المؤلفون: Milo, Ron¹ (AUTHOR), Korczyn, Amos D² (AUTHOR), Manouchehri, Navid³ (AUTHOR), Stüve, Olaf⁴ (AUTHOR)

المصدر: Multiple Sclerosis Journal. Jul2020, Vol. 26 Issue 8, p876-886. 11p. 1 Chart.

مصطلحات موضوعية: *MULTIPLE sclerosis, *NEURODEGENERATION, *CENTRAL nervous system, *PATHOLOGY, *INFLAMMATION, *MYELIN sheath diseases

المؤلفون: Ben Assayag, Einor¹, Korczyn, Amos D.², Giladi, Nir^1,2, Goldbourt, Uri², Berliner, A. Sholmo^1,2, Shenhar-Tsarfaty, Shani^1,2, Kliper, Efrat^1,2, Hallevi, Hen¹, Shopin, Ludmila¹, Hendler, Talma^1,3, Baashat, Dafna Ben¹, Aizenstein, Orna¹, Soreq, Hermona⁴, Katz, Noomi⁵, Solomon, Zahava⁶, Mike, Anat¹, Usher, Sali¹, Hausdorff, Jeff M.^1,2, Auriel, Eitan¹, Shapira, Itzhak^1,2

المصدر: International Journal of Stroke. Jun2012, Vol. 7 Issue 4, p341-347. 7p. 1 Chart.

مصطلحات موضوعية: *STROKE treatment, *RESEARCH protocols, *COGNITION disorders research, *COHORT analysis, *GENETIC markers, *BRAIN imaging

المؤلفون: Korczyn, Amos D.¹ amoskor@post.tau.ac.il

المصدر: Journal of the Neurological Sciences. Nov2011, Vol. 310 Issue 1/2, p2-3. 2p.

مصطلحات موضوعية: *PARKINSON'S disease, *NEURONS, *SUBSTANTIA nigra, *PARKINSONIAN disorders, *GENETIC mutation, *LEWY body dementia, *ETIOLOGY of diseases

المؤلفون: Benninger, Felix¹, Afawi, Zaid², Korczyn, Amos D.³, Oliver, Karen L.⁴, Pendziwiat, Manuela⁵, Nakamura, Masayuki⁶, Sano, Akira⁶, Helbig, Ingo^5,7, Berkovic, Samuel F.⁸, Blatt, Ilan⁹

المصدر: Epilepsia (Series 4). Apr2016, Vol. 57 Issue 4, p549-556. 8p.

مصطلحات موضوعية: *ERYTHROCYTE disorders, *CHOREA, *GENETIC mutation, *MAGNETIC resonance imaging, *ELECTROENCEPHALOGRAPHY, *GENETIC disorders, *SPASMS

المؤلفون: Afawi, Zaid¹ afawi@bgu.ac.il, Mandelstam, Simone² s.mandelstam@brain.org.au, Korczyn, Amos D.³ amoskor@post.tau.ac.il, Kivity, Sara⁴ sarakv@bezeqint.net, Walid, Simri⁵ waleeds@netvision.net.il, Shalata, Adel⁶ adel.shalata@gmail.com, Oliver, Karen L.⁷ oliverkl@unimelb.edu.au, Corbett, Mark⁸ mark.corbett@adelaide.edu.au, Gecz, Jozef^8,9 jozef.gecz@adelaide.edu.au, Berkovic, Samuel F.⁷ s.berkovic@unimelb.edu.au, Jackson, Graeme D.² gjackson@brain.org.au

المصدر: Epilepsy Research. Jul2013, Vol. 105 Issue 1/2, p240-244. 5p.

مصطلحات موضوعية: *GENETIC mutation, *EPILEPSY, *COGNITION disorders, *CEREBROCEREBELLAR system, *PHENOTYPES, *CEREBRAL atrophy

المؤلفون: Nitsan, Zeev^1,2 (AUTHOR) zeevn@bmc.gov.il, Cohen, Oren S.^3,4 (AUTHOR), Chapman, Joab^4,5 (AUTHOR), Kahana, Esther^1,2 (AUTHOR), Korczyn, Amos D.⁴ (AUTHOR), Appel, Shmuel^1,2 (AUTHOR), Osherov, Michael^1,2 (AUTHOR), Rosenmann, Hanna⁶ (AUTHOR), Milo, Ron^1,2 (AUTHOR)

المصدر: Journal of Neurology. Aug2020, Vol. 267 Issue 8, p2455-2458. 4p. 3 Charts.

