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Gustavo Malinger

Showing results (51-60 of 97) with videos related to

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Journal of Perinatology : Official Journal of the California Perinatal Association|August 16, 2018
Whole-exome sequencing in fetuses with central nervous system abnormalitiesAdi Reches, Liran Hiersch, Sharon Simchoni, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|December 6, 2012
The fetal vermis, pons and brainstem: normal longitudinal development as shown by dedicated neurosonographyShimon Ginath, Tally Lerman-Sagie, Karina Haratz Krajden, et al.
Prenatal Diagnosis|October 5, 2024
Prenatal Diagnosis of a KIDINS220 De Novo Heterozygous Variant in a Fetus With a Complex CNS AnomalyHadas Miremberg, Roee Birnbaum, Dorin Trigubov, et al.
Fetal Diagnosis and Therapy|October 6, 2024
Callosal Injuries in Cytomegalovirus Fetopathy: A Neurosonographic StudyKarina Krajden Haratz, Gustavo Malinger, Hadas Miremberg, et al.
Prenatal Diagnosis|March 18, 2011
Does normal fetal brain ultrasound predict normal neurodevelopmental outcome in congenital cytomegalovirus infection?Natalie Farkas, Chen Hoffmann, Liat Ben-Sira, et al.
Prenatal Diagnosis|October 11, 2022
Upgrading an intronic TMEM67 variant of unknown significance to likely pathogenic through RNA studies and community data sharingAlina Kurolap, Adi Mory, Sharon Simchoni, et al.
Virchows Archiv : an International Journal of Pathology|November 18, 2015
Agenesis of the corpus callosum. An autopsy study in fetusesDebora Kidron, Daniel Shapira, Liat Ben Sira, et al.
Prenatal Diagnosis|August 28, 2023
SMARCC1 is a susceptibility gene for congenital hydrocephalus with an autosomal dominant inheritance mode and incomplete penetranceNoa Hourvitz, Alina Kurolap, Adi Mory, et al.
European Radiology|July 13, 2022
Improved differentiation between hypo/hypertelorism and normal fetuses based on MRI using automatic ocular biometric measurements, ocular ratios, and machine learning multi-parametric classificationNetanell Avisdris, Daphna Link Sourani, Liat Ben-Sira, et al.
AJNR. American Journal of Neuroradiology|January 21, 2003
Fetal cytomegalovirus infection of the brain: the spectrum of sonographic findingsGustavo Malinger, Dorit Lev, Neriman Zahalka, et al.
Pageof 10

Showing results (51-60 of 97) with videos related to

Sort By:
Pageof 10
Journal of Perinatology : Official Journal of the California Perinatal Association|August 16, 2018
Whole-exome sequencing in fetuses with central nervous system abnormalitiesAdi Reches, Liran Hiersch, Sharon Simchoni, et al.
The Journal of Maternal-Fetal & Neonatal Medicine : the Official Journal of the European Association of Perinatal Medicine, the Federation of Asia and Oceania Perinatal Societies, the International Society of Perinatal Obstetricians|December 6, 2012
The fetal vermis, pons and brainstem: normal longitudinal development as shown by dedicated neurosonographyShimon Ginath, Tally Lerman-Sagie, Karina Haratz Krajden, et al.
Prenatal Diagnosis|October 5, 2024
Prenatal Diagnosis of a KIDINS220 De Novo Heterozygous Variant in a Fetus With a Complex CNS AnomalyHadas Miremberg, Roee Birnbaum, Dorin Trigubov, et al.
Fetal Diagnosis and Therapy|October 6, 2024
Callosal Injuries in Cytomegalovirus Fetopathy: A Neurosonographic StudyKarina Krajden Haratz, Gustavo Malinger, Hadas Miremberg, et al.
Prenatal Diagnosis|March 18, 2011
Does normal fetal brain ultrasound predict normal neurodevelopmental outcome in congenital cytomegalovirus infection?Natalie Farkas, Chen Hoffmann, Liat Ben-Sira, et al.
Prenatal Diagnosis|October 11, 2022
Upgrading an intronic TMEM67 variant of unknown significance to likely pathogenic through RNA studies and community data sharingAlina Kurolap, Adi Mory, Sharon Simchoni, et al.
Virchows Archiv : an International Journal of Pathology|November 18, 2015
Agenesis of the corpus callosum. An autopsy study in fetusesDebora Kidron, Daniel Shapira, Liat Ben Sira, et al.
Prenatal Diagnosis|August 28, 2023
SMARCC1 is a susceptibility gene for congenital hydrocephalus with an autosomal dominant inheritance mode and incomplete penetranceNoa Hourvitz, Alina Kurolap, Adi Mory, et al.
European Radiology|July 13, 2022
Improved differentiation between hypo/hypertelorism and normal fetuses based on MRI using automatic ocular biometric measurements, ocular ratios, and machine learning multi-parametric classificationNetanell Avisdris, Daphna Link Sourani, Liat Ben-Sira, et al.
AJNR. American Journal of Neuroradiology|January 21, 2003
Fetal cytomegalovirus infection of the brain: the spectrum of sonographic findingsGustavo Malinger, Dorit Lev, Neriman Zahalka, et al.
Pageof 10