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    Research 631–660 of 1000+

    1. Inborn Errors of Metabolism Pediatrics in review · 2009 · 3 citations
    2. Male androgenetic alopecia Human health handbooks · 2012 · 1 citations
    3. A Comprehensive Review on Alopecia: Mechanisms, Classification, and Therapeutic Strategies Zenodo (CERN European Organization for Nuclear Research) · 2026
    4. A Rare Case of Acrodermatitis Enteropathica in a One Year Old Child Journal of evolution of medical and dental sciences · 2020
    5. Trichothiodystrophy: Current Concepts Journal of Cutaneous Medicine and Surgery · 1996 · 5 citations
    6. Atypical Progeroid Syndrome due to Heterozygous Missense LMNA Mutations 2009 · 115 citations
    7. Down Syndrome and Autoimmune Disease Clinical Reviews in Allergy & Immunology · 2024 · 14 citations
    8. 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 Journal of dermatological science · 2017 · 5 citations
    9. Novel and recurrent mutations in the <i>AIRE</i> gene of autoimmune polyendocrinopathy syndrome type 1 (APS1) patients Clinical genetics · 2009 · 26 citations
    10. Twenty-Five and Up (25Up) Study: A New Wave of the Brisbane Longitudinal Twin Study Twin research and human genetics · 2019 · 18 citations
    11. Skin Pigmentation Types, Causes and Treatment—A Review Molecules · 2023 · 138 citations
    12. Pseudoxanthoma Elasticum: Progress in Research Toward Treatment: Summary of the 2012 PXE International Research Meeting 2013 · 46 citations
    13. Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix Journal of Investigative Dermatology · 1999 · 20 citations
    14. Analysis of breast health outcomes in women on oral 5-alpha reductase inhibitors: A single-center retrospective cohort study Journal of the American Academy of Dermatology · 2024 · 6 citations
    15. A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies 2022 · 2 citations
    16. THE MULTIFACETED APPROACH TO POLYCYSTIC OVARIAN SYNDROME: A REVIEW OF TRADITIONAL AND ALLOPATHIC MEDICINE International Journal for Research Trends and Innovation · 2025
    17. Case report: Acrodermatitis enteropathica result from a novel SLC39A4 gene mutation Frontiers in pediatrics · 2022
    18. Contents Vol. 2, 2016 Skin appendage disorders · 2016
    19. Surgical approach of ectropion in lamellar ichthyosis Journal of The American Academy of Dermatology · 2010
    20. Dermoscopy: A rapid bedside tool to assess monilethrix Indian journal of dermatology, venereology, and leprology · 2015 · 11 citations
    21. Polycystic Ovary Syndrome: Clinical Presentation, Diagnostic Challenges, and Evolving Management Approaches International Journal for Research in Applied Science and Engineering Technology · 2026
    22. Weeping Wound, Disgruntled Gut and Fading Hunger: Acrodermatitis Enteropathica in an Infant Cureus · 2025
    23. An updated review on acne World Journal of Biology Pharmacy and Health Sciences · 2023
    24. Netherton Syndrome Harper's Textbook of Pediatric Dermatology · 2019
    25. Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis 2022 · 6 citations
    26. Polycystic ovary syndrome The Lancet · 2007 · 989 citations
    27. Generalized Vitiligo Associated Autoimmune Diseases in Japanese Patients Their Families Allergology International · 2011 · 81 citations
    28. Using the zebrafish lateral line to uncover novel mechanisms of action and prevention in drug-induced hair cell death Frontiers in Cellular Neuroscience · 2015 · 34 citations
    29. Hair and Nail Relationship Skinmed · 2005 · 21 citations
    30. Type 1 Diabetes Mellitus and Autoimmune Diseases: A Critical Review of the Association and the Application of Personalized Medicine Journal of Personalized Medicine · 2023 · 12 citations