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Research 91–120 of 1000+
- Hair physiology and its disorders
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- New CDH3 mutation in the first Spanish case of hypotrichosis with juvenile macular dystrophy, a case report
- Four hypotrichosis families with mutations in the gene <i>LSS</i> presenting with and without neurodevelopmental phenotypes
- Hypotrichosis with juvenile macular dystrophy
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Autosomal recessive woolly hair/hypotrichosis caused by LIPH mutations: a case report
- BH15 Nonsyndromic hypotrichosis: a rare case of congenital hypotrichosis 15 and management with minoxidil
- Treatment of hypotrichosis simplex of the scalp with the combination of botanic extracts and minoxidil: a case report
- Autosomal recessive hereditary hypotrichosis simplex: A case report
- Hypotrichosis in a child with olmsted syndrome
- Odd-Looking Hair and Progressive Alopecia in Mother and Son
- Madarosis, milphosis, eyelash trichomegaly, and dermatochalasis
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- Drug-Induced Hair Loss and Hair Growth
- Drug Reactions Affecting Hair: Diagnosis
- Understanding and Management of Female Pattern Alopecia
- Acquired Generalized Hypertrichosis Due to Diazoxide
- Hair Disorders
- Describing the Hair and Related Abnormalities
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- HAIR AND SYSTEMATIC DISEASE
- Hair disorders in patients with cancer
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Management of hypotrichosis of the eyelashes: Focus on bimatoprost
- Hair Changes due to Drugs
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Biology and Genetics of Hair
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis