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Knut Brockmann

Showing results (41-50 of 125) with videos related to

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Brain & Development|May 12, 2009
Leukodystrophies and other genetic metabolic leukoencephalopathies in children and adultsAlfried Kohlschütter, Annette Bley, Knut Brockmann, et al.
Journal of Clinical Medicine|November 26, 2022
Health-Related Quality of Life after Pediatric Traumatic Brain Injury: A Qualitative Comparison of Perspectives of Children and Adolescents after TBI and a Comparison Group without a History of TBIDagmar Timmermann, Ugne Krenz, Silke Schmidt, et al.
American Journal of Medical Genetics. Part A|September 12, 2020
Evidence of pathogenicity for the leaky splice variant c.1066-6T>G in ATMSimone Schröder, Britta Wieland, Andreas Ohlenbusch, et al.
Journal of Neurology|March 15, 2003
Cerebral proton magnetic resonance spectroscopy in infantile Alexander diseaseKnut Brockmann, Peter Dechent, Moritz Meins, et al.
Journal of the Neurological Sciences|May 28, 2013
Acute onset of adult Alexander diseaseHolger Schmidt, Benedikt Kretzschmar, Paul Lingor, et al.
Journal of Magnetic Resonance Imaging : JMRI|August 23, 2012
Assessment of myelination in hypomyelinating disorders by quantitative MRISteffi F Dreha-Kulaczewski, Knut Brockmann, Marco Henneke, et al.
Orphanet Journal of Rare Diseases|September 22, 2012
Leukoencephalopathy with accumulated succinate is indicative of SDHAF1 related complex II deficiencyAndreas Ohlenbusch, Simon Edvardson, Johannes Skorpen, et al.
Pediatric Research|March 22, 2008
Early reduction of total N-acetyl-aspartate-compounds in patients with classical vanishing white matter disease. A long-term follow-up MRS studySteffi F Dreha-Kulaczewski, Peter Dechent, Jürgen Finsterbusch, et al.
European Journal of Pediatrics|March 5, 2005
Malignant ectomesenchymoma of the cerebrum. Case report and discussion of therapeutic optionsElisabeth Weiss, Clemens F Albrecht, Jochen Herms, et al.
Photodermatology, Photoimmunology & Photomedicine|November 19, 2015
Photosensitive form of trichothiodystrophy associated with a novel mutation in the XPD geneBirka Brauns, Steffen Schubert, Janin Lehmann, et al.
Pageof 13

Showing results (41-50 of 125) with videos related to

Sort By:
Pageof 13
Brain & Development|May 12, 2009
Leukodystrophies and other genetic metabolic leukoencephalopathies in children and adultsAlfried Kohlschütter, Annette Bley, Knut Brockmann, et al.
Journal of Clinical Medicine|November 26, 2022
Health-Related Quality of Life after Pediatric Traumatic Brain Injury: A Qualitative Comparison of Perspectives of Children and Adolescents after TBI and a Comparison Group without a History of TBIDagmar Timmermann, Ugne Krenz, Silke Schmidt, et al.
American Journal of Medical Genetics. Part A|September 12, 2020
Evidence of pathogenicity for the leaky splice variant c.1066-6T>G in ATMSimone Schröder, Britta Wieland, Andreas Ohlenbusch, et al.
Journal of Neurology|March 15, 2003
Cerebral proton magnetic resonance spectroscopy in infantile Alexander diseaseKnut Brockmann, Peter Dechent, Moritz Meins, et al.
Journal of the Neurological Sciences|May 28, 2013
Acute onset of adult Alexander diseaseHolger Schmidt, Benedikt Kretzschmar, Paul Lingor, et al.
Journal of Magnetic Resonance Imaging : JMRI|August 23, 2012
Assessment of myelination in hypomyelinating disorders by quantitative MRISteffi F Dreha-Kulaczewski, Knut Brockmann, Marco Henneke, et al.
Orphanet Journal of Rare Diseases|September 22, 2012
Leukoencephalopathy with accumulated succinate is indicative of SDHAF1 related complex II deficiencyAndreas Ohlenbusch, Simon Edvardson, Johannes Skorpen, et al.
Pediatric Research|March 22, 2008
Early reduction of total N-acetyl-aspartate-compounds in patients with classical vanishing white matter disease. A long-term follow-up MRS studySteffi F Dreha-Kulaczewski, Peter Dechent, Jürgen Finsterbusch, et al.
European Journal of Pediatrics|March 5, 2005
Malignant ectomesenchymoma of the cerebrum. Case report and discussion of therapeutic optionsElisabeth Weiss, Clemens F Albrecht, Jochen Herms, et al.
Photodermatology, Photoimmunology & Photomedicine|November 19, 2015
Photosensitive form of trichothiodystrophy associated with a novel mutation in the XPD geneBirka Brauns, Steffen Schubert, Janin Lehmann, et al.
Pageof 13