-
2
-
-
12944278608
-
Goniotomy for glaucoma associated with nevus flammeus
-
O. Barkan Goniotomy for glaucoma associated with nevus flammeus Am J Ophthalmol 43 1957 545 549
-
(1957)
Am J Ophthalmol
, vol.43
, pp. 545-549
-
-
Barkan, O.1
-
3
-
-
0023244033
-
Gene for von Recklinghausen neurofibromatosis is in the pericentromeric region of chromosome 17
-
D. Barker E. Wright K. Nguyen Gene for von Recklinghausen neurofibromatosis is in the pericentromeric region of chromosome 17 Science 236 1987 1100 1102
-
(1987)
Science
, vol.236
, pp. 1100-1102
-
-
Barker, D.1
Wright, E.2
Nguyen, K.3
-
4
-
-
0021069143
-
Ocular neurofibromatosis
-
S.L. Brownstein Ocular neurofibromatosis Ophthalmology 90 1983 1595 1599
-
(1983)
Ophthalmology
, vol.90
, pp. 1595-1599
-
-
Brownstein, S.L.1
-
5
-
-
33646802927
-
Cerebral sclerosis
-
A.W. Campbell Cerebral sclerosis Brain 28 1905 382 396
-
(1905)
Brain
, vol.28
, pp. 382-396
-
-
Campbell, A.W.1
-
6
-
-
0025326726
-
A major segment of the neurofibromatosis Type I gene: cDNA sequence, genomic structure, and point mutations
-
R.M. Cawthon M. Weiss G. Xu A major segment of the neurofibromatosis Type I gene: cDNA sequence, genomic structure, and point mutations Cell 62 1990 193 201
-
(1990)
Cell
, vol.62
, pp. 193-201
-
-
Cawthon, R.M.1
Weiss, M.2
Xu, G.3
-
7
-
-
0028981766
-
Germline mutations in the von Hippel-Lindau disease tumor suppresor gene: Correlations with phenotype
-
F. Chen T. Kishida M. Yao Germline mutations in the von Hippel-Lindau disease tumor suppresor gene: Correlations with phenotype Hum Mutat 5 1995 66 75
-
(1995)
Hum Mutat
, vol.5
, pp. 66-75
-
-
Chen, F.1
Kishida, T.2
Yao, M.3
-
8
-
-
33847007950
-
National Institues of Health Consensus Development Panel. National Institutes of Health Consensus Development Conference Statement on Acoustic Neuroma, December 11–13, 1991
-
Consensus Development Panel National Institues of Health Consensus Development Panel. National Institutes of Health Consensus Development Conference Statement on Acoustic Neuroma, December 11–13, 1991 Arch Neurol 51 1994 201 207
-
(1994)
Arch Neurol
, vol.51
, pp. 201-207
-
-
Consensus Development Panel1
-
9
-
-
0028219324
-
Identification of intragenic mutations in the von Hippel-Lindau disease tumour supressor gene and correlation with disease phenotype
-
P.A. Crossey F.M. Richards M.E. Phipps Identification of intragenic mutations in the von Hippel-Lindau disease tumour supressor gene and correlation with disease phenotype Hum Mol Genet 3 1994 595 598
-
(1994)
Hum Mol Genet
, vol.3
, pp. 595-598
-
-
Crossey, P.A.1
Richards, F.M.2
Phipps, M.E.3
-
10
-
-
75549095018
-
Atypical eye changes in four cases of Bourneville's tuberous sclerosis
-
A. DiTizio Atypical eye changes in four cases of Bourneville's tuberous sclerosis Bollettino D'Oculistica 42 1963 32 52
-
(1963)
Bollettino D'Oculistica
, vol.42
, pp. 32-52
-
-
DiTizio, A.1
-
11
-
-
0028219563
-
Gliomas of the anterior visual pathway
-
J.J. Dutton Gliomas of the anterior visual pathway Surv Ophthalmol 38 1994 427 452
