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A Abicht

Showing results (11-20 of 34) with videos related to

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Journal of Neurology|March 4, 2000
Leber's hereditary optic neuropathy presenting as multiple sclerosis-like disease of the CNSR Horváth, A Abicht, E A Shoubridge, et al.
Neuromuscular Disorders : NMD|July 17, 2020
Rare intronic mutation between Exon 62 and 63 (c.9225-285A>G) of the dystrophin gene associated with atypical BMD phenotypeS C Schüssler, T Gerhalter, A Abicht, et al.
Neurology|August 10, 2005
An intronic base alteration of the CHRNE gene leading to a congenital myasthenic syndromeJ S Müller, R Stucka, S Neudecker, et al.
Neuromuscular Disorders : NMD|April 20, 2006
Long-term improvement of slow-channel congenital myasthenic syndrome with fluoxetineJ Colomer, J S Müller, A Vernet, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 20, 2005
Leigh syndrome caused by mutations in the flavoprotein (Fp) subunit of succinate dehydrogenase (SDHA)R Horváth, A Abicht, E Holinski-Feder, et al.
Orphanet Journal of Rare Diseases|October 23, 2016
Novel homozygous RARS2 mutation in two siblings without pontocerebellar hypoplasia - further expansion of the phenotypic spectrumS Lühl, H Bode, W Schlötzer, et al.
Der Nervenarzt|July 6, 2018
[Congenital myasthenic syndromes in adulthood : Challenging, rare but treatable]G Wunderlich, A Abicht, A Brunn, et al.
European Journal of Medical Research|March 14, 1998
Congenital myasthenic syndromes: clinical and genetic analysis of 18 patientsA Abicht, W Müller-Felber, P Fischer, et al.
Neuropediatrics|July 13, 2004
Synaptic congenital myasthenic syndrome in three patients due to a novel missense mutation (T441A) of the COLQ geneJ S Müller, S Petrova, R Kiefer, et al.
Neurology|August 26, 2006
Impaired receptor clustering in congenital myasthenic syndrome with novel RAPSN mutationsJ S Müller, S K Baumeister, V M Rasic, et al.
Pageof 4

Showing results (11-20 of 34) with videos related to

Sort By:
Pageof 4
Journal of Neurology|March 4, 2000
Leber's hereditary optic neuropathy presenting as multiple sclerosis-like disease of the CNSR Horváth, A Abicht, E A Shoubridge, et al.
Neuromuscular Disorders : NMD|July 17, 2020
Rare intronic mutation between Exon 62 and 63 (c.9225-285A>G) of the dystrophin gene associated with atypical BMD phenotypeS C Schüssler, T Gerhalter, A Abicht, et al.
Neurology|August 10, 2005
An intronic base alteration of the CHRNE gene leading to a congenital myasthenic syndromeJ S Müller, R Stucka, S Neudecker, et al.
Neuromuscular Disorders : NMD|April 20, 2006
Long-term improvement of slow-channel congenital myasthenic syndrome with fluoxetineJ Colomer, J S Müller, A Vernet, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|December 20, 2005
Leigh syndrome caused by mutations in the flavoprotein (Fp) subunit of succinate dehydrogenase (SDHA)R Horváth, A Abicht, E Holinski-Feder, et al.
Orphanet Journal of Rare Diseases|October 23, 2016
Novel homozygous RARS2 mutation in two siblings without pontocerebellar hypoplasia - further expansion of the phenotypic spectrumS Lühl, H Bode, W Schlötzer, et al.
Der Nervenarzt|July 6, 2018
[Congenital myasthenic syndromes in adulthood : Challenging, rare but treatable]G Wunderlich, A Abicht, A Brunn, et al.
European Journal of Medical Research|March 14, 1998
Congenital myasthenic syndromes: clinical and genetic analysis of 18 patientsA Abicht, W Müller-Felber, P Fischer, et al.
Neuropediatrics|July 13, 2004
Synaptic congenital myasthenic syndrome in three patients due to a novel missense mutation (T441A) of the COLQ geneJ S Müller, S Petrova, R Kiefer, et al.
Neurology|August 26, 2006
Impaired receptor clustering in congenital myasthenic syndrome with novel RAPSN mutationsJ S Müller, S K Baumeister, V M Rasic, et al.
Pageof 4