Results 61 to 70 of about 5,991 (177)
Pediatric Neurology Briefs, 1993 The clinical and EEG features and reasons for frequent misdiagnosis of juvenile myoclonic epilepsy are reviewed by the Epilepsy Research Group, Institute of Neurology, National Hospital, and St Thomas’ Hospital, London, England.
J Gordon Millichap
doaj +1 more source
Exteroceptive Reflexes in Stiff Person Syndrome, Other Neurological Conditions and Healthy Controls
Movement Disorders Clinical Practice, EarlyView.Abstract Background Stiff person syndrome (SPS) is a rare disabling neurological condition with overlapping symptomatology with more common neurological conditions. Exaggerated exteroceptive reflex mechanisms are thought to play a role in its pathophysiology.
Belinda Cruse +8 more
wiley +1 more source
National Board of Examinations Journal of Medical SciencesBackground: A Wu type X-linked syndromic intellectual developmental disorder is caused by mutations in the GRIA3 gene This disorder is characterised by autistic features, hyporeflexia, intellectual disability and facial dysmorphism.
A Priya Margaret +3 more
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Journal 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
A case of early onset subacute sclerosing panencephalitis presented as juvenile myoclonic epilepsy
Indian Journal of Psychological Medicine, 2017 A 7.5 years girl presented with myoclonic jerks with prolonged duration coming progressively at shorter intervals for last six moinths. There was declining academic performances.
Ranjan Bhattacharyya +2 more
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Journal of Veterinary Emergency and Critical Care, EarlyView.ABSTRACT Objective To describe the clinical presentation of presumptive acute post‐hypoxic myoclonus in a cat and a dog after cardiopulmonary arrest (CPA). In people, acute post‐hypoxic myoclonus is a transient focal, multifocal, or generalized rhythmic myoclonus that results from global hypoxic–ischemic brain injury and may be cortical or subcortical ...
Theofanis Liatis +2 more
wiley +1 more source
The 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
Myoclonic Jerks and Ataxia: A Case of Rare Neurological Side Effects of Amiodarone. [PDF]
Cureus, 2022 Milan-Ortiz V +4 more
europepmc +1 more source
Genetic landscape of patients with atypical absence status epilepticus: A systematic review
Epilepsia Open, Volume 11, Issue 4, Page 1111-1125, August 2026.Abstract Atypical absence status epilepticus (AASE) is a rare subtype of nonconvulsive status epilepticus (NCSE), characterized by clouding of consciousness and continuous or fluctuating epileptiform activity, generally at a frequency below 3 Hz. Only sparse literature exists on the genetic conditions associated with it.
Maria Cristina Cioclu +2 more
wiley +1 more source