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Pascal Laforêt

Showing results (51-60 of 164) with videos related to

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Cell Death Discovery|April 14, 2025
Galectin-3: a novel biomarker of glycogen storage disease type IIILucille Rossiaud, Quentin Miagoux, Manon Benabides, et al.
Annals of Neurology|June 21, 2006
Cold extends electromyography distinction between ion channel mutations causing myotoniaEmmanuel Fournier, Karine Viala, Hélène Gervais, et al.
European Journal of Medical Research|July 24, 2023
French recommendations for the management of glycogen storage disease type IIICamille Wicker, Aline Cano, Valérie Decostre, et al.
European Heart Journal|July 31, 2015
Long-term cardiac prognosis and risk stratification in 260 adults presenting with mitochondrial diseasesKarim Wahbi, Wulfran Bougouin, Anthony Béhin, et al.
Neuromuscular Disorders : NMD|July 13, 2010
Investigating glycogenosis type III patients with multi-parametric functional NMR imaging and spectroscopyClaire Wary, Aleksandra Nadaj-Pakleza, Pascal Laforêt, et al.
Journal of Inherited Metabolic Disease|October 26, 2019
Incidence and predictors of total mortality in 267 adults presenting with mitochondrial diseasesConstantinos Papadopoulos, Karim Wahbi, Anthony Behin, et al.
Neuromuscular Disorders : NMD|December 14, 2011
High cardiovascular morbidity and mortality in myofibrillar myopathies due to DES gene mutations: a 10-year longitudinal studyKarim Wahbi, Anthony Béhin, Philippe Charron, et al.
Journal of Inherited Metabolic Disease|November 26, 2019
A high prevalence of arterial hypertension in patients with mitochondrial diseasesCaroline Chong-Nguyen, Caroline Stalens, Yves Goursot, et al.
Neuromuscular Disorders : NMD|September 3, 2019
X-linked Emery-Dreifuss muscular dystrophy manifesting with adult onset axial weakness, camptocormia, and minimal joint contracturesMarion Brisset, Rabah Ben Yaou, Robert-Yves Carlier, et al.
Neuromuscular Disorders : NMD|March 4, 2022
No effect of triheptanoin in patients with phosphofructokinase deficiencyDaniel Emil Raaschou-Pedersen, Karen Lindhardt Madsen, Nicoline Løkken, et al.
Pageof 17

Showing results (51-60 of 164) with videos related to

Sort By:
Pageof 17
Cell Death Discovery|April 14, 2025
Galectin-3: a novel biomarker of glycogen storage disease type IIILucille Rossiaud, Quentin Miagoux, Manon Benabides, et al.
Annals of Neurology|June 21, 2006
Cold extends electromyography distinction between ion channel mutations causing myotoniaEmmanuel Fournier, Karine Viala, Hélène Gervais, et al.
European Journal of Medical Research|July 24, 2023
French recommendations for the management of glycogen storage disease type IIICamille Wicker, Aline Cano, Valérie Decostre, et al.
European Heart Journal|July 31, 2015
Long-term cardiac prognosis and risk stratification in 260 adults presenting with mitochondrial diseasesKarim Wahbi, Wulfran Bougouin, Anthony Béhin, et al.
Neuromuscular Disorders : NMD|July 13, 2010
Investigating glycogenosis type III patients with multi-parametric functional NMR imaging and spectroscopyClaire Wary, Aleksandra Nadaj-Pakleza, Pascal Laforêt, et al.
Journal of Inherited Metabolic Disease|October 26, 2019
Incidence and predictors of total mortality in 267 adults presenting with mitochondrial diseasesConstantinos Papadopoulos, Karim Wahbi, Anthony Behin, et al.
Neuromuscular Disorders : NMD|December 14, 2011
High cardiovascular morbidity and mortality in myofibrillar myopathies due to DES gene mutations: a 10-year longitudinal studyKarim Wahbi, Anthony Béhin, Philippe Charron, et al.
Journal of Inherited Metabolic Disease|November 26, 2019
A high prevalence of arterial hypertension in patients with mitochondrial diseasesCaroline Chong-Nguyen, Caroline Stalens, Yves Goursot, et al.
Neuromuscular Disorders : NMD|September 3, 2019
X-linked Emery-Dreifuss muscular dystrophy manifesting with adult onset axial weakness, camptocormia, and minimal joint contracturesMarion Brisset, Rabah Ben Yaou, Robert-Yves Carlier, et al.
Neuromuscular Disorders : NMD|March 4, 2022
No effect of triheptanoin in patients with phosphofructokinase deficiencyDaniel Emil Raaschou-Pedersen, Karen Lindhardt Madsen, Nicoline Løkken, et al.
Pageof 17