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Beatrice Latal

Showing results (101-110 of 177) with videos related to

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The Journal of Pediatrics|August 3, 2015
Severe Congenital Heart Defects Are Associated with Global Reduction of Neonatal Brain VolumesMichael von Rhein, Andreas Buchmann, Cornelia Hagmann, et al.
Brain Communications|December 31, 2020
Delayed maturation of the structural brain connectome in neonates with congenital heart diseaseMaria Feldmann, Ting Guo, Steven P Miller, et al.
Acta Paediatrica (Oslo, Norway : 1992)|April 23, 2013
Development of neuromotor functions in very low birth weight children from six to 10 years of age: patterns of changeGiancarlo Natalucci, Michel Schneider, Helene Werner, et al.
Neuroimage. Clinical|December 16, 2021
Microstructural alterations of the corticospinal tract are associated with poor motor function in patients with severe congenital heart diseaseMelanie Ehrler, Michael von Rhein, Ladina Schlosser, et al.
International Journal of Cardiology|April 7, 2019
Smaller brain volumes at two years of age in patients with hypoplastic left heart syndrome - Impact of surgical approachWalter Knirsch, Kristina N Heye, Ruth O'Gorman Tuura, et al.
Developmental Medicine and Child Neurology|August 14, 2013
Neurodevelopmental outcome, psychological adjustment, and quality of life in adolescents with congenital heart diseaseChristina Schaefer, Michael von Rhein, Walter Knirsch, et al.
The Journal of Pediatrics|April 17, 2012
Health-related quality of life and behavior of triplets at adolescent ageGiancarlo Natalucci, Manuela Iten, Julia Hofmann, et al.
Early Human Development|December 10, 2015
Very preterm adolescents show impaired performance with increasing demands in executive function tasksFlavia M Wehrle, Liane Kaufmann, Laura D Benz, et al.
JAMA|May 18, 2016
Effect of Early Prophylactic High-Dose Recombinant Human Erythropoietin in Very Preterm Infants on Neurodevelopmental Outcome at 2 Years: A Randomized Clinical TrialGiancarlo Natalucci, Beatrice Latal, Brigitte Koller, et al.
Neuropediatrics|November 24, 2020
Thiamine Pyrophosphokinase Deficiency due to Mutations in the TPK1 Gene: A Rare, Treatable Neurodegenerative DisorderChristina T Rüsch, Saskia B Wortmann, Reka Kovacs-Nagy, et al.
Pageof 18

Showing results (101-110 of 177) with videos related to

Sort By:
Pageof 18
The Journal of Pediatrics|August 3, 2015
Severe Congenital Heart Defects Are Associated with Global Reduction of Neonatal Brain VolumesMichael von Rhein, Andreas Buchmann, Cornelia Hagmann, et al.
Brain Communications|December 31, 2020
Delayed maturation of the structural brain connectome in neonates with congenital heart diseaseMaria Feldmann, Ting Guo, Steven P Miller, et al.
Acta Paediatrica (Oslo, Norway : 1992)|April 23, 2013
Development of neuromotor functions in very low birth weight children from six to 10 years of age: patterns of changeGiancarlo Natalucci, Michel Schneider, Helene Werner, et al.
Neuroimage. Clinical|December 16, 2021
Microstructural alterations of the corticospinal tract are associated with poor motor function in patients with severe congenital heart diseaseMelanie Ehrler, Michael von Rhein, Ladina Schlosser, et al.
International Journal of Cardiology|April 7, 2019
Smaller brain volumes at two years of age in patients with hypoplastic left heart syndrome - Impact of surgical approachWalter Knirsch, Kristina N Heye, Ruth O'Gorman Tuura, et al.
Developmental Medicine and Child Neurology|August 14, 2013
Neurodevelopmental outcome, psychological adjustment, and quality of life in adolescents with congenital heart diseaseChristina Schaefer, Michael von Rhein, Walter Knirsch, et al.
The Journal of Pediatrics|April 17, 2012
Health-related quality of life and behavior of triplets at adolescent ageGiancarlo Natalucci, Manuela Iten, Julia Hofmann, et al.
Early Human Development|December 10, 2015
Very preterm adolescents show impaired performance with increasing demands in executive function tasksFlavia M Wehrle, Liane Kaufmann, Laura D Benz, et al.
JAMA|May 18, 2016
Effect of Early Prophylactic High-Dose Recombinant Human Erythropoietin in Very Preterm Infants on Neurodevelopmental Outcome at 2 Years: A Randomized Clinical TrialGiancarlo Natalucci, Beatrice Latal, Brigitte Koller, et al.
Neuropediatrics|November 24, 2020
Thiamine Pyrophosphokinase Deficiency due to Mutations in the TPK1 Gene: A Rare, Treatable Neurodegenerative DisorderChristina T Rüsch, Saskia B Wortmann, Reka Kovacs-Nagy, et al.
Pageof 18