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    Research 421–450 of 1000+

    1. Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness 2021
    2. Hair Anomalies in a 6-Year-Old Girl Case reports in clinical medicine · 2016
    3. Frontal Fibrosing Alopecia: A Comprehensive Review with Recent Updates Indian Journal of Dermatology · 2025
    4. Analysis of R199H Polymorphism of Canine Melanophilin Gene (MLPH) in Population of Czech Pointer in Slovakia DOAJ (DOAJ: Directory of Open Access Journals) · 2011 · 1 citations
    5. Central centrifugal cicatricial alopecia: retrospective case-control study of 54 patients from a tertiary care center International Journal of Women’s Dermatology · 2025
    6. Targeting integrin pathways: mechanisms and advances in therapy Signal Transduction and Targeted Therapy · 2023 · 54 citations
    7. Semidominant Inheritance in Epidermolytic Ichthyosis Journal of Investigative Dermatology · 2013 · 10 citations
    8. Bioengineering the Hair Follicle Organogenesis · 2007 · 26 citations
    9. Inflammatory Vegetative Lesions of the Perineum: A Rare and Severe Clinical Presentation of Netherton Syndrome Acta Dermato Venereologica · 2020 · 3 citations
    10. Rothmund Thomson syndrome with late onset and good preventive control of non-melanoma cancer with acitretin: case report Journal of Dermatology & Cosmetology · 2024
    11. WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes American journal of human genetics · 2009 · 197 citations
    12. Autoimmune Polyglandular Syndrome Type 1 in Russian Patients: Clinical Variants and Autoimmune Regulator Mutations Hormone research in paediatrics · 2010 · 62 citations
    13. Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy Journal of Investigative Dermatology · 2003 · 52 citations
    14. Rabson-Mendenhall syndrome: two case reports and a brief review of the literature Odontology · 2010 · 18 citations
    15. Effects of pre- and post-pubertal dihydrotestosterone treatment on penile length in 5α-reductase type 2 deficiency Endocrine journal · 2019 · 13 citations
    16. Case report of Schöpf–Schulz–Passarge syndrome resulting from a missense mutation, p.Arg104Cys, in <i>WNT10A</i> The Journal of Dermatology · 2017 · 5 citations
    17. A Case Report of Werner’s Syndrome With a Novel Mutation From India Cureus · 2020 · 4 citations
    18. Atrichia with papular lesions in a Taiwanese patient without hairless (HR) gene mutation Dermatologica Sinica · 2010 · 3 citations
    19. Papillon-Lefévre Syndrome: A Rare Case Report and a Brief Review of Literature Curēus · 2022 · 1 citations
    20. LAMELLAR ICHTHYOSIS: ONE CASE REPORT International Journal of Medical Reviews and Case Reports · 2019 · 1 citations
    21. Testosterone and dihydrotestosterone production in genetically furless and furred male rabbits and effects on growth. Proceedings of the 9th World Rabbit Congress, Verona, Italy, 10-13 June 2008 · 2008 · 1 citations
    22. Longitudinal clinical course in patients with 5α-reductase type 2 deficiency treated with testosterone and dihydrotestosterone during infancy and puberty Endocrine journal · 2022
    23. 575 An extract of Leontopodium alpinum prolongs anagen phase in human hair follicles ex vivo Journal of Investigative Dermatology · 2021
    24. A RARE CASE OF CHRONIC ACRODERMATITIS ENTEROPATHICA PERSISTING AND RECURRING IN THE ADULT AGE Journal of Evolution of Medical and Dental Sciences · 2016
    25. Cushing Syndrome from Percutaneous Absorption of 1% Hydrocortisone Ointment in Netherton Syndrome Pediatric dermatology · 2007 · 42 citations
    26. 272 Structural changes in human skin after topical application of glucocorticoids assessed by in vivo imaging technologies Journal of Investigative Dermatology · 2017 · 1 citations
    27. 269 Down-regulatory role of cholecystokinin on psoriatic epidermal inflammation Journal of Investigative Dermatology · 2017
    28. 270 A novel small compound HPH-15 antagonizes TGF-β/Smad signaling and ameliorates experimental skin fibrosis Journal of Investigative Dermatology · 2017
    29. 267 Deep phenotyping of patients with xeroderma pigmentosum and trichothiodystrophy Journal of Investigative Dermatology · 2017
    30. Thehairless gene of the mouse: Relationship of phenotypic effects with expression profile and genotype Developmental Dynamics · 1999 · 52 citations