
-
-
0030957310
-
The diagnostic evaluation and multidisciplinary management of neurofibromatosis 1 and neurofibromatosis 2
-
Gutmann DH, AylsworthA,Carey JC, et al. The diagnostic evaluation and multidisciplinary management of neurofibromatosis 1 and neurofibromatosis 2. JAMA. 1997;278:51-57. (Pubitemid 27274517)
-
(1997)
Journal of the American Medical Association
, vol.278
, Issue.1
, pp. 51-57
-
-
Gutmann, D.H.1
Aylsworth, A.2
Carey, J.C.3
Korf, B.4
Marks, J.5
Pyeritz, R.E.6
Rubenstein, A.7
Viskochil, D.8
-
40
-
-
0029931315
-
The management of brainstem gliomas in patients with neurofibromatosis 1
-
Pollack IF, Shultz B, Mulvihill JJ. The management of brainstem gliomas in patients with neurofibromatosis 1. Neurology. 1996;46:1652-1660. (Pubitemid 26185788)
-
(1996)
Neurology
, vol.46
, Issue.6
, pp. 1652-1660
-
-
Pollack, I.F.1
Shultz, B.2
Mulvihill, J.J.3
-
42
-
-
0036314750
-
Neurofibromatosis type 1 and sporadic optic gliomas
-
DOI 10.1136/adc.87.1.65
-
Singhal S, Birch JM, Kerr B, et al. Neurofibromatosis type 1 and sporadic optic gliomas. Arch Dis Child. 2002;87:65-70. (Pubitemid 34753778)
-
(2002)
Archives of Disease in Childhood
, vol.87
, Issue.1
, pp. 65-70
-
-
Singhal, S.1
Birch, J.M.2
Kerr, B.3
Lashford, L.4
Evans, D.G.R.5
-
43
-
-
0037226349
-
Prognostic factors of CNS tumours in Neurofibromatosis 1 (NF1): A retrospective study of 104 patients
-
DOI 10.1093/brain/awg016
-
Guillamo JS, Creange A, Kalifa C, et al. Prognostic factors of CNS tumours in Neurofibromatosis 1 (NF1): a retrospective study of 104 patients. Brain. 2003;126:152-160. (Pubitemid 36068565)
-
(2003)
Brain
, vol.126
, Issue.1
, pp. 152-160
-
-
Guillamo, J.-S.1
Creange, A.2
Kalifa, C.3
Grill, J.4
Rodriguez, D.5
Doz, F.6
Barbarot, S.7
Zerah, M.8
Sanson, M.9
Bastuji-Garin, S.10
Wolkenstein, P.11
-
44
-
-
0014649268
-
Optic glioma of childhood natural history and rationale for conservative management
-
Hoyt WF, Baghdassarian SA. Optic glioma of childhood. Natural history and rationale for conservative management. Br J Ophthalmol. 1969;53:793-798.
-
(1969)
Br. J. Ophthalmol.
, vol.53
, pp. 793-798
-
-
Hoyt, W.F.1
Baghdassarian, S.A.2
-
45
-
-
0034084847
-
Initial management of children with hypothalamic and thalamic tumors and the modifying role of neurofibromatosis-1
-
Allen JC. Initial management of children with hypothalamic and thalamic tumors and the modifying role of neurofibromatosis-1. Pediatric Neurosurg. 2000;32:154-162. (Pubitemid 30413204)
-
(2000)
Pediatric Neurosurgery
, vol.32
, Issue.3
, pp. 154-162
-
-
Allen, J.C.1
-
46
-
-
0026690907
-
Spontaneous regression of optic glioma in a patient with neurofibromatosis
-
Brzowski AE, Bazan C, 3rd, Mumma JV, et al. Spontaneous regression of optic glioma in a patient with neurofibromatosis. Neurology. 1992;42:679-681.
-
(1992)
Neurology
, vol.42
, pp. 679-681
-
-
Brzowski, A.E.1
Bazan III, C.2
Mumma, J.V.3
-
47
-
-
0032991588
-
Spontaneous partial regression of low-grade glioma in children with neurofibromatosis-1: A real possibility
-
Perilongo G, Moras P, Carollo C, et al. Spontaneous partial regression of low-grade glioma in children with neurofibromatosis-1: a real possibility. J Child Neurol. 1999;14:352-356. (Pubitemid 29321093)
-
(1999)
Journal of Child Neurology
, vol.14
, Issue.6
, pp. 352-356
-
-
Perilongo, G.1
Moras, P.2
Carollo, C.3
Battistella, A.4
Clementi, M.5
Laverda, A.6
Murgia, A.7
-
48
-
-
0029993431
-
Cerebro-vasculopathy and malignancy: Catastrophic complications of radiotherapy for optic nerve glioma in a von Recklinghausen neurofibromatosis patient
-
DOI 10.1007/BF00346610
-
Jamjoom AB, Malabarey T, Jamjoom ZA, et al. Cerebro-vasculopathy and malignancy: catastrophic complications of radiotherapy for optic nerve glioma in a von Recklinghausen neurofibromatosis patient. Neurosurg Rev. 1996;19:47-51. (Pubitemid 26147133)
-
(1996)
Neurosurgical Review
, vol.19
, Issue.1
, pp. 47-51
-
-
Jamjoom, A.B.1
Malabarey, T.2
Jamjoom, Z.A.B.3
Al-Sohaibani, M.4
Hulailah, A.5
Kolawole, T.6
-
49
-
-
34147172816
-
Optic pathway gliomas in neurofibromatosis-1: Controversies and recommendations
-
DOI 10.1002/ana.21107
-
Listernick R, Ferner RE, Liu GT, et al. Optic pathway gliomas in neurofibromatosis-1: controversies and recommendations. Ann Neurol. 2007;61:189-198. (Pubitemid 46557343)
-
(2007)
Annals of Neurology
, vol.61
, Issue.3
, pp. 189-198
-
-
Listernick, R.1
Ferner, R.E.2
Liu, G.T.3
Gutmann, D.H.4
-
50
-
-
0037389844
-
Do children with optic pathway tumors have an increased frequency of other central nervous system tumors?
-
DOI 10.1215/S1522851702000303
-
Korones DN, Padowski J, Factor BA, et al. Do children with optic pathway tumors have an increased frequency of other central nervous system tumors? Neuro-oncology. 2003;5:116-120. (Pubitemid 36416840)
-
(2003)
Neuro-Oncology
, vol.5
, Issue.2
, pp. 116-120
-
-
Korones, D.N.1
Padowski, J.2
Factor, B.A.3
Constine, L.S.4
-
51
-
-
33745001462
-
Second primary tumors in neurofibromatosis 1 patients treated for optic glioma: Substantial risks after radiotherapy
-
DOI 10.1200/JCO.2005.03.8349
-
Sharif S, Ferner R, Birch JM, et al. Second primary tumors in neurofibromatosis 1 patients treated for optic glioma: substantial risks after radiotherapy. J Clin Oncol. 2006;24:2570-2575. (Pubitemid 46630636)
-
(2006)
Journal of Clinical Oncology
, vol.24
, Issue.16
, pp. 2570-2575
-
-
Sharif, S.1
Ferner, R.2
Birch, J.M.3
Gillespie, J.E.4
Gattamaneni, H.R.5
Baser, M.E.6
Evans, D.G.R.7
-
52
-
-
0028176825
-
Neurofibromatosis type I andmalignancy: Review of 32 pediatric cases treated at a single institution
-
Shearer P, ParhamD,Kovnar E, et al. Neurofibromatosis type I andmalignancy: review of 32 pediatric cases treated at a single institution. Medical Pediatric Oncol. 1994;22:78-83.