-
(1994)
Surv Ophthalmol
, vol.38
, pp. 427-452
-
-
Dutton, J.J.1
-
12
-
-
85119787053
-
Neurofibromatosis 2: Evidence for clincal heterogeneity based on 54 affected individuals studied by MRI with gadolinium, 1987–1991
-
R. Eldridge D. Parry Neurofibromatosis 2: Evidence for clincal heterogeneity based on 54 affected individuals studied by MRI with gadolinium, 1987–1991 Conference Proceedings of the First International Conference on Acoustic Neuroma, Copenhagen, Denmark 1991 Kugler Publications New York
-
(1991)
-
-
Eldridge, R.1
Parry, D.2
-
13
-
-
0000103378
-
European Chromosome 16 Tuberous Sclerosis Consortium: Identification and characterization of the tuberous sclerosis gene on chromsome 16
-
European Chromosome 16 Tuberous Sclerosis Consortium: Identification and characterization of the tuberous sclerosis gene on chromsome 16 Cell 75 1993 1305 1315
-
(1993)
Cell
, vol.75
, pp. 1305-1315
-
-
-
14
-
-
0026746684
-
A clinical study of type 2 neurofibromatosis
-
D.G.R. Evans S.M. Huson D. Donnai A clinical study of type 2 neurofibromatosis QJM 84 1992 603 618
-
(1992)
QJM
, vol.84
, pp. 603-618
-
-
Evans, D.G.R.1
Huson, S.M.2
Donnai, D.3
-
15
-
-
85119815872
-
-
M.R. Gomez Tuberous Sclerosis 1988 Raven Press New York
-
(1988)
-
-
Gomez, M.R.1
-
16
-
-
0012974319
-
Tuberous Sclerosis: Description and report of 12 cases
-
R.D. Harley W.D. Grover Tuberous Sclerosis: Description and report of 12 cases Annals of Ophthalmology 1 1970 477 481
-
(1970)
Annals of Ophthalmology
, vol.1
, pp. 477-481
-
-
Harley, R.D.1
Grover, W.D.2
-
17
-
-
0021358959
-
von Hippel-Lindau disease: A familial, often lethal, multisystem phakomatosis
-
P. Hardwig D.M. Robertson von Hippel-Lindau disease: A familial, often lethal, multisystem phakomatosis Ophthalmology 91 1984 263 269
-
(1984)
Ophthalmology
, vol.91
, pp. 263-269
-
-
Hardwig, P.1
Robertson, D.M.2
-
19
-
-
0028230484
-
Neurofibromatosis type 1: the cognitive phenotype
-
K.J. Hoffman E.L. Harris N. Bryan Neurofibromatosis type 1: the cognitive phenotype J Pediatr 124 suppl 1994 S1 S8
-
(1994)
J Pediatr
, vol.124
, Issue.suppl
, pp. S1-S8
-
-
Hoffman, K.J.1
Harris, E.L.2
Bryan, N.3
-
20
-
-
0025666942
-
Localization of the von Hippel-Lindau disease gene to a small region of chromosome 3
-
S. Hosoe H. Brauch F. Latif Localization of the von Hippel-Lindau disease gene to a small region of chromosome 3 Genomics 8 1990 634 640
-
(1990)
Genomics
, vol.8
, pp. 634-640
-
-
Hosoe, S.1
Brauch, H.2
Latif, F.3
-
21
-
-
0024456038
-
A genetic study of von Recklinghausen neurofibromatosis in south east Wales. Prevalence, fitness, mutation rate, and effect of parental transmission on severity
-
S.M. Huson D.A.S. Compston P. Clark A genetic study of von Recklinghausen neurofibromatosis in south east Wales. Prevalence, fitness, mutation rate, and effect of parental transmission on severity J Med Genet 26 1989 704 711
-
(1989)
J Med Genet
, vol.26
, pp. 704-711
-
-
Huson, S.M.1
Compston, D.A.S.2
Clark, P.3
