Results 151 to 160 of about 1,055,007 (238)

Disrupted thalamic functional hierarchy on resting-state fMRI in idiopathic generalized epilepsy. [PDF]

Eur Radiol Exp
Chen J, Sun X, Yu K, Yang Z, Li H, Yang Z, Chen Y, Li J, Rodriguez-Labrada R, Yao D, Jiang S, Luo C.   +11 more
europepmc   +1 more source

Causality Analysis to the Abnormal Subcortical-Cortical Connections in Idiopathic-Generalized Epilepsy. [PDF]

Front Neurosci, 2022
Qin Y, Li S, Yao D, Luo C.
europepmc   +1 more source

Single‐Cell Integration of Mouse Models of Autism Reveals Conserved Transcriptomic Signatures of Excitatory‐Inhibitory Imbalance and Glial Dysfunction

Glia, Volume 74, Issue 12, December 2026.
Integrated scRNA‐seq from 11 ASD models reveals convergent E/I imbalance and glial dysfunction. Conserved astrocyte and oligodendrocyte dysregulation transcend model‐specific variability. Validated by human datasets. ABSTRACT The etiological heterogeneity of autism spectrum disorder (ASD) complicates identifying core molecular mechanisms.
João V. Nani, Victor J. Duque, Alysson R. Muotri, André S. Mecawi   +3 more
wiley   +1 more source

High‐Resolution IVIM MRI Characterizes Diffusion–Perfusion Properties of the Parasagittal Dura

NMR in Biomedicine, Volume 39, Issue 11, November 2026.
Parasagittal dura demonstrates intermediate diffusion and elevated perfusion‐related IVIM metrics compared with brain parenchyma, reflecting its unique microfluidic environment at the CSF–dura interface. IVIM imaging of the parasagittal dura provides a rapid, noncontrast MRI approach to assess dural fluid transport and may offer a potential imaging ...
Yi‐Jui Liu, Chun‐Han Liao, Shin‐Lei Peng, Shao‐Chieh Lin, Chao‐Chun Lin, Chia‐Wei Lin, Chia‐Hong Hsieh, Chun‐Wen Chen, Hing‐Chiu Chang   +8 more
wiley   +1 more source

Treatment outcomes in women with idiopathic generalized epilepsy. [PDF]

Acta Neurol Scand, 2022
Kiiski R, Basnyat P, Raitanen J, Rainesalo S, Peltola J, Mäkinen J.   +5 more
europepmc   +1 more source

Suspected hyperthyroidism‐associated myoclonus in a cat

Veterinary Record Case Reports, Volume 14, Issue 4, November 2026.
Abstract A 10‐year‐old, male, neutered domestic shorthair cat presented with a 2‐week history of progressively worsening myoclonic jerks predominantly involving the head. Jerks were continuous and marked at rest, but became less intense during activity.
Magdalena Maria Dyrka, Ian Ramsey, Fiona May Keir James, Grace Kadler, Jessica Zilli, Rodrigo Gutierrez Quintana   +5 more
wiley   +1 more source

GABRG2 C588T Polymorphism Is Associated with Idiopathic Generalized Epilepsy but Not with Antiepileptic Drug Resistance in Pakistani Cohort. [PDF]

Biomed Res Int, 2022
Saleem T, Maqbool H, Sheikh N, Tayyeb A, Mukhtar M, Ashfaq A.   +5 more
europepmc   +1 more source

Responsive stimulation of the thalamus for idiopathic generalized epilepsy: Results of the randomized controlled NAUTILUS trial through 18 months. [PDF]

Epilepsia
Uysal U, Landazuri P, Burdette DE, Patra S, Crudele AN, Englot DJ, Gavvala JR, Tandon N, Pati S, Kaye LC, Ojemann S, Barnett D, Neimat J, Palade AE, Rahimpour S, Arain AA, Richardson RM, Cash SS, Salanova V, Urban A, Welch WP, Gonzalez-Martinez JA, Van Gompel JJ, Starnes K, Spencer D, Ernst LD, Amin U, Rivera-Cruz A, Dugan P, Fajardo M, Lallas M, Jobst BC, Odom N, Roland JL, Willie JT, Sheth SA, Goldman AM, Skidmore CT, Wu C, Drees C, Parker J, Ganguly TM, Szaflarski J, Ghatan S, Johnson L, Norman J, Wingeier B, Seale CG, Morrell MJ, Nautilus Study Group.   +49 more
europepmc   +1 more source

Corrigendum: Alterations of cerebral perfusion and functional connectivity in children with idiopathic generalized epilepsy. [PDF]

Front Neurosci, 2022
Chen G, Hu J, Ran H, Nie L, Tang W, Li X, Li Q, He Y, Liu J, Song G, Xu G, Liu H, Zhang T.   +12 more
europepmc   +1 more source

Clinical and genetic characterization of intellectual disability

Developmental Medicine &Child Neurology, Volume 68, Issue 11, Page 1601-1609, November 2026.
This study examines the etiological factors and comorbidities in a large cohort of Finnish patients with intellectual disability. Genetic causes—including chromosomal abnormalities and pathogenic gene variants—were more frequently identified in individuals with moderate to profound intellectual disability.
Aarni Venetvaara, Minna Kraatari‐Tiri, Jussi‐Pekka Tolonen, Marko Merikukka, IDGEN Study Group, Hannaleena Kokkonen, Teija Paakkola, Susanna Varis, Antti Dahl, Jarmo Körkkö, Jonna Komulainen‐Ebrahim, Jukka Moilanen, Johanna Uusimaa, Outi Kuismin, Elisa Rahikkala   +14 more
wiley   +1 more source