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Nav1.7-related small fiber neuropathy: impaired slow-inactivation and DRG neuron hyperexcitability

Neurology, 2012-05, Vol.78 (21), p.1635

2012

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Inulin significantly improves serum magnesium levels in proton pump inhibitor‐induced hypomagnesaemia

Alimentary pharmacology & therapeutics, 2016-06, Vol.43 (11), p.1178-1185

2016

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Hepatic cyst penetration of cefazolin in patients receiving aspiration sclerotherapy

Journal of antimicrobial chemotherapy, 2016-09, Vol.71 (9), p.2547-2552

2016

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Long-term olive oil-based parenteral nutrition sustains innate immune function in home patients without active underlying disease

Clinical nutrition (Edinburgh, Scotland), 2013-08, Vol.32 (4), p.643-649

2013

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Mutations in serine protease inhibitor Kazal type 1 are strongly associated with chronic pancreatitis

Gut, 2002-05, Vol.50 (5), p.687-692

2002

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Secondary and tertiary structure modeling reveals effects of novel mutations in polycystic liver disease genes PRKCSH and SEC63

Clinical genetics, 2010-07, Vol.78 (1), p.47-56

2010

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Genetic polymorphisms in UDP-glucuronosyltransferases and glutathione S-transferases and colorectal cancer risk

Carcinogenesis (New York), 2004-12, Vol.25 (12), p.2407-2415

2004

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UGT1A7 polymorphisms in chronic pancreatitis: an example of genotyping pitfalls

The pharmacogenomics journal, 2008-02, Vol.8 (1), p.34-41

2008

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Genetic heterogeneity and exclusion of a modifying locus at 2q in a family with autosomal dominant primary erythermalgia

British journal of dermatology (1951), 2005-07, Vol.153 (1), p.174-177

2005

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Catechol-O-methyltransferase (COMT) gene variants and pain in chronic pancreatitis

Netherlands journal of medicine, 2011-07, Vol.69 (7-8), p.330-334

2011

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Prevalence of hepatitis C in the general population in the Netherlands

Netherlands journal of medicine, 2008, Vol.66 (1), p.13-17

2008

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Detoxification enzyme polymorphisms are not involved in duodenal adenomatosis in familial adenomatous polyposis

British journal of surgery, 2008-04, Vol.95 (4), p.499-505

2008

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Genetic polymorphism in UDP-glucuronosyltransferase 2B7 and colorectal cancer risk

Oncology research, 2009, Vol.17 (7), p.323

2009

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Paternal contribution to the risk for pre-eclampsia

Journal of medical genetics, 2002-01, Vol.39 (1), p.44-45

2002

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

Journal of medical genetics, 2005-10, Vol.42 (10), p.e62-e62

2005

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Deletion mutation of sodium channel NaV1.7 in inherited erythromelalgia: enhanced slow inactivation modulates dorsal root ganglion neuron hyperexcitability

Brain (London, England : 1878), 2011-07, Vol.134 (7), p.1972-1986

2011

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

Netherlands journal of medicine, 2010-10, Vol.68 (10), p.310-315

2010

Volltextzugriff (PDF)

Candida-specific interferon-γ deficiency and Toll-like receptor polymorphisms in patients with chronic mucocutaneous candidiasis

Netherlands journal of medicine, 2003-11, Vol.61 (11), p.365-369

2003

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No genetic association between EPHX1 and Crohn’s disease

Gut, 2005-11, Vol.54 (11), p.1659-1660

2005

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Haptoglobin and its association with the HELLP syndrome

Journal of medical genetics, 2003-03, Vol.40 (3), p.214-216

2003

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Genetic Basis of Chronic Pancreatitis

Scandinavian journal of gastroenterology, 2002, Vol.37 (236), p.91-94

2002

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Paroxysmal extreme pain disorder: a molecular lesion of peripheral neurons

Nature reviews. Neurology, 2011-01, Vol.7 (1), p.51

2011

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Characterization of the reactivity pattern of murine monoclonal antibodies against wild‐type hepatitis B surface antigen to g145r and other naturally occurring “a” loop escape mutations

Hepatology (Baltimore, Md.), 1999-11, Vol.30 (5), p.1287-1292

1999

Volltextzugriff (PDF)

Polymorphism in the promoter region of the bilirubin UDP‐glucuronosyltransferase (Gilbert's syndrome) in healthy Dutch subjects

Hepatology (Baltimore, Md.), 2001-03, Vol.33 (3), p.765-765

2001

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Gilbert's syndrome is not associated with HELLP syndrome

BJOG : an international journal of obstetrics and gynaecology, 2001-09, Vol.108 (9), p.1003-1004

2001

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Nav1.7-related small fiber neuropathy: impaired slow-inactivation and DRG neuron hyperexcitability

Inulin significantly improves serum magnesium levels in proton pump inhibitor‐induced hypomagnesaemia

Hepatic cyst penetration of cefazolin in patients receiving aspiration sclerotherapy

Long-term olive oil-based parenteral nutrition sustains innate immune function in home patients without active underlying disease

Mutations in serine protease inhibitor Kazal type 1 are strongly associated with chronic pancreatitis

Secondary and tertiary structure modeling reveals effects of novel mutations in polycystic liver disease genes PRKCSH and SEC63

Genetic polymorphisms in UDP-glucuronosyltransferases and glutathione S-transferases and colorectal cancer risk

UGT1A7 polymorphisms in chronic pancreatitis: an example of genotyping pitfalls

Genetic heterogeneity and exclusion of a modifying locus at 2q in a family with autosomal dominant primary erythermalgia

Catechol-O-methyltransferase (COMT) gene variants and pain in chronic pancreatitis

Prevalence of hepatitis C in the general population in the Netherlands

Detoxification enzyme polymorphisms are not involved in duodenal adenomatosis in familial adenomatous polyposis

Genetic polymorphism in UDP-glucuronosyltransferase 2B7 and colorectal cancer risk

Paternal contribution to the risk for pre-eclampsia

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

Deletion mutation of sodium channel NaV1.7 in inherited erythromelalgia: enhanced slow inactivation modulates dorsal root ganglion neuron hyperexcitability

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

Candida-specific interferon-γ deficiency and Toll-like receptor polymorphisms in patients with chronic mucocutaneous candidiasis

No genetic association between EPHX1 and Crohn’s disease

Haptoglobin and its association with the HELLP syndrome

Genetic Basis of Chronic Pancreatitis

Paroxysmal extreme pain disorder: a molecular lesion of peripheral neurons

Characterization of the reactivity pattern of murine monoclonal antibodies against wild‐type hepatitis B surface antigen to g145r and other naturally occurring “a” loop escape mutations

Polymorphism in the promoter region of the bilirubin UDP‐glucuronosyltransferase (Gilbert's syndrome) in healthy Dutch subjects

Gilbert's syndrome is not associated with HELLP syndrome

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