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    Research 751–780 of 1000+

    1. Recently Identified Forms of Epidermolysis Bullosa 2015 · 39 citations
    2. Cellular and Metabolic Basis for the Ichthyotic Phenotype in NIPAL4 (Ichthyin)–Deficient Canines American Journal Of Pathology · 2018 · 21 citations
    3. When Recurrent Strokes, Back Pain, and Alopecia Constitute a Hereditary Cause of Small-Vessel Disease, CARASIL in an Arabic Woman The Neurologist · 2022 · 3 citations
    4. Uncombable hair syndrome due to maternal uniparental disomy of chromosome 1 American journal of medical genetics. Part A · 2022
    5. Clinical Snippets Journal of Investigative Dermatology · 2015
    6. Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility 2009 · 189 citations
    7. Cantú Syndrome Is Caused by Mutations in ABCC9 The American Journal of Human Genetics · 2012 · 148 citations
    8. Sebaceous Gland, Hair Shaft, and Epidermal Barrier Abnormalities in Keratosis Pilaris with and without Filaggrin Deficiency ˜The œAmerican journal of pathology · 2015 · 23 citations
    9. Werner′s syndrome Indian Journal of Dermatology Venereology and Leprology · 2012 · 5 citations
    10. Is the Loose Anagen Hair Syndrome a Keratin Disorder? Archives of Dermatology · 2002 · 84 citations
    11. Semidominant Inheritance in Epidermolytic Ichthyosis Journal of Investigative Dermatology · 2013 · 10 citations
    12. Editors' Picks Journal of Investigative Dermatology · 2010
    13. Loose anagen hair syndrome: Treatment with systemic minoxidil characterised by marked hair colour change Australasian Journal of Dermatology · 2018 · 12 citations
    14. Role of caffeine in the management of androgenetic alopecia International Journal of Trichology · 2012 · 11 citations
    15. Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene Journal of Veterinary Medical Science · 2010 · 45 citations
    16. Trichorhinophalangeal syndrome with low expression of TRPS1 on epidermal and hair follicle epithelial cells The Journal of Dermatology · 2013 · 16 citations
    17. Skin and hair abnormalities of Cantu syndrome: A congenital hypertrichosis due to a genetic alteration mimicking the pharmacological effect of minoxidil Journal of Dermatology · 2020 · 7 citations
    18. Hair shaft structures in EDAR induced ectodermal dysplasia BMC Medical Genetics · 2015 · 5 citations
    19. Diabetes, ovarian tumor, hyperparathyroidism, and papillary cancer: A chance association? Endocrinología y nutrición · 2014
    20. Hormonal Control of Cardiac Action Potential Phase 1 Currents in the Brugada Syndrome Revista Argentina de Cardiología · 2014
    21. Adams–Oliver syndrome: new evidence in variable expressivity? International Journal of Dermatology · 2013
    22. A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia Archives of Dermatological Research · 2015 · 2 citations
    23. Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis Nature Genetics · 2009 · 181 citations
    24. HAIR REGROWTH Dermatologic Clinics · 1998 · 118 citations
    25. The Effect of Plasma Rich in Growth Factors on Pattern Hair Loss: A Pilot Study Dermatologic Surgery · 2017 · 70 citations
    26. Practical Guidelines for Evaluation of Loose Anagen Hair Syndrome Archives of Dermatology · 2009 · 46 citations
    27. Trichoscopy in Hair Shaft Disorders Dermatologic Clinics · 2018 · 36 citations
    28. A role for the Tgf-β/Bmp co-receptor Endoglin in the molecular oscillator that regulates the hair follicle cycle Journal of Molecular Cell Biology · 2018 · 26 citations
    29. Monilethrix Treated with Minoxidil International Journal of Immunopathology and Pharmacology · 2011 · 23 citations
    30. PTCH1 Germline Mutations and the Basaloid Follicular Hamartoma Values in the Tumor Spectrum of Basal Cell Carcinoma Syndrome (NBCCS) Anticancer Research · 2018 · 21 citations