Literature DB >> 5948649

Homocystinuria. A recently discovered cause of mental defect and cerebrovascular thrombosis.

H G Dunn, T L Perry, C L Dolman.   

Abstract

Entities:  

Mesh:

Substances:

Year:  1966        PMID: 5948649     DOI: 10.1212/wnl.16.4.407

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


× No keyword cloud information.
  15 in total

1.  Intracranial venous thrombosis.

Authors:  M Parsons
Journal:  Postgrad Med J       Date:  1967-06       Impact factor: 2.401

Review 2.  The skin in genetically-controlled metabolic disorders.

Authors:  P C Newbold
Journal:  J Med Genet       Date:  1973-06       Impact factor: 6.318

3.  Detection of heterozygotes for homocystinuria. Study of sulphur-containing amino acids in plasma and urine after L-methionine loading.

Authors:  I B Sardharwalla; B Fowler; A J Robins; G M Komrower
Journal:  Arch Dis Child       Date:  1974-07       Impact factor: 3.791

4.  Skeletal fingings in homocystinuria: a collaborative study.

Authors:  H Schedewie; E Willich; H Gröbe; H Schmidt; K M Müller
Journal:  Pediatr Radiol       Date:  1973-03

5.  Iherited abnormalities affecting the nervous system: genetic and psychiatric aspects.

Authors:  J Stern; V Cowie
Journal:  Biochem J       Date:  1969-02       Impact factor: 3.857

6.  Homocystinuria.

Authors:  N A Carson
Journal:  Proc R Soc Med       Date:  1970-01

Review 7.  Hyperhomocysteinaemia; with reference to its neuroradiological aspects.

Authors:  M van den Berg; M S van der Knaap; G H Boers; C D Stehouwer; J A Rauwerda; J Valk
Journal:  Neuroradiology       Date:  1995-07       Impact factor: 2.804

8.  Homocystinuria and dystonia.

Authors:  P Davous; P Rondot
Journal:  J Neurol Neurosurg Psychiatry       Date:  1983-03       Impact factor: 10.154

9.  Improved identification of heterozygotes for homocystinuria due to cystathionine synthase deficiency by the combination of methionine loading and enzyme determination in cultured fibroblasts.

Authors:  G H Boers; B Fowler; A G Smals; F J Trijbels; A I Leermakers; W J Kleijer; P W Kloppenborg
Journal:  Hum Genet       Date:  1985       Impact factor: 4.132

10.  Arachnodactyly, aminoaciduria, congenital cataracts, cerebellar ataxia, and delayed developmental milestones.

Authors:  P A Bhaskar; K Jagannathan; K Valmikinathan
Journal:  J Neurol Neurosurg Psychiatry       Date:  1974-12       Impact factor: 10.154

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.