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Publications by D. Osei-Hyiaman
Association of a Novel Point Mutation (C159G) of the CTLA4 Gene With Type 1 Diabetes in West Africans but Not in Chinese
Diabetes
Internal Medicine
Endocrinology
Metabolism
Diabetes
Related publications
Remapping the Type I Diabetes Association of the CTLA4 Locus
Genes and Immunity
Immunology
Genetics
A Novel Dominant Mutation in the SOX10 Gene in a Chinese Family With Waardenburg Syndrome Type�II
Molecular Medicine Reports
Oncology
Genetics
Molecular Biology
Biochemistry
Cancer Research
Molecular Medicine
Association of 2184AG Polymorphism in the RAGE Gene With Diabetic Nephropathy in Chinese Patients With Type 2 Diabetes
Journal of Diabetes Research
Endocrinology
Metabolism
Diabetes
A Point Mutation in the Albumin Gene in a Chinese Patient With Familial Dysalbuminemic Hyperthyroxinemia
European Journal of Endocrinology
Medicine
Endocrinology
Metabolism
Diabetes
Sex-Specific Association of PTPN22 1858T With Type 1 Diabetes but Not With Hashimoto's Thyroiditis or Addison's Disease in the German Population
European Journal of Endocrinology
Medicine
Endocrinology
Metabolism
Diabetes
Ehlers-Danlos Syndrome Type IV, Vascular Type, Which Demonstrated a Novel Point Mutation in the COL3A1 Gene
Internal Medicine
Internal Medicine
Medicine
C-Peptide Persistence in Type 1 Diabetes: ‘Not Drowning, but Waving’?
BMC Medicine
Medicine
Association of a Serotonin Transporter Gene (SLC6A4) 5-HTTLPR Polymorphism With Body Mass Index Categories but Not Type 2 Diabetes Mellitus in Mexicans
Genetics and Molecular Biology
Genetics
Molecular Biology
A Novel Compound Heterozygous Mutation of the AIRE Gene in a Patient With Autoimmune Polyendocrine Syndrome Type 1
Annals of Pediatric Endocrinology and Metabolism
Child Health
Endocrinology
Perinatology
Pediatrics
Metabolism
Diabetes