-
(1994)
Medical Pediatric Oncol.
, vol.22
, pp. 78-83
-
-
Shearer, P.1
Parham, D.2
Kovnar, E.3
-
53
-
-
0028560007
-
Follow-up of optic pathway gliomas in children with neurofibromatosis type 1
-
Kuenzle C, Weissert M, Roulet E, et al. Follow-up of optic pathway gliomas in children with neurofibromatosis type 1. Neuropediatrics. 1994;25:295-300.
-
(1994)
Neuropediatrics
, vol.25
, pp. 295-300
-
-
Kuenzle, C.1
Weissert, M.2
Roulet, E.3
-
54
-
-
0032982865
-
A clinical study of type 1 neurofibromatosis in north west England
-
McGaughran JM, Harris DI, Donnai D, et al. A clinical study of type 1 neurofibromatosis in northwest England. J Med Genet. 1999;36:197-203. (Pubitemid 29110448)
-
(1999)
Journal of Medical Genetics
, vol.36
, Issue.3
, pp. 197-203
-
-
McGaughran, J.M.1
Harris, D.I.2
Donnai, D.3
Teare, D.4
MacLeod, R.5
Westerbeek, R.6
Kingston, H.7
Super, M.8
Harris, R.9
Evans, D.G.R.10
-
55
-
-
0028069689
-
The NF1 gene in myelopoiesis and childhood myelodysplastic syndromes
-
DOI 10.1056/NEJM199403033300912
-
Brodeur GM. The NF1 gene in myelopoiesis and childhood myelodysplastic syndromes. N Engl J Med. 1994;330:637-639. (Pubitemid 24065802)
-
(1994)
New England Journal of Medicine
, vol.330
, Issue.9
, pp. 637-639
-
-
Brodeur, G.M.1
-
56
-
-
0032825694
-
Von recklinghausens disease and pheochromocytomas
-
Walther MM, Herring J, Enquist E, et al. von Recklinghausen's disease and pheochromocytomas. J Urol. 1999;162:1582-1586.
-
(1999)
J. Urol.
, vol.162
, pp. 1582-1586
-
-
Walther, M.M.1
Herring, J.2
Enquist, E.3
-
57
-
-
0036096489
-
Malignant peripheral nerve sheath tumours in neurofibromatosis
-
Evans DG, Baser ME, McGaughran J, et al. Malignant peripheral nerve sheath tumours in neurofibromatosis 1. J Med Genet. 2002;39:311-314. (Pubitemid 34526349)
-
(2002)
Journal of Medical Genetics
, vol.39
, Issue.5
, pp. 311-314
-
-
Evans, D.G.R.1
Baser, M.E.2
McGaughran, J.3
Sharif, S.4
Howard, E.5
Moran, A.6
-
58
-
-
33745768214
-
Role of the neurofibromatosis type 2 gene in the development of tumors of the nervous system
-
RuttledgeMH, RouleauGA. Role of the neurofibromatosis type 2 gene in the development of tumors of the nervous system. Neurosurg Focus. 2005;19:E6.
-
(2005)
Neurosurg. Focus.
, vol.19
-
-
Ruttledge, M.H.1
Rouleau, G.A.2
-
59
-
-
0027405720
-
A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor
-
DOI 10.1016/0092-8674(93)90406-G
-
Trofatter JA, MacCollin MM, Rutter JL, et al. A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor. Cell. 1993;72:791-800. (Pubitemid 23093886)
-
(1993)
Cell
, vol.72
, Issue.5
, pp. 791-800
-
-
Trofatter, J.A.1
MacCollin, M.M.2
Rutter, J.L.3
Murrell, J.R.4
Duyao, M.P.5
Parry, D.M.6
Eldridge, R.7
Kley, N.8
Menon, A.G.9
Pulaski, K.10
Haase, V.H.11
Ambrose, C.M.12
Munroe, D.13
Bove, C.14
Haines, J.L.15
Martuza, R.L.16
MacDonald, M.E.17
Seizinger, B.R.18
Short, M.P.19
-
60
-
-
2942689618
-
The role of von Hippel-Lindau tumor suppressor protein and hypoxia in renal clear cell carcinoma
-
DOI 10.1152/ajprenal.00424.2003
-
Sufan RI, Jewett MA, Ohh M. The role of von Hippel-Lindau tumor suppressor protein and hypoxia in renal clear cell carcinoma. Am J Physiol. 2004;287:F1-F6. (Pubitemid 38780576)
-
(2004)
American Journal of Physiology - Renal Physiology
, vol.287
, Issue.1
-
-
Sufan, R.I.1
Jewett, M.A.S.2
Ohh, M.3
-
61
-
-
7844234770
-
Improved detection of germline mutations in the von Hippel-Lindau disease tumor suppressor gene
-
DOI 10.1002/(SICI)1098-1004(1998)12:6<417::AID-HUMU8>3.0.CO;2-K
-
Stolle C, Glenn G, Zbar B, et al. Improved detection of germline mutations in the von Hippel-Lindau disease tumor suppressor gene. Human Mutation. 1998;12:417-423. (Pubitemid 28512618)
-
(1998)
Human Mutation
, vol.12
, Issue.6
, pp. 417-423
-
-
Stolle, C.1
Glenn, G.2
Zbar, B.3
Humphrey, J.S.4
Choyke, P.5
Walther, M.6
Pack, S.7
Hurley, K.8
Andrey, C.9
Klausner, R.10
Marston Linehan, W.11
-
62
-
-
0028938702
-
Von hippel-lindau disease: genetic clinical and imaging features
-
Choyke PL, Glenn GM, Walther MM, et al. von Hippel-Lindau disease: genetic, clinical, and imaging features. Radiology. 1995;194:629-642.
-
(1995)
Radiology
, vol.194
, pp. 629-642
-
-
Choyke, P.L.1
Glenn, G.M.2
Walther, M.M.3
-
63
-
-
0033577985
-
Plasma normetanephrine and metanephrine for detecting pheochromocytoma in von Hippel-Lindau disease and multiple endocrine neoplasia type 2
-
DOI 10.1056/NEJM199906173402404
-
Eisenhofer G, Lenders JW, Linehan WM, et al. Plasma normetanephrine and metanephrine for detecting pheochromocytoma in von Hippel-Lindau disease and multiple endocrine neoplasia type 2. N Engl J Med. 1999;340:1872-1879. (Pubitemid 29272667)
-
(1999)
New England Journal of Medicine
, vol.340
, Issue.24
, pp. 1872-1879
-
-
Eisenhofer, G.1
Lenders, J.W.M.2
Linehan, W.M.3
Walther, M.M.4
Goldstein, D.S.5
Keiser, H.R.6
-
64
-
-
72849181879
-
Multiple nevoid basal-cell epithelioma jaw cysts and bifid rib a syndrome
-
Gorlin RJ, Goltz RW. Multiple nevoid basal-cell epithelioma, jaw cysts and bifid rib. A syndrome. N Engl J Med. 1960;262:908-912.
