Gert Matthijs

Gert Matthijs

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Gert Matthijs

Publications by authors named "Gert Matthijs"

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Clinical Utility Gene Card for: PGM3 defective congenital disorder of glycosylation.

Eur J Hum Genet 2019 Nov 23;27(11):1757-1760. Epub 2019 Jun 23.

Department of Human Genetics, KU Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1038/s41431-019-0453-yDOI Listing
November 2019

Use of Endoglycosidase H as a diagnostic tool for MAN1B1-CDG patients.

Electrophoresis 2018 12 2;39(24):3133-3141. Epub 2018 Aug 2.

CNRS, UMR 8576-UGSF-Unité de Glycobiologie Structurale et Fonctionnelle, Univ. Lille, Lille, France.

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http://dx.doi.org/10.1002/elps.201800020DOI Listing
December 2018

Congenital disorders of glycosylation (CDG): Quo vadis?

Eur J Med Genet 2018 Nov 25;61(11):643-663. Epub 2017 Oct 25.

Center for Metabolic Diseases, KU Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1016/j.ejmg.2017.10.012DOI Listing
November 2018

Clinical Utility Gene Card For: GALNT3 defective congenital disorder of glycosylation.

Eur J Hum Genet 2018 08 23;26(8):1230-1233. Epub 2018 Apr 23.

Department of Human Genetics, KU Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1038/s41431-017-0002-5DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6057978PMC
August 2018

Consensus document on the implementation of next generation sequencing in the genetic diagnosis of hereditary cancer.

Med Clin (Barc) 2018 07 10;151(2):80.e1-80.e10. Epub 2018 Feb 10.

Molecular Diagnostic Unit, Hereditary Cancer Program, IDIBELL-Catalan Institute of Oncology, L'Hospitalet del Llobregat, Barcelona, Spain. Electronic address:

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http://dx.doi.org/10.1016/j.medcli.2017.12.010DOI Listing
July 2018

Investigating the function of Gdt1p in yeast Golgi glycosylation.

Biochim Biophys Acta Gen Subj 2018 Mar 3;1862(3):394-402. Epub 2017 Nov 3.

Univ. Lille, CNRS, UMR 8576 - UGSF - Unité de Glycobiologie Structurale et Fonctionnelle, F-59000 Lille, France; LIA GLYCOLAB4CDG France/Belgium (International Associated Laboratory "Laboratory for the Research on Congenital Disorders of Glycosylation - from cellular mechanisms to cure", France. Electronic address:

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http://dx.doi.org/10.1016/j.bbagen.2017.11.006DOI Listing
March 2018

Patient with confirmed LEOPARD syndrome developing multiple melanoma.

Dermatol Pract Concept 2018 Jan 31;8(1):59-62. Epub 2018 Jan 31.

Department of Dermatology, Cliniques Universitaires Saint-Luc, Université Catholique de Louvain, Brussels, Belgium.

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http://dx.doi.org/10.5826/dpc.0801a14DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5808376PMC
January 2018

PMM2-CDG and sensorineural hearing loss.

J Inherit Metab Dis 2017 09 31;40(5):629-630. Epub 2017 Jul 31.

Department of Development and Regeneration, KU Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1007/s10545-017-0073-zDOI Listing
September 2017

Manganese-induced turnover of TMEM165.

Biochem J 2017 04 19;474(9):1481-1493. Epub 2017 Apr 19.

CNRS, UMR 8576 - UGSF - Unité de Glycobiologie Structurale et Fonctionnelle, Université de Lille, Lille F-59000, France and the LIA GLYCOLAB4CDG France/ Belgium (International Associated Laboratory "Laboratory for the Research on Congenital Disorders of Glycosylation - from cellular mechanisms to cure")

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http://dx.doi.org/10.1042/BCJ20160910DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5595065PMC
April 2017

Galactose Supplementation in Patients With TMEM165-CDG Rescues the Glycosylation Defects.

J Clin Endocrinol Metab 2017 Apr;102(4):1375-1386

Université Lille, Centre National de la Recherche Française, UMR 8576-Unité de Glycobiologie Structurale et Fonctionnelle-Unité de Glycobiologie Structurale et Fonctionnelle, F-59000 Lille, France.

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http://dx.doi.org/10.1210/jc.2016-3443DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6283449PMC
April 2017

Detecting AGG Interruptions in Male and Female FMR1 Premutation Carriers by Single-Molecule Sequencing.

Hum Mutat 2017 03 17;38(3):324-331. Epub 2017 Jan 17.

