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Research 691–720 of 1000+
- Follikelhormone
- Development of polycystic ovary syndrome: involvement of genetic and environmental factors
- Hair Depigmentation Is a Biological Readout for Pharmacological Inhibition of KIT in Mice and Humans
- Loose anagen hair syndrome in children of Upper Egypt
- A Child with Nonscarring Alopecia
- Analisis IMT Terhadap Alopesia Androgenik Fakultas Kedokteran, RS Ibnu Sina Dan Menara UMI Makassar
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- Hormonal Therapy for Acne
- Endocrine evaluation of hirsutism
- Fatty acids and related lipid mediators in the regulation of cutaneous inflammation
- Consequences of steroid-5α-reductase deficiency and inhibition in vertebrates
- Serum level of interleukin-15 in active alopecia areata patients and its relation to age, sex, and disease severity
- Acne in Dark Skin
- Endocrine evaluation of hirsutism
- Muscle pain in a woman with congenital adrenal hyperplasia due to 21-hydroxylase deficiency resolved with testosterone therapy. A case report with 10 years of follow-up
- 毛乳頭細胞と毛包上皮細胞間の細胞内・細胞外情報伝達
- Polycystic Ovary Syndrome in Adolescents
- Management of androgenetic alopecia
- GABRA2 Alleles Moderate the Subjective Effects of Alcohol, Which are Attenuated by Finasteride
- Farmácia Azevedo Carvalho, Cabeceiras de Bastos
- Efectos de la disminución de los depósitos tisulares de hierro sobre los factores de riesgo cardiovascular en pacientes con hiperandrogenismo ovárico funcional
- Comprehensive analysis of circRNAs from cashmere goat skin by next generation RNA sequencing (RNA-seq)
- Nanocarrier Systems for Transdermal Drug Delivery
- Potential of Leucaena leucocephala and Leucaena esculenta Seeds in Human Nutrition: Composition, Techno-functional Properties, Toxicology and Pretreatment Technologies
- Two Different Mutations in the Same Codon of a Type II Hair Keratin (hHb6) in Patients with Monilethrix
- Establishment of Tsc2-deficient rat embryonic stem cells
- Hair cross-sectioning in uncombable hair syndrome: An easy tool for complex diagnosis
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia
- Long-Term Effects of Sirolimus on Human Skin TSC2-Null Fibroblast‒Like Cells
- Clinico-epidemiology of Keratosis Pilaris with Histopathologic and Dermoscopic Evaluation – A Cross-sectional Study in a Rural Tertiary Hospital