Publications by authors named "Nicol C Voermans"

87Publications

[Exertional heat stroke in athletes and soldiers].

Ned Tijdschr Geneeskd 2020 Aug 20;164. Epub 2020 Aug 20.

Radboudumc, afd. Neurologie,Nijmegen.

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August 2020

Reduced specific force in patients with mild and severe facioscapulohumeral muscular dystrophy.

Muscle Nerve 2020 Sep 22. Epub 2020 Sep 22.

Department of Neurology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.

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http://dx.doi.org/10.1002/mus.27074DOI Listing
September 2020

Correlation Between Quantitative MRI and Muscle Histopathology in Muscle Biopsies from Healthy Controls and Patients with IBM, FSHD and OPMD.

J Neuromuscul Dis 2020 ;7(4):495-504

Department of Neurology, Donders Institute for Brain, Cognition and Behaviour, Radboud university medical center, Nijmegen, The Netherlands.

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http://dx.doi.org/10.3233/JND-200543DOI Listing
January 2020

Muscle ultrasound is a responsive biomarker in facioscapulohumeral dystrophy.

Neurology 2020 04 4;94(14):e1488-e1494. Epub 2020 Mar 4.

From the Department of Neurology, Donders Centre for Neuroscience, Radboud University Medical Center, Nijmegen, the Netherlands.

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http://dx.doi.org/10.1212/WNL.0000000000009211DOI Listing
April 2020

Preserved single muscle fiber specific force in facioscapulohumeral muscular dystrophy.

Neurology 2020 03 21;94(11):e1157-e1170. Epub 2020 Jan 21.

From the Department of Neurology, Donders Institute for Brain, Cognition and Behaviour (S.L., N.C.V., B.G.M.v.E.), Department of Radiology (A.H.), and Department of Pulmonary Diseases (H.V.H.), Radboud University Medical Center, Nijmegen; Department of Physiology (S.L., R.v.d.P., M.v.d.B., C.A.C.O.) and Department of Pathology, Institute for Cardiovascular Research (B.K.), Amsterdam University Medical Center, the Netherlands; Department of Cellular and Molecular Medicine (R.v.d.P., C.A.C.O.), University of Arizona, Tucson; and Department of Human Genetics (S.M.v.d.M.), Leiden University Medical Centre, the Netherlands.

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http://dx.doi.org/10.1212/WNL.0000000000008977DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7220237PMC
March 2020

High incidence of falls in patients with myotonic dystrophy type 1 and 2: A prospective study.

Neuromuscul Disord 2019 10 28;29(10):758-765. Epub 2019 Aug 28.

Department of Neurology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Centre, Nijmegen, the Netherlands; Amsterdam UMC, University of Amsterdam, Department of Neurology, Amsterdam Neuroscience, Amsterdam, Netherlands.

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http://dx.doi.org/10.1016/j.nmd.2019.08.012DOI Listing
October 2019

Muscle fiber dysfunction contributes to weakness in inclusion body myositis.

Neuromuscul Disord 2019 06 7;29(6):468-476. Epub 2019 Mar 7.

Department of Physiology, Institute for Cardiovascular Research, VU University Medical Center, O/2 Building 11W53, 1081 HZ Amsterdam, The Netherlands.

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https://linkinghub.elsevier.com/retrieve/pii/S09608966183130
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http://dx.doi.org/10.1016/j.nmd.2019.03.001DOI Listing
June 2019

Early onset as a marker for disease severity in facioscapulohumeral muscular dystrophy.

Neurology 2019 01 19;92(4):e378-e385. Epub 2018 Dec 19.

From the Department of Neurology (R.J.M.G., K.M., C.R.v.K., T.H.A.S., C.E.E., G.W.P., N.C.V., B.G.M.v.E.), Donders Center for Neuroscience, Radboud University Medical Center, Nijmegen; Department of Human Genetics (R.J.L.F.L., S.M.v.d.M.), Leiden University Medical Center, the Netherlands; and Department of Neurology (J.M.S.), Kansas University Medical Center, Kansas City.

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http://dx.doi.org/10.1212/WNL.0000000000006819DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6345117PMC
January 2019

Experiences with bariatric surgery in patients with facioscapulohumeral dystrophy and myotonic dystrophy type 1: A qualitative study.

Neuromuscul Disord 2018 11 19;28(11):938-946. Epub 2018 Sep 19.

