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    Research 31–60 of 1000+

    1. Adverse events in patients treated with Jak‐inhibitors for alopecia areata: A systematic review 2023 · 2 citations
    2. Woodhouse-Sakati syndrome: genotype–phenotype review and case of intra-familial heterogeneity Journal of Rare Diseases · 2024
    3. Targeted transgenic expression of the mutation causing Hutchinson-Gilford progeria syndrome leads to proliferative and degenerative epidermal disease Journal of Cell Science · 2008 · 85 citations
    4. Finasteride improves motor, EEG, and cellular changes in rat brain in thioacetamide-induced hepatic encephalopathy American Journal of Physiology-gastrointestinal and Liver Physiology · 2014 · 17 citations
    5. Making the head: Caspases in life and death Frontiers in Cell and Developmental Biology · 2023 · 7 citations
    6. Variable expressivity of syndromic BMP4-related eye, brain, and digital anomalies: A review of the literature and description of three new cases European Journal of Human Genetics · 2019 · 7 citations
    7. Current Understanding of the Pathways Involved in Adult Stem and Progenitor Cell Migration for Tissue Homeostasis and Repair Stem Cell Reviews and Reports · 2016 · 24 citations
    8. Case 21-2012 The New England Journal of Medicine · 2012 · 16 citations
    9. Dictionary JAMA · 1998
    10. Normal Ultrasound Anatomy of the Skin, Nail, and Hair Springer eBooks · 2018 · 2 citations
    11. Zfp462 deficiency causes anxiety‐like behaviors with excessive self‐grooming in mice Genes Brain & Behavior · 2016 · 49 citations
    12. Disturbed Epidermal Structure in Mice with Temporally Controlled Fatp4 Deficiency 2005 · 39 citations
    13. Co-factors of LIM domains (Clims/Ldb/Nli) regulate corneal homeostasis and maintenance of hair follicle stem cells Developmental biology · 2007 · 25 citations
    14. Fortnightly review: Cosmetic surgery The BMJ · 1999 · 14 citations
    15. Biomechanical Factors in Psoriatic Disease: Defective Repair Exertion as a Potential Cause. Hypothesis Presentation and Literature Review ACR Open Rheumatology · 2019 · 8 citations
    16. Treatment of Satoyoshi syndrome: a systematic review Orphanet journal of rare diseases · 2019 · 8 citations
    17. Index of Suspicion Pediatrics in Review · 2007 · 2 citations
    18. Selective Pituitary Resistance to Thyroid Hormone: Clinical Hyperthyroidism with High TSH on Levothyroxine Administration in I-131 Ablated “Graves Disease” Open Journal of Endocrine and Metabolic Diseases · 2022 · 1 citations
    19. Parry–Romberg Syndrome: Radioclinical Dissociation in a Paucisymptomatic Form and a Proposed Diagnostic Framework Diagnostics · 2026
    20. Adult Onset Isolated Hypogonadotropic Hypogonadism- a Cause of Secondary Amenorrhea Journal of the Endocrine Society · 2021
    21. The Role of the Hairless (hr) Gene in the. Regulation of Hair Follicle Catagen Transformation American Journal Of Pathology · 1999 · 166 citations
    22. Dlx3 is a crucial regulator of hair follicle differentiation and cycling Development · 2008 · 132 citations
    23. Furnishing Wound Repair by the Subcutaneous Fascia International Journal of Molecular Sciences · 2021 · 40 citations
    24. Targeted inactivation of integrin-linked kinase in hair follicle stem cells reveals an important modulatory role in skin repair after injury Molecular Biology of the Cell · 2011 · 22 citations
    25. Emergence of the natural history of Myhre syndrome: 47 patients evaluated in the Massachusetts General Hospital Myhre Syndrome Clinic (2016–2023) American Journal of Medical Genetics Part A · 2024 · 21 citations
    26. Applications of Plasma-Activated Liquid in the Medical Field Biomedicines · 2021 · 13 citations
    27. Tooth Development Associated with Mutations in Hereditary Vitamin D–Resistant Rickets JDR Clinical & Translational Research · 2017 · 12 citations
    28. Expanding the phenotype: Four new cases and hope for treatment in Bachmann‐Bupp syndrome American Journal of Medical Genetics Part A · 2021 · 11 citations
    29. Congenital atrichia with papular lesions Indian Journal of Paediatric Dermatology · 2014 · 8 citations
    30. Mandibulofacial dysostosis with alopecia results from ETAR gain-of-function mutations via allosteric effects on ligand binding Journal of Clinical Investigation · 2023 · 4 citations