Search
for
Sort by
Research 511–540 of 1000+
- Hyperandrogenism in Women: Polycystic Ovary Syndrome
- Anagen Effluvium in Association With Extracorporeal Membrane Oxygenation
- Inherited Disorders of the Hair
- The Role of Histone Demethylases in Disease
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- 574 Murine sebaceous gland homeostasis requires intact cutaneous innervation in a hair cycle-dependent context
- 573 Hair follicles employ a 2-dimensional healing strategy to repair 3-dimensional injuries
- Follikelhormone
- Androgen effects on the skin
- The pathogenesis of alopecia areata
- First case of V281+I172N/V281L CYP21A2 genotype associated with congenital adrenal hyperplasia form. A case report from South Italy
- Obesity and the skin
- Keratin disorders: from gene to therapy
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Biallelic HEPHL1 variants impair ferroxidase activity and cause an abnormal hair phenotype
- A novel nonsense mutation in the STS gene in a Pakistani family with X-linked recessive ichthyosis: including a very rare case of two homozygous female patients
- An immune regulatory CCT repeat containing oligodeoxynucleotide capable of causing hair loss in male mice
- Genetic Variation at the MC1R Locus and the Time since Loss of Human Body Hair
- Neurosteroidogenesis Today: Novel Targets for Neuroactive Steroid Synthesis and Action and Their Relevance for Translational Research
- Adverse effects of common medications on male fertility
- Alopecia areata: a review on diagnosis, immunological etiopathogenesis and treatment options
- Absorption sites of orally administered drugs in the small intestine
- Differential Expression of miR-93 and miR-21 in Granulosa Cells and Follicular Fluid of Polycystic Ovary Syndrome Associating with Different Phenotypes
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- A Practical Approach to the Diagnosis and Management of Hair Loss in Children and Adolescents
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- ANDROGENETIC ALOPECIA
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- Long COVID syndrome: An unfolding enigma