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J Gärtner

Showing results (71-80 of 106) with videos related to

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Neuropediatrics|March 12, 2010
Unilateral dilation of virchow-robin spaces in early childhoodK Brockmann, S Gröschel, S Dreha-Kulaczewski, et al.
Neurology|November 10, 2010
Neuromyelitis optica and NMO-IgG in European pediatric patientsP Huppke, M Blüthner, O Bauer, et al.
Neuropediatrics|September 16, 2003
Consciousness disturbances in megalencephalic leukoencephalopathy with subcortical cystsM Bugiani, I Moroni, A Bizzi, et al.
Pediatric Research|February 1, 1991
The 22-kD peroxisomal integral membrane protein in Zellweger syndrome--presence, abundance, and association with a peroxisomal thiolase precursor proteinJ Gärtner, W W Chen, R I Kelley, et al.
Neuropediatrics|April 29, 1998
Clinical and genetic aspects of X-linked adrenoleukodystrophyJ Gärtner, A Braun, A Holzinger, et al.
Neuropediatrics|September 3, 2005
Complicated hereditary spastic paraplegia with thin corpus callosum (HSP-TCC) and childhood onsetK Brockmann, M A Simpson, A Faber, et al.
Pharmacopsychiatry|July 1, 1987
Differential effects of a new dibenzo-epine neuroleptic compared with haloperidol. Results of an open and crossover studyK Mann, M Bartels, H J Gärtner, et al.
Neuropediatrics|July 4, 2007
Infratentorial meningioma in an 8-year-old child as first sign of neurofibromatosis type 2G M Stettner, K M Rostasy, H C Ludwig, et al.
Biochemical and Biophysical Research Communications|February 19, 2000
The human PEX3 gene encoding a peroxisomal assembly protein: genomic organization, positional mapping, and mutation analysis in candidate phenotypesA C Muntau, A Holzinger, P U Mayerhofer, et al.
Neurology|June 2, 2010
Clinical neurophysiology in GJA12-related hypomyelination vs Pelizaeus-Merzbacher diseaseM Henneke, S Gegner, A Hahn, et al.
Pageof 11

Showing results (71-80 of 106) with videos related to

Sort By:
Pageof 11
Neuropediatrics|March 12, 2010
Unilateral dilation of virchow-robin spaces in early childhoodK Brockmann, S Gröschel, S Dreha-Kulaczewski, et al.
Neurology|November 10, 2010
Neuromyelitis optica and NMO-IgG in European pediatric patientsP Huppke, M Blüthner, O Bauer, et al.
Neuropediatrics|September 16, 2003
Consciousness disturbances in megalencephalic leukoencephalopathy with subcortical cystsM Bugiani, I Moroni, A Bizzi, et al.
Pediatric Research|February 1, 1991
The 22-kD peroxisomal integral membrane protein in Zellweger syndrome--presence, abundance, and association with a peroxisomal thiolase precursor proteinJ Gärtner, W W Chen, R I Kelley, et al.
Neuropediatrics|April 29, 1998
Clinical and genetic aspects of X-linked adrenoleukodystrophyJ Gärtner, A Braun, A Holzinger, et al.
Neuropediatrics|September 3, 2005
Complicated hereditary spastic paraplegia with thin corpus callosum (HSP-TCC) and childhood onsetK Brockmann, M A Simpson, A Faber, et al.
Pharmacopsychiatry|July 1, 1987
Differential effects of a new dibenzo-epine neuroleptic compared with haloperidol. Results of an open and crossover studyK Mann, M Bartels, H J Gärtner, et al.
Neuropediatrics|July 4, 2007
Infratentorial meningioma in an 8-year-old child as first sign of neurofibromatosis type 2G M Stettner, K M Rostasy, H C Ludwig, et al.
Biochemical and Biophysical Research Communications|February 19, 2000
The human PEX3 gene encoding a peroxisomal assembly protein: genomic organization, positional mapping, and mutation analysis in candidate phenotypesA C Muntau, A Holzinger, P U Mayerhofer, et al.
Neurology|June 2, 2010
Clinical neurophysiology in GJA12-related hypomyelination vs Pelizaeus-Merzbacher diseaseM Henneke, S Gegner, A Hahn, et al.
Pageof 11