Zobrazeno 1 - 10 of 21 pro vyhledávání: '"Leonardo, Vedolin"'
1
Akademický článek
Depressive symptoms in Fabry disease: the importance of coping, subjective health perception and pain
Autor: Simon Körver, Gert J. Geurtsen, Carla E. M. Hollak, Ivo N. van Schaik, Maria G. F. Longo, Marjana R. Lima, Leonardo Vedolin, Marcel G. W. Dijkgraaf, Mirjam Langeveld
Publikováno v: Orphanet Journal of Rare Diseases, Vol 15, Iss 1, Pp 1-9 (2020)
Abstract Background Despite the high prevalence of depressive symptoms in Fabry disease (FD), it is unclear which patient characteristics are important in relation to these symptoms. Additionally, the impact of coping styles in relation to depressive
Externí odkaz: https://doaj.org/article/202c9fc1b485482fbb298d9457d1fcd5
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2
Akademický článek
Leigh Syndrome Due to mtDNA Pathogenic Variants
Autor: Cristina Pereira, Carolina Fischinger de Souza, Leonardo Vedolin, Filippo Vairo, Cláudia Lorea, Cláudia Sobreira, Célia Nogueira, Laura Vilarinho
Publikováno v: Journal of Inborn Errors of Metabolism and Screening, Vol 7 (2019)
Abstract Leigh syndrome is a devastating neurodegenerative disease, typically manifesting in infancy or early childhood. Hallmarks of the disease are symmetrical lesions in the basal ganglia or brain stem on MRI, and a clinical course with rapid dete
Externí odkaz: https://doaj.org/article/ce40c206914844c1962e64438f2b8b31
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3
Akademický článek
Acute cerebellitis caused by Herpes Simplex virus
Autor: Lillian Gonçalves Campos, Juliana Avila Duarte, Roberto Rossato, Rodrigo Pires dos Santos, Leonardo Vedolin
Publikováno v: Clinical and Biomedical Research, Vol 39, Iss 1 (2019)
Case presentation A 29 year-old woman presented to the emergency with gait imbalance and dysarthria. At admission, neurologic examination revealed normal cognition, ataxia, dysarthria, dysmetria on both sides of the body, bilateral vertical nystagmu
Externí odkaz: https://doaj.org/article/0a10bf01e6604636baf18da37b5a3aa6
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4
Determinants of cerebral radiological progression in Fabry disease
Autor: Carla E. M. Hollak, Marcel G. W. Dijkgraaf, Marjana R. Lima, Mirjam Langeveld, Ivo N. van Schaik, Maria Gabriela Figueiro Longo, Simon Körver, Leonardo Vedolin, Mohamed El Sayed
Publikováno v: Journal of Neurology, Neurosurgery and Psychiatry, 91(7), 756-763. BMJ Publishing Group
Background and aimIt is unclear which patients with Fabry disease (FD) are at risk for progression of white matter lesions (WMLs) and brain infarctions and whether enzyme replacement therapy (ERT) changes this risk. The aim of this study was to deter
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::861272e1616160cb1c7920176ff1cb15
https://doi.org/10.1136/jnnp-2019-322268
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7
Akademický článek
Intra-Arterial Infusion of Autologous Bone Marrow Mononuclear Cells in Patients with Moderate to Severe Middle Cerebral Artery Acute Ischemic Stroke
Autor: Maurício A. G. Friedrich M.D., Ph.D., Maurer P. Martins, Mariana D. Araújo, Charles Klamt, Leonardo Vedolin, Bernardo Garicochea, Eduardo F. Raupp, Jeber Sartori El Ammar, Denise Cantarelli Machado, Jaderson C. Da Costa, Raul G. Nogueira, Paulo Henrique Rosado-De-Castro, Rosalia Mendez-Otero M.D., Ph.D., Gabriel R. De Freitas
Publikováno v: Cell Transplantation, Vol 21 (2012)
Transplantation of autologous bone marrow mononuclear cells (BMMCs) has been proven safe in animal and human studies. However, there are very few studies in stroke patients. In this study, intra-arterial autologous BMMCs were infused in patients with
Externí odkaz: https://doaj.org/article/4bed5886801248348a38a30105193ba6
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8
Verificação da reprodutibilidade de um sistema quantitativo de avaliação da qualidade de exames de ultrassonografia diagnóstica
Autor: Leonardo Vedolin, Wagner Iared, Paulo Roberto Bettini, Andrea Puchnick, Maria Cristina Chammas, Eduardo Bancovsky
Publikováno v: Radiologia Brasileira
Radiologia Brasileira v.51 n.3 2018
Colégio Brasileiro de Radiologia e Diagnóstico por Imagem (CBR)
instacron:CBR
Radiologia Brasileira, Issue: ahead, Published: 14 MAY 2018
Radiologia Brasileira, Iss 0 (2018)
Objective: To present a quantitative system for assessing the quality of ultrasound examinations-SQUALUS-and to determine its reproducibility, taking into consideration the images on file, as well as the consistency between the images obtained and th
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6df2da005f875959ef67b94d12ff206b
https://doi.org/10.1590/0100-3984.2017.0021
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9
Akademický článek
Mal de Pott: Uma Doença Milenar em um Novo Século
Autor: Frederico Soares Falcetta, Angélica Dal Pizzol, Juliana Bohn Assmann, Andreia Della Giustina, Mateus Franzoi, Alvaro Ernani Georg, Alan Christmann Fröhlich, Apio Claúdio Martins Antunes, Leonardo Vedolin, Marino Muxfeldt Bianchin
Publikováno v: Clinical and Biomedical Research, Vol 29, Iss 2 (2009)
A tuberculose espinhal, também conhecida como Mal de Pott ou Doença de Pott, caracteriza-se como a forma mais frequente de tuberculose extrapulmonar. Apresentamos aqui o caso de uma paciente encaminhada ao Serviço de Neurologia do Hospital de Clí
Externí odkaz: https://doaj.org/article/2f1d528c35e44477992e78fea123c1ce
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10
Leigh Syndrome Due to mtDNA Pathogenic Variants
Autor: Carolina Fischinger Moura de Souza, Cláudia Lorea, Laura Vilarinho, Leonardo Vedolin, Cláudia Ferreira da Rosa Sobreira, Cristina Pereira, Célia Nogueira, Filippo Pinto e Vairo
Publikováno v: Journal of Inborn Errors of Metabolism and Screening v.7 2019
Journal of Inborn Errors of Metabolism and Screening
Instituto Genética para Todos (IGPT)
instacron:IGPT
Journal of Inborn Errors of Metabolism and Screening, Vol 7 (2019)
Journal of Inborn Errors of Metabolism and Screening, Volume: 7, Article number: e20180003, Published: 05 AUG 2019
Leigh syndrome is a devastating neurodegenerative disease, typically manifesting in infancy or early childhood. Hallmarks of the disease are symmetrical lesions in the basal ganglia or brain stem on MRI, and a clinical course with rapid deterioration
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f1ec22dc9e3502e2de1851c4958b2aac
https://doi.org/10.1590/2326-4594-jiems-2018-0003
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