-
22
-
-
85119794832
-
-
S.M. Huson R.A.C. Hughes The Neurofibromatoses: A Pathogenetic and Clinical Overview 1994 Chapman and Hall London
-
(1994)
-
-
Huson, S.M.1
Hughes, R.A.C.2
-
23
-
-
0025851951
-
Magnetic resonance imaging signs of optic nerve gliomas in neurofibromatosis 1
-
R.K. Imes W.F. Hoyt Magnetic resonance imaging signs of optic nerve gliomas in neurofibromatosis 1 Am J Ophthalmol 111 1991 729 734
-
(1991)
Am J Ophthalmol
, vol.111
, pp. 729-734
-
-
Imes, R.K.1
Hoyt, W.F.2
-
24
-
-
0025313105
-
Analysis of surgical and medical management of glaucoma in Sturge-Weber syndrome
-
A.G. Iwach H.D. Hoskins J. Hetherington Analysis of surgical and medical management of glaucoma in Sturge-Weber syndrome Ophthalmology 97 1990 904 909
-
(1990)
Ophthalmology
, vol.97
, pp. 904-909
-
-
Iwach, A.G.1
Hoskins, H.D.2
Hetherington, J.3
-
25
-
-
0024521939
-
The association of posterior capsular lens opacities with bilateral acoustic neuromas in patients with neurofibromatosis type 2
-
M.I. Kaiser-Kupfer V. Freidlin M.B. Datiles The association of posterior capsular lens opacities with bilateral acoustic neuromas in patients with neurofibromatosis type 2 Arch Ophthalmology 107 1989 541 544
-
(1989)
Arch Ophthalmology
, vol.107
, pp. 541-544
-
-
Kaiser-Kupfer, M.I.1
Freidlin, V.2
Datiles, M.B.3
-
26
-
-
0026779944
-
Ocular findings associated with neurofibromatosis type 2
-
L. Kaye A. Rothner G. Beuchamp Ocular findings associated with neurofibromatosis type 2 Ophthalmology 99 1992 1424 1429
-
(1992)
Ophthalmology
, vol.99
, pp. 1424-1429
-
-
Kaye, L.1
Rothner, A.2
Beuchamp, G.3
-
27
-
-
0022655376
-
Tuberous sclerosis: A clinicoradiological evaluation of 110 cases with particular reference to atypical presentation
-
D.P. Kingsley B.E. Kendall C.R. Fitz Tuberous sclerosis: A clinicoradiological evaluation of 110 cases with particular reference to atypical presentation Neuroradiology 28 1986 38 46
-
(1986)
Neuroradiology
, vol.28
, pp. 38-46
-
-
Kingsley, D.P.1
Kendall, B.E.2
Fitz, C.R.3
-
29
-
-
33645000662
-
Eine familiare hereditare Form von tuberosen Sklerose
-
J. Koenen Eine familiare hereditare Form von tuberosen Sklerose Acta Psychiatr Scand 1 1932 813 821
-
(1932)
Acta Psychiatr Scand
, vol.1
, pp. 813-821
-
-
Koenen, J.1
-
30
-
-
0017687602
-
Depigmented iris sector in tuberous sclerosis
-
G.K. Kranias P.E. Romano Depigmented iris sector in tuberous sclerosis Am J Ophthalmol 83 1977 758 759
-
(1977)
Am J Ophthalmol
, vol.83
, pp. 758-759
-
-
Kranias, G.K.1
Romano, P.E.2
-
31
-
-
0027425657
-
Ocular fundus in neurofibromatosis type 2
-
K. Landau G.M. Yasargil Ocular fundus in neurofibromatosis type 2 Br J Ophthalmol 77 1993 646 649
-
(1993)
Br J Ophthalmol
, vol.77
, pp. 646-649
-
-
Landau, K.1
Yasargil, G.M.2
-
32
-
-
0027240519
-
Identification of the Hippel-Lindau disease tumour suppressor gene
-
F. Latif K. Tory J. Gnarra Identification of the Hippel-Lindau disease tumour suppressor gene Science 260 1993 1317 1320
-
(1993)
Science
, vol.260
, pp. 1317-1320
