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M Pfister

Showing results (161-170 of 752) with videos related to

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Pediatric Research|August 17, 2016
ERP evidence of preserved early memory function in term infants with neonatal encephalopathy following therapeutic hypothermiaKatie M Pfister, Lei Zhang, Neely C Miller, et al.
Science Signaling|March 16, 2017
Molecular mechanisms and therapeutic targets in pediatric brain tumorsKun-Wei Liu, Kristian W Pajtler, Barbara C Worst, et al.
Nature Reviews. Cancer|December 11, 2019
Medulloblastomics revisited: biological and clinical insights from thousands of patientsVolker Hovestadt, Olivier Ayrault, Fredrik J Swartling, et al.
The American Journal of Tropical Medicine and Hygiene|March 11, 1999
Differential immunodiagnosis between cystic hydatid disease and other cross-reactive pathologiesD Poretti, E Felleisen, F Grimm, et al.
Journal of Chromatography. B, Biomedical Applications|February 3, 1995
Immunoadsorption procedure as a potential method for the specific beta 2-microglobulin removal from plasma of patients with chronic renal failureL Vallar, P M Costa, A Teixeira, et al.
Zeitschrift Fur Die Gesamte Innere Medizin Und Ihre Grenzgebiete|October 15, 1990
[Possibilities for increasing the elimination rate of Bonnecor]C Fleck, L Schilder, U Schulze, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|October 17, 2018
Preserved speed of processing and memory in infants with a history of moderate neonatal encephalopathy treated with therapeutic hypothermiaElizabeth P Zorn, Lei Zhang, Kristin Sandness, et al.
International Journal of Molecular Medicine|July 11, 2001
Frequency of the recessive 30delG mutation in the GJB2 gene in Northeast-Hungarian individuals and patients with hearing impairmentT Tóth, S Kupka, H Esmer, et al.
Neuroscience|July 1, 1996
Extracellular adenosine levels in neostriatum and hippocampus during rest and activity periods of ratsJ P Huston, H L Haas, F Boix, et al.
HNO|August 28, 2003
[Clinical and molecular genetic analysis of monozygotic twins displaying stapes gusher syndrome (DFN3)]N Oh, S Kupka, F Mirghomizadeh, et al.
Pageof 76

Showing results (161-170 of 752) with videos related to

Sort By:
Pageof 76
Pediatric Research|August 17, 2016
ERP evidence of preserved early memory function in term infants with neonatal encephalopathy following therapeutic hypothermiaKatie M Pfister, Lei Zhang, Neely C Miller, et al.
Science Signaling|March 16, 2017
Molecular mechanisms and therapeutic targets in pediatric brain tumorsKun-Wei Liu, Kristian W Pajtler, Barbara C Worst, et al.
Nature Reviews. Cancer|December 11, 2019
Medulloblastomics revisited: biological and clinical insights from thousands of patientsVolker Hovestadt, Olivier Ayrault, Fredrik J Swartling, et al.
The American Journal of Tropical Medicine and Hygiene|March 11, 1999
Differential immunodiagnosis between cystic hydatid disease and other cross-reactive pathologiesD Poretti, E Felleisen, F Grimm, et al.
Journal of Chromatography. B, Biomedical Applications|February 3, 1995
Immunoadsorption procedure as a potential method for the specific beta 2-microglobulin removal from plasma of patients with chronic renal failureL Vallar, P M Costa, A Teixeira, et al.
Zeitschrift Fur Die Gesamte Innere Medizin Und Ihre Grenzgebiete|October 15, 1990
[Possibilities for increasing the elimination rate of Bonnecor]C Fleck, L Schilder, U Schulze, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|October 17, 2018
Preserved speed of processing and memory in infants with a history of moderate neonatal encephalopathy treated with therapeutic hypothermiaElizabeth P Zorn, Lei Zhang, Kristin Sandness, et al.
International Journal of Molecular Medicine|July 11, 2001
Frequency of the recessive 30delG mutation in the GJB2 gene in Northeast-Hungarian individuals and patients with hearing impairmentT Tóth, S Kupka, H Esmer, et al.
Neuroscience|July 1, 1996
Extracellular adenosine levels in neostriatum and hippocampus during rest and activity periods of ratsJ P Huston, H L Haas, F Boix, et al.
HNO|August 28, 2003
[Clinical and molecular genetic analysis of monozygotic twins displaying stapes gusher syndrome (DFN3)]N Oh, S Kupka, F Mirghomizadeh, et al.
Pageof 76