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Dorit Lev

Showing results (51-60 of 176) with videos related to

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Journal of Child Neurology|March 29, 2006
Nonprogressive familial leukoencephalopathy with porencephalic cyst and focal seizuresLubov Blumkin, Nathan Watemberg, Dorit Lev, et al.
Molecular Genetics and Metabolism|March 6, 2010
Leigh disease presenting in utero due to a novel missense mutation in the mitochondrial DNA-ND3Esther Leshinsky-Silver, Dorit Lev, Gustavo Malinger, et al.
Neuropediatrics|May 26, 2018
Multiple Causes of Pediatric Early Onset Chorea-Clinical and Genetic ApproachLubov Blumkin, Tally Lerman-Sagie, Ana Westenberger, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 14, 2018
Progressive cerebello-cerebral atrophy and progressive encephalopathy with edema, hypsarrhythmia and optic atrophy may be allelic syndromesRonen Hady-Cohen, Hila Ben-Pazi, Vardit Adir, et al.
Journal of Perinatal Medicine|December 8, 2019
Microarray findings in pregnancies with oligohydramnios - a retrospective cohort study and literature reviewAmihood Singer, Idit Maya, Rivka Sukenik-Halevy, 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|January 21, 2003
Prenatal exclusion of Leigh syndrome due to T8993C mutation in the mitochondrial DNAEsther Leshinsky-Silver, Michal Perach, Erena Basilevsky, et al.
American Journal of Medical Genetics. Part A|August 19, 2003
Familial optic atrophy with white matter changesChana Vinkler, Dorit Lev, Hadas Kalish, et al.
American Journal of Medical Genetics. Part A|April 9, 2009
Significant overlap and possible identity of macrocephaly capillary malformation and megalencephaly polymicrogyria-polydactyly hydrocephalus syndromesKaren W Gripp, Elizabeth Hopkins, Chana Vinkler, et al.
European Journal of Human Genetics : EJHG|May 29, 2002
MEHMO (Mental retardation, Epileptic seizures, Hypogenitalism, Microcephaly, Obesity): a new X-linked mitochondrial disorderEsther Leshinsky-Silver, Ami Zinger, Chaim N Bibi, et al.
Pageof 18

Showing results (51-60 of 176) with videos related to

Sort By:
Pageof 18
Journal of Child Neurology|March 29, 2006
Nonprogressive familial leukoencephalopathy with porencephalic cyst and focal seizuresLubov Blumkin, Nathan Watemberg, Dorit Lev, et al.
Molecular Genetics and Metabolism|March 6, 2010
Leigh disease presenting in utero due to a novel missense mutation in the mitochondrial DNA-ND3Esther Leshinsky-Silver, Dorit Lev, Gustavo Malinger, et al.
Neuropediatrics|May 26, 2018
Multiple Causes of Pediatric Early Onset Chorea-Clinical and Genetic ApproachLubov Blumkin, Tally Lerman-Sagie, Ana Westenberger, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|August 14, 2018
Progressive cerebello-cerebral atrophy and progressive encephalopathy with edema, hypsarrhythmia and optic atrophy may be allelic syndromesRonen Hady-Cohen, Hila Ben-Pazi, Vardit Adir, et al.
Journal of Perinatal Medicine|December 8, 2019
Microarray findings in pregnancies with oligohydramnios - a retrospective cohort study and literature reviewAmihood Singer, Idit Maya, Rivka Sukenik-Halevy, 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|January 21, 2003
Prenatal exclusion of Leigh syndrome due to T8993C mutation in the mitochondrial DNAEsther Leshinsky-Silver, Michal Perach, Erena Basilevsky, et al.
American Journal of Medical Genetics. Part A|August 19, 2003
Familial optic atrophy with white matter changesChana Vinkler, Dorit Lev, Hadas Kalish, et al.
American Journal of Medical Genetics. Part A|April 9, 2009
Significant overlap and possible identity of macrocephaly capillary malformation and megalencephaly polymicrogyria-polydactyly hydrocephalus syndromesKaren W Gripp, Elizabeth Hopkins, Chana Vinkler, et al.
European Journal of Human Genetics : EJHG|May 29, 2002
MEHMO (Mental retardation, Epileptic seizures, Hypogenitalism, Microcephaly, Obesity): a new X-linked mitochondrial disorderEsther Leshinsky-Silver, Ami Zinger, Chaim N Bibi, et al.
Pageof 18