Long-term outcomes in Ornithine Transcarbamylase deficiency: a series of 90 patients-Reference-Cited by-同舟云学术

Long-term outcomes in Ornithine Transcarbamylase deficiency: a series of 90 patients

Published:2015-05-10 Issue:1 Volume:10 Page:
ISSN:1750-1172
Container-title:Orphanet Journal of Rare Diseases
language:en
Short-container-title:Orphanet J Rare Dis

Author:

Brassier Anais,Gobin Stephanie,Arnoux Jean Baptiste,Valayannopoulos Vassili,Habarou Florence,Kossorotoff Manoelle,Servais Aude,Barbier Valerie,Dubois Sandrine,Touati Guy,Barouki Robert,Lesage Fabrice,Dupic Laurent,Bonnefont Jean Paul,Ottolenghi Chris,De Lonlay Pascale

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),Genetics(clinical),General Medicine

Link

http://link.springer.com/content/pdf/10.1186/s13023-015-0266-1.pdf

Reference32 articles.

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2. Keskinen P, Siitonen A, Salo M. Hereditary urea cycle diseases in Finland. Acta Paediatr. 2008;97:1412–9.

3. Gordon N. Ornithine transcarbamylase deficiency: a urea cycle defect. Eur J Paediatr Neurol EJPN Off J Eur Paediatr Neurol Soc. 2003;7:115–21.

4. Wraith JE. Ornithine carbamoyltransferase deficiency. Arch Dis Child. 2001;84:84–8.

5. Nicolaides P, Liebsch D, Dale N, Leonard J, Surtees R. Neurological outcome of patients with ornithine carbamoyltransferase deficiency. Arch Dis Child. 2002;86:54–6.

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