Department of Human Genetics, KU Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1002/humu.23150DOI Listing
March 2017

Galactose Epimerase Deficiency: Expanding the Phenotype.

JIMD Rep 2017 1;37:19-25. Epub 2017 Mar 1.

Unidade de Doenças Metabólicas, Centro de Desenvolvimento da Criança, Hospital Pediátrico - Centro Hospitalar e Universitário de Coimbra, EPE, Avenida Afonso Romão, Coimbra, 3000-206, Portugal.

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http://dx.doi.org/10.1007/8904_2017_10DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5740041PMC
March 2017

Clinical utility gene card for: B4GALT7-defective congenital disorder of glycosylation.

Eur J Hum Genet 2017 02 9;25(2). Epub 2016 Nov 9.

Department of Human Genetics, Centre for Human Genetics, KULeuven, Leuven, Belgium.

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http://dx.doi.org/10.1038/ejhg.2016.151DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5255951PMC
February 2017

Clinical utility gene card for: Peters plus syndrome.

Eur J Hum Genet 2016 08 6;24(8). Epub 2016 Apr 6.

Centre for Human Genetics, KU Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1038/ejhg.2016.32DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4970696PMC
August 2016

Clinical utility gene card for: MAN1B1 defective congenital disorder of glycosylation.

Eur J Hum Genet 2016 07 18;24(7). Epub 2015 Nov 18.

Centre for Human Genetics, KULeuven, Leuven, Belgium.

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http://dx.doi.org/10.1038/ejhg.2015.248DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5070899PMC
July 2016

Glycosylation abnormalities in Gdt1p/TMEM165 deficient cells result from a defect in Golgi manganese homeostasis.

Hum Mol Genet 2016 Apr 1;25(8):1489-500. Epub 2016 Feb 1.

Univ. Lille, CNRS, UMR 8576 - UGSF - Unité de Glycobiologie Structurale et Fonctionnelle, F-59000 Lille, France,

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http://dx.doi.org/10.1093/hmg/ddw026DOI Listing
April 2016

Serum transferrin carrying the xeno-tetrasaccharide NeuAc-Gal-GlcNAc2 is a biomarker of ALG1-CDG.

J Inherit Metab Dis 2016 Jan 3;39(1):107-14. Epub 2015 Sep 3.

Department of Pediatrics, Clinical Sciences, Lund University, BMC D12, 221 84, Lund, Sweden.

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http://dx.doi.org/10.1007/s10545-015-9884-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4822552PMC
January 2016

Guidelines for diagnostic next-generation sequencing.

Eur J Hum Genet 2016 Jan 28;24(1):2-5. Epub 2015 Oct 28.

University Hospital of Tübingen, Institute of Medical Genetics and Applied Genomics, Tübingen, Germany.

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http://dx.doi.org/10.1038/ejhg.2015.226DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4795226PMC
January 2016

New EuroGentest/ESHG guidelines and a new clinical utility gene card format for NGS-based testing.

Eur J Hum Genet 2016 Jan 28;24(1). Epub 2015 Oct 28.

Institute of Human Genetics, Hannover Medical School, Hannover, Germany.

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http://dx.doi.org/10.1038/ejhg.2015.229DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4795236PMC
January 2016

Clinical utility gene card for: DPAGT1 defective congenital disorder of glycosylation.

Eur J Hum Genet 2015 Dec 5;23(12). Epub 2015 Aug 5.

Department of Human Genetics, Centre for Human Genetics, KU Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1038/ejhg.2015.177DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4795212PMC
December 2015

ALG3-CDG: Report of two siblings with antenatal features carrying homozygous p.Gly96Arg mutation.

Am J Med Genet A 2015 Nov 30;167A(11):2748-54. Epub 2015 Jun 30.

Centre de Référence des Anomalies du Développement, Service de Génétique, Hôpital Femme Mère Enfant, Hospices Civils de Lyon, Bron, France.

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http://dx.doi.org/10.1002/ajmg.a.37232DOI Listing
November 2015

Key features and clinical variability of COG6-CDG.

Mol Genet Metab 2015 Nov 29;116(3):163-70. Epub 2015 Jul 29.

Berlin-Brandenburg Center for Regenerative Therapies, Charité-Universitaetsmedizin Berlin, Berlin, Germany; Institute of Medical Genetics and Human Genetics, Charité-Universitaetsmedizin Berlin, Berlin, Germany; Max Planck Institute for Molecular Genetics, Berlin, Germany. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S10967192153003
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http://dx.doi.org/10.1016/j.ymgme.2015.07.003DOI Listing
November 2015

Clinical utility gene card for: ALG1 defective congenital disorder of glycosylation.

