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    Research 331–360 of 1000+

    1. 8242 A Case of Ayme Gripp Syndrome Journal of the Endocrine Society · 2024
    2. Alopecia with Vitamin D-Dependent Rickets Type 2 A: A Case Report Clinical, cosmetic and investigational dermatology · 2024
    3. Ichthyosiform Erythroderma, a Multifaceted Syndromic Entity Pediatrics in review · 2021
    4. Salt-losing tubulopathy and chronic dermatitis Kidney international · 2018
    5. Urological Oncology: Prostate Cancer 2010
    6. Social selection favours offspring prone to the development of androgenetic alopecia. PubMed · 2018
    7. Immune-Molecular Link between Thyroid and Skin Autoimmune Diseases: A Narrative Review Journal of Clinical Medicine · 2024 · 6 citations
    8. Di-Genic Inheritance in Genodermatoses: Insights from Two Consanguineous Cases in a Reference Lebanese Center within the Middle East and North Africa (MENA) Region Dermatology Practical & Conceptual · 2025
    9. Sex differences in COVID-19: the role of androgens in disease severity and progression Endocrine · 2020 · 121 citations
    10. Complex genetic dependencies among growth and neurological phenotypes in healthy children: Towards deciphering developmental mechanisms PLoS ONE · 2020 · 13 citations
    11. Exploring Variation in Ovine KRTAP19-5 and Its Effect on Fine Wool Fibre Curvature in Chinese Tan Sheep Animals · 2024 · 4 citations
    12. Concept of tinea capitis Gadua Journal of Pure and Allied Science · 2022
    13. Epstein-Barr virus associated with high-grade B-cell lymphoma in nude severe combined immunodeficiency BMJ case reports · 2019 · 3 citations
    14. Perspectives of Kennedy's disease Journal of the Neurological Sciences · 2010 · 65 citations
    15. Genetic Polymorphisms of Immunity Regulatory Genes and Alopecia Areata Susceptibility in Jordanian Patients Medicina · 2024 · 1 citations
    16. Recessive Mutation in FAM83G Associated with Palmoplantar Keratoderma and Exuberant Scalp Hair Journal of Investigative Dermatology · 2017 · 10 citations
    17. Two novel MBTPS2 missense mutations impairing S2P proteolytic activity lead to IFAP syndrome with new phenotypic anomalies Journal of dermatological science · 2023
    18. Comprehensive Program Planning for the Integration of 21st Century Learning Center After-School Programs with Regular Day Programs and Community Partners. American Journal of Medical Genetics Part A · 1999
    19. Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023) American Journal of Medical Genetics Part A · 2024 · 21 citations
    20. A General Paediatric Approach to Ankyloblepharon–Ectodermal Dysplasia–Cleft Lip/Palate Syndrome in Infancy: A Case Report Journal of Paediatrics and Child Health · 2025
    21. Evidence for a functional interaction of WNT10A and EBF1 in male-pattern baldness PLoS ONE · 2021 · 12 citations
    22. The efficacy and safety of valproic acid medications with controlled active ingredient release in adults in real clinical practice from the position of pharmacokinetic and pharmacogenetic approaches Nevrologiâ, nejropsihiatriâ, psihosomatika · 2017 · 5 citations
    23. Recent positive selection of a human androgen receptor/ectodysplasin A2 receptor haplotype and its relationship to male pattern baldness Human Genetics · 2009 · 42 citations
    24. Registrars’ Symposium: Summaries of Papers British Journal of Dermatology · 2006
    25. RNA interference of NtNCED3 reduces drought tolerance and impairs plant growth through feedback regulation of isoprenoids in Nicotiana tabacum Environmental and Experimental Botany · 2018 · 17 citations
    26. <i>NIPAL4</i> deletion identified in an American Bully with autosomal recessive congenital ichthyosis and response to topical therapy Veterinary medicine and science · 2019 · 7 citations
    27. Loss‐of‐function of Endothelin receptor type A results in Oro‐Oto‐Cardiac syndrome American Journal of Medical Genetics Part A · 2020 · 11 citations
    28. Clinical and Molecular Genetic Findings of Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy Turkish Journal Of Neurology · 2021 · 3 citations
    29. A Missense Mutation within the Helix Termination Motif of KRT25 Causes Autosomal Dominant Woolly Hair/Hypotrichosis Journal of Investigative Dermatology · 2017 · 33 citations
    30. Variation in Ovine KRTAP13-3 and Its Association with Wool Characteristics in Chinese Tan Sheep Animals · 2025 · 1 citations