Ornithine aminotransferase deficiency: Diagnostic difficulties in neonatal presentation

Author： Cleary M.   Dorland L.   Koning T.   Poll-The B.   Duran M.   Mandell R.   Shih V.   Berger R.   Olpin S.   Besley G.  

Publisher： Springer Publishing Company

ISSN： 0141-8955

Source： Journal of Inherited Metabolic Disease, Vol.28, Iss.5, 2005-09, pp. : 673-679

Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Previous Menu Next

Abstract

Related content

Fatal presentation of ornithine transcarbamylase deficiency in a 62-year-old man and family studies

By Rohininath T.   Costello D. J.   Lynch T.   Monavari A.   Tuchman M.   Treacy E. P.  

Journal of Inherited Metabolic Disease, Vol. 27, Iss. 2, 2004-01 ,pp. : 285-288

Springer Publishing Company

Access to resources Recommend Favorite

Ornithine transcarbamylase deficiency in pregnancy

By Cordero D.   Baker J.   Dorinzi D.   Toffle R.  

Journal of Inherited Metabolic Disease, Vol. 28, Iss. 2, 2005-04 ,pp. : 237-240

Springer Publishing Company

Access to resources Recommend Favorite

LATE ONSET ORNITHINE TRANSCARBAMYLASE DEFICIENCY: A CASE REPORT

By Fessatou S.  

Pediatric Pathology & Molecular Medicine, Vol. 22, Iss. 2, 2003-03 ,pp. : 153-157

Informa Healthcare

Access to resources Recommend Favorite

Factor V Deficiency: A Subtle Presentation

By Sanklecha Mukesh   Sundaresan Suba   Charde Vivek  

The Indian Journal of Pediatrics, Vol. 81, Iss. 3, 2014-03 ,pp. : 283-284

Springer Publishing Company

Access to resources Recommend Favorite

How reliable is the allopurinol load in detecting carriers for ornithine transcarbamylase deficiency?

By Grünewald S.   Fairbanks L.   Genet S.   Cranston T.   Hüsing J.   Leonard J. V.   Champion M. P.  

Journal of Inherited Metabolic Disease, Vol. 27, Iss. 2, 2004-01 ,pp. : 179-186

Springer Publishing Company

Access to resources Recommend Favorite