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    Research 91–120 of 1000+

    1. The expanding significance of keratin intermediate filaments in normal and diseased epithelia Current opinion in cell biology · 2012 · 186 citations
    2. Cantú Syndrome Is Caused by Mutations in ABCC9 The American Journal of Human Genetics · 2012 · 148 citations
    3. Is thyrotropin-releasing hormone a novel neuroendocrine modulator of keratin expression in human skin? British Journal of Dermatology · 2013 · 10 citations
    4. Alopecia in children Clinics in Dermatology · 2000 · 7 citations
    5. Novel small‐insertion mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis Journal of dermatology · 2020 · 1 citations
    6. Hairless: A nuclear receptor corepressor essential for skin function Advances in developmental biology · 2006
    7. Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome Orphanet Journal of Rare Diseases · 2011 · 71 citations
    8. Polycystic Ovary Syndrome and NC-CAH: Distinct Characteristics and Common Findings. A Systematic Review Frontiers in Endocrinology · 2019 · 32 citations
    9. Hirsutism in Children: A Comprehensive Review of Etiology, Clinical Evaluation and Contemporary Management World Journal of Biology Pharmacy and Health Sciences · 2025 · 1 citations
    10. 7745 Hirsutism in young girls, Beyond PCOS Journal of the Endocrine Society · 2024
    11. Congenital Hair Anomaly in Association with Hypodontia of Permanent Teeth: A Quiz Acta dermato-venereologica · 2020
    12. An Approach to the Patient With Hirsutism Obstetrical & gynecological survey · 2013
    13. Steroidogenesis of the testis – new genes and pathways Annales d'endocrinologie · 2014 · 70 citations
    14. Clinical and molecular genetic studies in hereditary hair loss 2021
    15. Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle Scientific Reports · 2011 · 9 citations
    16. Atrichia congenita with papular lesions: A rare cause of pediatric alopecia TURKDERM · 2025
    17. Hair Shaft Disorders CRC Press eBooks · 2021
    18. Molecular basis of congenital atrichia in humans and mice. PubMed · 1999 · 15 citations
    19. ODP398 A Novel NR5A1 Gene Mutation Causing 46, XY DSD Without Adrenal Insufficiency in an Immigrant Boy from Dominican Republic Journal of the Endocrine Society · 2022
    20. An Update of Congenital Adrenal Hyperplasia Annals of the New York Academy of Sciences · 2004 · 151 citations
    21. Congenital Adrenal Hyperplasia IntechOpen eBooks · 2022
    22. A syndrome of congenital ichthyosis, mental retardation, myopathy and anemia in dizygotic twin sisters 2012
    23. Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families The Journal of Dermatology · 2011 · 11 citations
    24. Congenital Atrichia: A Case Report International journal of science and healthcare research · 2023
    25. The hairless (hr) gene is involved in the congential hypotrichosis of Valle del Belice sheep Agritrop (Cirad) · 2002
    26. Plasma levels of C19 steroid glucuronides in pre-menopausal women with non-classical congenital adrenal hyperplasia 1992 · 7 citations
    27. A newborn presenting with congenital blistering International Journal of Dermatology · 2004 · 7 citations
    28. ALOPECIA TRIANGULAR CONGÉNITA BILATERAL EN UN NEONATO: REPORTE DE CASO LA CIENCIA AL SERVICIO DE LA SALUD Y NUTRICIÓN · 2024
    29. Epidermal dysplasia and <i>Malassezia</i> infection in two West Highland White Terrier siblings: an inherited skin disorder or reaction to severe <i>Malassezia</i> infection? Veterinary dermatology · 2001 · 17 citations
    30. Clinical report of a Holstein's calf with ichthyosis. Veterinary research forum · 2021