Transcobalamin codon 259 polymorphism in HT-29 and Caco-2 cells and in Caucasians: relation to transcobalamin and homocysteine concentration in blood

Farès Namour, Jean‐Luc Olivier, Idrissia Abdelmouttaleb, +4

Blood

High prevalence of hyperhomocysteinemia related to folate deficiency and the 677C→T mutation of the gene encoding methylenetetrahydrofolate reductase in coastal West Africa

Emile Amouzou, Nicodème Chabi, Charles Adjalla, +5

American Journal of Clinical Nutrition

GeneticsInherited Metabolic DiseaseGenetic EpidemiologyCoastal West AfricaMethylenetetrahydrofolate Reductase +2

Alcoholic Cirrhosis and Cobalamin Metabolism

D Lambert, S. Benhayoun, Charles Adjalla, +8

Digestion

Identification of vitamin B12 and analogues by high- performance capillary electrophoresis and comparison with high-performance liquid chromatography

D Lambert, Charles Adjalla, F. Felden, +3

Journal of Chromatography A

Capillary ElectrophoresisBiochemistryGas ChromatographyMedicineBioanalysis +9

Association of MTRR A66G polymorphism (but not of MTHFR C677T and A1298C, MTR A2756G, TCN C776G) with homocysteine and coronary artery disease in the French population

Yves Juillière, M. Candito, Charles Adjalla, +5

Thrombosis and Haemostasis

Increased C-reactive protein levels in patients with in-stent restenosis and its implications

Michaël Angioı̈, Idrissia Abdelmouttaleb, Rosa-Maria Rodriguez, +4

The American Journal of Cardiology

InflammationMetabolic SyndromeVascular DiseaseCardiovascular DiseaseAtherosclerosis +9

Crohn's disease and vitamin B12 metabolism

Daniel Lambert, S. Benhayoun, Charles Adjalla, +8

Digestive Diseases and Sciences

InflammationNutritionImmunologyGastroenterologyPathology +4

Seven novel mutations inmut methylmalonic aciduria

Charles Adjalla, Angela Hosack, Brian M. Gilfix, +6

Human Mutation

Hyperhomocysteinemia Is Related to Residual Glomerular Filtration and Folate, but not to Methylenetetrahydrofolate-Reductase and Methionine Synthase Polymorphisms, in Supplemented End-Stage Renal Disease Patients Undergoing Hemodialysis

Jean-Louis Guéant, Idrissia Abdelmouttaleb, Charles Adjalla, +5

Clinical Chemistry and Laboratory Medicine (CCLM)

Renal PathologyMethionine Synthase PolymorphismsCystatin CResidual Glomerular FiltrationGlomerulonephritis +14

A common mutation among blacks with mut− methylmalonic aciduria

Charles Adjalla, Angela Hosack, Nora V. Matiaszuk, +1

Human Mutation

Common MutationGenetic DisorderGeneticsGenetic EpidemiologyHuman Polymorphism +1