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    Research 211–240 of 1000+

    1. Leukokoria sebagai Tanda Peringatan Penyakit Coats dan Gangguan Retina Lainnya Cermin Dunia Kedokteran · 2025
    2. Hair loss Pharmacy Today · 2021
    3. STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity Orphanet Journal of Rare Diseases · 2014 · 65 citations
    4. The vitamin D receptor functions as a transcription regulator in the absence of 1,25-dihydroxyvitamin D3 The Journal of Steroid Biochemistry and Molecular Biology · 2015 · 37 citations
    5. Study of Postpartum Alopecia Archives of Dermatology · 1963 · 24 citations
    6. Molecular Genetics of Alopecias Current problems in dermatology · 2015 · 9 citations
    7. Mutation in 5′ upstream region of <i>GCH</i> I gene causes familial dopa-responsive dystonia Movement Disorders · 2011 · 7 citations
    8. Autosomal Dominant Obstructive Sleep Apnea Syndrome Due to the New Variant c.980_984dup in COL1A2: A Case Report Cureus · 2026
    9. Serum markers thrombophilia in pregnant women with Systemic Lupus Erythematosus Revista Brasileira de Saúde Materno Infantil · 2017
    10. Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome The American Journal of Human Genetics · 2012 · 71 citations
    11. Familial Cortisol Resistance: Differential Diagnostic and Therapeutic Aspects The Journal of Clinical Endocrinology & Metabolism · 1986 · 65 citations
    12. A gene for monilethrix is closely linked to the type II keratin gene cluster at 12q13 Human Molecular Genetics · 1995 · 54 citations
    13. Tryptophan Missense Mutation in the Ligand‐Binding Domain of the Vitamin D Receptor Causes Severe Resistance to 1,25‐Dihydroxyvitamin D Journal of Bone and Mineral Research · 2002 · 47 citations
    14. Functional analyses of a novel missense and other mutations of the vitamin D receptor in association with alopecia Scientific Reports · 2017 · 20 citations
    15. Pathology in Practice Journal of the American Veterinary Medical Association · 2018
    16. Serine palmitoyltransferase and peripheral neuropathy: studies on neuropathy-causing mutations and their biochemical hallmarks Zurich Open Repository and Archive (University of Zurich) · 2016
    17. Studies on basal cell carcinoma with emphasis on the role of the human homologue of the Drosophila patched gene Open Archive (Karolinska Institutet) · 1997
    18. Female Androgenetic (?) Alopecia Hair transplant forum international · 2015
    19. Monilethrix in monozygotic twins with very rare mutation in KRT 86 gene Journal of the European Academy of Dermatology and Venereology · 2017 · 6 citations
    20. Alopecia X em cães: revisão PubVet · 2020 · 4 citations
    21. P‐35 
Nonlethal junctional epidermolysis bullosa in a dog Veterinary Dermatology · 2004 · 2 citations
    22. Description of clinical aspects and microscopy of the hair shaft of a carrier of familial monilethrix Jornal Brasileiro de Patologia e Medicina Laboratorial · 2018 · 1 citations
    23. Monilethrix: Beaded hair and hypotrichosis in a child Cosmoderma · 2026
    24. Critical Evaluation of Concept of Genetics in Ayurveda WSR to Eight Undesired Body Types (Ashta Nindit) Journal of complementary medicine & alternative healthcare · 2023
    25. Mutation analysis of type II hair keratin gene in a pedigree with monilethrix Chinese Journal of Dermatology · 2010
    26. Rates of polycystic ovary syndrome (PCOS) symptoms in relatives of patients with PCOS Fertility and sterility · 2002
    27. What Ages Hair? International Journal of Women's Dermatology · 2017 · 15 citations
    28. Factors affecting the development of alopecia areata in children Health care of Tajikistan · 2022
    29. Biology and Genetics of Hair Annual Review of Genomics and Human Genetics · 2010 · 89 citations
    30. Keratin K6irs is specific to the inner root sheath of hair follicles in mice and humans British Journal of Dermatology · 2001 · 38 citations