Publications by authors named "Kristl G Claeys"

88Publications

Clinical and muscle MRI features in a family with tubular aggregate myopathy and novel STIM1 mutation.

Neuromuscul Disord 2020 Sep 1;30(9):709-718. Epub 2020 Aug 1.

Department of Neurology, Neuromuscular Reference Centre, University Hospitals Leuven, Herestraat 49, 3000, Leuven, Belgium; Laboratory for Muscle diseases and Neuropathies, Department of Neurosciences, KU Leuven, Herestraat 49, 3000, Leuven, Belgium. Electronic address:

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http://dx.doi.org/10.1016/j.nmd.2020.07.010DOI Listing
September 2020

White matter brain lesions in infantile-onset Pompe disease are not metabolically active using F-FDG PET/MR imaging.

Neuromuscul Disord 2020 Sep 4;30(9):732-733. Epub 2020 Aug 4.

Department of Radiology, University Hospitals Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1016/j.nmd.2020.07.013DOI Listing
September 2020

Myositis as a neuromuscular complication of immune checkpoint inhibitors.

Acta Neurol Belg 2020 Apr 29;120(2):355-364. Epub 2020 Jan 29.

Department of Neurology, University Hospitals Leuven, Herestraat 49, 3000, Leuven, Belgium.

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http://dx.doi.org/10.1007/s13760-020-01282-wDOI Listing
April 2020

Congenital myopathies: an update.

Authors:
Kristl G Claeys

Dev Med Child Neurol 2020 03 2;62(3):297-302. Epub 2019 Oct 2.

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

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http://dx.doi.org/10.1111/dmcn.14365DOI Listing
March 2020

Serum neurofilament heavy chains as early marker of motor neuron degeneration.

Ann Clin Transl Neurol 2019 10 13;6(10):1971-1979. Epub 2019 Sep 13.

Laboratory for Molecular Neurobiomarker Research, Department of Neurosciences, KU Leuven, Leuven, Belgium.

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http://dx.doi.org/10.1002/acn3.50890DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6801162PMC
October 2019

Inflammatory markers in cerebrospinal fluid: independent prognostic biomarkers in amyotrophic lateral sclerosis?

J Neurol Neurosurg Psychiatry 2019 12 7;90(12):1338-1346. Epub 2019 Jun 7.

Department of Neurosciences, Laboratory for Molecular Neurobiomarker Research, KU Leuven, Leuven, Belgium

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http://dx.doi.org/10.1136/jnnp-2018-319586DOI Listing
December 2019

Clinical spectrum of the anti-GQ1b antibody syndrome: a case series of eight patients.

Acta Neurol Belg 2019 Mar 12;119(1):29-36. Epub 2019 Feb 12.

Department of Neurology, University Hospitals Leuven, Herestraat 49, 3000, Leuven, Belgium.

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http://dx.doi.org/10.1007/s13760-019-01093-8DOI Listing
March 2019

Malignant hyperthermia: still an issue for neuromuscular diseases?

Curr Opin Neurol 2018 10;31(5):628-634

Department of Neurology, University Hospitals Leuven.

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http://dx.doi.org/10.1097/WCO.0000000000000592DOI Listing
October 2018

Late onset necrotizing autoimmune myopathy 1 year after cessation of statin treatment.

Acta Neurol Belg 2019 Sep 14;119(3):487-489. Epub 2018 Jul 14.

Klinik und Poliklinik für Neurologie, Universitätsklinik Köln, Kerpener Straße 62, 50937, Cologne, Germany.

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http://dx.doi.org/10.1007/s13760-018-0985-xDOI Listing
September 2019

Detection of myositis-specific antibodies.

Ann Rheum Dis 2019 01 25;78(1):e7. Epub 2018 Jan 25.

Department of Microbiology and Immunology, Experimental Laboratory Immunology, KU Leuven, Leuven, Belgium.

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http://ard.bmj.com/lookup/doi/10.1136/annrheumdis-2017-21291
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http://dx.doi.org/10.1136/annrheumdis-2017-212915DOI Listing
January 2019

Anterior interosseous mononeuropathy associated with HEV infection.

