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Publications by J. Oshima
A Novel LMNA Mutation Causes Altered Nuclear Morphology and Symptoms of Familial Partial Lipodystrophy (Dunnigan Variety) With Progeroid Features
Molecular Syndromology
Genetics
Related publications
Obstructive Sleep Apnea in 2 Women With Familial Partial Lipodystrophy Due to a Heterozygous LMNA R482Q Mutation
CMAJ
Medicine
Effectiveness of Insulin Pump Therapy in a Patient With Familial Partial Lipodystrophy of Dunnigan Type
Journal of Diabetes & Metabolism
Familial Partial Lipodystrophy Type 3: A New Mutation on the PPARG Gene
Hormones
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Endocrinology
Metabolism
Diabetes
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
Evaluation of Epicardial Adipose Tissue in Familial Partial Lipodystrophy
Diabetology and Metabolic Syndrome
Internal Medicine
Endocrinology
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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