Disorders of the degradation of branched chain amino acids: What is new in clinics and laboratories?

ISSN： 0141-8955

Source： Journal of Inherited Metabolic Disease, Vol.35, Iss.1, 2012-01, pp. : 1-1

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

Enzymology of the branched-chain amino acid oxidation disorders: the valine pathway

By Wanders Ronald

Journal of Inherited Metabolic Disease, Vol. 35, Iss. 1, 2012-01 ,pp. : 5-12

Springer Publishing Company

Access to resources Recommend Favorite

Catabolism of Branched-Chain Amino Acids in Heart Failure: Insights from Genetic Models

By Sun Haipeng

Pediatric Cardiology, Vol. 32, Iss. 3, 2011-03 ,pp. : 305-310

Springer Publishing Company

Access to resources Recommend Favorite

Advances and challenges in the treatment of branched-chain amino/keto acid metabolic defects

By Knerr Ina

Journal of Inherited Metabolic Disease, Vol. 35, Iss. 1, 2012-01 ,pp. : 29-40

Springer Publishing Company

Access to resources Recommend Favorite

Treatment with amino acids in serine deficiency disorders

By de Koning T.

Journal of Inherited Metabolic Disease, Vol. 29, Iss. 2-3, 2006-04 ,pp. : 347-351

Springer Publishing Company

Access to resources Recommend Favorite

Long-Chain Polyunsaturated Fatty Acids

Neonatology, Vol. 74, Iss. 2, 1998-07 ,pp. : 106-120

Karger

Access to resources Recommend Favorite