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H Goebel

Showing results (411-420 of 483) with videos related to

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Annals of Neurology|September 8, 2000
Severe congenital myasthenic syndrome due to homozygosity of the 1293insG epsilon-acetylcholine receptor subunit mutationJ P Sieb, S Kraner, B Schrank, et al.
European Journal of Pediatrics|November 1, 1984
Mitochondrial myopathy with lactic acidosis and deficient activity of muscle succinate cytochrome-c-oxidoreductaseA W Behbehani, H Goebel, G Osse, et al.
Neuropathology and Applied Neurobiology|January 18, 2013
Juvenile autophagic vacuolar myopathy - a new entity or variant?W Stenzel, I Nishino, A von Moers, et al.
Journal of Neurology|November 1, 1993
Amyloidoma of the gasserian ganglion as a cause of symptomatic neuralgia of the trigeminal nerve: report of three casesA Bornemann, J Bohl, O Hey, et al.
Journal of Neuropathology and Experimental Neurology|January 1, 1992
Adult polyglucosan body myopathyH H Goebel, Y S Shin, F Gullotta, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 8, 2005
Camptocormia associated with focal myositis in multiple-system atrophyNico J Diederich, Hans H Goebel, Georges Dooms, et al.
Neurology|August 19, 2009
Consequences of mutations within the C terminus of the FHL1 geneB Schoser, H H Goebel, I Janisch, et al.
Acta Neuropathologica|June 1, 1997
Friedreich's ataxia with isolated vitamin E deficiency: a neuropathological study of a Tunisian patientA Larnaout, S Belal, M Zouari, et al.
Strabismus|September 13, 2008
Eye movement involvement in Parry-Romberg Syndrome: a clinicopathologic case reportA A Zubcov-Iwantscheff, F Thomke, H H Goebel, et al.
Lymphology|January 14, 2011
Immunohistochemical study of remodeling of myocardial lymphatic and blood microvascular structures in terminal heart failure: differences between ischemic and dilated cardiomyopathyA Dashkevich, W Bloch, A Antonyan, et al.
Pageof 49

Showing results (411-420 of 483) with videos related to

Sort By:
Pageof 49
Annals of Neurology|September 8, 2000
Severe congenital myasthenic syndrome due to homozygosity of the 1293insG epsilon-acetylcholine receptor subunit mutationJ P Sieb, S Kraner, B Schrank, et al.
European Journal of Pediatrics|November 1, 1984
Mitochondrial myopathy with lactic acidosis and deficient activity of muscle succinate cytochrome-c-oxidoreductaseA W Behbehani, H Goebel, G Osse, et al.
Neuropathology and Applied Neurobiology|January 18, 2013
Juvenile autophagic vacuolar myopathy - a new entity or variant?W Stenzel, I Nishino, A von Moers, et al.
Journal of Neurology|November 1, 1993
Amyloidoma of the gasserian ganglion as a cause of symptomatic neuralgia of the trigeminal nerve: report of three casesA Bornemann, J Bohl, O Hey, et al.
Journal of Neuropathology and Experimental Neurology|January 1, 1992
Adult polyglucosan body myopathyH H Goebel, Y S Shin, F Gullotta, et al.
Movement Disorders : Official Journal of the Movement Disorder Society|October 8, 2005
Camptocormia associated with focal myositis in multiple-system atrophyNico J Diederich, Hans H Goebel, Georges Dooms, et al.
Neurology|August 19, 2009
Consequences of mutations within the C terminus of the FHL1 geneB Schoser, H H Goebel, I Janisch, et al.
Acta Neuropathologica|June 1, 1997
Friedreich's ataxia with isolated vitamin E deficiency: a neuropathological study of a Tunisian patientA Larnaout, S Belal, M Zouari, et al.
Strabismus|September 13, 2008
Eye movement involvement in Parry-Romberg Syndrome: a clinicopathologic case reportA A Zubcov-Iwantscheff, F Thomke, H H Goebel, et al.
Lymphology|January 14, 2011
Immunohistochemical study of remodeling of myocardial lymphatic and blood microvascular structures in terminal heart failure: differences between ischemic and dilated cardiomyopathyA Dashkevich, W Bloch, A Antonyan, et al.
Pageof 49