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Hanna Mandel

Showing results (1-10 of 127) with videos related to

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Advances in Experimental Medicine and Biology|January 10, 2004
Phenotypic variability (heterogeneity) of peroxisomal disordersHanna Mandel, Stanley H Korman
Journal of Molecular Medicine (Berlin, Germany)|July 12, 2002
Depletion of the other genome-mitochondrial DNA depletion syndromes in humansOrly Elpeleg, Hanna Mandel, Ann Saada
Child Neurology Open|May 16, 2017
Guillain Barré Syndrome in a Child With X-Linked AdrenoleukodystrophyRon Jacob, Hanna Mandel, Naim Shehadeh
The Israel Medical Association Journal : IMAJ|March 26, 2025
Molybdenum Cofactor Deficiency Type A disease in Northern IsraelEliyahu Fund, Hanna Mandel, Yoav Zehavi, et al.
Neurology|July 26, 2013
Subependymal mass lesions and peripheral polyneuropathy in adult-onset glutaric aciduria type IMoshe Herskovitz, Dorith Goldsher, Ben-Ami Sela, et al.
Pediatric Pulmonology|January 25, 2005
Splicing mutation in the fibrillin-1 gene associated with neonatal Marfan syndrome and severe pulmonary emphysema with tracheobronchomalaciaMarwan Shinawi, Catherine Boileau, Riva Brik, et al.
American Journal of Medical Genetics. Part A|October 18, 2016
TBCK-related intellectual disability syndrome: Case study of two patientsHanna Mandel, Morad Khayat, Elana Chervinsky, et al.
The Journal of Biological Chemistry|August 27, 2009
The MitCHAP-60 disease is due to entropic destabilization of the human mitochondrial Hsp60 oligomerAvital Parnas, Michal Nadler, Shahar Nisemblat, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 27, 2005
Secondary diabetes mellitus: late complication of glycogen storage disease type 1bRonen Spiegel, Yardena Rakover-Tenenbaum, Hanna Mandel, et al.
Ultrastructural Pathology|July 7, 2007
The liver in congenital disorders of glycosylation: ultrastructural featuresTheodore C Iancu, Muhammad Mahajnah, Irena Manov, et al.
Pageof 13

Showing results (1-10 of 127) with videos related to

Sort By:
Pageof 13
Advances in Experimental Medicine and Biology|January 10, 2004
Phenotypic variability (heterogeneity) of peroxisomal disordersHanna Mandel, Stanley H Korman
Journal of Molecular Medicine (Berlin, Germany)|July 12, 2002
Depletion of the other genome-mitochondrial DNA depletion syndromes in humansOrly Elpeleg, Hanna Mandel, Ann Saada
Child Neurology Open|May 16, 2017
Guillain Barré Syndrome in a Child With X-Linked AdrenoleukodystrophyRon Jacob, Hanna Mandel, Naim Shehadeh
The Israel Medical Association Journal : IMAJ|March 26, 2025
Molybdenum Cofactor Deficiency Type A disease in Northern IsraelEliyahu Fund, Hanna Mandel, Yoav Zehavi, et al.
Neurology|July 26, 2013
Subependymal mass lesions and peripheral polyneuropathy in adult-onset glutaric aciduria type IMoshe Herskovitz, Dorith Goldsher, Ben-Ami Sela, et al.
Pediatric Pulmonology|January 25, 2005
Splicing mutation in the fibrillin-1 gene associated with neonatal Marfan syndrome and severe pulmonary emphysema with tracheobronchomalaciaMarwan Shinawi, Catherine Boileau, Riva Brik, et al.
American Journal of Medical Genetics. Part A|October 18, 2016
TBCK-related intellectual disability syndrome: Case study of two patientsHanna Mandel, Morad Khayat, Elana Chervinsky, et al.
The Journal of Biological Chemistry|August 27, 2009
The MitCHAP-60 disease is due to entropic destabilization of the human mitochondrial Hsp60 oligomerAvital Parnas, Michal Nadler, Shahar Nisemblat, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|July 27, 2005
Secondary diabetes mellitus: late complication of glycogen storage disease type 1bRonen Spiegel, Yardena Rakover-Tenenbaum, Hanna Mandel, et al.
Ultrastructural Pathology|July 7, 2007
The liver in congenital disorders of glycosylation: ultrastructural featuresTheodore C Iancu, Muhammad Mahajnah, Irena Manov, et al.
Pageof 13