-
-
Latif, F.1
Tory, K.2
Gnarra, J.3
-
33
-
-
0021220635
-
von Recklinghausen neurofibromatosis: Incidence of optic gliomata
-
R.A. Lewis L.P. Gerson K.A. Axelson von Recklinghausen neurofibromatosis: Incidence of optic gliomata Ophthalmology 91 1984 929 935
-
(1984)
Ophthalmology
, vol.91
, pp. 929-935
-
-
Lewis, R.A.1
Gerson, L.P.2
Axelson, K.A.3
-
34
-
-
0019433931
-
Von Recklinghausen neurofibromatosis: Incidence of iris hamartomas
-
R.A. Lewis V.M. Riccardi Von Recklinghausen neurofibromatosis: Incidence of iris hamartomas Ophthalmology 88 1981 348 354
-
(1981)
Ophthalmology
, vol.88
, pp. 348-354
-
-
Lewis, R.A.1
Riccardi, V.M.2
-
35
-
-
0024517513
-
Optic gliomas in children with neurofibromatosis type 1
-
R. Listernick J. Charrow M. Greenwald Optic gliomas in children with neurofibromatosis type 1 J Pediatr 114 1989 788 792
-
(1989)
J Pediatr
, vol.114
, pp. 788-792
-
-
Listernick, R.1
Charrow, J.2
Greenwald, M.3
-
36
-
-
0026656090
-
Emergence of optic pathway gliomas in children with neurofibromatosis type I after normal neuroimaging results
-
R. Listernick J. Charrow M. Greenwald Emergence of optic pathway gliomas in children with neurofibromatosis type I after normal neuroimaging results J Pediatr 121 1992 584 587
-
(1992)
J Pediatr
, vol.121
, pp. 584-587
-
-
Listernick, R.1
Charrow, J.2
Greenwald, M.3
-
37
-
-
0028304193
-
Natural history of optic pathway tumors in children with neurofibromatosis type 1: A longitudinal study
-
R. Listernick J. Charrow M. Greenwald Natural history of optic pathway tumors in children with neurofibromatosis type 1: A longitudinal study J Pediatr 125 1994 584 587
-
(1994)
J Pediatr
, vol.125
, pp. 584-587
-
-
Listernick, R.1
Charrow, J.2
Greenwald, M.3
-
38
-
-
19144371868
-
A genetic register for von Hippel-Lindau disease
-
I.R. Maddock A. Moran E.R. Maher A genetic register for von Hippel-Lindau disease J Med Genet 33 1996 120 127
-
(1996)
J Med Genet
, vol.33
, pp. 120-127
-
-
Maddock, I.R.1
Moran, A.2
Maher, E.R.3
-
39
-
-
0025000210
-
Clinical features and natural history of von Hippel-Lindau disease
-
E.R. Maher J.R. Yates R. Harries Clinical features and natural history of von Hippel-Lindau disease QJM 77 1990 1151 1163
-
(1990)
QJM
, vol.77
, pp. 1151-1163
-
-
Maher, E.R.1
Yates, J.R.2
Harries, R.3
-
41
-
-
0025816317
-
Mapping of the von Hippel-Lindau disease locus to a small region of chromosome 3p by genetic linkage analysis
-
E.R. Maher E. Bentley J.R.W. Yates Mapping of the von Hippel-Lindau disease locus to a small region of chromosome 3p by genetic linkage analysis Genomics 10 1991 957 960
-
(1991)
Genomics
, vol.10
, pp. 957-960
-
-
Maher, E.R.1
Bentley, E.2
Yates, J.R.W.3
-
42
-
-
0029940856
-
Phenotypic expression in von Hippel-Lindau disease: Correlations with germline VHL gene mutations
-
E.R. Maher A.R. Webster F.M. Richards Phenotypic expression in von Hippel-Lindau disease: Correlations with germline VHL gene mutations J Med Genet 33 1996 328 332
-
(1996)
J Med Genet
, vol.33
, pp. 328-332
