Zobrazeno 1 - 10
of 85
pro vyhledávání: '"Michael E. Behen"'
Autor:
Csaba Juhász, Aimee F. Luat, Michael E. Behen, Nore Gjolaj, Jeong-Won Jeong, Harry T. Chugani, Ajay Kumar
Publikováno v:
Pediatric Neurology. 139:49-58
Enlarged deep medullary veins (EDMVs) in patients with Sturge-Weber syndrome (SWS) may provide compensatory venous drainage for brain regions affected by the leptomeningeal venous malformation (LVM). We evaluated the prevalence, extent, hemispheric d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7571598c901907a99e6c5fc4c5b59db
https://doi.org/10.1016/j.pediatrneurol.2022.11.011
https://doi.org/10.1016/j.pediatrneurol.2022.11.011
Autor:
Ming Dong, Nolan O'Hara, Csaba Juhász, Michael E. Behen, Min-Hee Lee, Jeong-Won Jeong, Soumyanil Banerjee
Publikováno v:
Human Brain Mapping
This study investigated whether current state‐of‐the‐art deep reasoning network analysis on psychometry‐driven diffusion tractography connectome can accurately predict expressive and receptive language scores in a cohort of young children wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5ff16adebe81b0989a6308ac30538c24
https://doi.org/10.1002/hbm.25437
https://doi.org/10.1002/hbm.25437
Publikováno v:
Frontiers in Human Neuroscience, Vol 8 (2014)
Postmortem neuropathology studies report reduced number and size of Purkinje cells (PC) in a majority of cerebellum specimens from persons with autism spectrum disorders (ASD). In this study using diffusion weighted MRI, we investigated whether struc
Externí odkaz:
https://doaj.org/article/605f519fcafd4d12b7fc62dcf93f4052
Publikováno v:
Epilepsia. 59:1307-1315
Objective We analyzed long-term changes of lobar glucose metabolic abnormalities in relation to clinical seizure variables and development in a large group of children with medically refractory epilepsy. Methods Forty-one children (25 males) with dru
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::439b58bdb5e7fc22ce9aa1e1674c6ba8
https://doi.org/10.1111/epi.14404
https://doi.org/10.1111/epi.14404
Autor:
Flóra John, Jeong-Won Jeong, Rajkumar Agarwal, Mohsin Maqbool, Csaba Juhász, Michael E. Behen
Publikováno v:
Annals of Clinical and Translational Neurology
We present longitudinal imaging data of a child with Sturge–Weber syndrome (SWS). At age 8 months, 3 weeks after initial seizures and prolonged motor deficit, MRI showed extensive right hemispheric SWS involvement with severe glucose hypometabolism
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::74b0b75d139dd6845cd1c3414f8c833b
http://europepmc.org/articles/PMC5899918
http://europepmc.org/articles/PMC5899918
Publikováno v:
Brain Lang
To characterize structural white matter substrates associated with language functions in children with language disorders (LD), a psychometry-driven diffusion tractography network was investigated with canonical correlation analysis (CCA), which can
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54c333d11751bae4a177e4f51af6b43f
https://pubmed.ncbi.nlm.nih.gov/32004807
https://pubmed.ncbi.nlm.nih.gov/32004807
Publikováno v:
Human Brain Mapping. 37:3946-3956
To determine brain plasticity changes due to resective epilepsy surgery in children, we performed a longitudinal connectome analysis on the pattern of axonal connectivity in the contralateral hemisphere. Pre- and postoperative diffusion tensor imagin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6fdd4e47f7192fb0e5d9600ad4cae983
https://doi.org/10.1002/hbm.23287
https://doi.org/10.1002/hbm.23287
Publikováno v:
Journal of Magnetic Resonance Imaging. 44:1504-1512
PURPOSE To investigate whether different genetic mutations observed in children with global developmental delay (GD) are associated with unique patterns of the arcuate fasciculus dysmorphology. MATERIALS AND METHODS Six children with GD (age: 36.8 ±
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2134d6166f04f5978226969285dc90d1
https://doi.org/10.1002/jmri.25306
https://doi.org/10.1002/jmri.25306
Publikováno v:
American Journal of Neuroradiology. 37:1170-1177
Pure speech delay is a common developmental disorder which, according to some estimates, affects 5%-8% of the population. Speech delay may not only be an isolated condition but also can be part of a broader condition such as global developmental dela
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f8f8319d5b716f254d9c2968c85d5e82
https://doi.org/10.3174/ajnr.a4662
https://doi.org/10.3174/ajnr.a4662
Evolution of Brain Glucose Metabolic Abnormalities in Children With Epilepsy and SCN1A Gene Variants
Autor:
Tuhina Govil-Dalela, Csaba Juhász, Harry T. Chugani, Melissa A. Hicks, Aimee F. Luat, Michael E. Behen, Ananyaa Kumar
Publikováno v:
Journal of child neurology. 33(13)
Three children with drug-refractory epilepsy, normal magnetic resonance image (MRI), and a heterozygous SCN1A variant underwent 2-deoxy-2-[18F]fluoro-d-glucose positron emission tomography (FDG-PET) scanning between age 6 months and 1 year and then a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a0dd36903fc75c668fd26eaa15bca805
https://pubmed.ncbi.nlm.nih.gov/30182801
https://pubmed.ncbi.nlm.nih.gov/30182801