Zobrazeno 1 - 10
of 11
pro vyhledávání: '"Christopher W. Beatty"'
Autor:
Kristen Arredondo, Adam P. Ostendorf, Stephanie Ahrens, Christopher W. Beatty, Jonathan Pindrik, Ammar Shaikhouni
Publikováno v:
Journal of Clinical Neurophysiology.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f4639544e3f32da16169f804e11ef7e4
https://doi.org/10.1097/wnp.0000000000000991
https://doi.org/10.1097/wnp.0000000000000991
Autor:
Janelle, Wagner, Sonal, Bhatia, B Oyinkan, Marquis, Imelda, Vetter, Christopher W, Beatty, Rebecca, Garcia, Charuta, Joshi, Gogi, Kumar, Kavya, Rao, Nilika, Singhal, Karen, Skjei
Publikováno v:
Journal of Clinical Psychology in Medical Settings.
Epilepsy affects 1% of youth and is associated with neurocognitive and psychosocial comorbidities, increased risk of mortality, and poor health-related outcomes. Health disparities in children and youth with epilepsy (CYE) have been understudied. A S
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9a16405a21f640c7f626ce558e443d04
https://doi.org/10.1007/s10880-022-09898-1
https://doi.org/10.1007/s10880-022-09898-1
Autor:
John R Mytinger, William Parker, Steven W Rust, Stephanie M. Ahrens, Dara VF Albert, Christopher W. Beatty, Julie Chrisman, Daniel J Clark, Andrea Debs, Danielle Denney, Mary Karn, James Herbst, Adam P. Ostendorf, Mary C Taylor, Jaime DE Twanow, Jorge Vidaurre, Anup D. Patel
Publikováno v:
Neurology. 99(19)
Background and Objectives:Infantile spasms (IS) are early childhood seizures with potentially devastating consequences. Standard therapies (adrenocorticotropic hormone [ACTH], high-dose prednisolone, and vigabatrin) are strongly recommended as the fi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b36c7829ceb76a6ba5eda97e922547ec
https://pubmed.ncbi.nlm.nih.gov/36038276
https://pubmed.ncbi.nlm.nih.gov/36038276
Autor:
Adam P. Ostendorf, Alison Gehred, Christopher W. Beatty, Satyanarayana Gedela, Jason P. Lockrow
Publikováno v:
Seminars in pediatric neurology. 39
Pediatric epilepsy surgery is underutilized. Only 1%-11% of children with drug resistant epilepsy (DRE) undergo surgical treatment, or less than half of those estimated to benefit. We conducted a systematic review of articles published in PubMed, EMB
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f7ff8308c95903a24f8501aa11e2aba6
https://pubmed.ncbi.nlm.nih.gov/34620465
https://pubmed.ncbi.nlm.nih.gov/34620465
Autor:
Anup D. Patel, Christopher W. Beatty
Publikováno v:
Neurology. 98:475-476
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4fb105591e99ae12da3022bf5d1cebeb
https://doi.org/10.1212/wnl.0000000000200104
https://doi.org/10.1212/wnl.0000000000200104
Publikováno v:
Journal of Child Neurology. 33:153-157
Neonatal seizures are treated with phenobarbital and prolonged treatment does not prevent postneonatal epilepsy. The authors documented factors influencing phenobarbital use and determined whether published data changed practice. A total of 83 neonat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fadec425e26f845fd657c66b334e0c4d
https://doi.org/10.1177/0883073817745990
https://doi.org/10.1177/0883073817745990
Publikováno v:
Seizure. 45:184-188
Purpose To determine if there are differences in the timing of diagnosis and response to treatment between infants with infantile spasms (IS) and Trisomy 21 (T21) and those with idiopathic IS. Method This was a retrospective study evaluating the time
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::444e2b838d415a9c5574f68c4ba0b971
https://doi.org/10.1016/j.seizure.2016.12.016
https://doi.org/10.1016/j.seizure.2016.12.016
Publikováno v:
Pediatric Neurology. 60:79-82
Background Channelopathies are a group of monogenic disorders that affect a single ion channel and can result in neurological disease. While a rare cause of epilepsy, channelopathies offer unique insight to the molecular basis of epilepsy and treatme
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7eee413052417ef8451e476aa508ebb5
https://doi.org/10.1016/j.pediatrneurol.2016.03.012
https://doi.org/10.1016/j.pediatrneurol.2016.03.012
Juvenile Alpers-Huttenlocher syndrome is a mitochondrial deoxyribonucleic acid (mtDNA) depletion syndrome that results in a typical clinical course of headache with visual auras leading to explosive seizure onset and eventual hepatopathy. Elevations
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::53312d1b0bca74c1b897bccc7099e042
https://doi.org/10.1016/b978-0-12-800877-5.00017-6
https://doi.org/10.1016/b978-0-12-800877-5.00017-6
Publikováno v:
Seminars in pediatric neurology. 21(2)
We present the case of a 14-year-old girl with a biphasic course after oxycodone ingestion. Clinically, she had a rapid return to baseline after initial ingestion and presented a week later with new-onset ballism, akathisia, and encephalopathy. Neuro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::268b241133f463c42d04dada9e30f6ed
https://pubmed.ncbi.nlm.nih.gov/25149955
https://pubmed.ncbi.nlm.nih.gov/25149955