-
-
Maher, E.R.1
Webster, A.R.2
Richards, F.M.3
-
44
-
-
0025455386
-
Neurofibromatosis 1 (Recklinghaus disease) and neurofibromatosis 2 (bilateral acoustic neurofibromatosis). An update. (NIH Conference)
-
J.J. Mulvihill D.M. Parry J.I. Sherman Neurofibromatosis 1 (Recklinghaus disease) and neurofibromatosis 2 (bilateral acoustic neurofibromatosis). An update. (NIH Conference) Ann Intern Med 113 1990 39 52
-
(1990)
Ann Intern Med
, vol.113
, pp. 39-52
-
-
Mulvihill, J.J.1
Parry, D.M.2
Sherman, J.I.3
-
45
-
-
0002875040
-
Capillary haemangioma of the retina and von Hippel-Lindau disease
-
D.H. Nicholson Capillary haemangioma of the retina and von Hippel-Lindau disease Retina 1 1994 633 640
-
(1994)
Retina
, vol.1
, pp. 633-640
-
-
Nicholson, D.H.1
-
48
-
-
0027937181
-
Neurofibromatosis 2 (NF 2): Clinical characteristics of 63 affected individuals and clinical evidence for heterogeneity
-
D.M. Parry R. Eldridge M.I. Kaiser-Kupfer Neurofibromatosis 2 (NF 2): Clinical characteristics of 63 affected individuals and clinical evidence for heterogeneity Am J Med Genet 52 1994 450 461
-
(1994)
Am J Med Genet
, vol.52
, pp. 450-461
-
-
Parry, D.M.1
Eldridge, R.2
Kaiser-Kupfer, M.I.3
-
49
-
-
0022893557
-
Eye findings in bilateral acoustic (central) neurofibromatosis: Association with presenile lens opacties and cataract but absence of Lisch nodules
-
M.A. Pearson-Webb M.E. Kaiser-Kupfer R. Eldridge Eye findings in bilateral acoustic (central) neurofibromatosis: Association with presenile lens opacties and cataract but absence of Lisch nodules N Engl J Med 315 1986 1553 1554
-
(1986)
N Engl J Med
, vol.315
, pp. 1553-1554
-
-
Pearson-Webb, M.A.1
Kaiser-Kupfer, M.E.2
Eldridge, R.3
-
50
-
-
0017938941
-
The pathogenesis of glaucoma in Sturge-Weber syndrome
-
C.D. Phelps The pathogenesis of glaucoma in Sturge-Weber syndrome Ophthalmology 85 1978 276 286
-
(1978)
Ophthalmology
, vol.85
, pp. 276-286
-
-
Phelps, C.D.1
-
51
-
-
0028168936
-
Two loci for tuberous sclerosis: One on 9q34 and one on 16p13
-
S. Povey M.W. Burley J. Attwood Two loci for tuberous sclerosis: One on 9q34 and one on 16p13 Ann Hum Genet 58 1994 107 127
-
(1994)
Ann Hum Genet
, vol.58
, pp. 107-127
-
-
Povey, S.1
Burley, M.W.2
Attwood, J.3
-
52
-
-
0028877411
-
Ocular abnormalities in neurofibromatosis 2
-
N.K. Ragge M.E. Baser J. Klein Ocular abnormalities in neurofibromatosis 2 Am J Ophthalmol 120 1995 634 641
-
(1995)
Am J Ophthalmol
, vol.120
, pp. 634-641
-
-
Ragge, N.K.1
Baser, M.E.2
Klein, J.3
-
53
-
-
0025762426
-
Neurofibromatosis: Past, present, and future
-
V.M. Riccardi Neurofibromatosis: Past, present, and future N Engl J Med 324 1991 1283 1285
-
(1991)
N Engl J Med
, vol.324
, pp. 1283-1285
-
-
Riccardi, V.M.1
-
54
-
-
85119788187
-
-
V.M. Riccardi J.E. Eichner Neurofibromatosis: Phenotype, natural history and pathogenesis ed 2 1992 Johns Hopkins University Press Baltimore
-
(1992)
-
-
Riccardi, V.M.1
Eichner, J.E.2
-
56
-
-
0028064856
-
Early diagnosis of optic glioma in children with neurofibromatosis type 1
