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    Research 931–960 of 977

    1. 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
    2. An Occult Leydig Cell Tumour in a Postmenopausal Woman Presenting with Alopecia and Hirsutism: A Case Report touchREVIEWS in Endocrinology · 2021 · 3 citations
    3. The Rare Occurrence of a Left Atrial Thrombus in a Dog Case Reports in Veterinary Medicine · 2020 · 3 citations
    4. Diagnostic imaging in congenital adrenal hyperplasia – how does it help? Clinical endocrinology and metabolism journal · 2020 · 3 citations
    5. Isochromosome Mosaic Turner Syndrome: A Case Report Journal of the ASEAN Federation of Endocrine Societies · 2019 · 3 citations
    6. Alopecia Areata of the Nails: Diagnosis and Management Journal of Clinical Medicine · 2024 · 2 citations
    7. An adolescent girl with coexisting ovarian mature cystic teratoma and HAIR-AN syndrome, an extreme subtype of polycystic ovarian syndrome Endocrinology, diabetes & metabolism case reports · 2021 · 2 citations
    8. 66-Year-Old Woman With Painless Vesicular Lesions Mayo Clinic Proceedings · 2009 · 2 citations
    9. Steatocystoma Multiplex Indian Dermatology Online Journal · 2023 · 1 citations
    10. Unveiling a Shared Precursor Condition for Acne Keloidalis Nuchae and Primary Cicatricial Alopecias Clinical, Cosmetic and Investigational Dermatology · 2023 · 1 citations
    11. Post severe COVID-19 infection lung damages study. The experience of early three months multidisciplinary follow-up Monaldi archives for chest disease · 2022 · 1 citations
    12. Prevalence, Symptomatology and Herbal Management of Polycystic Ovarian Syndrome IntechOpen eBooks · 2021 · 1 citations
    13. Clinical and histological recovery of non-thymoma-associated exfoliative dermatitis in a cat treated with ciclosporin A Journal of Feline Medicine and Surgery Open Reports · 2020 · 1 citations
    14. Proliferative diabetic retinopathy as onset of type 1 diabetes Canadian journal of ophthalmology · 2019 · 1 citations
    15. A Novel Androgen Receptor Gene Mutation in a 46,XY Patient: Complete Androgen Insensitivity Syndrome AACE Clinical Case Reports · 2015 · 1 citations
    16. A young male with kidney damage from genetic mitochondrial disease: case report and literature review BMC Nephrology · 2026
    17. Multimodal Non-Invasive Skin Imaging in Dermatology: Current Modalities, Clinical Applications, and Future Integration Diagnostics · 2026
    18. Geleneksel Derleme: Dermatoloji ve Kozmetolojide Eksozomlar Akdeniz Medical Journal · 2026
    19. Idiopathic isolated adrenocorticotropic hormone deficiency combined with testicular germ cell tumor: Case report Medicine · 2025
    20. #3665 Glyoxylic acid induce crystalline nephropathy and hair-straightening products: a case report Nephrology Dialysis Transplantation · 2025
    21. Black Hairy Tongue Syndrome: Case Report and Review of the Literature BioMed · 2025
    22. Pilomatricoma in the Infraorbital Region 2025
    23. Identifying 17-β-HSD3 Deficiency in Patients with Karyotype 46,XY Misdiagnosed with Androgen Insensitivity Syndrome: A Pediatric Case Report American Journal of Case Reports · 2025
    24. Biomedical Applications of Bee Venom: A Natural Approach to Cancer, Infections, and Inflammatory Diseases Journal of Pure and Applied Microbiology · 2025
    25. Understanding Polycystic Ovary Syndrome: A Comprehensive Guide IntechOpen eBooks · 2025
    26. Lichen Planus Pigmentosus as a Cutaneous Extrahepatic Manifestation of Chronic Hepatitis C Virus Infection: A Case Report International Medical Case Reports Journal · 2025
    27. The role of ingrown hairs in persistent kerion of children: A clinical study The Journal of Dermatology · 2024
    28. P13 DMARD preconception counselling and reinforcement should be a norm in all rheumatology clinics Rheumatology Advances in Practice · 2024
    29. Pilomatricoma in the infraorbital region Clinical Case Reports · 2024
    30. Botanical extract combined with minoxidil improve hidrotic ectodermal dysplasia caused by p.G11R mutations: a case report Journal of Dermatological Treatment · 2024