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nephritis/seizures

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Presence of anti-La autoantibody is associated with a lower risk of nephritis and seizures in lupus patients.

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Previous reports suggest a protective role for anti-La autoantibody against the development of lupus nephritis. We studied the effect of anti-La on the prevalence of nephritis in a large cohort of lupus patients. In addition, we determined the association between anti-La and the presence of the

Prognosis and predictors of convulsion among pediatric lupus nephritis patients.

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In this study, we aimed to analyze features and outcome of convulsion in pediatric lupus nephritis patients. We retrospectively reviewed data of 14 Iranian children with lupus nephritis who developed seizures and compared them with a group of the same number of well matched pediatric lupus nephritis

Case of Epidemic Mumps: Complicated with Parotitis, Orchitis, Nephritis, Albuminuria, Convulsions: Recovery.

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Transient blindness and seizures in severe lupus nephritis.

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Convulsions in Acute Nephritis in Childhood.

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Case of Scarlet Fever, Nephritis, Anasarca, Convulsions, Death: Temporary Relief by Wet Packing.

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A CASE OF CEREBRO-SPINAL FEVER SIMULATING ACUTE NEPHRITIS WITH URAEMIC CONVULSIONS.

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Clinical features and mortality in Chinese with lupus nephritis and neuropsychiatric lupus: A 124-patient study.

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BACKGROUND Few investigation has focused on the patients with lupus nephritis (LN) and neuropsychiatric systemic lupus erythematosus (NPSLE). This study was aimed to investigate the clinical features, mortality, and the predictors for mortality of this group of patients. METHODS Medical records were

Anti-C1q antibodies: association with nephritis and disease activity in systemic lupus erythematosus.

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BACKGROUND Anti-C1q antibodies have been described in systemic lupus erythematosus (SLE) as well as in other connective tissue diseases. They have been considered as a marker for disease activity and presence of nephritis. OBJECTIVE The aim of this study was to determine the prevalence of anti-C1q
Lupus nephritis (LN) is an immune-complex glomerulonephritis that is usually manifested by proteinuria, active urinary sediment, hypertension, and renal failure. The objective of this study is to study the clinical and histopathological profile of LN and the response to treatment with

[A case report of chronic tubulo-interstitial nephritis].

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We report a case of 10-year-old boy with chronic tubulo-interstitial nephritis (TIN). He had febrile convulsion and received sodium valproate (VPA) treatment. 18 months later, he had developed Fanconi syndrome. On admission, he also had evidence of tubular and glomerular dysfunction. Renal biopsy

Henoch-Schönlein purpura nephritis complicated by reversible posterior leukoencephalopathy syndrome.

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We report a young female patient with Henoch-Schönlein purpura (HSP) nephritis complicated by reversible posterior leukoencephalopathy syndrome (RPLS). The patient suddenly showed generalized seizures and cortical blindness with severe hypertension due to renal insufficiency approximately 1 year

Association between SLE nephritis and polymorphic variants of the CRP and FcgammaRIIIa genes.

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OBJECTIVE To study the relationship between clinical manifestations in systemic lupus erythematosus (SLE) with polymorphisms in suggested susceptibility genes encoding FcgammaRIIa, FcgammaRIIIa, FcgammaRIIIb, CRP and IL-1Ra. METHODS Genetic polymorphisms were analysed in 323 unrelated SLE patients
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