-
L.N. Rossi G. Pastorino G. Scotti Early diagnosis of optic glioma in children with neurofibromatosis type 1 Childs Nerv Sys 10 1994 426 429
-
(1994)
Childs Nerv Sys
, vol.10
, pp. 426-429
-
-
Rossi, L.N.1
Pastorino, G.2
Scotti, G.3
-
57
-
-
0023204436
-
Genetic linkage of bilateral acoustic neurofibromatosis to a DNA marker on chromosome 22
-
G.A. Rouleau W. Werleleck J.L. Haines Genetic linkage of bilateral acoustic neurofibromatosis to a DNA marker on chromosome 22 Nature 329 1987 246 248
-
(1987)
Nature
, vol.329
, pp. 246-248
-
-
Rouleau, G.A.1
Werleleck, W.2
Haines, J.L.3
-
58
-
-
0028189424
-
Discrete and confluent Lisch nodules in neurofibromatosis type 1
-
S. Saxena R.C. Saxena Discrete and confluent Lisch nodules in neurofibromatosis type 1 Ann Ophthalmol 26 1994 23 24
-
(1994)
Ann Ophthalmol
, vol.26
, pp. 23-24
-
-
Saxena, S.1
Saxena, R.C.2
-
59
-
-
0023865666
-
von Hippel-Lindau disease maps to the region of chromosome 3 associated with renal cell carcinoma
-
B.R. Seizinger G.A. Rouleau L.J. Ozelius von Hippel-Lindau disease maps to the region of chromosome 3 associated with renal cell carcinoma Nature 332 1988 268 269
-
(1988)
Nature
, vol.332
, pp. 268-269
-
-
Seizinger, B.R.1
Rouleau, G.A.2
Ozelius, L.J.3
-
60
-
-
0025872333
-
Genetic flanking markers refine diagnostic criteria and provide insights into the genetics of von Hippel-Lindau disease
-
B.R. Seizinger K.I. Smithe M.R. Filling-Katz Genetic flanking markers refine diagnostic criteria and provide insights into the genetics of von Hippel-Lindau disease Proc Natl Acad Sci U S A 88 1991 2864 2868
-
(1991)
Proc Natl Acad Sci U S A
, vol.88
, pp. 2864-2868
-
-
Seizinger, B.R.1
Smithe, K.I.2
Filling-Katz, M.R.3
-
61
-
-
0026096189
-
Causes of death in patients with tuberous sclerosis
-
C.W. Shepard M.R. Gomez J.T. Lie Causes of death in patients with tuberous sclerosis Mayo Clin Proc 66 1991 792 296
-
(1991)
Mayo Clin Proc
, vol.66
, pp. 792-296
-
-
Shepard, C.W.1
Gomez, M.R.2
Lie, J.T.3
-
63
-
-
0009555847
-
A case of partial epilepsy apparently due to a lesion of one of the vasomotor centres of the brain
-
W.A. Sturge A case of partial epilepsy apparently due to a lesion of one of the vasomotor centres of the brain Trans Clin Soc London 12 1879 162 167
-
(1879)
Trans Clin Soc London
, vol.12
, pp. 162-167
-
-
Sturge, W.A.1
-
65
-
-
0016138059
-
The “tomato-catsup” fundus in Sturge-Weber syndrome
-
J.P. Susac J.L. Smith R.J. Scelfo The “tomato-catsup” fundus in Sturge-Weber syndrome Arch Ophthalmol 92 1974 69 70
-
(1974)
Arch Ophthalmol
, vol.92
, pp. 69-70
-
-
Susac, J.P.1
Smith, J.L.2
Scelfo, R.J.3
-
66
-
-
0038520329
-
Sturge-Weber syndrome. Encephalotrigeminal angiomatosis
-
B.J. Tripathi R.C. Tripathi G.H. Cibis Sturge-Weber syndrome. Encephalotrigeminal angiomatosis D.H. Gold T.A. Wieingist The Eye in Systemic Disease 1990 Lippincott Philadelphia 443 447
-
(1990)
, pp. 443-447
-
-
Tripathi, B.J.1
Tripathi, R.C.2
Cibis, G.H.3
-
67
-
-
0027405720
-
