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A Poretti

Showing results (31-40 of 35) with videos related to

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Neuropediatrics|March 12, 2010
Cerebellar cleft: confirmation of the neuroimaging patternA Poretti, T A G M Huisman, F M Cowan, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|November 27, 2015
Transfontanellar duplex brain ultrasonography resistive indices as a prognostic tool in neonatal hypoxic-ischemic encephalopathy before and after treatment with therapeutic hypothermiaG J Gerner, V J Burton, A Poretti, et al.
Neuropediatrics|December 29, 2017
Congenital Neuronal Ceroid Lipofuscinosis with a Novel CTSD Gene Mutation: A Rare Cause of Neonatal-Onset Neurodegenerative DisorderK Varvagiannis, S Hanquinet, M H Billieux, et al.
Clinical Genetics|September 7, 2016
Further evidence that de novo missense and truncating variants in ZBTB18 cause intellectual disability with variable featuresJ S Cohen, S Srivastava, K D Farwell Hagman, et al.
AJNR. American Journal of Neuroradiology|August 30, 2014
Apparent diffusion coefficient scalars correlate with near-infrared spectroscopy markers of cerebrovascular autoregulation in neonates cooled for perinatal hypoxic-ischemic injuryA Tekes, A Poretti, M M Scheurkogel, et al.
Pageof 4

Showing results (31-40 of 35) with videos related to

Sort By:
Pageof 4
You have reached the last page of results.This site can display upto 35 results.
Neuropediatrics|March 12, 2010
Cerebellar cleft: confirmation of the neuroimaging patternA Poretti, T A G M Huisman, F M Cowan, et al.
Journal of Perinatology : Official Journal of the California Perinatal Association|November 27, 2015
Transfontanellar duplex brain ultrasonography resistive indices as a prognostic tool in neonatal hypoxic-ischemic encephalopathy before and after treatment with therapeutic hypothermiaG J Gerner, V J Burton, A Poretti, et al.
Neuropediatrics|December 29, 2017
Congenital Neuronal Ceroid Lipofuscinosis with a Novel CTSD Gene Mutation: A Rare Cause of Neonatal-Onset Neurodegenerative DisorderK Varvagiannis, S Hanquinet, M H Billieux, et al.
Clinical Genetics|September 7, 2016
Further evidence that de novo missense and truncating variants in ZBTB18 cause intellectual disability with variable featuresJ S Cohen, S Srivastava, K D Farwell Hagman, et al.
AJNR. American Journal of Neuroradiology|August 30, 2014
Apparent diffusion coefficient scalars correlate with near-infrared spectroscopy markers of cerebrovascular autoregulation in neonates cooled for perinatal hypoxic-ischemic injuryA Tekes, A Poretti, M M Scheurkogel, et al.
Pageof 4