Neurol Neuroimmunol Neuroinflamm 2018 Mar 22;5(2):e429. Epub 2017 Dec 22.

Department of Neurosciences, Experimental Neurology (B.S., S.B., P.V.D.), KU Leuven-University of Leuven; Laboratory of Neurobiology (B.S., S.B., P.V.D.), Center for Brain & Disease Research, VIB; Departments of Neurology (B.S., M.S., K.G.C., P.V.D.), and Laboratory Medicine (V.S.), University Hospitals Leuven; and Laboratory for Cognitive Neurology (M.S.), Department of Neurosciences, Department of Microbiology and Immunology (V.S.), Laboratory for Muscle Diseases and Neuropathies (K.G.C.), Department of Neurosciences, Experimental Neurology, KU Leuven-University of Leuven, Belgium.

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http://dx.doi.org/10.1212/NXI.0000000000000429DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5745356PMC
March 2018

Comparison of elevated phosphorylated neurofilament heavy chains in serum and cerebrospinal fluid of patients with amyotrophic lateral sclerosis.

J Neurol Neurosurg Psychiatry 2018 04 20;89(4):367-373. Epub 2017 Oct 20.

Department of Neurosciences, Laboratory for Molecular Neurobiomarker Research, KU Leuven (University of Leuven), Leuven, Belgium.

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http://dx.doi.org/10.1136/jnnp-2017-316605DOI Listing
April 2018

Neurofilament markers for ALS correlate with extent of upper and lower motor neuron disease.

Neurology 2017 Jun 12;88(24):2302-2309. Epub 2017 May 12.

From the Laboratory for Molecular Neurobiomarker Research (K.P., M.D.S., B.G.), Laboratory for Cognitive Neurology (R.V.) and Laboratory of Neurobiology (Center for Brain & Disease Research, VIB, Leuven) (P.V.D.), Department of Neurosciences, KU Leuven (University of Leuven); Laboratory Medicine (K.P., M.D.S.) and Department of Neurology (O.S., K.G.C., G.C., A.D., N.L., P.T., D.V.R., R.V., P.V.D.), University Hospitals Leuven, Belgium; Hans Berger Department of Neurology (B.S., T.P., T.M.R., N.F., B.H., M.R., A.R., A.G., O.W.W., J.G.) and Institute for Biochemistry (P.M., S.W., H.R.), Jena University Hospital, Germany; INSERM, U942 (S.G., C.P.), Groupe Hospitalier Lariboisière Fernand-Widal Saint-Louis, CMRR Paris Nord AP-HP, Université Paris Diderot, France.

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http://dx.doi.org/10.1212/WNL.0000000000004029DOI Listing
June 2017

Towards a functional pathology of hereditary neuropathies.

Acta Neuropathol 2017 04 28;133(4):493-515. Epub 2016 Nov 28.

Friedrich-Baur-Institute, Department of Neurology, Ludwig-Maximilians-University, Ziemssenstr. 1a, 80336, Munich, Germany.

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http://link.springer.com/10.1007/s00401-016-1645-y
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http://dx.doi.org/10.1007/s00401-016-1645-yDOI Listing
April 2017

Diagnostic Challenges and Clinical Characteristics of Hepatitis E Virus-Associated Guillain-Barré Syndrome.

JAMA Neurol 2017 Jan;74(1):26-33

Department of Neurology, University Hospitals Leuven, Leuven, Belgium2Department of Neurosciences, Experimental Neurology, KU Leuven, University of Leuven, Leuven, Belgium5VIB, Vesalius Research Center, Leuven, Belgium.

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http://dx.doi.org/10.1001/jamaneurol.2016.3541DOI Listing
January 2017

Widening the spectrum of filamin-C myopathy: Predominantly proximal myopathy due to the p.A193T mutation in the actin-binding domain of FLNC.

Neuromuscul Disord 2017 Jan 27;27(1):73-77. Epub 2016 Sep 27.

