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Research 571–600 of 1000+
- Taking advantage from phenotype variability in a local animal genetic resource: identification of genomic regions associated with the hairless phenotype in Casertana pigs
- Hereditary vitamin D resistant rickets (HVDRR) case series: phenotype, genotype, conventional treatment, and adjunctive cinacalcet therapy
- Coexistence of Woolly Hair and Monilethrix: A Cases Study
- Protoporphyrin IX: the Good, the Bad, and the Ugly
- Keratosis pilaris atrophicans faciei: An observational, descriptive, retrospective clinical study
- Oral vitamin A as an adjunct treatment for canine sebaceous adenitis
- Anabolic-androgenic steroids and cardiovascular risk
- The Transmembrane Serine Protease HAT-like 4 Is Important for Epidermal Barrier Function to Prevent Body Fluid Loss
- Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders
- <i>DSG4</i> Gene Variants as a Cause of Hypotrichosis in the Child with Severe Atopic Dermatitis: Clinical Case
- Autoimmune polyglandular syndrome type 4 – case report
- Follikelhormone
- The Majority of Multipotent Epidermal Stem Cells Do Not Protect Their Genome by Asymmetrical Chromosome Segregation
- How to Speak Postmodern: Medicine, Illness, and Cultural Change
- Supplementary material from "Giant axonal neuropathy alters the structure of keratin intermediate filaments in human hair"
- HtrA1L364P leads to cognitive dysfunction and vascular destruction through TGF‐β/Smad signaling pathway in CARASIL model mice
- Successful management of Netherton syndrome using IVIG and dupilumab: A case report
- Alopecia in a Novel Mouse Model RCO3 Is Caused by mK6irs1 Deficiency
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- MON-194 A Case Of Sertoli Cell Tumor In A Patient With Familial Partial Lipodystrophy Type 2
- Atrichia with papular lesions resulting from mutations in the rhesus macaque (<i>Macaca mulatta</i>) <i>hairless</i> gene
- Expanding the Phenotypic Spectrum of APMR4 Syndrome Caused by a Novel Variant in LSS Gene
- Novel Mutation in the Hemojuvelin Gene (HJV) in a Patient with Juvenile Hemochromatosis Presenting with Insulin-dependent Diabetes Mellitus, Secondary Hypothyroidism and Hypogonadism
- Dental considerations in acrodermatitis enteropathica: A report of two cases
- Treatment of erythromelanosis follicularis faciei et colli with a 595‐nm pulsed dye laser
- A Rare Case of Severe Acrodermatitis Enteropathica During Covid-19 Lockdown.
- Causes and Management of Hypertrichosis
- Case Report: 7 Year-Old Saudi Female with Monilethrix
- Hair promotion effect of Beta vulgaris L. fruit extracts; physicochemical, and analytical evaluation
- Ichthyosis