A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor
-
J.A. Trofatter M.M. MacCollin J.L. Rutter A novel moesin-, ezrin-, radixin-like gene is a candidate for the neurofibromatosis 2 tumor suppressor Cell 72 1993 791 800
-
(1993)
Cell
, vol.72
, pp. 791-800
-
-
Trofatter, J.A.1
MacCollin, M.M.2
Rutter, J.L.3
-
68
-
-
0030879277
-
Identification of the tuberous sclerosis gene TSC 1 on chromosome 9q34
-
The TSC Consortium Identification of the tuberous sclerosis gene TSC 1 on chromosome 9q34 Science 277 1997 805 808
-
(1997)
Science
, vol.277
, pp. 805-808
-
-
The TSC Consortium1
-
70
-
-
0000631996
-
Les phacomatoses de Burneville, de Recklinghausen et de von Hippel-Lindau
-
J. van der Hoev Les phacomatoses de Burneville, de Recklinghausen et de von Hippel-Lindau Journal of Belgian Neurology and Psychiatry 33 1933 752 762
-
(1933)
Journal of Belgian Neurology and Psychiatry
, vol.33
, pp. 752-762
-
-
van der Hoev, J.1
-
71
-
-
0025369709
-
Deletions and a transolocation interrupt a cloned gene at the neuofibromatosis type I locus
-
K. Viskochil A.M. Buchberg G. Xu Deletions and a transolocation interrupt a cloned gene at the neuofibromatosis type I locus Cell 62 1990 187 192
-
(1990)
Cell
, vol.62
, pp. 187-192
-
-
Viskochil, K.1
Buchberg, A.M.2
Xu, G.3
-
72
-
-
0004265579
-
Ueber die multiplen fibrome der haut und ihre beziehung zu den multiplen neuromen
-
F. von Recklinghausen Ueber die multiplen fibrome der haut und ihre beziehung zu den multiplen neuromen Festschrift fur Rudolph Virchow 1882 Hirshwald Berlin
-
(1882)
-
-
von Recklinghausen, F.1
-
73
-
-
0015767319
-
Dial origin of glaucoma in encephalotrigeminal haemangiomatosis: A pathogenetic concept based upon histopathologic and haemodynamic consideratons
-
D.I. Weiss Dial origin of glaucoma in encephalotrigeminal haemangiomatosis: A pathogenetic concept based upon histopathologic and haemodynamic consideratons Trans Am Ophthalmol Soc 93 1973 477 493
-
(1973)
Trans Am Ophthalmol Soc
, vol.93
, pp. 477-493
-
-
Weiss, D.I.1
-
74
-
-
0025297599
-
Type I Neurofibromatosis gene: Identification of a large transcript disrupted in three NFI patients
-
M.R. Wallace K.A. Marchuk L.B. Andersen Type I Neurofibromatosis gene: Identification of a large transcript disrupted in three NFI patients Science 249 1990 181 186
-
(1990)
Science
, vol.249
, pp. 181-186
-
-
Wallace, M.R.1
Marchuk, K.A.2
Andersen, L.B.3
-
75
-
-
0014889473
-
von Hippel-Lindau disease
-
R.B. Welch von Hippel-Lindau disease Trans Am Ophthalmol Soc 68 1970 367 371
-
(1970)
Trans Am Ophthalmol Soc
, vol.68
, pp. 367-371
-
-
Welch, R.B.1
-
76
-
-
0022913655
-
von Hippel-Lindau disease: Case report of a patient with spontaneous regression of retinal angioma
-
J.T. Whitson R.B. Welch W.R. Green von Hippel-Lindau disease: Case report of a patient with spontaneous regression of retinal angioma Retina 6 1986 253 259
-
(1986)
Retina
, vol.6
, pp. 253-259
-
-
Whitson, J.T.1
Welch, R.B.2
Green, W.R.3
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