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Research 181–210 of 1000+
- Mutations in the vitamin D receptor and hereditary vitamin D-resistant rickets
- Congenital Adrenal Hyperplasia
- Recently Identified Forms of Epidermolysis Bullosa
- Treatment of monilethrix with oral minoxidil
- Asebia-2J (Scd1ab2J): A New Allele and a Model for Scarring Alopecia
- Epidermolysis bullosa simplex: a paradigm for disorders of tissue fragility
- Cantú Syndrome Is Caused by Mutations in ABCC9
- Is the Loose Anagen Hair Syndrome a Keratin Disorder?
- Werner′s syndrome
- Semidominant Inheritance in Epidermolytic Ichthyosis
- Clinical Snippets
- Nonclassic congenital adrenal hyperplasia
- Clinical Snippets
- Exploring the possibility of predicting human head hair greying from DNA using whole-exome and targeted NGS data
- Assessment of scalp hair survivin in patients with premature greying of hair
- Dermatopathia pigmentosa reticularis: A report of a case with delayed onset alopecia and onychodystrophy
- Baker′s dozen on the scalp: An interesting case of multiple trichilemmal cyst
- Hair That Is Difficult to Manage in a Hispanic Girl
- Targeting integrin pathways: mechanisms and advances in therapy
- Identification of the Rat Rex Mutation as a 7-bp Deletion at Splicing Acceptor Site of the Krt71 Gene
- Skin and hair abnormalities of Cantu syndrome: A congenital hypertrichosis due to a genetic alteration mimicking the pharmacological effect of minoxidil
- A distinct gene close to the hairless locus on chromosome 8p underlies hereditary Marie Unna type hypotrichosis in a German family
- Genetics of Structural Hair Disorders
- Molecular Genetics of Alopecias
- A novel homozygous variant in the dsp gene underlies the first case of non-syndromic form of alopecia
- Autosomal recessive hypotrichosis simplex with woolly hair: a report of a new family
- Mutations in the Keratin 85 (KRT85/hHb5) Gene Underlie Pure Hair and Nail Ectodermal Dysplasia
- Reversal of andro-genetic alopecia in a male. A spironolactone effect?
- Mutational spectrum of EDA, EDAR, EDARADD, and WNT10A genes in the largest cohort of Russian patients with hypohidrotic ectodermal dysplasia
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions