Publications by authors named "George W Padberg"

49Publications

Ophthalmological findings in facioscapulohumeral dystrophy.

Brain Commun 2019 11;1(1):fcz023. Epub 2019 Oct 11.

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

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http://dx.doi.org/10.1093/braincomms/fcz023DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7425335PMC
October 2019

26th Annual Facioscapulohumeral Dystrophy International Research Congress Marseille, France, 19-20 June 2019.

Neuromuscul Disord 2019 10 3;29(10):811-817. Epub 2019 Sep 3.

Radboud UMC, Nijmegen, The Netherlands.

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http://dx.doi.org/10.1016/j.nmd.2019.08.015DOI Listing
October 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

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

A 22-year follow-up reveals a variable disease severity in early-onset facioscapulohumeral dystrophy.

Eur J Paediatr Neurol 2018 Sep 3;22(5):782-785. Epub 2018 May 3.

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

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http://dx.doi.org/10.1016/j.ejpn.2018.04.013DOI Listing
September 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

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

Clinical trial preparedness in facioscapulohumeral muscular dystrophy: Clinical, tissue, and imaging outcome measures 29-30 May 2015, Rochester, New York.

Neuromuscul Disord 2016 Feb 9;26(2):181-6. Epub 2015 Nov 9.

Division of Human Biology, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.

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http://dx.doi.org/10.1016/j.nmd.2015.10.005DOI Listing
February 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

Population-based incidence and prevalence of facioscapulohumeral dystrophy.

Neurology 2014 Sep 13;83(12):1056-9. Epub 2014 Aug 13.

From the Department of Neurology (J.C.W.D., H.A., G.W.P., B.G.M.v.E.) and Department for Health Evidence (A.L.M.V.), Radboud University Medical Center, Nijmegen, the Netherlands; Department of Human Genetics (S.M.v.d.M.), Department of Neurology (J.J.G.M.V.), and Department of Clinical Genetics (E.B.), Leiden University Medical Center, Leiden, the Netherlands; and VU University Medical Center (S.S.W.), Amsterdam, the Netherlands.

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http://dx.doi.org/10.1212/WNL.0000000000000797DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4166358PMC
September 2014

Best practice guidelines on genetic diagnostics of Facioscapulohumeral muscular dystrophy: workshop 9th June 2010, LUMC, Leiden, The Netherlands.

Neuromuscul Disord 2012 May 16;22(5):463-70. Epub 2011 Dec 16.

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

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http://dx.doi.org/10.1016/j.nmd.2011.09.004DOI Listing
May 2012

Effect of aerobic exercise training and cognitive behavioural therapy on reduction of chronic fatigue in patients with facioscapulohumeral dystrophy: protocol of the FACTS-2-FSHD trial.

BMC Neurol 2010 Jun 30;10:56. Epub 2010 Jun 30.

Nijmegen Centre for Evidence Based Practice; Department of Rehabilitation, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.

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http://dx.doi.org/10.1186/1471-2377-10-56DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2906431PMC
June 2010

171st ENMC international workshop: Standards of care and management of facioscapulohumeral muscular dystrophy.

Neuromuscul Disord 2010 Jul;20(7):471-5

Fields Center for FSHD and Neuromuscular Research, Department of Neurology, University of Rochester Medical Center, Box 673, 601 Elmwood Avenue, Rochester, NY 14642, USA.

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http://dx.doi.org/10.1016/j.nmd.2010.04.007DOI Listing
July 2010

Facioscapulohumeral muscular dystrophy.

Curr Opin Neurol 2009 Oct;22(5):539-42

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

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https://insights.ovid.com/crossref?an=00019052-200910000-000
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http://dx.doi.org/10.1097/WCO.0b013e328330a572DOI Listing
October 2009

Quantitative MR imaging of individual muscle involvement in facioscapulohumeral muscular dystrophy.

Neuromuscul Disord 2009 May 28;19(5):357-62. Epub 2009 Mar 28.

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

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http://dx.doi.org/10.1016/j.nmd.2009.02.009DOI Listing
May 2009

Confirmation of dyslexia susceptibility loci on chromosomes 1p and 2p, but not 6p in a Dutch sib-pair collection.

Am J Med Genet B Neuropsychiatr Genet 2008 Apr;147(3):294-300

Department of Human Genetics, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands.

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http://dx.doi.org/10.1002/ajmg.b.30598DOI Listing
April 2008

Refinement of the locus for hereditary congenital facial palsy on chromosome 3q21 in two unrelated families and screening of positional candidate genes.

Eur J Hum Genet 2006 Dec 16;14(12):1306-12. Epub 2006 Aug 16.

