Results 91 to 100 of about 1,096,365 (243)

A Two‐Stage Questionnaire and Actigraphy Screening for iRBD in a Multicenter Retrospective Cohort

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Isolated rapid‐eye‐movement sleep behavior disorder is a prodromal marker of synucleinopathies. However, most cases remain undiagnosed due to the insufficient predictive value of questionnaires and limited access to confirmatory video‐polysomnography. We assessed a two‐stage screening strategy combining a brief questionnaire on rapid‐
Caleb A. Massimi, Giorgio Ricciardiello Mejia, Andre Metzger, Kang Hyun Ryu, Salonee Marwaha, Eva Grzegorczyk, Li Zhou, Eliana Jacobs, Boris Gilyadov, Claudia Kunney, Liqhwa Ncube, Ankit Parekh, Emmanuel Mignot, Fanny M. Elahi, Joseph Winer, Kathleen Poston, Andreas Brink‐Kjaer, Emmanuel H. During   +17 more
wiley   +1 more source

Nucleotide Excision Repair: From Molecular Defects to Neurological Abnormalities. [PDF]

Int J Mol Sci, 2021
Krasikova Y, Rechkunova N, Lavrik O.
europepmc   +1 more source

Isolated, Subtle, Neurological Abnormalities in Mild Cognitive Impairment Types.

, 2019
Background: Isolated, subtle neurological abnormalities (ISNA) are commonly seen in aging, and have been related to cerebral Small Vessel Disease (SVD) and subcortical atrophy in neurologically and cognitively healthy aging subjects.
Rosolino Camarda, Carmela Pipia, Cecili Camarda, Giovanna Cilluffo, Emanuele Grassedonio, Paola Torelli, DELIA Azzarello, Gianluca Sottile   +7 more
core  

White Matter Microstructural Abnormalities in Neonatal Onset Genetic Epilepsy

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Recent evidence indicates that epilepsy is associated with abnormal white matter. If seizures alter white matter, then the impact upon network function, epileptogenesis, and cognition could be pronounced in neonates undergoing rapid developmental myelination. Neonates with epilepsy due to nonstructural genetic causes provide a unique
Amanda G. Sandoval Karamian, Tianjia Zhu, Hao Huang, Shavonne L. Massey, Mark P. Fitzgerald, Darshana Parikh, Arastoo Vossough, Ingo Helbig, Nicholas S. Abend   +8 more
wiley   +1 more source

Investigation of Electroencephalographic Aspects, Adaptive Features, and Clinical Phenotypes in a Group of Children with Autism—A Pilot Study

Clinics and Practice
(1) Background: Autism, as an important global problem that affects many phenotypically different individuals, is associated with electroencephalographic (EEG) abnormalities and adaptability impairment.
Alexandru Capisizu, Leon Zăgrean, Elena Poenaru, Elena Tudorache, Mihaela Anca Bulf, Adriana Sorina Capisizu   +5 more
doaj   +1 more source

Diverse Neurological Symptoms in Chronic Liver Failure: Difficulties in Etiological Diagnosis

, 2013
Acquired hepatocerebral degeneration (AHCD) describes a neurological disorder in the context of chronic hepatic failure which is not related to acute encephalopathy and not explained by an alternative cause. Patients with AHCD may have cognitive deficits,
Ertan, Sibel, Kiziltan, Güneş, Altan, Nihan, Apaydin, Hulya, Gunduz, Aysegul, Freiwald, Tilo   +5 more
core  

Subclinical Optic Nerve Involvement in Radiologically Isolated Syndrome: Multimodal Detection and Diagnostic Impact

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objectives We aimed to determine the frequency of subclinical optic nerve (ON) lesions using MRI, optical coherence tomography (OCT), and visual evoked potentials (VEP) in radiologically isolated syndrome (RIS), and to assess their diagnostic and prognostic significance.
Christine Lebrun‐Frenay, Cassandre Landes‐Château, Lydiane Mondot, Mikael Cohen, Margherita Popolo, Jérôme de Seze, Bertrand Bourre, Françoise Durand‐Dubief, Olivier Casez, Orhun H. Kantarci, Aksel Siva, Stephanie Baillif, Darin T. Okuda, Letizia Leocani   +13 more
wiley   +1 more source

Neurological soft signs and EEG findings in children and adolescents with Gilles de la Tourette syndrome

The Turkish Journal of Pediatrics, 2000
Gilles de la Tourette syndrome (GTS) is a childhood-onset neuropsychiatric disorder, characterized by multiple motor and vocal tics. The presence of EEG abnormalities and neurological soft signs are reported in patients with GTS.
Z B Semerci
doaj  

Latrophilin-2 is a novel receptor of LRG1 that rescues vascular and neurological abnormalities and restores diabetic erectile function. [PDF]

Exp Mol Med, 2022
Yin GN, Kim DK, Kang JI, Im Y, Lee DS, Han AR, Ock J, Choi MJ, Kwon MH, Limanjaya A, Jung SB, Yang J, Min KW, Yun J, Koh Y, Park JE, Hwang D, Suh JK, Ryu JK, Kim HM.   +19 more
europepmc   +1 more source

Insular volume abnormalities associated with different transition probabilities to psychosis [PDF]

, 2011
Background Although individuals vulnerable to psychosis show brain volumetric abnormalities, structural alterations underlying different probabilities for later transition are unknown.
McGuire, P., A. Riecher-Rössler, Simon, A., Simon, A, P. Fusar-Poli, Lenz, C., Fusar-Poli P., Riecher-Rössler, A., Bendfeldt, K, Stieglitz, R D, Riecher-Rössler, A, S. J. Borgwardt, McGuire, P, Borgwardt, S. J., J. Aston, Smieskova R., Bendfeldt K., Lenz C., Smieskova, R., Borgwardt, S J, Riecher-Rossler A., R. Smieskova, Riecher-Roessler, A., P. McGuire, Fusar-Poli, P, Simon A., A. Simon, Borgwardt S. J., K. Bendfeldt, Aston, J, Bendfeldt, K., Stieglitz, R. -D., Lenz, C, Stieglitz R. -D., Stieglitz, R.-D., R.-D. Stieglitz, Fusar-Poli, P., Aston J., McGuire P., Fusar-Poli, P.; id_orcid, Smieskova, R, C. Lenz, Aston, J., Stieglitz RD, Borgwardt SJ, Bendfeldt K, Fusar-Poli P, Riecher-Rössler A, McGuire P, Aston J, Simon A, Smieskova R, Lenz C   +52 more
core   +2 more sources