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Research 631–660 of 1000+
- A Comprehensive Review on Alopecia: Mechanisms, Classification, and Therapeutic Strategies
- Polycystic Ovary Syndrome: A Complex Interplay of Hormones and Metabolism
- A Rare Case of Acrodermatitis Enteropathica in a One Year Old Child
- Red Blood Cells Folate Level in Patients with Alopecia Areata
- Inborn Errors of Metabolism
- Trichothiodystrophy: Current Concepts
- A combination of low-dose systemic etretinate and topical calcipotriol/betamethasone dipropionate treatment for hyperkeratosis and itching in Olmsted syndrome associated with a TRPV3 mutation
- Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations
- Novel and recurrent mutations in the <i>AIRE</i> gene of autoimmune polyendocrinopathy syndrome type 1 (APS1) patients
- Down Syndrome and Autoimmune Disease
- Dermoscopy: A rapid bedside tool to assess monilethrix
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Case report: Acrodermatitis enteropathica result from a novel SLC39A4 gene mutation
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Twenty-Five and Up (25Up) Study: A New Wave of the Brisbane Longitudinal Twin Study
- Surgical approach of ectropion in lamellar ichthyosis
- Skin Pigmentation Types, Causes and Treatment—A Review
- Pseudoxanthoma Elasticum: Progress in Research Toward Treatment: Summary of the 2012 PXE International Research Meeting
- Analysis of breast health outcomes in women on oral 5-alpha reductase inhibitors: A single-center retrospective cohort study
- Polycystic Ovary Syndrome: Clinical Presentation, Diagnostic Challenges, and Evolving Management Approaches
- Weeping Wound, Disgruntled Gut and Fading Hunger: Acrodermatitis Enteropathica in an Infant
- THE MULTIFACETED APPROACH TO POLYCYSTIC OVARIAN SYNDROME: A REVIEW OF TRADITIONAL AND ALLOPATHIC MEDICINE
- An updated review on acne
- Netherton Syndrome
- Contents Vol. 2, 2016
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Exome analysis for Cronkhite-Canada syndrome: A case report
- ODP408 Elevated DHEAS and Acute Hair Loss in an Adult Male with Trichorhinophalangeal Syndrome Type 1: a Case of Male PCOS
- Polycystic ovary syndrome
- Generalized Vitiligo Associated Autoimmune Diseases in Japanese Patients Their Families