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F Stögbauer

Showing results (11-20 of 56) with videos related to

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Muscle & Nerve|July 6, 2001
Brachial plexus involvement as the only expression of hereditary neuropathy with liability to pressure palsiesK Ørstavik, M Skard Heier, P Young, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 23, 2003
Placing nasogastric tubes in stroke patients with dysphagia: efficiency and tolerability of the reflex placementR Dziewas, M Schilling, C Konrad, et al.
European Radiology|August 25, 1999
Craniocervical artery dissection: MR imaging and MR angiographic findingsM Oelerich, F Stögbauer, G Kurlemann, et al.
The Cochrane Database of Systematic Reviews|February 7, 2008
Treatment for Charcot-Marie-Tooth diseaseP Young, P De Jonghe, F Stögbauer, et al.
Molecular Cell Biology Research Communications : MCBRC|November 30, 1999
Activation of Jak-Stat and MAPK2 pathways by oncostatin M leads to growth inhibition of human glioma cellsH Halfter, M Friedrich, C Postert, et al.
Brain Research. Molecular Brain Research|October 19, 2000
Activation of the Jak-Stat- and MAPK-pathways by oncostatin M is not sufficient to cause growth inhibition of human glioma cellsH Halfter, C Postert, M Friedrich, et al.
Neurology|February 19, 2000
Hereditary recurrent focal neuropathies: clinical and molecular featuresF Stögbauer, P Young, G Kuhlenbäumer, et al.
Deutsche Medizinische Wochenschrift (1946)|June 21, 1996
[Meralgia paresthetica. A rare differential diagnosis of circumscribed alopecia]D G Nabavi, D Georgiadis, F Stögbauer, et al.
Neurology|February 1, 1997
A novel frameshift mutation in PMP22 accounts for hereditary neuropathy with liability to pressure palsiesP Young, H Wiebusch, F Stögbauer, et al.
Der Nervenarzt|October 3, 1998
[X-chromosomal recessive spinobulbar muscular atrophy (Kennedy type). Description of a family, clinical aspects, molecular genetics, differential diagnosis and therapy]G Kuhlenbäumer, M Bocchicchio, W Kress, et al.
Pageof 6

Showing results (11-20 of 56) with videos related to

Sort By:
Pageof 6
Muscle & Nerve|July 6, 2001
Brachial plexus involvement as the only expression of hereditary neuropathy with liability to pressure palsiesK Ørstavik, M Skard Heier, P Young, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|October 23, 2003
Placing nasogastric tubes in stroke patients with dysphagia: efficiency and tolerability of the reflex placementR Dziewas, M Schilling, C Konrad, et al.
European Radiology|August 25, 1999
Craniocervical artery dissection: MR imaging and MR angiographic findingsM Oelerich, F Stögbauer, G Kurlemann, et al.
The Cochrane Database of Systematic Reviews|February 7, 2008
Treatment for Charcot-Marie-Tooth diseaseP Young, P De Jonghe, F Stögbauer, et al.
Molecular Cell Biology Research Communications : MCBRC|November 30, 1999
Activation of Jak-Stat and MAPK2 pathways by oncostatin M leads to growth inhibition of human glioma cellsH Halfter, M Friedrich, C Postert, et al.
Brain Research. Molecular Brain Research|October 19, 2000
Activation of the Jak-Stat- and MAPK-pathways by oncostatin M is not sufficient to cause growth inhibition of human glioma cellsH Halfter, C Postert, M Friedrich, et al.
Neurology|February 19, 2000
Hereditary recurrent focal neuropathies: clinical and molecular featuresF Stögbauer, P Young, G Kuhlenbäumer, et al.
Deutsche Medizinische Wochenschrift (1946)|June 21, 1996
[Meralgia paresthetica. A rare differential diagnosis of circumscribed alopecia]D G Nabavi, D Georgiadis, F Stögbauer, et al.
Neurology|February 1, 1997
A novel frameshift mutation in PMP22 accounts for hereditary neuropathy with liability to pressure palsiesP Young, H Wiebusch, F Stögbauer, et al.
Der Nervenarzt|October 3, 1998
[X-chromosomal recessive spinobulbar muscular atrophy (Kennedy type). Description of a family, clinical aspects, molecular genetics, differential diagnosis and therapy]G Kuhlenbäumer, M Bocchicchio, W Kress, et al.
Pageof 6