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A case of diabetic amyotrophy with severe atrophy and weakness of shoulder girdle muscles showing good response to intravenous immune globulin.
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A 45-year-old man with insulin-dependent diabetic mellitus developed progressive asymmetrical weakness and atrophy of both shoulder girdle muscles within 1 year. In the last month, he also developed slight weakness of both thighs. Neuropathology of the sural nerve showed an axonal degeneration and
Hepatic alpha(2u)-globulin mRNA levels and diethylstilbestrol-associated testicular atrophy in rats.
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Biosynthesis of alpha(2u)-Globulin (alpha(2u)-g) is under multihormonal regulation. In this study, we investigated histopathologic changes in the testis and hepatic alpha(2u)-g messenger ribonucleic acid (mRNA) levels in male rats after administration of the potent estrogen diethylstilbestrol (DES)
Familial spinocerebellar ataxia with cerebellar atrophy, peripheral neuropathy, and elevated level of serum creatine kinase, gamma-globulin, and alpha-fetoprotein.
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Here, we report a familial spinocerebellar ataxia (FSCA), which has clinical features similar to Friedreich's ataxia, an ataxia with isolated vitamin E deficiency, and ataxia telangiectasia. However, the serum levels of creatine kinase, gamma-globulin, and alpha-fetoprotein were elevated, and
Antioxidants may mitigate the deterioration of coronary arteritis in patients with Kawasaki disease unresponsive to high-dose intravenous gamma-globulin.
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During the early stages of Kawasaki disease, a marked increase in oxygen-free-radicals (OFRs), which are produced by activated polymorphonuclear cells, may induce coronary arteritis. Early use of high-dose intravenous gamma-globulin (IVIG) and aspirin effectively blocked this deteriorating course of
[Neuritic atrophy of the optic nerve in gamma globulin deficiency syndrome].
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Early diagnosis and intravenous immune globulin therapy in paraneoplastic cerebellar degeneration.
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[Emergence of new antigenicity due to degeneration of immuno gamma globulin].
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Early diagnosis and intravenous immune globulin therapy in paraneoplastic cerebellar degeneration.
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[Abnormal serum gamma globulin level in spinocerebellar degenerations].
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[Cerebrospinal fluid beta globulin and brain atrophy].
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Albumin & gamma-globulin modulation of activity levels of selected dehydrogenases in the denervation atrophy of amphibian gastrocnemius muscle.
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Severe Guillain-Barré syndrome in childhood treated with human immune globulin.
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Thirteen children with severe Guillain-Barré syndrome were treated with human immune globulin. Patients received a mean total dose of 1.9 gm/kg of human immune globulin for 2 or 5 days. To evaluate the relationship between the response to human immune globulin and electrodiagnostic findings, we
Paraneoplastic cerebellar degeneration caused by ovarian clear-cell carcinoma.
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Paraneoplastic cerebellar degeneration is a paraneoplastic neurological syndrome caused by the remote effect of certain systemic cancers and is characterized by subacute cerebellar symptoms. A 62-year-old woman suffering from unidentified cerebellar symptoms was admitted to our hospital.
[The assessment of the lipidogram and the proteinogram profile in patients with nonexudative age-related macular degeneration (AMD)].
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The aim of the study was to assess the change in lipid and protein fraction patterns in patients with dry age-related macular degeneration (AMD) when compared against a control group.
METHODS
Sample/research group: 37 nonexudative AMD patients; 14 men at the age of 52-80 and 23 women at the age of
[A case of perinatal cytomegalovirus infection with severe progressive brain atrophy].
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A 2-month-old girl had focal tonic convulsions. Brain CT showed no abnormalities on admission. Three weeks later she got a severe epileptic status. T 1-weighted MRI demonstrated low intensity areas in the right occipital and left frontal regions, and enhanced CT demonstrated low density areas in the
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