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Vilá, Luis M.
One or more keywords matched the following items that are connected to Vilá, Luis M.
Item TypeName
Academic Article Efficacy of low-dose intravenous cyclophosphamide in systemic lupus erythematosus presenting with Guillain-Barre syndrome-like acute axonal neuropathies: report of two cases.
Academic Article Recurrent venous thrombosis in Ehlers-Danlos syndrome type III: an atypical manifestation.
Academic Article Value of isolated IgA anti-?2 -glycoprotein I positivity in the diagnosis of the antiphospholipid syndrome.
Academic Article Multifocal osteonecrosis in systemic lupus erythematosus: case report and review of the literature.
Academic Article Infective endocarditis initially presenting with a dermatomyositis-like syndrome.
Academic Article Factors associated with tender point count in Puerto Ricans with fibromyalgia syndrome.
Academic Article Clinical Manifestations Associated with Overweight/Obesity in Puerto Ricans with Fibromyalgia Syndrome.
Academic Article Sustained Improvement of Fibromyalgia Syndrome After Electroconvulsive Therapy for Intractable Depression.
Academic Article Efficacy of intravenous immunoglobulins in a patient with systemic lupus erythematosus presenting with Stevens-Johnson syndrome.
Academic Article Severe systemic inflammatory response syndrome immediately after spinal surgery in a patient with axial gout.
Academic Article Efficacy of Cyclosporine in the Induction and Maintenance of Remission in a Systemic Lupus Erythematosus Patient Presenting with Macrophage-Activating Syndrome.
Academic Article Factors Associated With Disease Damage in Puerto Ricans With Primary Sj?gren Syndrome.
Academic Article Klinefelter's syndrome (47,XXY) in male systemic lupus erythematosus patients: support for the notion of a gene-dose effect from the X chromosome.
Concept Ehlers-Danlos Syndrome
Concept Klinefelter Syndrome
Concept Sjogren's Syndrome
Concept Stevens-Johnson Syndrome
Concept Antiphospholipid Syndrome
Concept Systemic Inflammatory Response Syndrome
Concept Guillain-Barre Syndrome
Academic Article Characterization of a subset of patients with primary Sj?gren's syndrome initially presenting with C3 or C4 hypocomplementemia.
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