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    Research 481–510 of 1000+

    1. Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome American journal of human genetics · 2020 · 34 citations
    2. Telogen Effluvium Cosmetics · 2016 · 18 citations
    3. A disease-causing novel missense mutation in the ST14 gene underlies autosomal recessive ichthyosis with hypotrichosis syndrome in a consanguineous family 2018 · 9 citations
    4. Hair diseases: a big problem on a small surface Postepy Dermatologii I Alergologii · 2016 · 4 citations
    5. Highlights of Gene and Cell Therapy for Epidermolysis Bullosa and Ichthyosis Dermatology and Therapy · 2024 · 3 citations
    6. Navaratnas in Dermatology Indian Dermatology Online Journal · 2024
    7. Investigating the role of keratin proteins and microbial associations in hereditary and pathogenic alopecia Archives of Dermatological Research · 2024
    8. Evidence for Novel Functions of the Keratin Tail Emerging from a Mutation Causing Ichthyosis Hystrix Journal of Investigative Dermatology · 2001 · 130 citations
    9. Expression of MK6a dominant-negative and C-terminal mutant transgenes in mice has distinct phenotypic consequences in the epidermis and hair follicle Differentiation · 1999 · 30 citations
    10. Hair Anomalies in a 6-Year-Old Girl Case reports in clinical medicine · 2016
    11. Chitin and Chitosans: Characteristics, Eco-Friendly Processes, and Applications in Cosmetic Science Marine Drugs · 2019 · 298 citations
    12. British Association of Dermatologists guidelines on the efficacy and use of acitretin in dermatology British Journal of Dermatology · 2010 · 136 citations
    13. Therapeutic Use of Botulinum Neurotoxins in Dermatology: Systematic Review Toxins · 2021 · 58 citations
    14. Psychological interventions in the management of common skin conditions Psychology Research and Behavior Management · 2010 · 41 citations
    15. Inherited epidermolysis bullosa: clinical and therapeutic aspects Anais Brasileiros de Dermatologia · 2013 · 32 citations
    16. Genomewide analysis of copy number variants in alopecia areata in a Central European cohort reveals association with <i>MCHR2</i> Experimental Dermatology · 2016 · 29 citations
    17. The Phenotypic and Genotypic Spectra of Ichthyosis With Confetti Plus Novel Genetic Variation in the 3′ End of<i>KRT10</i> JAMA dermatology · 2014 · 22 citations
    18. A novel PLEC nonsense homozygous mutation (c.7159G > T; p.Glu2387*) causes epidermolysis bullosa simplex with muscular dystrophy and diffuse alopecia: a case report BMC dermatology · 2018 · 18 citations
    19. Eruptive vellus hair cyst: An uncommon and underdiagnosed entity International journal of trichology · 2018 · 10 citations
    20. Atrichia with papular lesions International journal of trichology · 2011 · 8 citations
    21. Primary idiopathic pseudopelade of brocq: Five case reports International Journal of Trichology · 2014 · 7 citations
    22. Topical corticosteroid in foam vehicle offers comparable coverage compared with traditional vehicles Journal of the American Academy of Dermatology · 2000 · 7 citations
    23. Hair Keratin 1990 · 7 citations
    24. Confluent and Reticulated Papillomatosis Associated with Polycystic Ovarian Syndrome Cureus · 2019 · 3 citations
    25. Acute chylous peritonitis due to idiopathic pancreatitis mimicking acute appendicitis Journal of Mind and Medical Sciences · 2021 · 2 citations
    26. Scarring Alopecia With Coexisting Lichen Planus in a Child: A Rare Phenomenon Curēus · 2021 · 1 citations
    27. ROS-responsive hydrogel-delivered miR-665 targets STAT3 to alleviate inflammation and promote hair follicle regeneration in alopecia areata Journal of Nanobiotechnology · 2026
    28. Culinary Clues: Unraveling Dermatological Signs through Kitchen Analogies Indian Dermatology Online Journal · 2025
    29. Delicious Dermatology: Baked-Up Eponyms Indian Dermatology Online Journal · 2025
    30. Netherton Syndrome – Responding to Oral Retinoids International Journal of Trichology · 2025