Ingrid Tein

Toronto, ON, Canada

Last Updated: 09/26/2026

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Found 30 publications

Broadening the phenotypic and molecular spectrum of PRS deficiency in females.

Broadening the phenotypic and molecular spectrum of PRS deficiency in females.

Journal: HGG advances

Published: December 10, 2025

Broadening the phenotypic and molecular spectrum of PRS deficiency in females.

Broadening the phenotypic and molecular spectrum of PRS deficiency in females.

Journal: HGG advances

Published: December 10, 2025

Levodopa-Responsive Dystonia Secondary to CTNNB1 Neurodevelopmental Disorder.

Levodopa-Responsive Dystonia Secondary to CTNNB1 Neurodevelopmental Disorder.

Journal: Movement disorders clinical practice

Published: August 23, 2024

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.

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.

Journal: The Neurohospitalist

Published: September 23, 2022

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

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

Journal: Epilepsy & behavior : E&B

Published: June 28, 2022

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.

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.

Journal: The Neurohospitalist

Published: December 24, 2021

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

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

Journal: The Journal of rheumatology

Published: July 13, 2020

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

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

Journal: Molecular genetics and metabolism

Published: September 12, 2019

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

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

Journal: PloS one

Published: July 26, 2019

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.

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.

Journal: Clinica chimica acta; international journal of clinical chemistry

Published: June 23, 2019

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

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

Journal: Movement disorders : official journal of the Movement Disorder Society

Published: October 28, 2017

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

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

Journal: Journal of inherited metabolic disease

Published: October 06, 2017

Showing 1-12 of 30

Last Updated: 09/26/2026