Results 121 to 130 of about 255,164 (264)

Prevalence and determinants of language impairment in non-demented amyotrophic lateral sclerosis patients. [PDF]

Eur J Neurol, 2023
Solca F, Aiello EN, Torre S, Carelli L, Ferrucci R, Verde F, Ticozzi N, Silani V, Monti A, Poletti B.   +9 more
europepmc   +1 more source

Early Clinical, Imaging, and Pathological Characteristics of SRPK3/TTN‐Digenic Myopathy

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective SRPK3/TTN‐digenic myopathy was recently established as a skeletal muscle myopathy caused by digenic inheritance. This study characterizes the early clinical presentation of SRPK3/TTN‐digenic myopathy in one previously reported and seven newly identified pediatric patients.
Rotem Orbach, Sandra Donkervoort, Carola Hedberg‐Oldfors, Giovanni Baranello, Dimah Saade, Precilla D'Souza, Ruchee Patel, Eva Michael, A. Reghan Foley, Diana Bharucha‐Goebel, S. Jin Haugland, Meghan McAnally, Omer Abdul Hamid, Katherine Chao, Ellen F. Macnamara, Alan H. Beggs, Anna Sarkozy, Juliane Mueller, Steven A. Moore, Richard S. Finkel, Cynthia J. Tifft, Francesco Muntoni, Anders Oldfors, Carsten G. Bönnemann   +23 more
wiley   +1 more source

Using the Quantifying Bilingual Language Experience Questionnaire to Identify Risk for Language Impairment in Bilingual Children. [PDF]

J Speech Lang Hear Res
De Cat C, Tuller L, Gusnanto A, Kašćelan D, Prévost P, Serratrice L, Unsworth S.   +6 more
europepmc   +1 more source

Correction: Pleiotropy between language impairment and broader behavioral disorders-an investigation of both common and rare genetic variants. [PDF]

J Neurodev Disord, 2023
Nudel R, Appadurai V, Buil A, Nordentoft M, Werge T.   +4 more
europepmc   +1 more source

Problematic Internet Use in Frontotemporal Dementia: A Case Series

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT The present study investigated problematic internet use (PIU) among 61 patients with frontotemporal dementia (FTD) compared to a cohort of 354 patients with mild cognitive impairment (MCI) and Alzheimer's dementia. PIU was identified in 22.9% of FTD patients compared to only 0.8% of AD patients (p < 0.001). Behaviors included compulsive social
Daniele Urso, Giuseppe Volpe, Agnese Valguarnera, Davide Vilella, Alessandra Vitulli, Valentina Gnoni, Alessia Giugno, Eleonora Rollo, Mark D. Griffiths, Giancarlo Logroscino   +9 more
wiley   +1 more source

Impacts of Caregiver Stress on the Receptive Language Skills of Children With Language Impairment During the COVID-19 Pandemic. [PDF]

Int J Lang Commun Disord
Hutchins C, Poudel S, Tambyraja S, Schmitt MB.   +3 more
europepmc   +1 more source

Task-based profiles of language impairment and their relationship to cognitive dysfunction in Parkinson's disease. [PDF]

PLoS One, 2022
Lowit A, Thies T, Steffen J, Scheele F, Roheger M, Kalbe E, Barbe M.   +6 more
europepmc   +1 more source

Association Between Motor Pathway Damage and Motor Deficit in Upper and Lower Limb in People With MS

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Corticospinal tract damage is common in people with MS, but the degree of clinical symptoms varies. We hypothesize that corticospinal tract lesions are more extensive and severe in people with MS with motor impairments in both upper and lower limbs.
Mathilde Liffran, Malo Gaubert, Alice Dufey, Elise Bannier, Audrey Rico, Jean‐Christophe Ferré, Raphaël Chouteau, Laure Michel, Emmanuelle Le Page, Virginie Callot, Bertrand Audoin, Sarah Demortière, Benoît Combès, Anne Kerbrat   +13 more
wiley   +1 more source

Exploring Language Impairment in Catalan-Dominant Bilinguals with Primary Progressive Aphasia: Preliminary Data. [PDF]

Brain Sci
Salmons I, Muntané-Sánchez H.
europepmc   +1 more source

Language impairment in the genetic forms of behavioural variant frontotemporal dementia. [PDF]

J Neurol, 2023
Samra K, MacDougall AM, Bouzigues A, Bocchetta M, Cash DM, Greaves CV, Convery RS, van Swieten JC, Seelaar H, Jiskoot L, Moreno F, Sanchez-Valle R, Laforce R, Graff C, Masellis M, Tartaglia MC, Rowe JB, Borroni B, Finger E, Synofzik M, Galimberti D, Vandenberghe R, de Mendonça A, Butler CR, Gerhard A, Ducharme S, Le Ber I, Tiraboschi P, Santana I, Pasquier F, Levin J, Otto M, Sorbi S, Rohrer JD, Russell LL, Genetic FTD Initiative (GENFI).   +35 more
europepmc   +1 more source