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Research 91–120 of 346
- The Who’s, What’s, and “Y”s: Y Sex Chromosome Loss and Methylation for Analysis in Male Aging and Mortality and Forensic Science Applications
- Intrinsic and Extrinsic Factors Associated with Hair Graying (Canities) and Therapeutic Potential of Plant Extracts and Phytochemicals
- E-Poster
- Endocrinology
- Pre-Clinical Cell-Based Therapy for Limbal Stem Cell Deficiency
- Paternal Finasteride Treatment Can Influence the Testicular Transcriptome Profile of Male Offspring—Preliminary Study
- Paternal finasteride exposure and its impact on offspring testicular histopathology and intracellular junctions: the role of occludin and N-cadherin
- Infertility and teratogenicity after paternal exposure to systemic dermatologic medications: A systematic review
- Counselling regarding paternal exposures: Can we do better?
- Pregnancy Outcomes with Paternal Exposure to Finasteride, a Synthetic 5-Alpha-Reductase Inhibitor: A Case Series
- Safety concerns of paternal drug exposure on fertility, pregnancy and offspring: An analysis based on the FDA adverse event reporting system
- A pilot study of paternal drug exposure: the Motherisk experience
- Comparison of Androgenetic Alopecia Prevalence in Paternal and Maternal Male Family Members of Male Androgenetic Alopecia Patients
- Application of the basic and specific classification on patterned hair loss in Indians
- Early onset androgenetic alopecia in men and associated risk factors: a hospital based study
- 남성형탈모증 환자들의 생활습관에 대한 고찰
- Androgen levels and apoptosis in the testis during postnatal development of finasteride-treated male rat offspring
- The postnatal offspring of finasteride-treated male rats show altered ERα and PCNA expression in the liver
- Family History and Risk of Hair Loss
- New changes in pregnancy and lactation labelling: Review of dermatologic drugs
- Relationship between diet, atopy, family history, and premature hair graying
- Early-onset androgenetic alopecia in China: a descriptive study of a large outpatient cohort
- Mutations in the Desmoglein 4 Gene Are Associated with Monilethrix-like Congenital Hypotrichosis
- Genetic and other epidemiological risk factors of infants and children with hypospadias: a case control study
- Delving into diversity: exploring different risk factors of premature greying of hair
- Male pattern hair loss: Taking one for the team: The selfless gene
- Prevalence of Type II diabetes mellitus and insulin resistance in parents of women with polycystic ovary syndrome
- A new compound heterozygous frameshift mutation in the type II 3 beta-hydroxysteroid dehydrogenase (3 beta-HSD) gene causes salt-wasting 3 beta-HSD deficiency congenital adrenal hyperplasia.
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- The Annual Changes of Clinical Manifestation of Androgenetic Alopecia Clinic in Korean Males and Females: A Outpatient-Based Study