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Research 31–60 of 347
- The Genetics of Human Skin Disease
- Evaluation of hair loss
- Candidate SNP markers of reproductive potential are predicted by a significant change in the affinity of TATA-binding protein for human gene promoters
- Clinical-exome sequencing unveils the genetic landscape of polycystic ovarian syndrome (PCOS) focusing on lean and obese phenotypes: implications for cost-effective diagnosis and personalized treatment
- Dermatologic manifestations of endocrine disorders
- Cross sectional quality of life assessment in patients with androgenetic alopecia
- Toward Optimal Health: The Experts Discuss Facial Skin and Related Concerns in Women
- Molecular Mechanisms and Therapeutic Advances in Androgenetic Alopecia
- Bridging psychoneuroimmunology and homeopathy: Modulating the cellular and emotional cascades in refractory alopecia
- Case Report: Compound heterozygous variants in LSS and TSPEAR genes causing hypotrichosis type 14 complicated with ectodermal dysplasia type 14
- Autosomal Recessive Woolly Hair Caused by LIPH Mutations: A Case Series of Six Chinese Patients
- Versatility of autologous growth factor concentrate therapy in early-stage androgenetic alopecia: A case report
- A review of Kesha as diagnostic and prognostic tool in Ayurveda
- Les hormones sexuelles et la peau : questionnaire à l'attention des vétérinaires praticiens. Mise à jour bibliographique et synthèse
- Australasian Society for Dermatology Research Meeting, May 2006
- A ALOPECIA AREATA E SUA RELAÇÃO COM A GEOGRAFIA E A PROMOÇÃO DA SAÚDE
- Study of Association of Dyslipidemia in Male Androgenetic Alopecia Patients in a Tertiary Care Hospital
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- The Pathogenesis and Treatment Progress of Androgenic Alopecia
- Premature graying of hairs: Ayurveda perspective
- Sex-limited chromosomes and non-reproductive traits
- Genetic Analysis of Male Pattern Baldness and the 5α-Reductase Genes
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- Characteristics of Androgenetic Alopecia in Asian
- Autosomal Recessive Hypotrichosis with Woolly Hair Caused by a Mutation in the Keratin 25 Gene Expressed in Hair Follicles
- Myotonic Dystrophy—A Progeroid Disease?
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Complete Pseudo-Anodontia in an Adult Woman with Pseudo-Hypoparathyroidism Type 1a: A New Additional Nonclassical Feature?
- RSPO1-mutated keratinocytes from palmoplantar keratoderma display impaired differentiation, alteration of cell–cell adhesion, EMT-like phenotype and invasiveness properties: implications for squamous cell carcinoma susceptibility in patients with 46XX disorder of sexual development