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

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

By Sass Jörn  

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

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

Niemann–Pick disease type C and defective peroxisomal &bgr;-oxidation of branched-chain substrates

By Sequeira J.S.S.   Vellodi A.   vanier M.T.   Clayton P.T.  

Journal of Inherited Metabolic Disease, Vol. 21, Iss. 2, 1998-04 ,pp. : 149-154

Springer Publishing Company

Access to resources Recommend Favorite

Mitochondrial fatty acid oxidation disorders: clinical presentation of long-chain fatty acid oxidation defects before and after newborn screening

By Spiekerkoetter Ute  

Journal of Inherited Metabolic Disease, Vol. 33, Iss. 5, 2010-10 ,pp. : 527-532

Springer Publishing Company

Access to resources Recommend Favorite