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Research 91–120 of 1000+
- Presence of a Deletion Mutation (c.716delA) in the Ligand Binding Domain of the Vitamin D Receptor in an Indian Patient with Vitamin D-Dependent Rickets Type II
- Case Report: A Deletion Variant in the DCAF17 Gene Underlying Woodhouse-Sakati Syndrome in a Chinese Consanguineous Family
- Approach to the adult female patient with diffuse nonscarring alopecia
- Syphilis: A great imitator
- Research progress on mechanisms of skin aging and anti-aging strategies
- Identification of a Rare Variant in the <i>SRD5A2</i> Gene in Siblings With 46,XY Disorders of Sexual Development
- Novel Mutations in X-Linked Dominant Chondrodysplasia Punctata (CDPX2)
- Worldwide cohort study of 46, XY differences/disorders of sex development genetic diagnoses: geographic and ethnic differences in variants
- Adrenocortical Adenocarcinoma in a Syrian Golden Hamster ( <i>Mesocricetus auratus)</i> With Suspected Hyperadrenocorticism
- Clinical, biochemical and mutational findings in biotinidase deficiency among Malaysian population
- Extracellular Vesicles: Emerging Therapeutics in Cutaneous Lesions
- Circadian rhythm sleep-wake disorders (CRSWDs): Linking circadian misalignment to adverse health outcomes.
- Androgenetic alopecia: An update
- Phenotyping mice with skin, hair, or nail abnormalities: A systematic approach and methodologies from simple to complex
- Beyond Coincidence in Neurofibromatosis Type 1: Becker Nevus Adjacent to Plexiform Neurofibroma with Brachial Plexus Involvement and Integrated Mechanistic Illustration
- Expanding the Clinical and Mutational Spectrum of Recessive AEBP1-Related Classical-Like Ehlers-Danlos Syndrome
- Pulmonary manifestations of Birt-Hogg-Dubé syndrome
- Organoid‐Guided Precision Medicine: From Bench to Bedside
- Glucocorticoid Resistance Syndrome in 2 Patients With Diverse Genotype
- Painful thickened skin on the soles of the feet
- Exploring the clinical implications of novel SRD5A2 variants in 46,XY disorders of sex development
- Selective Pituitary Resistance to Thyroid Hormone: Clinical Hyperthyroidism with High TSH on Levothyroxine Administration in I-131 Ablated “Graves Disease”
- A Rare Case of Generalized Staphylococcal Dermatitis in European Bison
- LBODP010 A Case of Glucocorticoid Resistance Syndrome
- Performance of an interferon-γ release assay-based test for cell-mediated immunity to SARS-CoV-2
- The Search for the Causes of Common Hyperandrogenism, 1965 to Circa 2015
- Heterogeneity in the genetic alterations and in the clinical presentation of acrodermatitis enteropathic: Case report and review of the literature
- Targeting a fibrotic bottleneck may provide an opening in the treatment of LUTS
- Concurrent hepatitis B and autoimmune hepatitis a rare presentation of acute liver failure: a case report
- Pachyonychia congenita: Sporadic onset with mutation analysis