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    Research 31–60 of 1000+

    1. Trichodystrophies: A hair-raising differential diagnosis Clinics in Dermatology · 2015 · 1 citations
    2. Hirsutism: diagnosis and treatment Arquivos Brasileiros De Endocrinologia E Metabologia · 2014 · 26 citations
    3. Genetics of Structural Hair Disorders Journal of Investigative Dermatology · 2012 · 17 citations
    4. HAIR AND SYSTEMATIC DISEASE Dermatologic Clinics · 2001 · 58 citations
    5. Association of Topical Minoxidil With Autosomal Recessive Woolly Hair/Hypotrichosis Caused by <i>LIPH</i> Pathogenic Variants JAMA Dermatology · 2020 · 5 citations
    6. Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex The American Journal of Human Genetics · 2012 · 39 citations
    7. The Genetics of Human Skin Disease Cold Spring Harbor Perspectives in Medicine · 2014 · 24 citations
    8. Diseases of Periocular Hair Survey of Ophthalmology · 2011 · 7 citations
    9. A KRT71 Loss-of-Function Variant Results in Inner Root Sheath Dysplasia and Recessive Congenital Hypotrichosis of Hereford Cattle Genes · 2021 · 2 citations
    10. Genetic Hair Disorders: A Review Dermatology and Therapy · 2019 · 26 citations
    11. More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players Journal of Investigative Dermatology · 2006 · 35 citations
    12. A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient Journal of Dermatological Science · 2009 · 13 citations
    13. Clinical Case Notes. Castleman's disease of the lacrimal gland Clinical and Experimental Ophthalmology · 2004 · 9 citations
    14. Hair shaft disorders in children – An update Indian Dermatology Online Journal · 2023 · 12 citations
    15. Congenital hypotrichosis due to short anagen British Journal of Dermatology · 2000 · 42 citations
    16. Short anagen syndrome Journal of The American Academy of Dermatology · 2005 · 37 citations
    17. Deficient Plakophilin-1 Expression Due to a Mutation in PKP1 Causes Ectodermal Dysplasia-Skin Fragility Syndrome in Chesapeake Bay Retriever Dogs PLoS ONE · 2012 · 28 citations
    18. Do you know this syndrome? * Você conhece esta síndrome? * 2006
    19. Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family Acta Scientific Paediatrics · 2023
    20. Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14 Frontiers in Medicine · 2026
    21. Diagnosis and treatment of isolated autosomal recessive woolly hair/hypotrichosis Frontiers in Medicine · 2025
    22. Clinical Case Notes. Retinoblastoma, microphthalmia and the chromosome 13q deletion syndrome Clinical and Experimental Ophthalmology · 2004 · 6 citations
    23. Hair loss in infancy and childhood Paediatrics and Child Health · 2014 · 1 citations
    24. Telogen Effluvium: A Review Journal of Clinical and Diagnostic Research · 2015 · 70 citations
    25. Madarosis Survey of Ophthalmology · 2006 · 33 citations
    26. Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses Archives of Dermatology · 2001 · 23 citations
    27. Hair loss and its management in children Expert Review of Dermatology · 2011 · 5 citations
    28. Male fertility and skin diseases Reviews in Endocrine and Metabolic Disorders · 2016 · 12 citations
    29. Canine alopecia X-Like disorder Brazilian Journal of Veterinary Pathology · 2024
    30. Alopecia and its association with coronary heart disease and cardiovascular risk factors: A meta-analysis International Journal of Cardiology · 2014 · 48 citations