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Leonardo Vedolin

Observed names: L Vedolin, L. M. Vedolin, L. Vedolin, Leonardo M. Vedolin, Leonardo Modesti Vedolin, Leonardo VEDOLIN, LeonardoM Vedolin, LeonardoModesti Vedolin, Vedolin, Leonardo, Vedolin, Leonardo Modesti
Observed institutions: Brigham and Women's Hospital, Universidade Federal do Rio Grande do Sul, Mayo Clinic, Universidade Federal Fluminense, University of California, San Francisco, Hospital Moinhos de Vento, Massachusetts General Hospital, Centre Hospitalier Universitaire Amiens-Picardie, Hospital de Clínicas de Porto Alegre, Fundação Universitária de Cardiologia, Hospital São Lucas da PUCRS, Hospital Mãe de Deus, DASA (Brazil), Pontifícia Universidade Católica do Rio Grande do Sul, Universidade Luterana do Brasil
ORCID: 0000-0001-6682-5070
Observed ORCIDs: 0000-0001-6682-5070, 0000-0002-1653-5582
OpenAlex ID: A5011179487
Intra-Arterial Infusion of Autologous Bone Marrow Mononuclear Cells in Patients with Moderate to Severe Middle Cerebral Artery Acute Ischemic Stroke
2012 · Maurício A. G. Friedrich, Maurer P. Martins, et al. · Cell Transplantation · 161
Intrathecal enzyme replacement therapy in a patient with mucopolysaccharidosis type I and symptomatic spinal cord compression
2008 · Maria‐Veronica Munoz‐Rojas, Taiane Vieira, et al. · American Journal of Medical Genetics Part A · 133
Validation of a Smartphone Application in the Evaluation and Treatment of Acute Stroke in a Comprehensive Stroke Center
2019 · Sheila C.O. Martins, Gustavo Weiss, et al. · Stroke · 81
CNS involvement in Fabry disease: Clinical and imaging studies before and after 12 months of enzyme replacement therapy
2004 · L. Jardim, L. Vedolin, et al. · Journal of Inherited Metabolic Disease · 78
Brain MRI in mucopolysaccharidosis
2007 · L. Vedolin, I.V.D. Schwartz, et al. · Neurology · 73
Neuroimaging of Dandy-Walker Malformation
2011 · Gustavo Gumz Correa, Lázaro Faria Amaral, et al. · Topics in Magnetic Resonance Imaging · 72
Guidelines for acute ischemic stroke treatment: part I
2012 · Jamary Oliveira-Filho, Sheila Cristina Ouriques Martins, et al. · Arquivos de Neuro-Psiquiatria · 71
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Correlation of MR Imaging and MR Spectroscopy Findings with Cognitive Impairment in Mucopolysaccharidosis II
2007 · L. Vedolin, I.V.D. Schwartz, et al. · American Journal of Neuroradiology · 70
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Neuroimaging Findings in Patients with Mucopolysaccharidosis: What You Really Need to Know
2016 · Roberta Reichert, Lillian Gonçalves Campos, et al. · Radiographics · 67
MR Imaging in Spinocerebellar Ataxias: A Systematic Review
2016 · A. Klaes, E. Reckziegel, et al. · American Journal of Neuroradiology · 57
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Hydrocephalus in Children
2016 · Lillian Gonçalves Campos, Rafael Menegatti, et al. · Springer eBooks · 52
Rhombencephalitis: pictorial essay
2016 · Líllian Gonçalves Campos, Régis Augusto Reis Trindade, et al. · Radiologia Brasileira · 46
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Body Mass Index is Inversely Correlated with the Expanded CAG Repeat Length in SCA3/MJD Patients
2011 · Jonas Alex Morales Saute, Andrew Chaves Feitosa da Silva, et al. · The Cerebellum · 46
Location of Periventricular Nodular Heterotopia Is Related to the Malformation Phenotype on MRI
2012 · G. González, L. Vedolin, et al. · American Journal of Neuroradiology · 45
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Serum insulin‐like system alterations in patients with spinocerebellar ataxia type 3
2010 · Jonas Alex Morales Saute, Andrew Chaves Feitosa da Silva, et al. · Movement Disorders · 41
White matter lesions in Fabry disease before and after enzyme replacement therapy: a 2-year follow-up
2006 · Laura B. Jardim, Flávio Aesse, et al. · Arquivos de Neuro-Psiquiatria · 40
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Surgical management of neurological manifestations of mucopolysaccharidosis disorders
2017 · Tord D. Alden, Hernán Amartino, et al. · Molecular Genetics and Metabolism · 39
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Methylphenidate Alters Functional Connectivity of Default Mode Network in Drug-Naive Male Adults With ADHD
2018 · Felipe Almeida Picon, João Ricardo Sato, et al. · Journal of Attention Disorders · 34
Depressive symptoms in Fabry disease: the importance of coping, subjective health perception and pain
2020 · Simon Körver, Gert J. Geurtsen, et al. · Orphanet Journal of Rare Diseases · 32
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Inherited Cerebellar Ataxia in Childhood: A Pattern-Recognition Approach Using Brain MRI
2012 · L. Vedolin, G. Gonzalez, et al. · American Journal of Neuroradiology · 32
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Huntington disease‐like 2: the first patient with apparent European ancestry
2008 · C Santos, H Wanderley, et al. · Clinical Genetics · 29
Identification of a premature stop codon mutation in the PHGDH gene in severe Neu‐Laxova syndrome—evidence for phenotypic variability
2015 · Eduardo P. Mattos, André Anjos da Silva, et al. · American Journal of Medical Genetics Part A · 27
Brain magnetic resonance imaging findings in patients with mucopolysaccharidosis VI
2012 · Ana C. M. Azevedo, Osvaldo Artigalás, et al. · Journal of Inherited Metabolic Disease · 27
Magnetic resonance imaging findings in Hunter syndrome
2008 · Chelsea T Finn, Leonardo Vedolin, et al. · Acta Paediatrica · 26
X-linked adrenoleukodystrophy: Clinical course and minimal incidence in South Brazil
2009 · Laura Bannach Jardim, Andrew Chaves Feitosa da Silva, et al. · Brain and Development · 24
Works count: 112
Citation count: 1,774
H-index: 24
I10-index: 42
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