Hypocomplementemic Type II Membranoproliferative Glomerulonephritis in a Male Patient with Familial Lecithin-Cholesterol Acyltransferase Deficiency due to Two Different Allelic Mutations

Publisher： Karger

E-ISSN： 2235-3186|88|3|268-272

ISSN： 1660-8151

Source： Nephron, Vol.88, Iss.3, 2001-06, pp. : 268-272

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

Familial Lecithin:Cholesterol Acyltransferase Deficiency with Renal Failure in Two Siblings

By  

Nephron, Vol. 81, Iss. 1, 1999-01 ,pp. : 89-93

Karger

Access to resources Recommend Favorite

Marked Atherosclerosis in a Patient with Familiar Lecithin: Cholesterol Acyltransferase Deficiency Associated with End-Stage Renal Disease and Diabetes Mellitus

By  

American Journal of Nephrology, Vol. 21, Iss. 5, 2001-10 ,pp. : 415-419

Karger

Access to resources Recommend Favorite

Cyclosporin A Treatment for Membranoproliferative Glomerulonephritis Type II

By  

Nephron, Vol. 91, Iss. 3, 2002-07 ,pp. : 509-511

Karger

Access to resources Recommend Favorite

Membranoproliferative Glomerulonephritis Associated with Hypocomplementemic Urticarial Vasculitis after Complete Remission of Membranous Nephropathy

By  

Nephron, Vol. 88, Iss. 2, 2001-05 ,pp. : 174-177

Karger

Access to resources Recommend Favorite

Membranoproliferative Glomerulonephritis Type I, Mixed Cryoglobulinemia and Lymphoma in the Absence of Hepatitis C Infection

By  

American Journal of Nephrology, Vol. 19, Iss. 5, 1999-11 ,pp. : 599-604

Karger

Access to resources Recommend Favorite