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Esther Granot

Showing results (11-20 of 21) with videos related to

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Pediatrics|March 4, 2003
Medical treatment of recurrent intussusception associated with intestinal lymphoid hyperplasiaEyal Shteyer, Benjamin Z Koplewitz, Eitan Gross, 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|March 12, 2015
Is there a difference in breast milk fatty acid composition of mothers of preterm and term infants?Esther Granot, Keren Ishay-Gigi, Lea Malaach, et al.
Mediators of Inflammation|September 24, 2011
DHA supplementation during pregnancy and lactation affects infants' cellular but not humoral immune responseEsther Granot, Einat Jakobovich, Ruth Rabinowitz, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|March 18, 2011
Serum transaminases as a prognostic factor in children post cardiac surgeryEyal Shteyer, Ido Yatsiv, Muhamad Sharkia, et al.
Acta Paediatrica (Oslo, Norway : 1992)|May 15, 2007
Look-back study of Hepatitis C in teenagers after blood transfusions as neonatesMichal Kori, Orna Flidel-Rimon, Erica Sigler, et al.
Journal of Clinical Gastroenterology|March 22, 2002
Intestinal protein loss in acute and persistent diarrhea of early childhoodZvi Weizman, Mauricio Binsztok, Drora Fraser, et al.
American Journal of Medical Genetics. Part A|August 23, 2015
Homozygous deletion of TRMT10A as part of a contiguous gene deletion in a syndrome of failure to thrive, delayed puberty, intellectual disability and diabetes mellitusAmnon Zung, Michal Kori, Ella Burundukov, et al.
Journal of Pediatric Gastroenterology and Nutrition|June 15, 2012
Continuous 13C-methacetin breath test differentiates biliary atresia from other causes of neonatal cholestasisEyal Shteyer, Gadi Lalazar, Nilla Hemed, et al.
Molecular Genetics and Metabolism|February 6, 2007
Abetalipoproteinemia in Israel: evidence for a founder mutation in the Ashkenazi Jewish population and a contiguous gene deletion in an Arab patientLiat Benayoun, Esther Granot, Leah Rizel, et al.
American Journal of Medical Genetics|September 20, 2002
Jagged1 gene mutation for abdominal coarctation of the aorta in Alagille syndromeAnnick Raas-Rothschild, Eyal Shteyer, Israela Lerer, et al.
Pageof 3

Showing results (11-20 of 21) with videos related to

Sort By:
Pageof 3
Pediatrics|March 4, 2003
Medical treatment of recurrent intussusception associated with intestinal lymphoid hyperplasiaEyal Shteyer, Benjamin Z Koplewitz, Eitan Gross, 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|March 12, 2015
Is there a difference in breast milk fatty acid composition of mothers of preterm and term infants?Esther Granot, Keren Ishay-Gigi, Lea Malaach, et al.
Mediators of Inflammation|September 24, 2011
DHA supplementation during pregnancy and lactation affects infants' cellular but not humoral immune responseEsther Granot, Einat Jakobovich, Ruth Rabinowitz, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|March 18, 2011
Serum transaminases as a prognostic factor in children post cardiac surgeryEyal Shteyer, Ido Yatsiv, Muhamad Sharkia, et al.
Acta Paediatrica (Oslo, Norway : 1992)|May 15, 2007
Look-back study of Hepatitis C in teenagers after blood transfusions as neonatesMichal Kori, Orna Flidel-Rimon, Erica Sigler, et al.
Journal of Clinical Gastroenterology|March 22, 2002
Intestinal protein loss in acute and persistent diarrhea of early childhoodZvi Weizman, Mauricio Binsztok, Drora Fraser, et al.
American Journal of Medical Genetics. Part A|August 23, 2015
Homozygous deletion of TRMT10A as part of a contiguous gene deletion in a syndrome of failure to thrive, delayed puberty, intellectual disability and diabetes mellitusAmnon Zung, Michal Kori, Ella Burundukov, et al.
Journal of Pediatric Gastroenterology and Nutrition|June 15, 2012
Continuous 13C-methacetin breath test differentiates biliary atresia from other causes of neonatal cholestasisEyal Shteyer, Gadi Lalazar, Nilla Hemed, et al.
Molecular Genetics and Metabolism|February 6, 2007
Abetalipoproteinemia in Israel: evidence for a founder mutation in the Ashkenazi Jewish population and a contiguous gene deletion in an Arab patientLiat Benayoun, Esther Granot, Leah Rizel, et al.
American Journal of Medical Genetics|September 20, 2002
Jagged1 gene mutation for abdominal coarctation of the aorta in Alagille syndromeAnnick Raas-Rothschild, Eyal Shteyer, Israela Lerer, et al.
Pageof 3