Amanote Research
Register
Sign In
Discover open access scientific publications
Search, annotate, share and cite publications
Publications by Marilda Souza Gonçalves
A C677T Methylenetetrahydrofolate Reductase (MTHFR) Polymorphism and G20210A Mutation in the Prothrombin Gene of Sickle Cell Anemia Patients From Northeast Brazil
Hemoglobin
Biochemistry
Genetics
Clinical Biochemistry
Hematology
Related publications
Serum Homocysteine Levels and Its Methylenetetrahydrofolate Gene (MTHFR) C677t Polymorphism in Patients With Hemodialysis
Journal of Medical Sciences
Medicine
Methylenetetrahydrofolate Reductase C677T Polymorphism and Colorectal Cancer Susceptibility: A Meta-Analysis
Bioscience Reports
Biochemistry
Cell Biology
Molecular Biology
Biophysics
Investigation of MTHFR Gene C677T Polymorphism in Cardiac Syndrome X Patients
Journal of Clinical Laboratory Analysis
Allergy
Immunology
Biochemistry
Public Health
Medical Laboratory Technology
Clinical Biochemistry
Hematology
Microbiology
Environmental
Occupational Health
The 844ins68 Cystathionine Beta-Synthase and C677T MTHFR Gene Polymorphism and the Vaso-Occlusive Event Risk in Sickle Cell Disease
Archives of Medical Science
Medicine
Serum Homocysteine, Vitamin B12, Folic Acid Levels and Methylenetetrahydrofolate Reductase (MTHFR) Gene Polymorphism in Vitiligo
Disease Markers
Biochemistry
Medicine
Clinical Biochemistry
Molecular Biology
Genetics
Meta-Analysis of the Methylenetetrahydrofolate Reductase C677T Polymorphism and Susceptibility to Pre-Eclampsia
Hypertension Research
Internal Medicine
Cardiovascular Medicine
Physiology
Cardiology
Clinical Significance of Prothrombin G20210A Mutation in Homozygous Patients
American Journal of Hematology
Hematology
Polymorphism of Methylenetetrahydrofolate Reductase Gene (C677T MTHFR) Is Not a Confounding Factor of the Relationship Between Serum Uric Acid Level and the Prevalence of Hypertension in Japanese Men
Circulation Journal
Medicine
Cardiovascular Medicine
Cardiology
Methylenetetrahydrofolate Reductase C677T and A1298C Polymorphism in Iranian Women With Idiopathic Recurrent Pregnancy Losses
Iranian Red Crescent Medical Journal
Medicine