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Research 301–330 of 1000+
- Female pattern hair loss
- Variant <i>PADI3</i> in Central Centrifugal Cicatricial Alopecia
- Unraveling the Molecular Mechanisms of Hair and Nail Genodermatoses
- Congenital atrichia and hypotrichosis
- Embryologic layers in dermatology: Developmental checkpoint disorders, diagnostic insight, and regenerative futures
- Polymorphisms of the Androgen Receptor Gene and the Estrogen Receptor β Gene Are Associated with Androgen Levels in Women1
- Diagnostic approach to low‐renin hypertension
- Congenital adrenal hyperplasia
- Healthy individuals genetically at-risk for the development of Pemphigus vulgaris or Alopecia areata share disease-like cytokine dysregulation
- A New Heterozygous Variant of c.1225_1227delTTC (p.Phe409del) in Insulin Receptor Gene Associated with Severe Insulin Resistance and Hyperandrogenemia in an Adolescent Female with Type A Severe Insulin Resistance Syndrome
- Novel splice site mutation in the <i>LIPH</i> gene in a patient with autosomal recessive woolly hair/hypotrichosis: Case report and published work review
- Associations between sun sensitive pigmentary genes and serum prostate specific antigen levels
- CDH3 Mutation in Saudi Arabia: A Case of Hypotrichosis With Juvenile Macular Dystrophy
- Precision therapeutics in non-scarring alopecia: a systemic genomic and pathway-based framework for targeted interventions
- Hashimoto Thyroiditis - A Comprehensive Review
- Autosomal Recessive Transmission of a Rare KRT74 Variant Causes Hair and Nail Ectodermal Dysplasia: Allelism with Dominant Woolly Hair/Hypotrichosis
- Progeria (Hutchinson-Gilford Syndrome): Literature Review and Clinical Case
- Clinical Manifestation and Classification of Japanese patients with Inherited Keratinizing Disorders
- Woodhouse-Sakati Syndrome Due to the Rare DCAF17 c.321+1G>A Mutation: The Second Case Report Worldwide
- Adrenal causes of endocrine hypertension in childhood or adolescence
- Deficiency of the human cysteine protease inhibitor cystatin M/E causes hypotrichosis and dry skin
- Association study reveals a susceptibility locus with male pattern baldness in the Han Chinese population
- 302 Availability of mRNA Obtained from Peripheral Blood Mononuclear Cells for Mutational Analysis in Dystrophic Epidermolysis Bullosa
- The Chicken Frizzle Feather Is Due to an α-Keratin (KRT75) Mutation That Causes a Defective Rachis
- Molecular–clinical correlations in a family with variable tissue mitochondrial DNA T8993G mutant load
- Chronic overlapping pain conditions and nociplastic pain
- New case of trichorinophalangeal syndrome-like phenotype with a de novo t(2;8)(p16.1;q23.3) translocation which does not disrupt the TRPS1 gene
- A Homozygous Missense Variant in K25 Underlying Overlapping Phenotype with Woolly Hair and Dental Anomalies
- Pathogenic variants affecting peptidyl arginine deiminase 3 and its major substrates underlie central centrifugal cicatricial alopecia
- Trichoscopy in Unveiling the Triad of Netherton Syndrome