المؤلفون: Stocchi, F., Espay, A., Albanese, A., Ellenbogen, A., Ferreira, J. J, Giladi, N., Gurevich, T., Hassin-Baer, S., Hernandez-Vara, J., Isaacson, S., Kieburtz, K., LeWitt, Peter A, Lopez-Manzanares, L., Olanow, C. W, Pahwa, R., Poewe, W., Sarva, H., Yardeni, T., Adar, L., Lopes, N., Sasson, N., Case, R., Rascol, O.

المصدر: Neurology Meeting Abstracts

Relation: https://scholarlycommons.henryford.com/neurology_mtgabstracts/176; https://sfxhosted.exlibrisgroup.com/hfhs?sid=EMBASE&issn=18735126&id=doi:10.1016%2Fj.parkreldis.2024.106149&atitle=Continuous+subcutaneous+levodopa%2Fcarbidopa+infusion+%28ND0612%29+for+patients+with+Parkinson%27s+disease+and+motor+fluctuations%3A+A+Phase+3,+active-controlled+study+%28BouNDless%29&stitle=Parkinsonism+Relat.+Disord.&title=Parkinsonism+and+Related+Disorders&volume=122&issue=&spage=&epage=&aulast=Stocchi&aufirst=F.&auinit=F.&aufull=Stocchi+F.&coden=&isbn=&pages=-&date=2024&auinit1=F&auinitm=

الاتاحة: https://scholarlycommons.henryford.com/neurology_mtgabstracts/176
https://sfxhosted.exlibrisgroup.com/hfhs?sid=EMBASE&issn=18735126&id=doi:10.1016%2Fj.parkreldis.2024.106149&atitle=Continuous+subcutaneous+levodopa%2Fcarbidopa+infusion+%28ND0612%29+for+patients+with+Parkinson%27s+disease+and+motor+fluctuations%3A+A+Phase+3,+active-controlled+study+%28BouNDless%29&stitle=Parkinsonism+Relat.+Disord.&title=Parkinsonism+and+Related+Disorders&volume=122&issue=&spage=&epage=&aulast=Stocchi&aufirst=F.&auinit=F.&aufull=Stocchi+F.&coden=&isbn=&pages=-&date=2024&auinit1=F&auinitm=

المؤلفون: Fasano, A., Henchcliffe, C., Sarva, H., Lozano, A., Kalia, S., Yu, K.K.H., Brennan, C., Stemple, W., Abid, N., Yountz, M., Enayetallah, A., Lampron, A., Tabar, V.

المصدر: Parkinsonism & Related Disorders ; volume 122, page 106129 ; ISSN 1353-8020

الاتاحة: http://dx.doi.org/10.1016/j.parkreldis.2024.106129
https://api.elsevier.com/content/article/PII:S135380202400141X?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S135380202400141X?httpAccept=text/plain

المؤلفون: Gatto E. M., Walker R. H., Gonzalez C., Cesarini M., Cossu G., Stephen C. D., Balint B., Rodriguez-Violante M., Jankovic J., Morgante F., Jinnah H. A., Albanese A., Amorin I., Bhatia K., Brandabur M., Canals F., Cardoso F., Cardozo A., Carvalho V., Chade A., Chana P., Darling A., Correia Guedes L., De la Cerda A., de Koning-Tijssen M., Della Coletta M. V., Duquette A., Espay A., Etcheverry J., Ferreira J., Friedman J., Fung V., Ganos C., Ruiz P. G., Gershanik O., Gross K. B. V., Han-Joon K., Kaji R., Kotschet K., Rosa A. L. D., Litvan I., Lubarr N., Marano M., Josep Marti M., Martinez Ramirez D., Miyasaki J., Munchau A., Chesta D. M., Pal P., Peralta M. C., Phielipp N., Maria Riboldi G., Oroz M. C. R., Rodriguez-Porcel F., Sarva H., Schoels L., Stamelou M., Uribe Roca C.

المساهمون: Gatto, E. M., Walker, R. H., Gonzalez, C., Cesarini, M., Cossu, G., Stephen, C. D., Balint, B., Rodriguez-Violante, M., Jankovic, J., Morgante, F., Jinnah, H. A., Albanese, A., Amorin, I., Bhatia, K., Brandabur, M., Canals, F., Cardoso, F., Cardozo, A., Carvalho, V., Chade, A., Chana, P., Darling, A., Correia Guedes, L., De la Cerda, A., de Koning-Tijssen, M., Della Coletta, M. V., Duquette, A., Espay, A., Etcheverry, J., Ferreira, J., Friedman, J., Fung, V., Ganos, C., Ruiz, P. G., Gershanik, O., Gross, K. B. V., Han-Joon, K., Kaji, R., Kotschet, K., Rosa, A. L. D., Litvan, I., Lubarr, N., Marano, M., Josep Marti, M., Martinez Ramirez, D., Miyasaki, J., Munchau, A., Chesta, D. M., Pal, P., Peralta, M. C., Phielipp, N., Maria Riboldi, G., Oroz, M. C. R., Rodriguez-Porcel, F., Sarva, H., Schoels, L., Stamelou, M., Uribe Roca, C.

