Tadeu A. Fantaneanu

ORCID: 0000-0003-4218-068X
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About
Contact & Profiles
Research Areas
  • Epilepsy research and treatment
  • EEG and Brain-Computer Interfaces
  • Pharmacological Effects and Toxicity Studies
  • Adolescent and Pediatric Healthcare
  • Neonatal and fetal brain pathology
  • Traumatic Brain Injury and Neurovascular Disturbances
  • Cardiac Arrest and Resuscitation
  • Cerebrospinal fluid and hydrocephalus
  • Childhood Cancer Survivors' Quality of Life
  • Peripheral Neuropathies and Disorders
  • Neurosurgical Procedures and Complications
  • Pregnancy and Medication Impact
  • Cerebrovascular and Carotid Artery Diseases
  • Metabolism and Genetic Disorders
  • Infectious Encephalopathies and Encephalitis
  • Empathy and Medical Education
  • Cellular transport and secretion
  • Infant Development and Preterm Care
  • Acute Ischemic Stroke Management
  • Autoimmune Neurological Disorders and Treatments
  • Intensive Care Unit Cognitive Disorders
  • Innovations in Medical Education
  • Occupational and Professional Licensing Regulation
  • Vagus Nerve Stimulation Research
  • Moyamoya disease diagnosis and treatment

Ottawa Hospital
2012-2025

University of Ottawa
2011-2025

Ottawa Hospital Research Institute
2019-2024

Deleted Institution
2023

Brigham and Women's Hospital
2015-2020

Massachusetts General Hospital
2016-2020

Boston Children's Hospital
2020

Harvard University
2016

In-Q-Tel
2016

Hôpital du Valais
2015

<h3>Importance</h3> Periodic and rhythmic electroencephalographic patterns have been associated with risk of seizures in critically ill patients. However, specific features that confer higher seizure remain unclear. <h3>Objective</h3> To analyze the association distinct characteristics periodic seizures. <h3>Design, Setting, Participants</h3> We reviewed recordings from 4772 adults 3 academic medical centers February 2013 to September 2015 performed a multivariate analysis determine...

10.1001/jamaneurol.2016.4990 article EN JAMA Neurology 2016-12-20

Machado–Joseph disease (MJD), the most common dominantly inherited ataxia worldwide, is caused by a polyglutamine (polyQ) expansion in deubiquitinating (DUB) enzyme ataxin-3. Interestingly, MJD can present clinically with features of Parkinsonism. In this study, we identify parkin, an E3 ubiquitin-ligase responsible for familial form Parkinson's disease, as novel ataxin-3 binding partner. The interaction between and parkin direct, involves multiple domains greatly enhanced...

10.1093/hmg/ddq452 article EN Human Molecular Genetics 2010-10-11

Objectives: We wanted to examine the extent which “neurophobia” exists among medical students and determine if students’ perceptions of neurology differ by year study while exploring factors that contribute development “neurophobia”. Methods: used a two-phase, sequential, mixed-methods explanatory design in this single centre study. Phase 1 involved collection analysis questionnaire administered first three years school. 2 focus groups subgroup who demonstrated evidence neurophobia 1....

10.1017/s0317167100018436 article EN Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 2014-07-01

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10.1017/cjn.2025.8 article EN Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques 2025-01-24

Abstract Objective Dravet syndrome (DS) is a severe developmental and epileptic encephalopathy caused by SCN1A haploinsufficiency in the majority of cases. Caregivers adults with DS often complain about loss previously acquired skills. We set out to explore these perceptions determine whether abnormalities reported were detectable validated tests. also investigated possible correlations between symptoms, age, exposure sodium channel blockers (SCBs). Methods This cross‐sectional, multicenter...

10.1111/epi.18329 article EN cc-by-nc-nd Epilepsia 2025-03-04

We present a novel epilepsy fellow–driven transfer clinic model and discuss the challenges experienced in finding sustainability; this is timely as many pioneering transition clinics are dissolving across North America. The goal of was to improve patient care satisfaction, measured by post-visit telephone survey. Unfortunately, our proved unsustainable due several factors, broadly categorized (1) cultural-societal differences between pediatric adult health environments, (2) staffing issues,...

10.1212/cpj.0000000000000727 article EN Neurology Clinical Practice 2020-01-06

This report discusses a case of nonconvulsive status epilepticus, caused by cerebral amyloid angiopathy-related inflammation. Brain biopsy demonstrated angiopathy, with clinical and radiographic features indicative fluctuating inflammatory process. Immunomodulatory treatment pulse steroids resulted in rapid dramatic improvement. Cerebral inflammation should be considered the differential diagnosis new-onset seizures after age 40, when associated multifocal T2 hyperintensities petechial...

10.1016/j.ebcr.2016.05.003 article EN cc-by-nc-nd Epilepsy & Behavior Case Reports 2016-01-01

Epilepsy is most common in lower-income settings where access to electroencephalography (EEG) generally poor. A low-cost tablet-based EEG device may be valuable, but the quality and reproducibility of output are not established.Tablet-based was deployed a heterogeneous epilepsy cohort Republic Guinea (2018-2019), consisting tablet wirelessly connected 14-electrode cap. Participants underwent twice (EEG1 EEG2), separated by variable time interval. Recordings were scored remotely experts...

10.1111/ene.14291 article EN European Journal of Neurology 2020-05-02

Tandem occlusions, characterized by the simultaneous presence of an intracranial large vessel occlusion and extracranial carotid artery stenosis or occlusion,1 pose a unique endovascular challenge.2 3 Typically, is result atherosclerotic plaque; however, dissections are also possible cause. It currently uncertain whether first approach should be employed.4 5 A new technique has been developed which allows for treatment both lesion.6 We describe variation this technique: stent retriever...

10.1136/jnis-2023-021011 article EN Journal of NeuroInterventional Surgery 2023-10-30

There are few data on adults living with tuberous sclerosis complex (TSC), most studies focusing pediatric populations. The objective of our study was to examine a large national cohort TSC, and describe the clinical characteristics these nature multidisciplinary care that they receive.Six Canadian medical centers collaborated in this study. Data were collected using standardized form, descriptive statistics used for analyses.Our included 181 definite TSC (mean age = 33.6 years [SD 13.7])....

10.1111/epi.17159 article EN Epilepsia 2021-12-29

This case report describes a 57-year-old man with hemochromatosis and panhypopituitarism who presented 6-month history of word-finding difficulty, short-term memory loss, rapidly cycling symptoms.

10.1001/jamaneurol.2016.1085 article EN JAMA Neurology 2016-07-11

Introduction In donation after circulatory determination of death, death is declared 5 min arrest. This practice assumes, but does not explicitly confirm, permanent loss brain activity. While this assumption rooted a strong physiological rationale, paucity direct human data regarding temporal relationship between cessation activity and arrest during the dying process threatens public healthcare provider trust in deceased organ donation. Methods analysis cohort study, we will prospectively...

10.1136/bmjopen-2023-073643 article EN cc-by-nc BMJ Open 2023-04-01
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