مصطلحات موضوعية: *CREUTZFELDT-Jakob disease, *GENETIC disorders, *DISEASE progression, *AGE of onset, *BEHAVIOR, *FRONTAL lobe diseases

المؤلفون: Di Donato, Ilaria¹, Bianchi, Silvia¹, De Stefano, Nicola¹, Dichgans, Martin^2,3, Dotti, Maria Teresa¹, Duering, Marco², Jouvent, Eric^4,5,6, Korczyn, Amos D.⁷, Lesnik-Oberstein, Saskia A. J.⁸, Malandrini, Alessandro¹, Markus, Hugh S.⁹, Pantoni, Leonardo¹⁰, Penco, Silvana¹¹, Rufa, Alessandra¹, Sinanović, Osman¹², Stojanov, Dragan¹³, Federico, Antonio¹ federico@unisi.it

المصدر: BMC Medicine. 2/24/2017, Vol. 15, p1-12. 12p. 1 Black and White Photograph, 1 Diagram, 3 Charts, 1 Graph.

مصطلحات موضوعية: *CADASIL syndrome, *NEUROLOGICAL disorders, *BRAIN imaging, *MONOGENIC & polygenic inheritance (Genetics), *GENETIC disorders, *DIAGNOSIS, *CEREBRAL small vessel diseases, *DISEASE complications

المؤلفون: Grinton, Bronwyn E.¹, Heron, Sarah E.^2,3, Pelekanos, James T.^1,4,5, Zuberi, Sameer M.⁶, Kivity, Sara⁷, Afawi, Zaid⁸, Williams, Tristiana C.⁹, Casalaz, Dan M.¹⁰, Yendle, Simone¹, Linder, Ilan^11,12,13, Lev, Dorit^12,13,14, Lerman‐Sagie, Tally^11,12,13, Malone, Stephen¹⁵, Bassan, Haim¹⁶, Goldberg‐Stern, Hadassa⁷, Stanley, Thorsten¹⁷, Hayman, Michael^18,19, Calvert, Sophie¹⁵, Korczyn, Amos D.²⁰, Shevell, Michael²¹

المصدر: Epilepsia (Series 4). Jul2015, Vol. 56 Issue 7, p1071-1080. 10p.

مصطلحات موضوعية: *CHILDHOOD epilepsy, *NEONATAL diseases, *GENETIC mutation, *DEVELOPMENTAL delay, EPILEPSY research

المؤلفون: Reznik-Wolf, Haike, Treves, Therese A, Shabtai, Herzel, Aharon-Peretz, Judith, Chapman, Joab, Davidson, Michael, Barkai, Gad, St George Hyslop, Peter H, Goldman, Boleslaw, Korczyn, Amos D, Friedman, Eitan

المصدر: European Journal of Human Genetics. Mar1998, Vol. 6 Issue 2, p176. 5p.

مصطلحات موضوعية: *GENETIC mutation, *GENETICS of Alzheimer's disease, *FAMILIAL diseases, *GENETICS

مصطلحات جغرافية: ISRAEL

المؤلفون: Yahalom, Gilad¹, Kaplan, Natalie^1,2, Vituri, Aya³, Cohen, Oren S.^1,2, Inzelberg, Rivka^1,2, Kozlova, Evgenia¹, Korczyn, Amos D.⁴, Rosset, Saharon³, Friedman, Eitan^2,5, Hassin-Baer, Sharon^1,2 shassin@post.tau.ac.il

المصدر: Parkinsonism & Related Disorders. Nov2012, Vol. 18 Issue 9, p1039-1041. 3p.

مصطلحات موضوعية: *MOVEMENT disorders, *PARKINSON'S disease, *DARDARIN, *DOPA, *KAPLAN-Meier estimator, *PROPORTIONAL hazards models, *FOLLOW-up studies (Medicine)

مصطلحات جغرافية: ISRAEL