Partial response to biotin therapy in a patient with holocarboxylase synthetase deficiency: clinical, biochemical, and molecular genetic aspects

By Santer R.   Muhle H.   Suormala T.   Baumgartner E.R.   Duran M.   Yang X.   Aoki Y.   Suzuki Y.   Stephani U.  

Molecular Genetics and Metabolism, Vol. 79, Iss. 3, 2003-07 ,pp. : 160-166

Elsevier

Access to resources Recommend Favorite

Sialuria in a Portuguese Girl: Clinical, Biochemical, and Molecular Characteristics

By Ferreira H.   Seppala R.   Pinto R.   Huizing M.   Martins E.   Braga A.C.   Gomes L.   Krasnewich D.M.   Sa Miranda M.C.   Gahl W.A.  

Molecular Genetics and Metabolism, Vol. 67, Iss. 2, 1999-06 ,pp. : 131-137

Academic Press

Access to resources Recommend Favorite

Molecular and Genetic Mechanisms of Obesity: Implications for Future Management

By  

Current Molecular Medicine, Vol. 3, Iss. 4, 2003-06 ,pp. : 325-340

Bentham Science Publishers

Access to resources Recommend Favorite

Hereditary erythrocyte pyrimidine 5′-nucleotidase deficiency: A biochemical, genetic and clinical overview

By Chiarelli Laurent R.   Fermo Elisa   Zanella Alberto   Valentini Giovanna  

Hematology, Vol. 11, Iss. 1, 2006-02 ,pp. : 67-72

Maney Publishing

Access to resources Recommend Favorite

Biochemical, Enzymatic and Molecular Properties of Renin/Prorenin Mediated by (Pro)Renin Receptor

By  

Immunology, Endocrine & Metabolic Agents in Medicinal Chemistry (Formerly Current Medicinal Chemistry - Immunology, Endocrine and Metabolic Agents), Vol. 12, Iss. 1, 2012-03 ,pp. : 53-63

Bentham Science Publishers

Access to resources Recommend Favorite