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F Stögbauer

Showing results (41-50 of 56) with videos related to

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Nuclear Medicine and Biology|April 27, 2001
Kinetic parameters of 3-[(123)I]iodo-L-alpha-methyl tyrosine ([(123)I]IMT) transport in human GOS3 glioma cellsB Riemann, K Kopka, F Stögbauer, et al.
Genomics|December 28, 1999
A sequence-ready BAC/PAC contig and partial transcript map of approximately 1.5 Mb in human chromosome 17q25 comprising multiple disease genesG Kuhlenbäumer, A Schirmacher, J Meuleman, et al.
Journal of Neuro-Oncology|March 17, 2000
CNTF and its receptor subunits in human gliomasJ Weis, L M Schönrock, S L Züchner, et al.
Stroke|November 20, 2004
Protease inhibitors in spontaneous cervical artery dissectionsCarsten Konrad, C Langer, G A Müller, et al.
Neuroscience Letters|March 6, 1998
Absence of mutations in peripheral myelin protein-22, myelin protein zero, and connexin 32 in autosomal recessive Dejerine-Sottas syndromeF Stögbauer, P Young, H Wiebusch, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 17, 1999
Autosomal dominant burning feet syndromeF Stögbauer, P Young, G Kuhlenbäumer, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 18, 2006
Evaluation of single nucleotide polymorphisms in the phosphodiesterase 4D gene (PDE4D) and their association with ischaemic stroke in a large German cohortG Kuhlenbäumer, K Berger, A Huge, et al.
Human Genetics|June 21, 2001
Mutation analysis of 4 candidate genes for hereditary neuralgic amyotrophy (HNA)J Meuleman, G Kuhlenbäumer, D Audenaert, et al.
Neurology|May 11, 2005
Generalized arteriopathy in patients with cervical artery dissectionW Völker, M Besselmann, R Dittrich, et al.
Journal of Neurology|November 18, 2000
PMP22 Thr118Met is not a clinically relevant CMT1 markerP Young, F Stögbauer, B Eller, et al.
Pageof 6

Showing results (41-50 of 56) with videos related to

Sort By:
Pageof 6
Nuclear Medicine and Biology|April 27, 2001
Kinetic parameters of 3-[(123)I]iodo-L-alpha-methyl tyrosine ([(123)I]IMT) transport in human GOS3 glioma cellsB Riemann, K Kopka, F Stögbauer, et al.
Genomics|December 28, 1999
A sequence-ready BAC/PAC contig and partial transcript map of approximately 1.5 Mb in human chromosome 17q25 comprising multiple disease genesG Kuhlenbäumer, A Schirmacher, J Meuleman, et al.
Journal of Neuro-Oncology|March 17, 2000
CNTF and its receptor subunits in human gliomasJ Weis, L M Schönrock, S L Züchner, et al.
Stroke|November 20, 2004
Protease inhibitors in spontaneous cervical artery dissectionsCarsten Konrad, C Langer, G A Müller, et al.
Neuroscience Letters|March 6, 1998
Absence of mutations in peripheral myelin protein-22, myelin protein zero, and connexin 32 in autosomal recessive Dejerine-Sottas syndromeF Stögbauer, P Young, H Wiebusch, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|June 17, 1999
Autosomal dominant burning feet syndromeF Stögbauer, P Young, G Kuhlenbäumer, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|March 18, 2006
Evaluation of single nucleotide polymorphisms in the phosphodiesterase 4D gene (PDE4D) and their association with ischaemic stroke in a large German cohortG Kuhlenbäumer, K Berger, A Huge, et al.
Human Genetics|June 21, 2001
Mutation analysis of 4 candidate genes for hereditary neuralgic amyotrophy (HNA)J Meuleman, G Kuhlenbäumer, D Audenaert, et al.
Neurology|May 11, 2005
Generalized arteriopathy in patients with cervical artery dissectionW Völker, M Besselmann, R Dittrich, et al.
Journal of Neurology|November 18, 2000
PMP22 Thr118Met is not a clinically relevant CMT1 markerP Young, F Stögbauer, B Eller, et al.
Pageof 6