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    Research 31–60 of 1000+

    1. Disorders of hair in children Current Paediatrics · 2003
    2. Differential expression and functionality of ATP-binding cassette transporters in the human hair follicle British Journal of Dermatology · 2014 · 25 citations
    3. Congenital hair loss disorders: Rare, but not too rare The Journal of Dermatology · 2011 · 41 citations
    4. Clinical and genetic investigation of ichthyosis in familial and sporadic cases in south of Tunisia: genotype–phenotype correlation BMC Medical Genomics · 2022 · 6 citations
    5. Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin Genetics in medicine · 2018 · 10 citations
    6. Inherited ichthyoses/generalized Mendelian disorders of cornification European journal of human genetics · 2012 · 81 citations
    7. Autosomal-Dominant Woolly Hair Resulting from Disruption of Keratin 74 (KRT74), a Potential Determinant of Human Hair Texture The American Journal of Human Genetics · 2010 · 97 citations
    8. Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes American Journal of Medical Genetics Part A · 2021 · 16 citations
    9. Cystatin M/E Variant Causes Autosomal Dominant Keratosis Follicularis Spinulosa Decalvans by Dysregulating Cathepsins L and V Frontiers in Genetics · 2021 · 6 citations
    10. Hypotrichosis in a child with olmsted syndrome Indian Dermatology Online Journal · 2018
    11. First Symposium of Ichthyosis Experts 2013 · 1 citations
    12. Ichthyosis with confetti: clinics, molecular genetics and management Orphanet Journal of Rare Diseases · 2015 · 36 citations
    13. Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome American journal of human genetics · 2020 · 34 citations
    14. Severe Skin Permeability Barrier Dysfunction in Knockout Mice Deficient in a Fatty Acid ω-Hydroxylase Crucial to Acylceramide Production Journal of Investigative Dermatology · 2019 · 40 citations
    15. Genetic Hair Disorders: A Review Dermatology and Therapy · 2019 · 26 citations
    16. Metabolic and pathologic profiles of human LSS deficiency recapitulated in mice PLOS genetics · 2020 · 23 citations
    17. New clinico‐genetic classification of trichothiodystrophy American Journal of Medical Genetics Part A · 2009 · 68 citations
    18. Localisation and regulation of cholesterol transporters in the human hair follicle: mapping changes across the hair cycle Histochemistry and Cell Biology · 2021 · 13 citations
    19. Trichoscopy in Hair Shaft Disorders Dermatologic Clinics · 2018 · 36 citations
    20. SCALP HAIR CHARACTERISTICS IN THE NEWBORN INFANT Advances in neonatal care · 2003 · 46 citations
    21. Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses Archives of Dermatology · 2001 · 23 citations
    22. Male fertility and skin diseases Reviews in Endocrine and Metabolic Disorders · 2016 · 12 citations
    23. Hair and Nail Relationship Skinmed · 2005 · 21 citations
    24. Secondary cicatricial and other permanent alopecias Dermatologic Therapy · 2008 · 20 citations
    25. Skin signs of systemic diseases Clinics in Dermatology · 2011 · 21 citations
    26. Diseases of the Hair and Nails Medical Clinics of North America · 2009 · 4 citations
    27. Prognosis and Management of Congenital Hair Shaft Disorders without Fragility—Part II Pediatric Dermatology · 2016 · 14 citations
    28. Hair Shaft Dysplasias International Journal of Dermatology · 1988 · 19 citations
    29. Oral Presentations Pediatric Dermatology · 2017
    30. Role of trichoscopy in diagnosis of different hair and scalp disorders in pediatrics International Journal of Dermatology Venereology and Leprosy Sciences · 2024