Department of Neurology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, the Netherlands. Electronic address:

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https://linkinghub.elsevier.com/retrieve/pii/S09608966183102
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http://dx.doi.org/10.1016/j.nmd.2018.09.003DOI Listing
November 2018

Phenotype-genotype relations in facioscapulohumeral muscular dystrophy type 1.

Clin Genet 2018 12 8;94(6):521-527. Epub 2018 Oct 8.

Department of Neurology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, Nijmegen, The Netherlands.

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http://dx.doi.org/10.1111/cge.13446DOI Listing
December 2018

Quantitative muscle MRI and ultrasound for facioscapulohumeral muscular dystrophy: complementary imaging biomarkers.

J Neurol 2018 Nov 6;265(11):2646-2655. Epub 2018 Sep 6.

Department of Neurology and Clinical Neurophysiology, Radboud University Medical Center, PO Box 9101, 6500 HB, Nijmegen, The Netherlands.

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http://dx.doi.org/10.1007/s00415-018-9037-yDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6182682PMC
November 2018

MRI-Guided Biopsy as a Tool for Diagnosis and Research of Muscle Disorders.

J Neuromuscul Dis 2018;5(3):315-319

Department of Neurology, Donders Institute for Brain, Cognition and Behaviour, Radboud University Medical Center, The Netherlands.

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http://dx.doi.org/10.3233/JND-180318DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6087442PMC
November 2018

Intact transferrin and total plasma glycoprofiling for diagnosis and therapy monitoring in phosphoglucomutase-I deficiency.

Transl Res 2018 09 10;199:62-76. Epub 2018 May 10.

Department of Neurology and Translational Metabolic Laboratory, Donders Institute for Brain, Cognition, and Behavior, Radboud University Medical Center, Nijmegen, The Netherlands. Electronic address:

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http://dx.doi.org/10.1016/j.trsl.2018.04.008DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7041963PMC
September 2018

A family-based study into penetrance in facioscapulohumeral muscular dystrophy type 1.

Neurology 2018 07 11;91(5):e444-e454. Epub 2018 Jul 11.

From the Department of Neurology (M.W., C.G.H., B.G.v.E., G.W.P., N.C.V.), Donders Institute for Brain, Cognition and Behavior, and Radboud Institute for Health Sciences (M.J.), Radboud University Medical Center, Nijmegen; Department of Neurology (M.W.), ETZ, Tilburg; Department of Human Genetics (R.J.L., S.M.v.d.M.), Leiden University Medical Center; and Department of Neurology (E.v.d.K.), MCL, Leeuwarden, the Netherlands.

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http://dx.doi.org/10.1212/WNL.0000000000005915DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6093768PMC
July 2018

FSHD type 2 and Bosma arhinia microphthalmia syndrome: Two faces of the same mutation.

Neurology 2018 08 6;91(6):e562-e570. Epub 2018 Jul 6.

From the Department of Neurology (K.M., N.C.V., B.G.M.v.E., C.G.C.H.), Radboud University Medical Center, Nijmegen; Departments of Human Genetics (R.J.L.F.L., P.J.v.d.V., M.L.v.d.B., S.M.v.d.M.), Clinical Genetics (M.K.), and Neurology (U.A.B.), Leiden University Medical Center, Leiden, the Netherlands; Department of Pediatrics (J.M.G.), Cedars Sinai Medical Center, Los Angeles, CA; Department of Medical Genetics (A.E.L.), MassGeneral Hospital for Children, Boston, MA; Center for Genomic Medicine and Department of Neurology (H.B.), Massachusetts General Hospital, Boston; Department of Pathology (S.A.M.), University of Iowa Hospitals and Clinics, Iowa City; The John Walton Muscular Dystrophy Research Centre (K.J., T.E., A.T., V.S.), Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne, UK; Neuromuscular Consult Unit (S.K.G.), Bilbo-Basurtu Erakunde Sanitario Integratua, Organización Sanitaria Integrada Bilbao-Basurto, Spain; Centre de Référence des Maladies Neuromusculaires (S.S.), Nice, France; Department of Neurology (R.T.), University of Rochester Medical Center, NY; Division of Human Biology (S.J.T.), Fred Hutchinson Cancer Research Center, Seattle, WA; and National Institute of Environmental Health Sciences (N.D.S.), Research Triangle Park, NC.

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http://dx.doi.org/10.1212/WNL.0000000000005958DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6105048PMC
August 2018

MPZL2, Encoding the Epithelial Junctional Protein Myelin Protein Zero-like 2, Is Essential for Hearing in Man and Mouse.

