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    Research 241–270 of 1000+

    1. Three cases of hair loss analyzed by the point of view of the analytical psychology International Journal of Trichology · 2017 · 1 citations
    2. Overlap Between Ulerythema Ophryogenes and Keratosis Follicularis Spinulosa Decalvans: a Case Report 2015 · 1 citations
    3. Nevoid basal carcinoma syndrome (Gorlin syndrome) and pronounced androgenic alopecia in a woman with a novel mutation p.Leu1159fsx32 in the PTCH gene Journal of Dermatology · 2011 · 1 citations
    4. 61349 The Development of Vitiligo After Cessation of Finasteride: Is this Part of Post-Finasteride Syndrome or an Adverse Event of Finasteride? Journal of the American Academy of Dermatology · 2025
    5. Case Report: A novel KRT74 variant in an eight-year-old boy with alopecia totalis successfully treated with baricitinib Frontiers in Medicine · 2025
    6. Precocious Pubarche in a 7-Year-Old Patient. A Case Report Revista de Investigación y Educación en Ciencias de la Salud (RIECS) · 2024
    7. Hyperpigmentation in a child as a clue to chikungunya Karnataka Pediatric Journal · 2024
    8. Pure Leydig cell tumor of the ovary: a rare presentation of a rare entity in a pregnant patient Future Science OA · 2024
    9. Research Trend of Studies Regarding the Change and Treatment of the Skin on Pregnant Women in the Last Decade: A Systematic Review and Bibliometric Analysis 2023
    10. Pearly Pinna Papules in a Young Female Indian dermatology online journal · 2023
    11. Tourniquet syndrome in children (literature review and own observation) Ukraïnsʹkij žurnal Perinatologìâ ì pedìatrìâ · 2023
    12. Pediatric Features of Genetic Predisposition to Polycystic Ovary Syndrome ˜The œJournal of clinical endocrinology and metabolism · 2023
    13. An overview of risk factors for androgenetic alopecia among women at Pasar Ambacang, Kuranji, Padang Journal of General Procedural Dermatology and Venereology Indonesia · 2023
    14. CPC12 Coinheritance of <i>BRCA2</i> and <i>CYLD</i> germline pathogenic variants associated with targetable metastatic malignant cylindroma British Journal of Dermatology · 2023
    15. Case report: Acrodermatitis enteropathica result from a novel SLC39A4 gene mutation Frontiers in pediatrics · 2022
    16. The First Report of Isolated Clitoral Hood Hair-Thread Tourniquet Syndrome: A Study of Six Patients Cureus · 2022
    17. A rare case of pemphigus vulgaris in pregnancy Journal of Pakistan Association of Dermatologists · 2022
    18. Interrelationships between Skin Structure, Function, and Microbiome of Pregnant Females and Their Newborns: Study Protocol for a Prospective Cohort Study Dermatology Research and Practice · 2021
    19. Precocious puberty in a 24 month old Nigerian girl: case report Nigerian journal of paediatrics · 2020
    20. SAT0200 UNUSUAL SYSTEMIC LUPUS ERYTHEMATOSUS/SJOEGREN'S SYNDROME PHENOTYPE IN A PATIENT WITH A TNFAIP3 GENE MUTATION 2019
    21. 017 Lichen Planus Colocalized with Vitiligo: Coincidence? Journal of Investigative Dermatology Symposium Proceedings · 2017
    22. Chemotherapy-Induced Alopecia and Quality-of-Life: Ovarian and Uterine Cancer Patients and the Aesthetics of Disease Digital Commons - University of South Florida (University of South Florida) · 2017
    23. Diffuse hypotrichosis from early childhood Journal of The American Academy of Dermatology · 2016
    24. G367(P) A chubby child: is this a sign of health or malnutrition? Archives of disease in childhood · 2015
    25. Topical fluocinolone acetonide acetate ointment in autosomal dominant congenital hypotrichosis 2012
    26. Scleromyxedema with neurologic involvement: Therapy with intravenous immunoglobulin Journal of the American Academy of Dermatology · 2010
    27. Incidence and risk factors for neonatal occipital alopecia: A retrospective study Journal of The American Academy of Dermatology · 2010
    28. Management of pregnancy in a carrier of the Donohue mutation Prenatal Diagnosis · 2009
    29. Perancangan buku esai fotografi tentang kesenian ludruk di Surabaya International Journal of Trichology · 2008
    30. First case of V281+I172N/V281L CYP21A2 genotype associated with congenital adrenal hyperplasia form. A case report from South Italy Clinical Biochemistry · 2007