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

H Goebel

Showing results (471-480 of 483) with videos related to

Pageof 49
Sort By:
The Thoracic and Cardiovascular Surgeon|February 8, 2007
Actual management of patients with familial ascending aortic aneurysms and type-A aortic dissectionsE Weigang, X-C Chang, S Munk-Schulenburg, et al.
Neurology|March 10, 2015
Nuclear actin aggregation is a hallmark of anti-synthetase syndrome-induced dysimmune myopathyWerner Stenzel, Corinna Preuße, Yves Allenbach, et al.
Neuromuscular Disorders : NMD|January 20, 2016
De novo exonic mutation in MYH7 gene leading to exon skipping in a patient with early onset muscular weakness and fiber-type disproportionSander Pajusalu, Inga Talvik, Klari Noormets, et al.
Neuromuscular Disorders : NMD|December 20, 2022
Pathogenic variants in three families with distal muscle involvementMarian A J Weterman, Marieke Bronk, Aldo Jongejan, et al.
Journal of the Neurological Sciences|December 14, 2002
Filamin C accumulation is a strong but nonspecific immunohistochemical marker of core formation in muscleC G Bönnemann, T G Thompson, P F M van der Ven, et al.
Neuromuscular Disorders : NMD|August 2, 2015
GNE myopathy in Roma patients homozygous for the p.I618T founder mutationTeodora Chamova, Velina Guergueltcheva, Mariana Gospodinova, et al.
Biomed Research International|November 10, 2015
ATP synthase deficiency due to TMEM70 mutation leads to ultrastructural mitochondrial degeneration and is amenable to treatmentAnne K Braczynski, Stefan Vlaho, Klaus Müller, et al.
Neuromuscular Disorders : NMD|October 29, 2000
Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies)L V Anderson, R M Harrison, R Pogue, et al.
European Journal of Human Genetics : EJHG|December 4, 2008
In-frame deletion in the seventh immunoglobulin-like repeat of filamin C in a family with myofibrillar myopathyAlexey Shatunov, Montse Olivé, Zagaa Odgerel, et al.
Neuromuscular Disorders : NMD|July 20, 2010
Myopathy with hexagonally cross-linked crystalloid inclusions: delineation of a clinico-pathological entityKristl G Claeys, Jean-François Pellissier, Federico Garcia-Bragado, et al.
Pageof 49

Showing results (471-480 of 483) with videos related to

Sort By:
Pageof 49
The Thoracic and Cardiovascular Surgeon|February 8, 2007
Actual management of patients with familial ascending aortic aneurysms and type-A aortic dissectionsE Weigang, X-C Chang, S Munk-Schulenburg, et al.
Neurology|March 10, 2015
Nuclear actin aggregation is a hallmark of anti-synthetase syndrome-induced dysimmune myopathyWerner Stenzel, Corinna Preuße, Yves Allenbach, et al.
Neuromuscular Disorders : NMD|January 20, 2016
De novo exonic mutation in MYH7 gene leading to exon skipping in a patient with early onset muscular weakness and fiber-type disproportionSander Pajusalu, Inga Talvik, Klari Noormets, et al.
Neuromuscular Disorders : NMD|December 20, 2022
Pathogenic variants in three families with distal muscle involvementMarian A J Weterman, Marieke Bronk, Aldo Jongejan, et al.
Journal of the Neurological Sciences|December 14, 2002
Filamin C accumulation is a strong but nonspecific immunohistochemical marker of core formation in muscleC G Bönnemann, T G Thompson, P F M van der Ven, et al.
Neuromuscular Disorders : NMD|August 2, 2015
GNE myopathy in Roma patients homozygous for the p.I618T founder mutationTeodora Chamova, Velina Guergueltcheva, Mariana Gospodinova, et al.
Biomed Research International|November 10, 2015
ATP synthase deficiency due to TMEM70 mutation leads to ultrastructural mitochondrial degeneration and is amenable to treatmentAnne K Braczynski, Stefan Vlaho, Klaus Müller, et al.
Neuromuscular Disorders : NMD|October 29, 2000
Secondary reduction in calpain 3 expression in patients with limb girdle muscular dystrophy type 2B and Miyoshi myopathy (primary dysferlinopathies)L V Anderson, R M Harrison, R Pogue, et al.
European Journal of Human Genetics : EJHG|December 4, 2008
In-frame deletion in the seventh immunoglobulin-like repeat of filamin C in a family with myofibrillar myopathyAlexey Shatunov, Montse Olivé, Zagaa Odgerel, et al.
Neuromuscular Disorders : NMD|July 20, 2010
Myopathy with hexagonally cross-linked crystalloid inclusions: delineation of a clinico-pathological entityKristl G Claeys, Jean-François Pellissier, Federico Garcia-Bragado, et al.
Pageof 49