Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Annette Grefe"'
Publikováno v:
Journal of Child Neurology. :088307382311726
Background Children of minority race/ethnicity face barriers to accessing specialty services. During the COVID pandemic, health insurance companies reimbursed telehealth services. Our objective was to evaluate the effect of audio versus video visits
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7a76e17921c7d64be7a5616594b21eb1
https://doi.org/10.1177/08830738231172633
https://doi.org/10.1177/08830738231172633
Autor:
Marta Hernandez-Chavez, Cheryl Bushnell, Matthew E. Fink, Mark T Mackay, Christhunesa S. Christudass, Betsy Ostrander, Lisa Leffert, Beth Anne Cavanaugh, Jennifer J. Majersik, Adam Kirton, So Lee, Annette Grefe, Sanjith Aaron
Publikováno v:
Stroke. 50
Background: There is evidence that male neonates have higher incidences of ischemic stroke and associated limitations in brain repair compared to female neonates. We used data from the International Maternal Newborn Stroke Registry (IMNSR) to further
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4b480293330b7e410eb3ab24e29ce6fb
https://doi.org/10.1161/str.50.suppl_1.tp507
https://doi.org/10.1161/str.50.suppl_1.tp507
Autor:
Deborah L. Renaud, Emma Glamuzina, Catherine Fallet-Bianco, Bader Alhaddad, Laurence Gauquelin, Mackenzie A. Michell-Robinson, Kether Guerrero, Tobias B. Haack, Norberto Rodriguez-Espinosa, Geneviève Bernard, Ingrid Tejera-Martin, Kevin Petrecca, S. Leiz, Michael Saito, Fernando I. Monton, Savithri Nageswaran, Daniela Pohl, Annette Grefe, Luan T. Tran, Seth Cohen, Megan K. Dishop, Stefanie Perrier, Lama Darbelli, Myriam Srour
Publikováno v:
Neurology: Genetics
ObjectiveTo expand the phenotypic spectrum of severity of POLR3-related leukodystrophy and identify genotype-phenotype correlations through study of patients with extremely severe phenotypes.MethodsWe performed an international cross-sectional study
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::27d74b9a27980ea96f2be41d64d3fb34
https://doi.org/10.1212/nxg.0000000000000425
https://doi.org/10.1212/nxg.0000000000000425
Autor:
Saul A. Mullen, Steven Petrou, Mohamad A. Mikati, Vandana Shashi, Melanie J. Bonner, Yong-hui Jiang, Annette Grefe, Melody Li, Samuel F. Berkovic, Allyn McConkie, Ingrid E. Scheffer, Rebecca C. Spillmann, Slavé Petrovski, Michael P. Carboni, David Goldstein, Carol J. Milligan
Publikováno v:
Annals of Neurology. 78:995-999
We report 2 patients with drug-resistant epilepsy caused by KCNT1 mutations who were treated with quinidine. Both mutations manifested gain of function in vitro, showing increased current that was reduced by quinidine. One, who had epilepsy of infanc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::60230fe297825e82334b75202670968d
https://doi.org/10.1002/ana.24520
https://doi.org/10.1002/ana.24520
Autor:
Cormac A. O'Donovan, W. Vaughn McCall, Peter B. Rosenquist, Jane G. Boggs, Amy Harper, Hae W. Shin, William L. Bell, Annette Grefe
Publikováno v:
Seizure. 20(5):433-436
Status epilepticus is a life threatening condition with a high mortality rate in spite of aggressive treatment. There is little consensus on third and fourth line approaches in refractory cases. While electroconvulsive therapy (ECT) has been employed
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c54ef7941dd18d770bd8cd02526fb1e7
Autor:
Mohamad A, Mikati, Yong-Hui, Jiang, Michael, Carboni, Vandana, Shashi, Slave, Petrovski, Rebecca, Spillmann, Carol J, Milligan, Melody, Li, Annette, Grefe, Allyn, McConkie, Samuel, Berkovic, Ingrid, Scheffer, Saul, Mullen, Melanie, Bonner, Steven, Petrou, David, Goldstein
Publikováno v:
Annals of neurology. 78(6)
We report 2 patients with drug-resistant epilepsy caused by KCNT1 mutations who were treated with quinidine. Both mutations manifested gain of function in vitro, showing increased current that was reduced by quinidine. One, who had epilepsy of infanc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::448a7a4b4465cee2e986179e471c23ed
https://pubmed.ncbi.nlm.nih.gov/26369628
https://pubmed.ncbi.nlm.nih.gov/26369628
Publikováno v:
Neurology. 79(14)
A 15-year-old, right-handed Hispanic boy with B-cell acute lymphoblastic leukemia (ALL) was transferred for acute onset of stroke-like symptoms. Appoximately 6.5 hours prior to arrival, the patient was in his normal state of health. At that time, he
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c06cf3c66c733d0655452342f24f74f0
https://pubmed.ncbi.nlm.nih.gov/23033507
https://pubmed.ncbi.nlm.nih.gov/23033507
Publikováno v:
Journal of neuroscience methods. 79(1)
In the present study, a novel combination of techniques was used to identify the genes that may be involved in the lack of axonal regeneration in the mammalian adult central nervous system (CNS). The key features of this approach are: (1) a functiona
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::756d24dc242b6b8b84dd88a4b982a0a3
https://pubmed.ncbi.nlm.nih.gov/9531456
https://pubmed.ncbi.nlm.nih.gov/9531456