J. Drenth

发表

Endurance run increases circulating IL-6 and IL-1ra but downregulates ex vivo TNF-alpha and IL-1 beta production.

S. Van Uum, J. V. D. van der Meer, M. Deuren, 1995, Journal of applied physiology.

Genetic analysis as a valuable key to diagnosis and treatment of periodic Fever.

P. Tighe, J. V. D. van der Meer, M. van Deuren, 2001, Archives of internal medicine.

Specific glycosylation of α1-acid glycoprotein characterises patients with familial Mediterranean fever and obligatory carriers of MEFV

J. Bijzet, W. van Dijk, J. Drenth, 2001, Annals of the rheumatic diseases.

Familial periodic fever and amyloidosis due to a new mutation in the TNFRSF1A gene.

C. Dodé, J. V. D. van der Meer, A. Simon, 2001, The American journal of medicine.

Cytokine activation during attacks of the hyperimmunoglobulinemia D and periodic fever syndrome.

C. Schalkwijk, J. V. D. van der Meer, M. van Deuren, 1995, Blood.

Mevalonate kinase deficiency

H. Scheffer, R. Wevers, H. Kremer, 2004, Neurology.

The revised Atlanta criteria more accurately reflect severity of post-ERCP pancreatitis compared to the consensus criteria

E. van Geenen, N.G. Venneman, J. Buxbaum, 2019, United European gastroenterology journal.

Safety and efficacy of different lanreotide doses in the treatment of polycystic liver disease: pooled analysis of individual patient data

F. Nevens, B. Bammens, R. Vanslembrouck, 2013, Alimentary pharmacology & therapeutics.

Safety and ef fi cacy of different lanreotide doses in the treatment of polycystic liver disease : pooled analysis of individual patient data

F. Nevens, B. Bammens, R. Vanslembrouck, 2013 .

Somatostatin analogues reduce liver volume in polycystic liver disease

L. van Keimpema, R. D. de Man, J. Drenth, 2008, Gut.

Anti-cyclic citrullinated peptide positivity in non-rheumatoid arthritis disease samples: citrulline-dependent or not?

A. Dall'aglio, W. V. van Venrooij, F. Bianchi, 2006, Annals of the rheumatic diseases.

Receptor-mediated C-kinase activation contributes to alpha-adrenergic tone in rat mesenteric resistance artery.

V. Nouailhetas, J. Nishimura, J. Drenth, 1989, Journal of hypertension. Supplement : official journal of the International Society of Hypertension.

Familial Mediterranean fever and hyperimmunoglobulinemia D syndrome: two diseases with distinct clinical, serologic, and genetic features.

M. Pras, E. Pras, J. V. D. van der Meer, 1997, The Journal of rheumatology.

Serum amyloid A serum concentrations and genotype do not explain low incidence of amyloidosis in Hyper-IgD syndrome

J. Meer, A. Simon, J. Bijzet, 2005, Amyloid : the international journal of experimental and clinical investigation : the official journal of the International Society of Amyloidosis.

Nav1.7-related small fiber neuropathy

S. Dib-Hajj, S. Waxman, G. Lauria, 2012, Neurology.

Cutaneous manifestations and histologic findings in the hyperimmunoglobulinemia D syndrome. International Hyper IgD Study Group.

J. V. D. van der Meer, J. Drenth, B. W. Boom, 1994, Archives of dermatology.

Occurrence of arthritis in hyperimmunoglobulinaemia D.

A. Prieur, J. Drenth, 1993, Annals of the rheumatic diseases.

Approach to genetic analysis in the diagnosis of hereditary autoinflammatory syndromes.

A. Simon, K. Yoshimura, J. Drenth, 2006, Rheumatology.

Effect of inflammatory attacks in the classical type hyper‐IgD syndrome on immunoglobulin D, cholesterol and parameters of the acute phase response

J. van der Meer, A. Simon, J. Bijzet, 2004, Journal of internal medicine.

More on clinical renal genetics.

F. Nevens, C. Antignac, M. Kalbáčová, 2010, Clinical journal of the American Society of Nephrology : CJASN.

University of Birmingham A Placebo-Controlled Trial of Obeticholic Acid in Primary Biliary Cholangitis

A. Floreani, K. Kowdley, M. Trauner, 2016 .

Lovastatin inhibits formation of AA amyloid

J. Meer, B. Kluve-Beckerman, A. Simon, 2008, Journal of leukocyte biology.

Unstimulated peripheral blood mononuclear cells from patients with the hyper-IgD syndrome produce cytokines capable of potent induction of C-reactive protein and serum amyloid A in Hep3B cells.

J. V. D. van der Meer, I. Kushner, J. Drenth, 1996, Journal of immunology.

Immunoglobulin D enhances the release of tumour necrosis factor‐α, and interleukin‐1β as well as interleukin‐1 receptor antagonist from human mononuclear cells

M. Daha, J. V. D. van der Meer, J. van der Meer, 1996, Immunology.

A semi-quantitative reverse transcriptase polymerase chain reaction method for measurement of MRNA for TNF-alpha and IL-1 beta in whole blood cultures: its application in typhoid fever and exentric exercise.

M. Netea, E. Dharmana, J. V. D. van der Meer, 1996, Cytokine.

Milder clinical hyperimmunoglobulin E syndrome phenotype is associated with partial interleukin‐17 deficiency

B. Kullberg, F. L. van de Veerdonk, F. Veerdonk, 2010, Clinical and experimental immunology.

Increased susceptibility of serum amyloid A 1.1 to degradation by MMP-1: potential explanation for higher risk of type AA amyloidosis.

H. O. D. op den Camp, T. Yamada, A. Simon, 2008, Rheumatology.

Chronic anemia due to gastrointestinal bleeding: when do gastroenterologists transfuse?