-
(1960)
N. Engl. J. Med.
, vol.262
, pp. 908-912
-
-
Gorlin, R.J.1
Goltz, R.W.2
-
65
-
-
28244499878
-
The syndrome of jaw cysts basal cell tumours and skeletal abnormalities
-
Cawson RA, Kerr GA. The Syndrome of Jaw Cysts, Basal Cell Tumours and Skeletal Abnormalities. Proc Roy Soc Med. 1964;57:799-801.
-
(1964)
Proc. Roy. Soc. Med.
, vol.57
, pp. 799-801
-
-
Cawson, R.A.1
Kerr, G.A.2
-
66
-
-
0013879215
-
Basal cell nevus syndrome combined clinical staff conference at the national institutes of health
-
Berlin NI, Van Scott EJ, Clendenning WE, et al. Basal cell nevus syndrome. Combined clinical staff conference at the National Institutes of Health. Ann Int Med. 1966;64:403-421.
-
(1966)
Ann. Int. Med.
, vol.64
, pp. 403-421
-
-
Berlin, N.I.1
Van Scott, E.J.2
Clendenning, W.E.3
-
67
-
-
9644264182
-
Nevoid basal cell carcinoma (Gorlin) syndrome
-
DOI 10.1097/01.GIM.0000144188.15902.C4
-
Gorlin RJ. Nevoid basal cell carcinoma (Gorlin) syndrome. Genet Med. 2004;6:530-539. (Pubitemid 39576548)
-
(2004)
Genetics in Medicine
, vol.6
, Issue.6
, pp. 530-539
-
-
Gorlin, R.J.1
-
68
-
-
0027231001
-
Complications of the naevoid basal cell carcinoma syndrome: Results of a population based study
-
Evans DG, Ladusans EJ, Rimmer S, et al. Complications of the naevoid basal cell carcinoma syndrome: results of a population based study. JMed Genet. 1993;30:460-464. (Pubitemid 23197262)
-
(1993)
Journal of Medical Genetics
, vol.30
, Issue.6
, pp. 460-464
-
-
Evans, D.G.R.1
Ladusans, E.J.2
Rimmer, S.3
Burnell, L.D.4
Thakker, N.5
Farndon, P.A.6
-
69
-
-
0033486354
-
Nevoid basal cell carcinoma gorlin syndrome: Unanswered issues
-
Gorlin RJ. Nevoid basal cell carcinoma (Gorlin) syndrome: unanswered issues. J Lab Clin Med. 1999;134:551-552.
-
(1999)
J. Lab. Clin. Med.
, vol.134
, pp. 551-552
-
-
Gorlin, R.J.1
-
70
-
-
0031002840
-
Clinical manifestations in 105 persons with nevoid basal cell carcinoma syndrome
-
DOI 10.1002/(SICI)1096-8628(19970331)69:3<299::AID-AJMG16>3.0.CO;2- M
-
Kimonis VE, Goldstein AM, Pastakia B, et al. Clinical manifestations in 105 persons with nevoid basal cell carcinoma syndrome. Am J Med Genet. 1997;69:299-308. (Pubitemid 27154674)
-
(1997)
American Journal of Medical Genetics
, vol.69
, Issue.3
, pp. 299-308
-
-
Kimonis, V.E.1
Goldstein, A.M.2
Pastakia, B.3
Yang, M.L.4
Kase, R.5
Digiovanna, J.J.6
Bale, A.E.7
Bale, S.J.8
-
71
-
-
15844381336
-
Human homolog of patched, a candidate gene for the basal cell nevus syndrome
-
Johnson RL, Rothman AL, Xie J, et al. Human homolog of patched, a candidate gene for the basal cell nevus syndrome. Scienc (New York, NY). 1996;272:1668-1671. (Pubitemid 26200029)
-
(1996)
Science
, vol.272
, Issue.5268
, pp. 1668-1671
-
-
Johnson, R.L.1
Rothman, A.L.2
Xie, J.3
Goodrich, L.V.4
Bare, J.W.5
Bonifas, J.M.6
Quinn, A.G.7
Myers, R.M.8
Cox, D.R.9
Epstein Jr., E.H.10
Scott, M.P.11
-
72
-
-
16044363842
-
The role of the human homologue of Drosophila patched in sporadic basal cell carcinomas
-
DOI 10.1038/ng0996-78
-
Gailani MR, Stahle-Backdahl M, Leffell DJ, et al. The role of the human homologue of Drosophila patched in sporadic basal cell carcinomas. Nature Genet. 1996;14:78-81. (Pubitemid 26301550)
-
(1996)
Nature Genetics
, vol.14
, Issue.1
, pp. 78-81
-
-
Gailani, M.R.1
Stahle-Backdahl, M.2
Leffell, D.J.3
Glynn, M.4
Zaphiropoulos, P.G.5
Pressman, C.6
Unden, A.B.7
Dean, M.8
Brash, D.E.9
Bale, A.E.10
Toftgard, R.11
-
73
-
-
0033252592
-
Acquired and inherited basal cell carcinomas and the patched gene
-
discussion 84.
-
Gailani MR, Bale AE. Acquired and inherited basal cell carcinomas and the patched gene. Adv Dermatol. 1999;14:261-283; discussion 84.
-
(1999)
Adv. Dermatol.
, vol.14
, pp. 261-283
-
-
Gailani, M.R.1
Bale, A.E.2
-
75
-
-
15844386165
-
Mutations of the human homolog of drosophila patched in the nevoid basal cell carcinoma syndrome
-
DOI 10.1016/S0092-8674(00)81268-4
-
Hahn H, Wicking C, Zaphiropoulous PG, et al. Mutations of the human homolog of Drosophila patched in the nevoid basal cell carcinoma syndrome. Cell. 1996;85:841-851. (Pubitemid 26192135)
-
(1996)
Cell
, vol.85
, Issue.6
, pp. 841-851
-
-
Hahn, H.1
Wicking, C.2
Zaphiropoulos, P.G.3
Gailani, M.R.4
Shanley, S.5
Chidambaram, A.6
Vorechovsky, I.7
Holmberg, E.8
Unden, A.B.9
Gillies, S.10
Negus, K.11
Smyth, I.12
Pressman, C.13
Leffell, D.J.14
Gerrard, B.15
Goldstein, A.M.16
Dean, M.17
Toftgard, R.18
Chenevix-Trench, G.19
Wainwright, B.20
Bale, A.E.21
more..
-
76
-
-
0030866154
-
Altered neural cell fates and medulloblastoma in mouse patched mutants
-
DOI 10.1126/science.277.5329.1109
-
Goodrich LV, Milenkovic L, Higgins KM, et al. Altered neural cell fates and medulloblastoma in mouse patched mutants. Scienc (New York, NY). 1997;277:1109-1113. (Pubitemid 27371635)
-
(1997)
Science
, vol.277
, Issue.5329
, pp. 1109-1113
-
-
Goodrich, L.V.1
Milenkovic, L.2
Higgins, K.M.3
Scott, M.P.4
-
77
-
-
0031036694
-
Sporadic medulloblastomas contain PTCH mutations
-
Raffel C, Jenkins RB, Frederick L, et al. Sporadic medulloblastomas contain PTCH mutations. Cancer Res. 1997;57:842-845. (Pubitemid 27098006)
-
(1997)
Cancer Research
, vol.57
, Issue.5
, pp. 842-845
-
-
Raffel, C.1
Jenkins, R.B.2
Frederick, L.3
Hebrink, D.4
Alderete, B.5
Fults, D.W.6
David James, C.7
-
78
-
-
0033990220
-
Analysis of PTCH/SMO/SHH pathway genes in medulloblastoma
-
Zurawel RH, Allen C, Chiappa S, et al. Analysis of PTCH/SMO/SHH pathway genes in medulloblastoma. Genes, Chromosomes Cancer. 2000;27:44-51.
