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K Brockmann

Showing results (31-40 of 44) with videos related to

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Neuropediatrics|November 5, 2003
Quantitative proton magnetic resonance spectroscopy of children with adrenoleukodystrophy before and after hematopoietic stem cell transplantationB Wilken, P Dechent, K Brockmann, et al.
Neurology|December 21, 2007
GJA12 mutations are a rare cause of Pelizaeus-Merzbacher-like diseaseM Henneke, P Combes, S Diekmann, et al.
European Journal of Neurology|July 26, 2019
Orthostatic hypotension as a risk factor for longitudinal deterioration of cognitive function in the elderlyM Zimmermann, I Wurster, S Lerche, et al.
European Journal of Neurology|November 10, 2015
GBA-associated parkinsonism and dementia: beyond α-synucleinopathies?A Pilotto, C Schulte, A K Hauser, et al.
European Journal of Neurology|September 6, 2017
Progression of prodromal motor and non-motor symptoms in the premotor phase study - 2-year follow-up dataI Liepelt-Scarfone, B Brändle, R Yilmaz, et al.
JIMD Reports|November 6, 2013
A Novel SLC6A8 Mutation in a Large Family with X-Linked Intellectual Disability: Clinical and Proton Magnetic Resonance Spectroscopy Data of Both Hemizygous Males and Heterozygous FemalesS Dreha-Kulaczewski, V Kalscheuer, A Tzschach, et al.
NMR in Biomedicine|February 23, 2010
In vivo proton MR spectroscopy findings specific for adenylosuccinate lyase deficiencyM Henneke, S Dreha-Kulaczewski, K Brockmann, et al.
Neurology|July 11, 2007
Hypomyelination with atrophy of the basal ganglia and cerebellum: follow-up and pathologyM S van der Knaap, T Linnankivi, A Paetau, et al.
Brain : a Journal of Neurology|June 9, 2006
Morphological basis for the spectrum of clinical deficits in spinocerebellar ataxia 17 (SCA17)K Lasek, R Lencer, C Gaser, et al.
Annals of Neurology|October 18, 2001
Autosomal dominant glut-1 deficiency syndrome and familial epilepsyK Brockmann, D Wang, C G Korenke, et al.
Pageof 5

Showing results (31-40 of 44) with videos related to

Sort By:
Pageof 5
Neuropediatrics|November 5, 2003
Quantitative proton magnetic resonance spectroscopy of children with adrenoleukodystrophy before and after hematopoietic stem cell transplantationB Wilken, P Dechent, K Brockmann, et al.
Neurology|December 21, 2007
GJA12 mutations are a rare cause of Pelizaeus-Merzbacher-like diseaseM Henneke, P Combes, S Diekmann, et al.
European Journal of Neurology|July 26, 2019
Orthostatic hypotension as a risk factor for longitudinal deterioration of cognitive function in the elderlyM Zimmermann, I Wurster, S Lerche, et al.
European Journal of Neurology|November 10, 2015
GBA-associated parkinsonism and dementia: beyond α-synucleinopathies?A Pilotto, C Schulte, A K Hauser, et al.
European Journal of Neurology|September 6, 2017
Progression of prodromal motor and non-motor symptoms in the premotor phase study - 2-year follow-up dataI Liepelt-Scarfone, B Brändle, R Yilmaz, et al.
JIMD Reports|November 6, 2013
A Novel SLC6A8 Mutation in a Large Family with X-Linked Intellectual Disability: Clinical and Proton Magnetic Resonance Spectroscopy Data of Both Hemizygous Males and Heterozygous FemalesS Dreha-Kulaczewski, V Kalscheuer, A Tzschach, et al.
NMR in Biomedicine|February 23, 2010
In vivo proton MR spectroscopy findings specific for adenylosuccinate lyase deficiencyM Henneke, S Dreha-Kulaczewski, K Brockmann, et al.
Neurology|July 11, 2007
Hypomyelination with atrophy of the basal ganglia and cerebellum: follow-up and pathologyM S van der Knaap, T Linnankivi, A Paetau, et al.
Brain : a Journal of Neurology|June 9, 2006
Morphological basis for the spectrum of clinical deficits in spinocerebellar ataxia 17 (SCA17)K Lasek, R Lencer, C Gaser, et al.
Annals of Neurology|October 18, 2001
Autosomal dominant glut-1 deficiency syndrome and familial epilepsyK Brockmann, D Wang, C G Korenke, et al.
Pageof 5