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    Research 211–240 of 788

    1. Male-Pattern Baldness Is Common in Men with X-Linked Recessive Ichthyosis Dermatology · 2003 · 6 citations
    2. Topical polyhydroxy acid treatment for autosomal recessive congenital ichthyosis in the golden retriever: a prospective pilot study Veterinary dermatology · 2018 · 5 citations
    3. Superficial Epidermolytic Ichthyosis—Hypertrichosis as a Clue to Diagnosis Pediatric Dermatology · 2016 · 3 citations
    4. NIPAL4 mutation c.527C˃A identified in Romanian patients with autosomal recessive congenital ichthyosis Revista română de medicină de laborator · 2016 · 1 citations
    5. 152 Alopecia patterns in patients with autosomal receesive congenital ichthyosis Journal of Investigative Dermatology · 2024
    6. Alopecia patterns and trichoscopic findings in patients with autosomal recessive congenital ichthyosis International Journal of Women’s Dermatology · 2024
    7. Advances in the treatment of autosomal recessive congenital ichthyosis, a look towards the repositioning of drugs Frontiers in pharmacology · 2023
    8. Prenatal Screening for Bathing-suit Ichthyosis After Diagnosis in an Older Sibling Actas Dermo-Sifiliográficas · 2015 · 1 citations
    9. Updated mutational spectrum and genotype-phenotype correlations in ichthyosis patients with ABCA12 pathogenic variants Institutional Repositories DataBase (IRDB) · 2024
    10. Chronic Ulceration of the Scalp Associated with Genetically Different Types of Congenital Ichthyosis: A Series of Four Cases Acta dermato-venereologica · 2020 · 1 citations
    11. Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection Biomedicines · 2025
    12. 478 Mutation-specific siRNA Knockdown of GJB2 − Potential gene therapy for Keratitis-ichthyosis-deafness Syndrome Journal of Investigative Dermatology · 2017
    13. Netherton's syndrome: A syndrome of elevated IgE and characteristic skin and hair findings 1995 · 124 citations
    14. Overexpression of Hoxc13 in differentiating keratinocytes results in downregulation of a novel hair keratin gene cluster and alopecia Development · 2001 · 114 citations
    15. Noncalcemic actions of 1,25-dihydroxyvitamin D3 and clinical applications Bone · 1995 · 96 citations
    16. Cutaneous Syndromes Produced as Side Effects of Triparanol Therapy Archives of Dermatology · 1963 · 74 citations
    17. MULTIPLE DEFECTS OF THE HAIR SHAFT IN NETHERTON'S DISEASE. British Journal of Dermatology · 1969 · 58 citations
    18. Oral Retinoids in Dermatology International Journal of Dermatology · 1981 · 52 citations
    19. Skin diseases in the alpaca (<i>Vicugna pacos</i>): a literature review and retrospective analysis of 68 cases (Cornell University 1997–2006) Veterinary Dermatology · 2010 · 46 citations
    20. Disorders of Keratinization American journal of clinical dermatology · 2004 · 44 citations
    21. Hair Shaft Videodermoscopy in Netherton Syndrome Pediatric Dermatology · 2008 · 41 citations
    22. 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
    23. Retinoids and Keratinization International Journal of Dermatology · 1988 · 32 citations
    24. Chemotherapy of psoriasis and other skin disorders with oral retinoids Pharmacology & Therapeutics · 1981 · 31 citations
    25. Trichoscopy as a diagnostic tool in trichorrhexis invaginata and Netherton syndrome Anais Brasileiros de Dermatologia · 2015 · 30 citations
    26. Off-Label Uses of Topical Vitamin D in Dermatology: A Systematic Review Journal of cutaneous medicine and surgery · 2014 · 26 citations
    27. Trichothiodystrophy with Dysmyelination and Central Osteosclerosis American Journal of Neuroradiology · 2010 · 16 citations
    28. Sjogren-Larsson syndrome Journal of The American Academy of Dermatology · 2005 · 16 citations
    29. Biological significance of FoxN1 gain-of-function mutations during T and B lymphopoiesis in juvenile mice Cell death and disease · 2014 · 16 citations
    30. Symmetrical acrokeratoderma: A peculiar entity in China? Clinicopathologic and immunopathologic study of 34 new cases Journal of The American Academy of Dermatology · 2014 · 14 citations