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Michael Mull

Showing results (11-20 of 28) with videos related to

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AJNR. American Journal of Neuroradiology|February 16, 2002
Contrast-enhanced three-dimensional transcranial color-coded sonography of intracranial stenosesChristof Klötzsch, Alessandro Bozzato, Gero Lammers, et al.
Stroke|June 19, 2004
Three-dimensional assessment of extracranial Doppler sonography in carotid artery stenosis compared with digital subtraction angiographyTiemo Wessels, Judith U Harrer, Susanne Stetter, et al.
Neurocritical Care|October 12, 2012
Intrathecal saline infusion: an emergency procedure in a patient with spontaneous intracranial hypotensionChristian Sass, Christoph Kosinski, Patrick Schmidt, et al.
Neurosurgical Focus|July 28, 2022
Arteriovenous malformations of the filum terminale: clinical characteristics, angioarchitecture, and management of a rare spinal vascular pathologyMichael Mull, Manuel Dafotakis, Gerrit Alexander Schubert, et al.
Journal of Neurosurgery. Spine|October 20, 2006
Spinal epidural arteriovenous fistula with perimedullary drainage. Case report and pathomechanical considerationsTimo Krings, Michael Mull, Azize Bostroem, et al.
Neuropediatrics|December 27, 2016
Stroke as Initial Manifestation of Adenosine Deaminase 2 DeficiencyMiriam Elbracht, Michael Mull, Norbert Wagner, et al.
Journal of Neurosurgery. Spine|April 1, 2006
Spinal dural arteriovenous fistula associated with a spinal perimedullary fistula: case reportTimo Krings, Volker A Coenen, Martin Weinzierl, et al.
Journal of Neurology|October 13, 2009
Episodic dysarthria related to vascular medullary compressionChristina Haubrich, Nina Kleiser, Christoph Kosinski, et al.
Stroke|January 7, 2006
The hyperdense posterior cerebral artery sign: a computed tomography marker of acute ischemia in the posterior cerebral artery territoryTimo Krings, Dagmar Noelchen, Michael Mull, et al.
Brain : a Journal of Neurology|June 14, 2003
Oligophrenin 1 (OPHN1) gene mutation causes syndromic X-linked mental retardation with epilepsy, rostral ventricular enlargement and cerebellar hypoplasiaCarsten Bergmann, Klaus Zerres, Jan Senderek, et al.
Pageof 3

Showing results (11-20 of 28) with videos related to

Sort By:
Pageof 3
AJNR. American Journal of Neuroradiology|February 16, 2002
Contrast-enhanced three-dimensional transcranial color-coded sonography of intracranial stenosesChristof Klötzsch, Alessandro Bozzato, Gero Lammers, et al.
Stroke|June 19, 2004
Three-dimensional assessment of extracranial Doppler sonography in carotid artery stenosis compared with digital subtraction angiographyTiemo Wessels, Judith U Harrer, Susanne Stetter, et al.
Neurocritical Care|October 12, 2012
Intrathecal saline infusion: an emergency procedure in a patient with spontaneous intracranial hypotensionChristian Sass, Christoph Kosinski, Patrick Schmidt, et al.
Neurosurgical Focus|July 28, 2022
Arteriovenous malformations of the filum terminale: clinical characteristics, angioarchitecture, and management of a rare spinal vascular pathologyMichael Mull, Manuel Dafotakis, Gerrit Alexander Schubert, et al.
Journal of Neurosurgery. Spine|October 20, 2006
Spinal epidural arteriovenous fistula with perimedullary drainage. Case report and pathomechanical considerationsTimo Krings, Michael Mull, Azize Bostroem, et al.
Neuropediatrics|December 27, 2016
Stroke as Initial Manifestation of Adenosine Deaminase 2 DeficiencyMiriam Elbracht, Michael Mull, Norbert Wagner, et al.
Journal of Neurosurgery. Spine|April 1, 2006
Spinal dural arteriovenous fistula associated with a spinal perimedullary fistula: case reportTimo Krings, Volker A Coenen, Martin Weinzierl, et al.
Journal of Neurology|October 13, 2009
Episodic dysarthria related to vascular medullary compressionChristina Haubrich, Nina Kleiser, Christoph Kosinski, et al.
Stroke|January 7, 2006
The hyperdense posterior cerebral artery sign: a computed tomography marker of acute ischemia in the posterior cerebral artery territoryTimo Krings, Dagmar Noelchen, Michael Mull, et al.
Brain : a Journal of Neurology|June 14, 2003
Oligophrenin 1 (OPHN1) gene mutation causes syndromic X-linked mental retardation with epilepsy, rostral ventricular enlargement and cerebellar hypoplasiaCarsten Bergmann, Klaus Zerres, Jan Senderek, et al.
Pageof 3