Literature DB >> 24627279

Stroke as a rare manifestation of classical citrullinemia.

Ankur Singh1, Seema Kapoor, Nitin Maheshwari.   

Abstract

Entities:  

Mesh：

Year:  2014        PMID： 24627279     DOI： 10.1007/s12098-014-1373-z

Source DB:  PubMed          Journal:  Indian J Pediatr        ISSN： 0019-5456            Impact factor:   1.967


× No keyword cloud information.
  5 in total

1.  Mutation analysis of Indian patients with urea cycle defects.

Authors:  Neerja Gupta; Madhulika Kabra; J Häberle
Journal:  Indian Pediatr       Date:  2012-07       Impact factor: 1.411

2.  Two cases of citrullinaemia presenting with stroke.

Authors:  J H Choi; H Kim; H W Yoo
Journal:  J Inherit Metab Dis       Date:  2006-02       Impact factor: 4.982

3.  Acute extrapyramidal syndrome in mild ornithine transcarbamylase deficiency: metabolic stroke involving the caudate and putamen without metabolic decompensation.

Authors:  C E Keegan; D M Martin; D J Quint; J L Gorski
Journal:  Eur J Pediatr       Date:  2003-02-07       Impact factor: 3.183

4.  Heterogeneity of mutations in argininosuccinate synthetase causing human citrullinemia.

Authors:  K Kobayashi; M J Jackson; D B Tick; W E O'Brien; A L Beaudet
Journal:  J Biol Chem       Date:  1990-07-05       Impact factor: 5.157

5.  Neuropathology of propionic acidemia: a report of two patients with basal ganglia lesions.

Authors:  R L Hamilton; R H Haas; W L Nyhan; H C Powell; M R Grafe
Journal:  J Child Neurol       Date:  1995-01       Impact factor: 1.987
  5 in total
  1 in total

1.  Hyperammonemic Encephalopathy in an Adolescent Patient of Citrullinemia Type 1 With an Atypical Presentation.

Authors:  Samir Ruxmohan; Jonathan Quinonez; Jinal Choudhari; Sujan Poudel; Krunal Pandav
Journal:  Cureus       Date:  2021-05-19
  1 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.