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Virchows Archiv : an International Journal of Pathology
|
November 18, 2015
Agenesis of the corpus callosum. An autopsy study in fetuses
Debora Kidron, Daniel Shapira, Liat Ben Sira, et al.
Journal of Child Neurology
|
June 24, 2005
Mitochondrial myopathy, sideroblastic anemia, and lactic acidosis: an autosomal recessive syndrome in Persian Jews caused by a mutation in the PUS1 gene
Avraham Zeharia, Nathan Fischel-Ghodsian, Kari Casas, et al.
Developmental Medicine and Child Neurology
|
September 11, 2024
Parental magnetic resonance imaging for the evaluation of fetuses with brain anomalies
Stephanie Libzon, Michal Gafner, Dorit Lev, et al.
Epilepsia
|
October 16, 2012
Resolution of epileptic encephalopathy following treatment with transdermal nicotine
Ayelet Zerem, Daniella Nishri, Yael Yosef, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
July 21, 2015
Atypical presentation of Costeff syndrome-severe psychomotor involvement and electrical status epilepticus during slow wave sleep
Nirit Carmi, Dorit Lev, Esther Leshinsky-Silver, 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.
AJNR. American Journal of Neuroradiology
|
January 21, 2003
Fetal cytomegalovirus infection of the brain: the spectrum of sonographic findings
Gustavo Malinger, Dorit Lev, Neriman Zahalka, et al.
Harefuah
|
April 7, 2004
[Ketogenic diet as antiepileptic therapy: a description of the clinical experience and the multidisciplinary approach at the metabolic-neurogenetic clinic at the Wolfson Medical Center]
Mira Ginzberg, Nathan Watemberg, Anat Levi, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
April 19, 2014
Diagnosis by whole exome sequencing of atypical infantile onset Alexander disease masquerading as a mitochondrial disorder
Daniella Nishri, Simon Edvardson, Dorit Lev, et al.
Fetal Diagnosis and Therapy
|
April 7, 2016
The 'Brain Shadowing Sign': A Novel Marker of Fetal Craniosynostosis
Karina Krajden Haratz, Zvi Leibovitz, Ran Svirsky, et al.
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of 18
Search research articles
Search
Showing results (61-70 of 176) with videos related to
Sort By:
Page
of 18
Virchows Archiv : an International Journal of Pathology
|
November 18, 2015
Agenesis of the corpus callosum. An autopsy study in fetuses
Debora Kidron, Daniel Shapira, Liat Ben Sira, et al.
Journal of Child Neurology
|
June 24, 2005
Mitochondrial myopathy, sideroblastic anemia, and lactic acidosis: an autosomal recessive syndrome in Persian Jews caused by a mutation in the PUS1 gene
Avraham Zeharia, Nathan Fischel-Ghodsian, Kari Casas, et al.
Developmental Medicine and Child Neurology
|
September 11, 2024
Parental magnetic resonance imaging for the evaluation of fetuses with brain anomalies
Stephanie Libzon, Michal Gafner, Dorit Lev, et al.
Epilepsia
|
October 16, 2012
Resolution of epileptic encephalopathy following treatment with transdermal nicotine
Ayelet Zerem, Daniella Nishri, Yael Yosef, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
July 21, 2015
Atypical presentation of Costeff syndrome-severe psychomotor involvement and electrical status epilepticus during slow wave sleep
Nirit Carmi, Dorit Lev, Esther Leshinsky-Silver, 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.
AJNR. American Journal of Neuroradiology
|
January 21, 2003
Fetal cytomegalovirus infection of the brain: the spectrum of sonographic findings
Gustavo Malinger, Dorit Lev, Neriman Zahalka, et al.
Harefuah
|
April 7, 2004
[Ketogenic diet as antiepileptic therapy: a description of the clinical experience and the multidisciplinary approach at the metabolic-neurogenetic clinic at the Wolfson Medical Center]
Mira Ginzberg, Nathan Watemberg, Anat Levi, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
April 19, 2014
Diagnosis by whole exome sequencing of atypical infantile onset Alexander disease masquerading as a mitochondrial disorder
Daniella Nishri, Simon Edvardson, Dorit Lev, et al.
Fetal Diagnosis and Therapy
|
April 7, 2016
The 'Brain Shadowing Sign': A Novel Marker of Fetal Craniosynostosis
Karina Krajden Haratz, Zvi Leibovitz, Ran Svirsky, et al.
Page
of 18