Works matching AU Goebel, Hans H.


Results: 67
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    Infantile Intranuclear Rod Myopathy.

    Published in:
    Journal of Child Neurology, 1997, v. 12, n. 1, p. 22
    By:
    • Goebel, Hans H.;
    • Piirsoo, Anders;
    • Warlo, Irene;
    • Schofer, Otto;
    • Kehr, Stephan;
    • Gaude, Michael
    Publication type:
    Article
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    Introduction.

    Published in:
    Brain Pathology, 2009, v. 19, n. 3, p. 480, doi. 10.1111/j.1750-3639.2009.00291.x
    By:
    • Goebel, Hans H.
    Publication type:
    Article
    12

    Actinopathies and Myosinopathies.

    Published in:
    Brain Pathology, 2009, v. 19, n. 3, p. 516, doi. 10.1111/j.1750-3639.2009.00287.x
    By:
    • Goebel, Hans H.;
    • Laing, Nigel G.
    Publication type:
    Article
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    Introduction.

    Published in:
    Brain Pathology, 2004, v. 14, n. 1, p. 59, doi. 10.1111/j.1750-3639.2004.tb00498.x
    By:
    • Goebel, Hans H.
    Publication type:
    Article
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    Primary desminopathies.

    Published in:
    Journal of Cellular & Molecular Medicine, 2007, v. 11, n. 3, p. 416, doi. 10.1111/j.1582-4934.2007.00057.x
    By:
    • Schröder, Rolf;
    • Vrabie, Alexandra;
    • Goebel, Hans H.
    Publication type:
    Article
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    Desmin-related myopathy with mallory body–like inclusions is caused by mutations of the selenoprotein N gene (Accession numbers are listed in the <APPR HREF="app1">Appendix</APPR> on the last page of this article.).

    Published in:
    Annals of Neurology, 2004, v. 55, n. 5, p. 676
    By:
    • Ana Ferreiro;
    • Chantal Ceuterick-de Groote;
    • Jared J. Marks;
    • Nathalie Goemans;
    • Gudrun Schreiber;
    • Folker Hanefeld;
    • Michel Fardeau;
    • Jean-Jacques Martin;
    • Hans H. Goebel;
    • Pascale Richard;
    • Pascale Guicheney;
    • Carsten G. Bönnemann
    Publication type:
    Article
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    ATP Synthase Deficiency due to TMEM70 Mutation Leads to Ultrastructural Mitochondrial Degeneration and Is Amenable to Treatment.

    Published in:
    BioMed Research International, 2015, v. 2015, p. 1, doi. 10.1155/2015/462592
    By:
    • Braczynski, Anne K.;
    • Vlaho, Stefan;
    • Müller, Klaus;
    • Wittig, Ilka;
    • Blank, Anna-Eva;
    • Tews, Dominique S.;
    • Drott, Ulrich;
    • Kleinle, Stephanie;
    • Abicht, Angela;
    • Horvath, Rita;
    • Plate, Karl H.;
    • Stenzel, Werner;
    • Goebel, Hans H.;
    • Schulze, Andreas;
    • Harter, Patrick N.;
    • Kieslich, Matthias;
    • Mittelbronn, Michel
    Publication type:
    Article
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    Workshop Report.

    Published in:
    Neuropathology & Applied Neurobiology, 1997, v. 23, n. 3, p. 262, doi. 10.1111/j.1365-2990.1997.tb01210.x
    By:
    • Ruchoux, Marie-Magdeleine;
    • Goebel, Hans H.
    Publication type:
    Article
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    Spheroid body myopathy revisited.

    Published in:
    1997
    By:
    • Goebel, Hans H.;
    • D'Agostino, Anthony N.;
    • Wilson, Jacob;
    • Cole, George;
    • Foroud, Tatiana;
    • Koller, Daniel;
    • Farlow, Martin;
    • Azzarelli, Biagio;
    • Muller, Jans;
    • Goebel, H H;
    • D'Agostino, A N;
    • Wilson, J;
    • Cole, G;
    • Foroud, T;
    • Koller, D;
    • Farlow, M;
    • Azzarelli, B;
    • Muller, J
    Publication type:
    journal article
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    Focal myositis of the temporal muscle.

    Published in:
    Muscle & Nerve, 1993, v. 16, n. 12, p. 1374, doi. 10.1002/mus.880161216
    By:
    • Naumann, Markus;
    • Toyka, Laus Viktor;
    • Goebel, Hans H.;
    • Hofmann, Erich;
    • Reichmann, Heinz
    Publication type:
    Article
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    Mutations in the skeletal muscle α-actin gene in patients with actin myopathy and nemaline myopathy.

