Search
for

    Sort by

    Research 601–630 of 1000+

    1. Marie Unna hereditary hypotrichosis caused by a novel mutation in the human hairless transcript Experimental Dermatology · 2010 · 14 citations
    2. Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation American Journal of Medical Genetics - Part A · 2010 · 11 citations
    3. Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless Journal of Investigative Dermatology · 2000 · 4 citations
    4. Congenital and Hereditary Skin Diseases 2018
    5. Congenital and Hereditary Skin Diseases 2018
    6. 6874 A Rare Case Of Hereditary 1,25 (OH)2D Resistant Rickets Journal of the Endocrine Society · 2024
    7. SUN-332 A Rare Case Of Hereditary 1,25 (OH)2D Resistant Rickets Journal of the Endocrine Society · 2024
    8. Associaton of Insulin Resistance Linked Diseases and Hair Loss in Elderly Men. Finnish Population-based Study Central European Journal of Public Health · 2006 · 55 citations
    9. 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
    10. A Novel Type II Cytokeratin, mK6irs, is Expressed in the Huxley and Henle Layers of the Mouse Inner Root Sheath Journal of Investigative Dermatology · 2001 · 45 citations
    11. Characterization of Human Keratin-Associated Protein 1 Family Members 2003 · 17 citations
    12. Congenital atrichia and hypotrichosis World Journal of Pediatrics · 2011 · 11 citations
    13. Nutritive Beeinflussung des Haarwachstums Aktuelle Dermatologie · 2011 · 7 citations
    14. A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia Archives of Dermatological Research · 2015 · 2 citations
    15. Triphasic Progressive : une nouvelle formule pour une efficacité accrue contre la chute progressive des cheveux Dermato Mag · 2022
    16. Editors' Picks Journal of Investigative Dermatology · 2010
    17. Reversal of Baldness in Patient Receiving Minoxidil for Hypertension The New England Journal of Medicine · 1980 · 95 citations
    18. Two siblings with a novel nonsense mutation, p.R50X, in the vitamin D receptor gene Endocrine · 2011 · 8 citations
    19. Commonly associated disorders with complete scalp alopecia in early childhood: A review International journal of trichology · 2023
    20. Coat Problems 2021
    21. Clinical Snippets 2003
    22. Androgenetic Alopecia: Stress of Discovery Psychological Reports · 2006 · 7 citations
    23. Hur effektivt är finasteridbehandling mot ärftligt manligt håravfall 2013
    24. Androgenetic Alopecia (AGA) 2018
    25. The human keratins: biology and pathology Histochemistry and Cell Biology · 2008 · 1398 citations
    26. The Nuclear Vitamin D Receptor: Biological and Molecular Regulatory Properties Revealed Journal of bone and mineral research · 1998 · 1308 citations
    27. Genetic Disorders and Defects in Vitamin D Action Endocrinology and metabolism clinics of North America · 2010 · 151 citations
    28. The role of vitamin D receptor mutations in the development of alopecia Molecular and Cellular Endocrinology · 2011 · 109 citations
    29. Functional Analysis of VDR Gene Mutation R343H in A Child with Vitamin D-Resistant Rickets with Alopecia Scientific reports · 2017 · 6 citations
    30. Diseases of the skin. Treatment of scalp disorders. The BMJ · 1974 · 6 citations