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Anne-Dorte Sperfeld

Showing results (21-30 of 34) with videos related to

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Nature Clinical Practice. Neurology|June 19, 2008
Diagnosis and treatment of bulbar symptoms in amyotrophic lateral sclerosisPeter Kühnlein, Hans-Jürgen Gdynia, Anne-Dorte Sperfeld, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|April 23, 2008
Palliative care and circumstances of dying in German ALS patients using non-invasive ventilationPeter Kühnlein, Andrea Kübler, Sabine Raubold, et al.
Plos One|February 25, 2012
The cerebro-morphological fingerprint of a progeroid syndrome: white matter changes correlate with neurological symptoms in xeroderma pigmentosumJan Kassubek, Anne-Dorte Sperfeld, Elmar H Pinkhardt, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance|November 6, 2008
Cardiac involvement in patients with Becker muscular dystrophy: new diagnostic and pathophysiological insights by a CMR approachAli Yilmaz, Hans-Jürgen Gdynia, Hannibal Baccouche, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 13, 2010
Four familial ALS pedigrees discordant for two SOD1 mutations: are all SOD1 mutations pathogenic?Ansgar Felbecker, William Camu, Paul N Valdmanis, et al.
Journal of the Neurological Sciences|January 15, 2008
Screening of hereditary spastic paraplegia patients for alterations at NIPA1 mutational hotspotsChristian Beetz, Rebecca Schüle, Stephan Klebe, et al.
Archives of Neurology|September 10, 2008
Two German kindreds with familial amyotrophic lateral sclerosis due to TARDBP mutationsPeter Kühnlein, Anne-Dorte Sperfeld, Ben Vanmassenhove, et al.
Annals of Neurology|October 22, 2005
Heterozygous R1101K mutation of the DCTN1 gene in a family with ALS and FTDChristoph Münch, Angela Rosenbohm, Anne-Dorte Sperfeld, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|August 4, 2009
Concentrations of beta-amyloid precursor protein processing products in cerebrospinal fluid of patients with amyotrophic lateral sclerosis and frontotemporal lobar degenerationPetra Steinacker, Corinna Hendrich, Anne-Dorte Sperfeld, et al.
Journal of Neurology|April 14, 2009
Identification of novel Angiogenin (ANG) gene missense variants in German patients with amyotrophic lateral sclerosisRubén Fernández-Santiago, Sabine Hoenig, Peter Lichtner, et al.
Pageof 4

Showing results (21-30 of 34) with videos related to

Sort By:
Pageof 4
Nature Clinical Practice. Neurology|June 19, 2008
Diagnosis and treatment of bulbar symptoms in amyotrophic lateral sclerosisPeter Kühnlein, Hans-Jürgen Gdynia, Anne-Dorte Sperfeld, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|April 23, 2008
Palliative care and circumstances of dying in German ALS patients using non-invasive ventilationPeter Kühnlein, Andrea Kübler, Sabine Raubold, et al.
Plos One|February 25, 2012
The cerebro-morphological fingerprint of a progeroid syndrome: white matter changes correlate with neurological symptoms in xeroderma pigmentosumJan Kassubek, Anne-Dorte Sperfeld, Elmar H Pinkhardt, et al.
Journal of Cardiovascular Magnetic Resonance : Official Journal of the Society for Cardiovascular Magnetic Resonance|November 6, 2008
Cardiac involvement in patients with Becker muscular dystrophy: new diagnostic and pathophysiological insights by a CMR approachAli Yilmaz, Hans-Jürgen Gdynia, Hannibal Baccouche, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 13, 2010
Four familial ALS pedigrees discordant for two SOD1 mutations: are all SOD1 mutations pathogenic?Ansgar Felbecker, William Camu, Paul N Valdmanis, et al.
Journal of the Neurological Sciences|January 15, 2008
Screening of hereditary spastic paraplegia patients for alterations at NIPA1 mutational hotspotsChristian Beetz, Rebecca Schüle, Stephan Klebe, et al.
Archives of Neurology|September 10, 2008
Two German kindreds with familial amyotrophic lateral sclerosis due to TARDBP mutationsPeter Kühnlein, Anne-Dorte Sperfeld, Ben Vanmassenhove, et al.
Annals of Neurology|October 22, 2005
Heterozygous R1101K mutation of the DCTN1 gene in a family with ALS and FTDChristoph Münch, Angela Rosenbohm, Anne-Dorte Sperfeld, et al.
Journal of Neural Transmission (Vienna, Austria : 1996)|August 4, 2009
Concentrations of beta-amyloid precursor protein processing products in cerebrospinal fluid of patients with amyotrophic lateral sclerosis and frontotemporal lobar degenerationPetra Steinacker, Corinna Hendrich, Anne-Dorte Sperfeld, et al.
Journal of Neurology|April 14, 2009
Identification of novel Angiogenin (ANG) gene missense variants in German patients with amyotrophic lateral sclerosisRubén Fernández-Santiago, Sabine Hoenig, Peter Lichtner, et al.
Pageof 4