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Long-term safety of withholding standard prophylaxis in patients with moderate chronic kidney disease

European radiology, 2023-01, Vol.33 (1), p.627-632

2023

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Effects of Morphology of Cerium Oxide Catalysts for Reverse Water Gas Shift Reaction

Catalysis letters, 2016-04, Vol.146 (4), p.770-777

2016

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Impact on clinical practice of updated guidelines on iodinated contrast material: CINART

European radiology, 2020-07, Vol.30 (7), p.4005-4013

2020

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Serum matrix metalloproteinase-9 (MMP-9) as a biomarker for monitoring disease progression in Duchenne muscular dystrophy (DMD)

Neuromuscular disorders : NMD, 2011-08, Vol.21 (8), p.569-578

2011

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Deleterious alleles in the human genome are on average younger than neutral alleles of the same frequency

PLoS genetics, 2013-02, Vol.9 (2), p.e1003301

2013

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MDCT evaluation of aortic root and aortic valve prior to TAVI. What is the optimal imaging time point in the cardiac cycle?

European radiology, 2015-07, Vol.25 (7), p.1975-1983

2015

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Low contrast media volume in pre-TAVI CT examinations

European radiology, 2016-08, Vol.26 (8), p.2426-2435

2016

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Limb-girdle muscular dystrophy in the Netherlands: gene defect identified in half the families

Neurology, 2007-06, Vol.68 (24), p.2125

2007

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Relative power and sample size analysis on gene expression profiling data

BMC genomics, 2009-09, Vol.10 (1), p.439-439, Article 439

2009

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Comparative analysis of antisense oligonucleotide analogs for targeted DMD exon 46 skipping in muscle cells

Gene therapy, 2004-09, Vol.11 (18), p.1391-1398

2004

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Muscle regeneration in dystrophin-deficient mdx mice studied by gene expression profiling

BMC genomics, 2005-07, Vol.6 (1), p.98-98, Article 98

2005

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Complexity of gap junctions between horizontal cells of the carp retina

Neuroscience, 2017-01, Vol.340, p.8-22

2017

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Common pathological mechanisms in mouse models for muscular dystrophies

The FASEB journal, 2006-01, Vol.20 (1), p.127-129

2006

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WHSC1, a 90 kb SET Domain-Containing Gene, Expressed in Early Development and Homologous to a Drosophila Dysmorphy Gene Maps in the Wolf-Hirschhorn Syndrome Critical Region and is Fused to IgH in t(1;14) Multiple Myeloma

Human molecular genetics, 1998-07, Vol.7 (7), p.1071-1082

1998

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Value of the electrocardiogram in localizing the occlusion site in the left anterior descending coronary artery in acute anterior myocardial infarction

Journal of the American College of Cardiology, 1999-08, Vol.34 (2), p.389-395

1999

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Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP

Nature (London), 1995-07, Vol.376 (6538), p.348-351

1995

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Toward a roadmap in global biobanking for health

European journal of human genetics : EJHG, 2012-11, Vol.20 (11), p.1105-1111

2012

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Biobanking for Europe

Briefings in bioinformatics, 2008-01, Vol.9 (1), p.14-24

2008

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Fluorescent labelling of cRNA for microarray applications

Nucleic acids research, 2003-03, Vol.31 (5), p.e20

2003

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Development of monolith with a carbon-nanofiber-washcoat as a structured catalyst support in liquid phase

Catalysis today, 2003-04, Vol.79, p.29-33

2003

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Huntingtin with an expanded polyglutamine repeat affects the Jab1-p27(Kip1) pathway

Neurobiology of disease, 2012-06, Vol.46 (3), p.673-681

2012

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Mechanistic aspects of the formation of carbon-nanofibers on the surface of Ni foam: A new microstructured catalyst support

Journal of catalysis, 2006-04, Vol.239 (2), p.460-469

2006

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The effects of morphology of cerium oxide catalysts for dehydrogenation of ethylbenzene to styrene

Applied catalysis. A, General, 2015-09, Vol.505, p.354-364

2015

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Nearly all hereditary paragangliomas in The Netherlands are caused by two founder mutations in the SDHD gene

Genes chromosomes & cancer, 2001-07, Vol.31 (3), p.274-281

2001

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FcγRI (CD64) Contributes Substantially to Severity of Arthritis, Hypersensitivity Responses, and Protection from Bacterial Infection

Immunity (Cambridge, Mass.), 2002-03, Vol.16 (3), p.391-402

2002

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Long-term safety of withholding standard prophylaxis in patients with moderate chronic kidney disease

Effects of Morphology of Cerium Oxide Catalysts for Reverse Water Gas Shift Reaction

Impact on clinical practice of updated guidelines on iodinated contrast material: CINART

Serum matrix metalloproteinase-9 (MMP-9) as a biomarker for monitoring disease progression in Duchenne muscular dystrophy (DMD)

Deleterious alleles in the human genome are on average younger than neutral alleles of the same frequency

MDCT evaluation of aortic root and aortic valve prior to TAVI. What is the optimal imaging time point in the cardiac cycle?

Low contrast media volume in pre-TAVI CT examinations

Limb-girdle muscular dystrophy in the Netherlands: gene defect identified in half the families

Relative power and sample size analysis on gene expression profiling data

Comparative analysis of antisense oligonucleotide analogs for targeted DMD exon 46 skipping in muscle cells

Muscle regeneration in dystrophin-deficient mdx mice studied by gene expression profiling

Complexity of gap junctions between horizontal cells of the carp retina

Common pathological mechanisms in mouse models for muscular dystrophies

WHSC1, a 90 kb SET Domain-Containing Gene, Expressed in Early Development and Homologous to a Drosophila Dysmorphy Gene Maps in the Wolf-Hirschhorn Syndrome Critical Region and is Fused to IgH in t(1;14) Multiple Myeloma

Value of the electrocardiogram in localizing the occlusion site in the left anterior descending coronary artery in acute anterior myocardial infarction

Rubinstein-Taybi syndrome caused by mutations in the transcriptional co-activator CBP

Toward a roadmap in global biobanking for health

Biobanking for Europe

Fluorescent labelling of cRNA for microarray applications

Development of monolith with a carbon-nanofiber-washcoat as a structured catalyst support in liquid phase

Huntingtin with an expanded polyglutamine repeat affects the Jab1-p27(Kip1) pathway

Mechanistic aspects of the formation of carbon-nanofibers on the surface of Ni foam: A new microstructured catalyst support

The effects of morphology of cerium oxide catalysts for dehydrogenation of ethylbenzene to styrene

Nearly all hereditary paragangliomas in The Netherlands are caused by two founder mutations in the SDHD gene

FcγRI (CD64) Contributes Substantially to Severity of Arthritis, Hypersensitivity Responses, and Protection from Bacterial Infection

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