-
(2000)
Genes Chromosomes Cancer
, vol.27
, pp. 44-51
-
-
Zurawel, R.H.1
Allen, C.2
Chiappa, S.3
-
79
-
-
0033389196
-
The hedgehog signalling pathway and its role in basal cell carcinoma
-
DOI 10.1023/A:1006377425099
-
Booth DR. The hedgehog signaling pathway and its role in basal cell carcinoma. Cancer Metastasis Rev. 1999;18:261-284. (Pubitemid 30043862)
-
(1999)
Cancer and Metastasis Reviews
, vol.18
, Issue.2
, pp. 261-284
-
-
Booth, D.R.1
-
80
-
-
0030913738
-
The gene for the naevoid basal cell carcinoma syndrome acts as a tumour-suppressor gene in medulloblastoma
-
Cowan R, Hoban P, Kelsey A, et al. The gene for the naevoid basal cell carcinoma syndrome acts as a tumour-suppressor gene in medulloblastoma. Br J Cancer. 1997;76:141-145. (Pubitemid 27279651)
-
(1997)
British Journal of Cancer
, vol.76
, Issue.2
, pp. 141-145
-
-
Cowan, R.1
Hoban, P.2
Kelsey, A.3
Birch, J.M.4
Gattamaneni, R.5
Evans, D.G.R.6
-
81
-
-
0030960708
-
Nevoid basal cell carcinoma syndromewith medulloblastoma in an african-american boy: A rare case illustrating gene-environment interaction
-
Korczak JF, Brahim JS,DiGiovanna JJ, et al.Nevoid basal cell carcinoma syndromewith medulloblastoma in an African-American boy: a rare case illustrating gene-environment interaction. Am J Med Genet. 1997;69:309-314.
-
(1997)
Am. J. Med. Genet.
, vol.69
, pp. 309-314
-
-
Korczak, J.F.1
Brahim, J.S.2
DiGiovanna, J.J.3
-
82
-
-
0031007587
-
Complications of the nevoid basal cell carcinoma syndrome: A case report
-
DOI 10.1097/00043426-199705000-00016
-
Walter AW, Pivnick EK, Bale AE, et al. Complications of the nevoid basal cell carcinoma syndrome: a case report. J Pediatr Hematol Oncol. 1997;19:258-262. (Pubitemid 27276296)
-
(1997)
Journal of Pediatric Hematology/Oncology
, vol.19
, Issue.3
, pp. 258-262
-
-
Walter, A.W.1
Pivnick, E.K.2
Bale, A.E.3
Kun, L.E.4
-
83
-
-
0035117108
-
Germ-line p53 mutations predispose to a wide spectrum of early-onset cancers
-
Nichols KE, Malkin D, Garber JE, et al. Germ-line p53 mutations predispose to a wide spectrum of early-onset cancers. Cancer Epidemiol Biomarkers Prev. 2001;10:83-87. (Pubitemid 32172424)
-
(2001)
Cancer Epidemiology Biomarkers and Prevention
, vol.10
, Issue.2
, pp. 83-87
-
-
Nichols, K.E.1
Malkin, D.2
Garber, J.E.3
Fraumeni Jr., J.F.4
Li, F.P.5
-
85
-
-
0034650718
-
Predominance of brain tumors in an extended Li-Fraumeni (SBLA) kindred, including a case of Sturge-Weber syndrome
-
DOI 10.1002/(SICI)1097-0142(20000115)88:2<433::AID-CNCR26>3.0.CO;2- 0
-
Lynch HT, McComb RD, Osborn NK, et al. Predominance of brain tumors in an extended Li-Fraumeni (SBLA) kindred, including a case of Sturge-Weber syndrome. Cancer. 2000;88:433-439. (Pubitemid 30051830)
-
(2000)
Cancer
, vol.88
, Issue.2
, pp. 433-439
-
-
Lynch, H.T.1
McComb, R.D.2
Osborn, N.K.3
Wolpert, P.A.4
Lynch, J.F.5
Wszolek, Z.K.6
Sidransky, D.7
Steg, R.E.8
-
86
-
-
0031031049
-
Tumors associated with p53 germline mutations: A synopsis of 91 families
-
Kleihues P, Schauble B, zur Hausen A, et al. Tumors associated with p53 germline mutations: a synopsis of 91 families. Am J Pathol. 1997;150:1-13. (Pubitemid 27027090)
-
(1997)
American Journal of Pathology
, vol.150
, Issue.1
, pp. 1-13
-
-
Kleihues, P.1
Schauble, B.2
Zur Hausen, A.3
Esteve, J.4
Ohgaki, H.5
-
87
-
-
0036255776
-
The Li-Fraumeni syndrome
-
DOI 10.1016/S0300-9084(01)01361-X, PII S030090840101361X
-
Chompret A. The Li-Fraumeni syndrome. Biochimie. 2002;84:75-82. (Pubitemid 34477095)
-
(2002)
Biochimie
, vol.84
, Issue.1
, pp. 75-82
-
-
Chompret, A.1
-
88
-
-
0027315653
-
P53 and the Li-Fraumeni syndrome
-
DOI 10.1016/0165-4608(93)90233-C
-
Malkin D. p53 and the Li-Fraumeni syndrome. Cancer Genet Cytogenet. 1993;66:83-92. (Pubitemid 23155343)
-
(1993)
Cancer Genetics and Cytogenetics
, vol.66
, Issue.2
, pp. 83-92
-
-
Malkin, D.1
-
89
-
-
0025633582
-
Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms
-
Malkin D, Li FP, Strong LC, et al. Germ line p53 mutations in a familial syndrome of breast cancer, sarcomas, and other neoplasms. Scienc (New York, NY). 1990;250:1233-1238. (Pubitemid 120031831)
-
(1990)
Science
, vol.250
, Issue.4985
, pp. 1233-1238
-
-
Malkin, D.1
Li, F.P.2
Strong, L.C.3
Fraumeni Jr., J.F.4
Nelson, C.E.5
Kim, D.H.6
Kassel, J.7
Gryka, M.A.8
Bischoff, F.Z.9
Tainsky, M.A.10
Friend, S.H.11
-
90
-
-
0032522623
-
Multiple primary cancers in families with Li-Fraumeni syndrome
-
Hisada M, Garber JE, Fung CY, et al. Multiple primary cancers in families with Li-Fraumeni syndrome. J Natl Cancer Inst. 1998;90:606-611. (Pubitemid 28204804)
-
(1998)
Journal of the National Cancer Institute
, vol.90
, Issue.8
, pp. 606-611
-
-
Hisada, M.1
Garber, J.E.2
Fung, C.Y.3
Fraumeni Jr., J.F.4
Li, F.P.5
-
91
-
-
0025648762
-
Germ-line transmission of a mutated p53 gene in a cancer-prone family with Li-Fraumeni syndrome
-
Srivastava S, Zou ZQ, Pirollo K, et al. Germ-line transmission of a mutated p53 gene in a cancer-prone family with Li-Fraumeni syndrome. Nature. 1990;348:747-749. (Pubitemid 120015153)
-
(1990)
Nature
, vol.348
, Issue.6303
, pp. 747-749
-
-
Srivastava, S.1
Zou, Z.2
Pirollo, K.3
Blattner, W.4
Chang, E.H.5
-
92
-
-
0028953433
-
Germ-line p53 mutations in 15 families with li-fraumeni syndrome
-
Frebourg T, Barbier N, Yan YX, et al. Germ-line p53 mutations in 15 families with Li-Fraumeni syndrome. Am J Human Genet. 1995;56:608-615.
