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    Research 151–180 of 1000+

    1. Dermatopathia Pigmentosa Reticularis with Salzmann’s nodular degeneration of cornea: A rare association Nepalese journal of ophthalmology · 2015 · 5 citations
    2. P-19 A case of Birt Hogg Dube syndrome presented with parathyroid carcinoma JCEM case reports · 2024
    3. A missense mutation in the type II hair keratin hHb3 is associated with monilethrix Journal of Medical Genetics · 2005 · 79 citations
    4. A newborn presenting with congenital blistering International Journal of Dermatology · 2004 · 7 citations
    5. Monilethrix, a rare inherited hair shaft disorder in siblings Indian dermatology online journal · 2014 · 4 citations
    6. Delayed-onset pachyonychia congenita caused by a novel mutation in the V2 domain of keratin 6b The Journal of Dermatology · 2013 · 4 citations
    7. 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
    8. 199 Impairment of notch 1 signaling is a common defect in lesions from patients with hidradenitis suppurativa Journal of Investigative Dermatology · 2017 · 2 citations
    9. A 40-Year-Old Woman With Facial Papules and Flank Pain Archives of Pathology & Laboratory Medicine · 2006 · 2 citations
    10. ADULT (acro–dermato–ungual–lacrimal–tooth) syndrome: A case report from India Indian dermatology online journal · 2018 · 1 citations
    11. Androgenic alopecia and differential diagnoses of alopecia University of Zadar Institutional Repository · 2023
    12. Clinical cases of Darier-White follicular dyskeratosis Medičnì perspektivi · 2022
    13. Moniletrix of the scalp from almost normal aspect to total alopecia: variable intrafamilial expressiveness 2021
    14. Loose anagen syndrome in one identical twin girl. PubMed · 2021
    15. Loose Anagen Syndrome 2019
    16. Hair Anomalies in a 6-Year-Old Girl Case reports in clinical medicine · 2016
    17. Hair dysplasias 2015
    18. The Case | Bilateral kidney tumors and lung cysts Kidney international · 2013
    19. Novel frameshift mutation in TRPS1 in a ukrainian patient with trichorhinophalangeal syndrome type I International Journal of Trichology · 2013
    20. Targeting integrin pathways: mechanisms and advances in therapy Signal Transduction and Targeted Therapy · 2023 · 54 citations
    21. Diagnostic approach to low‐renin hypertension Clinical Endocrinology · 2018 · 29 citations
    22. Delayed Puberty Pediatrics in Review · 2010 · 21 citations
    23. Dermatopathia pigmentosa reticularis: A rare reticulate pigmentary disorder Indian dermatology online journal · 2013 · 12 citations
    24. Multicentric calcified trichilemmal cysts with alopecia universalis affecting siblings Indian Journal of Dermatology Venereology and Leprology · 2012 · 9 citations
    25. A review of genotrichoses and hair pathology associated with inherited skin diseases British Journal of Dermatology · 2023 · 8 citations
    26. Central Centrifugal Cicatricial Alopecia in the Adolescent Population: An Overview of Available Literature Life · 2023 · 5 citations
    27. Baker′s dozen on the scalp: An interesting case of multiple trichilemmal cyst Journal of Cutaneous and Aesthetic Surgery · 2014 · 5 citations
    28. A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report Revista Paulista de Pediatria · 2024 · 2 citations
    29. Corneodesmosin: Structure, Function and Involvement in Pathophysiology The Open Dermatology Journal · 2010 · 2 citations
    30. Hair That Is Difficult to Manage in a Hispanic Girl Skin appendage disorders · 2017 · 1 citations