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    Research 871–900 of 1000+

    1. Ocular and Mucocutaneous Sequelae among Survivors of Stevens-Johnson Syndrome and Toxic Epidermal Necrolysis in Togo Dermatology Research and Practice · 2019 · 6 citations
    2. Parry-Romberg Syndrome Augmented by Hyaluronic Acid Filler 2018 · 6 citations
    3. Hair Follicle Regeneration by Transplantation of a Bioengineered Hair Follicle Germ Methods in molecular biology · 2016 · 6 citations
    4. Cell-Based Model Systems for Validation of Various Efficacy-Based Claims for Cosmetic Ingredients Cosmetics · 2022 · 5 citations
    5. Hypotrichosis with juvenile macular dystrophy: a case report with molecular study Arquivos Brasileiros de Oftalmologia · 2017 · 5 citations
    6. Focal palmoplantar callosities in non-Herlitz junctional epidermolysis bullosa Journal of the American Academy of Dermatology · 2005 · 5 citations
    7. Child with De Novo t(1;6)(p22.1;p22.1) translocation and features of ectodermal dysplasia with hypodontia and developmental delay American Journal of Medical Genetics Part A · 2003 · 5 citations
    8. The dental needs of children with Epidermolysis Bullosa and service delivery: a scoping review BMC Oral Health · 2024 · 4 citations
    9. Hypotrichosis with juvenile macular dystrophy International Journal of Trichology · 2018 · 4 citations
    10. Substance P in keratosis follicularis spinulosa decalvans JAAD case reports · 2015 · 4 citations
    11. Monilethrix, a rare inherited hair shaft disorder in siblings Indian dermatology online journal · 2014 · 4 citations
    12. Monilethrix International Journal of Trichology · 2013 · 4 citations
    13. A study of phenotypic correlation with the genotypic status of HTM regions of KRTHB6 and KRTHB1 genes in monilethrix families of Indian origin Annales de Génétique · 2003 · 4 citations
    14. Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless Journal of Investigative Dermatology · 2000 · 4 citations
    15. Molecular Evolution and Protein Structure Variation of Dkk Family Genes · 2023 · 3 citations
    16. Congenital triangular alopecia - A case report International journal of trichology · 2020 · 3 citations
    17. Idiopathic hypoparathyroidism with extensive intracranial calcification in children Medicine · 2017 · 3 citations
    18. Acquired Generalized Hypertrichosis Due to Diazoxide 2013 · 3 citations
    19. Alopecia and Periodontitis: Exploring the connecting dots Journal of Indian Society of Periodontology · 2023 · 2 citations
    20. Gene detection in a family with monilethrix and treatment with 5% topical minoxidil Skin research and technology · 2022 · 2 citations
    21. A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies 2022 · 2 citations
    22. Treatment of Alopecia in Children Journal of Drugs in Dermatology · 2021 · 2 citations
    23. A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia 2020 · 2 citations
    24. Gene Expression Analysis of Chondrogenic Markers in Hair Follicle Dermal Papillae Cells Under the Effect of Laser Photobiomodulation and the Synovial Fluid Journal of lasers in medical sciences · 2019 · 2 citations
    25. Spontaneous Quick Resolution of Uncombable Hair Syndrome-Like Disease Skin appendage disorders · 2018 · 2 citations
    26. Trichothiodystrophy without associated neuroectodermal features in two siblings International Journal of Trichology · 2018 · 2 citations
    27. Dysfunction of keratinocyte adhesion Experimental Dermatology · 2004 · 2 citations
    28. The Roles of EDA2R in Ageing and Disease Aging Cell · 2025 · 1 citations
    29. Cosmeceutical Applications of Phlorotannins from Brown Seaweeds Phycology · 2025 · 1 citations
    30. Exploring the Differentiation Abilities of Hair Follicle and Dental Pulp Stem Cells Into Islet Like Cells Cell Biology International · 2025 · 1 citations