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Research 61–90 of 1000+
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- A pathophysiological and clinical review of androgenetic , areata, anagen effluvium, telogen effluvium and traction alopecia’s
- Triphasic Progressive : une nouvelle formule pour une efficacité accrue contre la chute progressive des cheveux
- Editors' Picks
- Two siblings with a novel nonsense mutation, p.R50X, in the vitamin D receptor gene
- Alopécie androgénogénétique chez la femme
- Clinical Snippets
- A Novel Type II Cytokeratin, mK6irs, is Expressed in the Huxley and Henle Layers of the Mouse Inner Root Sheath
- Coat Problems
- Androgenetic Alopecia: Stress of Discovery
- Androgenetic Alopecia (AGA)
- The Nuclear Vitamin D Receptor: Biological and Molecular Regulatory Properties Revealed
- Genetic Disorders and Defects in Vitamin D Action
- Focal and Generalized Alopecia
- Functional Analysis of VDR Gene Mutation R343H in A Child with Vitamin D-Resistant Rickets with Alopecia
- Androgenetic alopecia – is contact dermatitis an accelerating factor?
- New Publications
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Hereditary, Congenital, and Acquired Alopecias
- LibGuides: L3Y2 Tutorial 2022 - critical thinking: Claim 5: Caffeine reduces hair loss
- THE EXPRESSION AND INTERACTION OF HEREDITARY FACTORS PRODUCING HYPOTRICHOSIS IN THE MOUSE: HISTOLOGY AND EXPERIMENTAL RESULTS
- A rare hair loss in children: Monilethrix
- Marie Unna hereditary hypotrichosis caused by a novel mutation in the human hairless transcript
- Identification of a novel heterozygous mutation in the first Japanese case of Marie Unna hereditary hypotrichosis
- Disorders of the hair and scalp.
- What Ages Hair?
- ABC of Dermatology: Diseases of the hair and scalp
- Understanding Pattern Hair Loss—Hair Biology Impacted by Genes, Androgens, Prostaglandins and Epigenetic Factors
- Hair loss in children.
- Hair Loss in Children