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    Research 631–660 of 1000+

    1. Hair That Is Difficult to Manage in a Hispanic Girl Skin appendage disorders · 2017 · 1 citations
    2. Acne-Associated Syndromes InTech eBooks · 2017 · 1 citations
    3. Monilethrix: the use of tricoscopy in clinical diagnosis Medicina · 2016 · 1 citations
    4. Monilethrix: Beaded hair and hypotrichosis in a child Cosmoderma · 2026
    5. Assessment of scalp hair survivin in patients with premature greying of hair International Journal of Dermatology Venereology and Leprosy Sciences · 2025
    6. Painful thickened skin on the soles of the feet JAAD case reports · 2022
    7. Central Centrifugal Cicatricial Alopecia (CCCA) CRC Press eBooks · 2021
    8. Polycystic ovarian disease in adult and perimenopausal women Healthy aging research · 2014
    9. Office Diagnosis of Hair Shaft Defects Seminars in cutaneous medicine and surgery · 2006 · 33 citations
    10. A missense mutation in the P2RY5 gene leading to autosomal recessive woolly hair in a Syrian patient Journal of Dermatological Science · 2009 · 13 citations
    11. Sjogren-Larsson syndrome Journal of The American Academy of Dermatology · 2005 · 16 citations
    12. A homozygous nonsense mutation identified in <i>COL7A1</i> in a family with autosomal recessive dystrophic epidermolysis bullosa Journal of Medicine and Life · 2024
    13. Whole-genome SNP genotyping mapped a novel locus for hereditary hypotrichosis on chromosome 2q31.1–q32.2 Journal of Dermatological Science · 2015
    14. Clomiphene Citrate versus Letrozole for Ovulation Induction in PCOS: A Comparative Study Journal of South Asian Federation of Obstetrics and Gynaecology · 2018 · 3 citations
    15. A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis Journal of Investigative Dermatology · 2004 · 44 citations
    16. Desmoglein 4 Mutations Underlie Localized Autosomal Recessive Hypotrichosis in Humans, Mice, and Rats Journal of Investigative Dermatology Symposium Proceedings · 2005 · 13 citations
    17. Case report: Heterozygous mutation in HTRA1 causing typical cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy Frontiers in Genetics · 2023 · 1 citations
    18. Transplantation of autologous single hair units heals chronic wounds in autosomal recessive dystrophic epidermolysis bullosa: A proof-of-concept study Journal of Tissue Viability · 2020 · 7 citations
    19. Retinol dehydrogenase 12 (RDH12): Role in vision, retinal disease and future perspectives Experimental Eye Research · 2019 · 10 citations
    20. The medusa head: Dermoscopic diagnosis of woolly hair syndrome International Journal of Trichology · 2012 · 7 citations
    21. Genetics of Inherited Ichthyoses and Related Diseases Acta Dermato Venereologica · 2020 · 66 citations
    22. Asebia-2J (Scd1ab2J): A New Allele and a Model for Scarring Alopecia ˜The œAmerican journal of pathology · 2000 · 179 citations
    23. Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets BoneKEy Reports · 2014 · 107 citations
    24. Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines American Journal Of Pathology · 2018 · 21 citations
    25. Clinical Snippets Journal of Investigative Dermatology · 2015
    26. Biologically Driven Innovations in Aesthetic Surgery: Advances in Regenerative and Cellular Therapies IECCMEXICO · 2025
    27. Keratin disorders: from gene to therapy 2011 · 109 citations
    28. Congenital Adrenal Hyperplasia Journal of Pediatric and Adolescent Gynecology · 2017 · 88 citations
    29. Hair: more than just an appendage International journal of research in dermatology · 2021
    30. Genetics and Pathophysiology of Congenital Adrenal Hyperplasia Contemporary Endocrinology · 2017