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Research 511–540 of 1000+
- Clinical Conditions Targeted by OnabotulinumtoxinA in Different Ways in Medicine
- Atypical post-finasteride syndrome: A pharmacological riddle
- Renal tubular dysfunction presenting as recurrent hypokalemic periodic quadriparesis in systemic lupus erythematosus
- Intravesical instillation of platelet-rich plasma for treatment of interstitial cystitis/bladder pain syndrome: A pilot study
- A hairy fall: syncope resulting from topical application of minoxidil
- Endocrine abnormalities in ring chromosome 11: a case report and review of the literature
- Clinical Features and Treatment Options of Vogt-Koyanagi-Harada Disease
- Muscle weakness of the lower limbs after epidural anesthesia in a pregnant woman with undiscovered systemic lupus erythematosus
- Overnight loss of pigmented hair in autoimmune autonomic neuropathy treated with IVIg
- Incidence, complications and therapeutic evaluation of clinical hypothyroidism in different breeds of dogs
- Repurposing With Purpose: Treatment of Bachmann–Bupp Syndrome With Eflornithine and Implications for Other Polyaminopathies
- Sodium Valproate Induced Alopecia: A Case Series
- Vogt-Koyanagi-Harada Disease with Oral Manifestations: A Rare Case Report
- Do Syrian conflict survivors show novel chronic cutaneous sequelae from chlorine gas exposure: A case report and literature review
- Tata Laksana Refluks Gastroesofageal pada Anak
- Analysis of the finasteride treatment and its withdrawal in the rat hypothalamus and hippocampus at whole-transcriptome level
- Referee report. For: Case Report: Extensive digital gangrene as a primary manifestation of late-onset systemic lupus erythematosus [version 2; peer review: 1 approved]
- Primary Essential Cutis Verticis Gyrata: A Case Report with a Review of Literature
- Case Report: Extensive digital gangrene as a primary manifestation of late-onset systemic lupus erythematosus
- Low Serum Biotinidase Activity in Children with Valproic Acid Monotherapy
- Diffuse Alopecia in a Child Due to Dietary Zinc Deficiency
- Congenital insensitivity to pain with anhidrosis and progressing acro-osteolysis: a case report with 7-year follow-up
- Mutation in 5′ upstream region of <i>GCH</i> I gene causes familial dopa-responsive dystonia
- The Spectrum of Cutaneous Manifestations in Lupus Erythematosus: A Comprehensive Review
- Two Hypomorphic Alleles of Mouse Ass1 as a New Animal Model of Citrullinemia Type I and Other Hyperammonemic Syndromes
- ABCD1 Gene Mutations: Mechanisms and Management of Adrenomyeloneuropathy
- Mitochondrial DNA 10158T>C mutation in a patient with mitochondrial encephalomyopathy with lactic acidosis, and stroke-like episodes syndrome
- A young male with kidney damage from genetic mitochondrial disease: case report and literature review
- Management of long COVID-19 in children and adolescents: from diagnosis to therapeutically approaches
- A Systematic Scoping Review and Conceptual Analysis of New-Onset Fibromyalgia Manifestations After Non-Hospitalized COVID-19: Empirics, Definitions, Methodologies, Pathophysiology, Mapping of Literature, and Knowledge Gaps