-
(1995)
Am. J. Human. Genet.
, vol.56
, pp. 608-615
-
-
Frebourg, T.1
Barbier, N.2
Yan, Y.X.3
-
93
-
-
0028220688
-
Prevalence and diversity of constitutional mutations in the p53 gene among 21 Li-Fraumeni families
-
Birch JM, Hartley AL, Tricker KJ, et al. Prevalence and diversity of constitutional mutations in the p53 gene among 21 Li-Fraumeni families. Cancer Res. 1994;54:1298-1304. (Pubitemid 24108072)
-
(1994)
Cancer Research
, vol.54
, Issue.5
, pp. 1298-1304
-
-
Birch, J.M.1
Hartley, A.L.2
Tricker, K.J.3
Prosser, J.4
Condie, A.5
Kelsey, A.M.6
Harris, M.7
Morris Jones, P.H.8
Binchy, A.9
Crowther, D.10
Craft, A.W.11
Eden, O.B.12
Evans, D.G.R.13
Thompson, E.14
Mann, J.R.15
Martin, J.16
Mitchell, E.L.D.17
Santibanez-Koref, M.F.18
-
94
-
-
0028198314
-
Alterations of the TP53 gene in human gliomas
-
Rasheed BK, McLendon RE, Herndon JE, et al. Alterations of the TP53 gene in human gliomas. Cancer Res. 1994;54:1324-1330. (Pubitemid 24108076)
-
(1994)
Cancer Research
, vol.54
, Issue.5
, pp. 1324-1330
-
-
Rasheed, B.K.A.1
McLendon, R.E.2
Herndon, J.E.3
Friedman, H.S.4
Friedman, A.H.5
Bigner, D.D.6
Bigner, S.H.7
-
95
-
-
37349055876
-
TP53 mutations and survival in squamous-cell carcinoma of the head and neck
-
DOI 10.1056/NEJMoa073770
-
PoetaML,Manola J,GoldwasserMA, et al. TP53mutations and survival in squamous-cell carcinoma of the head and neck. N Engl J Med. 2007;357:2552-2561. (Pubitemid 350294222)
-
(2007)
New England Journal of Medicine
, vol.357
, Issue.25
, pp. 2552-2561
-
-
Poeta, M.L.1
Manola, J.2
Goldwasser, M.A.3
Forastiere, A.4
Benoit, N.5
Califano, J.A.6
Ridge, J.A.7
Goodwin, J.8
Kenady, D.9
Saunders, J.10
Westra, W.11
Sidransky, D.12
Koch, W.M.13
-
96
-
-
0033709501
-
A patient with 17 primary tumours and a germ line mutation in TP53: Tumour induction by adjuvant therapy
-
Royal College of Radiologists (Great Britain)).
-
Nutting C, Camplejohn RS, Gilchrist R, et al. A patient with 17 primary tumours and a germ line mutation in TP53: tumour induction by adjuvant therapy? Clin Onco (Royal College of Radiologists (Great Britain)). 2000;12:300-304.
-
(2000)
Clin. Onco.
, vol.12
, pp. 300-304
-
-
Nutting, C.1
Camplejohn, R.S.2
Gilchrist, R.3
-
97
-
-
0035921190
-
Two metachronous tumors in the radiotherapy fields of a patient with Li-Fraumeni syndrome
-
DOI 10.1002/ijc.1021
-
Limacher JM, Frebourg T, Natarajan-Ame S, et al. Two metachronous tumors in the radiotherapy fields of a patient with Li-Fraumeni syndrome. Int J Cancer. 2001;96:238-242. (Pubitemid 33081228)
-
(2001)
International Journal of Cancer
, vol.96
, Issue.4
, pp. 238-242
-
-
Limacher, J.-M.1
Frebourg, T.2
Natarajan-Ame, S.3
Jean-Pierre, B.M.D.4
-
98
-
-
0032032865
-
Malignant ependymomas in a patient with Turcot's Syndrome: Case report and management guidelines
-
DOI 10.1016/S0090-3019(97)00299-1, PII S0090301997002991
-
MullinsKJ,RubioA,Myers SP, et al. Malignant ependymomas in a patient with Turcot's syndrome: case report and management guidelines. Surg Neurol. 1998;49:290-294. (Pubitemid 28106874)
-
(1998)
Surgical Neurology
, vol.49
, Issue.3
, pp. 290-294
-
-
Mullins, K.J.1
Rubio, A.2
Myers, S.P.3
Korones, D.N.4
Pilcher, W.H.5
-
99
-
-
0023197201
-
Turcot syndrome: Autosomal dominant or recessive transmission?
-
DOI 10.1007/BF02555461
-
Costa OL, Silva DM, Colnago FA, et al. Turcot syndrome. Autosomal dominant or recessive transmission? Dis Colon Rectum. 1987;30:391-394. (Pubitemid 17078526)
-
(1987)
Diseases of the Colon and Rectum
, vol.30
, Issue.5
, pp. 391-394
-
-
Costa, O.L.1
Silva, D.M.2
Colnago, F.A.3
-
100
-
-
0029587042
-
A tale of four syndromes: Familial adenomatous polyposis, Gardner syndrome, attenuated APC and Turcot syndrome
-
Foulkes WD. A tale of four syndromes: familial adenomatous polyposis, Gardner syndrome, attenuated APC and Turcot syndrome. Qjm. 1995;88:853-863. (Pubitemid 26009653)
-
(1995)
QJM - Monthly Journal of the Association of Physicians
, vol.88
, Issue.12
, pp. 853-863
-
-
Foulkes, W.D.1
-
101
-
-
0028350888
-
Germ-line and somatic mutations of the APC gene in patients with Turcot syndrome and analysis of APC mutations in brain tumors
-
Mori T, Nagase H, Horii A, et al. Germ-line and somatic mutations of the APC gene in patients with Turcot syndrome and analysis of APC mutations in brain tumors. Genes Chromosomes Cancer. 1994;9:168-172. (Pubitemid 24074733)
-
(1994)
Genes Chromosomes and Cancer
, vol.9
, Issue.3
, pp. 168-172
-
-
Mori, T.1
Nagase, H.2
Horii, A.3
Miyoshi, Y.4
Shimano, T.5
Nakatsuru, S.6
Aoki, T.7
Arakawa, H.8
Yanagisawa, A.9
Ushio, Y.10
Takano, S.11
Ogawa, M.12
Nakamura, M.13
Shibuya, M.14
Nishikawa, R.15
Matsutani, M.16
Hayashi, Y.17
Takahashi, H.18
Ikuta, F.19
-
103
-
-
0001510499
-
Evidence for a recessive inheritance of Turcot's syndrome caused by compound heterozygous mutations within the PMS2 gene
-
De Rosa M, Fasano C, Panariello L, et al. Evidence for a recessive inheritance of Turcot's syndrome caused by compound heterozygous mutations within the PMS2 gene. Oncogene. 2000;19:1719-1723. (Pubitemid 30200974)
-
(2000)
Oncogene
, vol.19
, Issue.13
, pp. 1719-1723
-
-
De Rosa, M.1
Fasano, C.2
Panariello, L.3
Scarano, M.I.4
Belli, G.5
Iannelli, A.6
Ciciliano, F.7
Izzo, P.8
-
104
-
-
0032138226
-
Editorial: Multiple endocrine neoplasia - Syndromes of the twentieth century
