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Research 781–810 of 1000+
- Preparation and Evaluation of Curcumin Nanocrystals for Topical Administration: Cell Line Analysis and Histopathological Examination
- Nouvelles thérapeutiques dans la prise en charge de l’alopécie androgénétique
- Severe Post-Bariatric Kwashiorkor Syndrome: A Case Report
- Treatment of frontal fibrosing alopecia: literature review 2020-2025
- UTILIDADES DE LA ESPIRONOLACTONA COMO FÁRMACO ANTIANDROGÉNICO
- Noval advance of histone modification in inflammatory skin diseases and related treatment methods
- Síndrome postfinasterida y disfunción eréctil. Caso clínico y revisión de la literatura
- The stag as an historical source of materia medica
- El papel de los inhibidores de JAK en la alopecia areata: revisión de la literatura
- A MINI REVIEW ON PHOTO- BIOMODULATION- Novel approach
- SKIN SURFACE CHEMISTRY AS A DIAGNOSTIC TOOL FOR SKIN DISEASES
- Distancia promedio de la línea de implantación pilosa frontal y sus estructuras en una población de mujeres colombianas
- Psychiatry, Medicine
- Dictionary
- Health Messages
- National scientific medical meeting 1996 abstracts
- Comparative analysis of therapeutic outcomes in pediatric versus adult ophiasis-pattern alopecia areata: A review of treatment modalities and disease course
- Structure and biochemistry of mammalian hard keratin
- Androgenic Activity in Autism
- <i>egfl6</i> expression in the pharyngeal pouch is dispensable for craniofacial development
- Causal effects of glutamine and lipid-related metabolites on alopecia areata: A 2-sample Mendelian randomization study
- The effects of sonic, desert and Indian hedgehog signalling in skin
- Restoration of skin pigmentation after deep partial or full-thickness burn injury
- Evidence for 1,25-Dihydroxyvitamin D3-independent Transactivation by the Vitamin D Receptor
- Comparison clinical and metabolic effects of metformin and pioglitazone in polycystic ovary syndrome
- Abstract 14
- Mutational spectrum associated with oculocutaneous albinism and Hermansky-Pudlak syndrome in nine Pakistani families
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- P326: Cardiovascular features in adult individuals affected with Tatton-Brown-Rahman syndrome
- Trichoscopy of aplasia cutis congenita of the scalp in skin of color