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Research 301–330 of 1000+
- Novel Vitamin D Receptor Mutations in Hereditary Vitamin D Resistant Rickets in Chinese
- Evolving approaches to profiling the microbiome in skin disease
- ESGCT and FSGT Collaborative Congress Helsinki, Finland September 17–20, 2015 Abstracts
- A genome-wide association scan in admixed Latin Americans identifies loci influencing facial and scalp hair features
- K <sub>ATP</sub> Channels and Cardiovascular Disease
- Acne-associated syndromes: models for better understanding of acne pathogenesis
- Beyond Expectations
- Influence of TRPV3 mutation on hair growth cycle in mice
- Congenital hair loss disorders: Rare, but not too rare
- Morphological Approach to Hair Disorders
- <i>WNT10A</i> , dermatology and dentistry
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Harnessing neuroendocrine controls of keratin expression: A new therapeutic strategy for skin diseases?
- Genome-wide association study of skin complex diseases
- Alopecia Areata
- Cantú syndrome with coexisting familial pituitary adenoma
- Acromegaloidism with normal growth hormone secretion associated with X-Tetrasomy
- Ichthyosis in Unani Medicine: A Comprehensive Review of Disorders of Cornification and their Modern Dermatological Correlates
- Familial Pure Hair–Nail Ectodermal Dysplasia in Yemen: A Father–Son Case Report with Clinical Correlation
- Central centrifugal cicatricial alopecia: a subtype of lichen planopilaris in African descent?
- Patched-assoziierte Tumoren: Modifikatorgene und Pathogenese
- Inherited Epidermolysis Bullosa: A Clinical Case
- Pathogenesis and clinical features of alopecia in epidermolysis bullosa: A systematic review
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- British Society for Dermatopathology: Summaries of Papers
- Protoporphyrin IX: the Good, the Bad, and the Ugly
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- The rare association of congenital glaucoma, giant melanocytic nevus, alopecia, and hypospadias in an Egyptian child with neurofibromatosis type 1: a case report
- The prevalence and types of androgenetic alopecia in Korean men and women
- Biology of the wool follicle: an excursion into a unique tissue interaction system waiting to be re‐discovered