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Primary tumor sidedness has an impact on prognosis and treatment outcome in metastatic colorectal cancer: results from two randomized first-line panitumumab studies

Annals of oncology, 2017-08, Vol.28 (8), p.1862-1868

2017

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Genetics of microtia and associated syndromes

Journal of Medical Genetics, 2009-06, Vol.46 (6), p.361-369

2009

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The Complexity of Age-Related Hearing Impairment: Contributing Environmental and Genetic Factors

Audiology & neurotology, 2007-01, Vol.12 (6), p.345-358

2007

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Hotspot DAXX, PTCH2 and CYFIP2 mutations in pancreatic neuroendocrine neoplasms

Endocrine-related cancer, 2019-01, Vol.26 (1), p.1-12

2019

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Broadening the phenotype of LRP2 mutations: a new mutation in LRP2 causes a predominantly ocular phenotype suggestive of Stickler syndrome

Clinical genetics, 2014-09, Vol.86 (3), p.282-286

2014

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Cardiovascular disease prevention

Acta clinica belgica (English ed. Online), 2014-12, Vol.69 (6), p.407-411

Van Camp, G.

2014

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KCNQ4: a gene for age-related hearing impairment?

Human mutation, 2006-10, Vol.27 (10), p.1007-1016

2006

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Risk of valvular heart disease associated with the use of dopamine agonists in Parkinson’s disease: a systematic review

Journal of Neural Transmission, 2009-02, Vol.116 (2), p.179-191

2009

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Candidate Gene Association Study for Noise‐induced Hearing Loss in Two Independent Noise‐exposed Populations

Annals of human genetics, 2009-03, Vol.73 (2), p.215-224

2009

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A large deletion in GPR98 causes type IIC Usher syndrome in male and female members of an Iranian family

Journal of medical genetics, 2009-04, Vol.46 (4), p.272-276

2009

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Search for a genetic cause in children with unilateral isolated microtia and congenital aural atresia

European archives of oto-rhino-laryngology, 2023-02, Vol.280 (2), p.623-631

2023

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Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11

Clinical genetics, 2008-09, Vol.74 (3), p.223-232

2008

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P038 Early detection of breast cancer in liquid biopsies using DNA methylation markers

Breast (Edinburgh), 2023-04, Vol.68, p.S30-S31

2023

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Heart failure with preserved ejection fraction or non-cardiac dyspnea in paroxysmal atrial fibrillation: The role of left atrial strain

International journal of cardiology, 2021-01, Vol.323, p.161-167

2021

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The reduction in glutamate release is predictive of cognitive and emotional alterations that are corrected by the positive modulator of AMPA receptors S 47445 in perinatal stressed rats

Neuropharmacology, 2018-06, Vol.135, p.284-296

2018

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Involvement of T-cell receptor-beta alterations in the development of otosclerosis linked to OTSC2

Genes and immunity, 2010-04, Vol.11 (3), p.246-253

2010

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The prognostic value of KRAS, NRAS, BRAF and DNA mismatch repair (MMR) status in left- and right-sided metastatic colorectal cancer (mCRC): A Belgian population-based study

Annals of oncology, 2018-10, Vol.29, p.viii196-viii196

2018

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Comparing survival in left-sided and right-sided colorectal carcinoma: A Belgian population-based study

Annals of oncology, 2018-06, Vol.29, p.v98-v98

2018

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Mitral regurgitation in patients with aortic stenosis undergoing valve replacement

Heart, 2010-01, Vol.96 (1), p.9-14

2010

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Detection of mutations and copy number alterations in circulating DNA from pancreatic neuroendocrine tumor patients

Annals of oncology, 2018-10, Vol.29, p.viii477-viii477

2018

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Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss

Human mutation, 1998, Vol.11 (5), p.387-394

1998

Volltextzugriff (PDF)

Potentiometric sensors doped with biomolecules as a new approach to small molecule/biomolecule binding kinetics analysis

Biosensors & bioelectronics, 2014-04, Vol.54, p.515-520

2014

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Characterization of the resistome and predominant genetic lineages of Gram-positive bacteria causing keratitis

Antimicrobial agents and chemotherapy, 2024-03, Vol.68 (3), p.e0124723

2024

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A genotype-phenotype correlation for GJB2 (connexin 26) deafness

Journal of medical genetics, 2004-03, Vol.41 (3), p.147-154

2004

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Heart valvular disease in patients with Parkinson's disease treated with high-dose pergolide

Neurology, 2003-09, Vol.61 (6), p.859

2003

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Primary tumor sidedness has an impact on prognosis and treatment outcome in metastatic colorectal cancer: results from two randomized first-line panitumumab studies

Genetics of microtia and associated syndromes

The Complexity of Age-Related Hearing Impairment: Contributing Environmental and Genetic Factors

Hotspot DAXX, PTCH2 and CYFIP2 mutations in pancreatic neuroendocrine neoplasms

Broadening the phenotype of LRP2 mutations: a new mutation in LRP2 causes a predominantly ocular phenotype suggestive of Stickler syndrome

Cardiovascular disease prevention

KCNQ4: a gene for age-related hearing impairment?

Risk of valvular heart disease associated with the use of dopamine agonists in Parkinson’s disease: a systematic review

Candidate Gene Association Study for Noise‐induced Hearing Loss in Two Independent Noise‐exposed Populations

A large deletion in GPR98 causes type IIC Usher syndrome in male and female members of an Iranian family

Search for a genetic cause in children with unilateral isolated microtia and congenital aural atresia

Mutation analysis of TMC1 identifies four new mutations and suggests an additional deafness gene at loci DFNA36 and DFNB7/11

P038 Early detection of breast cancer in liquid biopsies using DNA methylation markers

Heart failure with preserved ejection fraction or non-cardiac dyspnea in paroxysmal atrial fibrillation: The role of left atrial strain

The reduction in glutamate release is predictive of cognitive and emotional alterations that are corrected by the positive modulator of AMPA receptors S 47445 in perinatal stressed rats

Involvement of T-cell receptor-beta alterations in the development of otosclerosis linked to OTSC2

The prognostic value of KRAS, NRAS, BRAF and DNA mismatch repair (MMR) status in left- and right-sided metastatic colorectal cancer (mCRC): A Belgian population-based study

Comparing survival in left-sided and right-sided colorectal carcinoma: A Belgian population-based study

Mitral regurgitation in patients with aortic stenosis undergoing valve replacement

Detection of mutations and copy number alterations in circulating DNA from pancreatic neuroendocrine tumor patients

Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss

Potentiometric sensors doped with biomolecules as a new approach to small molecule/biomolecule binding kinetics analysis

Characterization of the resistome and predominant genetic lineages of Gram-positive bacteria causing keratitis

A genotype-phenotype correlation for GJB2 (connexin 26) deafness

Heart valvular disease in patients with Parkinson's disease treated with high-dose pergolide

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