Results 91 to 100 of about 6,575 (206)
Voluntary stimulus-sensitive jerks and jumps mimicking myoclonus or pathological startle syndromes. [PDF]
Five patients who presented with stimulus-induced jerking as part of an apparent myoclonic or pathological startle syndrome are reported. Neurophysiological observations in these patients suggested the jerks were voluntary in origin.
Marsden, CD +14 more
core +1 more source
Summary Dreaming, a common yet mysterious cognitive phenomenon, is an involuntary process experienced by individuals during sleep. Although the fascination with dreams dates back to ancient times and gained therapeutic significance through psychoanalysis in the early twentieth century, its scientific investigation only gained momentum with the ...
Carlotta Mutti +2 more
wiley +1 more source
Adult myoclonic epilepsy: A distinct syndrome of idiopathic generalized epilepsy [PDF]
The authors present 11 cases of idiopathic generalized epilepsy that began in adulthood at a mean age of 39 years. All patients had myoclonic jerks, five had absence seizures, and nine had infrequent generalized tonic-clonic seizures.
Kuzniecky, R. +5 more
core
Myoclonic Jerks and Ataxia: A Case of Rare Neurological Side Effects of Amiodarone. [PDF]
Milan-Ortiz V +4 more
europepmc +1 more source
Abstract figure legend The Kcna1 knockout mouse model of sudden unexpected death in epilepsy (SUDEP) exhibits sex‐specific differences in SUDEP risk. Female mice exhibit a lower SUDEP risk than males, despite similar seizure characteristics and interictal cardiac function across sexes.
Kelsey Paulhus +11 more
wiley +1 more source
Analysis of the tremor in juvenile myoclonic epilepsy [PDF]
WOS: 000390742500019PubMed ID: 27835783Purpose: We aimed to investigate juvenile myoclonic epilepsy (JME) patients complaining of tremor unrelated to valproate (VPA) treatment and evaluate if there were differences between JME patients with and without ...
Oge, Ali Emre +6 more
core +1 more source
ABSTRACT Biallelic pathogenic variants in PNPT1 cause combined oxidative phosphorylation deficiency 13 (COXPD13) (MIM #614932), linking mitochondrial dysfunction to type I interferon (IFN) activation through cytosolic leakage of mitochondrial double‐stranded RNA (mt‐dsRNA).
Dan Ross Brooks +15 more
wiley +1 more source
Abstract Aim This study aimed to elucidate the nature and structure of the decision‐making experiences surrounding illness disclosure and concealment among people with epilepsy (PWE) who have experienced generalized tonic–clonic seizures (GTCS). Methods Giorgi's descriptive phenomenological method was employed. Data were collected between March and May
Young‐Min Shon, Woo Joung Joung
wiley +1 more source
Scotosensitive and photosensitive myoclonic seizures in an infant with trisomy 13. [PDF]
We describe a male carrier of trisomy 13 with scotosensitive and photosensitive myoclonic seizures appearing at the age of 8 months and persisting until death at 20 months.
TORNIERO C. +3 more
core +1 more source
Atypical Presentation of Subacute Sclerosing Panencephalitis in a Child
Background: Subacute sclerosing panencephalitis (SSPE) is a rare complication of measles, which emerges long after the initial infection. The diagnosis of SSPE can be challenging, especially when initial presentation is atypical.
Monika Hooda +3 more
doaj +1 more source

