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Research 31–60 of 1000+
- Marie-unna hereditary hypotrichosis
- Autosomal Recessive Woolly Hair Caused by LIPH Mutations: A Case Series of Six Chinese Patients
- Inherited Disorders of the Hair
- Autosomal recessive monilethrix: Novel variants of the <i>DSG4</i> gene in three Chinese families
- A Missense Mutation in the Zinc-Finger Domain of the Human Hairless Gene Underlies Congenital Atrichia in a Family of Irish Travellers
- A Missense Mutation within the Helix Initiation Motif of the Keratin K71 Gene Underlies Autosomal Dominant Woolly Hair/Hypotrichosis
- Mutations in SNRPE, which Encodes a Core Protein of the Spliceosome, Cause Autosomal-Dominant Hypotrichosis Simplex
- Marie Unna Hereditary Hypotrichosis Gene Maps to Human Chromosome 8p21 Near Hairless
- Successful induction of oral tolerance in Netherton syndrome
- Tricorrexis nudosa localizada por aplicación compulsiva de minoxidil
- Treatment of monilethrix with oral minoxidil
- A new locus for hereditary hypotrichosis simplex maps to chromosome 13q12.12∼12.3 in a Chinese family
- Loss-of-Function Mutations in HOXC13 Cause Pure Hair and Nail Ectodermal Dysplasia
- Diseases of Periocular Hair
- Corneodesmosin: Structure, Function and Involvement in Pathophysiology
- Clinical effects of non-ablative and ablative fractional lasers on various hair disorders: a case series of 17 patients
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Congenital atrichia and hypotrichosis
- Mutations in SREBF1, Encoding Sterol Regulatory Element Binding Transcription Factor 1, Cause Autosomal-Dominant IFAP Syndrome
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Acquired trichomegaly of the eyelashes and hypertrichosis induced by bimatoprost
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- HAIR AND SYSTEMATIC DISEASE
- Hirsutism: diagnosis and treatment
- Genetics of Alopecia
- Differential diagnosis of hair loss in children. Differentialdiagnose des Haarausfalls bei Kindern
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Differential expression and functionality of ATP-binding cassette transporters in the human hair follicle
- Ichthyosis, Follicular Atrophoderma, and Hypotrichosis Caused by Mutations in ST14 Is Associated with Impaired Profilaggrin Processing
- Phenotypic Diversity and Mutation Spectrum in Hypotrichosis with Juvenile Macular Dystrophy