Matthias Vorgerd

Matthias Vorgerd

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Matthias Vorgerd

Matthias Vorgerd

Publications by authors named "Matthias Vorgerd"

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Chaperones in sporadic inclusion body myositis-Validation of proteomic data.

Muscle Nerve 2020 Jan 8;61(1):116-121. Epub 2019 Nov 8.

Department of Neurology, Heimer Institute for Muscle Research, University Hospital Bergmannsheil, Ruhr University Bochum, Bochum, Germany.

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http://dx.doi.org/10.1002/mus.26742DOI Listing
January 2020

A metastable subproteome underlies inclusion formation in muscle proteinopathies.

Acta Neuropathol Commun 2019 Dec 3;7(1):197. Epub 2019 Dec 3.

Department of Neurology and Hope Center for Neurological Disease, Washington University School of Medicine, Saint Louis, MO, USA.

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http://dx.doi.org/10.1186/s40478-019-0853-9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6891963PMC
December 2019

Diffusion tensor imaging of the human thigh: consideration of DTI-based fiber tracking stop criteria.

MAGMA 2019 Nov 27. Epub 2019 Nov 27.

Department of Neurology, BG-University Hospital Bergmannsheil, Ruhr-University Bochum, Bürkle-de-la-Camp-Platz 1, 44789, Bochum, Germany.

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http://dx.doi.org/10.1007/s10334-019-00791-xDOI Listing
November 2019

Label-free identification of myopathological features with coherent anti-Stokes Raman scattering.

Muscle Nerve 2018 09 17;58(3):456-459. Epub 2018 May 17.

Neurological Clinic Bergmannsheil, Ruhr-University Bochum, Bochum, Germany.

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http://dx.doi.org/10.1002/mus.26140DOI Listing
September 2018

Diffusion tensor imaging of the human calf: Variation of inter- and intramuscle-specific diffusion parameters.

J Magn Reson Imaging 2017 10 2;46(4):1137-1148. Epub 2017 Feb 2.

Department of Neurology BG-University Hospital Bergmannsheil, Ruhr-University Bochum, Bochum, Germany.

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http://dx.doi.org/10.1002/jmri.25650DOI Listing
October 2017

The novel αB-crystallin (CRYAB) mutation p.D109G causes restrictive cardiomyopathy.

Hum Mutat 2017 08 21;38(8):947-952. Epub 2017 Jun 21.

Department of Thoracic and Cardiovascular Surgery, Heart and Diabetes Centre NRW, University Hospital of the Ruhr-University Bochum, Erich and Hanna Klessmann Institute for Cardiovascular Research & Development (EHKI), Bad Oeynhausen, Germany.

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http://dx.doi.org/10.1002/humu.23248DOI Listing
August 2017

Unveiling of miRNA Expression Patterns in Purkinje Cells During Development.

Cerebellum 2017 04;16(2):376-387

Department of Cytology, Institute of Anatomy, Ruhr-University Bochum, Universitätsstr. 150, 44801, Bochum, Germany.

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http://dx.doi.org/10.1007/s12311-016-0814-9DOI Listing
April 2017

Expanding the phenotype of BICD2 mutations toward skeletal muscle involvement.

Neurology 2016 Nov 26;87(21):2235-2243. Epub 2016 Oct 26.

From the Department of Cardiovascular Physiology (A.U., T.D., W.A.L.), Center for Rare Diseases Ruhr (A.U., G.D., A.G., T.D., R.K., M.T., C.H., W.A.L., S.H., M.V.), Department of Human Genetics (G.D., S.H.), Department of Neurology, Heimer Institute for Muscle Research, University Hospital Bergmannsheil (A.G., R.K., M.T., M.V.), and Institute for Pediatric Radiology, Katholisches Klinikum Bochum (C.H.), Ruhr University Bochum; Klinikum Kassel (A.F.), Kassel Medical School; Institute of Neuropathology (J.W.), RWTH University Hospital Aachen; and Institute of Human Genetics (L.M.-C., M.S., B.W.), Center for Molecular Medicine and Institute for Genetics, University of Cologne, Germany.

