-
1
-
-
2642601107
-
Software and database for the analysis of mutations in the VHL gene
-
Beroud C, Joly D, Gallon C, Staroz F, Orfanelli MT, Junien C: Software and database for the analysis of mutations in the VHL gene. Nucleic Acids Res 26:256-258, 1998.
-
(1998)
Nucleic Acids Res
, vol.26
, pp. 256-258
-
-
Beroud, C.1
Joly, D.2
Gallon, C.3
Staroz, F.4
Orfanelli, M.T.5
Junien, C.6
-
2
-
-
0000168230
-
Von Hippel Lindau disease and capillary hemangioblastoma
-
Kleihues P, Cavenee (eds). Lyon, IARC Press, ed 2
-
Böhling T, Plate KH, Haltia M: Von Hippel Lindau disease and capillary hemangioblastoma, in Kleihues P, Cavenee (eds): Pathology and Genetics of Tumors of the Nervous System: World Health Organization Classification Of Tumours. Lyon, IARC Press, 2000, ed 2, pp 223-226.
-
(2000)
Pathology and Genetics of Tumors of the Nervous System: World Health Organization Classification of Tumours
, pp. 223-226
-
-
Böhling, T.1
Plate, K.H.2
Haltia, M.3
-
3
-
-
0032729680
-
Two distinct phenotypes caused by two different missense mutations in the same codon of the VHL gene
-
Bradley JF, Collins DL, Schimke RN, Parrott HN, Rothberg PG: Two distinct phenotypes caused by two different missense mutations in the same codon of the VHL gene. Am J Med Genet 87:163-167, 1999.
-
(1999)
Am J Med Genet
, vol.87
, pp. 163-167
-
-
Bradley, J.F.1
Collins, D.L.2
Schimke, R.N.3
Parrott, H.N.4
Rothberg, P.G.5
-
4
-
-
0029742035
-
Genotype-phenotype correlation in von Hippel-Lindau disease: Identification of a mutation associated with VHL type 2A
-
Chen F, Slife L, Kishida T, Mulvihill J, Tisherman SE, Zbar B: Genotype-phenotype correlation in von Hippel-Lindau disease: Identification of a mutation associated with VHL type 2A. J Med Genet 33:716-717, 1996.
-
(1996)
J Med Genet
, vol.33
, pp. 716-717
-
-
Chen, F.1
Slife, L.2
Kishida, T.3
Mulvihill, J.4
Tisherman, S.E.5
Zbar, B.6
-
5
-
-
0028938702
-
Von Hippel-Lindau disease: Genetic, clinical and imaging features
-
Choyke PL, Glenn GM, Walther MM: Von Hippel-Lindau disease: Genetic, clinical and imaging features. Radiology 194:629-642, 1995.
-
(1995)
Radiology
, vol.194
, pp. 629-642
-
-
Choyke, P.L.1
Glenn, G.M.2
Walther, M.M.3
-
6
-
-
0029838624
-
PCR fidelity of pfu DNA polymerase and other thermostable DNA polymerase
-
Cline J, Bramam JC, Hogrefe HH: PCR fidelity of pfu DNA polymerase and other thermostable DNA polymerase. Nucleic Acids Res 24:3546-3551, 1996.
-
(1996)
Nucleic Acids Res
, vol.24
, pp. 3546-3551
-
-
Cline, J.1
Bramam, J.C.2
Hogrefe, H.H.3
-
7
-
-
0022658443
-
Posterior fossa hemangioblastomas
-
Constans JP, Meder F, Maiuri F, Donzelli R, Spaziante R, de Divitiis E: Posterior fossa hemangioblastomas. Surg Neurol 25:269-275, 1986.
-
(1986)
Surg Neurol
, vol.25
, pp. 269-275
-
-
Constans, J.P.1
Meder, F.2
Maiuri, F.3
Donzelli, R.4
Spaziante, R.5
De Divitiis, E.6
-
8
-
-
0035155525
-
Hemangioblastomas of the central nervous system in von Hippel-Lindau syndrome and sporadic disease
-
Conway JE, Chou D, Clatterbuck RE, Brem H, Long DM, Rigamonti D: Hemangioblastomas of the central nervous system in von Hippel-Lindau syndrome and sporadic disease. Neurosurgery 48:55-63, 2001.