-
DOI 10.1210/jc.83.8.2617
-
Thakker RV. Multiple endocrine neoplasia - syndromes of the twentieth century. J Clin Endocrinol Metabolism. 1998;83:2617-2620. (Pubitemid 28493749)
-
(1998)
Journal of Clinical Endocrinology and Metabolism
, vol.83
, Issue.8
, pp. 2617-2620
-
-
Thakker, R.V.1
-
105
-
-
0029928102
-
The spectrum of RB1 germ-line mutations in hereditary retinoblastoma
-
Lohmann DR, Brandt B, Hopping W, et al. The spectrum of RB1 germ-line mutations in hereditary retinoblastoma. Am J Human Genet. 1996;58:940-949. (Pubitemid 26115165)
-
(1996)
American Journal of Human Genetics
, vol.58
, Issue.5
, pp. 940-949
-
-
Lohmann, D.R.1
Brandt, B.2
Hopping, W.3
Passarge, E.4
Horsthemke, B.5
-
106
-
-
0037322272
-
Sensitive and efficient detection of RB1 gene mutations enhances care for families with retinoblastoma
-
DOI 10.1086/345651
-
Richter S, Vandezande K, Chen N, et al. Sensitive and efficient detection of RB1 gene mutations enhances care for families with retinoblastoma. Am J Human Genet. 2003;72:253-269. (Pubitemid 36194237)
-
(2003)
American Journal of Human Genetics
, vol.72
, Issue.2
, pp. 253-269
-
-
Richter, S.1
Vandezande, K.2
Chen, N.3
Zhang, K.4
Sutherland, J.5
Anderson, J.6
Han, L.7
Panton, R.8
Branco, P.9
Gallie, B.10
-
107
-
-
34548684366
-
Expansion of the deletion 13q syndrome phenotype: A case report
-
DOI 10.1177/0883073807306257
-
Lance EI, DuPont BR, Holden KR. Expansion of the deletion 13q syndrome phenotype: a case report. J Child Neurol. 2007;22:1124-1127. (Pubitemid 47412688)
-
(2007)
Journal of Child Neurology
, vol.22
, Issue.9
, pp. 1124-1127
-
-
Lance, E.I.1
DuPont, B.R.2
Holden, K.R.3
-
108
-
-
0022977663
-
Trilateral retinoblastoma
-
DOI 10.1002/mpo.2950140609
-
Meadows A. Trilateral retinoblastoma. Med Pediatric Oncol. 1986;14:323-326. (Pubitemid 17217050)
-
(1986)
Medical and Pediatric Oncology
, vol.14
, Issue.6
, pp. 323-326
-
-
Meadows, A.1
-
109
-
-
0033064337
-
Trilateral retinoblastoma: A meta-analysis of hereditary retinoblastoma associated with primary ectopic intracranial retinoblastoma
-
Kivela T. Trilateral retinoblastoma: ameta-analysis of hereditary retinoblastoma associated with primary ectopic intracranial retinoblastoma. J Clin Oncol. 1999;17:1829-1837. (Pubitemid 29269254)
-
(1999)
Journal of Clinical Oncology
, vol.17
, Issue.6
, pp. 1829-1837
-
-
Kivela, T.1
-
110
-
-
0034803968
-
Third (fourth and fifth) nonocular tumors in survivors of retinoblastoma
-
DOI 10.1016/S0161-6420(01)00713-8, PII S0161642001007138
-
Abramson DH, Melson MR, Dunkel IJ, et al. Third (fourth and fifth) nonocular tumors in survivors of retinoblastoma. Ophthalmology. 2001;108:1868-1876. (Pubitemid 32905948)
-
(2001)
Ophthalmology
, vol.108
, Issue.10
, pp. 1868-1876
-
-
Abramson, D.H.1
Melson, M.R.2
Dunkel, I.J.3
Frank, C.M.4
-
112
-
-
0031917294
-
Second nonocular tumors in survivors of bilateral retinoblastoma: A possible age effect on radiation-related risk
-
573-579; discussion
-
Abramson DH, Frank CM. Second nonocular tumors in survivors of bilateral retinoblastoma: a possible age effect on radiation-related risk. Ophthalmology. 1998;105:573-579; discussion 9-80.
-
(1998)
Ophthalmology
, vol.105
, pp. 9-80
-
-
Abramson, D.H.1
Frank, C.M.2
-
113
-
-
0030808308
-
Cerebral primitive neuro-ectodermal tumour following treatment of a unilateral retinoblastoma
-
DOI 10.1007/BF01420048
-
Dorfmuller G, Wurtz FG, Kleinert R, et al. Cerebral primitive neuro-ectodermal tumour following treatment of a unilateral retinoblastoma. Acta Neurochirurgica. 1997;139:749-755. (Pubitemid 27354722)
-
(1997)
Acta Neurochirurgica
, vol.139
, Issue.8
, pp. 749-755
-
-
Dorfmuller, G.1
Wurtz, F.G.2
Kleinert, R.3
Lanner, G.4
-
114
-
-
0023714356
-
Cutaneous malignant melanoma in survivors of heritable retinoblastoma
-
Traboulsi EI, Zimmerman LE, Manz HJ. Cutaneous malignant melanoma in survivors of heritable retinoblastoma. Arc Ophthalmol. 1988;106:1059-1061.
-
(1988)
Arc. Ophthalmol.
, vol.106
, pp. 1059-1061
-
-
Traboulsi, E.I.1
Zimmerman, L.E.2
Manz, H.J.3
-
115
-
-
0036256293
-
The triad of bilateral retinoblastoma, dysplastic naevus syndrome and multiple cutaneous malignant melanomas: A case report and review of the literature
-
DOI 10.1097/00008390-200204000-00012
-
Belt PJ, Smithers M, Elston T. The triad of bilateral retinoblastoma, dysplastic naevus syndrome and multiple cutaneous malignant melanomas: a case report and review of the literature. Melanoma Res. 2002;12:179-182. (Pubitemid 34478460)
-
(2002)
Melanoma Research
, vol.12
, Issue.2
, pp. 179-182
-
-
Belt, P.J.1
Smithers, M.2
Elston, T.3
-
116
-
-
33846942292
-
Risk of soft tissue sarcomas by individual subtype in survivors of hereditary retinoblastoma
-
Kleinerman RA, Tucker MA, Abramson DH, et al. Risk of soft tissue sarcomas by individual subtype in survivors of hereditary retinoblastoma. J Natl Cancer Inst. 2007;99:24-31.
-
(2007)
J. Natl. Cancer Inst.
, vol.99
, pp. 24-31
-
-
Kleinerman, R.A.1
Tucker, M.A.2
Abramson, D.H.3
-
117
-
-
0035115961
-
Second malignant neoplasms of the head and neck in survivors of retinoblastoma
-
Wenzel CT, Halperin EC, Fisher SR. Second malignant neoplasms of the head and neck in survivors of retinoblastoma. Ear Nose Throat J. 2001;80:106, 9-12.
