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Research 451–480 of 1000+
- Pseudallescheria boydii infection associated with IgG4-related disease
- Therapeutic effect of finasteride through its antiandrogenic and antioxidant role in a propionic acid-induced autism model: Demonstrated by behavioral tests, histological findings and MR spectroscopy
- Clinical and Molecular Genetic Findings of Cerebral Arteriopathy with Subcortical Infarcts and Leukoencephalopathy
- Childhood‐onset systemic lupus erythematosus with trisomy X and the increased risk for bone complications: a case report
- Novel Mutation in the Hemojuvelin Gene (HJV) in a Patient with Juvenile Hemochromatosis Presenting with Insulin-dependent Diabetes Mellitus, Secondary Hypothyroidism and Hypogonadism
- Scalp Arteriovenous Fistula following Hair Transplantation: A Case Report and Review of the Literature
- Diffuse hair loss in Addison disease: A reason for X-linked adrenoleukodystrophy screening
- Balint’s syndrome—missed or mistaken?
- Mania in Hyperandrogenism, Insulin Resistance, and Nigricans Acanthosis Syndrome
- Staphylococcus aureus Sepsis Complicating Hair Transplant
- Nonsurgical Facial Esthetic Procedures
- Muscle weakness of the lower limbs after epidural anesthesia in a pregnant woman with undiscovered systemic lupus erythematosus
- Folliculotropic CD8+ mycosis fungoides associated with diffuse mucosal involvement
- Congenital Generalized Hypertrichosis Terminalis with Gingival Hyperplasia and a Coarse Face: a Case Report
- Primary vitreoretinal lymphoma masquerading as refractory uveitis—just go with the flow
- Leveraging deep neural networks to uncover unprecedented levels of precision in the diagnosis of hair and scalp disorders
- Case report: Heterozygous mutation in HTRA1 causing typical cerebral autosomal recessive arteriopathy with subcortical infarcts and leukoencephalopathy
- Impending central retinal vein occlusion and granulomatous uveitis in a patient with Satoyoshi syndrome
- DSP c.6310delA p.(Thr2104Glnfs*12) associates with arrhythmogenic cardiomyopathy, increased trabeculation, curly hair, and palmoplantar keratoderma
- A Case to Tear One's Hair Out: Trichotillomania in Wilson's Disease
- Metreleptin Treatment in a Boy with Congenital Generalized Lipodystrophy due to Homozygous c.465_468delGACT (p.T156Rfs*8) Mutation in the BSCL2 Gene: Results From the First-year
- 46, XY 5-Alpha Reductase Deficiency in a 36-Year-Old Phenotypic Female Patient
- Methotrexate injection site reactions: Case report and literature review
- Writer’s Cramp Presentation of Woodhouse–Sakati Syndrome – “Out of the Woods”
- 02 Management of difficult infections in SLE
- Epidermal cyst of temporal bone as a delayed complication of myringoplasty
- Hirsutism-A Comprehensive Update of Embryology, Aetiopathogenesis and Therapeutic Approach
- Viewpoint 7
- Influenza-like symptoms and thrombocytopenia in a teenager
- Trichoscopy of twisted hairs in a patient with unilateral ecchymoses: A case of modern-day scurvy