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High‐rate volatile fatty acid (VFA) production by a granular sludge process at low pH

Biotechnology and bioengineering, 2015-11, Vol.112 (11), p.2248-2255

2015

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IL-10 signaling in dendritic cells controls IL-1β-mediated IFNγ secretion by human CD4+ T cells: relevance to inflammatory bowel disease

Mucosal immunology, 2019-09, Vol.12 (5), p.1201-1211

2019

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Malignancy and mortality in paediatric‐onset inflammatory bowel disease: a 3‐year prospective, multinational study from the paediatric IBD Porto group of ESPGHAN

Alimentary pharmacology & therapeutics, 2018-09, Vol.48 (5), p.523-537

2018

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Invasive fungal infections in patients treated with Bruton's tyrosine kinase inhibitors

Netherlands journal of medicine, 2020-09, Vol.78 (5), p.294-296

2020

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Recurrent cholangitis in a 65-year-old man

Gut, 2015-06, Vol.64 (6), p.883-883

2015

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Phenotypic variation in hereditary frontotemporal dementia with tau mutations

Annals of neurology, 1999-10, Vol.46 (4), p.617-626

1999

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P063 Expression of the coinhibitory receptor TIGIT on memory CD4+ T cells is induced by TCR ligation and retinoic acid co-stimulation and is elicited during microbial colonization of the intestine

Journal of Crohn's and colitis, 2022-01, Vol.16 (Supplement_1), p.i172-i172

2022

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Mutations in the DJ-1 Gene Associated with Autosomal Recessive Early-Onset Parkinsonism

Science (American Association for the Advancement of Science), 2003-01, Vol.299 (5604), p.256-259

2003

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Frontotemporal dementia in The Netherlands: patient characteristics and prevalence estimates from a population‐based study

Brain (London, England : 1878), 2003-09, Vol.126 (9), p.2016-2022

2003

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P045 TIGIT expression differentiates regulatory from inflammatory Th1 gut-homing effector CD4+ T cells in inflammatory bowel disease patients

Journal of Crohn's and colitis, 2022-01, Vol.16 (Supplement_1), p.i161-i161

2022

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Disruption of a Long-Range Cis-Acting Regulator for Shh Causes Preaxial Polydactyly

Proceedings of the National Academy of Sciences - PNAS, 2002-05, Vol.99 (11), p.7548-7553

2002

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P069 Elevated adaptive immune responses to multiple Lachnospiraceae bacterial flagellins in therapy-naïve pediatric CD patients are associated with distinct immune pathology

Journal of Crohn's and colitis, 2023-01, Vol.17 (Supplement_1), p.i235-i236

2023

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P012 Low frequencies of circulating inhibitory TIGIT+CD38+ effector T cells identify an immunologically distinct subgroup of pediatric patients with severe Crohn’s disease

Journal of Crohn's and colitis, 2021-05, Vol.15 (Supplement_1), p.S134-S134

2021

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A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis

Nature genetics, 2001-07, Vol.28 (3), p.213-214

2001

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Cntnap2 is disrupted in a family with gilles de la tourette syndrome and obsessive compulsive disorder

Genomics (San Diego, Calif.), 2003-07, Vol.82 (1), p.1-9

2003

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Quantitative visual fields under binocular viewing conditions in primary and consecutive divergent strabismus

Graefe's archive for clinical and experimental ophthalmology, 1999-07, Vol.237 (7), p.535-545

1999

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High Prevalence of Mutations in the Microtubule-Associated Protein Tau in a Population Study of Frontotemporal Dementia in the Netherlands

American journal of human genetics, 1999-02, Vol.64 (2), p.414-421

1999

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Quantitative perimetry under binocular viewing conditions in microstrabismus

Vision research (Oxford), 1997-10, Vol.37 (19), p.2801-2812

1997

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P819 Whole-exome sequencing in early-onset primary sclerosing cholangitis: first results of the WHELP study

