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Research 901–930 of 1000+
- Normal Hair Growth in Children
- Keratinocyte-specific ablation of the NF-κB regulatory protein A20 (TNFAIP3) reveals a role in the control of epidermal homeostasis
- A New Heterozygous Variant of c.1225_1227delTTC (p.Phe409del) in Insulin Receptor Gene Associated with Severe Insulin Resistance and Hyperandrogenemia in an Adolescent Female with Type A Severe Insulin Resistance Syndrome
- Revised 2003 consensus on diagnostic criteria and long-term health risks related to polycystic ovary syndrome
- Protoporphyrin IX: the Good, the Bad, and the Ugly
- PAK4 signaling in health and disease: defining the PAK4–CREB axis
- Hairless and Wnt Signaling: Allies in Epithelial Stem Cell Differentiation
- Management of congenital ichthyoses: European guidelines of care, part two
- Polycystic Ovary Syndrome and Its Differential Diagnosis
- Anabolic-androgenic steroids and cardiovascular risk
- Smad4-dependent desmoglein-4 expression contributes to hair follicle integrity
- Stem cells and aberrant signaling of molecular systems in skin aging
- The Transmembrane Serine Protease HAT-like 4 Is Important for Epidermal Barrier Function to Prevent Body Fluid Loss
- Perspectives in dermatopathology: telomeres and telomerase in ageing and cancer; with emphasis on cutaneous disease
- Physiology and Medical Treatments for Alopecia
- Novel Systematics of Nomenclature and Classification of Female Functional Androgenization (Including Polycystic Ovary Syndrome and Non-Classic Congenital Adrenal Hyperplasia)
- Nonscarring hair loss disorders
- Management OF Patients with Polycystic Ovary Syndrom
- Correlation between sebum level and severity of male androgenetic alopecia
- Disorders of the skin appendages
- Abstracts Pt.30
- A Case of Hair Structure Abnormality Associated with Iron Deficiency Anaemia
- Hair Depigmentation Is a Biological Readout for Pharmacological Inhibition of KIT in Mice and Humans
- 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
- Polycystic Ovary Syndrome in Adolescents
- Farmácia Azevedo Carvalho, Cabeceiras de Bastos
- 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
- De novo variation in ARID1B gene causes Coffin-Siris syndrome 1 in a Chinese family with excessive early-onset high myopia