    Published in:
    Nature Genetics, 1999, v. 23, n. 2, p. 208, doi. 10.1038/13837
    By:
    • Nowak, Kristen J.;
    • Wattanasirichaigoon, Duangrurdee;
    • Goebel, Hans H.;
    • Wilce, Matthew;
    • Pelin, Katarina;
    • Donner, Kati;
    • Jacob, Rebecca L.;
    • Hübner, Christoph;
    • Oexle, Konrad;
    • Anderson, Janice R.;
    • Verity, Christopher M.;
    • North, Kathryn N.;
    • Iannaccone, Susan T.;
    • Müller, Clemens R.;
    • Nürnberg, Peter;
    • Muntoni, Francesco;
    • Sewry, Caroline;
    • Hughes, Imelda;
    • Sutphen, Rebecca
    Publication type:
    Article
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    SIL1 mutations and clinical spectrum in patients with Marinesco-Sjogren syndrome.

    Published in:
    2013
    By:
    • Krieger, Michael;
    • Roos, Andreas;
    • Stendel, Claudia;
    • Claeys, Kristl G;
    • Sonmez, Fatma Mujgan;
    • Baudis, Michael;
    • Bauer, Peter;
    • Bornemann, Antje;
    • de Goede, Christian;
    • Dufke, Andreas;
    • Finkel, Richard S;
    • Goebel, Hans H;
    • Häussler, Martin;
    • Kingston, Helen;
    • Kirschner, Janbernd;
    • Medne, Livija;
    • Muschke, Petra;
    • Rivier, François;
    • Rudnik-Schöneborn, Sabine;
    • Spengler, Sabrina
    Publication type:
    Journal Article
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    SIL1 mutations and clinical spectrum in patients with Marinesco-Sjögren syndrome.

    Published in:
    Brain: A Journal of Neurology, 2013, v. 136, n. 12, p. 3634, doi. 10.1093/brain/awt283
    By:
    • Krieger, Michael;
    • Roos, Andreas;
    • Stendel, Claudia;
    • Claeys, Kristl G.;
    • Sonmez, Fatma Mujgan;
    • Baudis, Michael;
    • Bauer, Peter;
    • Bornemann, Antje;
    • de Goede, Christian;
    • Dufke, Andreas;
    • Finkel, Richard S.;
    • Goebel, Hans H.;
    • Häussler, Martin;
    • Kingston, Helen;
    • Kirschner, Janbernd;
    • Medne, Livija;
    • Muschke, Petra;
    • Rivier, François;
    • Rudnik-Schöneborn, Sabine;
    • Spengler, Sabrina
    Publication type:
    Article
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    McLeod myopathy revisited: more neurogenic and less benign.

    Published in:
    Brain: A Journal of Neurology, 2007, v. 130, n. 12, p. 3285, doi. 10.1093/brain/awm269
    By:
    • Ekkehard Hewer;
    • Adrian Danek;
    • Benedikt G. Schoser;
    • Marcelo Miranda;
    • Ross Reichard;
    • Claudia Castiglioni;
    • Matthias Oechsner;
    • Hans H. Goebel;
    • Frank L. Heppner;
    • Hans H. Jung
    Publication type:
    Article
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    Hamartoma of the triceps surae muscle.

    Published in:
    Acta Neuropathologica, 1997, v. 94, n. 1, p. 91, doi. 10.1007/s004010050677
    By:
    • Tews, D. S.;
    • Goebel, Hans H.;
    • Heffner, Reid R.;
    • Reitter, Bernd;
    • Vetter, Thomas;
    • Kreitner, Karl F.
    Publication type:
    Article
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    Autophagic vacuolar myopathy is a common feature of CLN3 disease.

    Published in:
    Annals of Clinical & Translational Neurology, 2018, v. 5, n. 11, p. 1385, doi. 10.1002/acn3.662
    By:
    • Radke, Josefine;
    • Koll, Randi;
    • Gill, Esther;
    • Wiese, Lars;
    • Schulz, Angela;
    • Kohlschütter, Alfried;
    • Schuelke, Markus;
    • Hagel, Christian;
    • Stenzel, Werner;
    • Goebel, Hans H.
    Publication type:
    Article
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    Storage Diseases: Diagnostic Position.

    Published in:
    Ultrastructural Pathology, 2013, v. 37, n. 1, p. 19, doi. 10.3109/01913123.2012.670060
    By:
    • Goebel, Hans H.;
    • Müller, Harald D.
    Publication type:
    Article
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