-
(2001)
Neurosurgery
, vol.48
, pp. 55-63
-
-
Conway, J.E.1
Chou, D.2
Clatterbuck, R.E.3
Brem, H.4
Long, D.M.5
Rigamonti, D.6
-
9
-
-
0034095068
-
Von Hippel-Lindau disease
-
Couch V, Lindor NM, Karnes PS, Michels W: Von Hippel-Lindau disease. Mayo Clin Proc 75:265-272, 2000.
-
(2000)
Mayo Clin Proc
, vol.75
, pp. 265-272
-
-
Couch, V.1
Lindor, N.M.2
Karnes, P.S.3
Michels, W.4
-
10
-
-
0033569787
-
Von Hippel-Lindau syndrome: A pleomorphic condition
-
Friedrich CA: Von Hippel-Lindau syndrome: A pleomorphic condition. Cancer 86:2478-2482, 1999.
-
(1999)
Cancer
, vol.86
, pp. 2478-2482
-
-
Friedrich, C.A.1
-
11
-
-
4143122357
-
Genotype-phenotype correlation in von Hippel-Lindau families with renal lesions
-
Gallou C, Chauveau D, Richard S, Joly D, Giraud S, Olschwang S, Martin N, Saquet C, Chretien Y, Mejean A, Correas JM, Benoit G, Colombeau P, Grunfeld JP, Junien C, Beroud C: Genotype-phenotype correlation in von Hippel-Lindau families with renal lesions. Hum Mutat 24:215-224, 2004.
-
(2004)
Hum Mutat
, vol.24
, pp. 215-224
-
-
Gallou, C.1
Chauveau, D.2
Richard, S.3
Joly, D.4
Giraud, S.5
Olschwang, S.6
Martin, N.7
Saquet, C.8
Chretien, Y.9
Mejean, A.10
Correas, J.M.11
Benoit, G.12
Colombeau, P.13
Grunfeld, J.P.14
Junien, C.15
Beroud, C.16
-
12
-
-
0032702779
-
The impact of molecular genetic analysis of the VHL gene in patients with hemangioblastomas of the central nervous system
-
Glasker S, Bender BU, Apel TW, Natt E, van Velthoven V, Scheremet R, Zentner J, Neumann HP: The impact of molecular genetic analysis of the VHL gene in patients with hemangioblastomas of the central nervous system. J Neurol Neurosurg Psychiatry 67:758-762, 1999.
-
(1999)
J Neurol Neurosurg Psychiatry
, vol.67
, pp. 758-762
-
-
Glasker, S.1
Bender, B.U.2
Apel, T.W.3
Natt, E.4
Van Velthoven, V.5
Scheremet, R.6
Zentner, J.7
Neumann, H.P.8
-
13
-
-
4644270437
-
Frequent somatic mutations of the von Hippel Lindau tumor suppressor gene and its meaning in sporadic human clear cell carcinoma
-
Gong K, Zhang N, Guo HF, Zhang ZW, Xin DQ, Na YQ: Frequent somatic mutations of the von Hippel Lindau tumor suppressor gene and its meaning in sporadic human clear cell carcinoma [in Chinese]. Beijing Da Xue Xue Bao 36:169-172, 2004.
-
(2004)
Beijing Da Xue Xue Bao
, vol.36
, pp. 169-172
-
-
Gong, K.1
Zhang, N.2
Guo, H.F.3
Zhang, Z.W.4
Xin, D.Q.5
Na, Y.Q.6
-
14
-
-
3543151306
-
Somatic mutations of VHL gene and HIF-1α expression in primary renal clear cell carcinomas
-
Guo HF, Gong K, Zou SM, Zhang ZW, Liu XY, Na X, Wu G, Na Y: Somatic mutations of VHL gene and HIF-1α expression in primary renal clear cell carcinomas [in Chinese]. Zhonghua Wai Ke Za Zhi 42:196-200, 2004.
-
(2004)
Zhonghua Wai Ke Za Zhi
, vol.42
, pp. 196-200
-
-
Guo, H.F.1
Gong, K.2
Zou, S.M.3
Zhang, Z.W.4
Liu, X.Y.5
Na, X.6
Wu, G.7
Na, Y.8
-
15
-
-
0034635882
-
Von Hippel-Lindau disease: Protocols for diagnosis and periodical clinical monitoring-National Von Hippel-Lindau Disease Working Group
-
Hes FJ, van der Luijt RB: Von Hippel-Lindau disease: Protocols for diagnosis and periodical clinical monitoring-National Von Hippel-Lindau Disease Working Group [in Dutch]. Ned Tijdschr Geneeskd 144:505-509, 2000.
