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1دورية أكاديمية
المؤلفون: Zorian Radomyslsky, Sara Kivity, Yaniv Alon, Mor Saban
المصدر: BMC Geriatrics, Vol 24, Iss 1, Pp 1-11 (2024)
مصطلحات موضوعية: Cognitive impairment, Older adults, COVID-19 vaccination, Mortality, Predictive analytics, Geriatrics, RC952-954.6
وصف الملف: electronic resource
Relation: https://doaj.org/toc/1471-2318
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2دورية أكاديمية
المؤلفون: Limor Adler, Mor Saban, Ilan Yehoshua, Miri Mizrahi Reuveni, Zorian Radomyslsky, Eduardo Schejter, Yakov Segal, Sara Kivity, Etti Naimi
المصدر: Family Medicine and Community Health, Vol 12, Iss 2 (2024)
مصطلحات موضوعية: Medicine (General), R5-920
وصف الملف: electronic resource
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3دورية أكاديمية
المؤلفون: Zorian Radomyslsky, Sara Kivity, Shira Lidar, Netta Bentur, Liat Korn, Rachel Nissanholtz-Gannot, Shelley Sternberg, Inbal Halevi Hochwald, Orna Reges, Yaniv Alon, Mor Saban
المصدر: Frontiers in Public Health, Vol 11 (2023)
مصطلحات موضوعية: dementia, COVID-19, mild cognitive impairment, vaccination, psychiatric disorder diagnosis, Public aspects of medicine, RA1-1270
وصف الملف: electronic resource
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4دورية أكاديمية
المؤلفون: Sara Kivity, Sivia Barnoy
المصدر: SAGE Open, Vol 13 (2023)
مصطلحات موضوعية: History of scholarship and learning. The humanities, AZ20-999, Social Sciences
وصف الملف: electronic resource
Relation: https://doaj.org/toc/2158-2440
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المؤلفون: Orrin Devinsky, Samuel F. Berkovic, Catharine Freyer, Annapurna Poduri, Eric B. Geller, Amos D. Korczyn, Heidi E. Kirsch, Nathan B. Fountain, Rosemary Burgess, Jack M. Parent, Jocelyn F. Bautista, Susannah T. Bellows, Robert C. Knowlton, David Goldstein, Dennis J. Dlugos, Heather C Mefford, Anthony G Marson, Mike Smith, Sabrina Cristofaro, Erin L. Heinzen, Bassel Abou-Khalil, Michael P. Epstein, Douglas E. Crompton, Eileen P.G. Vining, Kevin McKenna, Steven Petrou, Anu Venkat, Eric H. Kossoff, Gretchen Von Allmen, Sheryl R. Haut, Ruben Kuzniecky, Juliann M. Paolicchi, Colin A Ellis, Rani K. Singh, Simon Glynn, Daniel H. Lowenstein, Liu Lin Thio, Lynette G. Sadleir, Rebecca Loeb, Norman Delanty, Terence J. O'Brien, Paul V. Motika, Peter Widdess-Walsh, Sara Kivity, Gregory D. Cascino, Slavé Petrovski, Ruth Ottman, Micheline Gravel, Andrew S. Allen, Jerry J. Shih, Ingrid E. Scheffer, Joseph I Sirven, William O. Pickrell, Tracy A. Glauser, Judith L.Z. Weisenberg, Judith Bluvstein, Zaid Afawi, Phil Smith, Kevin F. Haas, Mark McCormack, Hadassa Goldberg-Stern, Sarah Paterson, Melodie R. Winawer, Mark I. Rees, Saul A. Mullen, Patrick Cossette, Rhys H. Thomas
المصدر: Epilepsia
مصطلحات موضوعية: Male, 0301 basic medicine, Concordance, Electroencephalography, Article, 03 medical and health sciences, Epilepsy, 0302 clinical medicine, medicine, Humans, Medical history, Generalized epilepsy, medicine.diagnostic_test, Seizure types, business.industry, Family aggregation, medicine.disease, Latent class model, Pedigree, Phenotype, 030104 developmental biology, Neurology, Latent Class Analysis, Female, Neurology (clinical), business, Epileptic Syndromes, 030217 neurology & neurosurgery, Clinical psychology
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المؤلفون: Sara Kivity, Sivia Barnoy
مصطلحات موضوعية: medicine.medical_specialty, Fetus, business.industry, Obstetrics, Abort, embryonic structures, Medicine, Disease, business, reproductive and urinary physiology
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_________::6fa553951e5fad524d7d24897902a356
https://doi.org/10.21203/rs.3.rs-136856/v1 -
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المؤلفون: Ayelet Halevy, Rony Cohen, Rachel Straussberg, Sara Kivity, Sharon Aharoni, Liora Kornreich, Hadassah Goldberg-Stern
المصدر: Neuropediatrics. 51(6)
مصطلحات موضوعية: 0301 basic medicine, Pediatrics, medicine.medical_specialty, Epileptologist, Movement disorders, Adolescent, Pontocerebellar hypoplasia, 030105 genetics & heredity, Electroencephalography, 03 medical and health sciences, Epilepsy, 0302 clinical medicine, Medicine, Humans, Spasticity, Child, Progressive microcephaly, medicine.diagnostic_test, business.industry, Brain, Magnetic resonance imaging, General Medicine, medicine.disease, Pediatrics, Perinatology and Child Health, Disease Progression, Olivopontocerebellar Atrophies, Female, Neurology (clinical), medicine.symptom, business, 030217 neurology & neurosurgery