Eur J Hum Genet 2015 Oct 4;23(10). Epub 2015 Feb 4.

Centre for Human Genetics, KU Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1038/ejhg.2015.9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4592101PMC
October 2015

Abnormal cartilage development and altered N-glycosylation in Tmem165-deficient zebrafish mirrors the phenotypes associated with TMEM165-CDG.

Glycobiology 2015 Jun 21;25(6):669-82. Epub 2015 Jan 21.

Complex Carbohydrate Research Center, Department of Biochemistry and Molecular Biology, University of Georgia, Athens, GA 30602, USA

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http://dx.doi.org/10.1093/glycob/cwv009DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4410832PMC
June 2015

Clinical utility gene card for: ALG6 defective congenital disorder of glycosylation.

Eur J Hum Genet 2015 Feb 23;23(2). Epub 2014 Jul 23.

Centre for Human Genetics, KU Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1038/ejhg.2014.146DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4297893PMC
February 2015

Clinical utility gene card for: Phosphomannose isomerase deficiency.

Eur J Hum Genet 2014 Sep 26;22(9). Epub 2014 Feb 26.

Centre for Human Genetics, KU Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1038/ejhg.2014.29DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4135420PMC
September 2014

Clinical utility gene card for: Phosphomannomutase 2 deficiency.

Eur J Hum Genet 2014 Aug 15;22(8). Epub 2014 Jan 15.

Centre for Human Genetics, KU Leuven, Leuven, Belgium.

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http://www.nature.com/articles/ejhg2013298
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http://dx.doi.org/10.1038/ejhg.2013.298DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4350603PMC
August 2014

Exome sequencing reveals HINT1 mutations as a cause of distal hereditary motor neuropathy.

Eur J Hum Genet 2014 Jun 9;22(6):847-50. Epub 2013 Oct 9.

1] Vesalius Research Center, VIB, Leuven, Belgium [2] Department of Experimental Neurology, Leuven Research Institute for Neurodegenerative Diseases (LIND), KU Leuven, Leuven, Belgium [3] Department of Neurology, University Hospital Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1038/ejhg.2013.231DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4023208PMC
June 2014

Asymptomatic phosphomannose isomerase deficiency (MPI-CDG) initially mistaken for excessive alcohol consumption.

Clin Chim Acta 2014 Apr 6;431:15-8. Epub 2014 Feb 6.

Karolinska Institutet, Department of Laboratory Medicine, Stockholm, Sweden; Karolinska University Laboratory, Clinical Chemistry, Stockholm, Sweden.

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http://dx.doi.org/10.1016/j.cca.2014.01.018DOI Listing
April 2014

ALG3-CDG (CDG-Id): clinical, biochemical and molecular findings in two siblings.

Mol Genet Metab 2013 Sep-Oct;110(1-2):170-5. Epub 2013 Jun 7.

Developmental Medicine, Royal Children's Hospital, Melbourne, Australia.

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http://dx.doi.org/10.1016/j.ymgme.2013.05.020DOI Listing
March 2014

Frequency of C9orf72 repeat expansions in amyotrophic lateral sclerosis: a Belgian cohort study.

Neurobiol Aging 2013 Dec 17;34(12):2890.e7-2890.e12. Epub 2013 Jul 17.

Department of Neurology, University of Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1016/j.neurobiolaging.2013.06.009DOI Listing
December 2013

Dolichol kinase deficiency (DOLK-CDG) with a purely neurological presentation caused by a novel mutation.

Mol Genet Metab 2013 Nov 10;110(3):342-4. Epub 2013 Jul 10.

Department of Laboratory Medicine, Karolinska Institutet, Stockholm, Sweden; Karolinska University Laboratory, Stockholm, Sweden. Electronic address:

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http://dx.doi.org/10.1016/j.ymgme.2013.07.002DOI Listing
November 2013

EPCAM germline and somatic rearrangements in Lynch syndrome: identification of a novel 3'EPCAM deletion.

Genes Chromosomes Cancer 2013 Sep 26;52(9):845-54. Epub 2013 Jun 26.

Department of Human Genetics, University Hospital Leuven, 3000 Leuven, Belgium.

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http://dx.doi.org/10.1002/gcc.22080DOI Listing
September 2013

The European BRCA patent oppositions and appeals: coloring inside the lines.

Nat Biotechnol 2013 Aug;31(8):704-10

Center for Human Genetics of the University of Leuven, Belgium.

