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    Research 541–570 of 1000+

    1. Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements Journal of Human Genetics · 2016 · 30 citations
    2. Familial frontal fibrosing alopecia: A cross‐sectional study of 20 cases from nine families Australasian Journal of Dermatology · 2018 · 8 citations
    3. A Comprehensive Review on Alopecia: Mechanisms, Classification, and Therapeutic Strategies Zenodo (CERN European Organization for Nuclear Research) · 2026
    4. Non-surgical treatments for androgenetic alopecia: a literature review Zenodo (CERN European Organization for Nuclear Research) · 2023
    5. Alopecia Totalis/Universalis Springer eBooks · 2018
    6. КЛІНІЧНІ ФЕНОТИПИ ВИСОКОГО РИЗИКУ НАЯВНОСТІ ПЕРВИННИХ МІТОХОНДРІАЛЬНИХ ЦИТОПАТІЙ (частина 2) The Scientific Issues of Ternopil Volodymyr Hnatiuk National Pedagogical University Series pedagogy · 2025
    7. Ulcerative colitis and total alopecia in a mother and her son Gastroenterology · 1993 · 23 citations
    8. Chromosomal localization of acidic and basic keratin genes of the domestic dog Mammalian Genome · 1999 · 9 citations
    9. The Etiological Correlation of Seven Common Types of Alopecia 2025
    10. Demodicidose generalizada em cão da raça Teckel: Relato de caso Lume (Universidade Federal do Rio Grande do Sul) · 2015
    11. Molecular studies of Hutchinson-Gilford progeria syndrome OPAL (Open@LaTrobe) (La Trobe University) · 2009
    12. GLOMERULAR MEMBRANOUS NEPHROPATHY AND WERNER SYNDROME: A CASE REPORT Journal of the American Geriatrics Society · 2011 · 1 citations
    13. Alopecia Areata Update Dermatologic Clinics · 2012 · 85 citations
    14. A Case of Frontal Fibrosing Alopecia in a Patient with Primary Biliary Cirrhosis and Polymyalgia Rheumatica Skin appendage disorders · 2016 · 5 citations
    15. A rare manifestation of STING-associated vasculopathy with onset in infancy: a case report Pediatric rheumatology online journal · 2024
    16. Hair physiology and its disorders Drug Discovery Today: Disease Mechanisms · 2008 · 31 citations
    17. Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1 American journal of medical genetics. Part A · 2022
    18. Man made disease: Clinical manifestations of low phenylalanine levels in an inadequately treated phenylketonuria patient and mouse study Molecular genetics and metabolism · 2013 · 13 citations
    19. P4 Outcome following switch between brand name and generic tacrolimus in paediatric population Archives of Disease in Childhood · 2018 · 3 citations
    20. Nitroxide pharmaceutical development for age-related degeneration and disease Frontiers in Genetics · 2015 · 24 citations
    21. Kératose pilaire Pan African Medical Journal · 2019 · 1 citations
    22. Alopecia Areata is associated with MICA and an extended HLA haplotype Journal of the American Academy of Dermatology · 2004 · 1 citations
    23. Familial Frontal Fibrosing Alopecia Sultan Qaboos University medical journal · 2021 · 2 citations
    24. Male androgenetic alopecia Turkderm · 2014 · 3 citations
    25. Topikal %1 Pimekrolimus Tedavisine Cevap Veren Bir Alopesi Areata Olgusu Çağdaş tıp dergisi · 2016
    26. Alopecia Areata InTech eBooks · 2017 · 1 citations
    27. Progress of Integrated Medicine in the Treatment of Androgenic Alopecia 2016
    28. Drug Repurposing Patent Applications April–June 2021 Assay and drug development technologies · 2021
    29. Contents Dermatologic Clinics · 2019
    30. Application of multi-omics techniques to androgenetic alopecia: Current status and perspectives Computational and Structural Biotechnology Journal · 2024