Familial central nervous system neoplasia. Case report of a family with von Recklinghausen's neurofibromatosis.

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作者信息

Lee D K, Abbott M L

出版信息

Arch Neurol. 1969 Feb;20(2):154-60. doi: 10.1001/archneur.1969.00480080054006.

DOI:10.1001/archneur.1969.00480080054006

PMID:4975015

Abstract

摘要

相似文献

Familial central nervous system neoplasia. Case report of a family with von Recklinghausen's neurofibromatosis.

Arch Neurol. 1969 Feb;20(2):154-60. doi: 10.1001/archneur.1969.00480080054006.

A family with coexistent von Recklinghausen's neurofibromatosis and von Hippel-Lindau's disease. Diseases possibly derived from a common gene.一个同时患有冯·雷克林霍增氏神经纤维瘤病和冯·希佩尔－林道病的家族。这两种疾病可能源自同一个共同基因。

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Von Hippel's disease in association with von Recklinghausen's neurofibromatosis.冯·希佩尔病与冯·雷克林豪森神经纤维瘤病相关。

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Oftalmol Zh. 1978(6):473-6.

[Von Recklinghausen's neurofibromatosis and pregnancy. Apropos of a case].

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Germ-line mutations in the neurofibromatosis 2 gene: correlations with disease severity and retinal abnormalities.神经纤维瘤病2基因的种系突变：与疾病严重程度及视网膜异常的相关性

Am J Hum Genet. 1996 Sep;59(3):529-39.

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A genetic study of type 2 neurofibromatosis in the United Kingdom. I. Prevalence, mutation rate, fitness, and confirmation of maternal transmission effect on severity.英国2型神经纤维瘤病的遗传学研究。I. 患病率、突变率、适合度以及母系遗传对严重程度影响的确认。

J Med Genet. 1992 Dec;29(12):841-6. doi: 10.1136/jmg.29.12.841.

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