-
(2000)
Ned Tijdschr Geneeskd
, vol.144
, pp. 505-509
-
-
Hes, F.J.1
Van Der Luijt, R.B.2
-
16
-
-
0035149725
-
Molecular genetic aspects of von Hippel-Lindau disease and criteria for DNA analysis in subject at risk
-
Hes FJ, Lips CJ, van der Luijt RB: Molecular genetic aspects of von Hippel-Lindau disease and criteria for DNA analysis in subject at risk. Neth J Med 59:235-243, 2001.
-
(2001)
Neth J Med
, vol.59
, pp. 235-243
-
-
Hes, F.J.1
Lips, C.J.2
Van Der Luijt, R.B.3
-
17
-
-
0034535884
-
Cryptic von Hippel-Lindau disease: Germline mutation in patients with hemangioblastoma only
-
Hes FJ, McKee S, Taphoorn MJ, Rehal P, van der Luijt RB, McMahon R, van der Smagt JJ, Dow D, Zewald RA, Whittaker J, Lips CJ, MacDonald F, Pearson PL, Maher ER: Cryptic von Hippel-Lindau disease: Germline mutation in patients with hemangioblastoma only. J Med Genet 37:939-943, 2000.
-
(2000)
J Med Genet
, vol.37
, pp. 939-943
-
-
Hes, F.J.1
McKee, S.2
Taphoorn, M.J.3
Rehal, P.4
Van Der Luijt, R.B.5
McMahon, R.6
Van Der Smagt, J.J.7
Dow, D.8
Zewald, R.A.9
Whittaker, J.10
Lips, C.J.11
MacDonald, F.12
Pearson, P.L.13
Maher, E.R.14
-
18
-
-
0034753757
-
Clinical management of von Hippel-Lindau (VHL) disease
-
Hes FJ, van der Luijt RB, Lips CJ: Clinical management of von Hippel-Lindau (VHL) disease. Neth J Med 59:225-234, 2001.
-
(2001)
Neth J Med
, vol.59
, pp. 225-234
-
-
Hes, F.J.1
Van Der Luijt, R.B.2
Lips, C.J.3
-
19
-
-
0030321178
-
Von Hippel-Lindau syndrome: Hereditary cancer arising from inherited mutations of the VHL tumor suppressor gene
-
Humphrey JS, Klausner RD, Linehan WM: Von Hippel-Lindau syndrome: Hereditary cancer arising from inherited mutations of the VHL tumor suppressor gene. Cancer Treat Res 88:13-22, 1996.
-
(1996)
Cancer Treat Res
, vol.88
, pp. 13-22
-
-
Humphrey, J.S.1
Klausner, R.D.2
Linehan, W.M.3
-
20
-
-
0027938458
-
Somatic mutations of the von Hippel-Lindau tumor suppressor gene in sporadic central nervous system hemangioblastomas
-
Kanno H, Kondo K, Ito S, Yamamoto I, Fujii S, Torigoe S, Sakai N, Hosaka M, Shuin T, Yao M: Somatic mutations of the von Hippel-Lindau tumor suppressor gene in sporadic central nervous system hemangioblastomas. Cancer Res 54:4845-4847, 1994.
-
(1994)
Cancer Res
, vol.54
, pp. 4845-4847
-
-
Kanno, H.1
Kondo, K.2
Ito, S.3
Yamamoto, I.4
Fujii, S.5
Torigoe, S.6
Sakai, N.7
Hosaka, M.8
Shuin, T.9
Yao, M.10
-
22
-
-
0024493153
-
Von Hippel-Lindau disease affecting 43 members of a single kindred
-
Lamiell JM, Salazar FG, Hsia YE: Von Hippel-Lindau disease affecting 43 members of a single kindred. Medicine 68:1-29, 1989.
