Urinary Lactate Excretion to Monitor the Efficacy of Treatment of Type I Glycogen Storage Disease

Author： Hagen T.   Korson M.S.   Wolfsdorf J.I.  

Publisher： Academic Press

ISSN： 1096-7192

Source： Molecular Genetics and Metabolism, Vol.70, Iss.3, 2000-07, pp. : 189-195

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

Molecular Genetics of Type 1 Glycogen Storage Disease

By Janecke A.R.   Mayatepek E.   Utermann G.  

Molecular Genetics and Metabolism, Vol. 73, Iss. 2, 2001-06 ,pp. : 117-125

Academic Press

Access to resources Recommend Favorite

Late-Onset Glycogen Storage Disease Type 2

By  

Current Molecular Medicine, Vol. 14, Iss. 8, 2014-09 ,pp. : 971-978

Bentham Science Publishers

Access to resources Recommend Favorite

Molecular Characterization of Glycogen Storage Disease Type III

By  

Current Molecular Medicine, Vol. 2, Iss. 2, 2002-03 ,pp. : 167-175

Bentham Science Publishers

Access to resources Recommend Favorite

Type I Glycogen Storage Diseases: Disorders of the Glucose-6- Phosphatase Complex

By  

Current Molecular Medicine, Vol. 2, Iss. 2, 2002-03 ,pp. : 121-143

Bentham Science Publishers

Access to resources Recommend Favorite

Molecular Genetics of Glycogen-Storage Disease Type 1a in Chinese Patients of Taiwan

By Wong L-J.C.   Hwu W-L.   Dai P.   Chen T-J.  

Molecular Genetics and Metabolism, Vol. 72, Iss. 2, 2001-02 ,pp. : 175-180

Academic Press

Access to resources Recommend Favorite