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    Research 61–90 of 805

    1. A Heritable Keratinization Defect of the Superficial Epidermis in Norfolk Terriers Journal of Comparative Pathology · 2004 · 11 citations
    2. 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
    3. Alopecia developed in a transitional case from pemphigus foliaceus to pemphigus vulgaris The Journal of Dermatology · 2017 · 7 citations
    4. 3D organotypic skin models recapitulate autoantibody-driven pemphigus pathomechanisms and targeted therapeutic response Science Advances · 2026 · 1 citations
    5. Hemidesmosomes and Notch signaling regulate epidermal differentiation via delamination Development · 2026
    6. Secondary Cicatricial Scalp Alopecia Caused by Brunsting-Perry Pemphigoid: A Case Report Cureus · 2025
    7. Scarring Alopecia in a 66‐Year‐Old Woman JEADV Clinical Practice · 2025
    8. A Comprehensive Review on Trichogram and Trichoscopy in Dermatology Pakistan Journal of Medical and Health Sciences · 2021
    9. SnapshotDx Quiz: May 2020 2020
    10. Hair follicle stem cell progeny heal blisters while pausing skin development bioRxiv (Cold Spring Harbor Laboratory) · 2020
    11. 441 RPGRIP1L facilitates desmosomal adhesion through suppressing PKCβII-mediated desmoglein endocytosis: Implication in pemphigus 2016
    12. The role of Kindlin-1 in skin homeostasis and tumor development Max Planck Digital Library · 2014
    13. In this Issue Journal of Investigative Dermatology · 2002
    14. Clinical Patterns and Frequency of Dermatological Manifestations Associated with Pregnancy Pakistan Journal of Medical and Health Sciences · 2023
    15. Abstracts Veterinary Dermatology · 2020
    16. Localized Epidermolysis Bullosa Simplex (Weber-Cockayne type) Journal of Pediatric and Adolescent Gynecology · 2011
    17. Case report: Pseudoporphyria in a 56-year-old man as a result of finasteride intake Journal of the American Academy of Dermatology · 2011
    18. The Functional Diversity of Epidermal Keratins Revealed by the Partial Rescue of the Keratin 14 Null Phenotype by Keratin 16 1999 · 53 citations
    19. Pseudo Pemphigus Phenotypes in Mice with Inactivated Desmoglein 3 ˜The œAmerican journal of pathology · 2015 · 5 citations
    20. Pathological Mechanisms Involved in Epidermolysis Bullosa Simplex: Current Knowledge and Therapeutic Perspectives International Journal of Molecular Sciences · 2024 · 9 citations
    21. Diagnosis, treatment, and long‐term outcomes of pediatric pemphigus: a retrospective study at tertiary medical centers International Journal of Dermatology · 2024 · 3 citations
    22. The Case Files Emergency Medicine News · 2014
    23. Identification of somatic and germline mosaicism for a keratin 5 mutation in epidermolysis bullosa simplex in a family of which the proband was previously regarded as a sporadic case Clinical Genetics · 2004 · 26 citations
    24. Keratolysis in a patient with pemphigus vulgaris British Journal of Ophthalmology · 2001 · 14 citations
    25. 259 Scalp hair follicle dermal sheath fibroblasts express genes associated with promotion of skin integrity/wound healing and prevention of autoimmune responses in Recessive Dystrophic Epidermolysis Bullosa Journal of Investigative Dermatology · 2024
    26. 603 Pathological modeling of epidermolysis bullosa simplex (EBS) using induced pluripotent stem cells (iPSC) Journal of Investigative Dermatology · 2019
    27. Generalized atrophic benign epidermolysis bullosa. PubMed · 1997 · 51 citations
    28. The Significance of Scalp Involvement in Pemphigus: A Literature Review BioMed Research International · 2018 · 13 citations
    29. The dental needs of children with Epidermolysis Bullosa and service delivery: a scoping review BMC Oral Health · 2024 · 4 citations
    30. Loose anagen hair syndrome in two patients with epidermolysis bullosa simplex, Dowling-Meara type Journal of the American Academy of Dermatology · 2012 · 2 citations