Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

Hans-Hilmar Goebel

Showing results (41-50 of 80) with videos related to

Pageof 8
Sort By:
Journal of Child Neurology|December 17, 2013
A paucisymptomatic neuromuscular disease mimicking type III 5q-SMA with complex rearrangements in the SMN geneLaura Nanna Lohkamp, Katja von Au, Hans-Hilmar Goebel, et al.
Neuropathology and Applied Neurobiology|May 11, 2021
Inflammation, fibrosis and skeletal muscle regeneration in LGMDR9 are orchestrated by macrophagesHeike Kölbel, Corinna Preuße, Lukas Brand, et al.
Neuromuscular Disorders : NMD|December 1, 2006
MRI in DNM2-related centronuclear myopathy: evidence for highly selective muscle involvementJoachim Schessl, Livija Medne, Ying Hu, et al.
Rheumatology (Oxford, England)|September 21, 2022
Eosinophilic fasciitis (Shulman syndrome)-recognition of the histological spectrum allows for new insights into possible pathomechanismsDebora Pehl, Corinna Preuße, Yves Allenbach, et al.
Acta Neuropathologica|January 12, 2024
Complement and MHC patterns can provide the diagnostic framework for inflammatory neuromuscular diseasesChristopher Nelke, Simone Schmid, Felix Kleefeld, et al.
Neuropathology and Applied Neurobiology|May 10, 2021
Successful plasmapheresis and immunoglobulin treatment for severe lipid storage myopathy: Doing the right thing for the wrong reasonFelix Kleefeld, Anja von Renesse, Carsten Dittmayer, et al.
Brain Pathology (Zurich, Switzerland)|May 27, 2021
NanoString technology distinguishes anti-TIF-1γ<sup>+</sup> from anti-Mi-2<sup>+</sup> dermatomyositis patientsCorinna Preusse, Pascale Eede, Lucie Heinzeling, et al.
Archives of Pathology & Laboratory Medicine|July 2, 2015
Common Data Elements for Muscle Biopsy ReportingJahannaz Dastgir, Anne Rutkowski, Rachel Alvarez, et al.
Muscle & Nerve|February 3, 2004
Muscle pathology in 57 patients with myotonic dystrophy type 2Benedikt G H Schoser, Christiane Schneider-Gold, Wolfram Kress, et al.
Acta Neuropathologica|April 17, 2021
Systemic sclerosis-associated myositis features minimal inflammation and characteristic capillary pathologyElise Siegert, Akinori Uruha, Hans-Hilmar Goebel, et al.
Pageof 8

Showing results (41-50 of 80) with videos related to

Sort By:
Pageof 8
Journal of Child Neurology|December 17, 2013
A paucisymptomatic neuromuscular disease mimicking type III 5q-SMA with complex rearrangements in the SMN geneLaura Nanna Lohkamp, Katja von Au, Hans-Hilmar Goebel, et al.
Neuropathology and Applied Neurobiology|May 11, 2021
Inflammation, fibrosis and skeletal muscle regeneration in LGMDR9 are orchestrated by macrophagesHeike Kölbel, Corinna Preuße, Lukas Brand, et al.
Neuromuscular Disorders : NMD|December 1, 2006
MRI in DNM2-related centronuclear myopathy: evidence for highly selective muscle involvementJoachim Schessl, Livija Medne, Ying Hu, et al.
Rheumatology (Oxford, England)|September 21, 2022
Eosinophilic fasciitis (Shulman syndrome)-recognition of the histological spectrum allows for new insights into possible pathomechanismsDebora Pehl, Corinna Preuße, Yves Allenbach, et al.
Acta Neuropathologica|January 12, 2024
Complement and MHC patterns can provide the diagnostic framework for inflammatory neuromuscular diseasesChristopher Nelke, Simone Schmid, Felix Kleefeld, et al.
Neuropathology and Applied Neurobiology|May 10, 2021
Successful plasmapheresis and immunoglobulin treatment for severe lipid storage myopathy: Doing the right thing for the wrong reasonFelix Kleefeld, Anja von Renesse, Carsten Dittmayer, et al.
Brain Pathology (Zurich, Switzerland)|May 27, 2021
NanoString technology distinguishes anti-TIF-1γ<sup>+</sup> from anti-Mi-2<sup>+</sup> dermatomyositis patientsCorinna Preusse, Pascale Eede, Lucie Heinzeling, et al.
Archives of Pathology & Laboratory Medicine|July 2, 2015
Common Data Elements for Muscle Biopsy ReportingJahannaz Dastgir, Anne Rutkowski, Rachel Alvarez, et al.
Muscle & Nerve|February 3, 2004
Muscle pathology in 57 patients with myotonic dystrophy type 2Benedikt G H Schoser, Christiane Schneider-Gold, Wolfram Kress, et al.
Acta Neuropathologica|April 17, 2021
Systemic sclerosis-associated myositis features minimal inflammation and characteristic capillary pathologyElise Siegert, Akinori Uruha, Hans-Hilmar Goebel, et al.
Pageof 8