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f21b922226453621fb86970f407462d3
https://pubmed.ncbi.nlm.nih.gov/32629522 -
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المؤلفون: Leanne M. Dibbens, Anna-Elina Lehesjoki, Roberto Michelucci, Aarno Palotie, Barbara Castellotti, Jillian M. Cameron, Amos D. Korczyn, Loretta Giuliano, Davide Uccellini, Alessandro Filla, Edith Said, Karen Oliver, Zaid Afawi, William C. Sessa, Hui Bein Chew, Silvana Franceschetti, Carlo Di Bonaventura, Eva Andermann, Anna Teresa Giallonardo, Angelo Labate, Samuel F. Berkovic, Betül Baykan, Kariona A. Grabińska, Carolina Courage, Patrizia Riguzzi, Melanie Bahlo, Antonio Gambardella, John A. Damiano, Laura Canafoglia, Tarja Joensuu, Pasquale Striano, Christopher B. Jackson, Mikko Muona, Christian Brandt, Chiara Criscuolo, Sara Kivity, Eon Joo Park, Ingrid E. Scheffer, Géza Berecki
المساهمون: HUSLAB, Medicum, Department of Medical and Clinical Genetics, University of Helsinki, Clinicum, Research Programs Unit, STEMM - Stem Cells and Metabolism Research Program, Faculty of Medicine, Centre of Excellence in Complex Disease Genetics, Aarno Palotie / Principal Investigator, Institute for Molecular Medicine Finland, Genomics of Neurological and Neuropsychiatric Disorders, Helsinki Institute of Life Science HiLIFE, Courage, Carolina, Oliver, Karen L, Park, Eon Joo, Cameron, Jillian M, Dibbens, Leanne M, Lehesjoki, Anna Elina
المصدر: Am J Hum Genet
مصطلحات موضوعية: 0301 basic medicine, Male, Glycosylation, medicine.disease_cause, Whole Exome Sequencing, Cohort Studies, 0302 clinical medicine, Dolichols, whole-exome sequencing, Age of Onset, Child, Genetics (clinical), Exome sequencing, Genetics, Mutation, 1184 Genetics, developmental biology, physiology, dolichol-dependent glycosylation, Middle Aged, 3. Good health, Child, Preschool, ASAH1, Female, medicine.symptom, Adult, Adolescent, DNA Copy Number Variations, Progressive myoclonus epilepsy, Biology, progressive myoclonus epilepsy, Article, 03 medical and health sciences, Young Adult, Progressive, Myoclonic Epilepsies, Exome Sequencing, medicine, Humans, epilepsy genetics, Preschool, Gene, Genetic heterogeneity, Intron, Introns, Myoclonic Epilepsies, Progressive, medicine.disease, 030104 developmental biology, 3111 Biomedicine, Myoclonus, 030217 neurology & neurosurgery
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1f932a416de210b04bfdbaee703d7f1d
https://pubmed.ncbi.nlm.nih.gov/33798445 -
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المؤلفون: Samuel F. Berkovic, Andrew Bleasel, Hadassa Goldberg-Stern, Bronwyn E. Grinton, Sara Kivity, Leanne M. Dibbens, Elizabeth K. Ruzzo, John A. Damiano, Lata Vadlamudi, Zaid Afawi, Georgie C. Glubb, Jodie P. Malone, Rosemary Burgess, Padraic Grattan-Smith, Yue-Hua Zhang, Danya F. Vears, Katherine L. Helbig, Amos D. Korczyn, Ingrid E. Scheffer, Susannah T. Bellows, Michael S. Hildebrand
المصدر: Neurology. 89:1210-1219
مصطلحات موضوعية: Adult, Male, 0301 basic medicine, Adolescent, Seizures, Febrile, Genetic epilepsy, Young Adult, 03 medical and health sciences, Epilepsy, 0302 clinical medicine, Childhood absence epilepsy, medicine, Humans, Age of Onset, Focal Epilepsies, Generalized epilepsy, Child, business.industry, Infant, Genetic data, Middle Aged, medicine.disease, Pedigree, Phenotype, 030104 developmental biology, Child, Preschool, Immunology, Epilepsy, Generalized, Female, Epilepsies, Partial, Neurology (clinical), Age of onset, business, Generalized epilepsy with febrile seizures plus, 030217 neurology & neurosurgery
URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::18390db2eb361bf30fba2f9cd97e9d43
https://doi.org/10.1212/wnl.0000000000004384 -
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المؤلفون: Rosemary Burgess, John A. Damiano, Zaid Afawi, Ingrid E. Scheffer, Tally Lerman-Sagie, Samuel F. Berkovic, Michael S. Hildebrand, Sara Kivity
المصدر: Epilepsia. 58:e40-e43
مصطلحات موضوعية: Male, 0301 basic medicine, Proband, Genetic counseling, DNA Mutational Analysis, Nonsense mutation, Biology, Cohort Studies, 03 medical and health sciences, Epilepsy, 0302 clinical medicine, Aphasia, medicine, Humans, Adaptor Proteins, Signal Transducing, Family Health, Genetics, Point mutation, Infant, Electroencephalography, medicine.disease, Phenotype, 030104 developmental biology, Neurology, Mutation, Mutation (genetic algorithm), Speech delay, Female, CNKSR2, Neurology (clinical), medicine.symptom, Sleep, Spasms, Infantile, 030217 neurology & neurosurgery