Zobrazeno 1 - 10
of 50
pro vyhledávání: '"David Masur"'
Autor:
Arielle Hershkovich, Erica F Weiss, John McGinley, Diana Bronshteyn, David Masur, Ronda Facchini
Publikováno v:
Archives of Clinical Neuropsychology. 37:1429-1429
Objective: The KCNQ2 gene mutations (KCNQ2), a known cause of neuronal potassium channel dysfunction in brain cells, causes susceptibility to seizures beginning within the first days of life. Seizure semiology, severity and cognitive sequela can vary
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f8318ff794ca0b9c18a80bd60dc8b1dd
https://doi.org/10.1093/arclin/acac060.278
https://doi.org/10.1093/arclin/acac060.278
Publikováno v:
Archives of Clinical Neuropsychology. 37:1318-1318
Objective: We present the neuropsychological profile of a 9-year-old girl with a history of waxing and waning ataxia, initially diagnosed at 18 months of age, with Acute Disseminated Encephalomyelitis (ADEM), later thought to be axonal motor sensory
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cce44d0dc07ce8a25c0513818f76c1e5
https://doi.org/10.1093/arclin/acac060.163
https://doi.org/10.1093/arclin/acac060.163
Publikováno v:
Archives of Clinical Neuropsychology. 33:703-794
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f9e5d8b449d3a276c712abfee8f37369
https://doi.org/10.1093/arclin/acy061.113
https://doi.org/10.1093/arclin/acy061.113
Publikováno v:
Archives of Clinical Neuropsychology. 36:1099-1099
Objective Antiphospholipid Antibody Syndrome (APS), also known as Hughes Syndrome, is an autoimmune condition linked to various adverse medical and neurological outcomes affecting 5 in 100,000. APS results from antibodies (aPL) that attack blood prot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::951f6680519901ee4a93febf0e08a9ea
https://doi.org/10.1093/arclin/acab062.75
https://doi.org/10.1093/arclin/acab062.75
Publikováno v:
Archives of Clinical Neuropsychology. 36:1082-1082
Objective Developmental Discoordination Disorder (DCD) is an often overlooked and seldom diagnosed neurodevelopmental condition marked by impairments in motor skills. Lacking identifiable medical or neurological etiology, children with DCD often have
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d17403ca372cbaca1d60c7305f9f7773
https://doi.org/10.1093/arclin/acab062.59
https://doi.org/10.1093/arclin/acab062.59
Publikováno v:
Archives of Clinical Neuropsychology. 36:1126-1126
Objective Spinocerebellar ataxia 29 (SCA29) is a rare autosomal dominant disorder resulting in infantile-onset hypertonia, gross motor delay and cognitive impairment. SCA29 causes cerebellar dysfunction and atrophy manifested by poor hand coordinatio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::78b19b9f14fdf7c877d3c282e46f8a71
https://doi.org/10.1093/arclin/acab062.99
https://doi.org/10.1093/arclin/acab062.99
Autor:
Dennis Dlugos, David Masur, Erica F. Weiss, Chunyan Liu, Avital Cnaan, Ruth C. Shinnar, Fengming Hu, Shlomo Shinnar, Tracy A. Glauser, Deborah G. Hirtz, Peggy Clark
Publikováno v:
Neurology. 89:1698-1706
Objective:To characterize pretreatment behavioral problems and differential effects of initial therapy in children with childhood absence epilepsy (CAE).Methods:The Child Behavior Checklist (CBCL) was administered at baseline, week 16–20, and month
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c32f593c2079c3c11d788e07847c2181
https://doi.org/10.1212/wnl.0000000000004514
https://doi.org/10.1212/wnl.0000000000004514
Autor:
Shlomo Shinnar, Veronica J. Hinton, Ruth C. Shinnar, Douglas R. Nordli, Dale C. Hesdorffer, William Gallentine, David Masur, Shumei Sun, Julie Rinaldi, Leon G. Epstein, Syndi Seinfeld, Virginia Van de Water, Solomon L. Moshé, Melanie J. Bonner, James Culbert, L. Mathew Frank, Erica F. Weiss
Publikováno v:
Epilepsy & Behavior. 64:283-288
Objective The objective of this study was to determine early developmental and cognitive outcomes of children with febrile status epilepticus (FSE) one month and one year after FSE. Methods One hundred ninety four children with FSE were evaluated on
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e513d697f9dbfd5ec7b37bd1758b18db
https://doi.org/10.1016/j.yebeh.2016.09.013
https://doi.org/10.1016/j.yebeh.2016.09.013
Publikováno v:
Archives of Clinical Neuropsychology. 35:985-985
Objective 22q11.2 deletion syndrome (22q11DS) is a genetic microdeletion disorder linked to various adverse medical and psychiatric outcomes affecting 1 in every 1,000 to 4,000 births. 22q11DS results from a meiotic deletion of DNA at the q11.2 site
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f10b3dae6cd7e4e5c87ec213d3754d8f
https://doi.org/10.1093/arclin/acaa068.190
https://doi.org/10.1093/arclin/acaa068.190
Autor:
Dennis J. Dlugos, Deborah Hirtz, Shlomo Shinnar, Tracy A. Glauser, Peggy Clark, Avital Cnaan, F. Hu, Solomon L. Moshé, David Masur, Eli M. Mizrahi
Publikováno v:
Neurology. 85:1108-1114
To determine incidence and early predictors of generalized tonic-clonic seizures (GTCs) in children with childhood absence epilepsy (CAE).Occurrence of GTCs was determined in 446 children with CAE who participated in a randomized clinical trial compa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::588cf7e86c0e8418a7fd81b9bb89f8b2
https://doi.org/10.1212/wnl.0000000000001971
https://doi.org/10.1212/wnl.0000000000001971