Journal of Crohn's and colitis, 2019-01, Vol.13 (Supplement_1), p.S532-S532

2019

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DOP09 IgG responses to multiple bacterial flagellins identify a subgroup of paediatric therapy-naive Crohn’s disease patients with increased microbiota-specific T-cell reactivity

Journal of Crohn's and colitis, 2020-01, Vol.14 (Supplement_1), p.S046-S046

2020

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A novel presenilin 1 mutation (L174 M) in a large Cuban family with early onset Alzheimer disease

Neurogenetics, 2002-10, Vol.4 (2), p.97-104

2002

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Mutations in TITF-1 are associated with benign hereditary chorea

Human molecular genetics, 2002-04, Vol.11 (8), p.971-979

2002

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Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17

Nature (London), 1998-06, Vol.393 (6686), p.702-705

1998

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P095 Consequences of an IL2RA locus duplication in a very early onset inflammatory bowel disease patient

Journal of Crohn's and colitis, 2018-01, Vol.12 (supplement_1), p.S141-S142

2018

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A new gene, encoding an anion transporter, is mutated in sialic acid storage diseases

Nature genetics, 1999-12, Vol.23 (4), p.462-465

1999

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High‐rate volatile fatty acid (VFA) production by a granular sludge process at low pH

IL-10 signaling in dendritic cells controls IL-1β-mediated IFNγ secretion by human CD4+ T cells: relevance to inflammatory bowel disease

Malignancy and mortality in paediatric‐onset inflammatory bowel disease: a 3‐year prospective, multinational study from the paediatric IBD Porto group of ESPGHAN

Invasive fungal infections in patients treated with Bruton's tyrosine kinase inhibitors

Recurrent cholangitis in a 65-year-old man

Phenotypic variation in hereditary frontotemporal dementia with tau mutations

P063 Expression of the coinhibitory receptor TIGIT on memory CD4+ T cells is induced by TCR ligation and retinoic acid co-stimulation and is elicited during microbial colonization of the intestine

Mutations in the DJ-1 Gene Associated with Autosomal Recessive Early-Onset Parkinsonism

Frontotemporal dementia in The Netherlands: patient characteristics and prevalence estimates from a population‐based study

P045 TIGIT expression differentiates regulatory from inflammatory Th1 gut-homing effector CD4+ T cells in inflammatory bowel disease patients

Disruption of a Long-Range Cis-Acting Regulator for Shh Causes Preaxial Polydactyly

P069 Elevated adaptive immune responses to multiple Lachnospiraceae bacterial flagellins in therapy-naïve pediatric CD patients are associated with distinct immune pathology

P012 Low frequencies of circulating inhibitory TIGIT+CD38+ effector T cells identify an immunologically distinct subgroup of pediatric patients with severe Crohn’s disease

A mutation in SLC11A3 is associated with autosomal dominant hemochromatosis

Cntnap2 is disrupted in a family with gilles de la tourette syndrome and obsessive compulsive disorder

Quantitative visual fields under binocular viewing conditions in primary and consecutive divergent strabismus

High Prevalence of Mutations in the Microtubule-Associated Protein Tau in a Population Study of Frontotemporal Dementia in the Netherlands

Quantitative perimetry under binocular viewing conditions in microstrabismus

P819 Whole-exome sequencing in early-onset primary sclerosing cholangitis: first results of the WHELP study

DOP09 IgG responses to multiple bacterial flagellins identify a subgroup of paediatric therapy-naive Crohn’s disease patients with increased microbiota-specific T-cell reactivity

A novel presenilin 1 mutation (L174 M) in a large Cuban family with early onset Alzheimer disease

Mutations in TITF-1 are associated with benign hereditary chorea

Association of missense and 5′-splice-site mutations in tau with the inherited dementia FTDP-17

P095 Consequences of an IL2RA locus duplication in a very early onset inflammatory bowel disease patient

A new gene, encoding an anion transporter, is mutated in sialic acid storage diseases

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