Am J Hum Genet 2018 07 28;103(1):74-88. Epub 2018 Jun 28.

Hearing and Genes Division, Department of Otorhinolaryngology, Radboud University Medical Center, 6500 HB Nijmegen, the Netherlands; Donders Institute for Brain, Cognition and Behavior, Radboud University Medical Center, 6500 HB Nijmegen, the Netherlands; Department of Human Genetics, Radboud University Medical Center, 6500 HB Nijmegen, the Netherlands. Electronic address:

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http://dx.doi.org/10.1016/j.ajhg.2018.05.011DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6037131PMC
July 2018

Is fatigue a disease-specific or generic symptom in chronic medical conditions?

Health Psychol 2018 06;37(6):530-543

Expert Center for Chronic Fatigue, Department of Medical Psychology, Amsterdam Public Health Research Institute, VU University Medical Center.

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http://dx.doi.org/10.1037/hea0000598DOI Listing
June 2018

Dejerine-Sottas disease in childhood-Genetic and sonographic heterogeneity.

Brain Behav 2018 04 21;8(4):e00919. Epub 2018 Feb 21.

Neurology Department The Royal Children's Hospital Melbourne Parkville Vic. Australia.

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http://dx.doi.org/10.1002/brb3.919DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5893341PMC
April 2018

Lifetime endogenous estrogen exposure and disease severity in female patients with facioscapulohumeral muscular dystrophy.

Neuromuscul Disord 2018 06 8;28(6):508-511. Epub 2018 Mar 8.

Department of Neurology, Radboud University Medical Center, Nijmegen, The Netherlands.

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http://dx.doi.org/10.1016/j.nmd.2018.02.012DOI Listing
June 2018

Early onset facioscapulohumeral dystrophy - a systematic review using individual patient data.

Neuromuscul Disord 2017 Dec 21;27(12):1077-1083. Epub 2017 Sep 21.

Department of Neurology, Donders Centre for Medical Neuroscience, Radboud University Medical Centre, Nijmegen, The Netherlands.

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http://dx.doi.org/10.1016/j.nmd.2017.09.007DOI Listing
December 2017

Adding quantitative muscle MRI to the FSHD clinical trial toolbox.

Neurology 2017 Nov 13;89(20):2057-2065. Epub 2017 Oct 13.

From the Department of Neurology (K.M., S.C.C.V., N.C.V., G.W.P., C.G.C.H., B.G.M.v.E.), Radboud University Medical Center, Nijmegen; and Department of Human Genetics (R.J.L.F.L., P.J.v.d.V., S.M.v.d.M.), Leiden University Medical Center, the Netherlands.

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http://www.neurology.org/lookup/doi/10.1212/WNL.000000000000
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http://dx.doi.org/10.1212/WNL.0000000000004647DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5711504PMC
November 2017

Skeletal muscle morphology, protein synthesis, and gene expression in Ehlers-Danlos syndrome.

J Appl Physiol (1985) 2017 Aug 8;123(2):482-488. Epub 2017 Jun 8.

Institute of Sports Medicine, Department of Orthopedic Surgery, Bispebjerg Hospital, University of Copenhagen, Copenhagen, Denmark.

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http://dx.doi.org/10.1152/japplphysiol.01044.2016DOI Listing
August 2017

The diagnostic value of hyperammonaemia induced by the non-ischaemic forearm exercise test.

J Clin Pathol 2017 Oct 11;70(10):896-898. Epub 2017 Apr 11.

Paris-Est Neuromuscular Center, Institute of Myology, Pitié-Salpêtrière Hospital, Assistance Publique Hôpitaux de Paris, Paris, France.

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http://dx.doi.org/10.1136/jclinpath-2017-204324DOI Listing
October 2017

Exertional rhabdomyolysis: physiological response or manifestation of an underlying myopathy?

BMJ Open Sport Exerc Med 2016 7;2(1):e000151. Epub 2016 Sep 7.

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

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http://bmjopensem.bmj.com/lookup/doi/10.1136/bmjsem-2016-000
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http://dx.doi.org/10.1136/bmjsem-2016-000151DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5117086PMC
September 2016

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

Congenital myopathies: not only a paediatric topic.