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http://dx.doi.org/10.1212/WNL.0000000000003360DOI Listing
November 2016

Confocal Cornea Microscopy Detects Involvement of Corneal Nerve Fibers in a Patient with Light-Chain Amyloid Neuropathy Caused by Multiple Myeloma: A Case Report.

Case Rep Neurol 2016 May-Aug;8(2):134-9. Epub 2016 Jun 27.

Department of Neurology, Berufsgenossenschaftliches Universitätsklinikum Bergmannsheil, Ruhr University Bochum, Bochum, Germany.

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http://dx.doi.org/10.1159/000446538DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4945811PMC
August 2016

Th2-M2 immunity in lesions of muscular sarcoidosis and macrophagic myofasciitis.

Neuropathol Appl Neurobiol 2015 Dec 19;41(7):952-63. Epub 2015 May 19.

Department of Neuropathology, Charité-Universitätsmedizin Berlin, Germany.

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http://dx.doi.org/10.1111/nan.12231DOI Listing
December 2015

50 years to diagnosis: Autosomal dominant tubular aggregate myopathy caused by a novel STIM1 mutation.

Neuromuscul Disord 2015 Jul 16;25(7):577-84. Epub 2015 Apr 16.

Friedrich-Baur-Institute, Department of Neurology, Ludwig-Maximilians-University of Munich, Munich, Germany.

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http://dx.doi.org/10.1016/j.nmd.2015.04.005DOI Listing
July 2015

ATOH8: a novel marker in human muscle fiber regeneration.

Histochem Cell Biol 2015 May 17;143(5):443-52. Epub 2014 Dec 17.

Department of Neurology, Heimer-Institute at the BG University-Hospital Bergmannsheil GmbH, Ruhr University Bochum, Bürkle-de-la-Camp-Platz 1, 44789, Bochum, Germany,

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http://dx.doi.org/10.1007/s00418-014-1299-6DOI Listing
May 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

Long survival in Leigh syndrome: new cases and review of literature.

Neuropediatrics 2014 Dec 11;45(6):346-53. Epub 2014 Aug 11.

Department of Neuropediatrics, University Children's Hospital, Ruhr University, Bochum, Germany.

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http://dx.doi.org/10.1055/s-0034-1383823DOI Listing
December 2014

Effects of follicular versus luteal phase-based strength training in young women.

Springerplus 2014 11;3:668. Epub 2014 Nov 11.

Department of Sports Medicine and Sports Nutrition, Faculty of Sport Science, Ruhr-University Bochum, Gesundheitscampus Nord, Bochum, Haus 10, 44801 Germany.

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http://dx.doi.org/10.1186/2193-1801-3-668DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4236309PMC
December 2014

Pregnancy and delivery in women with Pompe disease.

Mol Genet Metab 2014 Jun 30;112(2):148-53. Epub 2014 Mar 30.

Department of Neurology, Martin-Luther-University Halle-Wittenberg, Ernst-Grube-Str. 40, 06120 Halle (Saale), Germany. Electronic address:

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http://ac.els-cdn.com/S1096719214001152/1-s2.0-S109671921400
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http://linkinghub.elsevier.com/retrieve/pii/S109671921400115
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http://dx.doi.org/10.1016/j.ymgme.2014.03.010DOI Listing
June 2014

Human β-defensin-3 correlates with muscle fibre degeneration in idiopathic inflammatory myopathies.

Innate Immun 2014 Jan 22;20(1):49-60. Epub 2013 Apr 22.

1Department of Neurology, BG University Hospital Bergmannsheil GmbH, Ruhr University Bochum, Germany.

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http://journals.sagepub.com/doi/10.1177/1753425913481820
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http://dx.doi.org/10.1177/1753425913481820DOI Listing
January 2014

Human myocytes are protected from titin aggregation-induced stiffening by small heat shock proteins.

J Cell Biol 2014 Jan 13;204(2):187-202. Epub 2014 Jan 13.

Department of Cardiovascular Physiology and 2 Neurological University Clinic Bergmannsheil, Ruhr University Bochum, 44780 Bochum, Germany.

