Results 131 to 140 of about 524,560 (351)

Defining Meyer's loop-temporal lobe resections, visual field deficits and diffusion tensor tractography

, 2009
Anterior temporal lobe resection is often complicated by superior quadrantic visual field deficits (VFDs). In some cases this can be severe enough to prohibit driving, even if a patient is free of seizures.
M Yogarajah (16050209), J S Duncan (16050227), McEvoy, A.W., M J Koepp (13602235), Focke, N.K., Koepp, M. J., Duncan, John S., M R Symms (16042382), Koepp, Matthias J., Duncan, J.S., Symms, M.R., Alexander, D. C., Parker, G. J M, Acheson, J., Bonelli, S., A W McEvoy (16050224), S Bonelli (16050215), G J M Parker (16050218), Mara Cercignani (4463104), Alexander, Daniel C., Alexander, D.C., Koepp, M.J., McEvoy, A. W., Parker, G.J.M., J Acheson (10343627), Yogarajah, Mahinda, Symms, Mark R., Bonelli, Silvia B., Cercignani, M., D C Alexander (16050221), Yogarajah, M., Focke, N. K., Symms, M. R., Focke, Niels K., Duncan, J. S., N K Focke (16050212), Parker, G. J. M.   +36 more
core   +1 more source

Memory and Resting‐State Connectivity in Acute Transient Global Amnesia: A Case–Control fMRI Study

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Background and Objectives Transient global amnesia (TGA) is a striking model of isolated amnesia. While hippocampal lesions are well described, the network‐level mechanisms and the precise neuropsychological profile remain debated. Our objective was thus to characterize functional and neuropsychological correlates of acute TGA and their ...
Elias El Otmani, Emmanuel Barbeau, Béatrice Lemesle, Emilie Milongo‐Rigal, Sophie Fernandez, Sandrine Charpentier, Jean‐François Albucher, Nicolas Raposo, Fabrice Bonneville, Patrice Péran, Jérémie Pariente   +10 more
wiley   +1 more source

Comparison of physiological triggering schemes for diffusion-weighted magnetic resonance imaging in kidneys

, 2010
To determine the potential benefit of combined respiratory-cardiac triggering for diffusion-weighted imaging (DWI) of kidneys compared to respiratory triggering alone (RT)
Thoeny, Harriet C, Peter Vermathen, Boesch, Chris, Ute Eisenberger, Stemmer, Alto, Harriet C. Thoeny, Eisenberger, Ute, Binser, Tobias, Tobias Binser, Vermathen, Peter, Alto Stemmer, Chris Boesch   +11 more
core   +1 more source

POAS4SPM: a toolbox for SPM to denoise diffusion MRI data [PDF]

, 2013
We present an implementation of a recently developed noise reduction algorithm for dMRI data, called multi-shell position orientation adaptive smoothing (msPOAS), as a toolbox for SPM.
Weiskopf, N, Polzehl, J, Weiskopf, N. ; https://orcid.org/, Polzehl, J., Nikolaus Weiskopf, Weiskopf, Nikolaus, Mohammadi, S, Karsten Tabelow, Tabelow, K., Mohammadi, S., Tabelow, Karsten, Jörg Polzehl, Tabelow, K, Polzehl, Jörg, Mohammadi, Siawoosh, Siawoosh Mohammadi   +15 more
core   +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

Subacute sclerosing panencephalitis relationship between clinical stage and diffusion weighted imaging findings

, 2006
To investigate the relationship between clinical stages and apparent diffusion coefficient (ADC) changes in the brain of patients with subacute sclerosing panencephalitis (SSPE).
Alkan, Alpay, Yoloğlu, Saim, Erdem, Gülnur, Korkmaz, Levent, Sığırcı, Ahmet, Yakıncı, Mehmet Cengiz, Kutlu, Ramazan   +6 more
core   +1 more source

Recurrent Hypothermia and Autonomic Dysfunction Secondary to Shapiro Syndrome

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT A 44‐year‐old man presented with recurrent hypothermia, diaphoresis and hypertension. Extensive investigation for infectious, inflammatory, metabolic and endocrine aetiologies was negative. MR scan of the brain demonstrated no lesions but revealed callosal dysgenesis, consistent with Shapiro syndrome.
Naveen Kumar, Jeremy Johnson, Susanne Watkins, Eoin Mulroy   +3 more
wiley   +1 more source

Longitudinal measurement of the developing grey matter in preterm subjects using multi-modal MRI.

, 2015
Preterm birth is a major public health concern, with the severity and occurrence of adverse outcome increasing with earlier delivery. Being born preterm disrupts a time of rapid brain development: in addition to volumetric growth, the cortex folds ...
Eaton-Rosen, Zach, Eaton-Rosen, Z, Kendall, Giles S., Alan Bainbridge, Marlow, N, Nicola J. Robertson, Marlow, Neil, Neil Marlow, Ourselin, Sebastien, Modat, Marc, M. Jorge Cardoso, Eliza Orasanu, Modat, M, Robertson, Nicola J., Zach Eaton-Rosen, Robertson, NJ, Melbourne, A, Orasanu, Eliza, Bainbridge, Alan, Melbourne, Andrew, Giles S. Kendall, Sebastien Ourselin, Cardoso, MJ, Ourselin, S, Kendall, GS, Orasanu, E, Bainbridge, A, Andrew Melbourne, Cardoso, M. Jorge, Marc Modat   +29 more
core   +1 more source

Comprehensive Characterization of 98 Chinese Cases of Genetic Creutzfeldt‐Jakob Disease With T188K Mutation

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective To characterize the demographic, clinical, and laboratory features of the Chinese patients of genetic Creutzfeldt‐Jakob disease with T188K variant (T188K‐gCJD), the most common subtype of genetic prion diseases (gPrDs) in China. Methods In this nationwide retrospective study, data from 98 genetically confirmed T188K‐gCJD patients ...
Chun‐Jie Li, Dong‐Lin Liang, Li‐Ping Gao, Wei‐Wei Zhang, Wei Zhou, A. Ruhan, Bing Xu, Run‐Dong Cao, Kang Xiao, Cao Chen, Qi Shi, Xiao‐Ping Dong   +11 more
wiley   +1 more source

A 17 Year Old With Developmental Delay Presenting With Increasing Confusion and Imbalance

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Methylmalonic acidemia is an autosomal recessive genetic disorder primarily caused by defects in methylmalonyl‐CoA mutase and cobalamin (vitamin B12) metabolism. These defects disrupt the tricarboxylic acid cycle and oxidative phosphorylation, leading to the abnormal accumulation of metabolic products such as methylmalonic acid, propionic acid,
Wei Zhao, Yingli Zhang, Hongliang Zheng
wiley   +1 more source