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Research 571–600 of 1000+
- E-Poster
- An adolescent girl presenting with primary amenorrhea: A case report of complete androgen insensitivity syndrome
- A novel pathogenic variant of NECTIN4 gene in a child with ectodermal dysplasia-syndactyly syndrome
- Clinical features of non‐classical 21‐hydroxylase deficiency after normal newborn mass screening
- Sarcoptic mange outbreak decimates South American camelid populations in San Guillermo National Park, Argentina
- Alymphoid cystic thymic dysgenesis - FOXN1 gene mutation: a rare case report of two siblings
- Moderne Untersuchungsmethoden zur Evaluation von Haarausfall und Alopezie bei Frauen
- A 9-month-old infant with severe scalp dermatosis
- Case of epidermolytic ichthyosis (bullous congenial ichthyosiform erythroderma) with a novel L157P mutation in KRT10 complicated by hypercalcemia
- Main Plenary Sessions: Summaries of Papers
- A cross-sectional study of clinical, dermoscopic, histopathological, and molecular patterns of scalp melanoma in patients with or without androgenetic alopecia
- Coordinated Activation of Wnt in Epithelial and Melanocyte Stem Cells Initiates Pigmented Hair Regeneration
- Asebia-2J (Scd1ab2J): A New Allele and a Model for Scarring Alopecia
- Obesity and Polycystic Ovary Syndrome: Implications for Pathogenesis and Novel Management Strategies
- Structure of human type II 5 alpha-reductase gene.
- Obesity and polycystic ovary syndrome
- The Nude Mutant Gene Foxn1 Is a HOXC13 Regulatory Target during Hair Follicle and Nail Differentiation
- Development and application of emotion recognition technology — a systematic literature review
- AGD1, a class 1 ARF‐GAP, acts in common signaling pathways with phosphoinositide metabolism and the actin cytoskeleton in controlling Arabidopsis root hair polarity
- Hyperplasia of Hair Follicles and Other Adnexal Structures in Cutaneous Lymphoproliferative Disorders
- A novel mutation in the connexin 26 gene (<i>GJB2</i>) in a child with clinical and histological features of keratitis–ichthyosis–deafness (KID) syndrome
- Hair follicle characteristics and fibre production in South American camelids
- Crystalline Cataract and Uncombable Hair
- <i>De novo</i> mutation in the mitochondrial tRNA<sup>Leu(UUR)</sup> gene (A3243G) with rapid segregation resulting in MELAS in the offspring
- Epidermolysis Bullosa in Calves in the United Kingdom
- Epidermolysis Bullosa Simplex Caused by Distal Truncation of BPAG1-e: An Intermediate Generalized Phenotype with Prurigo Papules
- Bloom's syndrome–‐a first report from India
- Association of atopic dermatitis with autoimmune diseases: A bidirectional and multivariable two-sample mendelian randomization study
- Molecular cloning, characterization, and expression of sheep FGF5 gene
- Clinical and histopathological characteristics in patients with scarring folliculitis type of acne inversa