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Research 661–690 of 1000+
- 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
- Halo Scalp Ring: An Annular Alopecia Associated with Birth Injury
- Committee on database of hair restoration results on patients with cicatricial alopecia and hair diseases other than androgenetic alopecia
- Keratin 17 null mice exhibit age- and strain-dependent alopecia
- 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
- Pachyonychia congenita: Sporadic onset with mutation analysis
- Ulerythema ophryogenes with multiple congenital anomalies
- Homozygous ALOXE3 Nonsense Variant Identified in a Patient with Non-Bullous Congenital Ichthyosiform Erythroderma Complicated by Superimposed Bullous Majocchi’s Granuloma: The Consequences of Skin Barrier Dysfunction
- Roux-en-Y gastric bypass in the treatment of non-classic congenital adrenal hyperplasia due to 11-hydroxylase deficiency
- Outcomes of Tissue Expander Application for Scalp Reconstruction in Extensive Aplasia Cutis Congenita
- Trichoscopy of aplasia cutis congenita of the scalp in skin of color
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Skin and hair abnormalities of Cantu syndrome: A congenital hypertrichosis due to a genetic alteration mimicking the pharmacological effect of minoxidil
- DIAGNOSTIC VALUE OF CHROMOSOMAL MICROARRAY ANALYSIS IN PATIENTS WITH CONGENITAL ANOMALIES AND DYSMORPHIC FEATURES; DETAILS OF TWO NEW PATIENTS WITH 2q33 DELETIONS
- FOXN1: A Master Regulator Gene of Thymic Epithelial Development Program
- Vitamin D<sub>3</sub>Analogs Stimulate Hair Growth in Nude Mice
- FOXN1 Deficiency: from the Discovery to Novel Therapeutic Approaches
- Human ClinicalPhenotype Associated with FOXN1 Mutations
- FOXN1 Italian founder mutation in Indian family: Implications in prenatal diagnosis
- Leptomeningeal angiomatosis accompanied by hair follicle nevus
- Side effects after artificial hair implants: 2 case reports
- Nevus psiloliparus: Newly described histopathological features from transverse sections
- Mechanism of JmjC-containing protein Hairless in the regulation of vitamin D receptor function
- Hair Shaft Abnormalities. Pili Bifurcati: A Scanning Electron Microscopy Analysis
- Hair loss disorders in domestic animals
- Novel small‐insertion mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis