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Hanna Mandel

Showing results (11-20 of 127) with videos related to

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Biochemical and Biophysical Research Communications|October 11, 2003
Mitochondrial deoxyribonucleoside triphosphate pools in thymidine kinase 2 deficiencyAnn Saada, Efrat Ben-Shalom, Rivka Zyslin, et al.
Journal of Child Neurology|February 3, 2011
Prenatal brain disruption in molybdenum cofactor deficiencyNirit Carmi-Nawi, Gustavo Malinger, Hanna Mandel, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 17, 2008
Familial leukoencephalopathy with slowly progressive dystonia and ataxiaLubov Blumkin, Hanna Mandel, Marieta Anca-Herschkovitsch, et al.
The American Journal of Dermatopathology|December 24, 2010
A case of H syndrome showing immunophenotye similarities to Rosai-Dorfman diseaseEmily Avitan-Hersh, Hanna Mandel, Margarita Indelman, et al.
Annals of Neurology|September 5, 2002
A novel mutation in the deoxyguanosine kinase gene causing depletion of mitochondrial DNAJan-Willem Taanman, Ihab Kateeb, Ania C Muntau, et al.
The Journal of Pediatrics|June 2, 2006
A retrospective, multinational, multicenter study on the natural history of infantile-onset Pompe diseasePriya S Kishnani, Wuh-Liang Hwu, Hanna Mandel, et al.
Archives of Disease in Childhood|July 27, 2007
The significance of isolated elevation of serum aminotransferases in infants and young childrenNina Bugeac, Avi Pacht, Hanna Mandel, et al.
Journal of Pediatric Hematology/Oncology|February 8, 2006
Myeloid dysplasia in familial 3-methylglutaconic aciduriaMotti Haimi, Ronit Elhasid, Ruth Gershoni-Baruch, et al.
Pediatric Pulmonology|January 23, 2018
Cardiopulmonary exercise test to quantify enzyme replacement response in pediatric Pompe diseaseRonen Bar-Yoseph, Hanna Mandel, Gur Mainzer, et al.
Journal of Pediatric Gastroenterology and Nutrition|October 29, 2003
Nonsyndromic paucity of interlobular bile ducts: report of 10 patientsVered Yehezkely-Schildkraut, Mariana Munichor, Hanna Mandel, et al.
Pageof 13

Showing results (11-20 of 127) with videos related to

Sort By:
Pageof 13
Biochemical and Biophysical Research Communications|October 11, 2003
Mitochondrial deoxyribonucleoside triphosphate pools in thymidine kinase 2 deficiencyAnn Saada, Efrat Ben-Shalom, Rivka Zyslin, et al.
Journal of Child Neurology|February 3, 2011
Prenatal brain disruption in molybdenum cofactor deficiencyNirit Carmi-Nawi, Gustavo Malinger, Hanna Mandel, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society|December 17, 2008
Familial leukoencephalopathy with slowly progressive dystonia and ataxiaLubov Blumkin, Hanna Mandel, Marieta Anca-Herschkovitsch, et al.
The American Journal of Dermatopathology|December 24, 2010
A case of H syndrome showing immunophenotye similarities to Rosai-Dorfman diseaseEmily Avitan-Hersh, Hanna Mandel, Margarita Indelman, et al.
Annals of Neurology|September 5, 2002
A novel mutation in the deoxyguanosine kinase gene causing depletion of mitochondrial DNAJan-Willem Taanman, Ihab Kateeb, Ania C Muntau, et al.
The Journal of Pediatrics|June 2, 2006
A retrospective, multinational, multicenter study on the natural history of infantile-onset Pompe diseasePriya S Kishnani, Wuh-Liang Hwu, Hanna Mandel, et al.
Archives of Disease in Childhood|July 27, 2007
The significance of isolated elevation of serum aminotransferases in infants and young childrenNina Bugeac, Avi Pacht, Hanna Mandel, et al.
Journal of Pediatric Hematology/Oncology|February 8, 2006
Myeloid dysplasia in familial 3-methylglutaconic aciduriaMotti Haimi, Ronit Elhasid, Ruth Gershoni-Baruch, et al.
Pediatric Pulmonology|January 23, 2018
Cardiopulmonary exercise test to quantify enzyme replacement response in pediatric Pompe diseaseRonen Bar-Yoseph, Hanna Mandel, Gur Mainzer, et al.
Journal of Pediatric Gastroenterology and Nutrition|October 29, 2003
Nonsyndromic paucity of interlobular bile ducts: report of 10 patientsVered Yehezkely-Schildkraut, Mariana Munichor, Hanna Mandel, et al.
Pageof 13