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Research 901–930 of 1000+
- Secondary Cicatricial and other Permanent Alopecias
- First case of V281+I172N/V281L CYP21A2 genotype associated with congenital adrenal hyperplasia form. A case report from South Italy
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Congenital atrichia with papular lesions
- Ichthyosis follicularis alopecia and photophobia syndrome:Transient improvement with oral isotretinoin
- Triangular Temporal Alopecia - Two Case Reports, Dermoscopy and Review
- Congenital Adrenal Hyperplasia
- Phenotypic profiling of parents with cryptic nonclassic congenital adrenal hyperplasia: findings in 145 unrelated families
- A Novel Missense Mutation Affecting the Human Hairless Thyroid Receptor Interacting Domain 2 Causes Congenital Atrichia
- Congenital Zinc Deficiency from Mutations of the<i>SLC39A4</i>Gene as the Genetic Background of Acrodermatitis Enteropathica
- Novel adenosine triphosphate (ATP)-binding cassette, subfamily A, member 12 (ABCA12) mutations associated with congenital ichthyosiform erythroderma
- Congenital atrichia with papular lesions resulting from novel mutations in human hairless gene in four consanguineous families
- A frameshift insertion in SGK3 leads to recessive hairlessness in Scottish Deerhounds: a candidate gene for human alopecia conditions
- Management Approaches to Congenital Adrenal Hyperplasia in Adolescents and Adults; Latest Therapeutic Developments
- Prioritization of therapy uncertainties in congenital ichthyosis: results from a Priority Setting Partnership
- Early diagnosis of ichthyosis, leukocyte vacuoles, alopecia, and sclerosing cholangitis syndrome: A case report
- Incidence of Congenital Goitre in Goats, in and Around Hyderabad, India
- Neuroimaging Findings in Congenital Biotinidase Deficiency: A Case Report
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- A syndrome of congenital ichthyosis, mental retardation, myopathy and anemia in dizygotic twin sisters
- Hypotrichosis congenita of Marie Unna
- Nonclassic Congenital Adrenal Hyperplasia
- Non-classic congenital adrenal hyperplasia
- Endo&Art why Diana is depicted with mild androgenic alopecia?
- Bullous Congenital Ichthyosiform Erythroderma with Tinea Capitis in Half-Siblings: Rare Phenomenon in Ichthyosis with Co-Existing Trichophyton rubrum Infection and Blocker Displacement Amplification for Mosaic Mutation Detection
- Alopecia in Patients with Collagen VI-Related Myopathies: A Novel/Unrecognized Scalp Phenotype
- Keratin 17 null mice exhibit age- and strain-dependent alopecia
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- KERATIN 17-related recessive atypical pachyonychia congenita with variable hair and tooth anomalies
- Resolution of the plantar hyperkeratosis of pachyonychia congenita during chemotherapy for Ewing sarcoma