-
(2001)
Ear. Nose. Throat. J.
, vol.80
, Issue.106
, pp. 9-12
-
-
Wenzel, C.T.1
Halperin, E.C.2
Fisher, S.R.3
-
118
-
-
0034694664
-
Hereditary retinoblastoma and risk of lung cancer
-
Kleinerman RA, Tarone RE, Abramson DH, et al. Hereditary retinoblastoma and risk of lung cancer. J Natl Cancer Inst. 2000;92:2037-2039. (Pubitemid 32045901)
-
(2000)
Journal of the National Cancer Institute
, vol.92
, Issue.24
, pp. 2037-2039
-
-
Kleinerman, R.A.1
Tarone, R.E.2
Abramson, D.H.3
Seddon, J.M.4
Li, F.P.5
Tucker, M.A.6
-
119
-
-
0013986675
-
Radiation-induced neoplasms following curative therapy for retinoblastoma
-
Soloway HB. Radiation-induced neoplasms following curative therapy for retinoblastoma. Cancer. 1966;19:1984-1988.
-
(1966)
Cancer
, vol.19
, pp. 1984-1988
-
-
Soloway, H.B.1
-
120
-
-
0021739401
-
Second nonocular tumors in retinoblastoma survivors. Are they radiation-induced?
-
Abramson DH, Ellsworth RM, Kitchin FD, et al. Second nonocular tumors in retinoblastoma survivors. Are they radiation-induced? Ophthalmology. 1984;91:1351-1355. (Pubitemid 15208903)
-
(1984)
Ophthalmology
, vol.91
, Issue.11
, pp. 1351-1355
-
-
Abramson, D.H.1
Ellsworth, R.M.2
Kitchin, F.D.3
Tung, G.4
-
121
-
-
17144398035
-
Risk of new cancers after radiotherapy in long-term survivors of retinoblastoma: An extended follow-up
-
DOI 10.1200/JCO.2005.05.054
-
Kleinerman RA, Tucker MA, Tarone RE, et al. Risk of new cancers after radiotherapy in long-term survivors of retinoblastoma: an extended follow-up. J Clin Oncol. 2005;23:2272-2279. (Pubitemid 46218720)
-
(2005)
Journal of Clinical Oncology
, vol.23
, Issue.10
, pp. 2272-2279
-
-
Kleinerman, R.A.1
Tucker, M.A.2
Tarone, R.E.3
Abramson, D.H.4
Seddon, J.M.5
Stovall, M.6
Li, F.P.7
Fraumeni Jr., J.F.8
-
122
-
-
33748029123
-
Mortality from second tumour among long-term survivors of retinoblastoma: A retrospective analysis of the Italian retinoblastoma registry
-
DOI 10.1038/sj.onc.1209786, PII 1209786
-
Acquaviva A, Ciccolallo L, Rondelli R, et al. Mortality from second tumour among long-term survivors of retinoblastoma: a retrospective analysis of the Italian retinoblastoma registry. Oncogene. 2006;25:5350-5357. (Pubitemid 44299097)
-
(2006)
Oncogene
, vol.25
, Issue.38
, pp. 5350-5357
-
-
Acquaviva, A.1
Ciccolallo, L.2
Rondelli, R.3
Balistreri, A.4
Ancarola, R.5
Cozza, R.6
Hadjistilianou, D.7
Francesco, S.D.8
Toti, P.9
Pastore, G.10
Haupt, R.11
Carli, M.12
Santoro, N.13
Cataldo, A.D.14
Fiorillo, A.15
Indolfi, P.16
Nucci, P.17
Sandri, A.18
Porta, F.19
Porcaro, A.B.20
Tamaro, P.21
Morgese, G.22
more..
-
124
-
-
0022613428
-
Second nonocular tumors in survivors of heritable retinoblastoma
-
Lueder GT, Judisch F, O'Gorman TW. Second nonocular tumors in survivors of heritable retinoblastoma. Arc Ophthalmol. 1986;104:372-373. (Pubitemid 16132996)
-
(1986)
Archives of Ophthalmology
, vol.104
, Issue.3
, pp. 372-373
-
-
Lueder, G.T.1
Judisch, G.F.2
O'Gorman, T.W.3
-
126
-
-
0023815309
-
Incidence of second neoplasms in patients with bilateral retinoblastoma
-
Roarty JD, McLean IW, Zimmerman LE. Incidence of second neoplasms in patients with bilateral retinoblastoma. Ophthalmology. 1988;95:1583-1587.
-
(1988)
Ophthalmology
, vol.95
, pp. 1583-1587
-
-
Roarty, J.D.1
McLean, I.W.2
Zimmerman, L.E.3
-
127
-
-
0027172571
-
Mortality from second tumors among long-term survivors of retinoblastoma
-
Eng C, Li FP, Abramson DH, et al. Mortality from second tumors among long-term survivors of retinoblastoma. J Natl Cancer Inst. 1993;85:1121-1128. (Pubitemid 23212278)
-
(1993)
Journal of the National Cancer Institute
, vol.85
, Issue.14
, pp. 1121-1128
-
-
Eng, C.1
Li, F.P.2
Abramson, D.H.3
Ellsworth, R.M.4
Wong, F.L.5
Goldman, M.B.6
Seddon, J.7
Tarbell, N.8
Boice Jr., J.D.9
-
128
-
-
0030989864
-
Second primary tumors in patients with retinoblastoma. A review of the literature
-
Moll AC, Imhof SM, Bouter LM, et al. Second primary tumors in patients with retinoblastoma. A review of the literature. Ophthalmic Genet. 1997;18:27-34. (Pubitemid 27222911)
-
(1997)
Ophthalmic Genetics
, vol.18
, Issue.1
, pp. 27-34
-
-
Moll, A.C.1
Imhof, S.M.2
Bouter, L.M.3
Tan, K.E.W.4
-
129
-
-
0031402818
-
Second primary tumours in hereditary- and nonhereditary retinoblastoma patients treated with megavoltage external beam irradiation
-
DOI 10.1007/BF02569071
-
Imhof SM, Moll AC, Hofman P, et al. Second primary tumours in hereditary- and nonhereditary retinoblastoma patients treated with megavoltage external beam irradiation. Documenta Ophthalmologica. 1997;93:337-344. (Pubitemid 28261028)
-
(1997)
Documenta Ophthalmologica
, vol.93
, Issue.4
, pp. 337-344
-
-
Imhof, S.M.1
Moll, A.C.2
Hofman, P.3
Mourits, M.P.H.4
Schipper, J.5
Tan, K.E.W.P.6
-
130
-
-
1542499463
-
For whom the bell tolls: Susceptibility to common adult cancers in retinoblastoma survivors
-
Kaye FJ, Harbour JW. For whom the bell tolls: susceptibility to common adult cancers in retinoblastoma survivors. J Natl Cancer Inst. 2004;96:342-343. (Pubitemid 38351289)
-
(2004)
Journal of the National Cancer Institute
, vol.96
, Issue.5
, pp. 342-343
-
-
Kay, F.J.1
Harbour, J.W.2
-
131
-
-
1542318327
-
Lifetime risks of common cancers among retinoblastoma survivors
-
Fletcher O, Easton D, Anderson K, et al. Lifetime risks of common cancers among retinoblastoma survivors. J Natl Cancer Inst. 2004;96:357-363. (Pubitemid 38401013)
-
(2004)
Journal of the National Cancer Institute