-
(1989)
Medicine
, vol.68
, pp. 1-29
-
-
Lamiell, J.M.1
Salazar, F.G.2
Hsia, Y.E.3
-
23
-
-
0027240519
-
Identification of the von Hippel-Lindau disease tumor suppressor gene
-
Latif F, Tory K, Gnarra J, Yao M, Duh FM, Orcutt ML, Stackouse T, Kuzmin I, Modi W, Geil L, Schmidt L, Zhou F, Li H, Wei MH, Chen F, Glenn G, Choyke P, Walther MM, Weng Y, Duan DR, Dean A, Glavac D, Richard FM, Crossey PA, Ferguson-Smith MA, Le Paslier D, Chumakov I, Cohen D, Chinault CA, Maher ER, Linehan WM, Zbar B: Identification of the von Hippel-Lindau disease tumor suppressor gene. Science 260:1317-1320, 1993.
-
(1993)
Science
, vol.260
, pp. 1317-1320
-
-
Latif, F.1
Tory, K.2
Gnarra, J.3
Yao, M.4
Duh, F.M.5
Orcutt, M.L.6
Stackouse, T.7
Kuzmin, I.8
Modi, W.9
Geil, L.10
Schmidt, L.11
Zhou, F.12
Li, H.13
Wei, M.H.14
Chen, F.15
Glenn, G.16
Choyke, P.17
Walther, M.M.18
Weng, Y.19
Duan, D.R.20
Dean, A.21
Glavac, D.22
Richard, F.M.23
Crossey, P.A.24
Ferguson-Smith, M.A.25
Le Paslier, D.26
Chumakov, I.27
Cohen, D.28
Chinault, C.A.29
Maher, E.R.30
Linehan, W.M.31
Zbar, B.32
more..
-
24
-
-
18844474899
-
Loss of heterozygosity and somatic mutation of the VHL suppressor gene in sporadic cerebellar hemangioblastomas
-
Lee JY, Dong SM, Park WS, Yoo NJ, Kim CS, Jang JJ, Chi JG, Zbar B, Lubensky LA, Linehan WM, Worrmeyer AO, Zhuang Z: Loss of heterozygosity and somatic mutation of the VHL suppressor gene in sporadic cerebellar hemangioblastomas. Cancer Res 58:504-508, 1998.
-
(1998)
Cancer Res
, vol.58
, pp. 504-508
-
-
Lee, J.Y.1
Dong, S.M.2
Park, W.S.3
Yoo, N.J.4
Kim, C.S.5
Jang, J.J.6
Chi, J.G.7
Zbar, B.8
Lubensky, L.A.9
Linehan, W.M.10
Worrmeyer, A.O.11
Zhuang, Z.12
-
25
-
-
0028887421
-
Identification of the von Hippel-Lindau gene: Its role in renal cancer
-
Linehan WM, Lerman MI, Zbar B: Identification of the von Hippel-Lindau gene: Its role in renal cancer. JAMA 273:564-570, 1995.
-
(1995)
JAMA
, vol.273
, pp. 564-570
-
-
Linehan, W.M.1
Lerman, M.I.2
Zbar, B.3
-
26
-
-
0033458843
-
Clinical impact of molecular genetic diagnosis, genetic counseling, and management of hereditary cancer
-
Lynch HT, Watson P, Shaw TG, Lynch JF, Harty AE, Franklin BA, Kapler CR, Tinley ST, Liu B: Clinical impact of molecular genetic diagnosis, genetic counseling, and management of hereditary cancer. Cancer 86:2449-2456, 1999.
-
(1999)
Cancer
, vol.86
, pp. 2449-2456
-
-
Lynch, H.T.1
Watson, P.2
Shaw, T.G.3
Lynch, J.F.4
Harty, A.E.5
Franklin, B.A.6
Kapler, C.R.7
Tinley, S.T.8
Liu, B.9
-
27
-
-
19144371868
-
A genetic register for von Hippel-Lindau disease
-
Maddock IR, Moran A, Maher ER, Teare MD, Normann A, Payne SJ, Whitehouse R, Dodd C, Lavin M, Hartley N, Super M, Evans DG: A genetic register for von Hippel-Lindau disease. J Med Genet 33:120-127, 1996.
-
(1996)
J Med Genet
, vol.33
, pp. 120-127
-
-
Maddock, I.R.1
Moran, A.2
Maher, E.R.3
Teare, M.D.4
Normann, A.5
Payne, S.J.6
Whitehouse, R.7
Dodd, C.8
Lavin, M.9
Hartley, N.10
Super, M.11
Evans, D.G.12
-
28
-
-
0025741681
-
Von Hippel-Lindau disease: A genetic study
-
Maher ER, Iselius L, Yates JR, Littler M, Benjamin C, Harris R, Sampson J, Williams A, Ferguson-Smith MA, Morton N: Von Hippel-Lindau disease: A genetic study. J Med Genet 28:443-447, 1991.
