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Dorit Lev

Showing results (101-110 of 176) with videos related to

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Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|June 8, 2018
Ultrasound Nomograms of the Fetal Optic Nerve Sheath DiameterKarina Krajden Haratz, Yaakov Melcer, Zvi Leibovitz, et al.
Molecular Genetics and Metabolism|April 15, 2009
NDUFS4 mutations cause Leigh syndrome with predominant brainstem involvementE Leshinsky-Silver, Anne-Sophie Lebre, Limor Minai, et al.
Pediatric Research|September 9, 2005
Is age of onset of Crohn's disease governed by mutations in NOD2/caspase recruitment domains 15 and Toll-like receptor 4? Evaluation of a pediatric cohortEsther Leshinsky-Silver, Amir Karban, Erena Buzhakor, et al.
American Journal of Medical Genetics. Part A|October 18, 2019
Brain white matter abnormalities associated with copy number variantsNitzan Vigdorovich, Liat Ben-Sira, Lubov Blumkin, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|October 27, 2018
Lacosamide for SCN2A-related intractable neonatal and infantile seizuresHadar Flor-Hirsch, Eli Heyman, Ayelet Livneh, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|January 26, 2018
Isolated fetal horseshoe kidney does not seem to increase the risk for abnormal chromosomal microarray resultsLena Sagi-Dain, Idit Maya, Tzipora Falik-Zaccai, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 23, 2015
The spinal muscular atrophy with pontocerebellar hypoplasia gene VRK1 regulates neuronal migration through an amyloid-β precursor protein-dependent mechanismHadar Vinograd-Byk, Tamar Sapir, Lara Cantarero, et al.
European Journal of Human Genetics : EJHG|November 25, 2010
A large homozygous deletion in the SAMHD1 gene causes atypical Aicardi-Goutiéres syndrome associated with mtDNA deletionsEsther Leshinsky-Silver, Gustavo Malinger, Liat Ben-Sira, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 14, 2016
RARS2 mutations cause early onset epileptic encephalopathy without ponto-cerebellar hypoplasiaDaniella Nishri, Hadassa Goldberg-Stern, Iris Noyman, et al.
Fetal Diagnosis and Therapy|June 19, 2017
Unique Imaging Features Enabling the Prenatal Diagnosis of Developmental Venous Anomalies: A Persistent Echogenic Brain Lesion Drained by a Collecting Vein in Contrast with Normal Brain Parenchyma on MRIKarina Krajden Haratz, Alon Peled, Boris Weizman, et al.
Pageof 18

Showing results (101-110 of 176) with videos related to

Sort By:
Pageof 18
Ultraschall in Der Medizin (Stuttgart, Germany : 1980)|June 8, 2018
Ultrasound Nomograms of the Fetal Optic Nerve Sheath DiameterKarina Krajden Haratz, Yaakov Melcer, Zvi Leibovitz, et al.
Molecular Genetics and Metabolism|April 15, 2009
NDUFS4 mutations cause Leigh syndrome with predominant brainstem involvementE Leshinsky-Silver, Anne-Sophie Lebre, Limor Minai, et al.
Pediatric Research|September 9, 2005
Is age of onset of Crohn's disease governed by mutations in NOD2/caspase recruitment domains 15 and Toll-like receptor 4? Evaluation of a pediatric cohortEsther Leshinsky-Silver, Amir Karban, Erena Buzhakor, et al.
American Journal of Medical Genetics. Part A|October 18, 2019
Brain white matter abnormalities associated with copy number variantsNitzan Vigdorovich, Liat Ben-Sira, Lubov Blumkin, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape|October 27, 2018
Lacosamide for SCN2A-related intractable neonatal and infantile seizuresHadar Flor-Hirsch, Eli Heyman, Ayelet Livneh, et al.
European Journal of Obstetrics, Gynecology, and Reproductive Biology|January 26, 2018
Isolated fetal horseshoe kidney does not seem to increase the risk for abnormal chromosomal microarray resultsLena Sagi-Dain, Idit Maya, Tzipora Falik-Zaccai, et al.
The Journal of Neuroscience : the Official Journal of the Society for Neuroscience|January 23, 2015
The spinal muscular atrophy with pontocerebellar hypoplasia gene VRK1 regulates neuronal migration through an amyloid-β precursor protein-dependent mechanismHadar Vinograd-Byk, Tamar Sapir, Lara Cantarero, et al.
European Journal of Human Genetics : EJHG|November 25, 2010
A large homozygous deletion in the SAMHD1 gene causes atypical Aicardi-Goutiéres syndrome associated with mtDNA deletionsEsther Leshinsky-Silver, Gustavo Malinger, Liat Ben-Sira, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|March 14, 2016
RARS2 mutations cause early onset epileptic encephalopathy without ponto-cerebellar hypoplasiaDaniella Nishri, Hadassa Goldberg-Stern, Iris Noyman, et al.
Fetal Diagnosis and Therapy|June 19, 2017
Unique Imaging Features Enabling the Prenatal Diagnosis of Developmental Venous Anomalies: A Persistent Echogenic Brain Lesion Drained by a Collecting Vein in Contrast with Normal Brain Parenchyma on MRIKarina Krajden Haratz, Alon Peled, Boris Weizman, et al.
Pageof 18