Search
for

    Sort by

    Research 151–180 of 1000+

    1. The Role of rs6152 Allele and Non-Genetic Factors in Androgenetic Alopecia: A Pilot Study in the Indonesian Local Population Bioscientia medicina · 2024
    2. P378: Expanding the phenotype of hyper-IgE syndrome: Heterozygous VUS in IL6ST with elevated serum IgE and isolated abscesses Genetics in Medicine Open · 2024
    3. A case of myasthenia gravis following alopecia areata Journal of Cutaneous Immunology and Allergy · 2023
    4. Pearly Pinna Papules in a Young Female Indian dermatology online journal · 2023
    5. Hypotrichosis and Hair Loss on the Occipital Scalp Cutis · 2023
    6. Clouston syndrome: A complete genotype–Phenotype correlation after four decades and six generations Indian Journal of Paediatric Dermatology · 2022
    7. Coexistence of Woolly Hair and Monilethrix: A Cases Study Mağallaẗ al-Muẖtar li-l-ʿulūm · 2021
    8. Clinical and molecular genetic studies in hereditary hair loss 2021
    9. Hair Shaft Defect in a Teenage Girl: Trichoscopy Saves the Day! Dermatology practical & conceptual · 2020
    10. Two females with hair loss Journal der Deutschen Dermatologischen Gesellschaft · 2019
    11. Common genetic hair shaft abnormalities may be visualized by light and electron microscope Global Dermatology · 2019
    12. Quoi de neuf en dermatologie pédiatrique ? Annales de dermatologie et de vénéréologie · 2017
    13. Monilethrix – Case report of a rare disease Nasza Dermatologia Online · 2015
    14. Odd-Looking Hair and Progressive Alopecia in Mother and Son JAMA Dermatology · 2014
    15. Hair Restoration Facial Plastic Surgery · 2008
    16. Monilethrix with Acitretin 2005
    17. Informàtica i Dret penal: Els delictes relatius a la informàtica Studia iuridica · 1996
    18. A University Center for the Performing Arts Clinical Cosmetic and Investigational Dermatology · 1982
    19. Gene detection in a family with monilethrix and observation of the treatment effect with 5% topical minoxidil Research Square (Research Square) · 2022
    20. The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis PLoS Genetics · 2012 · 99 citations
    21. N-terminal functional domain of Gasdermin A3 regulates mitochondrial homeostasis via mitochondrial targeting Journal of biomedical science · 2015 · 76 citations
    22. ADAM17 variant causes hair loss via ubiquitin ligase TRIM47 mediated degradation JCI insight · 2024
    23. 474 Stabilizing mutations of KLHL24 ubiquitin ligase cause loss of keratin 14 and human skin fragility Journal of Investigative Dermatology · 2017
    24. The Agouti Gene in Obesity: Central and Peripheral Mechanisms, and Therapeutic Implications 2001
    25. Exploring Mechanical Niches Identified by Hair Follicle Compression and How These Transduce Proliferation and Differentiation Cues in Epidermally Derived cells. Durham e-Theses (Durham University) · 2019
    26. Familial Cortisol Resistance: Differential Diagnostic and Therapeutic Aspects The Journal of Clinical Endocrinology & Metabolism · 1986 · 65 citations
    27. Keratosis follicularis spinulosa decalvans in a family Journal of the American Academy of Dermatology · 2008 · 32 citations
    28. Case Report: Androgen-secreting pediatric adrenocortical tumor of uncertain malignant potential presenting with virilization in a 19-month-old girl Frontiers in Endocrinology · 2026
    29. A Neonate with Blisters Pediatrics in Review · 2020
    30. Mykogene und piläre Faktoren des Haarabbaus durch Dermatomyzeten* (2. Mitteilung) Mycoses · 2009