Search
for

    Sort by

    Research 30 of 1000+

    1. Monilethrix: A rare hereditary condition Indian Journal of Dermatology · 2013 · 12 citations
    2. Identification of a novel heterozygous mutation in the first Japanese case of Marie Unna hereditary hypotrichosis The Journal of Dermatology · 2013 · 6 citations
    3. ST Premature Graying Hair in Seven Years Old Children Jurnal Biomedika dan Kesehatan · 2024
    4. Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity Pediatric Dermatology · 1986 · 5 citations
    5. Familial hypotrichosis of the scalp. Autosomal dominant inheritance in four generations. Acta Dermato Venereologica · 1991 · 17 citations
    6. Topical fluocinolone acetonide acetate ointment in autosomal dominant congenital hypotrichosis 2012
    7. Polycystic Ovaries Are Inherited as an Autosomal Dominant Trait: Analysis of 29 Polycystic Ovary Syndrome and 10 Control Families The Journal of Clinical Endocrinology & Metabolism · 1999 · 63 citations
    8. Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis PLoS ONE · 2014 · 21 citations
    9. Hereditary Mucoepithelial Dysplasia and Autosomal-Dominant IFAP Syndrome Is a Clinical Spectrum Due to SREBF1 Variants 2021 · 6 citations
    10. Heterozygous <i>KRT32</i> variant is responsible for autosomal dominant loose anagen hair syndrome 2025
    11. An incompletely penetrant novel MAFB (p.Ser56Phe) variant in autosomal dominant multicentric carpotarsal osteolysis syndrome International Journal of Molecular Medicine · 2013 · 20 citations
    12. A novel monilethrix mutation in coil 2A of KRT86 causing autosomal dominant monilethrix with incomplete penetrance British Journal of Dermatology · 2012 · 15 citations
    13. Monilethrix: a keratin hHb6 mutation is co‐dominant with variable expression Experimental Dermatology · 1998 · 26 citations
    14. PSEUDOPELADE: AN INHERITED ALOPECIA International Journal of Dermatology · 1996 · 19 citations
    15. Ugreelig hår Tidsskrift for Den norske legeforening · 2022 · 1 citations
    16. Odd-Looking Hair and Progressive Alopecia in Mother and Son JAMA Dermatology · 2014
    17. Familial Dyskeratotic Comedones: A Case Report and Literature Review Clinical Cosmetic and Investigational Dermatology · 2023 · 1 citations
    18. Congenital hypotrichosis due to short anagen British Journal of Dermatology · 2000 · 42 citations
    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. Acquired Uncombable Hair Archives of Dermatology · 1993 · 6 citations
    21. Banded Scalp Hair with an Unusual Glistening Appearance in a Teenager: A Quiz Acta dermato-venereologica · 2018 · 1 citations
    22. SASH1 Mutations and Hereditary Disorders of Pigmentation: Review of Literature Pigment Cell & Melanoma Research · 2025 · 1 citations
    23. Woolly hair generalizado: caso clínico e revisão da literatura Journal Archives of Health · 2024
    24. Masquerading of trichotillomania in a family with monilethrix European Journal of Dermatology · 2011 · 6 citations
    25. Loose Anagen Hair as a Cause of Hereditary Hair Loss in Children Archives of Dermatology · 1992 · 55 citations
    26. LOOSE ANAGEN SYNDROME AND LOOSE ANAGEN HAIR Dermatologic Clinics · 1996 · 25 citations
    27. Dermoscopic Features of Pili Annulati: Features of PA Skin Research and Technology · 2024
    28. Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations Indian Journal of Paediatric Dermatology · 2022
    29. Pitfalls of mapping a large Turkish consanguineous family with vertical monilethrix inheritance. PubMed · 2009 · 4 citations
    30. Inherited Disorders of the Hair Elsevier eBooks · 2013 · 2 citations