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research Decision Letter: Human Biallelic MFN2 Mutations Induce Mitochondrial Dysfunction, Upper Body Adipose Hyperplasia, and Suppression of Leptin Expression

January 2017

MFN2 mutations cause mitochondrial problems, unusual fat distribution, and low leptin despite high body fat.

research Dunnigan-Type Familial Partial Lipodystrophy: Understanding and Treating the Syndrome

January 2017 in “Open Journal of Endocrine and Metabolic Diseases”

The document concludes that managing Dunnigan-Type Familial Partial Lipodystrophy involves treating associated health issues and using medications like metformin and leptin replacement.

research Protein Profiling of Forehead Epidermal Corneocytes Distinguishes Frontal Fibrosing From Androgenetic Alopecia

March 2023 in “PLOS ONE”

Protein profiling of forehead skin can help distinguish between frontal fibrosing alopecia and androgenetic alopecia.

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