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Nicolai Preisler

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Neurology|April 3, 2015
Skeletal muscle metabolism is impaired during exercise in glycogen storage disease type IIINicolai Preisler, Pascal Laforêt, Karen Lindhardt Madsen, et al.
Molecular Genetics and Metabolism|September 18, 2012
Fat and carbohydrate metabolism during exercise in late-onset Pompe diseaseNicolai Preisler, Pascal Laforet, Karen Lindhardt Madsen, et al.
Endocrine Connections|May 12, 2017
Skeletal muscle metabolism during prolonged exercise in Pompe diseaseNicolai Preisler, Pascal Laforêt, Karen Lindhardt Madsen, et al.
American Journal of Physiology. Regulatory, Integrative and Comparative Physiology|November 21, 2014
Protein-carbohydrate supplements improve muscle protein balance in muscular dystrophy patients after endurance exercise: a placebo-controlled crossover studyGrete Andersen, Mette C Ørngreen, Nicolai Preisler, et al.
Molecular Genetics and Metabolism|September 10, 2013
Late-onset Pompe disease is prevalent in unclassified limb-girdle muscular dystrophiesNicolai Preisler, Zoltan Lukacs, Lotte Vinge, et al.
The Journal of Clinical Endocrinology and Metabolism|June 2, 2015
Lactate and Energy Metabolism During Exercise in Patients With Blocked Glycogenolysis (McArdle Disease)Mette Cathrine Ørngreen, Tina Dysgaard Jeppesen, Tanja Taivassalo, et al.
The Journal of Clinical Endocrinology and Metabolism|June 20, 2013
Fat and carbohydrate metabolism during exercise in phosphoglucomutase type 1 deficiencyNicolai Preisler, Pascal Laforêt, Andoni Echaniz-Laguna, et al.
JIMD Reports|September 6, 2021
Energy metabolism during exercise in patients with β-enolase deficiency (GSDXIII)Astrid Emilie Buch, Olimpia Musumeci, Ralph Wigley, et al.
Molecular Genetics and Metabolism|March 20, 2013
Exercise intolerance in Glycogen Storage Disease Type III: weakness or energy deficiency?Nicolai Preisler, Agnès Pradel, Edith Husu, et al.
Molecular Genetics and Metabolism|September 9, 2017
Impaired glycogen breakdown and synthesis in phosphoglucomutase 1 deficiencyNicolai Preisler, Jonathan Cohen, Christoffer Rasmus Vissing, et al.
Pageof 2

Showing results (11-20 of 20) with videos related to

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Neurology|April 3, 2015
Skeletal muscle metabolism is impaired during exercise in glycogen storage disease type IIINicolai Preisler, Pascal Laforêt, Karen Lindhardt Madsen, et al.
Molecular Genetics and Metabolism|September 18, 2012
Fat and carbohydrate metabolism during exercise in late-onset Pompe diseaseNicolai Preisler, Pascal Laforet, Karen Lindhardt Madsen, et al.
Endocrine Connections|May 12, 2017
Skeletal muscle metabolism during prolonged exercise in Pompe diseaseNicolai Preisler, Pascal Laforêt, Karen Lindhardt Madsen, et al.
American Journal of Physiology. Regulatory, Integrative and Comparative Physiology|November 21, 2014
Protein-carbohydrate supplements improve muscle protein balance in muscular dystrophy patients after endurance exercise: a placebo-controlled crossover studyGrete Andersen, Mette C Ørngreen, Nicolai Preisler, et al.
Molecular Genetics and Metabolism|September 10, 2013
Late-onset Pompe disease is prevalent in unclassified limb-girdle muscular dystrophiesNicolai Preisler, Zoltan Lukacs, Lotte Vinge, et al.
The Journal of Clinical Endocrinology and Metabolism|June 2, 2015
Lactate and Energy Metabolism During Exercise in Patients With Blocked Glycogenolysis (McArdle Disease)Mette Cathrine Ørngreen, Tina Dysgaard Jeppesen, Tanja Taivassalo, et al.
The Journal of Clinical Endocrinology and Metabolism|June 20, 2013
Fat and carbohydrate metabolism during exercise in phosphoglucomutase type 1 deficiencyNicolai Preisler, Pascal Laforêt, Andoni Echaniz-Laguna, et al.
JIMD Reports|September 6, 2021
Energy metabolism during exercise in patients with β-enolase deficiency (GSDXIII)Astrid Emilie Buch, Olimpia Musumeci, Ralph Wigley, et al.
Molecular Genetics and Metabolism|March 20, 2013
Exercise intolerance in Glycogen Storage Disease Type III: weakness or energy deficiency?Nicolai Preisler, Agnès Pradel, Edith Husu, et al.
Molecular Genetics and Metabolism|September 9, 2017
Impaired glycogen breakdown and synthesis in phosphoglucomutase 1 deficiencyNicolai Preisler, Jonathan Cohen, Christoffer Rasmus Vissing, et al.
Pageof 2