Department of Neurology, Radboud University Medical Centre, Nijmegen, The Netherlands. Electronic address:

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http://dx.doi.org/10.1016/j.nmd.2016.09.017DOI Listing
January 2017

Tubular aggregates in autoimmune Lambert-Eaton myasthenic syndrome.

Neuromuscul Disord 2016 Dec 20;26(12):880-884. Epub 2016 Sep 20.

Department of Neurology, RWTH Aachen University, Aachen, Germany; Institute of Neuropathology, RWTH Aachen University, Aachen, Germany; Department of Neurology, University Hospitals Leuven and University of Leuven (KU Leuven), Leuven, Belgium. Electronic address:

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http://dx.doi.org/10.1016/j.nmd.2016.09.011DOI Listing
December 2016

Underestimated associated features in CMT neuropathies: clinical indicators for the causative gene?

Brain Behav 2016 04 4;6(4):e00451. Epub 2016 Mar 4.

Department of Neurology University Hospital RWTH Aachen Aachen Germany; Institute of Neuropathology University Hospital RWTH Aachen Aachen Germany; Department of Neurology University Hospitals Leuven and University of Leuven (KU Leuven) Leuven Belgium.

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http://dx.doi.org/10.1002/brb3.451DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4782242PMC
April 2016

Nuclear actin aggregation is a hallmark of anti-synthetase syndrome-induced dysimmune myopathy.

Neurology 2015 Mar 6;84(13):1346-54. Epub 2015 Mar 6.

From the Departments of Neuropathology (W.S., C.P., D.P., F.L.H., H.H.G.) and Rheumatology (U.S.), Charité-Universitätsmedizin Berlin, Germany; the Département de Médecine Interne et Immunologie Clinique (Y.A., O.B.), Centre de Référence Maladies Neuro-Musculaires Paris Est, Assistance Public-Hôpitaux de Paris Université Pierre et Marie Curie, Hôpital Pitié-Salpêtrière, Paris, France; the Section of Neuropathology, Department of Anatomical Pathology (R.J.), Path West Laboratory Medicine, Royal Perth Hospital, Perth; School of Pathology and Laboratory Medicine (R.J.), University of Western Australia, Nedlands, Australia; the Institute of Neuropathology (K.N., K.G.C., J.W.) and the Department of Neurology (K.G.C.), RWTH Aachen, Germany; the Department of Pathology and Neuropathology (E.A.), AMC University, Amsterdam, the Netherlands; the Department of Neuropathology (V.K., E.R.), University of Zürich, Switzerland; and the Department of Neuropathology (H.H.G.), University Medicine, Johannes Gutenberg University, Mainz, Germany.

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http://dx.doi.org/10.1212/WNL.0000000000001422DOI Listing
March 2015

Two novel nebulin variants in an adult patient with congenital nemaline myopathy.

Neuromuscul Disord 2015 May 3;25(5):392-6. Epub 2015 Feb 3.

Neurologische Klinik, Heimer-Institut am Bergmannsheil, Ruhr-Universität Bochum, Bochum, Germany.

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http://dx.doi.org/10.1016/j.nmd.2015.01.013DOI Listing
May 2015

The proximal medial sural nerve biopsy model: a standardised and reproducible baseline clinical model for the translational evaluation of bioengineered nerve guides.

Biomed Res Int 2014 2;2014:121452. Epub 2014 Jun 2.

Department of Plastic Surgery, Reconstructive and Hand Surgery, Burn Centre, Medical Faculty, RWTH Aachen University Hospital, Pauwelsstraße 30, 52074 Aachen, Germany.

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http://dx.doi.org/10.1155/2014/121452DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4077352PMC
March 2015

Progressive cardiac dysfunction in Bethlem myopathy during pregnancy.

Obstet Gynecol 2014 Feb;123(2 Pt 2 Suppl 2):436-8

Departments of Obstetrics and Prenatal Medicine, Neurology, and Cardiology, University Medical School, Bonn, and the Department of Neurology and the Institute of Neuropathology, RWTH Aachen University, Aachen, Germany.

