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Sunita Venkateswaran

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Western University

Canada

Research Interests

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Professors in Canada

Recent Grants

Grant: Open

RareKids-CAN: Pediatric Rare Disease Clinical Trials and Treatment Network

Open Date: 2023-04-01

Close Date: 2028-03-31

Grant: Close

Development, Implementation and Dissemination of a Standardized Approach to the Care of Paediatric Multiple Sclerosis: A National Consensus Guideline of Management Strategies including Treatment of Acute Relapses, Immunomodulation and Escalation Therapy to Increase Patient Safety and Prevent Early-Onset Neurological Disability

Open Date: 2012-04-01

Close Date: 2013-03-31

Articles (16)

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2025

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Collaborators (6)

Alfonso Fasano

Humanitas University

ITALY

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Robert J. Klaassen

MD FRCPC

Children's Hospital of Eastern Ontario

CANADA

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Douglas Arnold

Distinguished James McGill Professor

McGill University

CANADA

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Ivan Ivanovski

Wissenschaftliche Mitarbeiter

University of Zurich

SWITZERLAND

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Patricia E. Longmuir

University of Ottawa

CANADA

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Amit Bar-Or

Professor

University of Pennsylvania

UNITED STATES

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ApplyKite TwinLearns as you apply

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Sunita Venkateswaran

Research Interests

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Recent Grants

Articles (16)

Early Onset Dystonia, Parkinsonism, and Spasticity in Siblings with VAC14‐Associated Neurodegeneration: A Case Report and Literature Review

Quick, Effective Screening Tasks Identify Children With Medical Conditions or Disabilities Needing Physical Literacy Support

Deep Brain Stimulation in a Child with Aicardi-Goutières Syndrome-7 (AGS7): A Case Report and Literature Review

Isolated leg weakness with painful spasms in an adolescent

POLR3-Related Leukodystrophy: A Qualitative Study on Parents’ Experiences With the Health Care System

Stress and Quality of Life of Parents of Children With POLR3-Related Leukodystrophy: A Cross-Sectional Pilot Study

Telemedicine in Pediatric Neurology: A Survey of Patient and Provider Experience

Choroid Plexus Volume in Pediatric-Onset Multiple Sclerosis

Congenital tremor and myopathy secondary to novel MYBPC1 variant

Head circumference values among Inuit children in Nunavut, Canada: a retrospective cohort study

IRF2BPL-Related Disorder, Causing Neurodevelopmental Disorder with Regression, Abnormal Movements, Loss of Speech and Seizures (NEDAMSS) Is Characterized by Pathology Consistent with DRPLA

The diagnostic workup of children with the radiologically isolated syndrome differs by age and by sex

Tone management: An environmental scan of current management practices across Canada

Deep phenotyping of the neuroimaging and skeletal features in KBG syndrome: A study of 53 patients and review of the literature

A Novel Homozygous Mutation Causing Complete TYK2 Deficiency, with Severe Respiratory Viral Infections, EBV-Driven Lymphoma, and Jamestown Canyon Viral Encephalitis

Generation of the human iPSC lines AKOSi011-A carrying the mutation p.Pro65Ser/p.Asp35T and AKOSi012-A, carrying the mutation p.Tyr231His, derived from FAHN patient fibroblasts

Collaborators (6)

Alfonso Fasano

Robert J. Klaassen

Douglas Arnold

Ivan Ivanovski

Patricia E. Longmuir

Amit Bar-Or

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