-
(1991)
J Med Genet
, vol.28
, pp. 443-447
-
-
Maher, E.R.1
Iselius, L.2
Yates, J.R.3
Littler, M.4
Benjamin, C.5
Harris, R.6
Sampson, J.7
Williams, A.8
Ferguson-Smith, M.A.9
Morton, N.10
-
29
-
-
0029940856
-
Phenotypic expression in von Hippel-Lindau disease: Correlations with germline VHL gene mutations
-
Maher ER, Webster AR, Richards FM, Green JS, Crossey PA, Payne SJ, Moore AT: Phenotypic expression in von Hippel-Lindau disease: Correlations with germline VHL gene mutations. J Med Genet 33:328-332, 1996.
-
(1996)
J Med Genet
, vol.33
, pp. 328-332
-
-
Maher, E.R.1
Webster, A.R.2
Richards, F.M.3
Green, J.S.4
Crossey, P.A.5
Payne, S.J.6
Moore, A.T.7
-
30
-
-
0025000210
-
Clinical features and natural history of Von Hippel-Lindau disease
-
Maher ER, Yates JR, Harries R, Benjamin C, Harris R, Moore AT, Ferguson-Smith MA: Clinical features and natural history of Von Hippel-Lindau disease. Q J Med 77:1151-1163, 1990.
-
(1990)
Q J Med
, vol.77
, pp. 1151-1163
-
-
Maher, E.R.1
Yates, J.R.2
Harries, R.3
Benjamin, C.4
Harris, R.5
Moore, A.T.6
Ferguson-Smith, M.A.7
-
31
-
-
0034880192
-
Rapid mutation scanning of genes associated with familial cancer syndromes using denaturing high-performance liquid chromatography
-
Marsh DJ, Theodosopoulos G, Howell V, Richardson AL, Benn DE, Proos AL, Eng C, Robinson BG: Rapid mutation scanning of genes associated with familial cancer syndromes using denaturing high-performance liquid chromatography. Neoplasia 3:236-244, 2001.
-
(2001)
Neoplasia
, vol.3
, pp. 236-244
-
-
Marsh, D.J.1
Theodosopoulos, G.2
Howell, V.3
Richardson, A.L.4
Benn, D.E.5
Proos, A.L.6
Eng, C.7
Robinson, B.G.8
-
32
-
-
50549195332
-
Lindau's disease: Review of the literature and study of a large kindred
-
Melmon KL, Rosen SW: Lindau's disease: Review of the literature and study of a large kindred. Am J Med 36:595-617, 1964.
-
(1964)
Am J Med
, vol.36
, pp. 595-617
-
-
Melmon, K.L.1
Rosen, S.W.2
-
33
-
-
0031834186
-
Genotype-phenotype correlations in von Hippel-Lindau disease
-
Neumann HP, Bender BU: Genotype-phenotype correlations in von Hippel-Lindau disease. J Intern Med 243:541-545, 1998.
-
(1998)
J Intern Med
, vol.243
, pp. 541-545
-
-
Neumann, H.P.1
Bender, B.U.2
-
34
-
-
0024525750
-
Hemangioblastoma of the central nervous system; A 10-year study with special reference to von Hippel-Lindau syndrome
-
Neumann HP, Eggert HR, Weigel K, Freidburg H, Wiestler OD, Schollmeyer P: Hemangioblastoma of the central nervous system; A 10-year study with special reference to von Hippel-Lindau syndrome. J Neurosurg 70:24-30, 1989.
-
(1989)
J Neurosurg
, vol.70
, pp. 24-30
-
-
Neumann, H.P.1
Eggert, H.R.2
Weigel, K.3
Freidburg, H.4
Wiestler, O.D.5
Schollmeyer, P.6
-
35
-
-
0032695163
-
Long-term prognosis of hemangioblastoma of the CNC: Impact of von Hippel-Lindau disease
-
Niemela M, Lemeta S, Summanen P, Bohling T, Sainio M, Kere J, Poussa K, Sankila R, Haapasalo H, Kaariainen H, Pukkala E, Jääskeläinen J: Long-term prognosis of hemangioblastoma of the CNC: Impact of von Hippel-Lindau disease. Acta Neurochir (Wien) 141:1147-1156, 1999.
