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Research 181–210 of 672
- Case report: Two individuals with AEBP1-related classical-like EDS: Further clinical characterisation and description of novel AEBP1 variants
- Commonly encountered symptoms and their management in patients with cirrhosis
- Pruritus in Lichen Planopilaris and Frontal Fibrosing Alopecia—Clinical Characteristics and Dermoscopic Correlations
- E-Poster
- Peculiarities of long-COVID-19 and treatment strategy: a clinical case
- 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
- Cutaneous manifestations and considerations in COVID ‐19 pandemic: A systematic review
- A Recurrent Intragenic Deletion in the Desmoglein 4 Gene Underlies Localized Autosomal Recessive Hypotrichosis
- Growth Hormone and the Human Hair Follicle
- Dermatopathia Pigmentosa Reticularis: Report of a New Cases and Literature Review
- Ontogeny of Skin Stem Cells and Molecular Underpinnings
- Multidisciplinary screening and diagnosis of obesity related diseases: an Arabic Association for the Study of Diabetes and metabolism position statement (AASD)
- Endocrinology
- Proceedings of the Ninth World Congress for Hair Research (2015)
- Early onset and novel features in a spinal and bulbar muscular atrophy patient with a 68 CAG repeat
- Metabolism and skin diseases
- Tinea Capitis Presenting as Diffuse Hair Loss and Significance of Trichoscopy: Four Case Reports
- Unusual Clinical Presentation of a Primary Cutaneous Follicle Center Lymphoma on the Scalp of a Middle-Aged Female: Case Report and Review of the Literature
- Histopathological and Ultrastructural Study of Ectodermal Dysplasia/Skin Fragility Syndrome
- Atrichia with papular lesions resulting from a novel insertion mutation in the human hairless gene
- Holistic Ayurvedic Management of Psoriasis with special reference to Eka Kustha
- Scaly Papular Lesions
- Symmetrical acrokeratoderma: A peculiar entity in China? Clinicopathologic and immunopathologic study of 34 new cases
- WNT10A Mutations Are a Frequent Cause of a Broad Spectrum of Ectodermal Dysplasias with Sex-Biased Manifestation Pattern in Heterozygotes
- A placebo-controlled, double-blind crossover study of fluoxetine in trichotillomania
- Is seborrhea a sign of autonomic impairment in Parkinson's disease?
- Congenital hypotrichosis due to short anagen
- Mutational spectrum in 101 patients with hypohidrotic ectodermal dysplasia and breakpoint mapping in independent cases of rare genomic rearrangements
- Wigs and hairpieces: Evaluating dermatologic issues
- Skin signs of systemic diseases