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J Christen

Showing results (71-80 of 85) with videos related to

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Annals of Neurology|August 1, 1992
Multiple sclerosis in children: cerebral metabolic alterations monitored by localized proton magnetic resonance spectroscopy in vivoH Bruhn, J Frahm, K D Merboldt, et al.
Journal of Chromatography|July 23, 1993
Quantitative organic acid analysis in cerebrospinal fluid and plasma: reference values in a pediatric populationG F Hoffmann, C K Seppel, B Holmes, et al.
Pediatric Research|February 1, 1997
Hypoparathyroidism and deafness associated with pleioplasmic large scale rearrangements of the mitochondrial DNA: a clinical and molecular genetic study of four children with Kearns-Sayre syndromeE Wilichowski, A Grüters, K Kruse, et al.
Journal of Pediatric Hematology/Oncology|January 4, 1998
Potential prognostic value of C-erbB-2 expression in medulloblastomas in very young childrenJ W Herms, J Behnke, M Bergmann, et al.
Nanotechnology|July 31, 2012
Single-photon emission from electrically driven InP quantum dots epitaxially grown on CMOS-compatible Si(001)M Wiesner, W-M Schulz, C Kessler, et al.
Internal Medicine Journal|May 7, 2015
Measures of acute physiology, comorbidity and functional status to differentiate illness severity and length of stay among acute general medical admissions: a prospective cohort studyP J Huggan, F Akram, B H D Er, et al.
Neuropediatrics|November 7, 2007
Novel mutations in exon 6 of the GFAP gene affect a highly conserved if motif in the rod domain 2B and are associated with early onset infantile Alexander diseaseH Hartmann, J Herchenbach, U Stephani, et al.
American Journal of Medical Genetics|October 27, 1998
Megalencephaly, mega corpus callosum, and complete lack of motor development: a previously undescribed syndromeG Göhlich-Ratmann, M Baethmann, P Lorenz, et al.
Nanotechnology|June 13, 2017
Selective area growth of AlN/GaN nanocolumns on (0001) and (11-22) GaN/sapphire for semi-polar and non-polar AlN pseudo-templatesA Bengoechea-Encabo, S Albert, M Müller, et al.
Human Genetics|January 27, 2017
Heterozygosity for ARID2 loss-of-function mutations in individuals with a Coffin-Siris syndrome-like phenotypeNuria C Bramswig, O Caluseriu, H-J Lüdecke, et al.
Pageof 9

Showing results (71-80 of 85) with videos related to

Sort By:
Pageof 9
Annals of Neurology|August 1, 1992
Multiple sclerosis in children: cerebral metabolic alterations monitored by localized proton magnetic resonance spectroscopy in vivoH Bruhn, J Frahm, K D Merboldt, et al.
Journal of Chromatography|July 23, 1993
Quantitative organic acid analysis in cerebrospinal fluid and plasma: reference values in a pediatric populationG F Hoffmann, C K Seppel, B Holmes, et al.
Pediatric Research|February 1, 1997
Hypoparathyroidism and deafness associated with pleioplasmic large scale rearrangements of the mitochondrial DNA: a clinical and molecular genetic study of four children with Kearns-Sayre syndromeE Wilichowski, A Grüters, K Kruse, et al.
Journal of Pediatric Hematology/Oncology|January 4, 1998
Potential prognostic value of C-erbB-2 expression in medulloblastomas in very young childrenJ W Herms, J Behnke, M Bergmann, et al.
Nanotechnology|July 31, 2012
Single-photon emission from electrically driven InP quantum dots epitaxially grown on CMOS-compatible Si(001)M Wiesner, W-M Schulz, C Kessler, et al.
Internal Medicine Journal|May 7, 2015
Measures of acute physiology, comorbidity and functional status to differentiate illness severity and length of stay among acute general medical admissions: a prospective cohort studyP J Huggan, F Akram, B H D Er, et al.
Neuropediatrics|November 7, 2007
Novel mutations in exon 6 of the GFAP gene affect a highly conserved if motif in the rod domain 2B and are associated with early onset infantile Alexander diseaseH Hartmann, J Herchenbach, U Stephani, et al.
American Journal of Medical Genetics|October 27, 1998
Megalencephaly, mega corpus callosum, and complete lack of motor development: a previously undescribed syndromeG Göhlich-Ratmann, M Baethmann, P Lorenz, et al.
Nanotechnology|June 13, 2017
Selective area growth of AlN/GaN nanocolumns on (0001) and (11-22) GaN/sapphire for semi-polar and non-polar AlN pseudo-templatesA Bengoechea-Encabo, S Albert, M Müller, et al.
Human Genetics|January 27, 2017
Heterozygosity for ARID2 loss-of-function mutations in individuals with a Coffin-Siris syndrome-like phenotypeNuria C Bramswig, O Caluseriu, H-J Lüdecke, et al.
Pageof 9