-
1
-
-
0019741677
-
Translation of case reports in Ueber die multiplen Fibrome der Haut und ihre Beziehung zu den multiplen Neuromen by F. v. Recklinghausen
-
Crump T. Translation of case reports in Ueber die multiplen Fibrome der Haut und ihre Beziehung zu den multiplen Neuromen by F. v. Recklinghausen [in Japanese]. Adv Neurol 1981;29:259-75.
-
(1981)
Adv Neurol
, vol.29
, pp. 259-275
-
-
Crump, T.1
-
2
-
-
0343596166
-
Veder "Centrale" Neurofibromatose und die Geschwulste-des Kleinhirnbruckenwinkels (acusticusneuromc)
-
Henneberg, Koch M: Veder "Centrale" Neurofibromatose und die Geschwulste-des Kleinhirnbruckenwinkels (acusticusneuromc). Arch Psychiatrie 1902;36:251.
-
(1902)
Arch Psychiatrie
, vol.36
, pp. 251
-
-
Henneberg1
Koch, M.2
-
3
-
-
0023885121
-
Neurofibromatosis
-
Conference Statement. National Institutes of Health Consensus Development Conference. Neurofibromatosis. Arch Neurol 1988;45:575-8.
-
(1988)
Arch Neurol
, vol.45
, pp. 575-578
-
-
-
4
-
-
0023244033
-
Gene for von Recklinghausen neurofibromatosis is in the pericentromereic region of chromosome 17
-
Barker D, Wright E, Nguyen K, et al. Gene for von Recklinghausen neurofibromatosis is in the pericentromereic region of chromosome 17. Science 1987;236:1100-2.
-
(1987)
Science
, vol.236
, pp. 1100-1102
-
-
Barker, D.1
Wright, E.2
Nguyen, K.3
-
5
-
-
0023204436
-
Genetic linkage of bilateral acoustic neurofibromatosis to a DNA marker on chromosome 22
-
Rouleau GA, Wertelecki W, Haines JL, et al. Genetic linkage of bilateral acoustic neurofibromatosis to a DNA marker on chromosome 22. Nature 1987;329:246-8.
-
(1987)
Nature
, vol.329
, pp. 246-248
-
-
Rouleau, G.A.1
Wertelecki, W.2
Haines, J.L.3
-
6
-
-
0019761388
-
Central neurofibromatosis with bilateral acoustic neuroma
-
Eldridge R. Central neurofibromatosis with bilateral acoustic neuroma. Adv Neurol 1981;29:57-65.
-
(1981)
Adv Neurol
, vol.29
, pp. 57-65
-
-
Eldridge, R.1
-
7
-
-
0023854155
-
Neurofibromatosis 2 (bilateral acoustic neurofibromatosis)
-
Martuza RL, Eldridge R. Neurofibromatosis 2 (bilateral acoustic neurofibromatosis). N Engl J Med 1988;318:684-8.
-
(1988)
N Engl J Med
, vol.318
, pp. 684-688
-
-
Martuza, R.L.1
Eldridge, R.2
-
8
-
-
0027937181
-
Neurofibromatosis 2 (NF2): Clinical characteristics of 63 affected individuals and clinical evidence for heterogeneity
-
Parry DM, Eldridge R, Kaiser-Kupfer MI, et al. Neurofibromatosis 2 (NF2): clinical characteristics of 63 affected individuals and clinical evidence for heterogeneity. Am J Med Genet 1994;52:450-61.
-
(1994)
Am J Med Genet
, vol.52
, pp. 450-461
-
-
Parry, D.M.1
Eldridge, R.2
Kaiser-Kupfer, M.I.3
-
9
-
-
0022893557
-
Eye findings in bilateral acoustic (central) neurofibromatosis: Association with presenile lens opacities and cataracts but absence of Lisch nodules
-
Pearson-Webb MA, Kaiser-Kupfer MI, Eldridge R. Eye findings in bilateral acoustic (central) neurofibromatosis: association with presenile lens opacities and cataracts but absence of Lisch nodules [letter]. N Engl J Med 1986;315:1553-4.
-
(1986)
N Engl J Med
, vol.315
, pp. 1553-1554
-
-
Pearson-Webb, M.A.1
Kaiser-Kupfer, M.I.2
Eldridge, R.3
-
10
-
-
0024521939
-
The association of posterior capsular lens opacities with bilateral acoustic neuromas in patients with neurofibromatosis type 2
-
Kaiser-Kupfer MI, Freidlin V, Datiles MB, et al. The association of posterior capsular lens opacities with bilateral acoustic neuromas in patients with neurofibromatosis type 2. Arch Ophthalmol 1989;107:541-4.
