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Published in 2022 at "Annals of Neurology"
DOI: 10.1002/ana.26520
Abstract: Cavitating Leukoencephalopathy in Fulminant Subacute Sclerosing Panencephalitis A 14-year-old girl presented with high-grade fever followed by recurrent episodes of generalized tonic–clonic seizures and altered sensorium, developing over a period of 2 weeks. She had a… read more here.
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Published in 2020 at "Journal of Neuroimmunology"
DOI: 10.1016/j.jneuroim.2019.577088
Abstract: Subacute sclerosing panencephalitis (SSPE) is a rare neurodegenerative disorder caused by a persistent infection with aberrant measles virus. Indoleamine-2, 3-dioxygenase (IDO) initiates the increased production of kynurenine pathway (KP) metabolites quinolinic acid (QUIN), which has… read more here.
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Published in 2022 at "Journal of Neurosciences in Rural Practice"
DOI: 10.1055/s-0041-1740612
Abstract: Introduction Subacute sclerosing panencephalitis (SSPE) is a devastating neurodegenerative disease occurring as a complication of measles infection that is still prevalent in low-resource countries. Clinical and electrographical variability in SSPE can lead to diagnostic delays.… read more here.
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Published in 2020 at "International Journal of Neuroscience"
DOI: 10.1080/00207454.2020.1759584
Abstract: Abstract Purpose/aim of the study Subacute sclerosing panencephalitis (SSPE) is a degenerative disease of the brain caused by a persistent measles virus infection occurring mostly in childhood or early adolescence. The spectrum of epileptic phenomena… read more here.
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Published in 2017 at "Clinical Infectious Diseases"
DOI: 10.1093/cid/cix302
Abstract: Background Subacute sclerosing panencephalitis (SSPE) is a fatal complication of measles. We reviewed California cases from 1998-2015 to understand risk factors for SPPE and estimate incidence. Methods SSPE cases had clinically compatible symptoms and measles… read more here.
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Published in 2020 at "Pediatrics International"
DOI: 10.1111/ped.14244
Abstract: Subacute sclerosing panencephalitis (SSPE) is a progressive neurologic disorder caused by the measles virus (MV) and is identified by positive MV‐specific antibody titers, detected mainly by hemagglutination inhibition (HI) tests in the cerebrospinal fluid (CSF).… read more here.
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Published in 2019 at "Journal of Child Neurology"
DOI: 10.1177/0883073819860631
Abstract: Subacute sclerosing panencephalitis (SSPE) is a progressive and fatal disease caused by reactivation of a mutated measles virus in brain tissue. The process of reactivation is yet to be elucidated. In this study, the possible… read more here.
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Published in 2022 at "Journal of Child Neurology"
DOI: 10.1177/08830738221144081
Abstract: Background: Subacute sclerosing panencephalitis is a progressive neurodegenerative disease that is a late complication of measles infection. However, to date, the pathogenesis of subacute sclerosing panencephalitis is still not explained; both viral and host factors… read more here.
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Published in 2022 at "Neurology"
DOI: 10.1212/wnl.0000000000201283
Abstract: Slow periodic myoclonus (up to 1 second in duration) is a distinctive phenomenology described in fulminant subacute sclerosing panencephalitis (SSPE).1 We describe slow axial myoclonus in 2 children having SSPE (Videos 1 and 2). The… read more here.
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Published in 2019 at "Neurosciences"
DOI: 10.17712/nsj.2019.1.20180020
Abstract: I have read the interesting case report by Khursheed et al,1 published in October 2018’s issue of Neurosciences (Riyadh). The authors nicely described a case of fulminant subacute sclerosing panencephalitis (SSPE) in a 20-month-old Indian… read more here.
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Published in 2022 at "Neurology India"
DOI: 10.4103/0028-3886.338737
Abstract: Background: Subacute sclerosing panencephalitis (SSPE) is a rare entity characterized by a protracted course and progressive neurological deterioration. Objective: We present patterns of diffusion restriction in eight cases of SSPE, a seldom described imaging attribute.… read more here.