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http://dx.doi.org/10.1097/AOG.0000000000000101DOI Listing
February 2014

Diagnostic challenge and therapeutic dilemma in necrotizing myopathy.

Neurology 2013 Sep 6;81(10):932-5. Epub 2013 Aug 6.

Department of Neurology, RWTH Aachen University, Aachen, Germany.

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http://dx.doi.org/10.1212/WNL.0b013e3182a35285DOI Listing
September 2013

Myofibrillar myopathies.

Handb Clin Neurol 2013 ;113:1337-42

Department of Neurology and Institute for Neuropathology, University Hospital RWTH Aachen, Aachen, Germany. Electronic address:

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http://dx.doi.org/10.1016/B978-0-444-59565-2.00005-8DOI Listing
March 2014

Myopathy with lobulated fibers, cores, and rods caused by a mutation in collagen VI.

Neurology 2012 Dec 21;79(23):2288-90. Epub 2012 Nov 21.

Department of Neurology, RWTH Aachen University, Aachen, Germany.

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http://dx.doi.org/10.1212/WNL.0b013e31827689fbDOI Listing
December 2012

Novel FHL1 mutation in a family with reducing body myopathy.

Muscle Nerve 2013 Jan 21;47(1):127-34. Epub 2012 Nov 21.

Institute of Neuropathology, University Hospital Aachen, Aachen, Germany.

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http://dx.doi.org/10.1002/mus.23500DOI Listing
January 2013

Acute but transient neurological deterioration revealing adult polyglucosan body disease.

J Neurol Sci 2013 Jan 10;324(1-2):179-82. Epub 2012 Nov 10.

AP-HP, Service de neurologie, Hôpital Avicenne, Bobigny, France.

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http://dx.doi.org/10.1016/j.jns.2012.10.015DOI Listing
January 2013

De novo RYR1 heterozygous mutation (I4898T) causing lethal core-rod myopathy in twins.

Eur J Med Genet 2011 Jan-Feb;54(1):29-33. Epub 2010 Oct 1.

Institut de Myologie, Unité de Morphologie Neuromusculaire, Groupe Hospitalier-Universitaire Pitié-Salpêtrière, Paris F-75013, France.

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http://dx.doi.org/10.1016/j.ejmg.2010.09.009DOI Listing
June 2011

DNAJB2 expression in normal and diseased human and mouse skeletal muscle.

Am J Pathol 2010 Jun 15;176(6):2901-10. Epub 2010 Apr 15.

Unité de Morphologie Neuromusculaire, and the Centre de Référence Neuromusculaire Paris-Est, Institut de Myologie, Groupe Hospitalier Pitié-Salpêtrière, AP-HP, Paris, France

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http://dx.doi.org/10.2353/ajpath.2010.090663DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2877851PMC
June 2010

Rigid spine syndrome revealing late-onset Pompe disease.

Neuromuscul Disord 2010 Feb 14;20(2):128-30. Epub 2009 Dec 14.

Centre de référence de pathologie neuromusculaire Paris-Est, Institut de Myologie, Groupe Hospitalier Pitié-Salpêtrière, Assistance Publique-Hôpitaux de Paris, Paris, France.

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http://dx.doi.org/10.1016/j.nmd.2009.11.006DOI Listing
February 2010

Magnetic resonance imaging findings of leg musculature in Charcot-Marie-Tooth disease type 2 due to dynamin 2 mutation.

J Neurol 2008 Jul 17;255(7):986-92. Epub 2008 Jun 17.

Services of Radiology, Clinical Neurophysiology and Neurology, University Hospital Marqués de Valdecilla, (CIBERNED and IFIMAV), Santander, Spain.

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http://dx.doi.org/10.1007/s00415-008-0808-8DOI Listing
July 2008

Tacrolimus-related polyneuropathy: case report and review of the literature.

Clin Neurol Neurosurg 2008 Mar 4;110(3):291-4. Epub 2007 Dec 4.

