-Tally Lerman-Sagie Researcher Activity Profile

Research Author Detailed Information 

Tally Lerman-Sagie Publication Rate By Year

Tally Lerman-Sagie has published 1 paper(s) in 2003, 2 paper(s) in 2004, 8 paper(s) in 2007, 4 paper(s) in 2008, for a total of 15 research publications in total.

Tally T Lerman-Sagie Author Information

LAST NAME: lerman-sagie

FIRST NAME: Tally

INITIALS: t

AFFILIATION:

Papers

Tally Lerman-Sagie's Publication Record

1. Autoimmune epilepsy: some epilepsy patients harbor autoantibodies to glutamate receptors and dsDNA on both sides of the blood-brain barrier, which may kill neurons and decrease in brain fluids after hemispherotomy. Year Published: 2004
Department of Neurobiology, The Weizmann Institute of Science, Rehovot, Israel.
2. Prenatal diagnosis of malformations of cortical development by dedicated neurosonography. Year Published: 2007
Fetal Neurology Clinic, Wolfson Medical Center, Holon, Israel. gmalinger@gmail.com
3. The fetal corpus callosum. 'The truth is out there'. Year Published: 2007
Fetal Neurology Clinic, Wolfson Medical Center, Holon, Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel. gmalinger@gmail.com
4. OC72: Prenatal diagnosis of cerebellar anomalies by dedicated neurosonography. Year Published: 2007
Women's Health Clinic, Batteer, Bethlehem, Palestinian Territory.
5. OC75: Thick corpus callosum: prenatal diagnosis and clinical significance. Year Published: 2007
Wolfson Medical Center, Sackler School of Medicine, Tel-Aviv University, Israel.
6. Developmental coordination disorder in children with attention-deficit-hyperactivity disorder and physical therapy intervention. Year Published: 2007
Child Neurology Unit and Child Development Center, Meir Medical Center, Kfar Saba, Israel.
7. The fetal corpus callosum. 'The truth is out there'. Year Published: 2007
Fetal Neurology Clinic, Wolfson Medical Center, Holon, Sackler School of Medicine, Tel-Aviv University, Tel-Aviv, Israel. gmalinger@gmail.com
8. Developmental coordination disorder in children with attention-deficit-hyperactivity disorder and physical therapy intervention. Year Published: 2007
Child Neurology Unit and Child Development Center, Meir Medical Center, Kfar Saba, Israel.
9. Short-chain acyl-CoA dehydrogenase gene mutation (c.319C>T) presents with clinical heterogeneity and is candidate founder mutation in individuals of Ashkenazi Jewish origin. Year Published: 2008
Division of Neurology, Department of Pediatrics, Laboratory Medicine and Pathobiology, Hospital for Sick Children, University of Toronto, Toronto, Canada M5G 1X8.
10. Developmental coordination disorder in children with attention-deficit-hyperactivity disorder and physical therapy intervention. Year Published: 2007
Child Neurology Unit and Child Development Center, Meir Medical Center, Kfar Saba, Israel.
11. Fetal cytomegalovirus infection of the brain: the spectrum of sonographic findings. Year Published: 2003
Fetal Neurology Clinic, the Prenatal Diagnoisis Unit, Department of Obstetrics and Gyneclogy, Edith Wolfson Medical Center, Holon, Israel.
12. Clinical presentations of mitochondrial cardiomyopathies. Year Published: 2004
Mitochondrial Disease Clinic, Metabolic Neurogenetic Service, Wolfson Medical Center, Holon, Israel. dorlev@post.tau.ac.il
13. Epilepsy and mental retardation limited to females: an under-recognized disorder. Year Published: 2008
Epilepsy Research Centre, Department of Medicine, University of Melbourne, Austin Health, Neurosciences Building, Level 1, Heidelberg Repatriation Hospital, Banksia Street, Heidelberg VIC 3081, Australia. scheffer@unimelb.edu.au.
14. Epilepsy and mental retardation limited to females: an under-recognized disorder. Year Published: 2008
Epilepsy Research Centre, Department of Medicine, University of Melbourne, Heidelberg Repatriation Hospital, Banksia Street, Heidelberg VIC 3081, Australia. scheffer@unimelb.edu.au
15. Short-chain acyl-CoA dehydrogenase gene mutation (c.319C>T) presents with clinical heterogeneity and is candidate founder mutation in individuals of Ashkenazi Jewish origin. Year Published: 2008
Division of Neurology, Department of Pediatrics, Laboratory Medicine and Pathobiology, Hospital for Sick Children, University of Toronto, Toronto, Canada M5G 1X8. ingrid.tein@sickkids.ca