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    Research 181–210 of 1000+

    1. Alymphoid cystic thymic dysgenesis - FOXN1 gene mutation: a rare case report of two siblings International journal of contemporary pediatrics · 2020
    2. Clinical Case Notes. Castleman's disease of the lacrimal gland Clinical and Experimental Ophthalmology · 2004 · 9 citations
    3. FOXN1 deficient nude severe combined immunodeficiency Orphanet journal of rare diseases · 2017 · 32 citations
    4. Gene detection in a family with monilethrix and treatment with 5% topical minoxidil Skin research and technology · 2022 · 2 citations
    5. Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness 2021
    6. Ichthyosis and Trichothiodystrophy: the Tay and PIBI(D)S Syndromes 1989 · 2 citations
    7. Ectodermal Dysplasia: Variable Expressions Indian Journal of Dermatology · 2025
    8. Hypotrichosis with juvenile macular dystrophy International Journal of Trichology · 2018 · 4 citations
    9. Werner′s syndrome Indian Journal of Dermatology Venereology and Leprology · 2012 · 5 citations
    10. PLACK syndrome associated with alopecia areata and a novel homozygous base pair insertion in exon 18 of CAST gene Indian Journal of Dermatology Venereology and Leprology · 2023 · 2 citations
    11. S3507 GI Bleed Leading to Discovery of Hereditary Hemochromatosis The American Journal of Gastroenterology · 2020
    12. A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report Revista Paulista de Pediatria · 2024 · 2 citations
    13. Erythromelanosis follicularis faciei et colli with reticulated hyperpigmentation of the extremities Clinical case reports · 2017 · 3 citations
    14. Frontal Alopecia after Repeated Botulinum Toxin Type A Injections for Forehead Wrinkles: An Underestimated Entity? Skin appendage disorders · 2016 · 12 citations
    15. Trichoscopy in Hair Shaft Disorders Dermatologic Clinics · 2018 · 36 citations
    16. Hair shaft disorders IP Indian Journal of Clinical and Experimental Dermatology · 2025
    17. Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome Genes · 2019 · 20 citations
    18. To grow or not to grow: Hair morphogenesis and human genetic hair disorders Seminars in Cell & Developmental Biology · 2013 · 43 citations
    19. Ichthyosis in Unani Medicine: A Comprehensive Review of Disorders of Cornification and their Modern Dermatological Correlates International Journal of Science and Research (IJSR) · 2026
    20. Hair shaft disorders: a rare case series International journal of research in dermatology · 2022
    21. Role of trichoscopy in diagnosis of different hair and scalp disorders in pediatrics International Journal of Dermatology Venereology and Leprosy Sciences · 2024
    22. Dermatoscopy of hair shaft disorders Journal of the American Academy of Dermatology · 2012 · 68 citations
    23. Mimicking Hair Disorders by Genetic Manipulation of Organ-Cultured Human Hair Follicles Journal of Investigative Dermatology · 2012 · 5 citations
    24. Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders 2012 · 1 citations
    25. Disorders of the skin appendages John Wiley & Sons, Ltd eBooks · 2016
    26. Disorders of hair in children Current Paediatrics · 2003
    27. Non-Neoplastic Disorders of Hair Elsevier eBooks · 2010
    28. MENSTRUAL DISORDERS IN ADOLESCENTS Pediatric Clinics of North America · 1999 · 75 citations
    29. Congenital hair loss disorders: Rare, but not too rare The Journal of Dermatology · 2011 · 41 citations
    30. Adrenal Disorders and the Paediatric Brain: Pathophysiological Considerations and Clinical Implications International Journal of Endocrinology · 2014 · 38 citations