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Research 151–180 of 1000+
- Hair follicles and their role in skin health
- A novel mutation in ST14 at a functionally significant amino acid residue expands the spectrum of ichthyosis-hypotrichosis syndrome
- Homozygous missense mutation in the<i>LIPH</i>gene causing autosomal recessive hypotrichosis simplex in a Chinese patient
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- ĮGIMTA NERANDĖJANTI SKALPO ALOPECIJA: KLINIKINIS ATVEJIS IR DIFERENCINĖ DIAGNOSTIKA
- Hypotrichosis in a child with olmsted syndrome
- Editors' Picks
- Hair Loss in Children
- Localized Acquired Hypertrichosis Associated with the Application of a Splint
- Minoxidil-induced hypertrichosis in a child with alopecia areata
- Malignancy and Cancer Treatment-Related Hair and Nail Changes
- Understanding and Management of Female Pattern Alopecia
- Low prevalence of twisted hair in anorexia nervosa
- BIOACTIVE AND PERIPHERAL ANDROGENS IN PREPUBERTAL SIMPLE HYPERTRICHOSIS
- Acquired Localized Hypertrichosis Induced by Rivastigmine
- Capryloyl glycine and soy isoflavonoids in hypertrichosis: An experimental and placebo‐controlled clinical study
- Hypertrichosis Induced by Minoxidil: A Case of Systemic Absorption from Scalp Occlusion
- Biology and Genetics of Hair
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- Loss-of-function mutations of an inhibitory upstream ORF in the human hairless transcript cause Marie Unna hereditary hypotrichosis
- HAIR AND SYSTEMATIC DISEASE
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- A novel mutation in Hr causes abnormal hair follicle morphogenesis in hairpoor mouse, an animal model for Marie Unna Hereditary Hypotrichosis
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Woolly Antics between the Sheaths
- Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report