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Anne-D Sperfeld

Showing results (1-10 of 12) with videos related to

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Journal of Neurology, Neurosurgery, and Psychiatry|March 3, 2007
Widespread white matter changes in Kennedy disease: a voxel based morphometry studyJan Kassubek, Freimut D Juengling, Anne-D Sperfeld
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|July 9, 2024
Combination therapy for Sneddon syndrome to reduce the incidence of cerebrovascular complicationsAlbert Narwutsch, Johannes Wohlrab, Anne-D Sperfeld, et al.
Neurochemical Research|March 25, 2010
Hypercapnia is a possible determinant of the function of the blood-cerebrospinal fluid barrier in amyotrophic lateral sclerosisSigurd D Süssmuth, Anne D Sperfeld, Albert C Ludolph, et al.
European Neurology|July 29, 2010
Amygdala size reduction is associated with memory deficits in complicated hereditary spastic paraparesis: an MRI studyElmar H Pinkhardt, Anne-D Sperfeld, Ingo Uttner, et al.
Biomedical Engineering Online|November 13, 2007
Diffusion tensor imaging and tractwise fractional anisotropy statistics: quantitative analysis in white matter pathologyHans-Peter Mueller, Alexander Unrath, Anne D Sperfeld, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|September 14, 2007
Different regional brain volume loss in pure and complicated hereditary spastic paraparesis: a voxel-based morphometric studyJan Kassubek, Freimut D Juengling, Annette Baumgartner, et al.
Brain : a Journal of Neurology|March 5, 2003
A novel nonsense mutation in the ABC1 gene causes a severe syringomyelia-like phenotype of Tangier diseaseStephan Züchner, Anne D Sperfeld, Jan Senderek, et al.
Archives of Neurology|December 10, 2002
X-linked bulbospinal neuronopathy: Kennedy diseaseAnne D Sperfeld, Jochem Karitzky, Dagmar Brummer, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|November 6, 2008
Identification of candidate genes for sporadic amyotrophic lateral sclerosis by array comparative genomic hybridizationSarah A Shoichet, Stefan Waibel, Sonja Endruhn, et al.
Journal of the Neurological Sciences|July 13, 2005
Spastin related hereditary spastic paraplegia with dysplastic corpus callosumBurkhard Alber, Magdalena Pernauer, Annemarie Schwan, et al.
Pageof 2

Showing results (1-10 of 12) with videos related to

Sort By:
Pageof 2
Journal of Neurology, Neurosurgery, and Psychiatry|March 3, 2007
Widespread white matter changes in Kennedy disease: a voxel based morphometry studyJan Kassubek, Freimut D Juengling, Anne-D Sperfeld
Journal Der Deutschen Dermatologischen Gesellschaft = Journal of the German Society of Dermatology : JDDG|July 9, 2024
Combination therapy for Sneddon syndrome to reduce the incidence of cerebrovascular complicationsAlbert Narwutsch, Johannes Wohlrab, Anne-D Sperfeld, et al.
Neurochemical Research|March 25, 2010
Hypercapnia is a possible determinant of the function of the blood-cerebrospinal fluid barrier in amyotrophic lateral sclerosisSigurd D Süssmuth, Anne D Sperfeld, Albert C Ludolph, et al.
European Neurology|July 29, 2010
Amygdala size reduction is associated with memory deficits in complicated hereditary spastic paraparesis: an MRI studyElmar H Pinkhardt, Anne-D Sperfeld, Ingo Uttner, et al.
Biomedical Engineering Online|November 13, 2007
Diffusion tensor imaging and tractwise fractional anisotropy statistics: quantitative analysis in white matter pathologyHans-Peter Mueller, Alexander Unrath, Anne D Sperfeld, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|September 14, 2007
Different regional brain volume loss in pure and complicated hereditary spastic paraparesis: a voxel-based morphometric studyJan Kassubek, Freimut D Juengling, Annette Baumgartner, et al.
Brain : a Journal of Neurology|March 5, 2003
A novel nonsense mutation in the ABC1 gene causes a severe syringomyelia-like phenotype of Tangier diseaseStephan Züchner, Anne D Sperfeld, Jan Senderek, et al.
Archives of Neurology|December 10, 2002
X-linked bulbospinal neuronopathy: Kennedy diseaseAnne D Sperfeld, Jochem Karitzky, Dagmar Brummer, et al.
Amyotrophic Lateral Sclerosis : Official Publication of the World Federation of Neurology Research Group on Motor Neuron Diseases|November 6, 2008
Identification of candidate genes for sporadic amyotrophic lateral sclerosis by array comparative genomic hybridizationSarah A Shoichet, Stefan Waibel, Sonja Endruhn, et al.
Journal of the Neurological Sciences|July 13, 2005
Spastin related hereditary spastic paraplegia with dysplastic corpus callosumBurkhard Alber, Magdalena Pernauer, Annemarie Schwan, et al.
Pageof 2