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Publications by M. Huda
Correction To: Adipokines and the Insulin Resistance Syndrome in Familial Partial Lipodystrophy Caused by a Mutation in Lamin a/C
Diabetologia
Internal Medicine
Endocrinology
Metabolism
Diabetes
Related publications
Familial Partial Lipodystrophy Type 3: A New Mutation on the PPARG Gene
Hormones
Medicine
Endocrinology
Metabolism
Diabetes
Electrophysiological and Histopathological Characteristics of Progressive Atrioventricular Block Accompanied by Familial Dilated Cardiomyopathy Caused by a Novel Mutation of Lamin a/C Gene
Journal of Cardiovascular Electrophysiology
Cardiovascular Medicine
Physiology
Cardiology
Obstructive Sleep Apnea in 2 Women With Familial Partial Lipodystrophy Due to a Heterozygous LMNA R482Q Mutation
CMAJ
Medicine
Familial Scaphocephaly Syndrome Caused by a Novel Mutation in the FGFR2 Tyrosine Kinase Domain
Journal of Medical Genetics
Genetics
Effectiveness of Insulin Pump Therapy in a Patient With Familial Partial Lipodystrophy of Dunnigan Type
Journal of Diabetes & Metabolism
LIPE-related Familial Partial Lipodystrophy
Familial Partial Lipodystrophy, Köbberling Type
CIDEC-related Familial Partial Lipodystrophy
Familial Partial Lipodystrophy Type 3 Due to PPARgamma Mutation: Presentation With Diabetes and Severe Hypertriglyceridemia
Endocrine Abstracts
