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Research 121–150 of 1000+
- Molecular Genetics of Alopecias
- Alopecia: Association with Resistance to Thyroid Hormones
- Hair shaft structures in EDAR induced ectodermal dysplasia
- Diagnostic challenges in determining alopecia areata
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- Alopecia and Its homoeopathic treatment
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- Functional mapping of the mouse <i>hairless</i> gene promoter region
- Disorders of the skin appendages
- Hair Today
- Abstracts from the Symposium on the Pathophysiology of Hair Growth Organized by the Institute of Dermatology at the Royal Society of Medicine, 29 October 1987
- Hirsutism and the Variable Response of the Pilosebaceous Unit to Androgen
- Erasing the methyl mark: histone demethylases at the center of cellular differentiation and disease
- Cutaneous Androgen Metabolism: Basic Research and Clinical Perspectives
- Learning from nudity: lessons from the nude phenotype
- Disruption of the hedgehog signaling pathway contributes to the hair follicle cycling deficiency in Vdr knockout mice
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy
- The spectrum of hair loss in patients with mycosis fungoides and Sézary syndrome
- MOUSE MODELS FOR THE STUDY OF HUMAN HAIR LOSS
- Black women’s hair: the main scalp dermatoses and aesthetic practices in women of African ethnicity
- Methods of hair loss evaluation: a comparison of TrichoScan<sup>®</sup>with the modified wash test
- A spermidine-based nutritional supplement prolongs the anagen phase of hair follicles in humans: a randomized, placebo-controlled, double-blind study
- Development of squamous cell carcinoma from erythroplasia of Queyrat following photodynamic therapy
- Selected topics in pediatric hair loss
- Alopecia Areata and Alopecia Areata Incognita
- Recurrent MBTPS2 variant c.970+5G>A in IFAP syndrome: a mutational hotspot
- Localized Hypotrichosis Type 1 Due to Intragenic Deletion of Exons 5-8 in Desmoglein Gene in a Neonate from Indian Family
- Clinical course of the first Japanese family with Marie Unna hereditary hypotrichosis: a follow-up report
- Contents Vol. 4, 2018
- Odd-Looking Hair and Progressive Alopecia in Mother and Son