Curr Opin Neurol 2016 10;29(5):642-50

aDepartment of Paediatric Neurology, Neuromuscular Service, Evelina's Children Hospital, Guy's & St. Thomas' Hospital NHS Foundation Trust bRandall Division of Cell and Molecular Biophysics, Muscle Signalling Section cDepartment of Clinical and Basic Neuroscience, IoPPN, King's College, London, UK dDepartment of Neurology, Radboud University Medical Centre, Nijmegen, The Netherlands.

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http://dx.doi.org/10.1097/WCO.0000000000000372DOI Listing
October 2016

[Overactive muscles: it can be more serious than common myalgia or cramp].

Ned Tijdschr Geneeskd 2016 ;160:A9675

Radboud Universitair Medisch Centrum, afd. Neurologie, Nijmegen.

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November 2017

The Dutch patients' perspective on oculopharyngeal muscular dystrophy: A questionnaire study on fatigue, pain and impairments.

Neuromuscul Disord 2016 Mar 13;26(3):221-6. Epub 2016 Feb 13.

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

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http://dx.doi.org/10.1016/j.nmd.2015.12.009DOI Listing
March 2016

What's in a name? The clinical features of facioscapulohumeral muscular dystrophy.

Pract Neurol 2016 Jun 9;16(3):201-7. Epub 2016 Feb 9.

Department of Neurology, Radboud University Medical Center, Nijmegen, The Netherlands.

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http://dx.doi.org/10.1136/practneurol-2015-001353DOI Listing
June 2016

Statin-Induced Myopathy Is Associated with Mitochondrial Complex III Inhibition.

Cell Metab 2015 Sep;22(3):399-407

Department of Pharmacology and Toxicology, Radboud University Medical Center, Nijmegen 6500HB, the Netherlands; Center for Systems Biology and Bioenergetics, Nijmegen Center for Mitochondrial Disorders, Radboud University Medical Center, Nijmegen 6500HB, the Netherlands. Electronic address:

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http://dx.doi.org/10.1016/j.cmet.2015.08.002DOI Listing
September 2015

Diagnosis of becker muscular dystrophy: Results of Re-analysis of DNA samples.

Muscle Nerve 2016 Jan 3;53(1):44-8. Epub 2015 Jun 3.

Department of Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.

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http://dx.doi.org/10.1002/mus.24691DOI Listing
January 2016

Facioscapulohumeral muscular dystrophy as a genetic cause of pectus excavatum.

Eur J Med Genet 2015 Apr 25;58(4):203-4. Epub 2015 Feb 25.

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

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http://dx.doi.org/10.1016/j.ejmg.2015.02.007DOI Listing
April 2015

Primary cataract as a key to recognition of myotonic dystrophy type 1.

Eur J Ophthalmol 2015 May 25;25(4):e46-9. Epub 2015 May 25.

1 Department of Neurology, Radboud University Medical Centre, Nijmegen - The Netherlands.

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http://dx.doi.org/10.5301/ejo.5000565DOI Listing
May 2015

Neurological manifestations of Ehlers-Danlos syndrome(s): A review.

Iran J Neurol 2014 Oct;13(4):190-208

Department of Neurology, Radboud University Medical Centre, Nijmegen, Netherlands.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4300794PMC
October 2014

Sporadic late-onset nemaline myopathy with MGUS: long-term follow-up after melphalan and SCT.

Neurology 2014 Dec 5;83(23):2133-9. Epub 2014 Nov 5.

From the Departments of Neurology (N.C.V., B.G.v.E.) and Pathology (M.L.), Radboud University Medical Centre, Nijmegen, the Netherlands; Department of Internal Medicine (O.B.), Hôpital Pitié Salpêtrière, UPMC, U974, DHU I2B, Paris, France; Department of Hematology (M.C.M., H.L.), University Medical Center Utrecht, the Netherlands; Department of Pathology (M.L.), Antwerp University Hospital, University of Antwerp, Edegem; Departments of Internal Medicine (W.M.) and Hematology (M.D.), University Hospital Leuven, Belgium; Neurology Service (T.K., J.N.), Lausanne University Hospital CHUV, Lausanne; Department of Medical Oncology (T.P.), University Hospital Bern, Switzerland; Electromyography and Neuromuscular Pathologies Department Lyon Est (F.B.), Bron Hospitals, France; Departments of Pathology (N.R.) and Neurology (B.E.), Hôpital Pitié Salpêtrière, Myology Institute, Paris; Department of Hematology (V.L., P.v.d.B.), Hôpital Pitié Salpêtrière, UPMC Univ Paris 6 GRC 11 GRECHY, Paris, France; Neuromuscular Reference Centre, Department of Neurology (V.L., P.v.d.B.), and Department of Hematology (M.C.V.), Cliniques Universitaires Saint-Luc, University of Louvain, Brussels, Belgium.