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http://dx.doi.org/10.1083/jcb.201306077DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3897184PMC
January 2014

Creatine for treating muscle disorders.

Cochrane Database Syst Rev 2013 Jun 5(6):CD004760. Epub 2013 Jun 5.

Department of Neurology, University Hospital Bergmannsheil, Ruhr University Bochum, Bochum, Germany.

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http://doi.wiley.com/10.1002/14651858.CD004760.pub4
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http://dx.doi.org/10.1002/14651858.CD004760.pub4DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6492334PMC
June 2013

Impairment of protein degradation in myofibrillar myopathy caused by FLNC/filamin C mutations.

Autophagy 2013 Mar 13;9(3):422-3. Epub 2012 Dec 13.

Department of Neurology, Neuromuscular Center Ruhrgebiet, University Hospital Bergmannsheil, Ruhr-University, Bochum, Germany.

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http://www.tandfonline.com/doi/abs/10.4161/auto.22921
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http://dx.doi.org/10.4161/auto.22921DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3590265PMC
March 2013

Filamin C-related myopathies: pathology and mechanisms.

Acta Neuropathol 2013 Jan 30;125(1):33-46. Epub 2012 Oct 30.

Institute for Cell Biology, University of Bonn, Ulrich-Haberland-Str. 61a, 53121 Bonn, Germany.

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http://link.springer.com/10.1007/s00401-012-1054-9
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http://dx.doi.org/10.1007/s00401-012-1054-9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5127197PMC
January 2013

Central mechanisms during fatiguing muscle exercise in muscular dystrophy and fibromyalgia syndrome: a study with transcranial magnetic stimulation.

Muscle Nerve 2011 Apr 8;43(4):479-84. Epub 2011 Feb 8.

Department of Neurology, BG-Universitätsklinikum Bergmannsheil, Ruhr University, Buerkle-de-la-Camp-Platz 1, Bochum D-44789, Germany.

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http://dx.doi.org/10.1002/mus.21920DOI Listing
April 2011

Creatine for treating muscle disorders.

Cochrane Database Syst Rev 2011 Feb 16(2):CD004760. Epub 2011 Feb 16.

Department of Neurology, University Hospital Bergmannsheil, Ruhr University Bochum, Buerkle-de-la-Camp-Platz 1, Bochum, Germany, 44789.

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http://doi.wiley.com/10.1002/14651858.CD004760.pub3
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http://dx.doi.org/10.1002/14651858.CD004760.pub3DOI Listing
February 2011

De novo desmin-mutation N116S is associated with arrhythmogenic right ventricular cardiomyopathy.

Hum Mol Genet 2010 Dec 9;19(23):4595-607. Epub 2010 Sep 9.

Herz- & Diabeteszentrum NRW, Klinik f. Thorax- und Kardiovaskularchirurgie, Erich und Hanna Klessmann-Institutfür Kardiovaskulaere Forschung und Entwicklung/Klinik fuer angeborene Herzfehler, Georgstrasse 11, Bad Oeynhausen, Germany.

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http://www.physik.uni-bielefeld.de/biophysik/uploads/hmg_kla
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http://www.hmg.oxfordjournals.org/cgi/doi/10.1093/hmg/ddq387
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http://dx.doi.org/10.1093/hmg/ddq387DOI Listing
December 2010

MRI in lipid-lowering agent-associated myopathy: a retrospective review of 21 cases.

AJR Am J Roentgenol 2010 Apr;194(4):W323-8

Department of Radiology, Ruhr University Bochum, Universitätsklinikum Bergmannsheil, Buerkle-de-la-Camp-Platz 1, 44789 Bochum, Germany.

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http://dx.doi.org/10.2214/AJR.09.2698DOI Listing
April 2010

Rippling muscle disease: variable phenotype in a family with five afflicted members.

Muscle Nerve 2010 Jan;41(1):128-32

Department of Neurology, University of Heidelberg, Im Neuenheimer Feld 400, 69120 Heidelberg, Germany.

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http://dx.doi.org/10.1002/mus.21446DOI Listing
January 2010

Congenital type IV glycogenosis: the spectrum of pleomorphic polyglucosan bodies in muscle, nerve, and spinal cord with two novel mutations in the GBE1 gene.

