Zobrazeno 1 - 10
of 17
pro vyhledávání: '"Helio A G Teive"'
Autor:
Vera Hashem, Anjana Tiwari, Brittani Bewick, Helio A G Teive, Mariana Moscovich, Birgitt Schüle, Khalaf Bushara, Matt Bower, Astrid Rasmussen, Yu-Chih Tsai, Tyson Clark, Karen McFarland, Tetsuo Ashizawa
Publikováno v:
PLoS ONE, Vol 15, Iss 4, p e0231746 (2020)
[This corrects the article DOI: 10.1371/journal.pone.0228789.].
Externí odkaz:
https://doaj.org/article/45e3af1af38b491598951674d9b00d16
Autor:
Vera Hashem, Anjana Tiwari, Brittani Bewick, Helio A G Teive, Mariana Moscovich, Birgitt Schüele, Khalaf Bushara, Matt Bower, Astrid Rasmussen, Yu-Chih Tsai, Tyson Clark, Karen McFarland, Tetsuo Ashizawa
Publikováno v:
PLoS ONE, Vol 15, Iss 3, p e0228789 (2020)
Large expansions of microsatellite DNA cause several neurological diseases. In Spinocerebellar ataxia type 10 (SCA10), the repeat interruptions change disease phenotype; an (ATTCC)n or a (ATCCT)n/(ATCCC)n interruption within the (ATTCT)n repeat is as
Externí odkaz:
https://doaj.org/article/abdc59366c454ec1a5adca9aba5d9623
Autor:
Inga Koneczny, Stefan Macher, Markus Hutterer, Thomas Seifert-Held, Evelyn Berger-Sieczkowski, Morten Blaabjerg, Markus Breu, Jens Dreyhaupt, Livia Almeida Dutra, Marcus Erdler, Ingrid Fae, Gottfried Fischer, Florian Frommlet, Anna Heidbreder, Birgit Högl, Veronika Klose, Sigrid Klotz, Herburg Liendl, Mette S. Nissen, Jasmin Rahimi, Raphael Reinecke, Gerda Ricken, Ambra Stefani, Marie Süße, Helio A. G. Teive, Serge Weis, Thomas Berger, Lidia Sabater, Carles Gaig, Jan Lewerenz, Romana Höftberger
Publikováno v:
Frontiers in Immunology, Vol 15 (2024)
BackgroundAnti-IgLON5 disease is a rare chronic autoimmune disorder characterized by IgLON5 autoantibodies predominantly of the IgG4 subclass. Distinct pathogenic effects were described for anti-IgLON5 IgG1 and IgG4, however, with uncertain clinical
Externí odkaz:
https://doaj.org/article/4973fe045006435cbdd85643ef22108a
Autor:
Francisco Manoel B, Germiniani, Mauricio, Roriz, Samir K, Nabhan, Helio A G, Teive, Lineu C, Werneck
Publikováno v:
Arquivos de neuro-psiquiatria. 60(4)
Central pontine myelinolysis (CPM) and extra-pontine myelinolysis (EPM) are different presentations of a demyelinating disorder of the brain more commonly associated with rapid correction of hyponatremia, spastic tetraparesia and pseudo-bulbar palsy.
Autor:
Helio A. G. Teive, Daniel S. Sa
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 59, Iss 1, Pp 123-124 (2001)
We describe a female patient with stable Parkinson's disease who has shown a marked worsening of her motor functions following therapy of menopause related symptoms with veralipride, as well as the improvement of her symptoms back to baseline after d
Autor:
Khalaf Bushara, Matthew Bower, Jilin Liu, Karen N McFarland, Ivette Landrian, Diane Hutter, Hélio A G Teive, Astrid Rasmussen, Connie J Mulligan, Tetsuo Ashizawa
Publikováno v:
PLoS ONE, Vol 8, Iss 11, p e81342 (2013)
Spinocerebellar ataxia type 10 (SCA10), an autosomal dominant cerebellar ataxia, is caused by the expansion of the non-coding ATTCT pentanucleotide repeat in the ATAXIN 10 gene. To date, all cases of SCA10 are restricted to patients with ancestral ti
Externí odkaz:
https://doaj.org/article/800c1b9d3bd847f1833bf28af624acc4
Autor:
Misti C White, Rui Gao, Weidong Xu, Santi M Mandal, Jung G Lim, Tapas K Hazra, Maki Wakamiya, Sharon F Edwards, Salmo Raskin, Hélio A G Teive, Huda Y Zoghbi, Partha S Sarkar, Tetsuo Ashizawa
Publikováno v:
PLoS Genetics, Vol 6, Iss 6, p e1000984 (2010)
We have identified a large expansion of an ATTCT repeat within intron 9 of ATXN10 on chromosome 22q13.31 as the genetic mutation of spinocerebellar ataxia type 10 (SCA10). Our subsequent studies indicated that neither a gain nor a loss of function of
Externí odkaz:
https://doaj.org/article/47d7208ba53542e4ac4ad4250a896680
Publikováno v:
Acta Médica Portuguesa, Vol 20, Iss 4 (2007)
Regarded as one of the best Brazilian writers, Machado de Assis was diagnosed with epilepsy since childhood. In his vast work, some of the main pieces are rich in describing neuropsychiatric disorders, including epilepsy, depression, dementia (most l
Externí odkaz:
https://doaj.org/article/7dff918cf84248db96c3d30456d2ed4c
Autor:
Stephanie Efthymiou, Luiz E. Novis, Georgios Koutsis, Chrysoula Koniari, Reza Maroofian, Valentina Turchetti, Georgios Velonakis, Luiz F. Vasconcellos, Salmo Raskin, Varunvenkat M. Srinivasan, Alistair T. Pagnamenta, Yaramanchanahalli B. Arun, Uddhava V. Kinhal, Vykuntaraju K. Gowda, Helio A. G. Teive, Henry Houlden
Publikováno v:
Annals of Clinical and Translational Neurology, Vol 10, Iss 10, Pp 1910-1916 (2023)
Abstract Bi‐allelic variants in peroxiredoxin 3 (PRDX3) have only recently been associated with autosomal recessive spinocerebellar ataxia characterized by early onset slowly progressive cerebellar ataxia, variably associated with hyperkinetic and
Externí odkaz:
https://doaj.org/article/a871963bb6444806854fed86a9acdb13
Autor:
Renato P Munhoz, Hélio A G Teive
Publikováno v:
Arquivos de Neuro-Psiquiatria, Vol 71, Iss 2, Pp 133-133 (2013)
Externí odkaz:
https://doaj.org/article/dcbba7828f5c44b7a7abdda2dd8cc3b0