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    Research 241–270 of 1000+

    1. National scientific medical meeting 1996 abstracts Irish Journal of Medical Science (1971 -) · 1996
    2. ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy The Application of Clinical Genetics · 2022 · 15 citations
    3. Inherited ichthyoses/generalized Mendelian disorders of cornification European journal of human genetics · 2012 · 81 citations
    4. Disorders of Keratinization American journal of clinical dermatology · 2004 · 44 citations
    5. Unveiling the Potential of Dermoscopy in Diagnosing Netherton Syndrome Indian Journal of Paediatric Dermatology · 2025
    6. Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility 2009 · 189 citations
    7. Bachmann–Bupp syndrome and treatment 2023
    8. Case Report:Pregnancy and birth in a mild phenotype of Alström syndrome Frontiers in Genetics · 2022 · 5 citations
    9. Dermatopathia pigmentosa reticularis: A rare case with adermatoglyphia Our Dermatology Online · 2025
    10. A Case of Trichorhinophalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the <i>TRPS1</i> Gene Clinical Case Reports · 2025
    11. Polycystic Ovary Syndrome: Etiology, Current Management, and Future Therapeutics Journal of Clinical Medicine · 2023 · 380 citations
    12. Inherited epidermolysis bullosa: clinical and therapeutic aspects Anais Brasileiros de Dermatologia · 2013 · 32 citations
    13. Dermatology resident comfort level treating hair conditions related to patients with skin of color International journal of women’s dermatology · 2024
    14. Post‐finasteride syndrome: real or myth? Trends in Urology & Men s Health · 2024
    15. Ehlers-Danlos syndrome: From bedside to bench Frontiers research topics · 2024
    16. Pulmonary manifestations of Birt-Hogg-Dubé syndrome Familial cancer · 2013 · 99 citations
    17. Perspectives of Chinese Adult Patients with Alopecia Areata on Janus Kinase Inhibitors Therapy: A Qualitative Analysis Based on Social Media Platforms Patient Preference and Adherence · 2025
    18. 8507 Misdiagnosis of Graves’ and RAI Treatment in Patient with THRB Gene Mutation Journal of the Endocrine Society · 2024
    19. Correlation of Trichoscopic Findings with Severity in Androgenetic Alopecia Indian Journal of Dermatology · 2024
    20. Dunnigan-Type Familial Partial Lipodystrophy: Understanding and Treating the Syndrome Open Journal of Endocrine and Metabolic Diseases · 2017
    21. A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome Orphanet Journal of Rare Diseases · 2017 · 11 citations
    22. Gene detection in a family with monilethrix and treatment with 5% topical minoxidil Skin research and technology · 2022 · 2 citations
    23. Fundamental Concepts and Novel Aspects of Polycystic Ovarian Syndrome: Expert Consensus Resolutions Frontiers in Endocrinology · 2020 · 138 citations
    24. Diagnosis and Management of Polycystic Ovary Syndrome in Adolescent Girls Pediatric Annals · 2015 · 20 citations
    25. Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome ˜The œAmerican journal of case reports · 2018 · 14 citations
    26. Minoxidil-induced hypertrichosis: Pathophysiology, clinical implications, and therapeutic strategies JAAD reviews. · 2024 · 7 citations
    27. Practices, Efficacy, and Reported Side Effects Associated with Isotretinoin Treatment in Palestine Patient Preference and Adherence · 2024 · 3 citations
    28. Listening to patients: A qualitative study on diagnostic delay, coping strategies and stigma in early‐onset colorectal cancer Colorectal Disease · 2025 · 1 citations
    29. Perspectives on the pharmacist’s “product”: a narrative review Pharmacy Practice (internet) · 2021 · 1 citations
    30. Impact of Reporter Type on Signal Detection of Cancer Therapy-Induced Alopecia: A Hypothesis-Generating Study Using the FDA Adverse Event Reporting System Pharmaceuticals · 2026