-
(1999)
Acta Neurochir (Wien)
, vol.141
, pp. 1147-1156
-
-
Niemela, M.1
Lemeta, S.2
Summanen, P.3
Bohling, T.4
Sainio, M.5
Kere, J.6
Poussa, K.7
Sankila, R.8
Haapasalo, H.9
Kaariainen, H.10
Pukkala, E.11
Jääskeläinen, J.12
-
36
-
-
0029811626
-
Gamma knife radiosurgery in 11 hemangioblastomas
-
Niemela M, Lim YJ, Soderman M, Jääskeläinen J, Lindquist C: Gamma knife radiosurgery in 11 hemangioblastomas. J Neurosurg 85:591-596, 1996.
-
(1996)
J Neurosurg
, vol.85
, pp. 591-596
-
-
Niemela, M.1
Lim, Y.J.2
Soderman, M.3
Jääskeläinen, J.4
Lindquist, C.5
-
37
-
-
0029893946
-
Mutation of the Von Hippel-Lindau tumour suppressor gene in capillary hemangioblastoma of the central nervous system
-
Oberstrass J, Reifenberger G, Reifenberger J, Wechsler W, Collins VP: Mutation of the Von Hippel-Lindau tumour suppressor gene in capillary hemangioblastoma of the central nervous system. J Pathol 179:151-156, 1996.
-
(1996)
J Pathol
, vol.179
, pp. 151-156
-
-
Oberstrass, J.1
Reifenberger, G.2
Reifenberger, J.3
Wechsler, W.4
Collins, V.P.5
-
38
-
-
0031762403
-
Germline mutation profile of the VHL gene in von Hippel-Lindau disease and in sporadic hemangioblastoma
-
Olschwang S, Richard S, Boisson C, Giraud S, Laurent-Puig P, Resche F, Thomas G: Germline mutation profile of the VHL gene in von Hippel-Lindau disease and in sporadic hemangioblastoma. Hum Mutat 12:424-430, 1998.
-
(1998)
Hum Mutat
, vol.12
, pp. 424-430
-
-
Olschwang, S.1
Richard, S.2
Boisson, C.3
Giraud, S.4
Laurent-Puig, P.5
Resche, F.6
Thomas, G.7
-
39
-
-
0030175495
-
Radiosurgery for hemangioblastoma: Results of a multi-institutional experience
-
Patrice SJ, Sneed PK, Flickinger JC, Shrieve DC, Pollock BE, Alexander E III, Larson DA, Kondziolka D, Gutin PH, Wara WM, McDermott MW, Lunsford LD, Loeffler JS: Radiosurgery for hemangioblastoma: Results of a multi-institutional experience. Int J Radiat Oncol Biol Phys 35:493-499, 1996.
-
(1996)
Int J Radiat Oncol Biol Phys
, vol.35
, pp. 493-499
-
-
Patrice, S.J.1
Sneed, P.K.2
Flickinger, J.C.3
Shrieve, D.C.4
Pollock, B.E.5
Alexander III, E.6
Larson, D.A.7
Kondziolka, D.8
Gutin, P.H.9
Wara, W.M.10
McDermott, M.W.11
Lunsford, L.D.12
Loeffler, J.S.13
-
40
-
-
0028169207
-
Does hemangioblastoma exist outside von Hippel-Lindau disease?
-
Richard S, Beigelman C, Gerber S, Van Effenterre R, Gaudric A, Sahel M: Does hemangioblastoma exist outside von Hippel-Lindau disease? [in French]. Neurochirurgie 40:145-154, 1994.
-
(1994)
Neurochirurgie
, vol.40
, pp. 145-154
-
-
Richard, S.1
Beigelman, C.2
Gerber, S.3
Van Effenterre, R.4
Gaudric, A.5
Sahel, M.6
-
41
-
-
0031837459
-
Hemangioblastoma of the central nervous system in von Hippel-Lindau disease: French VHL Study Group
-
Richard S, Campello C, Taillandier L, Parker F, Resche F: Hemangioblastoma of the central nervous system in von Hippel-Lindau disease: French VHL Study Group. J Intern Med 243:547-553, 1998.
