Results 81 to 90 of about 16,570 (207)

MELAS‐Like Mitochondrial Encephalopathy With Catatonia Associated With a Pathogenic MT‐ND3 (m.10158 T > C) Mutation: A Case Report and Literature Review

Progress in Neurology and Psychiatry, Volume 30, Issue 2, May 2026.
Abstract Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke‐like episodes (MELAS) is a rare multisystem mitochondrial disorder primarily caused by mutations in mitochondrial DNA. While it typically presents with stroke‐like episodes, seizures, and lactic acidosis, recent evidence highlights a broader clinical spectrum, including ...
Faezeh Khorshidian, Vajiheh Aghamollaii, Mohammadreza Mousavipour, Setareh Rassa   +3 more
wiley   +1 more source

Three views on economic information on television [PDF]

, 1989
Three views on economic information on ...
Castellet, Andreu, Missé, Andreu, Ureta, Josep M.   +2 more
core  

NMS, and Why We Should Call It (Malignant) Catatonia [PDF]

, 2006
See full ...
Johnson, Robert Arnold, M.D. (PGY4)
core   +2 more sources

Electroconvulsive Therapy in Schizophrenia: Exploratory Study on the Efficacy, Cognitive Effects, and Safety of Right Unilateral Versus Bitemporal Techniques

Brain and Behavior, Volume 16, Issue 4, April 2026.
The purpose of the study was to compare the effectiveness, safety, and cognitive effects of BTS versus RUS in hospitalized patients with schizophrenia. The results should be considered preliminary due to the sample size (n = 17) and lack of blinding of participants.
Héctor O. Castañeda‐González, Alexandra Magaña‐Ornelas, Aurea Ruby Santiago‐Maury, Sophia Sánchez López, Iván de Jesús Leonor‐Hernández, Hector Cabello‐Rangel   +5 more
wiley   +1 more source

Protocol for a prospective descriptive prevalence study of catatonia in an acute mental health unit in urban South Africa

BMJ Open, 2020
Introduction Catatonia arises from serious mental, medical, neurological or toxic conditions. The prevalence range depends on the setting and the range is anything from 7% to 63% in other countries.
Zukiswa Zingela, Louise Stroud, Johan Cronje, Max Fink, Stephanus van Wyk   +4 more
doaj   +1 more source

Catatonia

Journal of Psychiatrists' Association of Nepal, 2015
DOI: http://dx.doi.org/10.3126/jpan.v3i3 ...
openaire   +3 more sources

Malignant catatonia due to anti-NMDA-receptor encephalitis in a 17-year-old girl: case report [PDF]

, 2011
Anti-NMDA-Receptor encephalitis is a severe form of encephalitis that was recently identified in the context of acute neuropsychiatric presentation. Here, we describe the case of a 17-year-old girl referred for an acute mania with psychotic features and ...
Angèle Consoli, Karine Ronen, Isabelle An-Gourfinkel, Martine Barbeau, Donata Marra, Nathalie Costedoat-Chalumeau, Delphine Montefiore, Philippe Maksud, Olivier Bonnot, Adrien Didelot, Zahir Amoura, Marie Vidailhet, David Cohen   +12 more
core   +1 more source

Catatonia Development in a Patient with Bipolar Disorder Following Electroconvulsive Therapy: A Case Report

Iranian Journal of Psychiatry, 2018
Objective: Electroconvulsive therapy (ECT) is a major treatment of catatonia; and catatonia development during electroconvulsive therapy is a highly surprising phenomenon.
Alireza Ghayoumi, Azadeh Mashayekhi
doaj  

Case report: Recurrent catatonia in a patient with 17p13.3 microduplication syndrome

Frontiers in Psychiatry
Catatonia is a clinically significant syndrome with various etiologies, including genetic factors, that are increasingly recognized. We present a case of recurrent catatonia associated with 17p13.3 microduplication syndrome in a 47-year-old woman with a ...
Ilya Querter, Ilya Querter, Nika Schuermans, Nele Van de Velde, Cisse Geleyn, Annelies Dheedene, Kurt Audenaert, Kurt Audenaert, Chris Baeken, Chris Baeken, Bert Callewaert, Gilbert Lemmens, Gilbert Lemmens   +12 more
doaj   +1 more source

Neuroleptic Malignant Syndrome - Diagnostic Challenges in the Emergency Room [PDF]

, 2008
Introdução - Síndroma maligna dos neurolépticos (SMN) é um efeito secundário raro potencialmente fatal destes fármacos. Relato de caso - Sexo masculino, 18 anos, encefalopatia não progressiva, atraso global do desenvolvimento, epilepsia, perturbação do
Calado, E, Pimentel, S, Silva, R
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