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http://dx.doi.org/10.1212/WNL.0000000000001047DOI Listing
December 2014

Prior medical conditions and the risk of amyotrophic lateral sclerosis.

J Neurol 2014 Oct 25;261(10):1949-56. Epub 2014 Jul 25.

Department of Neurology, Brain Center Rudolf Magnus, University Medical Center Utrecht, Heidelberglaan 100, 3584 CX, Utrecht, The Netherlands.

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http://dx.doi.org/10.1007/s00415-014-7445-1DOI Listing
October 2014

Compound heterozygous mutations of the TNXB gene cause primary myopathy.

Neuromuscul Disord 2014 Jan 5;24(1):88-9. Epub 2013 Nov 5.

Research Institute MOVE, Faculty of Human Movement Sciences, VU University, Amsterdam, The Netherlands.

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https://linkinghub.elsevier.com/retrieve/pii/S09608966130098
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http://dx.doi.org/10.1016/j.nmd.2013.10.007DOI Listing
January 2014

[Increased CK activity in serum without symptoms: further investigations often unnecessary].

Ned Tijdschr Geneeskd 2013 ;157(41):A6315

Universitair Medisch Centrum St Radboud, afd. Neurologie, Nijmegen.

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May 2014

Exertional hyperckemia might be the first manifestation of a genetic disorder.

Muscle Nerve 2013 Sep 27;48(3):461-2. Epub 2013 Jul 27.

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

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http://dx.doi.org/10.1002/mus.23826DOI Listing
September 2013

Neuromuscular properties of the thigh muscles in patients with Ehlers-Danlos syndrome.

Muscle Nerve 2013 Jan 21;47(1):96-104. Epub 2012 Nov 21.

Research Institute MOVE, Faculty of Human Movement Sciences, VU University Amsterdam, van der Boechorststraat 9, 1081 BT Amsterdam, The Netherlands.

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http://dx.doi.org/10.1002/mus.23482DOI Listing
January 2013

Titin-based stiffening of muscle fibers in Ehlers-Danlos Syndrome.

J Appl Physiol (1985) 2012 Apr 5;112(7):1157-65. Epub 2012 Jan 5.

Laboratory for Physiology, Institute for Cardiovascular Research, VU University Medical Center, Amsterdam.

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http://jap.physiology.org/content/jap/112/7/1157.full.pdf
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http://jap.physiology.org/cgi/doi/10.1152/japplphysiol.01166
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http://dx.doi.org/10.1152/japplphysiol.01166.2011DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3774215PMC
April 2012

Well-defined clinical presentation of Ehlers-Danlos syndrome in patients with tenascin-X deficiency: a report of four cases.

Clin Dysmorphol 2012 Jan;21(1):15-8

Department of Dermatology, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.

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http://dx.doi.org/10.1097/MCD.0b013e32834c4bb7DOI Listing
January 2012

Rituximab treatment in patients with refractory inflammatory myopathies.

Rheumatology (Oxford) 2011 Dec 13;50(12):2206-13. Epub 2011 May 13.

Department of Rheumatology, Radboud University Nijmegen Medical Centre, HB Nijmegen, The Netherlands.

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http://dx.doi.org/10.1093/rheumatology/ker088DOI Listing
December 2011

Trachea rupture in tenascin-X-deficient type Ehlers-Danlos syndrome.

Anesthesiology 2010 Sep;113(3):746-9

Department of Critical Care Medicine, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.

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http://anesthesiology.pubs.asahq.org/Article.aspx?doi=10.109
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http://dx.doi.org/10.1097/ALN.0b013e3181e19c0fDOI Listing
September 2010

Pain in ehlers-danlos syndrome is common, severe, and associated with functional impairment.

J Pain Symptom Manage 2010 Sep 25;40(3):370-8. Epub 2010 Jun 25.

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

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http://dx.doi.org/10.1016/j.jpainsymman.2009.12.026DOI Listing
September 2010

Muscle characteristics and altered myofascial force transmission in tenascin-X-deficient mice, a mouse model of Ehlers-Danlos syndrome.

J Appl Physiol (1985) 2010 Oct 24;109(4):986-95. Epub 2010 Jun 24.

