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    Research 31–60 of 1000+

    1. A New Clinical Variant of Hereditary Localized Alopecia: Report of a Chinese Family Mapped to Chromosome 2p25.1–2p23.2 2007 · 2 citations
    2. AN UPDATE OF HAIR SHAFT DISORDERS Dermatologic clinics · 1996 · 12 citations
    3. Hair science and technology Micron · 2003 · 3 citations
    4. Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2 Journal of Dermatological Science · 2015
    5. Successful treatment of hereditary hypotrichosis simplex by platelet rich plasma injection with topical minoxidil 2% Journal of Dermatological Treatment · 2023
    6. APCDD1 is a novel Wnt inhibitor mutated in hereditary hypotrichosis simplex Nature · 2010 · 199 citations
    7. Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets BoneKEy Reports · 2014 · 107 citations
    8. Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia resulting from a novel missense mutation in the DNA-binding domain of the vitamin D receptor Molecular Genetics and Metabolism · 2009 · 50 citations
    9. Zinc‐responsive dermatosis in goats suggestive of hereditary malabsorption: two field cases Veterinary Dermatology · 2005 · 34 citations
    10. A Humanized Mouse Model of Hereditary 1,25-Dihydroxyvitamin D–Resistant Rickets Without Alopecia Endocrinology · 2014 · 25 citations
    11. A Girl with a Novel Splice Site Mutation in <i>VDR</i> Supports the Role of a Ligand-Independent VDR Function on Hair Cycling Hormone Research in Paediatrics · 2006 · 21 citations
    12. Hereditary 1,25-dihydroxyvitamin D-resistant rickets with alopecia in four Egyptian families: report of three novel mutations in the vitamin D receptor gene Journal of Pediatric Endocrinology and Metabolism · 2014 · 10 citations
    13. Molecular, immunological, enzymatic and biochemical studies of coproporphyrinogen oxidase deficiency in a family with hereditary coproporphyria. PubMed · 2002 · 9 citations
    14. Clinical and genetic findings in a Chinese family with VDR-associated hereditary vitamin D-resistant rickets Bone Research · 2016 · 7 citations
    15. Hereditary vitamin D rickets: a case series in a family 2014 · 6 citations
    16. Erythrocyte deformability and hereditary elliptocytosis Clinical hemorheology and microcirculation · 2014 · 6 citations
    17. A newly identified missense mutation of the HR gene is associated with a novel, unusual phenotype of Marie Unna Hereditary Hypotrichosis 1 including limb deformities Archives of Dermatological Research · 2012 · 6 citations
    18. Hereditary Vitamin D Resistant Rickets: Clinical, Laboratory, and Genetic Characteristics of 2 Iranian Siblings 2017 · 5 citations
    19. Hereditary vitamin D-resistant rickets in Lebanese patients: the p.R391S and p.H397P variants have different phenotypes 2017 · 4 citations
    20. Iron Screening in Alopecia Areata Patients May Catch Hereditary Hemochromatosis Early Cutis · 2022
    21. Hereditary, Congenital, and Acquired Alopecias Elsevier eBooks · 2016
    22. Odd-Looking Hair and Progressive Alopecia in Mother and Son JAMA Dermatology · 2014
    23. Marie-unna hereditary hypotrichosis International Journal of Trichology · 2014 · 4 citations
    24. TREATMENT OF HAIR LOSS วารสารเภสัชวิทยา (Thai Journal of Pharmacology) · 2000
    25. Congenital and Hereditary Skin Diseases 2018
    26. Hair loss Pharmacy Today · 2021
    27. 6874 A Rare Case Of Hereditary 1,25 (OH)2D Resistant Rickets Journal of the Endocrine Society · 2024
    28. SUN-332 A Rare Case Of Hereditary 1,25 (OH)2D Resistant Rickets Journal of the Endocrine Society · 2024
    29. Mutations in the vitamin D receptor gene in four patients with hereditary 1,25-dihydroxyvitamin D-resistant rickets Arquivos Brasileiros de Endocrinologia & Metabologia · 2008 · 24 citations
    30. Nutritive Beeinflussung des Haarwachstums Aktuelle Dermatologie · 2011 · 7 citations