Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Heidi Kirsch"'
Publikováno v:
BMC Neurology, Vol 21, Iss 1, Pp 1-7 (2021)
Abstract Background Epileptic seizures can be difficult to distinguish from other etiologies that cause cerebral hypoxia, especially cardiac diseases. Long QT syndrome (LQTS), especially LQTS type 2 (LQT2), frequently masquerades as seizures because
Externí odkaz:
https://doaj.org/article/5c15e0e472ee4f19a3aca9c2da66cad0
Autor:
Ann Poncelet, Seth Bokser, Brook Calton, Karen E. Hauer, Heidi Kirsch, Tracey Jones, Cindy J. Lai, Lindsay Mazotti, William Shore, Arianne Teherani, Lowell Tong, Maria Wamsley, Patricia Robertson
Publikováno v:
Medical Education Online, Vol 16, Iss 0, Pp 1-10 (2011)
In 2005, medical educators at the University of California, San Francisco (UCSF), began developing the Parnassus Integrated Student Clinical Experiences (PISCES) program, a year-long longitudinal integrated clerkship at its academic medical center. T
Externí odkaz:
https://doaj.org/article/6764fa56cf34450b90389ca26d7a9215
Publikováno v:
Journal of Alzheimer's Disease. 92:13-27
Cortical network hyperexcitability related to synaptic dysfunction in Alzheimer’s disease (AD) is a potential target for therapeutic intervention. In recent years, there has been increased interest in the prevalence of silent seizures and intericta
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ca2853255f1b1b6cb7083a2588e39e52
https://doi.org/10.3233/jad-220983
https://doi.org/10.3233/jad-220983
Autor:
Drew Cheng, Michael Zhu Chen, August Yue Huang, Junseok Park, Heidi Kirsch, Christopher Walsh, Diane Shao
Publikováno v:
Sunday, April 23.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4f108d7119750a22d72ce3677080b182
https://doi.org/10.1212/wnl.0000000000202083
https://doi.org/10.1212/wnl.0000000000202083
Autor:
Andreas Schulze-Bonhage, Patrick May, Samuel Berkovic, Lorenzo Ferri, Monica Gagliardi, Adam Strzelczyk, Oluyomi Modupe Adesoji, Vytautas Kasiulevicius, Heidi Kirsch, Algirdas Utkus, Bobby Koeleman, Gianpiero Cavalleri
Epilepsy is a highly heritable disorder affecting over 50 million people worldwide, of which about one-third are resistant to current treatments. Here, we report a trans-ethnic GWAS including 29,944 cases, stratified into three broad- and seven sub-t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8987c7a3b8658557c398255d13bf3cd6
https://doi.org/10.1101/2022.06.08.22276120
https://doi.org/10.1101/2022.06.08.22276120
Autor:
Ingrid Scheffer, Samuel Berkovic, Lynette Sadleir, Anthony Marson, Andrew Allen, Terence O'Brien, Heidi Kirsch, Kristen Park
Publikováno v:
Epilepsia. 62:973-983
Objective We sought to identify novel genes and to establish the contribution of known genes in a large cohort of patients with nonsyndromic sporadic polymicrogyria and epilepsy. Methods We enrolled participants with polymicrogyria and their parents
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::604d75eef70401bdd2ccfb65d252b12c
https://doi.org/10.1111/epi.16854
https://doi.org/10.1111/epi.16854
Publikováno v:
Journal of Clinical Oncology. 40:11028-11028
11028 Background: Cognitive integration (CI) connects foundational science (FS) to medical practice and improves clinical reasoning. While evidence supports CI in medical training, the clinical relevance of FS is often obscure to medical students, pa
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0d7de506e0221cf63b57422d0bfe0b61
https://doi.org/10.1200/jco.2022.40.16_suppl.11028
https://doi.org/10.1200/jco.2022.40.16_suppl.11028
Autor:
Cun Li, Hongbin Cai, Xu Zhao, Xincong Xi, Qing Zhou, Huiya Luo, Zhouping Tang, Kang Huicong, Heidi Kirsch
Background Anti-leucine-rich glioma-inactivated 1 (LGI1) encephalitis is clinically heterogeneous, especially at presentation, and though it is sometimes found in association with tumor, this is by no means the rule. Methods Clinical data for 10 peop
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::28092ef6c8daab03c48e1ac896f023e6
https://doi.org/10.22541/au.161538659.91902892/v1
https://doi.org/10.22541/au.161538659.91902892/v1
Autor:
Graham Neil Thomas, Remi Stevelink, Ingrid Scheffer, Andreja Avbersek, Thomas Ferraro, Costin Leu, Krishna Chinthapalli, Claudia B. Catarino, Peter Widdess-Walsh, Colin Doherty, Anthony Marson, Michele Iacomino, Martin Krenn, Aarno Palotie, Heidi Kirsch, Stefan Wolking, Gianpiero Cavalleri
Publikováno v:
MOLECULAR GENETICS AND METABOLISM REPORTS
Molecular Genetics and Metabolism Reports, 21. Elsevier BV
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports, Vol 21, Iss, Pp-(2019)
Molecular Genetics and Metabolism Reports, 21. Elsevier BV
Molecular Genetics and Metabolism Reports
Molecular Genetics and Metabolism Reports, Vol 21, Iss, Pp-(2019)
Altered vitamin B6 metabolism due to pathogenic variants in the gene PNPO causes early onset epileptic encephalopathy, which can be treated with high doses of vitamin B6. We recently reported that single nucleotide polymorphisms (SNPs) that influence
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd7c8c2629b12267d6450abecf614381
http://livrepository.liverpool.ac.uk/3061803/1/1-s2.0-S2214426919301570-main.pdf
http://livrepository.liverpool.ac.uk/3061803/1/1-s2.0-S2214426919301570-main.pdf