Results 221 to 230 of about 399,854 (379)

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

Synopsis of Neuropsychiatry

, 2001
Carl Salzman
openalex   +2 more sources

Jeffrey L. Cummings, Michael S. Mega: Neuropsychiatry and Behavioral Neuroscience [PDF]

, 2004
Frédéric Assal
openalex   +1 more source

Neuropsychiatry of epilepsy [PDF]

Irish Journal of Psychological Medicine, 2006
Mary Cannon, David Cotter, Frederick Sundram   +2 more
openaire   +3 more sources

Bridging neurology and psychiatry: establishing Latin America's first dedicated Neuropsychiatry Ward at IPq-HCFMUSP. [PDF]

Front Psychiatry
Lacerda DCR, Sousa LDP, Obeid M, Santos LS, Bozutti LA, Marchetti RL.   +5 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

Service innovations: Is there a market for neuropsychiatry? A year in the life of a district-based neuropsychiatry service [PDF]

, 2005
K. Barrett, S Sudharsan
openalex   +1 more source

Towards a second-person neuropsychiatry

Philosophical Transactions of the Royal Society B: Biological Sciences, 2016
L. Schilbach
semanticscholar   +1 more source

Simultaneous tDCS‐rTMS stimulation to regulate the language network and improve language ability in Landau–Kleffner syndrome

Epilepsia Open, EarlyView.
Abstract Landau–Kleffner syndrome (LKS) is a rare epileptic syndrome causing language regression. In this preliminary study, we investigated the effects of simultaneous transcranial direct current stimulation (tDCS) and transcranial magnetic stimulation (rTMS) on LKS patients and the underlying mechanism based on magnetoencephalography (MEG) network ...
Runze Chen, Xinyan Liu, Xiaohong Qi, Wenwen Shen, Xuerong Leng, Xiating Zhang, Liping Zhang, Yuexin Zhang, Xuan Zhao, Xingyu Wang, Jicong Zhang, Yuping Wang, Yicong Lin   +12 more
wiley   +1 more source

Correction: Cerebral Braak stage and amygdala granular fuzzy astrocyte status have independent effects on neuronal 3R-tau and 4R-tau accumulations in the olfactory bulb, respectively, in cases with low to intermediate AD neuropathologic change. [PDF]

Acta Neuropathol
Yokota O, Miki T, Nakashima-Yasuda H, Ishizu H, Haraguchi T, Miyashita A, Ikeuchi T, Hasegawa M, Nishikawa N, Takenoshita S, Terada S, Takaki M.   +11 more
europepmc   +1 more source