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Research 301–330 of 1000+
- Androgenetic Alopecia: Therapy Update
- Correlation between sebum level and severity of male androgenetic alopecia
- A REVIEW ARTICLE – PANCHAKARMA (DETOXIFICATION) SHODHAN KARMA
- Minoxidil oral en alopecia androgénica: estudio retrospectivo acerca de su seguridad en práctica clínica real
- Polycystic ovarian syndrome
- Hair Loss in Children
- Type 2 Diabetes, Metabolic Syndrome and Lipid Metabolism
- Syndromes of Severe Insulin Resistance (SSIRs)
- Disorders of hair in children
- Cutaneous signals of immune system disease
- Hair Loss in Children
- Selected topics in pediatric hair loss
- Avaliação do impacto da redução significativa de peso pela dieta cetogênica de muito baixa caloria nos parâmetros metabólicos, inflamatórios, hormonais e seminais de homens obesos
- Follikelhormone
- Dutasteride Micro-Injections in Androgenetic Alopecia
- Analysis of familial factors using the basic and specific (BASP) classification in Korean patients with androgenetic alopecia
- Recalcitrant Female Pattern Hair Loss Like Alopecia Unveils Unexpected Rare Entity
- Clinico-epidemiology of Keratosis Pilaris with Histopathologic and Dermoscopic Evaluation – A Cross-sectional Study in a Rural Tertiary Hospital
- Deciphering the pathogenesis of central centrifugal cicatricial alopecia
- 284 Deciphering the pathogenesis of central centrifugal cicatricial alopecia
- MON-194 A Case Of Sertoli Cell Tumor In A Patient With Familial Partial Lipodystrophy Type 2
- Central centrifugal cicatricial alopecia: challenges and solutions
- A Monoallelic Two-Hit Mechanism in PLCD1 Explains the Genetic Pathogenesis of Hereditary Trichilemmal Cyst Formation
- Correction of Hair Shaft Defects through Allele-Specific Silencing of Mutant Krt75
- Rapp-Hodgkin syndrome: A review of the aspects of hair and hair color
- Dermoscopy: A rapid bedside tool to assess monilethrix
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- Osseous Metaplasia and Mature Bone Formation With Extramedullary Hematopoiesis in Trichilemmal Cyst
- A TP63 Mutation Causes Prominent Alopecia with Mild Ectodermal Dysplasia
- TRPS1 haploinsufficiency results in increased STAT3 and SOX9 mRNA expression in hair follicles in trichorhinophalangeal syndrome