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    Research 181–210 of 1000+

    1. Novel missense mutation in the EDA gene in a family affected by oligodontia 2016 · 12 citations
    2. Androgenetic Alopecia Springer eBooks · 1996 · 8 citations
    3. Diagnostic challenges in determining alopecia areata Expert Review of Dermatology · 2013 · 1 citations
    4. Hereditary, Congenital, and Acquired Alopecias Elsevier eBooks · 2006 · 1 citations
    5. Case Report: PTCH1 splice-site mutation and sonidegib treatment in Gorlin-Goltz syndrome: clinical insights from a family case study Frontiers in Medicine · 2026
    6. Complications in follicular unit excision hair transplantation: current evidence and practical approaches Frontiers in Medicine · 2026
    7. Polarized microscopy in genetic hair disorders: case series 2025
    8. Woodhouse-Sakati Syndrome with Unique Unreported Previous Findings Scholars Journal of Medical Case Reports · 2021
    9. Lab Quality Management and Methodology Indian Journal of Medical Biochemistry · 2015
    10. Gonads John Wiley & Sons, Ltd eBooks · 2013
    11. Risk factors for prostate cancer: a case-control study investigating selected key exposures and their interactions with predisposition genes Jurnal Natural (Faculty of Mathematics and Natural Science, Syiah Kuala University) · 2010
    12. HAIR REGROWTH Dermatologic Clinics · 1998 · 118 citations
    13. Nonalcoholic fatty liver disease and polycystic ovary syndrome World Journal of Gastroenterology · 2014 · 114 citations
    14. Nonsurgical Management of Facial Masculinization and Feminization Aesthetic surgery journal · 2018 · 39 citations
    15. Subpericranial and epidural abscess with skull osteomyelitis as a complication of microneedling for alopecia: A singular case report Surgical Neurology International · 2026
    16. Poster Presentations at the 28th Joint Meeting of the International Society of Dermatopathology, March 5–6, 2025, Orlando, Florida, USA American Journal of Dermatopathology · 2025
    17. Cosmetic Treatment Using Botulinum Toxin in the Oral and Maxillofacial Area: A Narrative Review of Esthetic Techniques Toxins · 2023 · 52 citations
    18. Expanding phenotype of hereditary fibrosing poikiloderma with tendon contractures, myopathy, and pulmonary fibrosis caused by FAM111B mutations: Report of an additional family raising the question of cancer predisposition and a short review of early-onset poikiloderma JAAD case reports · 2017 · 23 citations
    19. Periorbital facial rejuvenation; applied anatomy and pre-operative assessment journal of current ophthalmology · 2017 · 36 citations
    20. The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation 2010 · 68 citations
    21. A rare LMNA missense mutation causing a severe phenotype of mandibuloacral dysplasia type A: a case report Revista Paulista de Pediatria · 2024 · 2 citations
    22. Exploring the Complexities of TGF-beta Signaling in Keloids: Beyond the Classical Smad Pathway International Journal of Molecular Sciences · 2026
    23. Reversible Vision Loss With Pituitary Microadenoma Following PRP Injection for Hair Growth: A Rare Case Report and a Mini‐Review of the Literature Clinical Case Reports · 2025
    24. An Unusual Case of Mycosis Fungoides Presenting with Multiple Atypical Morphologies in a Photoexacerbated Distribution Indian Dermatology Online Journal · 2025
    25. A Honey Trap for the Treatment of Acne: Manipulating the Follicular Microenvironment to Control<i>Propionibacterium acnes</i> BioMed research international · 2013 · 9 citations
    26. Menopause and hair loss in women: Exploring the hormonal transition Maturitas · 2025 · 1 citations
    27. Report on the 11th National Congress AICPE (Associazione Italiana di Chirurgia Plastica Estetica) Held in Rimini, Italy, 12–14 April 2024 Surgical Techniques Development · 2024
    28. Challenges in the Physical Characterization of Lipid Nanoparticles Pharmaceutics · 2021 · 92 citations
    29. Effects of microenvironment and biological behavior on the paracrine function of stem cells Genes & Diseases · 2023 · 44 citations
    30. Novel Mutation in Sjögren-Larsson Syndrome Is Associated With Divergent Neurologic Phenotypes Journal of child neurology · 2012 · 15 citations