INTERMITTENT ATAXIA AND BIOCHEMICAL DISORDERS-Reference-Cited by-同舟云学术

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INTERMITTENT ATAXIA AND BIOCHEMICAL DISORDERS

Published:2008-11-12 Issue:2 Volume:15 Page:208-210
ISSN:0012-1622
Container-title:Developmental Medicine & Child Neurology
language:en
Short-container-title:

Author:

Gordon Neil

Publisher

Wiley

Subject

Neurology (clinical),Developmental Neuroscience,Pediatrics, Perinatology and Child Health

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1469-8749.1973.tb15164.x/fullpdf

Reference10 articles.

1. The new approach to early diagnosis of handicaps in childhood;Ingram;Developmental Medicine and Child Neurology,1969

2. Hereditary pellagra-like skin rash with temporary cerebellar ataxia, constant renal amino-aciduria and other bizarre chemical features;Baron;Lancet,1956

3. Intermittent branched-chain ketoaciduria. Variant of maple-syrup-urine disease;Dancis;New England Journal of Medicine,1967

4. Thiamine-responsive progressive maple-syrup-urine disease;Scriver;Lancet,1971

5. Genetical theory and the “inborn error of metabolism”;Harris;British Medical Journal,1970

Cited by 2 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Recurrent Ataxia in Children and Adolescents;Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques;2017-01-03

2. Autosomal dominant recurrent encephalopathy of childhood;American Journal of Medical Genetics;1983-05

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