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    Research 301–330 of 1000+

    1. Dermatopathia pigmentosa reticularis: A report of a case with delayed onset alopecia and onychodystrophy JAAD Case Reports · 2019 · 4 citations
    2. SkIndia Quiz 24: Itchy papules over face Indian Dermatology Online Journal · 2016
    3. Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness 2021
    4. More than One Gene Involved in Monilethrix: Intracellular but also Extracellular Players Journal of Investigative Dermatology · 2006 · 35 citations
    5. Rare Coexistence of Monilethrix and Trichorrhexis Nodosa in a Pediatric Patient: A Case Report Clinical Case Reports · 2026
    6. Whole exome sequencing in Alopecia Areata identifies rare variants in KRT82 Nature communications · 2022 · 9 citations
    7. FOXN1 deficient nude severe combined immunodeficiency Orphanet journal of rare diseases · 2017 · 32 citations
    8. A Novel Mutation in the<i>MBTPS2</i>Gene Resulting in Ichthyosis Follicularis, Atrichia, and Photophobia Syndrome Annals of Dermatology · 2022 · 1 citations
    9. A Case of Tricho-rhino-phalangeal Syndrome Caused by a Novel Heterozygous Nonsense Mutation in the TRPS1 Gene 2024
    10. Animals in Dermatology 2024
    11. Ichthyosis and Trichothiodystrophy: the Tay and PIBI(D)S Syndromes 1989 · 2 citations
    12. Painful thickened skin on the soles of the feet JAAD case reports · 2022
    13. Morphologische und biochemische untersuchungen am Haar bei gestörtem Aminosäurestoffwechsel Archives of Dermatological Research · 1976 · 4 citations
    14. Deimination and Peptidylarginine Deiminases in Skin Physiology and Diseases International Journal of Molecular Sciences · 2020 · 57 citations
    15. Telogen Effluvium: A Review Journal of Clinical and Diagnostic Research · 2015 · 70 citations
    16. Molecular Genetic Characteristics of the Hoxc13 Gene and Association Analysis of Wool Traits International journal of molecular sciences · 2024
    17. A Novel Connexin 26 Mutation in a Patient Diagnosed with Keratitis–Ichthyosis–Deafness Syndrome 2002 · 152 citations
    18. Atrichia Caused by Mutations in the Vitamin D Receptor Gene is a Phenocopy of Generalized Atrichia Caused by Mutations in the Hairless Gene 2001 · 139 citations
    19. Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome The American Journal of Human Genetics · 2012 · 71 citations
    20. The developmental basis of fingerprint pattern formation and variation Cell · 2023 · 44 citations
    21. Ribonucleotide Excision Repair Is Essential to Prevent Squamous Cell Carcinoma of the Skin Cancer research · 2018 · 34 citations
    22. Novel missense mutation in the EDA gene in a family affected by oligodontia 2016 · 12 citations
    23. Remarks on Perfection in Plastic Surgery of the Face BioMed Research International · 2018 · 3 citations
    24. Ichthyosis follicularis alopecia and photophobia syndrome:Transient improvement with oral isotretinoin Indian journal of paediatric dermatology · 2015 · 3 citations
    25. Challenges associated with the identification of germline variants on myeloid malignancy genomic profiling—a Singaporean experience Frontiers in Oncology · 2023 · 1 citations
    26. Hypotrichosis in a child with olmsted syndrome Indian Dermatology Online Journal · 2018
    27. Secondary Syphilis in a 12-Year-Old Girl Misdiagnosed as Pityriasis lichenoides et varioliformis acuta: A Case Report Clinical Cosmetic and Investigational Dermatology · 2021 · 1 citations
    28. Treatment of pediatric alopecia areata: A systematic review Journal of the American Academy of Dermatology · 2021 · 48 citations
    29. Voice changes in reproductive disorders, thyroid disorders and diabetes: a review Endocrine connections · 2022
    30. Three Cases of Canine Dermatomyositis-Like Disease Acta Scientiae Veterinariae · 2018