Faculty profile

Ingrid Tein

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ProfessorDepartment of PaediatricsUniversity of Toronto

Ingrid Tein

Professor

Department of Paediatrics

Temerty Faculty of Medicine

University of Toronto

Toronto, Ontario, Canada

Supervision signals

Professors usually supervise graduate students in their department's programs.
4 publications in the last five years, latest in 2025.
Senior (last) author on 2 recent papers, a sign of leading a research group.
Principal investigator on 1 research grant (1 CIHR), most recently in 2009.

These signals come from public records, including federal and provincial funding decisions. Ask the professor or the graduate program whether they are taking new students.

Academic metrics

Publications

364

Citations

Collaborators

Grants

Publications by year

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Profiles and links

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Signals and details

Research

Read how they describe their research on their University of Toronto profile.

Latest papers

Levodopa-Responsive Dystonia Secondary to CTNNB1 Neurodevelopmental Disorder.
Movement disorders clinical practice · 2025
Recent advances in neurometabolic diseases: The genetic role in the modern era.
Epilepsy & behavior : E&B · 2023 · first author
Reversal of Stroke-Like Episodes With L-Arginine and Meticulous Perioperative Management of Renal Transplantation in a Patient With Mitochondrial Encephalomyopathy, Lactic Acidosis and Stroke-Like Episodes (MELAS) Syndrome. Case Report.
The Neurohospitalist · 2022 · senior author

All 29 publications

Latest funding

MITO2019 | The Power of Mitochondria to Transform Human Health
CIHR · 2019 · Co-investigator
$19,375
CIHR Team Grant in Exercise in Chronically Ill Children
CIHR · 2009 · Principal investigator
$10,000

All 2 grants and awards

29 publications.

Levodopa-Responsive Dystonia Secondary to CTNNB1 Neurodevelopmental Disorder.

Algethami H, Lim WK, Chitayat D, Tein I, Fasano A, Gorodetsky C

Movement disorders clinical practice20254 citationsOpen Access

DOI: 10.1002/mdc3.70166 PMID: 40525469

Recent advances in neurometabolic diseases: The genetic role in the modern era.

Tein I

Epilepsy & behavior : E&B2023First author

DOI: 10.1016/j.yebeh.2023.109338 PMID: 37453291

Reversal of Stroke-Like Episodes With L-Arginine and Meticulous Perioperative Management of Renal Transplantation in a Patient With Mitochondrial Encephalomyopathy, Lactic Acidosis and Stroke-Like Episodes (MELAS) Syndrome. Case Report.

Al Yazidi G, Mulder J, Licht C, Harvey E, Robertson J, Sondheimer N, Tein I

The Neurohospitalist20229 citationsSenior authorOpen Access

DOI: 10.1177/19418744211000512 PMID: 34950389

Response to the Letter to the Editor "The apparent beneficial effect of L-arginine for stroke-like lesions can be accidental" by Josef Finsterer and Sinda Zarrouk.

Al Yazidi G, Mulder J, Licht C, Harvey E, Tein I

The Neurohospitalist2022Senior authorOpen Access

DOI: 10.1177/19418744221090276 PMID: 36147768

The Effect of Creatine Supplementation on Muscle Function in Childhood Myositis: A Randomized, Double-blind, Placebo-controlled Feasibility Study

Dover S, Stephens S, Schneiderman JE, Pullenayegum E, Wells GD, Levy DM, Marcuz J-A, Whitney K, Schulze A, Tein I

Journal of Rheumatology202120 citationsOpen Access

DOI: 10.3899/jrheum.191375

L-arginine effects on cerebrovascular reactivity, perfusion and neurovascular coupling in MELAS (mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes) syndrome

Lance H. Rodan, Julien Poublanc, Joseph Arnold Fisher, Olivia Sobczyk, David John Mikulis, Ingrid Tein

PLoS ONE202026 citationsSenior authorOpen Access

DOI: 10.1371/journal.pone.0238224 PMID: 32881886

Carnitine uptake defect due to a 5'UTR mutation in a pedigree with false positives and false negatives on Newborn screening.

