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    Research 511–540 of 1000+

    1. Dermatopathia Pigmentosa Reticularis with Salzmann’s nodular degeneration of cornea: A rare association Nepalese journal of ophthalmology · 2015 · 5 citations
    2. Type II Vitamin D Dependent Rickets: A Case Report Journal of Nepal Paediatric Society · 1970 · 5 citations
    3. Hypotrichosis with juvenile macular dystrophy International Journal of Trichology · 2018 · 4 citations
    4. Telogen hair loss and androgenetic‐like alopecia in GAPO syndrome Australasian Journal of Dermatology · 2018 · 1 citations
    5. Inherited Acrodermatitis Enteropathica Indian Journal of Paediatric Dermatology · 2025
    6. Adli Uygulamalarda Yeni Nesil Dizileme Teknolojilerinin Yeri ve Önemi Turkish Journal of Forensic Medicine · 2024
    7. Atrichia with Papular Lesions: Dermoscopy to the Rescue Indian Journal of Dermatology · 2024
    8. P-19 A case of Birt Hogg Dube syndrome presented with parathyroid carcinoma JCEM case reports · 2024
    9. Case Report: Bi-allelic missense variant in the desmocollin 3 gene causes hypotrichosis and recurrent skin vesicles Frontiers in genetics · 2022
    10. Papular atrichia International journal of research in dermatology · 2020
    11. Photosensitive Trichothiodystrophy with Complex Cerebral Abnormalities Neuropediatrics · 2012
    12. Acrodermatitis enteropathica: Case report analyses of zinc metabolism electron microscopic examination and immune function The Journal of Trace Elements in Experimental Medicine · 2000
    13. A missense mutation in the type II hair keratin hHb3 is associated with monilethrix Journal of Medical Genetics · 2005 · 79 citations
    14. <i>C2orf37</i> mutational spectrum in Woodhouse–Sakati syndrome patients Clinical genetics · 2010 · 43 citations
    15. Congenital adrenal hyperplasia Dermatologic Therapy · 2008 · 16 citations
    16. A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis PLoS ONE · 2012 · 13 citations
    17. Successful induction of oral tolerance in Netherton syndrome Allergologia et immunopathologia · 2011 · 11 citations
    18. A novel mutation in the FERMT1 gene in a Spanish family with Kindler’s syndrome Journal of The European Academy of Dermatology and Venereology · 2009 · 8 citations
    19. A newborn presenting with congenital blistering International Journal of Dermatology · 2004 · 7 citations
    20. Hereditary vitamin D rickets: a case series in a family 2014 · 6 citations
    21. Werner′s syndrome Indian Journal of Dermatology Venereology and Leprology · 2012 · 5 citations
    22. Monilethrix, a rare inherited hair shaft disorder in siblings Indian dermatology online journal · 2014 · 4 citations
    23. Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b The Journal of Dermatology · 2013 · 4 citations
    24. Case Report: A Chinese Family of Woodhouse-Sakati Syndrome With Diabetes Mellitus, With a Novel Biallelic Deletion Mutation of the DCAF17 Gene Frontiers in endocrinology · 2021 · 3 citations
    25. Hutchinson-Gilford progeria syndrome: Report of 2 cases and a novel LMNA mutation of HGPS in China Journal of the American Academy of Dermatology · 2013 · 3 citations
    26. PLACK syndrome associated with alopecia areata and a novel homozygous base pair insertion in exon 18 of CAST gene Indian Journal of Dermatology Venereology and Leprology · 2023 · 2 citations
    27. 199 Impairment of notch 1 signaling is a common defect in lesions from patients with hidradenitis suppurativa Journal of Investigative Dermatology · 2017 · 2 citations
    28. A 40-Year-Old Woman With Facial Papules and Flank Pain Archives of Pathology & Laboratory Medicine · 2006 · 2 citations
    29. ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India Indian dermatology online journal · 2018 · 1 citations
    30. Rickets with Alopecia Signals Vitamin D Dependent Rickets Type II Journal of Nepal Paediatric Society · 2016 · 1 citations