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    Research 631–660 of 1000+

    1. Reversible hypopigmentation of hair secondary to Vitamin B12 deficiency Nasza Dermatologia Online · 2013 · 1 citations
    2. Clinical Snippets 2003 · 1 citations
    3. Exploring the landscape of hair and scalp disorders in the pediatric skin of color population: A scoping review JAAD reviews. · 2026
    4. Genotype-Phenotype Delineation of Autoimmune Polyendocrinopathy, Candidiasis, and Ectodermal Dystrophy in a Pediatric Patient: A Case Report Genes · 2026
    5. Surgical Treatment Combined With Concentrated Growth Factor Injection for a Case of Pseudopelade of Brocq Journal of Cosmetic Dermatology · 2025
    6. Olympic and Board Game Dermatology: Exploring Eponyms Linking Skin Conditions to Sports and Strategy Games Indian Dermatology Online Journal · 2025
    7. Perosomus elumbus fetal monster: a rare cause of dystocia in a beetal goat - a case report from Pakistan Journal of Animal Reproduciton and Biotechnology · 2024
    8. P326: Cardiovascular features in adult individuals affected with Tatton-Brown-Rahman syndrome Genetics in Medicine Open · 2024
    9. A case of <i>MBTPS1</i>‐related disorder due to compound heterozygous variants in <i>MBTPS1</i> gene: Genotype–phenotype expansion and the emergence of a novel syndrome American journal of medical genetics. Part A · 2023
    10. 547 CDK9 Kinase Activation in Association with AFF1-SEC Initiate Epidermal Progenitor differentiation Journal of Investigative Dermatology · 2022
    11. 671 Impaired follicular Nrf2 signaling: Potential early therapeutic target in hidradenitis suppurativa 2022
    12. Porokeratotic adnexal ostial nevus: a paradigm of cutaneous mosaicism Authorea (Authorea) · 2022
    13. G338(P) Dermatological manifestations in children with chronic kidney disease in a tertiary care center: a case-control study 2020
    14. SUN-287 A Case of Ectopic Neurohypophysis Journal of the Endocrine Society · 2020
    15. P095 The Very Interesting Small Bowel Lesions of Cronkhite-Canada Syndrome The American Journal of Gastroenterology · 2019
    16. Compound Heterozygous Mutations in <i>Forkhead Box N1</i> (<i>FOXN1</i>) Lead to a Severe Immunodeficiency but Normal Hair and Nail Development in Patients 2018
    17. O que sabemos sobre os inibidores da 5 alfa redutase? Surgical and Cosmetic Dermatology · 2018
    18. A Rare Case of Cronkhite-Canada Syndrome The American Journal of Gastroenterology · 2017
    19. Escobar syndrome (multiple pterygium syndrome) associated with osteogenesis imperfecta: a case report ORTHOPAEDICS TRAUMATOLOGY and PROSTHETICS · 2017
    20. Patients with Compound Heterozygous Mutations in Forkhead Box N1 have a Severe Immunodeficiency while Maintaining Normal Skin and Hair Development 2017
    21. Early Onset Werner Syndrome Turkish Journal of Endocrinology and Metabolism · 2015
    22. Nitrogen Mustard Induces DNA Damage and Structural Changes in Mouse Skin Hair Follicles The FASEB Journal · 2015
    23. A Very Unusual Cause of Diarrhea in a 60-Year-Old Man The American Journal of Gastroenterology · 2013
    24. Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities Neuropediatrics · 2012
    25. Preliminary studies on the phytochemistry and efficacy of extracts of the bark of <i>Spondias mombin</i> l. on induced cancer in rats Annals of Biomedical Sciences · 2008
    26. This Month in the Journal The American Journal of Human Genetics · 2005
    27. RE: EFFECT OF THE DUAL 5α-REDUCTASE INHIBITOR DUTASTERIDE ON MARKERS OF TUMOR REGRESSION IN PROSTATE CANCER 2005
    28. The Role of 5αR Inhibitors in the Early Growth of Pca Cells Urologia Journal · 2005
    29. Cantú Syndrome Is Caused by Mutations in ABCC9 The American Journal of Human Genetics · 2012 · 148 citations
    30. British Association of Dermatologists guidelines on the efficacy and use of acitretin in dermatology British Journal of Dermatology · 2010 · 136 citations