-
(1998)
J Intern Med
, vol.243
, pp. 547-553
-
-
Richard, S.1
Campello, C.2
Taillandier, L.3
Parker, F.4
Resche, F.5
-
42
-
-
0034098260
-
Central nervous system hemangioblastomas, endolymphatic sac tumors, and von Hippel-Lindau disease
-
Richard S, David P, Marsot-Dupuch K, Giraud S, Beroud C, Resche F: Central nervous system hemangioblastomas, endolymphatic sac tumors, and von Hippel-Lindau disease. Neurosurg Rev 23:1-24, 2000.
-
(2000)
Neurosurg Rev
, vol.23
, pp. 1-24
-
-
Richard, S.1
David, P.2
Marsot-Dupuch, K.3
Giraud, S.4
Beroud, C.5
Resche, F.6
-
43
-
-
10744222427
-
Generic characterization and structural analysis of VHL Spanish families to define genotype-phenotype correlations
-
Ruiz-Llorente S, Bravo J, Cebrian A, Cascon A, Pollan M, Telleria D, Leton R, Urioste M, Rodriguez-Lopez R, de Campos JM, Munoz MJ, Lacambra C, Benitez J, Robledo M: Generic characterization and structural analysis of VHL Spanish families to define genotype-phenotype correlations. Hum Mutat 23:160-169, 2004.
-
(2004)
Hum Mutat
, vol.23
, pp. 160-169
-
-
Ruiz-Llorente, S.1
Bravo, J.2
Cebrian, A.3
Cascon, A.4
Pollan, M.5
Telleria, D.6
Leton, R.7
Urioste, M.8
Rodriguez-Lopez, R.9
De Campos, J.M.10
Munoz, M.J.11
Lacambra, C.12
Benitez, J.13
Robledo, M.14
-
44
-
-
0034816143
-
Incidence of von Hippel-Lindau disease in hemangioblastoma patients: The University of Tokyo Hospital experience from 1954-1998
-
Sora S, Ueki K, Saito N, Kawahara N, Shitara N, Kirino T: Incidence of von Hippel-Lindau disease in hemangioblastoma patients: The University of Tokyo Hospital experience from 1954-1998. Acta Neurochir (Wien) 143: 893-896, 2001.
-
(2001)
Acta Neurochir (Wien)
, vol.143
, pp. 893-896
-
-
Sora, S.1
Ueki, K.2
Saito, N.3
Kawahara, N.4
Shitara, N.5
Kirino, T.6
-
45
-
-
7844234770
-
Improved detection of germline mutations in the von Hippel-Lindau disease tumor suppressor gene
-
Stolle C, Glenn G, Zbar B, Humphrey JS, Choyke P, Walther M: Improved detection of germline mutations in the von Hippel-Lindau disease tumor suppressor gene. Hum Mutat 12:417-423, 1998.
-
(1998)
Hum Mutat
, vol.12
, pp. 417-423
-
-
Stolle, C.1
Glenn, G.2
Zbar, B.3
Humphrey, J.S.4
Choyke, P.5
Walther, M.6
-
46
-
-
0032601052
-
Descriptive epidemiology of the primary brain and CNS tumors: Results from the Central Brain Tumor Registry of the United States, 1990-1994
-
Surawicz TS, McCarthy BJ, Kupelian V, Jukivh PJ, Bruner JM, Davs FG: Descriptive epidemiology of the primary brain and CNS tumors: Results from the Central Brain Tumor Registry of the United States, 1990-1994. Neurooncology 1:14-25, 1999.
-
(1999)
Neurooncology
, vol.1
, pp. 14-25
-
-
Surawicz, T.S.1
McCarthy, B.J.2
Kupelian, V.3
Jukivh, P.J.4
Bruner, J.M.5
Davs, F.G.6
-
47
-
-
0027327367
-
Preoperative embolization of brain and spinal hemangioblastoma
-
Tampieri D, Leblanc R, ter Brugge K: Preoperative embolization of brain and spinal hemangioblastoma. Neurosurgery 33:502-505, 1993.
-
(1993)
Neurosurgery
, vol.33
, pp. 502-505
-
-
Tampieri, D.1
Leblanc, R.2
Ter Brugge, K.3
-
48
-
-
0030958304
-
Von Hippel-Lindau gene deletion detected in the stromal cell component of a cerebellar hemangioblastoma associated with von Hippel-Lindau disease
-
Vortmeyer AO, Gnarra JR, Emmert-Buck MR, Katz D, Linehan WM, Oldfield EH: Von Hippel-Lindau gene deletion detected in the stromal cell component of a cerebellar hemangioblastoma associated with von Hippel-Lindau disease. Hum Pathol 28:540-543, 1997.
