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Research 61–90 of 1000+
- Hair loss among a group of Egyptian children
- Hair loss in infancy and childhood
- Hair Loss in Children
- Skin features in myotonic dystrophy type 1: An observational study
- Alopecia areata: Clinical presentation, diagnosis, and unusual cases
- General Dermatology
- Dermatoses of pregnancy
- The Skin and Subcutaneous Tissues
- Congenital atrichia associated with situs inversus and mesocardia
- Ectodermal Dysplasia: Variable Expressions
- A Brazilian case of IFAP syndrome with severe congenital ichthyosis and limb malformations caused by a rare variant in MBTPS2
- Case report: A novel splice-site mutation of MTX2 gene caused mandibuloacral dysplasia progeroid syndrome: the first report from China and literature review
- Biallelic Variants in Lanosterol Synthase (LSS) Cause Palmoplantar Keratoderma-Congenital Alopecia Syndrome Type 2
- Loss of Ten1 in mice induces telomere shortening and models human dyskeratosis congenita
- 414 A new form of ectodermal dysplasia caused by mutations in TSPEAR
- Novel mutations of the ABCA12, KRT1 and ST14 genes in three unrelated newborns showing congenital ichthyosis
- Pili Torti: A Feature of Numerous Congenital and Acquired Conditions
- Lichen Planopilaris with Pili Torti and Ectodermal Dysplasia: a hair curling case report.
- DIAGNOSTIC VALUE OF CHROMOSOMAL MICROARRAY ANALYSIS IN PATIENTS WITH CONGENITAL ANOMALIES AND DYSMORPHIC FEATURES; DETAILS OF TWO NEW PATIENTS WITH 2q33 DELETIONS
- Westwood Carolina Conference on Clinical Dermatology
- Wnt Signaling Across Adult Skin Mini-Organs: Interfollicular Epidermis, Hair Follicle, and Nail—Implications for Disease and Regeneration
- Further Insights in Trichothiodistrophy: A Clinical, Microscopic, and Ultrastructural Study of 20 Cases and Literature Review
- Ichthyosis Follicularis, Alopecia, and Photophobia Syndrome in a Saudi Child: A Case Report
- Hedgehog Signaling, Keratin 6 Induction, and Sebaceous Gland Morphogenesis
- A Review of the Use of Biotin for Hair Loss
- Germline Mutation in ATR in Autosomal- Dominant Oropharyngeal Cancer Syndrome
- Ichthyosis follicularis, alopecia, and photophobia (IFAP) syndrome
- Ichthyosis follicularis alopecia and photophobia syndrome:Transient improvement with oral isotretinoin
- When Rare Meets Risky: Clouston Syndrome with Cutaneous Squamous Cell Carcinoma
- Genetic Hair Disorders: A Review