Department of Critical Care Medicine, University Hospital of Antwerp, University of Antwerp, Wilrijkstraat 10, B 2650 Edegem, Belgium.

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http://dx.doi.org/10.1016/j.clineuro.2007.10.014DOI Listing
March 2008

Epilepsy as part of the phenotype associated with ATP1A2 mutations.

Epilepsia 2008 Mar 19;49(3):500-8. Epub 2007 Nov 19.

Neurogenetics Group, Department of Molecular Genetics, VIB; Antwerpen, Belgium.

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http://dx.doi.org/10.1111/j.1528-1167.2007.01415.xDOI Listing
March 2008

Epilepsy and migraine in a patient with Urbach-Wiethe disease.

Seizure 2007 Jul 2;16(5):465-8. Epub 2007 Apr 2.

Neurogenetics Group, Department of Molecular Genetics, Flanders Interuniversity Institute for Biotechnology (VIB), University of Antwerp, Universiteitsplein 1, B-2610 Antwerpen, Belgium.

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http://linkinghub.elsevier.com/retrieve/pii/S105913110700051
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http://dx.doi.org/10.1016/j.seizure.2007.02.014DOI Listing
July 2007

Unraveling the genetics of distal hereditary motor neuronopathies.

Neuromolecular Med 2006 ;8(1-2):131-46

Peripheral Neuropathy Group, Department of Molecular Genetics, Flanders Interuniversity Institute for Biotechnology, University of Antwerp, Antwerpen, Belgium.

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http://dx.doi.org/10.1385/nmm:8:1-2:131DOI Listing
March 2007

Novel frameshift and splice site mutations in the neurotrophic tyrosine kinase receptor type 1 gene (NTRK1) associated with hereditary sensory neuropathy type IV.

Neuromuscul Disord 2006 Jan 20;16(1):19-25. Epub 2005 Dec 20.

Department of Molecular Genetics, Flanders Interuniversity Institute for Biotechnology, Institute Born-Bunge, University of Antwerp, Universiteitsplein 1, B-2610 Antwerpen, Belgium.

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http://dx.doi.org/10.1016/j.nmd.2005.10.007DOI Listing
January 2006

Genome-wide linkage of febrile seizures and epilepsy to the FEB4 locus at 5q14.3-q23.1 and no MASS1 mutation.

Hum Genet 2006 Jan 5;118(5):618-25. Epub 2005 Nov 5.

Neurogenetics Group, Department of Molecular Genetics VIB8, University of Antwerp, Campus Drie Eiken, Universiteitsplein 1, 2610 Antwerpen, Belgium.

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http://dx.doi.org/10.1007/s00439-005-0077-xDOI Listing
January 2006

Color discrimination involves ventral and dorsal stream visual areas.

Cereb Cortex 2004 Jul 28;14(7):803-22. Epub 2004 Mar 28.

Laboratorium voor Neuro- en Psychofysiologie, K.U. Leuven, Medical School, Herestraat 49, B3000 Leuven, Belgium.

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http://dx.doi.org/10.1093/cercor/bhh040DOI Listing
July 2004

A higher order motion region in human inferior parietal lobule: evidence from fMRI.

Neuron 2003 Oct;40(3):631-42

Laboratorium voor Neuro- en Psychofysiologie, Katholieke Universiteit Leuven, Campus Gasthuisberg, Herestraat 49, B-3000 Leuven, Belgium.

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http://optometry.osu.edu/research/VisualPerceptionLaboratory
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http://dx.doi.org/10.1016/s0896-6273(03)00590-7DOI Listing
October 2003

Involvement of multiple functionally distinct cerebellar regions in visual discrimination: a human functional imaging study.

Neuroimage 2003 Oct;20(2):840-54

Laboratory of Theoretical Neurobiology, Born-Bunge Foundation, University of Antwerp-U.A., Universiteitsplein 1, B2610, Antwerpen, Belgium.

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http://dx.doi.org/10.1016/s1053-8119(03)00366-5DOI Listing
October 2003