Results 91 to 100 of about 8,854,237 (294)

KBG syndrome: A scoping review of electroclinical features of patients with epilepsy

Epileptic Disorders, EarlyView.
Abstract Background and Objectives KBG syndrome is a rare autosomal developmental disorder caused by pathogenic variants of the ANKRD11 gene. This scoping review aimed to explore all current literature data regarding clinical and electroencephalographic features of patients with KBG syndrome and epilepsy. Materials and Methods We conducted a literature
Stefania Kalampokini, Evripidis Pityrigkas, Zoi Kallia, Georgia Pepe, Antonis Frontistis, Dimitrios Profer, Vasilios Kimiskidis   +6 more
wiley   +1 more source

Diagnostic yield and copy number variants findings in 219 adult patients with developmental and epileptic encephalopathy

Epilepsia, EarlyView.
Abstract In a clinical setting, exome sequencing (ES) with copy number variant (CNV) analysis is currently the most effective approach for developmental and epileptic encephalopathies (DEE). However, trio‐based ES is often not feasible in adults, its costs remain prohibitive in certain health care settings, and computational tools for CNV calling still
Laura Licchetta, Giulia Bruschi, Tania Giangregorio, Carlotta Stipa, Elisa Mannini, Raffaella Minardi, Barbara Mostacci, Valentina Tontini, Tommaso Pippucci, Francesca Bisulli, Pamela Magini   +10 more
wiley   +1 more source

Impaired psychomotor ability and attention in patients with persistent pain: a cross-sectional comparative study

, 2016
Helena Gunnarsson,1,2 Birgitta Grahn,3–5 Jens Agerström1 1Department of Psychology, Faculty of Health and Life Sciences, Linnaeus University, Vaxjo, 2Hälsoringen, Neron HSU AB, Osby, 3Department of Clinical Sciences Lund-Orthopedics, Lund
Grahn B, Agerström J, Gunnarsson H
core  

Instrumental activities of daily living in older adults with epilepsy: A cross‐sectional and longitudinal multicenter study

Epilepsia, EarlyView.
Abstract Objective Instrumental activities of daily living (IADLs) represent a critical but understudied measure of day‐to‐day function in people with epilepsy (PWE). In the multicenter Brain Aging and Cognition in Epilepsy (BrACE) study of PWE ≥55 years of age, we examined the proportion, clinical correlates, epilepsy‐related predictors, and ...
Ifrah Zawar, Anny Reyes, Jonathan Helm, Kayela Arrotta, Bruce P. Hermann, Alena Stasenko, Robyn M. Busch, Mark Quigg, Jaideep Kapur, Aaron F. Struck, Vineet Punia, McKenna E. Williams, Katherine J. Bangen, Irene Wang, Jerry J. Shih, Lisa Ferguson, Jana E. Jones, Carrie R. McDonald   +17 more
wiley   +1 more source

Psychomotor performance in Alzheimer disease

, 1985
The clinical course of Alzheimer disease (AD) is primarily characterized by a progressive decline in intellectual functioning. Motor behavior is generally considered to remain intact until late in the course of the disease.
Mahurin, Roderick K.
core  

Norwegian Psychomotor Physiotherapy: A scoping review [PDF]

, 2022
Background: Norwegian Psychomotor Physiotherapy (NPMP) is an established treatment approach mainly applied to patients with long-lasting musculoskeletal pain. The research in the field of NPMP is gradually expanding.
Øien, Aud Marie, Dragesund, Tove
core  

Prenatal betamethasone–postnatal N‐methyl‐D‐aspartic acid model of spasms: Update on mechanisms and treatments

Epilepsia Open, EarlyView.
Abstract Infantile epilepsy spasms syndrome (IESS), formerly known as infantile spasms or West Syndrome, is a severe epilepsy syndrome affecting about 3 in 10,000 newborns in the United States. Characterized by clusters of epileptic spasms, interictal hypsarrhythmia, and developmental delays, IESS has diverse causes, including structural‐metabolic ...
Kayla Vieira, Antonia Schonwald, Chian‐Ru Chern, Kamya Shah, Jana Velíšková, Libor Velíšek   +5 more
wiley   +1 more source

Expanding the electroclinical spectrum of TANC2‐related disorders: Lennox–Gastaut syndrome and related developmental epileptic phenotypes

Epilepsia Open, EarlyView.
Abstract Objective Neurodevelopmental disorders (NDDs) and epilepsy are often associated. Increasing evidence highlights a pivotal role for pathogenic variants in genes encoding synaptic scaffolding proteins. Within this group, TANC2 has recently been implicated in intellectual developmental disorder with autistic features and language delay, with or ...
Lorenzo Perilli, Carlotta Stipa, Gianmichele Villano, Laura Licchetta, Leo Strothmann, Robin Tobias Jauss, Gerhard Josef Kluger, Raffaella Minardi, NETRE consortium, Giuseppe Gobbi, Salvatore Grosso, Francesca Bisulli, Pasquale Striano   +12 more
wiley   +1 more source

Long‐term developmental outcome in infantile epileptic spasms syndrome after high‐dose prednisolone and vigabatrin treatment

Epilepsia Open, EarlyView.
Abstract Objective To evaluate long‐term developmental outcomes and identify independent predictors of favorable developmental outcomes at 3 years of age in children with infantile epileptic spasms syndrome (IESS) treated with a standardized stepwise vigabatrin and high‐dose prednisolone protocol.
Soyoung Jang, Hui Jin Shin, Se Hee Kim, Joon Soo Lee, Ara Ko, Hoon‐Chul Kang   +5 more
wiley   +1 more source

Correlations of Selected Psychomotor and Visuomotor Tests with Initial Dynavision Performance

, 2008
The current study investigated the relationship between Dynavision scores for 36 men and 52 women ( M age = 20.5 yr.) and performance on six conventional psychomotor tests which presumably tap similar psychomotor abilities and visuomotor skills ...
Steve L. Prime, John Esposito, Michael Vesia, Peter Klavora   +3 more
core   +1 more source