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Rendu-Osler-Weber disease: update of medical and dental considerations

Oral surgery, oral medicine, oral pathology, oral radiology and endodontics, 2008-02, Vol.105 (2), p.e38-e41

2008

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A report on 10 new patients with heterozygous mutations in the COL11A1 gene and a review of genotype-phenotype correlations in type XI collagenopathies

American journal of medical genetics. Part A, 2007-02, Vol.143A (3), p.258-264

2007

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Contribution of CYLN2 and GTF2IRD1 to neurological and cognitive symptoms in Williams Syndrome

Neurobiology of disease, 2007-04, Vol.26 (1), p.112-124

2007

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Germline Mutations in RASA1 Are Not Found in Patients with Klippel-Trenaunay Syndrome or Capillary Malformation with Limb Overgrowth

Molecular syndromology, 2013-04, Vol.4 (4), p.173-178

2013

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Interstitial deletion in 3q in a patient with blepharophimosis‐ptosis‐epicanthus inversus syndrome (BPES) and microcephaly, mild mental retardation and growth delay: Clinical report and review of the literature

American journal of medical genetics. Part A, 2005-08, Vol.137A (1), p.81-87

2005

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Saccade dysmetria in Williams–Beuren syndrome

Neuropsychologia, 2004, Vol.42 (5), p.569-576

2004

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Interstitial deletion in 3q in a patient with blepharophimosis-ptosis-epicanthus inversus syndrome (BPES) and microcephaly, mild mental retardation and growth delay: Clinical report and review of the literature

American Journal of Medical Genetics Part A, 2005, Vol.137A (1), p.81-87

2005

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Therapietrouw versus therapiebewustzijn; een klein verschil met grote gevolgen

Pharmaceutisch Weekblad, 1980-12, Vol.2 (1), p.1449-1453

Van Hagen, J. J. M.

1980

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Verslag van een GVO-project ‘Omgaan met geneesmiddelen’

Pharmaceutisch Weekblad, 1980-12, Vol.2 (1), p.1578-1584

1980

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Ingezonden

Pharmaceutisch weekblad, 1981-12, Vol.3 (1), p.1201-1202

1981

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Ingezonden

Pharmaceutisch Weekblad, 1980-12, Vol.2 (1), p.1659-1664

1980

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Primary immunodeficiencies in the Netherlands: National patient data demonstrate the increased risk of malignancy

Clinical immunology (Orlando, Fla.), 2015-02, Vol.156 (2), p.154-162

2015

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Mild hyperthermia inhibits homologous recombination, induces BRCA2 degradation, and sensitizes cancer cells to poly (ADP-ribose) polymerase-1 inhibition

Proceedings of the National Academy of Sciences - PNAS, 2011-06, Vol.108 (24), p.9851-9856

2011

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Human IgE+ B cells are derived from T cell–dependent and T cell–independent pathways

Journal of allergy and clinical immunology, 2014-09, Vol.134 (3), p.688-697.e6

2014

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Morbidly Obese Human Subjects Have Increased Peripheral Blood CD4+ T Cells With Skewing Toward a Treg- and Th2-Dominated Phenotype

Diabetes (New York, N.Y.), 2012-02, Vol.61 (2), p.401-408

2012

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Multicolor Flowcytometric Immunophenotyping Is a Valuable Tool for Detection of Intraocular Lymphoma

Ophthalmology (Rochester, Minn.), 2013-05, Vol.120 (5), p.991-996

2013

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Common variable immunodeficiency and idiopathic primary hypogammaglobulinemia: two different conditions within the same disease spectrum

Haematologica (Roma), 2013-10, Vol.98 (10), p.1617-1623

2013

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Electron beam deposition for nanofabrication: Insights from surface science

Surface science, 2011-02, Vol.605 (3), p.257-266

2011

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B-cell replication history and somatic hypermutation status identify distinct pathophysiologic backgrounds in common variable immunodeficiency

Blood, 2011-12, Vol.118 (26), p.6814-6823

2011

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Shedding of klotho by ADAMs in the kidney

American journal of physiology. Renal physiology, 2015-08, Vol.309 (4), p.F359-F368

2015

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Genetic defects in PI3Kδ affect B-cell differentiation and maturation leading to hypogammaglobulineamia and recurrent infections

Clinical immunology (Orlando, Fla.), 2017-03, Vol.176, p.77-86

2017

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Psychological Symptoms in Primary Immunodeficiencies: a Common Comorbidity?

