Concepedia

The variant methylenetetrahydrofolate reductase c.1298A>C (p.E429A) is associated with multiple sclerosis in a German case-control study

Luisa Klotz, Melinda Farkas, Nadja Bain, Salla Keskitalo, A. Semmler, Benjamin Victor Ineichen, Thomas Klockgether, Heike Kölsch, Michael Weller, Michael Linnebank

Neuroscience Letters · 2009 · 29 citations · 9 references

DOI

Concepts

References

9

Diagnostic criteria for multiple sclerosis: 2010 Revisions to the McDonald criteria

Chris H. Polman, Stephen C. Reingold, Brenda Banwell et al. · Annals of Neurology · 2011 · 9.8K citations · Full text

, , +10

Risk Alleles for Multiple Sclerosis Identified by a Genomewide Study

New England Journal of Medicine · 2007 · 1.7K citations

, , +17

A Second Common Mutation in the Methylenetetrahydrofolate Reductase Gene: An Additional Risk Factor for Neural-Tube Defects?

N.M.J. van der Put, F. Gabreëls, E M Stevens et al. · The American Journal of Human Genetics · 1998 · 1.6K citations · Full text

, , +17

Association of demyelination with deficiency of cerebrospinal-fluid S-adenosylmethionine in inborn errors of methyl-transfer pathway

R. Surtees, J. Leonard, Stephanie Austin · The Lancet · 1991 · 234 citations

, , +15

Plasma homocysteine levels in multiple sclerosis

G. S. M. Ramsaransing · Journal of Neurology Neurosurgery & Psychiatry · 2006 · 107 citations · Full text

, , +11