Ghent University Academic Bibliography

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Correlation between faecal microbiota and serum levels of Hypoglycin A and MCPA-carnitine in horses with atypical myopathy

Carla Cesarini, Dominique Votion, François Boemer, Simona Cerri, Laurence Lefère (UGent) , Katrien Palmers, Gunther van Loon (UGent) , Helene Amory, Georges Daube and Bernard Taminiau

(2018) Proceedings of the 11th European College of Equine Internal Medicine congress. p.104-104
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- Journal Article
- A1
- open access
Acylcarnitines profile best predicts survival in horses with atypical myopathy

François Boemer, Johann Detilleux, Christophe Cello, Hélène Amory, Christel Marcillaud-Pitel, Eric Richard, Gaby van Galen, Gunther van Loon (UGent) , Laurence Lefère (UGent) and Dominique-Marie Votion

(2017) PLOS ONE. 12(8).
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Mitochondrial function is altered in horse atypical myopathy

Hélène Lemieux, François Boemer, Gaby van Galen, Didier Serteyn, Hélène Amory, Etienne Baise, Dominique Cassart, Gunther van Loon (UGent) , Christel Marcillaud-Pitel and Dominique-M Votion

(2016) MITOCHONDRION. 30. p.35-41
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Mutation of the iron-sulfur cluster assembly gene IBA57 causes fatal infantile leukodystrophy

François-Guillaume Debray, Claudia Stümpfig, Arnaud Vanlander (UGent) , Vinciane Dideberg, Claire Josse, Jean-Hubert Caberg, François Boemer, Vincent Bours, René Stevens, Sara Seneca, et al.

(2015) JOURNAL OF INHERITED METABOLIC DISEASE. 38(6). p.1147-1153
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Mitochondrial encephalomyopathy with cytochrome c oxidase deficiency caused by a novel mutation in the MTCO1 gene

François-Guillaume Debray, Sara Seneca, Michel Gonce, Kim Vancampenhaut, Elettra Bianchi, François Boemer, Laurent Weekers, Joél Smet (UGent) and Rudy Van Coster (UGent)

(2014) MITOCHONDRION. 17. p.101-105

Academic Bibliography

Correlation between faecal microbiota and serum levels of Hypoglycin A and MCPA-carnitine in horses with atypical myopathy

Acylcarnitines profile best predicts survival in horses with atypical myopathy

Mitochondrial function is altered in horse atypical myopathy

Mutation of the iron-sulfur cluster assembly gene IBA57 causes fatal infantile leukodystrophy

Mitochondrial encephalomyopathy with cytochrome c oxidase deficiency caused by a novel mutation in the MTCO1 gene

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