Hereditary defect of cobalamin metabolism (homocystinuria and methylmalonic aciduria) of juvenile onset

被引：26

作者：

Gold, R

Bogdahn, U

Kappos, L

Toyka, KV

Baumgartner, ER

Fowler, B

Wendel, U

机构：

[1] UNIV BASEL,CHILDRENS HOSP,BASEL,SWITZERLAND

[2] UNIV DUSSELDORF,DEPT PAEDIAT,DUSSELDORF,GERMANY

来源：

JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY | 1996年 / 60卷 / 01期

关键词：

D O I：

10.1136/jnnp.60.1.107

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

引用

收藏

页码：107 / 108

页数：2

相关论文

共 6 条

[1] ADAMS RD, 1993, PRINCIPLES NEUROLOGY, P864
[2] BAUMGARTNER ER, 1983, METHODS HEMATOLOGY, P181
[3] HEREDITARY DEFECT OF COBALAMIN METABOLISM (CBLG MUTATION) PRESENTING AS A NEUROLOGIC DISORDER IN ADULTHOOD
CARMEL, R
WATKINS, D
GOODMAN, SI
ROSENBLATT, DS
[J]. NEW ENGLAND JOURNAL OF MEDICINE, 1988, 318 (26) : 1738 - 1741
[4] FENTON WA, 1989, METABOLIC BASIS INHE, P2065
[5] ROSENBERG LE, 1989, METABOLIC BASIS INHE, P821
[6] COBALAMIN-C MUTATION (METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA) IN ADOLESCENCE - A TREATABLE CAUSE OF DEMENTIA AND MYELOPATHY
SHINNAR, S
SINGER, HS
[J]. NEW ENGLAND JOURNAL OF MEDICINE, 1984, 311 (07) : 451 - 454