E. van Geenen, W. Kievit, J. Drenth, 2017, United European gastroenterology journal.

Paediatric hypertension-associated erythromelalgia responds to corticosteroids and is not associated with SCN9A mutations.

A. Borzutzky, J. Salomon, J. Drenth, 2012, Rheumatology.

Interferon‐γ and urine neopterin in attacks of the hyperimmunoglobulinaemia D and periodic fever syndrome

J. Meer, J. Drenth, N. S. Brown, 1995, European journal of clinical investigation.

Elevated serum level and altered glycosylation of alpha 1-acid glycoprotein in hyperimmunoglobulinemia D and periodic fever syndrome: evidence for persistent inflammation.

J. V. D. van der Meer, J. van der Meer, E. C. van Ommen, 1995, Clinical immunology and immunopathology.

Activation of the cytokine network in familial Mediterranean fever.

D. Zemer, M. Pras, J. V. D. van der Meer, 1999, The Journal of rheumatology.

Iron saturation of serum ferritin in patients with adult onset Still's disease.

M. Kahn, J. Drenth, J. ten Kate, 2001, The Journal of rheumatology.

Efficacy of diltiazem in the treatment of diffuse oesophageal spasm

J. Drenth, L. Engels, L. Bos, 1990, Alimentary pharmacology & therapeutics.

Acute renal failure associated with paracetamol ingestion in an alcoholic patient.

J. V. D. van der Meer, J. Drenth, E. Wuis, 1994, Nephron.

Hereditary fevers.

M. Delpech, J. Drenth, G. Grateau, 1999, Current Opinion in Rheumatology.

Hyperimmunoglobulinaemia D syndrome in India: report of two siblings with a novel mutation

J. Drenth, A. Lawrence, F. Hol, 2006, Annals of the rheumatic diseases.

Limited efficacy of thalidomide in the treatment of febrile attacks of the hyper-IgD and periodic fever syndrome: a randomized, double-blind, placebo-controlled trial.

J. Meer, A. Vonk, R. Powell, 2001, The Journal of pharmacology and experimental therapeutics.

Hyper-IgD syndrome and familial Hibernian fever are true periodic fever syndromes.

J. Drenth, R. Powell, 2000, The Journal of pediatrics.

Hyper-IgD syndrome and pregnancy.

J. V. D. van der Meer, J. Drenth, J. D. de Hullu, 1996, European journal of obstetrics, gynecology, and reproductive biology.

Genetic linkage of the Muckle-Wells syndrome to chromosome 1q44.

J. Beckmann, D. Scott, David Steven Scott, 1999, American journal of human genetics.

Circulating and ex vivo production of pyrogenic cytokines and interleukin-1 receptor antagonist in 123 patients with fever of unknown origin. The Netherlands Fever of Unknown Origin Study Group.

J. V. D. van der Meer, P. Demacker, J. Drenth, 1997, Journal of Infectious Diseases.

Chronic yersiniosis due to defects in the TLR5 and NOD2 recognition pathways.

L. Joosten, M. Netea, D. Jong, 2010, The Netherlands journal of medicine.

Termination of ouabain-induced ventricular tachycardia by flunarizine in conscious dogs.

H. Wellens, M. Vos, A. Gorgels, 1989, European journal of pharmacology.

A Risk Assessment of Factors for the Presence of Angiodysplasias During Endoscopy and Factors Contributing to Symptomatic Bleeding and Rebleeds

E. V. van Geenen, J. Drenth, G. Holleran, 2019, Digestive Diseases and Sciences.

Whole‐blood cultures: a valid and reliable tool for studying cytokines in exercise

J. V. D. van der Meer, J. Drenth, 1999, European journal of clinical investigation.

[Hyperimmunoglobulin D syndrome].

A. Prieur, J. V. D. van der Meer, J. Drenth, 1995, Presse medicale.

AL amyloidosis enhances development of amyloid A amyloidosis

J. Meer, A. Simon, J. Drenth, 2007, The British journal of dermatology.

Premature escape beats. A model for triggered activity in the intact heart?

B. de Wit, H. Wellens, M. Vos, 1990, Circulation.

Hereditary periodic fever.

J. Drenth, J. V. D. van der Meer, J. Drenth, 2001, The New England journal of medicine.

Effect of etanercept and anakinra on inflammatory attacks in the hyper-IgD syndrome: introducing a vaccination provocation model.

J. Meer, J. Drenth, A. Simon, 2005, The Netherlands journal of medicine.

Mevalonate kinase deficiency: Evidence for a phenotypic continuum

A. Simon, J. Drenth, H. Scheffer, 2004 .

Heterozygous alpha-I antitrypsin deficiency as a co-factor in the development of chronic liver disease: a review.

R. D. de Man, J. Drenth, R. Houwen, 2007, The Netherlands journal of medicine.

NaV1.7 Gain-of-Function Mutations as a Continuum: A1632E Displays Physiological Changes Associated with Erythromelalgia and Paroxysmal Extreme Pain Disorder Mutations and Produces Symptoms of Both Disorders

S. Dib-Hajj, S. Waxman, J. Drenth, 2008, The Journal of Neuroscience.

Polymorphisms of UDP-glucuronosyltransferase 1A7 are not involved in pancreatic diseases

H. Friess, B. Künzli, A. Kage, 2005, Journal of Medical Genetics.

S. Dib-Hajj, S. Waxman, R. T. Morsche, 2008, The Journal of Neuroscience.

On-demand anakinra treatment is effective in mevalonate kinase deficiency

J. Drenth, J. Frenkel, E. Bodar, 2011, Annals of the rheumatic diseases.