Lysosomal Acid Lipase Mutations That Determine Phenotype in Wolman and Cholesterol Ester Storage Disease

By Anderson R.A.   Bryson G.M.   Parks J.S.  

Molecular Genetics and Metabolism, Vol. 68, Iss. 3, 1999-11 ,pp. : 333-345

Academic Press

Access to resources Recommend Favorite

The Variable Presentations of Glycogen Storage Disease Type IV: A Review of Clinical, Enzymatic and Molecular Studies

By  

Current Molecular Medicine, Vol. 2, Iss. 2, 2002-03 ,pp. : 177-188

Bentham Science Publishers

Access to resources Recommend Favorite

Chediak-Higashi Syndrome: a Clinical and Molecular View of a Rare Lysosomal Storage Disorder

By  

Current Molecular Medicine, Vol. 2, Iss. 5, 2002-08 ,pp. : 469-477

Bentham Science Publishers

Access to resources Recommend Favorite

Increasing High-Density Lipoprotein Cholesterol Through Cholesteryl Ester Transfer Protein Inhibition: A Next Step in the Fight Against Cardiovascular Disease?

By  

Current Drug Targets - Cardiovascular & Hematological Disorders, Vol. 5, Iss. 6, 2005-12 ,pp. : 481-488

Bentham Science Publishers

Access to resources Recommend Favorite

Molecular Characterization of a Novel Endonuclease (Xib) and Possible Involvement in Lysosomal Glycogen Storage Disorders

By Malferrari G.   Mazza U.   Tresoldi C.   Rovida E.   Nissim M.   Mirabella M.   Servidei S.   Biunno I.  

Experimental and Molecular Pathology, Vol. 66, Iss. 2, 1999-06 ,pp. : 123-130

Elsevier

Access to resources Recommend Favorite