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    Research 151–180 of 1000+

    1. Msx2 deficiency in mice causes pleiotropic defects in bone growth and ectodermal organ formation Nature genetics · 2000 · 694 citations
    2. Erosive pustular dermatosis of the scalp: challenges and solutions Clinical, Cosmetic and Investigational Dermatology · 2019 · 13 citations
    3. Valproate‐associated hair abnormalities: Pathophysiology and management strategies Human Psychopharmacology: Clinical and Experimental · 2021 · 2 citations
    4. Utility of trichoscopy in comparison to the standard methods for assessing the disease activity, severity, and therapeutic response in alopecia areata Cosmoderma · 2023 · 1 citations
    5. ALOPECIA FEMININA: UMA ABORDAGEM INTEGRADA DO DIAGNÓSTICO AO MANEJO TERAPÊUTICO Aracê. · 2026
    6. Importancia de la pseudopelada de Brocq en la práctica de la medicina estética capilar Medicina Estética Revista Científica de la Sociedad Española de Medicina Estética (SEME) · 2024
    7. An ancestral recipe of “Champigny Saumure” to be used tepid by topical way could be useful to combat Patton-Lynch’s Erosive pustular dermatosis of the scalp Our Dermatology Online · 2023
    8. Clinical and dermoscopic patterns of childhood alopecia areata in a tertiary care centre in North India International journal of research in dermatology · 2021
    9. An overview of scalp dermatoses in a tertiary care institute International Journal of Research in Dermatology · 2020
    10. Do we need hair follicle stem cells and hair follicle neogenesis to cure common hair loss disorders? Hair transplant forum international · 2008 · 3 citations
    11. Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters European Journal of Human Genetics · 2023 · 1 citations
    12. An overview on congenital alopecia in domestic animals Veterinary dermatology · 2006 · 32 citations
    13. Hair transplantation between identical twins Journal of The American Academy of Dermatology · 1988 · 1 citations
    14. Congenital Triangular Alopecia (Brauer Nevus) Pediatric Dermatology · 1995 · 34 citations
    15. Encephalocraniocutaneous lipomatosis: congenital alopecia treatment in a rare neurocutaneous syndrome Journal of Plastic Surgery and Hand Surgery · 2013 · 4 citations
    16. T Cell Immunodeficiency, Congenital Alopecia, and Nail Dystrophy 2022
    17. FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches Journal of clinical immunology · 2017 · 33 citations
    18. A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2 Revista Paulista de Pediatria · 2023
    19. Genetic Defects of Female Sexual Differentiation Elsevier eBooks · 2016
    20. Delayed Diagnosis of Ectopic Thyroid Due to Ignored Borderline Result of Newborn Screening for Congenital Hypothyroidism American Journal of Case Reports · 2025
    21. Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities Neuropediatrics · 2012
    22. FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program Frontiers in Immunology · 2013 · 69 citations
    23. FOXN1 deficient nude severe combined immunodeficiency Orphanet journal of rare diseases · 2017 · 32 citations
    24. Mammalian-specific ectodermal enhancers control the expression of <i>Hoxc</i> genes in developing nails and hair follicles Proceedings of the National Academy of Sciences · 2020 · 25 citations
    25. Teratogenic effect of isotretinoin in both fertile females and males (Review) Experimental and Therapeutic Medicine · 2021 · 19 citations
    26. Hepatitis C‐related mixed type vitiligo in a patient with Ivemark syndrome The Journal of Dermatology · 2014 · 1 citations
    27. Delayed Puberty Springer eBooks · 2016
    28. SUN-287 A Case of Ectopic Neurohypophysis Journal of the Endocrine Society · 2020
    29. Perosomus elumbus fetal monster: a rare cause of dystocia in a beetal goat - a case report from Pakistan Journal of Animal Reproduciton and Biotechnology · 2024
    30. Mesenchymal cell replacement corrects thymic hypoplasia in murine models of 22q11.2 deletion syndrome Journal of Clinical Investigation · 2022 · 9 citations