Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Mary Bertrand"'
Autor:
Mary Bertrand, Jennifer Strahle, Ananth K. Vellimana, David D. Limbrick, Matthew D. Smyth, Anna Jeong
Publikováno v:
Journal of Neurosurgery: Pediatrics. 19:56-62
OBJECTIVE Electrical status epilepticus of sleep (ESES) is a rare electrographic pattern associated with global regression, which is often poorly responsive to traditional epilepsy treatments and can have a devastating and permanent neurocognitive ou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9b499d8023af03b0a155d2d3480d7d18
https://doi.org/10.3171/2016.8.peds16319
https://doi.org/10.3171/2016.8.peds16319
Publikováno v:
International Journal of Pediatric Otorhinolaryngology. 102:154-156
Paradoxical vocal fold motion (PVFM) is characterized by vocal fold adduction during respiration. Benign Rolandic epilepsy (BRE) is the most common childhood epilepsy and can cause oropharyngolaryngeal or facial manifestations. A 9-year-old male pres
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8cf2fef3eaea828c7102259ed434cc6f
https://doi.org/10.1016/j.ijporl.2017.09.021
https://doi.org/10.1016/j.ijporl.2017.09.021
Autor:
James W. Wheless, Sohnee Ahmed, William B. Dobyns, Alex R. Paciorkowski, Mandy Ma, Laurie E. Seltzer, Mary Bertrand
Publikováno v:
Epilepsia. 55:1292-1300
SummaryObjective FOXG1-related disorders are associated with severe intellectual disability, absent speech with autistic features, and epilepsy. Children with deletions or intragenic mutations of FOXG1 also have postnatal microcephaly, morphologic ab
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b1a2deef254d78e474e8f7339db85b6
https://doi.org/10.1111/epi.12648
https://doi.org/10.1111/epi.12648
Autor:
David D. Limbrick, Matthew D. Smyth, Mary Bertrand, Brandon A. Miller, Anna Jeong, Brian J. Dlouhy
Publikováno v:
Child's nervous system : ChNS : official journal of the International Society for Pediatric Neurosurgery. 32(9)
Dravet syndrome (DS), also known as severe myoclonic epilepsy of infancy (SMEI), is a rare genetic disorder that results in severe childhood-onset epilepsy. Children with DS initially present with seizures in the first year of life that are often ass
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::925be84c0e289a614c2e7a00b993d2eb
https://pubmed.ncbi.nlm.nih.gov/27465677
https://pubmed.ncbi.nlm.nih.gov/27465677
Autor:
Jeffrey B. Titus, David D. Limbrick, Ian G. Dorward, Matthew D. Smyth, James M. Johnston, Mary Bertrand
Publikováno v:
Journal of Neurosurgery: Pediatrics. 7:179-188
Object Patients undergoing epilepsy surgery without evidence of a lesion on MR imaging and without a temporal source for seizure onset generally have less favorable outcomes than patients with structural lesions or temporal onset. However, many of th
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::efad50b92f5f3c39be1b5f2d91c2ffdb
https://doi.org/10.3171/2010.11.peds10265
https://doi.org/10.3171/2010.11.peds10265
Autor:
Prithvi Narayan, Tae Sung Park, David D. Limbrick, Mary Bertrand, Alexander K. Powers, Matthew D. Smyth, Jeffrey G. Ojemann
Publikováno v:
Journal of Neurosurgery: Pediatrics. 4:323-332
Object Hemispherotomy generally is performed in hemiparetic patients with severe, intractable epilepsy arising from one cerebral hemisphere. In this study, the authors evaluate the efficacy of hemispherotomy and present an analysis of the factors inf
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8d9dfdd9bd8c9110569cde4ace05b169
https://doi.org/10.3171/2009.5.peds0942
https://doi.org/10.3171/2009.5.peds0942
Publikováno v:
Epilepsia. 50:1450-1461
Summary Purpose: Medically intractable seizures arising from the sensorimotor (rolandic) cortex present a formidable challenge for epileptologists and epilepsy surgeons. The objective of this study was to evaluate the safety and efficacy of surgical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e3b4981104d406592856e4ea9404e777
https://doi.org/10.1111/j.1528-1167.2008.01868.x
https://doi.org/10.1111/j.1528-1167.2008.01868.x
Autor:
Vaishnavi Purusothaman, Donna B. Jeffe, Michael Wallendorf, Matthew D. Smyth, Robin C. C. Ryther, David D. Limbrick, Lisa A. Harker, Mary Bertrand
Publikováno v:
Epilepsybehavior : EB. 37
Purpose Up to 14% of children with epilepsy continue to experience seizures despite having appropriate medical therapy and develop medically refractory epilepsy (MRE) [8] , [9] . Assessing clinical outcomes and therapeutic efficacy in children with M
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8551df386acae4546da764fa600d25f0
https://pubmed.ncbi.nlm.nih.gov/24967697
https://pubmed.ncbi.nlm.nih.gov/24967697
Autor:
Karen Steger-May, Matthew D. Smyth, Laleh Jalilian, David D. Limbrick, Mary Bertrand, Aimen Kasasbeh
Publikováno v:
Neurosurgery. 74(1)
BACKGROUND Corpus callosotomy (CC) is a valuable palliative surgical option for children with medically refractory epilepsy due to generalized or multifocal cortical seizure onset. OBJECTIVE To investigate the extent of CC resulting in optimal seizur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::248b95de2932fee4dd96c09535b9b533
https://pubmed.ncbi.nlm.nih.gov/24089047
https://pubmed.ncbi.nlm.nih.gov/24089047
Autor:
Sau Wai Cheung, Katia Rocchetti, Chiara Pantaleoni, Pawel Stankiewicz, Maria Clara Bonaglia, Roberto Ciccone, Stefano D'Arrigo, Jeffrey R Hughes, Mary Bertrand, Thomy de Ravel, Nicola Brunetti-Pierri, Erika Della Mina, Christian P. Schaaf, Zhilian Xia, Naftha Jelluma, Orsetta Zuffardi, Renato Borgatti, Claudia A. L. Ruivenkamp, Parul Jayakar, Serena Belli, Alex R. Paciorkowski, V. Reid Sutton
Publikováno v:
European Journal of Human Genetics, 19(1), 102-107
Genome-wide high-resolution array analysis is rapidly becoming a reliable method of diagnostic investigation in individuals with mental retardation and congenital anomalies, leading to the identification of several novel microdeletion and microduplic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::200fbc29c64dcd4037a7753420903068
https://hdl.handle.net/1887/108675
https://hdl.handle.net/1887/108675