Acta Neuropathol 2008 Nov 26;116(5):491-506. Epub 2008 Jul 26.

Department of Neuropathology, RWTH Aachen University Hospital, Pauwelsstr. 30, 52074, Aachen, Germany.

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http://link.springer.com/10.1007/s00401-008-0417-8
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http://dx.doi.org/10.1007/s00401-008-0417-8DOI Listing
November 2008

Therapeutic options in other metabolic myopathies.

Authors:
Matthias Vorgerd

Neurotherapeutics 2008 Oct;5(4):579-82

Department of Neurology, Ruhr-University Bochum, Kliniken Bergmannsheil, Bochum, Germany.

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http://link.springer.com/10.1016/j.nurt.2008.08.006
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http://dx.doi.org/10.1016/j.nurt.2008.08.006DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4514707PMC
October 2008

The pathomechanism of filaminopathy: altered biochemical properties explain the cellular phenotype of a protein aggregation myopathy.

Hum Mol Genet 2007 Jun 5;16(11):1351-8. Epub 2007 Apr 5.

Department of Cell Biology, University of Potsdam, 14476 Potsdam-Golm, Germany.

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http://dx.doi.org/10.1093/hmg/ddm085DOI Listing
June 2007

Parkinson syndrome, neuropathy, and myopathy caused by the mutation A8344G (MERRF) in tRNALys.

Neurology 2007 Jan;68(1):56-8

Friedrich-Baur-Institute and Department of Neurology, Ludwig-Maximilians-University, Munich, Germany.

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http://www.neurology.org/cgi/doi/10.1212/01.wnl.0000250334.4
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http://dx.doi.org/10.1212/01.wnl.0000250334.48038.7aDOI Listing
January 2007

Muscle pain in myophosphorylase deficiency (McArdle's disease): the role of gender, genotype, and pain-related coping.

Pain 2006 Oct 21;124(3):295-304. Epub 2006 Jun 21.

Department of Neurology, Neuromuscular Center Ruhrgebiet, Kliniken Bergmannsheil, Ruhr-University, Bochum, Germany.

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http://dx.doi.org/10.1016/j.pain.2006.04.017DOI Listing
October 2006

The novel neurofilament light (NEFL) mutation Glu397Lys is associated with a clinically and morphologically heterogeneous type of Charcot-Marie-Tooth neuropathy.

Neuromuscul Disord 2004 Feb;14(2):147-57

Institut für Neuropathologie, Universitätsklinikum der RWTH Aachen, Pauwelsstrasse 32, 52074 Aachen, Germany.

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http://dx.doi.org/10.1016/j.nmd.2003.10.003DOI Listing
February 2004

Variable reduction of caveolin-3 in patients with LGMD2B/MM.

J Neurol 2003 Dec;250(12):1431-8

Gene Center, Friedrich-Baur-Institute & Dept. of Neurology, Ludwig Maximilians University of Munich, Munich, Germany.

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http://dx.doi.org/10.1007/s00415-003-0234-xDOI Listing
December 2003

Breakdown of adenine nucleotide pool in fatiguing skeletal muscle in McArdle's disease: a noninvasive 31P-MRS and EMG study.

Muscle Nerve 2003 Jun;27(6):728-36

Institute of Aerospace Medicine, German Aerospace Center (DLR e.V.), Linder Höhe, D-51170 Köln, Cologne, Germany.

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http://dx.doi.org/10.1002/mus.10377DOI Listing
June 2003

Carbohydrate oxidation disorders of skeletal muscle.

Curr Opin Clin Nutr Metab Care 2002 Nov;5(6):611-7

Kliniken Bergmannsheil, Department of Neurology, Ruhr-University Bochum, Germany.

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http://dx.doi.org/10.1097/00075197-200211000-00003DOI Listing
November 2002

Rippling muscle disease in childhood.

J Child Neurol 2002 Jul;17(7):483-90

Department of Pediatrics, Ruhr-University Bochum, Germany.

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http://dx.doi.org/10.1177/088307380201700703DOI Listing
July 2002