-
(1997)
Hum Pathol
, vol.28
, pp. 540-543
-
-
Vortmeyer, A.O.1
Gnarra, J.R.2
Emmert-Buck, M.R.3
Katz, D.4
Linehan, W.M.5
Oldfield, E.H.6
-
49
-
-
6544234532
-
Clinical and genetic characterization of pheochromocytoma in von Hippel-Lindau families: Comparison with sporadic pheochromocytoma gives insight into natural history of pheochromocytoma
-
Walther MM, Reiter R, Keiser HR, Choyke PL, Venzon D, Hurley K, Gnarra JR, Reynolds JC, Glenn GM, Zbar B, Linehan WM: Clinical and genetic characterization of pheochromocytoma in von Hippel-Lindau families: Comparison with sporadic pheochromocytoma gives insight into natural history of pheochromocytoma. J Urol 162[Suppl 3]:659-664, 1999.
-
(1999)
J Urol
, vol.162
, Issue.SUPPL. 3
, pp. 659-664
-
-
Walther, M.M.1
Reiter, R.2
Keiser, H.R.3
Choyke, P.L.4
Venzon, D.5
Hurley, K.6
Gnarra, J.R.7
Reynolds, J.C.8
Glenn, G.M.9
Zbar, B.10
Linehan, W.M.11
-
50
-
-
0037222647
-
The natural history of hemangioblastomas of the central nervous system in patients with von Hippel-Lindau disease
-
Wanebo JE, Lonser RR, Glenn GM, Oldfield EH: The natural history of hemangioblastomas of the central nervous system in patients with von Hippel-Lindau disease. J Neurosurg 98:82-94, 2003.
-
(2003)
J Neurosurg
, vol.98
, pp. 82-94
-
-
Wanebo, J.E.1
Lonser, R.R.2
Glenn, G.M.3
Oldfield, E.H.4
-
51
-
-
0034999807
-
Denaturing high-performance liquid chromatography: A review
-
Xiao W, Oefner PJ: Denaturing high-performance liquid chromatography: A review. Human Mutat 17:439-474, 2001.
-
(2001)
Human Mutat
, vol.17
, pp. 439-474
-
-
Xiao, W.1
Oefner, P.J.2
-
52
-
-
0033136031
-
Third International Meeting on von Hippel-Lindau disease
-
Zbar B, Kaelin W, Maher E, Richard S: Third International Meeting on von Hippel-Lindau disease. Cancer Res 59:2251-2253, 1999.
-
(1999)
Cancer Res
, vol.59
, pp. 2251-2253
-
-
Zbar, B.1
Kaelin, W.2
Maher, E.3
Richard, S.4
-
53
-
-
16144365122
-
Germline mutations in the Von Hippel-Lindau disease (VHL) gene in families from North America, Europe, and Japan
-
Zbar B, Kishida T, Chen F, Schmidt L, Maher ER, Richards FM, Crossey PA, Webster AR, Affara NA, Ferguson-Smith MA, Brauch H, Glavac D, Neumann HP, Tisherman S, Mulvihill JJ, Gross DJ, Shuin T, Whaley J, Seizinger B, Kley N, Olschwang S, Boisson C, Richard S, Lips CH, Lerman M, et al: Germline mutations in the Von Hippel-Lindau disease (VHL) gene in families from North America, Europe, and Japan. Hum Mutat 8:348-357, 1996.
-
(1996)
Hum Mutat
, vol.8
, pp. 348-357
-
-
Zbar, B.1
Kishida, T.2
Chen, F.3
Schmidt, L.4
Maher, E.R.5
Richards, F.M.6
Crossey, P.A.7
Webster, A.R.8
Affara, N.A.9
Ferguson-Smith, M.A.10
Brauch, H.11
Glavac, D.12
Neumann, H.P.13
Tisherman, S.14
Mulvihill, J.J.15
Gross, D.J.16
Shuin, T.17
Whaley, J.18
Seizinger, B.19
Kley, N.20
Olschwang, S.21
Boisson, C.22
Richard, S.23
Lips, C.H.24
Lerman, M.25
more..
|