Department of Neurology, University Medical Centre Nijmegen, 6500 HB Nijmegen, The Netherlands.

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http://dx.doi.org/10.1038/sj.ejhg.5201706DOI Listing
December 2006

Facioscapulohumeral muscular dystrophy.

Biochim Biophys Acta 2007 Feb 6;1772(2):186-94. Epub 2006 Jun 6.

Leiden University Medical Center (LUMC), Department of Human Genetics, Postal zone S-3-P, PO box 9600, 2300 RC Leiden, The Netherlands.

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http://linkinghub.elsevier.com/retrieve/pii/S092544390600100
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http://dx.doi.org/10.1016/j.bbadis.2006.05.009DOI Listing
February 2007

Electrophysiological assessment in patients with Möbius syndrome and clumsiness.

J Clin Neurophysiol 2005 Dec;22(6):422-5

Department of Neurology, Radboud University Nijmegen Medical Centre, PO Box 9101, 6500 HB Nijmegen, The Netherlands.

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http://dx.doi.org/10.1097/01.WNP.0000179965.94248.B3DOI Listing
December 2005

Variable hypomethylation of D4Z4 in facioscapulohumeral muscular dystrophy.

Ann Neurol 2005 Oct;58(4):569-76

Department of Human Genetics, Center for Human and Clinical Genetics, Leiden, The Netherlands.

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http://dx.doi.org/10.1002/ana.20625DOI Listing
October 2005

Nucleotide variation analysis does not support a causal role for plexin-A1 in hereditary congenital facial paresis.

Brain Res Dev Brain Res 2005 Aug;158(1-2):66-71

Department of Neurology, University Medical Centre Nijmegen, P.O. Box 9101, 6500 HB, Nijmegen, The Netherlands.

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http://dx.doi.org/10.1016/j.devbrainres.2005.06.004DOI Listing
August 2005

The spectrum of Mobius syndrome: an electrophysiological study.

Brain 2005 Jul 13;128(Pt 7):1728-36. Epub 2005 Apr 13.

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

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http://dx.doi.org/10.1093/brain/awh502DOI Listing
July 2005

Radiologic evidence for absence of the facial nerve in Möbius syndrome.

Neurology 2005 Mar;64(5):849-55

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

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http://dx.doi.org/10.1212/01.WNL.0000152980.92436.D9DOI Listing
March 2005

Contractions of D4Z4 on 4qB subtelomeres do not cause facioscapulohumeral muscular dystrophy.

Am J Hum Genet 2004 Dec 4;75(6):1124-30. Epub 2004 Oct 4.

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

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http://dx.doi.org/10.1086/426035DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1182148PMC
December 2004

Somatic mosaicism in FSHD often goes undetected.

Ann Neurol 2004 Jun;55(6):845-50

Center for Human and Clinical Genetics, Leiden University Medical Center, Leiden, The Netherlands.

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http://dx.doi.org/10.1002/ana.20106DOI Listing
June 2004

Oculopharyngeal muscular dystrophy with limb girdle weakness as major complaint.

J Neurol 2003 Nov;250(11):1307-12

Neuromuscular Centre Nijmegen, Dept. of Neurology, University Medical Centre Nijmegen, 9101, 6500 HB, Nijmegen, The Netherlands.

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http://link.springer.com/10.1007/s00415-003-0201-6
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http://dx.doi.org/10.1007/s00415-003-0201-6DOI Listing
November 2003

Hypomethylation of D4Z4 in 4q-linked and non-4q-linked facioscapulohumeral muscular dystrophy.

Nat Genet 2003 Dec 23;35(4):315-7. Epub 2003 Nov 23.

Department of Human Genetics, Center for Human and Clinical Genetics, Leiden University Medical Center, P.O. Box 9502, 2300 RA Leiden, The Netherlands.

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http://dx.doi.org/10.1038/ng1262DOI Listing
December 2003

Möbius syndrome redefined: a syndrome of rhombencephalic maldevelopment.

Neurology 2003 Aug;61(3):327-33

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

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http://dx.doi.org/10.1212/01.wnl.0000076484.91275.cdDOI Listing
August 2003

Facioscapulohumeral muscular dystrophy is uniquely associated with one of the two variants of the 4q subtelomere.

Nat Genet 2002 Oct 23;32(2):235-6. Epub 2002 Sep 23.

Department of Human Genetics, Center for Human and Clinical Genetics, Leiden University Medical Center, Wassenaarseweg 72, 2333 AL Leiden, The Netherlands.

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http://www.nature.com/articles/ng999
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http://dx.doi.org/10.1038/ng999DOI Listing
October 2002