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Literature DB >> 3150233

Cognitive development in children with inborn errors of urea synthesis.

M Msall, P S Monahan, N Chapanis, M L Batshaw.

Abstract

Entities: Disease Species

Mesh：

Substances：
Urea

Year: 1988 PMID： 3150233 DOI： 10.1111/j.1442-200x.1988.tb02534.x

Source DB: PubMed Journal: Acta Paediatr Jpn ISSN： 0374-5600

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Cited

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24 in total

1. Behavioural and emotional problems, intellectual impairment and health-related quality of life in patients with organic acidurias and urea cycle disorders.

Authors: Dagmar Jamiolkowski; Stefan Kölker; Esther M Glahn; Ivo Barić; Jiri Zeman; Matthias R Baumgartner; Chris Mühlhausen; Angels Garcia-Cazorla; Florian Gleich; Gisela Haege; Peter Burgard
Journal: J Inherit Metab Dis Date: 2015-08-27 Impact factor: 4.982

2. Ornithine transcarbamylase deficiency with persistent abnormality in cerebral glutamate metabolism in adults.

Authors: Andrea L Gropman; Napapon Sailasuta; Kent C Harris; Osama Abulseoud; Brian D Ross
Journal: Radiology Date: 2009-06-30 Impact factor: 11.105

Review 3. Brain imaging in urea cycle disorders.

Authors: Andrea Gropman
Journal: Mol Genet Metab Date: 2010-02-13 Impact factor: 4.797

4. Diffusion tensor imaging detects areas of abnormal white matter microstructure in patients with partial ornithine transcarbamylase deficiency.

Authors: A L Gropman; B Gertz; K Shattuck; I L Kahn; R Seltzer; L Krivitsky; J Van Meter
Journal: AJNR Am J Neuroradiol Date: 2010-05-20 Impact factor: 3.825

Review 5. Advances in urea cycle neuroimaging: Proceedings from the 4th International Symposium on urea cycle disorders, Barcelona, Spain, September 2013.

Authors: Ileana Pacheco-Colón; Stanley Fricke; John VanMeter; Andrea L Gropman
Journal: Mol Genet Metab Date: 2014-05-20 Impact factor: 4.797

Review 10. Profiling of astrocyte properties in the hyperammonaemic brain: shedding new light on the pathophysiology of the brain damage in hyperammonaemia.

Authors: U Lichter-Konecki
Journal: J Inherit Metab Dis Date: 2008-08-09 Impact factor: 4.982

Cognitive development in children with inborn errors of urea synthesis.

1. Behavioural and emotional problems, intellectual impairment and health-related quality of life in patients with organic acidurias and urea cycle disorders.

2. Ornithine transcarbamylase deficiency with persistent abnormality in cerebral glutamate metabolism in adults.

Review 3. Brain imaging in urea cycle disorders.

4. Diffusion tensor imaging detects areas of abnormal white matter microstructure in patients with partial ornithine transcarbamylase deficiency.

Review 5. Advances in urea cycle neuroimaging: Proceedings from the 4th International Symposium on urea cycle disorders, Barcelona, Spain, September 2013.

Review 6. A longitudinal study of urea cycle disorders.

Review 7. Recurrent encephalopathy: NAGS (N-acetylglutamate synthase) deficiency in adults.

8. 1H MRS identifies symptomatic and asymptomatic subjects with partial ornithine transcarbamylase deficiency.

9. Intellectual, adaptive, and behavioral functioning in children with urea cycle disorders.

Review 10. Profiling of astrocyte properties in the hyperammonaemic brain: shedding new light on the pathophysiology of the brain damage in hyperammonaemia.