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Unravelling faecal microbiota variations in equine atypical myopathy : correlation with blood markers and contribution of microbiome
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Large-scale study of blood markers in equine atypical myopathy reveals subclinical poisoning and advances in diagnostic and prognostic criteria
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- Journal Article
- A1
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Belgian rare diseases plan in clinical pathology : identification of key biochemical diagnostic tests and establishment of reference laboratories and financing conditions
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Outcome of publicly funded nationwide first-tier noninvasive prenatal screening
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Performance and diagnostic value of genome-wide noninvasive prenatal testing in multiple gestations
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Correlation between faecal microbiota and serum levels of Hypoglycin A and MCPA-carnitine in horses with atypical myopathy
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- Journal Article
- A1
- open access
Acylcarnitines profile best predicts survival in horses with atypical myopathy
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Mitochondrial function is altered in horse atypical myopathy
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Mutation of the iron-sulfur cluster assembly gene IBA57 causes fatal infantile leukodystrophy
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Mitochondrial encephalomyopathy with cytochrome c oxidase deficiency caused by a novel mutation in the MTCO1 gene