Zobrazeno 1 - 10
of 68
pro vyhledávání: '"Schteinschnaider A"'
Autor:
Bensi, C, Marrodan, M, González, A, Chertcoff, A, Osa Sanz, E, Chaves, H, Schteinschnaider, A, Correale, J, Farez, MF
Publikováno v:
In Multiple Sclerosis and Related Disorders October 2018 25:246-250
Autor:
Riva-Posse, Patricio, Busto-Marolt, Laura, Schteinschnaider, Ángeles, Martinez-Echenique, Lucia, Cammarota, Ángel, Merello, Marcelo
Publikováno v:
In Parkinsonism and Related Disorders 2008 14(5):415-419
Autor:
A. González, Anibal Chertcoff, A Schteinschnaider, Catalina Bensi, Mariano Marrodan, J. Correale, Mauricio F. Farez, Hernán Chaves, E Osa Sanz
Publikováno v:
Multiple Sclerosis and Related Disorders. 25:246-250
Objective Test the ability of a brain and spinal cord MRI criteria to differentiate neuromyelitis optica spectrum disorders and MOG-disease from MS. MRI criteria was further tested in patients with CIS and pediatric MS. Background MOG-disease and neu
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::988045b16dc6e55ee67e8e3bdb9f99ce
https://doi.org/10.1016/j.msard.2018.08.008
https://doi.org/10.1016/j.msard.2018.08.008
Autor:
Palmer, Elizabeth E., Hong, Seungbeom, Al Zahrani, Fatema, Hashem, Mais O., Aleisa, Fajr A., Ahmed, Heba M. Jalal, Kandula, Tejaswi, Macintosh, Rebecca, Minoche, Andre E., Puttick, Clare, Gayevskiy, Velimir, Drew, Alexander P., Cowley, Mark J., Dinger, Marcel, Rosenfeld, Jill A., Xiao, Rui, Cho, Megan T., Yakubu, Suliat F., Henderson, Lindsay B., Guillen Sacoto, Maria J., Begtrup, Amber, Hamad, Muddathir, Shinawi, Marwan, Andrews, Marisa V., Jones, Marilyn C., Lindstrom, Kristin, Bristol, Ruth E., Kayani, Saima, Snyder, Molly, Villanueva, María Mercedes, Schteinschnaider, Angeles, Faivre, Laurence, Thauvin, Christel, Vitobello, Antonio, Roscioli, Tony, Kirk, Edwin P., Bye, Ann, Merzaban, Jasmeen, Jaremko, Łukasz, Jaremko, Mariusz, Sachdev, Rani K., Alkuraya, Fowzan S., Arold, Stefan T.
Publikováno v:
In The American Journal of Human Genetics 7 March 2019 104(3):542-552
Autor:
Tejaswi Kandula, Maria J. Guillen Sacoto, Mais Hashem, Saima Kayani, André E. Minoche, Edwin P. Kirk, Łukasz Jaremko, Heba M. Jalal Ahmed, Marwan Shinawi, Elizabeth E. Palmer, Christel Thauvin, Molly Snyder, Mark J. Cowley, Muddathir H Hamad, Maria Mercedes Villanueva, Seungbeom Hong, Fatema Al Zahrani, Laurence Faivre, Suliat F. Yakubu, Ann M. E. Bye, Velimir Gayevskiy, Megan T. Cho, Jasmeen S. Merzaban, Marisa V. Andrews, Alexander P. Drew, Ruth E. Bristol, Jill A. Rosenfeld, Stefan T. Arold, Lindsay B. Henderson, Antonio Vitobello, Tony Roscioli, Clare Puttick, Mariusz Jaremko, Rui Xiao, Fajr A. Aleisa, Amber Begtrup, Marilyn C. Jones, Fowzan S. Alkuraya, Rebecca Macintosh, Marcel E. Dinger, Kristin Lindstrom, Rani Sachdev, Angeles Schteinschnaider
Publikováno v:
American journal of human genetics, vol 104, iss 3
Polyglutamine expansions in the transcriptional co-repressor Atrophin-1, encoded by ATN1, cause the neurodegenerative condition dentatorubral-pallidoluysian atrophy (DRPLA) via a proposed novel toxic gain of function. We present detailed phenotypic i
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::db127783b1fb1ce2a655ab86e5d0fed4
https://europepmc.org/articles/PMC6407605/
https://europepmc.org/articles/PMC6407605/
Autor:
A. Schteinschnaider, D. Dossi, L. Bembenuto, L. Aversa, S. Ameriso, C. Routaboul, H. Chavez, L. Biaggi, V. Fulco
Publikováno v:
Pediatric Critical Care Medicine. 22:47-47
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::adfcbab6092155c308d88a79d446c4e4
https://doi.org/10.1097/01.pcc.0000738432.44263.de
https://doi.org/10.1097/01.pcc.0000738432.44263.de
Publikováno v:
Pediatric Critical Care Medicine. 22:47-47
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5dc1d4ef64d8bcc8f740dabc46784dc4
https://doi.org/10.1097/01.pcc.0000738428.56100.07
https://doi.org/10.1097/01.pcc.0000738428.56100.07
Autor:
S. Jaimovich, G. Vazquez, A. Schteinschnaider, V. Aguerre, F. Dallesandro, S. Duhalde, C. Routaboul, M. Pinto, E. Cavassa
Publikováno v:
Neuromuscular Disorders. 28:S81
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::faa76d1f59830bfd6cd5725ead95e39f
https://doi.org/10.1016/j.nmd.2018.06.203
https://doi.org/10.1016/j.nmd.2018.06.203
Autor:
Ángeles Schteinschnaider, Laura Busto-Marolt, Lucia Martinez-Echenique, Patricio Riva-Posse, Marcelo Merello, Angel Cammarota
Publikováno v:
Parkinsonism & Related Disorders. 14:415-419
Background Stuttering is often accompanied by involuntary movements, abnormal gestures or changes in facial expression. Objective To describe the incidence and phenomenology of abnormal movements (AMs) in stuttering patients. Materials and methods Ei
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c6882375172a077e194c384ba8ca0175
https://doi.org/10.1016/j.parkreldis.2007.11.006
https://doi.org/10.1016/j.parkreldis.2007.11.006
Autor:
Angeles Schteinschnaider
Publikováno v:
European Journal of Paediatric Neurology. 21:7-8
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0a16f1fb0d4ecddd50039e9746f83808
https://doi.org/10.1016/j.ejpn.2016.11.007
https://doi.org/10.1016/j.ejpn.2016.11.007