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    Research 451–480 of 1000+

    1. Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population Molecular genetics and metabolism reports · 2019 · 8 citations
    2. Comparative Efficacy Study Combination of Oral Methotrexate and Prednisolone versus Oral Methotrexate in Patients with Lichen Planopilaris Dermatology Research and Practice · 2022 · 4 citations
    3. Short-Term Side Effects of Low Dose Valproate Monotherapy in Epileptic Children: A Prospective Study. PubMed · 2019 · 4 citations
    4. De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia BMC Medical Genomics · 2024 · 3 citations
    5. Abstracts from the 55th European Society of Human Genetics (ESHG) Conference: e-Posters European Journal of Human Genetics · 2023 · 1 citations
    6. Clinicopathologic features, demographics, disease burden, and therapeutics in alopecic sarcoidosis: a case series and systematic review International Journal of Women’s Dermatology · 2024
    7. Non‐biologic immunosuppressive drugs for inflammatory and autoimmune skin diseases Journal der Deutschen Dermatologischen Gesellschaft · 2024
    8. First-in-Man Clinical Trial of the Oral Pan-AKT Inhibitor MK-2206 in Patients With Advanced Solid Tumors Journal of clinical oncology · 2011 · 505 citations
    9. Biotinidase Deficiency: Prevalence, Impact And Management Strategies. PubMed · 2020 · 89 citations
    10. Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis Dermatology Online Journal · 2013 · 78 citations
    11. Morphea: progress to date and the road ahead Annals of Translational Medicine · 2021 · 50 citations
    12. Primary cicatricial alopecia: diagnosis and treatment Canadian Medical Association Journal · 2013 · 48 citations
    13. Dermatologic care for lesbian, gay, bisexual, and transgender persons Journal of The American Academy of Dermatology · 2019 · 47 citations
    14. Ptosis in childhood Medicine · 2018 · 15 citations
    15. Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes Journal of child neurology · 2012 · 15 citations
    16. Phenotypic Variability of c.436delC DCAF17 Gene Mutation in Woodhouse-Sakati Syndrome ˜The œAmerican journal of case reports · 2018 · 14 citations
    17. Cellular Senescence and Aging in Myotonic Dystrophy International Journal of Molecular Sciences · 2022 · 4 citations
    18. Novel Application of Light-Emitting Diode Therapy in the Treatment of Eyebrow Loss in Frontal Fibrosing Alopecia Sensors · 2021 · 4 citations
    19. Seborrheic Dermatitis Revisited: Pathophysiology, Diagnosis, and Emerging Therapies—A Narrative Review Biomedicines · 2025 · 3 citations
    20. The Use of Imaging Techniques in the Diagnosis of Dermatoses of the Scalp Medicina · 2025 · 1 citations
    21. Role of the Wnt/β-Catenin Signaling Pathway in Mediating Outer Root Sheath Stem Cells to Promote Hair Follicle Regeneration and Skin Wound Healing in Mice Cells · 2026
    22. Successfully Nonsurgical Epidermoid Cyst Management with Recombinant Hydrolytic Enzymes: A Case Report Clinical Cosmetic and Investigational Dermatology · 2024
    23. Critical Factors in Sample Collection and Preparation for Clinical Metabolomics of Underexplored Biological Specimens Metabolites · 2024
    24. The Spectrum of Scarring in Craniofacial Wound Repair Frontiers in Physiology · 2019 · 48 citations
    25. Research progress of post-acute sequelae after SARS-CoV-2 infection Cell death and disease · 2024
    26. Measures of Adult Systemic Lupus Erythematosus: Disease Activity and Damage Arthritis Care & Research · 2020 · 44 citations
    27. Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan Genes · 2016 · 9 citations
    28. Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation BMC Medical Genomics · 2022 · 6 citations
    29. A novel <i>MBTPS2</i> variant associated with BRESHECK syndrome impairs sterol‐regulated transcription and the endoplasmic reticulum stress response American Journal of Medical Genetics Part A · 2021 · 5 citations
    30. Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing Journal of Investigative Dermatology · 2008 · 99 citations