The Common Mutations C677T and A1298C in the Human Methylenetetrahydrofolate Reductase Gene Are Associated with Hyperhomocysteinemia and Cardiovascular Disease in Hemodialysis Patients

Publisher： Karger

E-ISSN： 2235-3186|92|1|120-126

ISSN： 1660-8151

Source： Nephron, Vol.92, Iss.1, 2002-08, pp. : 120-126

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

Methylenetetrahydrofolate Reductase Gene Polymorphism, Hyperhomocysteinemia, and Cardiovascular Diseases in Chronic Hemodialysis Patients

By  

Nephron, Vol. 90, Iss. 1, 2001-12 ,pp. : 43-50

Karger

Access to resources Recommend Favorite

Methylenetetrahydrofolate Reductase Gene C677T Polymorphism, Plasma Homocysteine and Folate in End-Stage Renal Disease Dialysis and Non-Dialysis Patients

By  

Nephron, Vol. 92, Iss. 1, 2002-08 ,pp. : 235-239

Karger

Access to resources Recommend Favorite

Urinary Tract Anomalies Associated with MTHFR Gene Polymorphism C677T in Girls

By  

Kidney and Blood Pressure Research, Vol. 34, Iss. 6, 2011-08 ,pp. : 465-471

Karger

Access to resources Recommend Favorite

Polymorphism in Methylenetetrahydrofolate Reductase Gene: Its Impact on Plasma Homocysteine Levels and Carotid Atherosclerosis in ESRD Patients Receiving Hemodialysis

By  

Nephron, Vol. 87, Iss. 3, 2001-03 ,pp. : 249-256

Karger

Access to resources Recommend Favorite

Lower Hydrogen Sulfide Is Associated with Cardiovascular Mortality, Which Involves cPKCβII/Akt Pathway in Chronic Hemodialysis Patients

By  

Blood Purification, Vol. 40, Iss. 3, 2015-0 ,pp. : 260-269

Karger

Access to resources Recommend Favorite