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Hans-Hilmar Goebel

Showing results (61-70 of 80) with videos related to

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The American Journal of Pathology|January 26, 2016
Dermatomyositis With or Without Anti-Melanoma Differentiation-Associated Gene 5 Antibodies: Common Interferon Signature but Distinct NOS2 ExpressionYves Allenbach, Gaëlle Leroux, Xavier Suárez-Calvet, et al.
Brain Pathology (Zurich, Switzerland)|June 15, 2022
Endoplasmic reticulum-stress and unfolded protein response-activation in immune-mediated necrotizing myopathyCorinna Preusse, Theodore Marteau, Norina Fischer, et al.
Neurology|July 31, 2019
Idiopathic inflammatory myopathy: Interrater variability in muscle biopsy readingPieter A Olivier, Boel De Paepe, Eleonora Aronica, et al.
Acta Neuropathologica|July 16, 2024
Anti-Ku + myositis: an acquired inflammatory protein-aggregate myopathyMarie-Therese Holzer, Akinori Uruha, Andreas Roos, et al.
Journal of Neurology|January 23, 2026
Exploring molecular signatures in PURA syndrome using muscle proteomics and serum biomarkersMagdalena Mroczek, Corinna Preusse, Andreas Hentschel, et al.
American Journal of Human Genetics|March 1, 2016
Mutations in Subunits of the Activating Signal Cointegrator 1 Complex Are Associated with Prenatal Spinal Muscular Atrophy and Congenital Bone FracturesEllen Knierim, Hiromi Hirata, Nicole I Wolf, et al.
Neurology|January 14, 2018
Necrosis in anti-SRP<sup>+</sup> and anti-HMGCR<sup>+</sup>myopathies: Role of autoantibodies and complementYves Allenbach, Louiza Arouche-Delaperche, Corinna Preusse, et al.
Annals of Neurology|April 1, 2003
Homozygous mutations in caveolin-3 cause a severe form of rippling muscle diseaseChristian Kubisch, Benedikt G H Schoser, Monika von Düring, et al.
Brain : a Journal of Neurology|April 7, 2025
Mitochondrial damage is associated with an early immune response in inclusion body myositisFelix Kleefeld, Emily Cross, Daniel Lagos, et al.
The Journal of Clinical Investigation|February 16, 2008
Proteomic identification of FHL1 as the protein mutated in human reducing body myopathyJoachim Schessl, Yaqun Zou, Meagan J McGrath, et al.
Pageof 8

Showing results (61-70 of 80) with videos related to

Sort By:
Pageof 8
The American Journal of Pathology|January 26, 2016
Dermatomyositis With or Without Anti-Melanoma Differentiation-Associated Gene 5 Antibodies: Common Interferon Signature but Distinct NOS2 ExpressionYves Allenbach, Gaëlle Leroux, Xavier Suárez-Calvet, et al.
Brain Pathology (Zurich, Switzerland)|June 15, 2022
Endoplasmic reticulum-stress and unfolded protein response-activation in immune-mediated necrotizing myopathyCorinna Preusse, Theodore Marteau, Norina Fischer, et al.
Neurology|July 31, 2019
Idiopathic inflammatory myopathy: Interrater variability in muscle biopsy readingPieter A Olivier, Boel De Paepe, Eleonora Aronica, et al.
Acta Neuropathologica|July 16, 2024
Anti-Ku + myositis: an acquired inflammatory protein-aggregate myopathyMarie-Therese Holzer, Akinori Uruha, Andreas Roos, et al.
Journal of Neurology|January 23, 2026
Exploring molecular signatures in PURA syndrome using muscle proteomics and serum biomarkersMagdalena Mroczek, Corinna Preusse, Andreas Hentschel, et al.
American Journal of Human Genetics|March 1, 2016
Mutations in Subunits of the Activating Signal Cointegrator 1 Complex Are Associated with Prenatal Spinal Muscular Atrophy and Congenital Bone FracturesEllen Knierim, Hiromi Hirata, Nicole I Wolf, et al.
Neurology|January 14, 2018
Necrosis in anti-SRP<sup>+</sup> and anti-HMGCR<sup>+</sup>myopathies: Role of autoantibodies and complementYves Allenbach, Louiza Arouche-Delaperche, Corinna Preusse, et al.
Annals of Neurology|April 1, 2003
Homozygous mutations in caveolin-3 cause a severe form of rippling muscle diseaseChristian Kubisch, Benedikt G H Schoser, Monika von Düring, et al.
Brain : a Journal of Neurology|April 7, 2025
Mitochondrial damage is associated with an early immune response in inclusion body myositisFelix Kleefeld, Emily Cross, Daniel Lagos, et al.
The Journal of Clinical Investigation|February 16, 2008
Proteomic identification of FHL1 as the protein mutated in human reducing body myopathyJoachim Schessl, Yaqun Zou, Meagan J McGrath, et al.
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