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http://dx.doi.org/10.1038/nbt.2644DOI Listing
August 2013

Impact of disease-causing mutations on TMEM165 subcellular localization, a recently identified protein involved in CDG-II.

Hum Mol Genet 2013 Jul 10;22(14):2914-28. Epub 2013 Apr 10.

CNRS-UMR 8576, Structural and Functional Glycobiology Unit, IFR 147, University of Lille 1, 59655 Villeneuve d’Ascq, France.

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http://dx.doi.org/10.1093/hmg/ddt146DOI Listing
July 2013

Approaches to homozygosity mapping and exome sequencing for the identification of novel types of CDG.

Glycoconj J 2013 Jan 15;30(1):67-76. Epub 2012 Sep 15.

Center for Human Genetics, University of Leuven, Herestraat 49, 3000, Leuven, Belgium.

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http://dx.doi.org/10.1007/s10719-012-9445-7DOI Listing
January 2013

DPAGT1-CDG: report of a patient with fetal hypokinesia phenotype.

Am J Med Genet A 2012 Aug 11;158A(8):2027-30. Epub 2012 Jul 11.

San Pedro de Alcántara Hospital, Neonatology Unit, Cáceres, Spain.

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http://dx.doi.org/10.1002/ajmg.a.35472DOI Listing
August 2012

TMEM165 deficiency causes a congenital disorder of glycosylation.

Am J Hum Genet 2012 Jul 7;91(1):15-26. Epub 2012 Jun 7.

Centre National de la Recherche Scientifique UMR, Structural and Functional Glycobiology Unit, University of Lille, Institut Fédératif de Recherche, Villeneuve D'Ascq, France.

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http://dx.doi.org/10.1016/j.ajhg.2012.05.002DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3397274PMC
July 2012

The fate and future of patents on human genes and genetic diagnostic methods.

Nat Rev Genet 2012 05 18;13(6):441-8. Epub 2012 May 18.

Faculty of Pharmaceutical Sciences and Centre for Intellectual Property Rights, University of Leuven, Herestraat 49, B-3000 Leuven, Belgium.

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http://dx.doi.org/10.1038/nrg3255DOI Listing
May 2012

Microfluidic amplification as a tool for massive parallel sequencing of the familial hypercholesterolemia genes.

Clin Chem 2012 Apr 31;58(4):717-24. Epub 2012 Jan 31.

Laboratory for Molecular Diagnosis, Center for Human Genetics, University of Leuven, Leuven, Belgium.

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http://www.clinchem.org/cgi/doi/10.1373/clinchem.2011.173963
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http://dx.doi.org/10.1373/clinchem.2011.173963DOI Listing
April 2012

Patent pools and clearinghouses in the life sciences.

Trends Biotechnol 2011 Nov 4;29(11):569-76. Epub 2011 Jul 4.

Centre for Intellectual Property Rights, University of Leuven, Minderbroedersstraat 5, 3000 Leuven, Belgium.

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http://dx.doi.org/10.1016/j.tibtech.2011.06.002DOI Listing
November 2011

Impact of gene patents on diagnostic testing: a new patent landscaping method applied to spinocerebellar ataxia.

Eur J Hum Genet 2011 Nov 3;19(11):1114-21. Epub 2011 Aug 3.

Centre for Intellectual Property Rights, Faculty of Law, University of Leuven, Herestraat 49, Leuven, Belgium.

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http://dx.doi.org/10.1038/ejhg.2011.109DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3198141PMC
November 2011

Gene and genetic diagnostic method patent claims: a comparison under current European and US patent law.

Eur J Hum Genet 2011 Oct 8;19(10):1104-7. Epub 2011 Jun 8.

Research Centre for Pharmaceutical Care and Pharmaco-Economics, Department of Pharmaceutical Sciences, University of Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1038/ejhg.2011.76DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3190248PMC
October 2011

The CAREGENE study: genetic variants of the endothelium and aerobic power in patients with coronary artery disease.

Acta Cardiol 2011 Aug;66(4):407-14

Cardiovascular Rehabilitation Unit, Department of Rehabilitation Sciences, Katholieke Universiteit Leuven, Belgium.

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http://dx.doi.org/10.2143/AC.66.4.2126586DOI Listing
August 2011

Differential effects of lobe A and lobe B of the Conserved Oligomeric Golgi complex on the stability of {beta}1,4-galactosyltransferase 1 and {alpha}2,6-sialyltransferase 1.

Glycobiology 2011 Jul 8;21(7):864-76. Epub 2010 Nov 8.

Unité de Glycobiologie Structurale et Fonctionnelle UMR/CNRS 8576, IFR147, Université des Sciences et Technologies de Lille, Villeneuve d'Ascq, France.