Journal of clinical immunology, 2022-04, Vol.42 (3), p.695-698

2022

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Immunoglobulin Replacement Therapy Versus Antibiotic Prophylaxis as Treatment for Incomplete Primary Antibody Deficiency

Journal of clinical immunology, 2021-02, Vol.41 (2), p.382-392

2021

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Diagnostic exome sequencing in 266 Dutch patients with visual impairment

European journal of human genetics : EJHG, 2017-05, Vol.25 (5), p.591-599

2017

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Molecular phenotyping and functional assessment of smooth muscle-like cells with pathogenic variants in aneurysm genes ACTA2, MYH11, SMAD3 and FBN1

Human molecular genetics, 2021-11, Vol.30 (23), p.2286-2299

2021

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Rendu-Osler-Weber disease: update of medical and dental considerations

A report on 10 new patients with heterozygous mutations in the COL11A1 gene and a review of genotype-phenotype correlations in type XI collagenopathies

Contribution of CYLN2 and GTF2IRD1 to neurological and cognitive symptoms in Williams Syndrome

Germline Mutations in RASA1 Are Not Found in Patients with Klippel-Trenaunay Syndrome or Capillary Malformation with Limb Overgrowth

Interstitial deletion in 3q in a patient with blepharophimosis‐ptosis‐epicanthus inversus syndrome (BPES) and microcephaly, mild mental retardation and growth delay: Clinical report and review of the literature

Saccade dysmetria in Williams–Beuren syndrome

Interstitial deletion in 3q in a patient with blepharophimosis-ptosis-epicanthus inversus syndrome (BPES) and microcephaly, mild mental retardation and growth delay: Clinical report and review of the literature

Therapietrouw versus therapiebewustzijn; een klein verschil met grote gevolgen

Verslag van een GVO-project ‘Omgaan met geneesmiddelen’

Ingezonden

Ingezonden

Primary immunodeficiencies in the Netherlands: National patient data demonstrate the increased risk of malignancy

Mild hyperthermia inhibits homologous recombination, induces BRCA2 degradation, and sensitizes cancer cells to poly (ADP-ribose) polymerase-1 inhibition

Human IgE+ B cells are derived from T cell–dependent and T cell–independent pathways

Morbidly Obese Human Subjects Have Increased Peripheral Blood CD4+ T Cells With Skewing Toward a Treg- and Th2-Dominated Phenotype

Multicolor Flowcytometric Immunophenotyping Is a Valuable Tool for Detection of Intraocular Lymphoma

Common variable immunodeficiency and idiopathic primary hypogammaglobulinemia: two different conditions within the same disease spectrum

Electron beam deposition for nanofabrication: Insights from surface science

B-cell replication history and somatic hypermutation status identify distinct pathophysiologic backgrounds in common variable immunodeficiency

Shedding of klotho by ADAMs in the kidney

Genetic defects in PI3Kδ affect B-cell differentiation and maturation leading to hypogammaglobulineamia and recurrent infections

Psychological Symptoms in Primary Immunodeficiencies: a Common Comorbidity?

Immunoglobulin Replacement Therapy Versus Antibiotic Prophylaxis as Treatment for Incomplete Primary Antibody Deficiency

Diagnostic exome sequencing in 266 Dutch patients with visual impairment

Molecular phenotyping and functional assessment of smooth muscle-like cells with pathogenic variants in aneurysm genes ACTA2, MYH11, SMAD3 and FBN1

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