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Indian Journal of Psychological Medicine, 2017 Subacute sclerosing panencephalitis (SSPE) is a rare slowly progressing neurological illness. Although patients with SSPE initially present with symptoms such as myoclonic jerks, cognitive decline, and personality/behavioral changes usually, rarely pure ...
Arpit Parmar +2 more
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Epilepsy with myoclonic atonic seizures: an electroclinical study of 69 patients. [PDF]
, 2013 Epilepsy with myoclonic-atonic seizures is characterized by myoclonic-atonic, absence, tonicclonic, and eventually tonic seizures, appearing in previously normal children at ages 18-60 months.
Fortini S +4 more
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Myoclonic status epilepticus in six patients without epilepsy [PDF]
, 2013 Myoclonic status epilepticus (MSE) is defined as prolonged period of myoclonic jerks that are correlated with epileptiform discharges on EEG. We here describe clinical features and video-EEG records of six adult patients with MSE who did not have a prior
Acarer A. +6 more
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Adult-onset autosomal dominant myoclonic epilepsy: Report of a family with an overlooked epileptic syndrome [PDF]
, 2006 SummaryObjectiveMyoclonic epilepsy is a common epileptic syndrome with high genetic contribution. We described a pedigree in which 10 individuals presented with a non-progressive, adult-onset myoclonic epilepsy.Materials and methodsThe pedigree was ...
Hsin, Yue-Loong +11 more
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Case Reports in Pediatrics, 2012 Subacute sclerosing panencephalitis is a neurodegenerative disease secondary to measles infection that usually has a typical presentation with progressive myoclonia, cognitive decline, and periodic slow-wave complexes on electroencephalography. We report
Pratibha Singhi +2 more
doaj +1 more source
Nonconvulsion status epilepticus in patients with juvenile myoclonic epilepsy: types and frequencies [PDF]
, 2002 Juvenile myoclonic epilepsy (JME) is an idiopathic, age-related generalized epileptic syndrome, featuring generalizedtonic–clonic and absence seizures as well as myoclonic jerks.
Rainer Dziewas +5 more
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Reflex writing seizures in two siblings with juvenile myoclonic epilepsy [PDF]
, 2004 We report on two siblings who presented with juvenile myoclonic epilepsy, and in whom myoclonic jerks of the right arm and hand were also triggered by writing tasks.
K. Turner +5 more
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Motor co-activation in siblings of patients with juvenile myoclonic epilepsy: an imaging endophenotype? [PDF]
, 2014 Juvenile myoclonic epilepsy is a heritable idiopathic generalized epilepsy syndrome, characterized by myoclonic jerks and frequently triggered by cognitive effort. Impairment of frontal lobe cognitive functions has been reported in patients with juvenile
Koepp, MJ +6 more
core
DystoniaGlobus pallidus internus (GPi) deep brain stimulation (DBS) was used to treat a stiff-person syndrome (SPS) patient. Prior to implantation, microelectrode recordings measured firing frequencies and patterns (burst index).
Ahmed Mohamed +18 more
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A case series on subacute sclerosing panencephalitis: Diagnostic challenges and clinical features
Indian Journal of PsychiatrySubacute sclerosing panencephalitis (SSPE), slowly progressive neurological disorder, commonly affects children who had past history of measles or if their parents forgot to provide measles vaccination.
Suparna Kumar, Govind Madhaw
doaj +1 more source