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J Finsterer

Showing results (291-300 of 336) with videos related to

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Acta Neurologica Belgica|September 21, 2020
Mitochondrial disorder should be considered as a differential of late-onset myasthenia gravisJ Finsterer, F A Scorza, C A Scorza, et al.
Herz|September 27, 2013
Mitochondrial tRNA glutamine variant in hypertrophic cardiomyopathyS Zarrouk-Mahjoub, S Mehri, F Ouarda, et al.
Neurobiology of Aging|July 13, 2021
Prove pathogenicity of OPTN variants before establishing a causal relation with amyotrophic lateral sclerosisJ Finsterer, F A Scorza, C A Scorza, et al.
Clinical Genetics|May 22, 2001
Relation of cardiac abnormalities and CTG-repeat size in myotonic dystrophyJ Finsterer, E Gharehbaghi-Schnell, C Stöllberger, et al.
Journal of Clinical Pathology|May 1, 1996
Anti-GM1 antibodies in polyneuropathies of unknown originJ Finsterer, W Muellbacher, W M Halbmayer, et al.
The Medical Journal of Malaysia|July 30, 2020
Periodic weakness of the diaphragm as the sole manifestation of bulbar onset myastheniaJ Finsterer, C A Scorza, F A Scorza, et al.
Case Reports in Neurological Medicine|July 30, 2019
Comment on "Proximal Myopathy due to m.5835G>A Mutation in Mitochondrial MT-TY Gene"J Finsterer, C A Scorza, A C Fiorini, et al.
Current Neurology and Neuroscience Reports|March 24, 2018
Takotsubo Syndrome: Clinical Features, Pathogenesis, Treatment, and Relationship with Cerebrovascular DiseasesM Ranieri, J Finsterer, G Bedini, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|June 26, 2008
Stroke as initial manifestation of a fulminant C. perfringens sepsisB Hess, P Hitzenberger, W Grisold, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|November 14, 1997
APC resistance and factor V Leiden (FV:Q506) mutation in patients with ischemic cerebral events. Vienna Thrombophilia in Stroke Study Group (VITISS)W M Halbmayer, A Haushofer, V Angerer, et al.
Pageof 34

Showing results (291-300 of 336) with videos related to

Sort By:
Pageof 34
Acta Neurologica Belgica|September 21, 2020
Mitochondrial disorder should be considered as a differential of late-onset myasthenia gravisJ Finsterer, F A Scorza, C A Scorza, et al.
Herz|September 27, 2013
Mitochondrial tRNA glutamine variant in hypertrophic cardiomyopathyS Zarrouk-Mahjoub, S Mehri, F Ouarda, et al.
Neurobiology of Aging|July 13, 2021
Prove pathogenicity of OPTN variants before establishing a causal relation with amyotrophic lateral sclerosisJ Finsterer, F A Scorza, C A Scorza, et al.
Clinical Genetics|May 22, 2001
Relation of cardiac abnormalities and CTG-repeat size in myotonic dystrophyJ Finsterer, E Gharehbaghi-Schnell, C Stöllberger, et al.
Journal of Clinical Pathology|May 1, 1996
Anti-GM1 antibodies in polyneuropathies of unknown originJ Finsterer, W Muellbacher, W M Halbmayer, et al.
The Medical Journal of Malaysia|July 30, 2020
Periodic weakness of the diaphragm as the sole manifestation of bulbar onset myastheniaJ Finsterer, C A Scorza, F A Scorza, et al.
Case Reports in Neurological Medicine|July 30, 2019
Comment on "Proximal Myopathy due to m.5835G>A Mutation in Mitochondrial MT-TY Gene"J Finsterer, C A Scorza, A C Fiorini, et al.
Current Neurology and Neuroscience Reports|March 24, 2018
Takotsubo Syndrome: Clinical Features, Pathogenesis, Treatment, and Relationship with Cerebrovascular DiseasesM Ranieri, J Finsterer, G Bedini, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques|June 26, 2008
Stroke as initial manifestation of a fulminant C. perfringens sepsisB Hess, P Hitzenberger, W Grisold, et al.
Blood Coagulation & Fibrinolysis : an International Journal in Haemostasis and Thrombosis|November 14, 1997
APC resistance and factor V Leiden (FV:Q506) mutation in patients with ischemic cerebral events. Vienna Thrombophilia in Stroke Study Group (VITISS)W M Halbmayer, A Haushofer, V Angerer, et al.
Pageof 34