Search
for
Sort by
Research 91–120 of 1000+
- 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
- Madarosis, milphosis, eyelash trichomegaly, and dermatochalasis
- Hairy Pinnae after Orchiectomy and Chemotherapy for Testicular Cancer: Acquired Localized Hypertrichosis of the Ears
- Reply
- Drug-Induced Hair Loss and Hair Growth
- Drug Reactions Affecting Hair: Diagnosis
- Acquired Generalized Hypertrichosis Due to Diazoxide
- Hair Disorders
- Mutations in the Desmoglein 4 Gene Underlie Localized Autosomal Recessive Hypotrichosis with Monilethrix Hairs and Congenital Scalp Erosions
- HAIR AND SYSTEMATIC DISEASE
- 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
- A position effect on TRPS1 is associated with Ambras syndrome in humans and the Koala phenotype in mice
- To grow or not to grow: Hair morphogenesis and human genetic hair disorders
- A Missense Mutation in the Cadherin Interaction Site of The Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- The β9 Loop Domain of PA-PLA1α Has a Crucial Role in Autosomal Recessive Woolly Hair/Hypotrichosis
- Novel D323G mutation of <i>DSG4</i> gene in a girl with localized autosomal recessive hypotrichosis clinically overlapped with monilethrix
- A newly identified missense mutation of the HR gene is associated with a novel, unusual phenotype of Marie Unna Hereditary Hypotrichosis 1 including limb deformities
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Novel compound heterozygous cadherin 3 mutations in hypotrichosis and juvenile macular dystrophy
- Complete defect in PA-PLA1α secretion function leading to autosomal recessive woolly hair and hypotrichosis: insights from a novel compound heterozygous LIPH variant study in a Chinese pedigree