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Successful surgical repair of a temporal and parietal bone fracture with associated traumatic brain injury in a fourteen-day-old foal = Succesvolle chirurgische behandeling van een os temporale en parietale fractuur met bijhorende hersenschade bij een twee weken oud veulen
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High seroprevalence against lawsonia intracellularis among adult horses in Belgium
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- Journal Article
- A1
- open access
Resolving the dark matter of ABCA4 for 1054 Stargardt disease probands through integrated genomics and transcriptomics
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Yellow fat disease (steatitis) in 20 equids : description of clinical and ultrasonographic findings
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Coding and non-coding structural variants of ABCA4 contribute to the missing heritability in Stargardt disease, a prevalent inherited retinal disease
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- Journal Article
- A1
- open access
ABCA4-associated disease as a model for missing heritability in autosomal recessive disorders : novel noncoding splice, cis-regulatory, structural, and recurrent hypomorphic variants
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- Journal Article
- A1
- open access
Deep-intronic ABCA4 variants explain missing heritability in Stargardt disease and allow correction of splice defects by antisense oligonucleotides
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Resolving the dark matter of ABCA4 for 1,054 Stargardt disease probands through integrated genomics and transcriptomics
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- Conference Paper
- C3
- open access
Bacterial blood culture isolates and their antimicrobial susceptibility obtained from 42 critically ill neonatal foals presented at Ghent University between 2011 and 2017
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- Journal Article
- A1
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The choroid plexus epithelium as a novel player in the stomach-brain axis during Helicobacter infection
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- Journal Article
- A1
- open access
Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations
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Hidden genetic variation in Stargardt disease : novel copy number variations, cis-regulatory and deep-intronic splice variants within the ABCA4 locus
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Effect of a gastral infection with zoonotic Helicobacter species on brain barrier integrity
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A novel isolation protocol and probe-based RT-PCR for diagnosis of gastric infections with the zoonotic pathogen Helicobacter suis
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- Journal Article
- A1
- open access
arrEYE : a customized platform for high-resolution copy number analysis of coding and noncoding regions of known and candidate retinal dystrophy genes and retinal noncoding RNAs
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Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations
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Mapping the genomic landscape of inherited retinal disease genes prioritizes genes prone to coding and noncoding copy-number variations
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Yellow fat disease (steatitis) : description of 20 cases with emphasis on typical ultrasounographic findings
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- Journal Article
- A1
- open access
Phenylephrine-induced epistaxis in a six-year-old Quarter horse with nephrosplenic entrapment
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Coding and non-coding copy number variations explaining unsolved retinal dystrophies : role of genomic architectural features and underlying mechanisms
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Coding and non-coding copy number variations explaining unsolved retinal dystrophies : role of genomic architectural features and underlying mechanisms
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Coding and non-coding copy number variations explaining unsolved retinal dystrophies : role of genomic architectural features and underlying mechanisms
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Coding and non-coding copy number variations explaining unsolved retinal dystrophies : role of genomic architectural features and underlying mechanisms
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Tetanus in equids: a survey over the period 2001–2013
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Influence of the stomach-brain axis in relation to an experimental Helicobacter suis infection in mice
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Involvement of the Helicobacter heilmannii locus encoding the HOF outer membrane proteins in binding to the gastric mucosa
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- Journal Article
- A1
- open access
Hidden genetic variation in LCA9-associated congenital blindness explained by 5′UTR mutations and copy-number variations of NMNAT1
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Novel FRMD7 mutations and genomic rearrangement expand the molecular pathogenesis of X-linked idiopathic infantile nystagmus
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Steatitis (Yellow Fat Disease) bij een tweejarige hengst
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Equine multisystemic eosinophilic epitheliotropic disease: a case report and review of literature
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A dual approach for comprehensive genetic testing of ABCA4 in Stargardt disease
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A dual approach for comprehensive genetic testing of ABCA4 in Stargardt disease
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A dual approach for comprehensive genetic testing of ABCA4 in Stargardt disease
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A dual approach for comprehensive genetic testing of ABCA4 in Stargardt disease
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Regulatory mutations in the 5'UTR of NMNAT1, encoding the nuclear isoform of nicotinamide nucleotide adenylyltransferase 1, cause Leber Congenital Amaurosis
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Regulatory mutations in the 5'UTR of NMNAT1, encoding the nuclear isoform of nicotinamide nucleotide adenylyltransferase 1, cause Leber Congenital Amaurosis
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Retrospective study of 44 cases of equine grass sickness in Belgium
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Regulatory mutations in the 5'UTR of NMNAT1, encoding the nuclear isoform of nicotinamide nucleotide adenylyltransferase 1, cause Leber Congenital Amaurosis
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Regulatory mutations in the 5'UTR of NMNAT1, encoding the nuclear isoform of nicotinamide nucleotide adenylyltransferase 1, cause Leber Congenital Amaurosis
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Hypocalcemia caused by primary hypoparathyroidism in a 3-month-old filly
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Leptospirosis as a cause of acute respiratory distress and renal failure in two foals
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- Journal Article
- A1
- open access
Evaluation of the pocH-100iV DIFF hematology analyzer for use in horses and cattle
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An atypical cause of respiratory distress in an adult dairy cow