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Research 211–240 of 360
- Trichoscopic Features, Clinical Correlates, and Risk Prediction in Female Pattern Hair Loss: A Retrospective Case-Control Study
- DEFINITION OF FRONTAL FIBROSING ALOPECIA IN THE GROUP OF SCARRING ALOPECIAS
- Secondary cicatricial and other permanent alopecias
- Cutaneous Androgen Metabolism: Basic Research and Clinical Perspectives
- Female pattern hair loss
- Biology of the Hair Follicle: The Basics
- Vitamin D metabolism and function in the skin
- Learning from nudity: lessons from the nude phenotype
- Approach to the adult female patient with diffuse nonscarring alopecia
- Female pattern hair loss: A clinical, pathophysiologic, and therapeutic review
- Clinical evaluation of alopecias using a handheld dermatoscope
- The cycling hair follicle as an ideal systems biology research model
- Hirsutism and the Variable Response of the Pilosebaceous Unit to Androgen
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy
- Alopecia Areata
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- The spectrum of hair loss in patients with mycosis fungoides and Sézary syndrome
- Scalp Dermatoscopic Findings in Androgenetic Alopecia and Their Relations with Disease Severity
- Towards a consensus on how to diagnose and quantify female pattern hair loss – The ‘Female Pattern Hair Loss Severity Index (FPHL-SI)’
- Electron paramagnetic resonance (EPR) spectroscopy for investigating murine telogen skin after spontaneous or depilation-induced hair growth
- Psychotrichology: psychosomatic aspects of hair diseases
- Short anagen syndrome: Case series and literature review
- Dermoscopic findings in female androgenetic alopecia
- Dermatoscopic findings of syphilitic alopecia
- A non-invasive study of alopecia in Japanese macaques Macaca fuscata
- Molecular evolution of HR, a gene that regulates the postnatal cycle of the hair follicle
- Alopecia: Association with Resistance to Thyroid Hormones
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Advances in Hair Diseases