Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Alona Gad"'
Autor:
Nir Giladi, Achinoam Faust-Socher, Alona Gad, Meir Kestenbaum, Dina Shpunt, Yael Oestreicher-Kedem, Jennifer Zitser, Tanya Gurevich, Noit Inbar, Yael Manor, Stav Naor
Publikováno v:
CNS Spectrums. 24:413-418
BackgroundHuntington’s disease (HD) is a neurodegenerative disease characterized by increasing dysphagia as the disease progresses. Specific characteristics of the HD dysphagia are not well defined.ObjectiveTo characterize the swallowing disturbanc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a6e3d511d9aabbcb1421c44af8540478
https://doi.org/10.1017/s1092852918001037
https://doi.org/10.1017/s1092852918001037
Autor:
Nira Dangoor, Diana Paleacu, Ludmila Merkin, Avi Orr-Urtreger, Marieta Anca-Herschkovitch, Nir Giladi, Tanya Gurevich, Aya Bar David, Achinoam Faust-Socher, Meir Kestenbaum, Y. Balash, Jennifer Zitser, Tova Naiman, Yael Manor, Noit Inbar, Avner Thaler, Elissa L. Ash, Hertzel Shabtai, Alona Gad, Anat Bar-Shira, Chava Peretz
Publikováno v:
Neurodegenerative Diseases. 17:281-285
Background: Worldwide prevalence estimates of Huntington disease (HD) vary widely, with no reliable information regarding the Jewish population in Israel. Methods: This specialized tertiary single-center cross-sectional study assessed clinical, cogni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::51b605ca37eb51b813bc8b0ecc4c166a
https://doi.org/10.1159/000479375
https://doi.org/10.1159/000479375
Autor:
David Grabli, Wendy H. Raskind, Oriane Trouillard, Steven Parrish Winesett, Domitille Gras, Thomas D. Bird, Bertrand Degos, Marie Y. Davis, Nathalie Damon-Perrière, Emily Bonkowski, Cyril Mignot, Phillip D. Swanson, Laura M. Amendola, Alona Gad, Michael O. Dorschner, Aurélie Méneret, Jennifer Friedman, Christine Tranchant, Marie Vidailhet, Evan E. Eichler, Holly A.F. Stessman, Mathieu Anheim, Ali Torkamani, Saunder Bernes, Dong Hui Chen, Olena Korvatska, Fuki M. Hisama, Katherine M. Mackenzie, Diane Doummar, Michael D. Weiss, Emmanuel Roze
Publikováno v:
Neurology. 85:2026-2035
Objective: To investigate the clinical spectrum and distinguishing features of adenylate cyclase 5 ( ADCY5 )–related dyskinesia and genotype–phenotype relationship. Methods: We analyzed ADCY5 in patients with choreiform or dystonic movements by e
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4eeebf4be977a4747fa5344b284ef1ba
https://doi.org/10.1212/wnl.0000000000002058
https://doi.org/10.1212/wnl.0000000000002058
Autor:
Eldad Melamed, Israel Steiner, Ilan Ziv, Ruth Djaldetti, Alexander Khlebtovsky, Amihai Rigbi, Alona Gad
Publikováno v:
Journal of Neural Transmission. 119:1367-1371
Parkinson's disease (PD) exacts a physical and emotional toll on both patients and family. The aim of this study was to compare patient and caregiver perceptions of the social consequences of basic symptoms of PD and levodopa-induced dyskinesias. For
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2ad31698856e1d5d49641bb0934b820d
https://doi.org/10.1007/s00702-012-0796-9
https://doi.org/10.1007/s00702-012-0796-9
Publikováno v:
American Journal of Medical Genetics Part A. :1880-1885
The Waardenburg syndromes (WS) account for approximately 2% of congenital sensorineural deafness. This heterogeneous group of diseases currently can be categorized into four major subtypes (WS types 1-4) on the basis of characteristic clinical featur
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::390989f89e6a9acef74d520e3a7cebb3
https://doi.org/10.1002/ajmg.a.32402
https://doi.org/10.1002/ajmg.a.32402
Autor:
Tanya Gurevich, Yael Oestriecher-Kedem, Alona Gad, Adi Ezra, Yael Manor, Michal Avniel, Judith Knaani, Dina Shpunt, Daniel Assa, Ahinoam Socher, Yael Torner
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 87:A57.2-A58
Background Huntington’s disease (HD) is a genetic neurodegenerative disease clinically manifested by motor, cognitive and psychiatric disturbances. With disease progress patients experience increasing swallowing difficulty. Objective To characteris
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6732fb2ed984c97291e38f05e0860b94
https://doi.org/10.1136/jnnp-2016-314597.161
https://doi.org/10.1136/jnnp-2016-314597.161
Autor:
Netta Sendler, Ahinoam Socher, Angel A Migirov, Judith Knaani, Lee Frydman, Stav Naor, Alona Gad, Adi Ezra, Tanya Gurevich, Dina Shpunt, Yael Manor
Publikováno v:
Journal of Neurology, Neurosurgery & Psychiatry. 87:A54.1-A54
Background Huntington’s disease (HD) is a genetic neurodegenerative disorder characterised with motor, cognitive and psychiatric disturbances. As it progress patients experience reduced language and communication skills. Objective To characterise t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1119691bedcbf57621691d5fcfa635a0
https://doi.org/10.1136/jnnp-2016-314597.151
https://doi.org/10.1136/jnnp-2016-314597.151
Publikováno v:
Harefuah. 141(1)
Somatization disorder in children and adolescents is a common anxiety disorder. Errors and delays in diagnosis may incur unnecessary expensive and sometimes dangerous medical workup. We review the epidemiology, clinical features, treatment approaches
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::288669bb8d1c571bd38dc91708cddd42
https://pubmed.ncbi.nlm.nih.gov/11851105
https://pubmed.ncbi.nlm.nih.gov/11851105