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    Research 421–450 of 1000+

    1. Hypotrichosis with juvenile macular dystrophy: a case report with molecular study 2018
    2. Monilethrix – Case report of a rare disease Nasza Dermatologia Online · 2015
    3. Disorders of Keratinization 2014
    4. Odd-Looking Hair and Progressive Alopecia in Mother and Son JAMA Dermatology · 2014
    5. Woolly Hair in Two Siblings International Journal of Trichology · 2012
    6. Curly : a new hair defect mutation in the SELH/bc mouse strain 2009
    7. INDENTIFICATION OF GENES INVOLVED IN INHERITED ECTODERMAL DYSPLASIAS 2008
    8. Tricotiodistrofia. Reporte de un caso Revista del Centro Dermatológico Pascua · 2007
    9. Research Snippets British Journal of Dermatology · 2005
    10. Monilethrix with Acitretin 2005
    11. Lanceolate hair-J (lahJ): a mouse model for human hair disorders [In Process Citation] The Mouseion at the JAXlibrary (Jackson Laboratory) · 2000
    12. Informàtica i Dret penal: Els delictes relatius a la informàtica Studia iuridica · 1996
    13. A genetic electrophoretic variant of high-sulfur hair proteins for forensic hair comparisons. I. Characterization of variant high-sulfur proteins of human hair. PubMed · 1989
    14. A University Center for the Performing Arts Clinical Cosmetic and Investigational Dermatology · 1982
    15. Gene detection in a family with monilethrix and observation of the treatment effect with 5% topical minoxidil Research Square (Research Square) · 2022
    16. Mutations in the Desmoglein 4 Gene Are Associated with Monilethrix-like Congenital Hypotrichosis 2006 · 74 citations
    17. The lanceolate hair rat phenotype results from a missense mutation in a calcium coordinating site of the desmoglein 4 gene Genomics · 2004 · 50 citations
    18. More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players Journal of Investigative Dermatology · 2006 · 35 citations
    19. When Recurrent Strokes, Back Pain, and Alopecia Constitute a Hereditary Cause of Small-Vessel Disease, CARASIL in an Arabic Woman The Neurologist · 2022 · 3 citations
    20. Current Genetics in Hair Diseases InTech eBooks · 2013 · 1 citations
    21. A New CARASIL Family: Recurrent Lobar Hemorrhage as a Novel Characteristic of the Disease Turkish Journal of Cerebrovascular Diseases · 2025
    22. Updated mutational spectrum and genotype-phenotype correlations in ichthyosis patients with ABCA12 pathogenic variants Institutional Repositories DataBase (IRDB) · 2024
    23. Lanceolate Hair (lah): A Recessive Mouse Mutation with Alopecia and Abnormal Hair 1996 · 36 citations
    24. Keratosis follicularis spinulosa decalvans in a family Journal of the American Academy of Dermatology · 2008 · 32 citations
    25. Nonclassic 21-hydroxylase deficiency Fertility and Sterility · 2006 · 13 citations
    26. Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1 American journal of medical genetics. Part A · 2022
    27. An Update of Congenital Adrenal Hyperplasia Annals of the New York Academy of Sciences · 2004 · 151 citations
    28. Familial Cortisol Resistance: Differential Diagnostic and Therapeutic Aspects The Journal of Clinical Endocrinology & Metabolism · 1986 · 65 citations
    29. Treatment of monilethrix with oral minoxidil JAAD case reports · 2016 · 37 citations
    30. Keratin 71 Mutations: From Water Dogs to Woolly Hair 2012 · 11 citations