, vol.96
, Issue.5
, pp. 357-363
-
-
Fletcher, O.1
Easton, D.2
Anderson, K.3
Gilham, C.4
Jay, M.5
Peto, J.6
-
132
-
-
0032142723
-
Second nonocular tumors in survivors of heritable retinoblastoma and prior radiation therapy
-
DOI 10.1016/S0002-9394(98)00146-9, PII S0002939498001469
-
Mohney BG, Robertson DM, Schomberg PJ, et al. Second nonocular tumors in survivors of heritable retinoblastoma and prior radiation therapy. Am J Ophthalmol. 1998;126:269-277. (Pubitemid 28397100)
-
(1998)
American Journal of Ophthalmology
, vol.126
, Issue.2
, pp. 269-277
-
-
Mohney, B.G.1
Robertson, D.M.2
Schomberg, P.J.3
Hodge, D.O.4
-
134
-
-
34648840189
-
Loss of the retinoblastoma tumor suppressor: Differential action on transcriptional programs related to cell cycle control and immune function
-
DOI 10.1038/sj.onc.1210450, PII 1210450
-
Markey MP, Bergseid J, Bosco EE, et al. Loss of the retinoblastoma tumor suppressor: differential action on transcriptional programs related to cell cycle control and immune function. Oncogene. 2007;26:6307-6318. (Pubitemid 47462102)
-
(2007)
Oncogene
, vol.26
, Issue.43
, pp. 6307-6318
-
-
Markey, M.P.1
Bergseid, J.2
Bosco, E.E.3
Stengel, K.4
Xu, H.5
Mayhew, C.N.6
Schwemberger, S.J.7
Braden, W.A.8
Jiang, Y.9
Babcock, G.F.10
Jegga, A.G.11
Aronow, B.J.12
Reed, M.F.13
Wang, J.Y.J.14
Knudsen, E.S.15
-
135
-
-
34447121974
-
Retinoblastoma tumor suppressor status is a critical determinant of therapeutic response in prostate cancer cells
-
DOI 10.1158/0008-5472.CAN-06-4424
-
Sharma A, Comstock CE, Knudsen ES, et al. Retinoblastoma tumor suppressor status is a critical determinant of therapeutic response in prostate cancer cells. Cancer Res. 2007;67:6192-6203. (Pubitemid 47037500)
-
(2007)
Cancer Research
, vol.67
, Issue.13
, pp. 6192-6203
-
-
Sharma, A.1
Comstock, C.E.S.2
Knudsen, E.S.3
Cao, K.H.4
Hess-Wilson, J.K.5
Morey, L.M.6
Barrera, J.7
Knudsen, K.E.8
-
136
-
-
34250889432
-
Retinoblastoma pathway dysregulation causes DNA methyltransferase 1 overexpression in cancer via MAD2-mediated inhibition of the anaphase-promoting complex
-
DOI 10.2353/ajpath.2007.060779
-
Agoston AT, Argani P, De Marzo AM, et al. Retinoblastoma pathway dysregulation causesDNAmethyltransferase 1 overexpression in cancer viaMAD2-mediated inhibition of the anaphase-promoting complex. Am J Pathol. 2007;170:1585-1593. (Pubitemid 47339303)
-
(2007)
American Journal of Pathology
, vol.170
, Issue.5
, pp. 1585-1593
-
-
Agoston, A.T.1
Argani, P.2
De Marzo, A.M.3
Hicks, J.L.4
Nelson, W.G.5
-
137
-
-
0022506980
-
A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma
-
Friend SH, Bernards R, Rogelj S, et al. A human DNA segment with properties of the gene that predisposes to retinoblastoma and osteosarcoma. Nature. 1986;323:643-646. (Pubitemid 16008560)
-
(1986)
Nature
, vol.323
, Issue.6089
, pp. 643-646
-
-
Friend, S.H.1
Bernards, R.2
Rogelj, S.3
-
138
-
-
0035906222
-
Second malignant neoplasms in five-year survivors of childhood cancer: Childhood cancer survivor study
-
Neglia JP, Friedman DL, Yasui Y, et al. Second malignant neoplasms in five-year survivors of childhood cancer: childhood cancer survivor study. J Natl Cancer Inst. 2001;93:618-629. (Pubitemid 32409629)
-
(2001)
Journal of the National Cancer Institute
, vol.93
, Issue.8
, pp. 618-629
-
-
Neglia, J.P.1
Friedman, D.L.2
Yasui, Y.3
Mertens, A.C.4
Hammond, S.5
Stovall, M.6
Donaldson, S.S.7
Meadows, A.T.8
Robison, L.L.9
-
140
-
-
0024428903
-
Non-ocular cancer in relatives of retinoblastoma patients
-
Sanders BM, Jay M, Draper GJ, et al. Non-ocular cancer in relatives of retinoblastoma patients. Br J Cancer. 1989;60:358-365. (Pubitemid 19227406)
-
(1989)
British Journal of Cancer
, vol.60
, Issue.3
, pp. 358-365
-
-
Sanders, B.M.1
Jay, M.2
Draper, G.J.3
Roberts, E.M.4
-
142
-
-
5044223691
-
Regarding chemoreduction for retinoblastoma and intracranial neoplasms [1] (multiple letters)
-
DOI 10.1001/archopht.122.10.1570
-
Meadows AT, Shields CL. Regarding chemoreduction for retinoblastoma and intracranial neoplasms. Arch Ophthalmol. 2004;122:1570-1571; author reply 1. (Pubitemid 39336571)
-
(2004)
Archives of Ophthalmology
, vol.122
, Issue.10
, pp. 1570-1571
-
-
Meadows, A.T.1
Shields, C.L.2
Schouten-Van Meeteren, A.Y.N.3
Moll, A.C.4
Imhof, S.M.5
Dommering, C.J.6
-
143
-
-
0028907719
-
Spectrum of germline mutations in the RB1 gene: A study of 232 patients with hereditary and non hereditary retinoblastoma
-
Blanquet V, Turleau C, Gross-Morand MS, et al. Spectrum of germline mutations in the RB1 gene: a study of 232 patients with hereditary and non hereditary retinoblastoma. Human Molecular Genet. 1995;4:383-388.
-
(1995)
Human Molecular. Genet.
, vol.4
, pp. 383-388
-
-
Blanquet, V.1
Turleau, C.2
Gross-Morand, M.S.3
-
144
-
-
33644846696
-
Risk of selected subsequent carcinomas in survivors of childhood cancer: A report from the childhood cancer survivor study
-
DOI 10.1200/JCO.2005.02.7235
-
Bassal M, Mertens AC, Taylor L, et al. Risk of selected subsequent carcinomas in survivors of childhood cancer: a report from the Childhood Cancer Survivor Study. J Clin Oncol. 2006;24:476-483. (Pubitemid 46630467)
-
(2006)
Journal of Clinical Oncology
, vol.24
, Issue.3
, pp. 476-483
-
-
Bassal, M.1
Mertens, A.C.2
Taylor, L.3
Neglia, J.P.4
Greffe, B.S.5
Hammond, S.6
Ronckers, C.M.7
Friedman, D.L.8
Stovall, M.9
Yasui, Y.Y.10
Robison, L.L.11
Meadows, A.T.12
Kadan-Lottick, N.S.13
|