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http://dx.doi.org/10.1093/glycob/cwq176DOI Listing
July 2011

How Golgi glycosylation meets and needs trafficking: the case of the COG complex.

Glycobiology 2011 Jul 26;21(7):853-63. Epub 2010 Nov 26.

Laboratory for Membrane Trafficking, Center for Human Genetics, KULeuven, Department for Molecular and Developmental Genetics (VIB), Leuven, Belgium.

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http://dx.doi.org/10.1093/glycob/cwq179DOI Listing
July 2011

Identification of phosphorylated oligosaccharides in cells of patients with a congenital disorders of glycosylation (CDG-I).

Biochimie 2011 May 16;93(5):823-33. Epub 2011 Feb 16.

Laboratory for Molecular Diagnosis, Center for Human Genetics, University of Leuven, B-3000 Leuven, Belgium.

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http://dx.doi.org/10.1016/j.biochi.2011.01.016DOI Listing
May 2011

A standardized framework for the validation and verification of clinical molecular genetic tests.

Eur J Hum Genet 2010 Dec 28;18(12):1276-88. Epub 2010 Jul 28.

National Genetics Reference Laboratory (Wessex), Salisbury District Hospital, Salisbury, UK.

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http://dx.doi.org/10.1038/ejhg.2010.101DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3002854PMC
December 2010

A novel mutation and first report of dilated cardiomyopathy in ALG6-CDG (CDG-Ic): a case report.

Orphanet J Rare Dis 2010 Apr 16;5. Epub 2010 Apr 16.

Department of Medical Genetics, King Faisal Specialist Hospital and Research Centre, Riyadh, Saudi Arabia.

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http://dx.doi.org/10.1186/1750-1172-5-7DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2861021PMC
April 2010

Screening for OST deficiencies in unsolved CDG-I patients.

Biochem Biophys Res Commun 2009 Dec 14;390(3):769-74. Epub 2009 Oct 14.

Laboratory for Molecular Diagnosis, Center for Human Genetics, University of Leuven, B-3000 Leuven, Belgium.

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http://dx.doi.org/10.1016/j.bbrc.2009.10.047DOI Listing
December 2009

A new mutation in COG7 extends the spectrum of COG subunit deficiencies.

Eur J Med Genet 2009 Sep-Oct;52(5):303-5. Epub 2009 Jul 3.

Department of Paediatrics, University Hospitals Leuven, Leuven BE-3000, Belgium.

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http://dx.doi.org/10.1016/j.ejmg.2009.06.006DOI Listing
November 2009

RFT1 deficiency in three novel CDG patients.

Hum Mutat 2009 Oct;30(10):1428-34

Laboratory for Molecular Diagnosis, Center for Human Genetics, University of Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1002/humu.21085DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3869400PMC
October 2009

Legal uncertainty in the area of genetic diagnostic testing.

Nat Biotechnol 2009 Oct;27(10):903-9

Centre for Intellectual Property Rights, Faculty of Law, Catholic University of Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1038/nbt1009-903DOI Listing
October 2009

Golgi function and dysfunction in the first COG4-deficient CDG type II patient.

Hum Mol Genet 2009 Sep 3;18(17):3244-56. Epub 2009 Jun 3.

and Department for Molecular and Developmental Genetics, Laboratory for Membrane Trafficking, Center for Human Genetics, University of Leuven VIB, B-3000 Leuven, Belgium.

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http://dx.doi.org/10.1093/hmg/ddp262DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2722986PMC
September 2009

From glycosylation to glycosylation diseases.

Biochim Biophys Acta 2009 Sep;1792(9):823

Center for Metabolic Diseases, University Hospital Gasthuisberg, Herestraat, 49, BE-3000 Leuven, Belgium.

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http://dx.doi.org/10.1016/j.bbadis.2009.08.003DOI Listing
September 2009

CDG nomenclature: time for a change!

Biochim Biophys Acta 2009 Sep;1792(9):825-6

Center for Metabolic Disease, Katholieke Universiteit Leuven, BE-3000 Leuven, Belgium.

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http://dx.doi.org/10.1016/j.bbadis.2009.08.005DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3917312PMC
September 2009

Quality control of glycoproteins bearing truncated glycans in an ALG9-defective (CDG-IL) patient.

Glycobiology 2009 Aug 18;19(8):910-7. Epub 2009 May 18.

Laboratory for Molecular Diagnosis, Center for Human Genetics, University of Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1093/glycob/cwp067DOI Listing
August 2009