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    Research 121–150 of 1000+

    1. Autoimmune Polyglandular Syndrome Type 3-D 2022
    2. Polycystic ovary syndrome [PCOS]: Comprehensive management in primary care Comprehensive Therapy · 2002
    3. Cutaneous manifestations of systemic infection in children Current problems in dermatology · 1993
    4. WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes American journal of human genetics · 2009 · 197 citations
    5. Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease Journal of Cell Science · 2008 · 85 citations
    6. Prevalence of the metabolic syndrome in African populations: A systematic review and meta-analysis PLoS ONE · 2023 · 59 citations
    7. Role of Endolysosomes in Severe Acute Respiratory Syndrome Coronavirus-2 Infection and Coronavirus Disease 2019 Pathogenesis: Implications for Potential Treatments Frontiers in Pharmacology · 2020 · 55 citations
    8. Epidermal expression of the truncated prelamin A causing Hutchinson-Gilford progeria syndrome: effects on keratinocytes, hair and skin Human Molecular Genetics · 2008 · 48 citations
    9. Hutchinson-Gilford Progeria Syndrome—Current Status and Prospects for Gene Therapy Treatment Cells · 2019 · 39 citations
    10. Impact of Combined Baricitinib and FTI Treatment on Adipogenesis in Hutchinson–Gilford Progeria Syndrome and Other Lipodystrophic Laminopathies Cells · 2023 · 4 citations
    11. Unusual acute lupus hemophagocytic syndrome – a test of diagnostic criteria: a case report Journal of Medical Case Reports · 2017 · 4 citations
    12. Skin and metabolic syndrome: A review of the possible associations Journal of Research in Medical Sciences · 2021 · 3 citations
    13. Effect of polycystic ovary syndrome on dysmenorrhea: a case-control study International Journal of Reproduction Contraception Obstetrics and Gynecology · 2024 · 2 citations
    14. Minoxidil restores thymic growth in 22q11.2 deletion syndrome by limiting Sox9+ chondrocyte expansion Journal of Human Immunity · 2025 · 1 citations
    15. An infant with congenital micrognathia and upper airway obstruction was diagnosed as Hutchinson-Gilford progeria syndrome caused by a novel LMNA mutation: Case report and literature review Heliyon · 2023 · 1 citations
    16. Impaired LEF1 Activation Accelerates iPSC-Derived Keratinocytes Differentiation in Hutchinson-Gilford Progeria Syndrome International journal of molecular sciences · 2022 · 1 citations
    17. Integration of Biochemical and Mechanical Signals at the Nuclear Periphery: Impacts on Skin Development and Disease Stem cell biology and regenerative medicine · 2018
    18. Repurposing With Purpose: Treatment of Bachmann–Bupp Syndrome With Eflornithine and Implications for Other Polyaminopathies American Journal of Medical Genetics Part C Seminars in Medical Genetics · 2025 · 1 citations
    19. Comparison of ovarian electrocautery and oral contraceptives in the treatment of hyperandrogenism in women with polycystic ovary syndrome Acta Obstetricia Et Gynecologica Scandinavica · 1999 · 9 citations
    20. Drug repurposing of cyclin-dependent kinase inhibitors for neutrophilic acute respiratory distress syndrome and psoriasis Journal of Advanced Research · 2024 · 8 citations
    21. Mesenchymal cell replacement corrects thymic hypoplasia in murine models of 22q11.2 deletion syndrome Journal of Clinical Investigation · 2022 · 9 citations
    22. Renal Carcinoma Presenting with Adrenocortical Insufficiency Due to a Pituitary Metastasis Annals of Clinical Biochemistry International Journal of Laboratory Medicine · 1998 · 20 citations
    23. Diseases associated with hidranitis suppurativa: part 2 of a series on hidradenitis Dermatology Online Journal · 2013 · 78 citations
    24. Dupilumab in Inflammatory Skin Diseases: A Systematic Review Biomolecules · 2023 · 72 citations
    25. Myotonic Dystrophy—A Progeroid Disease? Frontiers in Neurology · 2018 · 41 citations
    26. Regulation of Receptor Binding Specificity of FGF9 by an Autoinhibitory Homodimerization Structure · 2017 · 24 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. Histological and Gene Expression Analysis of the Effects of Menopause Status and Hormone Therapy on the Vaginal Introitus and Labia Majora Journal of clinical medicine research · 2019 · 7 citations
    29. Cardiovascular risk in patients with selected cutaneous diseases Journal of Education, Health and Sport · 2022
    30. Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases International Journal of Molecular Sciences · 2020 · 57 citations