Jove
Visualize
Contact Us
JoVE
x logofacebook logolinkedin logoyoutube logo
ABOUT JoVE
OverviewLeadershipBlogJoVE Help Center
AUTHORS
Publishing ProcessEditorial BoardScope & PoliciesPeer ReviewFAQSubmit
LIBRARIANS
TestimonialsSubscriptionsAccessResourcesLibrary Advisory BoardFAQ
RESEARCH
JoVE JournalMethods CollectionsJoVE Encyclopedia of ExperimentsArchive
EDUCATION
JoVE CoreJoVE BusinessJoVE Science EducationJoVE Lab ManualFaculty Resource CenterFaculty Site
Terms & Conditions of Use
Privacy Policy
Policies

Filters

F Stögbauer

Showing results (31-40 of 56) with videos related to

Pageof 6
Sort By:
Stroke|April 1, 1996
A novel technique for identification of doppler microembolic signals based on the coincidence method: in vitro and in vivo evaluationD Georgiadis, J Goeke, M Hill, et al.
Fortschritte Der Neurologie-Psychiatrie|April 8, 1998
[Hereditary neural amyotrophy (HNA): clinical and molecular genetic basis]F Stögbauer, P Young, G Kuhlenbäumer, et al.
Journal of Neurology|July 5, 2001
Mutation analysis in Chariot-Marie Tooth disease type 1: point mutations in the MPZ gene and the GJB1 gene cause comparable phenotypic heterogeneityP Young, K Grote, G Kuhlenbäumer, et al.
Journal of Neurochemistry|January 9, 2001
Characterization of 3-[(123)I]iodo-L-alpha-methyl tyrosine transport in astrocytes of neonatal ratsK Kopka, B Riemann, M Friedrich, et al.
European Annals of Otorhinolaryngology, Head and Neck Diseases|April 30, 2026
Evaluating the interpretation of neck CT/MRI scans by ChatGPT-4V for detecting primary oropharyngeal squamous cell carcinoma: An exploratory studyB Schmidl, R Walter, C C Hoch, et al.
Journal of Neurology|November 8, 2001
Hereditary Neuralgic Amyotrophy (HNA) is genetically heterogeneousG Kuhlenbäumer, J Meuleman, P De Jonghe, et al.
Neurology|April 1, 1998
PCR-based strategy for the diagnosis of hereditary neuropathy with liability to pressure palsies and Charcot-Marie-Tooth disease type 1AP Young, F Stögbauer, H Wiebusch, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 18, 2004
Pneumonia in acute stroke patients fed by nasogastric tubeR Dziewas, M Ritter, M Schilling, et al.
European Journal of Nuclear Medicine|December 14, 1999
Kinetics of 3-[(123)I]iodo-l-alpha-methyltyrosine transport in rat C6 glioma cellsB Riemann, F Stögbauer, K Kopka, et al.
European Journal of Clinical Investigation|June 4, 2009
Adiponectin downregulates CD163 whose cellular and soluble forms are elevated in obesityD Sporrer, M Weber, J Wanninger, et al.
Pageof 6

Showing results (31-40 of 56) with videos related to

Sort By:
Pageof 6
Stroke|April 1, 1996
A novel technique for identification of doppler microembolic signals based on the coincidence method: in vitro and in vivo evaluationD Georgiadis, J Goeke, M Hill, et al.
Fortschritte Der Neurologie-Psychiatrie|April 8, 1998
[Hereditary neural amyotrophy (HNA): clinical and molecular genetic basis]F Stögbauer, P Young, G Kuhlenbäumer, et al.
Journal of Neurology|July 5, 2001
Mutation analysis in Chariot-Marie Tooth disease type 1: point mutations in the MPZ gene and the GJB1 gene cause comparable phenotypic heterogeneityP Young, K Grote, G Kuhlenbäumer, et al.
Journal of Neurochemistry|January 9, 2001
Characterization of 3-[(123)I]iodo-L-alpha-methyl tyrosine transport in astrocytes of neonatal ratsK Kopka, B Riemann, M Friedrich, et al.
European Annals of Otorhinolaryngology, Head and Neck Diseases|April 30, 2026
Evaluating the interpretation of neck CT/MRI scans by ChatGPT-4V for detecting primary oropharyngeal squamous cell carcinoma: An exploratory studyB Schmidl, R Walter, C C Hoch, et al.
Journal of Neurology|November 8, 2001
Hereditary Neuralgic Amyotrophy (HNA) is genetically heterogeneousG Kuhlenbäumer, J Meuleman, P De Jonghe, et al.
Neurology|April 1, 1998
PCR-based strategy for the diagnosis of hereditary neuropathy with liability to pressure palsies and Charcot-Marie-Tooth disease type 1AP Young, F Stögbauer, H Wiebusch, et al.
Journal of Neurology, Neurosurgery, and Psychiatry|May 18, 2004
Pneumonia in acute stroke patients fed by nasogastric tubeR Dziewas, M Ritter, M Schilling, et al.
European Journal of Nuclear Medicine|December 14, 1999
Kinetics of 3-[(123)I]iodo-l-alpha-methyltyrosine transport in rat C6 glioma cellsB Riemann, F Stögbauer, K Kopka, et al.
European Journal of Clinical Investigation|June 4, 2009
Adiponectin downregulates CD163 whose cellular and soluble forms are elevated in obesityD Sporrer, M Weber, J Wanninger, et al.
Pageof 6