Verbeeten KC, Lamhonwah AM, Bulman D, Faghfoury H, Chakraborty P, Tein I, Geraghty MT

Molecular genetics and metabolism202016 citations

DOI: 10.1016/j.ymgme.2019.12.006 PMID: 31864849

Expression of the organic cation/carnitine transporter family (Octn1,-2 and-3) in mdx muscle and heart: Implications for early carnitine therapy in Duchenne muscular dystrophy to improve cellular carnitine homeostasis.

Lamhonwah AM, Tein I

Clinica chimica acta; international journal of clinical chemistry2020Senior author

DOI: 10.1016/j.cca.2020.02.015 PMID: 32070725

Rationale for dopa-responsive CTNNB1/ß-catenin deficient dystonia.

Pipo-Deveza J, Fehlings D, Chitayat D, Yoon G, Sroka H, Tein I

Movement disorders : official journal of the Movement Disorder Society201819 citationsSenior author

DOI: 10.1002/mds.27320 PMID: 29436745

Erratum to: Common data elements for clinical research in mitochondrial disease: a National Institute for Neurological Disorders and Stroke project

Karaa A, Rahman S, Lombès A, Yu‐Wai‐Man P, Sheikh MK, Alai‐Hansen S, Cohen BH, Dimmock D, Emrick L, Falk MJ

Journal of Inherited Metabolic Disease20181 citationsOpen Access

DOI: 10.1007/s10545-017-0081-z

Profile data last refreshed on September 29, 2026 from the university directory, publication records and public research funding records.

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Ingrid Tein

Research

Latest papers

Latest funding

Levodopa-Responsive Dystonia Secondary to CTNNB1 Neurodevelopmental Disorder.

Recent advances in neurometabolic diseases: The genetic role in the modern era.

Reversal of Stroke-Like Episodes With L-Arginine and Meticulous Perioperative Management of Renal Transplantation in a Patient With Mitochondrial Encephalomyopathy, Lactic Acidosis and Stroke-Like Episodes (MELAS) Syndrome. Case Report.

Response to the Letter to the Editor "The apparent beneficial effect of L-arginine for stroke-like lesions can be accidental" by Josef Finsterer and Sinda Zarrouk.

The Effect of Creatine Supplementation on Muscle Function in Childhood Myositis: A Randomized, Double-blind, Placebo-controlled Feasibility Study

L-arginine effects on cerebrovascular reactivity, perfusion and neurovascular coupling in MELAS (mitochondrial encephalomyopathy with lactic acidosis and stroke-like episodes) syndrome

Carnitine uptake defect due to a 5'UTR mutation in a pedigree with false positives and false negatives on Newborn screening.

Expression of the organic cation/carnitine transporter family (Octn1,-2 and-3) in mdx muscle and heart: Implications for early carnitine therapy in Duchenne muscular dystrophy to improve cellular carnitine homeostasis.

Rationale for dopa-responsive CTNNB1/&#xdf;-catenin deficient dystonia.

Erratum to: Common data elements for clinical research in mitochondrial disease: a National Institute for Neurological Disorders and Stroke project

MITO2019 | The Power of Mitochondria to Transform Human Health

CIHR Team Grant in Exercise in Chronically Ill Children

Frequent collaborators

Mark Tarnopolsky

Greg Wells

Andreas Schulze

Christoph Licht

David Chitayat

Arie Peliowski

Hanna Faghfoury

Grace Yoon

Carolina Gorodetsky

Elizabeth Harvey

Ray Buncic

David Mikulis

Jill Hamilton

Elysa Widjaja

Darcy Fehlings

Dennis Bulman

Brian Feldman

Laura Banks

Alfonso Fasano

Samantha Stephens

Michael Geraghty

Joseph Fisher

Michael Noseworthy

Eleanor Pullenayegum

Mary Sherlock

Benjamin Alman

Cynthia Hawkins

Rationale for dopa-responsive CTNNB1/ß-catenin deficient dystonia.