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Pediatric Research
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May 25, 2021
Combining advanced MRI and EEG techniques better explains long-term motor outcome after very preterm birth
Charlotte van 't Westende, Sylke J Steggerda, Lisette Jansen, et al.
Frontiers in Neurology
|
May 5, 2018
Nitric Oxide Synthase Inhibition as a Neuroprotective Strategy Following Hypoxic-Ischemic Encephalopathy: Evidence From Animal Studies
Laurent M A Favié, Arlette R Cox, Agnes van den Hoogen, et al.
Journal of Medical Genetics
|
December 20, 2023
Clinical phenotype of FOXP1 syndrome: parent-reported medical signs and symptoms in 40 individuals
Saskia Koene, Fabiënne Gwendolin Ropers, Jannelien Wieland, et al.
Frontiers in Pediatrics
|
July 8, 2021
Longitudinal Follow-Up of Children Born Preterm: Neurodevelopment From 2 to 10 Years of Age
Lisette Jansen, Cacha M P C D Peeters-Scholte, Annette A van den Berg-Huysmans, et al.
American Journal of Medical Genetics. Part A
|
March 16, 2013
GPSM2 and Chudley-McCullough syndrome: a Dutch founder variant brought to North America
Rowida Almomani, Yu Sun, Emmelien Aten, et al.
Journal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology
|
June 8, 2012
A fatal course of neonatal meningo-encephalitis
Gretha J van den Berg-van de Glind, Jutte J C de Vries, Katja C Wolthers, et al.
The Journal of Pediatrics
|
February 12, 2021
Associations between Neonatal Magnetic Resonance Imaging and Short- and Long-Term Neurodevelopmental Outcomes in a Longitudinal Cohort of Very Preterm Children
Lisette Jansen, Andrea van Steenis, Annette A van den Berg-Huysmans, et al.
Cancer Immunology, Immunotherapy : CII
|
March 10, 2026
Protein-level profiling of TIGIT axis components in human PDAC reveals immune-suppressive expression patterns
D Quatannens, Y Verhoeven, S van der Heijden, et al.
Clinical Genetics
|
October 6, 2021
Prenatal exome sequencing: A useful tool for the fetal neurologist
Maayke A de Koning, Mariëtte J V Hoffer, Esther A R Nibbeling, et al.
Clinical Case Reports
|
April 22, 2016
Polyhydramnios and cerebellar atrophy: a prenatal presentation of mitochondrial encephalomyopathy caused by mutations in the FBXL4 gene
Maartje C van Rij, Fenna A R Jansen, Debby M E I Hellebrekers, et al.
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Search research articles
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Showing results (101-110 of 132) with videos related to
Sort By:
Page
of 14
Pediatric Research
|
May 25, 2021
Combining advanced MRI and EEG techniques better explains long-term motor outcome after very preterm birth
Charlotte van 't Westende, Sylke J Steggerda, Lisette Jansen, et al.
Frontiers in Neurology
|
May 5, 2018
Nitric Oxide Synthase Inhibition as a Neuroprotective Strategy Following Hypoxic-Ischemic Encephalopathy: Evidence From Animal Studies
Laurent M A Favié, Arlette R Cox, Agnes van den Hoogen, et al.
Journal of Medical Genetics
|
December 20, 2023
Clinical phenotype of FOXP1 syndrome: parent-reported medical signs and symptoms in 40 individuals
Saskia Koene, Fabiënne Gwendolin Ropers, Jannelien Wieland, et al.
Frontiers in Pediatrics
|
July 8, 2021
Longitudinal Follow-Up of Children Born Preterm: Neurodevelopment From 2 to 10 Years of Age
Lisette Jansen, Cacha M P C D Peeters-Scholte, Annette A van den Berg-Huysmans, et al.
American Journal of Medical Genetics. Part A
|
March 16, 2013
GPSM2 and Chudley-McCullough syndrome: a Dutch founder variant brought to North America
Rowida Almomani, Yu Sun, Emmelien Aten, et al.
Journal of Clinical Virology : the Official Publication of the Pan American Society for Clinical Virology
|
June 8, 2012
A fatal course of neonatal meningo-encephalitis
Gretha J van den Berg-van de Glind, Jutte J C de Vries, Katja C Wolthers, et al.
The Journal of Pediatrics
|
February 12, 2021
Associations between Neonatal Magnetic Resonance Imaging and Short- and Long-Term Neurodevelopmental Outcomes in a Longitudinal Cohort of Very Preterm Children
Lisette Jansen, Andrea van Steenis, Annette A van den Berg-Huysmans, et al.
Cancer Immunology, Immunotherapy : CII
|
March 10, 2026
Protein-level profiling of TIGIT axis components in human PDAC reveals immune-suppressive expression patterns
D Quatannens, Y Verhoeven, S van der Heijden, et al.
Clinical Genetics
|
October 6, 2021
Prenatal exome sequencing: A useful tool for the fetal neurologist
Maayke A de Koning, Mariëtte J V Hoffer, Esther A R Nibbeling, et al.
Clinical Case Reports
|
April 22, 2016
Polyhydramnios and cerebellar atrophy: a prenatal presentation of mitochondrial encephalomyopathy caused by mutations in the FBXL4 gene
Maartje C van Rij, Fenna A R Jansen, Debby M E I Hellebrekers, et al.
Page
of 14