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Research 9
- Metreleptin Treatment in a Boy with Congenital Generalized Lipodystrophy due to Homozygous c.465_468delGACT (p.T156Rfs*8) Mutation in the BSCL2 Gene: Results From the First-year
- Berardinelli–Seip syndrome
- Progressive Metabolic Dysfunction-Associated Steatotic Liver Disease (MASLD) from a Young Age Due to a Rare Genetic Disorder, Familial Partial Lipodystrophy: A Case Report and Review of the Literature
- How to diagnose a lipodystrophy syndrome
- Rabson-Mendenhall syndrome: two case reports and a brief review of the literature
- Oxidative Stress in Alopecia Areata and its Association with Disease Severity, Treatment and Autoimmunity
- 2014 Female Athlete Triad Coalition Consensus Statement on Treatment and Return to Play of the Female Athlete Triad: 1st International Conference held in San Francisco, California, May 2012 and 2nd International Conference held in Indianapolis, Indiana, May 2013
- Where Have the Periods Gone? The Evaluation and Management of Functional Hypothalamic Amenorrhea
- Dunnigan-Type Familial Partial Lipodystrophy: Understanding and Treating the Syndrome