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Research 331–360 of 348
- Finasteride and Dutasteride for the Treatment of Male Androgenetic Alopecia: A Review of Efficacy and Reproductive Adverse Effects
- Epigenetic mechanism of Gtl2-miRNAs causes the primitive sheep characteristics found in purebred Merino sheep
- The mutational analysis of mitochondrial DNA in maternal inheritance of polycystic ovarian syndrome
- Female Pattern Hair Loss: An Overview with Focus on the Genetics
- Study on the Sexual Attractiveness of Male Beard and Female Long Hair to the Opposite Sex
- Congenital Adrenal Hyperplasia
- Folliculitis decalvans: a case report of satisfactory recovery after implementing isotretinoin therapy
- A study of micronutrient levels in premature canities in children
- Occurrence of Klinefelter Syndrome Mosaic 45,X/46,XY/47,XXY/48,XXYY/48,XXXY and Primary Hyperparathyroidism
- The First Visit: Consult and Workup Before Sperm Banking
- Genetics of Diabetes in Childhood
- Geographical Differences in Male Infertility between the United States and Canada: Insights from the Andrology Research Consortium
- Involvement of Follicular Stem Cells in Forming Not Only the Follicle but Also the Epidermis
- Regenerative Medicine-Based Treatment for Vitiligo: An Overview
- Defining compartmentalized stem cell populations with distinct cell division dynamics in the ocular surface epithelium
- Eyes open on stem cells
- Treatment of androgenetic alopecia in transgender people receiving testosterone therapy with sublingual minoxidil: A randomized, double-blind, placebo-controlled clinical trial
- Novel Vegan Exosome-like Biomimetic Vesicles for Skin and Hair Follicle Protection and Rejuvenation: Structural and Functional Characterization and Placebo-Controlled Clinical Efficacy Studies
- Associaton of Insulin Resistance Linked Diseases and Hair Loss in Elderly Men. Finnish Population-based Study
- Hair Loss, Insulin Resistance, and Heredity in Middle-aged Women. a Population-based Study
- The Interplay between Finasteride-Induced Androgen Imbalance, Endoplasmic Reticulum Stress, Oxidative Stress, and Liver Disorders in Paternal and Filial Generation
- Marie Unna hereditary hypotrichosis: A Turkish family with loss of eyebrows and a <i>U2HR</i> mutation
- Hereditary Hypotrichosis and Localized Morphea: A New Clinical Entity
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Critical Evaluation of Concept of Genetics in Ayurveda WSR to Eight Undesired Body Types (Ashta Nindit)
- STUB1 mutations in autosomal recessive ataxias – evidence for mutation-specific clinical heterogeneity
- Analysis of familial factors using the basic and specific (BASP) classification in Korean patients with androgenetic alopecia
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- National scientific medical meeting 1996 abstracts
- When Rare Meets Risky: Clouston Syndrome with Cutaneous Squamous Cell Carcinoma