Results 91 to 100 of about 6,575 (206)

Voluntary stimulus-sensitive jerks and jumps mimicking myoclonus or pathological startle syndromes. [PDF]

open access: yes, 1992
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

Dreaming conundrum

open access: yesJournal of Sleep Research, Volume 34, Issue 2, April 2025.
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]

open access: yes, 2000
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]

open access: yesCureus, 2022
Milan-Ortiz V   +4 more
europepmc   +1 more source

Sex‐specific differences in mortality and neurocardiac interactions in the Kv1.1 knockout mouse model of sudden unexpected death in epilepsy (SUDEP)

open access: yesThe Journal of Physiology, EarlyView.
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]

open access: yes, 2016
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

JAK Inhibition in PNPT1‐Related Mitochondrial Interferonopathy: A Case Report and Review of Mitochondrial–Immune Crosstalk

open access: yesJIMD Reports, Volume 67, Issue 4, July 2026.
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

Phenomenological insights into disclosure and concealment decision‐making among people with epilepsy experiencing generalized tonic–clonic seizures

open access: yesJapan Journal of Nursing Science, Volume 23, Issue 3, July 2026.
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]

open access: yes, 2007
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

open access: yesIndian Pediatrics Case Reports
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

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