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Research 361–390 of 1000+
- Segregation of Incomplete Achromatopsia and Alopecia Due to PDE6H and LPAR6 Variants in a Consanguineous Family from Pakistan
- Biotin: overview of the treatment of diseases of cutaneous appendages and of hyperseborrhea
- Index of Suspicion
- Disorders of the Hair and Nails
- Farmácia Avenida - Guimarães e nos Serviços Farmacêuticos da Unidade Local de Saúde do Alto Ave, EPE - Guimarães
- Linear and Unilateral Basaloid Follicular Hamartoma Along Blaschko’s Lines in an Elderly Patient: A Rare Presentation
- Eyelash Trichomegaly: Unusual Feature Associated with Systemic Lupus Erythematosus Patient
- Alopecias
- Cumulative Index
- Becker's Nevus Syndrome
- Acquired uncombable hair
- Acquired Localized Trichorrhexis Nodosa Secondary to Cultural Practices
- SPECIFIC ECTODERMAL ENHANCERS CONTROL THE EXPRESSION OF<i>Hoxc</i>GENES IN DEVELOPING MAMMALIAN INTEGUMENTS
- Hair and Scalp Dermatoscopy (Trichoscopy)
- Acquired progressive kinking of the hair in a Korean female adolescent
- Congenital Hypotrichosis in Japanese White Strain (JW-NIBS) Rabbits.
- A Spontaneous Fatp4/Scl27a4 Splice Site Mutation in a New Murine Model for Congenital Ichthyosis
- Cutaneous Mastocytosis Associated With Congenital Alopecia
- A Case of Basal Cell Carcinoma Arising in Congenital Triangular Alopecia
- Epicardial fat thickness in children with classic congenital adrenal hyperplasia
- The <i>hairless</i> gene mutated in congenital hair loss disorders encodes a novel nuclear receptor corepressor
- Management of congenital ichthyoses: European guidelines of care, part two
- Medical dermatologic conditions in transgender women
- Congenital atrichia with papular lesions: a rare cause of irreversible childhood alopecia
- Clinical and trichoscopic features of early congenital syphilis: a single-center cross-sectional study
- Neuroimaging Findings in Congenital Biotinidase Deficiency: A Case Report
- An Update of Congenital Adrenal Hyperplasia
- Polycystic Ovary Syndrome: Conditions, Genetics and Current Cure
- Conditional knock out of N-WASP in keratinocytes causes skin barrier defects and atopic dermatitis-like inflammation
- Nonclassic congenital adrenal hyperplasia and the heterozygote carrier