-
(1989)
Arch Ophthalmol
, vol.107
, pp. 541-544
-
-
Kaiser-Kupfer, M.I.1
Freidlin, V.2
Datiles, M.B.3
-
11
-
-
0025455386
-
NIH Conference. Neurofibromatosis 1 (Recklinghausen disease) and neurofibromatosis 2 (bilateral acoustic neurofibromatosis)
-
Mulvihill JJ, Parry DM, Sherman JL, et al. NIH Conference. Neurofibromatosis 1 (Recklinghausen disease) and neurofibromatosis 2 (bilateral acoustic neurofibromatosis). Ann Intern Med 1990;113:39-52.
-
(1990)
Ann Intern Med
, vol.113
, pp. 39-52
-
-
Mulvihill, J.J.1
Parry, D.M.2
Sherman, J.L.3
-
12
-
-
0026779944
-
Ocular findings associated with neurofibromatosis type II
-
Kaye LD, Rothner AD, Beauchamp GR, et al. Ocular findings associated with neurofibromatosis type II. Ophthalmology 1992;99:1424-9.
-
(1992)
Ophthalmology
, vol.99
, pp. 1424-1429
-
-
Kaye, L.D.1
Rothner, A.D.2
Beauchamp, G.R.3
-
13
-
-
0027425657
-
Ocular fundus in neurofibromatosis type 2
-
Landau K, Yasargil GM. Ocular fundus in neurofibromatosis type 2. Br J Ophthalmol 1993;77:646-9.
-
(1993)
Br J Ophthalmol
, vol.77
, pp. 646-649
-
-
Landau, K.1
Yasargil, G.M.2
-
15
-
-
0028877411
-
Ocular abnormalities in neurofibromatosis 2
-
Ragge NK, Baser ME, Klein J, et al. Ocular abnormalities in neurofibromatosis 2. Am J Ophthalmol 1995;120:634-41.
-
(1995)
Am J Ophthalmol
, vol.120
, pp. 634-641
-
-
Ragge, N.K.1
Baser, M.E.2
Klein, J.3
-
16
-
-
0017550023
-
Café-au-lait spots of the fundus in neurofibromatosis
-
Cotlier E. Café-au-lait spots of the fundus in neurofibromatosis. Arch Ophthalmol 1977;95:1990-3.
-
(1977)
Arch Ophthalmol
, vol.95
, pp. 1990-1993
-
-
Cotlier, E.1
-
18
-
-
0026763196
-
Familial occurrence of combined pigment epithelial and retinal hamartomas associated with neurofibromatosis 2
-
Bouzas EA, Parry DM, Eldridge R, Kaiser-Kupfer MI. Familial occurrence of combined pigment epithelial and retinal hamartomas associated with neurofibromatosis 2. Retina 1992;12:103-7.
-
(1992)
Retina
, vol.12
, pp. 103-107
-
-
Bouzas, E.A.1
Parry, D.M.2
Eldridge, R.3
Kaiser-Kupfer, M.I.4
-
19
-
-
0025984832
-
Combined hamartoma of the retina and retinal pigment epithelium in a patient with neurofibromatosis type 2
-
Sivalingam A, Augsburger J, Perilongo G, et al. Combined hamartoma of the retina and retinal pigment epithelium in a patient with neurofibromatosis type 2. J Pediatr Ophthalmol Strabismus 1991;28:320-2.
-
(1991)
J Pediatr Ophthalmol Strabismus
, vol.28
, pp. 320-322
-
-
Sivalingam, A.1
Augsburger, J.2
Perilongo, G.3
-
20
-
-
0029774092
-
Germline mutations in the neurofibromatosis 2 gene: Correlations with disease severity and retinal abnormalities
-
Parry DM, MacCollin MM, Kaiser-Kupfer MI, et al. Germline mutations in the neurofibromatosis 2 gene: correlations with disease severity and retinal abnormalities. Am J Hum Genet 1996;59:529-39.
-
(1996)
Am J Hum Genet
, vol.59
, pp. 529-539
-
-
Parry, D.M.1
MacCollin, M.M.2
Kaiser-Kupfer, M.I.3
-
22
-
-
0030248107
-
Blindness, deafness, quadriparesis, and a retinal malformation: The ravages of neurofibromatosis 2
-
Rettele GA, Brodsky MC, Merin LM, et al. Blindness, deafness, quadriparesis, and a retinal malformation: the ravages of neurofibromatosis 2. Surv Ophthalmol 1996;41:135-41.
-
(1996)
Surv Ophthalmol
, vol.41
, pp. 135-141
-
-
Rettele, G.A.1
Brodsky, M.C.2
Merin, L.M.3
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