مصطلحات موضوعية: chorea, dystonia, genetic and inherited disorder, genetic diagnosi, genetic testing, movement disorder, Parkinson's disease, whole exome sequencing, Asia, Europe, Human, Middle East, Movement Disorders

Relation: info:eu-repo/semantics/altIdentifier/pmid/33730413; info:eu-repo/semantics/altIdentifier/wos/WOS:000638078200001; volume:28; issue:6; firstpage:1901; lastpage:1909; numberofpages:9; journal:EUROPEAN JOURNAL OF NEUROLOGY; https://hdl.handle.net/11570/3207739; info:eu-repo/semantics/altIdentifier/scopus/2-s2.0-85104352984

الاتاحة: https://hdl.handle.net/11570/3207739
https://doi.org/10.1111/ene.14826

المؤلفون: Gatto, E. M., Walker, R. H., Gonzalez, C., Cesarini, M., Cossu, G., Stephen, C. D., Balint, B., Rodriguez-Violante, M., Jankovic, J., Morgante, F., Jinnah, H. A., Albanese, A., Amorin, I., Bhatia, K., Brandabur, M., Canals, F., Cardoso, F., Cardozo, A., Carvalho, V., Chade, A., Chana, P., Darling, A., Correia Guedes, L., De la Cerda, A., de Koning-Tijssen, M., Della Coletta, M. V., Duquette, A., Espay, A., Etcheverry, J., Ferreira, J., Friedman, J., Fung, V., Ganos, C., Ruiz, P. G., Gershanik, O., Gross, K. B. V., Han-Joon, K., Kaji, R., Kotschet, K., Rosa, A. L. D., Litvan, I., Lubarr, N., Marano, M., Josep Marti, M., Martinez Ramirez, D., Miyasaki, J., Munchau, A., Chesta, D. M., Pal, P., Peralta, M. C., Phielipp, N., Maria Riboldi, G., Oroz, M. C. R., Rodriguez-Porcel, F., Sarva, H., Schoels, L., Stamelou, M., Uribe Roca, C.

مصطلحات موضوعية: Asia, Movement disorders, Disease, Limited access, Middle East, 03 medical and health sciences, 0302 clinical medicine, medicine, Humans, Genetic Testing, 030212 general & internal medicine, Public funding, Genetic testing, Dystonia, Movement Disorders, medicine.diagnostic_test, business.industry, Chorea, medicine.disease, Europe, Neurology, Neurology (clinical), medicine.symptom, business, chorea, dystonia, genetic and inherited disorders, genetic diagnosis, genetic testing, movement disorders, Parkinson's disease, whole exome sequencing, 030217 neurology & neurosurgery, Demography

URL الوصول: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::23d0c9a614ddc13771d80d0285fec354
http://hdl.handle.net/11570/3207739

المؤلفون: Weaver, J., Sarva, H., Barone, D., Bobker, S., Bushara, K., Hiller, A., Ishii, M., Jankovic, J., Lakhani, S., Niotis, K., Scharre, D.W., Tuite, P., Stutz, A., Westhoff, C.M., Walker, R.H.

المصدر: Parkinsonism & Related Disorders ; volume 64, page 293-299 ; ISSN 1353-8020

الاتاحة: http://dx.doi.org/10.1016/j.parkreldis.2019.04.022
https://api.elsevier.com/content/article/PII:S1353802019302172?httpAccept=text/xml
https://api.elsevier.com/content/article/PII:S1353802019302172?httpAccept=text/plain

المؤلفون: Deuschl, G., Sarva, H., Jacoby, N.

المصدر: Reference Module in Neuroscience and Biobehavioral Psychology ; ISBN 9780128093245

الاتاحة: http://dx.doi.org/10.1016/b978-0-12-809324-5.00754-9
https://api.elsevier.com/content/article/PII:B9780128093245007549?httpAccept=text/plain
https://api.elsevier.com/content/article/PII:B9780128093245007549?httpAccept=text/xml

المؤلفون: Panichpisal, K., Omoregie, E., Rodriguez, A., Sarva, H., Law, S., Rojas-Soto, D., Dardis, C., Ramirez-Abreu, D., Nguyen, C., Sareen, A., Kotseva, M., Cherian, S., Moradiya, Y., Antezana, A., Bulic, S., Jadoo, C., Personna-Policard, J., Vulkanov, V., Emami, A., Arya, K., Jirasakuldej, S., Kozlova, O., McIntyre, S., Thomas, L., Rosenbaum, D., Levine, S., Baird, A.

المصدر: Neurology ; volume 78, issue Meeting Abstracts 1, page P07.050-P07.050 ; ISSN 0028-3878 1526-632X

الاتاحة: http://dx.doi.org/10.1212/wnl.78.1_meetingabstracts.p07.050
https://journals.lww.com/10.1212/WNL.78.1_MeetingAbstracts.P07.050

المؤلفون: Sarva, H¹, Graber, J², Remanan, R³, Rosenblum, M⁴, Omuro, A²

المصدر: Bone Marrow Transplantation. Feb2012, Vol. 47 Issue 2, p318-320. 3p. 1 Color Photograph, 1 Black and White Photograph.

مصطلحات موضوعية: *LETTERS to the editor, *CYTOMEGALOVIRUS diseases

المؤلفون: El-Sherif Y, Sarva H, Valsamis H

المصدر: Neurology; 1/10/2012, Vol. 78 Issue 2, pe4-7, 1p