Research Instituut MOVE, Faculteit Bewegingswetenschappen, Vrije Universiteit, Amsterdam, The Netherlands.

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http://dx.doi.org/10.1152/japplphysiol.00723.2009DOI Listing
October 2010

Dural ectasia in Marfan syndrome.

Neurology 2009 Dec;73(23):2047; author reply 2047-8

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http://dx.doi.org/10.1212/WNL.0b013e3181bd1ff8DOI Listing
December 2009

Fatigue is a frequent and clinically relevant problem in Ehlers-Danlos Syndrome.

Semin Arthritis Rheum 2010 Dec 30;40(3):267-74. Epub 2009 Oct 30.

Neuromuscular Centre Nijmegen, Department of Neurology, Nijmegen, The Netherlands.

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http://dx.doi.org/10.1016/j.semarthrit.2009.08.003DOI Listing
December 2010

Neuromuscular involvement in various types of Ehlers-Danlos syndrome.

Ann Neurol 2009 Jun;65(6):687-97

Department of Neurology, Neuromuscular Centre Nijmegen, Radboud University Nijmegen Medical Centre, Nijmegen, the Netherlands.

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http://doi.wiley.com/10.1002/ana.21643
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http://dx.doi.org/10.1002/ana.21643DOI Listing
June 2009

[Treatment of central and facial pain. First experience with motoric-cortical stimulation].

Ned Tijdschr Geneeskd 2009 Mar;153(12):538-42

Afd. Anesthesiologie, Universitair Medisch Centrum Groningen, Groningen.

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March 2009

[Light traumatic brain concussion in an older patient with oral antifibrinolytic agents].

Ned Tijdschr Geneeskd 2009 Jan;153(4):130-5

Universitair Medisch Centrum St Radboud, Nijmegen.

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January 2009

Computer-aided visualization of muscle weakness distribution.

J Neurol 2008 Nov 3;255(11):1670-8. Epub 2008 Sep 3.

Research Centre of Allied Health Sciences, Dept. of Rehabilitation Physical Therapy (code 897), Radboud University Nijmegen Medical Centre, 9101, 6500 HB Nijmegen, The Netherlands.

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http://dx.doi.org/10.1007/s00415-008-0959-7DOI Listing
November 2008

Caffeine and muscle cramps: a stimulating connection.

Am J Med 2007 Aug;120(8):e1-2

Neuromuscular Centre Nijmegen, Department of Neurology, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.

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http://dx.doi.org/10.1016/j.amjmed.2006.07.035DOI Listing
August 2007

Quantification of trunk rotations during turning and walking in Parkinson's disease.

Clin Neurophysiol 2007 Jul 23;118(7):1602-6. Epub 2007 Apr 23.

Department of Neurology, Radboud University Nijmegen Medical Centre, Parkinson Center Nijmegen, Nijmegen, The Netherlands.

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http://dx.doi.org/10.1016/j.clinph.2007.03.010DOI Listing
July 2007

Pediatric median neuropathy due to pruritus in Alagille syndrome.

Pediatr Neurol 2006 Sep;35(3):216-9

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

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http://dx.doi.org/10.1016/j.pediatrneurol.2006.02.011DOI Listing
September 2006

Secondary parkinsonism in childhood: A rare complication after radiotherapy.

Pediatr Neurol 2006 Jun;34(6):495-8

Department of Neurology, Radboud University Nijmegen Medical Centre, the Netherlands.

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http://dx.doi.org/10.1016/j.pediatrneurol.2005.10.021DOI Listing
June 2006

Rhabdomyolysis caused by an inherited metabolic disease: very long-chain acyl-CoA dehydrogenase deficiency.

Am J Med 2006 Feb;119(2):176-9

Neuromuscular Center Nijmegen, Department of Neurology, Radboud University Nijmegen Medical Center, The Netherlands.

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http://dx.doi.org/10.1016/j.amjmed.2005.07.064DOI Listing
February 2006

Fallacious falls.

J Neurol 2005 Oct 19;252(10):1271-3. Epub 2005 Sep 19.

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http://dx.doi.org/10.1007/s00415-005-0033-7DOI Listing
October 2005

Interaction between the human hippocampus and the caudate nucleus during route recognition.

Neuron 2004 Aug;43(3):427-35

Department of Medical Psychology, University Medical Center Nijmegen, P.O. Box 9101, 6500 HB Nijmegen, The Netherlands.

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http://dx.doi.org/10.1016/j.neuron.2004.07.009DOI Listing
August 2004