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European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
December 21, 2006
Treatment of epilepsy in Rett syndrome
Peter Huppke, Karola Köhler, Knut Brockmann, et al.
Clinical Chemistry
|
February 26, 2004
Tandem mass spectrometry for the direct assay of enzymes in dried blood spots: application to newborn screening for Krabbe disease
Yijun Li, Knut Brockmann, Frantisek Turecek, et al.
Journal of Neurology
|
April 19, 2005
X-linked paroxysmal dyskinesia and severe global retardation caused by defective MCT8 gene
Knut Brockmann, Alexandra M Dumitrescu, Thomas T Best, et al.
Brain & Development
|
December 19, 2006
Quantitative proton MRS of cerebral metabolites in laminin alpha2 chain deficiency
Knut Brockmann, Peter Dechent, Carsten Bönnemann, et al.
Pediatric Neurology
|
December 27, 2005
Magnetic resonance imaging and proton magnetic resonance spectroscopy of megalencephaly and dilated Virchow-Robin spaces
Samuel Groeschel, Knut Brockmann, Peter Dechent, et al.
American Journal of Medical Genetics. Part A
|
November 26, 2009
Overlap of Moebius and oromandibular limb hypogenesis syndrome with gastroschisis and pulmonary hypoplasia
Knut Brockmann, Heiko Backes, Bernd Auber, et al.
European Neurology
|
August 29, 2003
A novel GFAP mutation and disseminated white matter lesions: adult Alexander disease?
Knut Brockmann, Moritz Meins, Angelika Taubert, et al.
Neuromuscular Disorders : NMD
|
June 1, 2007
Sensitivity and specificity of qualitative muscle ultrasound in assessment of suspected neuromuscular disease in childhood
Knut Brockmann, Peter Becker, Gudrun Schreiber, et al.
American Journal of Medical Genetics. Part A
|
December 12, 2019
A novel homozygous nonsense mutation of VPS13B associated with previously unreported features of Cohen syndrome
Katrin Koehler, Markus Schuelke, Anna K Hell, et al.
Pediatric Neurology
|
November 25, 2003
Progressive muscle weakness after high-dose steroids in two children with CIDP
Kevin M Rostasy, Katharina Diepold, Johannes Buckard, et al.
Page
of 13
Search research articles
Search
Showing results (21-30 of 125) with videos related to
Sort By:
Page
of 13
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
December 21, 2006
Treatment of epilepsy in Rett syndrome
Peter Huppke, Karola Köhler, Knut Brockmann, et al.
Clinical Chemistry
|
February 26, 2004
Tandem mass spectrometry for the direct assay of enzymes in dried blood spots: application to newborn screening for Krabbe disease
Yijun Li, Knut Brockmann, Frantisek Turecek, et al.
Journal of Neurology
|
April 19, 2005
X-linked paroxysmal dyskinesia and severe global retardation caused by defective MCT8 gene
Knut Brockmann, Alexandra M Dumitrescu, Thomas T Best, et al.
Brain & Development
|
December 19, 2006
Quantitative proton MRS of cerebral metabolites in laminin alpha2 chain deficiency
Knut Brockmann, Peter Dechent, Carsten Bönnemann, et al.
Pediatric Neurology
|
December 27, 2005
Magnetic resonance imaging and proton magnetic resonance spectroscopy of megalencephaly and dilated Virchow-Robin spaces
Samuel Groeschel, Knut Brockmann, Peter Dechent, et al.
American Journal of Medical Genetics. Part A
|
November 26, 2009
Overlap of Moebius and oromandibular limb hypogenesis syndrome with gastroschisis and pulmonary hypoplasia
Knut Brockmann, Heiko Backes, Bernd Auber, et al.
European Neurology
|
August 29, 2003
A novel GFAP mutation and disseminated white matter lesions: adult Alexander disease?
Knut Brockmann, Moritz Meins, Angelika Taubert, et al.
Neuromuscular Disorders : NMD
|
June 1, 2007
Sensitivity and specificity of qualitative muscle ultrasound in assessment of suspected neuromuscular disease in childhood
Knut Brockmann, Peter Becker, Gudrun Schreiber, et al.
American Journal of Medical Genetics. Part A
|
December 12, 2019
A novel homozygous nonsense mutation of VPS13B associated with previously unreported features of Cohen syndrome
Katrin Koehler, Markus Schuelke, Anna K Hell, et al.
Pediatric Neurology
|
November 25, 2003
Progressive muscle weakness after high-dose steroids in two children with CIDP
Kevin M Rostasy, Katharina Diepold, Johannes Buckard, et al.
Page
of 13