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Bruno Maranda

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The Lancet. Infectious Diseases|August 24, 2023
Safety and efficacy of inhaled IBIO123 for mild-to-moderate COVID-19: a randomised, double-blind, dose-ascending, placebo-controlled, phase 1/2 trialBruno Maranda, Sébastien M Labbé, Magali Lurquin, et al.
Molecular Genetics and Metabolism|November 28, 2008
Citrin deficiency, a perplexing global disorderDavid Dimmock, Bruno Maranda, Carlo Dionisi-Vici, et al.
Journal of Medical Genetics|January 27, 2011
LRPPRC mutations cause a phenotypically distinct form of Leigh syndrome with cytochrome c oxidase deficiencyFrançois-Guillaume Debray, Charles Morin, Annie Janvier, et al.
International Journal of Molecular Sciences|August 29, 2020
Diurnal Variation of Urinary Fabry Disease Biomarkers during Enzyme Replacement Therapy CyclesMichel Boutin, Pamela Lavoie, Iskren Menkovic, et al.
Journal of Inherited Metabolic Disease|December 10, 2019
Nocturnal enteral nutrition is therapeutic for growth failure in Fanconi-Bickel syndromeAlessandra Pennisi, Bruno Maranda, Jean-François Benoist, et al.
Journal of Inherited Metabolic Disease|February 12, 2019
Combined malonic and methylmalonic aciduria due to ACSF3 mutations: Benign clinical course in an unselected cohortAlina Levtova, Paula J Waters, Daniela Buhas, et al.
The Lancet. Respiratory Medicine|April 20, 2019
Early-onset emphysema in a large French-Canadian family: a genetic investigationYohan Bossé, Maxime Lamontagne, Nathalie Gaudreault, et al.
Clinical Genetics|June 23, 2025
PMS2 c.2117del (p.Lys706Serfs*19) is the Most Frequent Cancer-Associated Founder Pathogenic Variant in the French-Canadian Population of Quebec, CanadaAnne-Laure Chong, Alejandro Mejia-Garcia, Supriya Behl, et al.
Familial Cancer|July 23, 2011
A survey of APC mutations in QuebecJonathan Jarry, Jean-Sébastien Brunet, Rachel Laframboise, et al.
Orphanet Journal of Rare Diseases|January 27, 2016
Diagnosis of late-onset Pompe disease and other muscle disorders by next-generation sequencingSébastien Lévesque, Christiane Auray-Blais, Elaine Gravel, et al.
Pageof 7

Showing results (31-40 of 63) with videos related to

Sort By:
Pageof 7
The Lancet. Infectious Diseases|August 24, 2023
Safety and efficacy of inhaled IBIO123 for mild-to-moderate COVID-19: a randomised, double-blind, dose-ascending, placebo-controlled, phase 1/2 trialBruno Maranda, Sébastien M Labbé, Magali Lurquin, et al.
Molecular Genetics and Metabolism|November 28, 2008
Citrin deficiency, a perplexing global disorderDavid Dimmock, Bruno Maranda, Carlo Dionisi-Vici, et al.
Journal of Medical Genetics|January 27, 2011
LRPPRC mutations cause a phenotypically distinct form of Leigh syndrome with cytochrome c oxidase deficiencyFrançois-Guillaume Debray, Charles Morin, Annie Janvier, et al.
International Journal of Molecular Sciences|August 29, 2020
Diurnal Variation of Urinary Fabry Disease Biomarkers during Enzyme Replacement Therapy CyclesMichel Boutin, Pamela Lavoie, Iskren Menkovic, et al.
Journal of Inherited Metabolic Disease|December 10, 2019
Nocturnal enteral nutrition is therapeutic for growth failure in Fanconi-Bickel syndromeAlessandra Pennisi, Bruno Maranda, Jean-François Benoist, et al.
Journal of Inherited Metabolic Disease|February 12, 2019
Combined malonic and methylmalonic aciduria due to ACSF3 mutations: Benign clinical course in an unselected cohortAlina Levtova, Paula J Waters, Daniela Buhas, et al.
The Lancet. Respiratory Medicine|April 20, 2019
Early-onset emphysema in a large French-Canadian family: a genetic investigationYohan Bossé, Maxime Lamontagne, Nathalie Gaudreault, et al.
Clinical Genetics|June 23, 2025
PMS2 c.2117del (p.Lys706Serfs*19) is the Most Frequent Cancer-Associated Founder Pathogenic Variant in the French-Canadian Population of Quebec, CanadaAnne-Laure Chong, Alejandro Mejia-Garcia, Supriya Behl, et al.
Familial Cancer|July 23, 2011
A survey of APC mutations in QuebecJonathan Jarry, Jean-Sébastien Brunet, Rachel Laframboise, et al.
Orphanet Journal of Rare Diseases|January 27, 2016
Diagnosis of late-onset Pompe disease and other muscle disorders by next-generation sequencingSébastien Lévesque, Christiane Auray-Blais, Elaine Gravel, et al.
Pageof 7