Results 321 to 330 of about 461,280 (380)

Genetic epilepsies with myoclonic seizures: Mechanisms and syndromes

Epilepsia Open, EarlyView.
Abstract Genetic epilepsy with myoclonic seizures encompasses a heterogeneous spectrum of conditions, ranging from benign and self‐limiting forms to severe, progressive disorders. While their causes are diverse, a significant proportion stems from genetic abnormalities.
Antonietta Coppola, Marica Rubino, Antonella Riva, Pasquale Striano   +3 more
wiley   +1 more source

Protocol for the isolation and characterization of porcine brain region-associated extracellular particles. [PDF]

PLoS One
De Avila A, Diaz M, Cisterna BA, Castillo S, Lezana JP, Molino J, Luis L, Venegas-Anaya M, Reginensi D.   +8 more
europepmc   +1 more source

Absence seizures: Update on signaling mechanisms and networks

Epilepsia Open, EarlyView.
Abstract Absence seizures (AS) are a hallmark of genetic generalized epilepsies (GGE), characterized by brief episodes of impaired consciousness accompanied by electroencephalographic spike‐and‐wave discharges (SWDs). Traditionally attributed to cortico‐thalamo‐cortical (CTC) dysrhythmia, emerging evidence suggests a more intricate pathophysiological ...
Ozlem Akman, Filiz Onat
wiley   +1 more source

Cortical excitability and analgesic effects of multisite transcranial direct current stimulation targeting the motor cortex and cerebellum in fibromyalgia. [PDF]

Sci Rep
Betancur DFA, da Graça Lopes Tarragó M, França BR, Bueno GB, Gomes J, Coelho ML, Venturini CL, Torres ILS, Fregni F, Bock H, Caumo W.   +10 more
europepmc   +1 more source

The challenge of ultra‐rarity: Dual diagnosis of Lafora disease and developmental encephalopathies linked to TRIO and SHANK3 pathogenic variants

Epilepsia Open, EarlyView.
Abstract We report two cases of dual genetic diagnoses involving Lafora disease (LD) and co‐occurring neurodevelopmental disorders caused by pathogenic variants in TRIO and SHANK3, respectively. LD is an ultra‐rare, autosomal recessive, severe form of progressive myoclonus epilepsy affecting previously healthy children or adolescents. In both patients,
Lorenzo Muccioli, Francesca Bisulli, Raffaella Minardi, Maria Lucia Valentino, Micaela De Simone, Rodrigo Almeida Paroni, Edward Cesnik, Elisa Fallica, Luigi Bonan, Eleonora Pizzi, DEFEAT‐LD Study Group, Cosimo Altomare, Massimo Carella, Cinzia Costa, Giuseppe Damante, Lidia Di Vito, Giuseppe d’Orsi, Nicola Gambacorta, Paola Imbrici, Valentina Imperatore, Antonella Liantonio, Laura Licchetta, Raffaele Lodi, Paola Mantuano, Orazio Palumbo, Elena Pasini, Paolo Prontera, Luca Vignatelli, Gaetano Cantalupo, Laura Licchetta   +29 more
wiley   +1 more source

Motor circuits and beyond: Functional connectivity related to psychomotor syndromes in depression. [PDF]

Psychol Med
Liang Q, Zhou Z, Li Y, Chen S, Lin S, Lin X, Zhang Y, Peng B, Xu Z, Hou G, Qiu Y.   +10 more
europepmc   +1 more source

Gallic acid alleviates hippocampus and cerebellum injuries in a rat model of hepatic encephalopathy. [PDF]

Sci Rep
Jafaripour L, Ahmadvand H, Babaeenezhad E, Esmaeilpour K, Maneshian M, Bashiri H, Asadi-Shekaari M.   +6 more
europepmc   +1 more source

Fractional Amplitude of Low-Frequency Fluctuations and Regional Homogeneity Analyses Revealed Altered Local Spontaneous Neural Activities in Ankylosing Spondylitis. [PDF]

J Pain Res
Lin C, Xie Y, Liu D, Liu B, Gu J, Wang X, Qin J.   +6 more
europepmc   +1 more source

PRDM13 is required for specification of PAX2 lineage inhibitory neurons in the developing cerebellum. [PDF]

Dev Biol
Ma ZZ, Hale MA, Mona B, Uruena A, Johnson JE.   +4 more
europepmc   +1 more source

Insights Into Creutzfeldt-Jakob Disease With a Case Series From a District General Hospital and a Literature Review. [PDF]

Cureus
Rai B, Nandish S, Randall M, Rajgopal A.
europepmc   +1 more source