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Ben Pode-Shakked

Showing results (11-20 of 85) with videos related to

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European Journal of Medical Genetics|April 1, 2021
Ophthalmic manifestations in Kabuki (make-up) syndrome: A single-center pediatric cohort and systematic review of the literatureRona Merdler-Rabinowicz, Daphna Prat, Ben Pode-Shakked, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine|December 10, 2016
Nonobstructive Diffuse Dilated Bowel Loops: Prenatal Diagnosis, Fetal Characteristics and Neonatal OutcomesGuy Katz, Ben Pode-Shakked, Michal Berkenstadt, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine|January 14, 2018
LMOD3-Associated Nemaline Myopathy: Prenatal Ultrasonographic, Pathologic, and Molecular FindingsMichal Berkenstadt, Ben Pode-Shakked, Ortal Barel, et al.
Molecular Genetics and Metabolism Reports|December 21, 2016
Cardiac failure in very long chain acyl-CoA dehydrogenase deficiency requiring extracorporeal membrane oxygenation (ECMO) treatment: A case report and review of the literatureSharon Katz, Yuval Landau, Ben Pode-Shakked, et al.
Molecular Genetics and Metabolism|November 12, 2013
Man made disease: clinical manifestations of low phenylalanine levels in an inadequately treated phenylketonuria patient and mouse studyBen Pode-Shakked, Lilach Shemer-Meiri, Alon Harmelin, et al.
Molecular Genetics and Metabolism Reports|November 30, 2016
Glutaric Aciduria type I and acute renal failure - Coincidence or causality?Ben Pode-Shakked, Dina Marek-Yagel, Marina Rubinshtein, et al.
Pediatric Nephrology (Berlin, Germany)|September 27, 2021
Kidney and urinary tract findings among patients with Kabuki (make-up) syndromeRona Merdler-Rabinowicz, Ben Pode-Shakked, Asaf Vivante, et al.
Nutrients|October 23, 2021
The Effects of a Ketogenic Diet on Patients with Dihydrolipoamide Dehydrogenase DeficiencyOrna Staretz-Chacham, Ben Pode-Shakked, Eyal Kristal, et al.
Italian Journal of Pediatrics|June 6, 2022
Hereditary neuropathy with liability to pressure palsies (HNPP): Intrafamilial phenotypic variability and early childhood refusal to walk as the presenting symptomShani Karklinsky, Shir Kugler, Omer Bar-Yosef, et al.
European Journal of Medical Genetics|November 1, 2015
A novel mutation in the C7orf11 gene causes nonphotosensitive trichothiodystrophy in a multiplex highly consanguineous kindredBen Pode-Shakked, Dina Marek-Yagel, Shoshana Greenberger, et al.
Pageof 9

Showing results (11-20 of 85) with videos related to

Sort By:
Pageof 9
European Journal of Medical Genetics|April 1, 2021
Ophthalmic manifestations in Kabuki (make-up) syndrome: A single-center pediatric cohort and systematic review of the literatureRona Merdler-Rabinowicz, Daphna Prat, Ben Pode-Shakked, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine|December 10, 2016
Nonobstructive Diffuse Dilated Bowel Loops: Prenatal Diagnosis, Fetal Characteristics and Neonatal OutcomesGuy Katz, Ben Pode-Shakked, Michal Berkenstadt, et al.
Journal of Ultrasound in Medicine : Official Journal of the American Institute of Ultrasound in Medicine|January 14, 2018
LMOD3-Associated Nemaline Myopathy: Prenatal Ultrasonographic, Pathologic, and Molecular FindingsMichal Berkenstadt, Ben Pode-Shakked, Ortal Barel, et al.
Molecular Genetics and Metabolism Reports|December 21, 2016
Cardiac failure in very long chain acyl-CoA dehydrogenase deficiency requiring extracorporeal membrane oxygenation (ECMO) treatment: A case report and review of the literatureSharon Katz, Yuval Landau, Ben Pode-Shakked, et al.
Molecular Genetics and Metabolism|November 12, 2013
Man made disease: clinical manifestations of low phenylalanine levels in an inadequately treated phenylketonuria patient and mouse studyBen Pode-Shakked, Lilach Shemer-Meiri, Alon Harmelin, et al.
Molecular Genetics and Metabolism Reports|November 30, 2016
Glutaric Aciduria type I and acute renal failure - Coincidence or causality?Ben Pode-Shakked, Dina Marek-Yagel, Marina Rubinshtein, et al.
Pediatric Nephrology (Berlin, Germany)|September 27, 2021
Kidney and urinary tract findings among patients with Kabuki (make-up) syndromeRona Merdler-Rabinowicz, Ben Pode-Shakked, Asaf Vivante, et al.
Nutrients|October 23, 2021
The Effects of a Ketogenic Diet on Patients with Dihydrolipoamide Dehydrogenase DeficiencyOrna Staretz-Chacham, Ben Pode-Shakked, Eyal Kristal, et al.
Italian Journal of Pediatrics|June 6, 2022
Hereditary neuropathy with liability to pressure palsies (HNPP): Intrafamilial phenotypic variability and early childhood refusal to walk as the presenting symptomShani Karklinsky, Shir Kugler, Omer Bar-Yosef, et al.
European Journal of Medical Genetics|November 1, 2015
A novel mutation in the C7orf11 gene causes nonphotosensitive trichothiodystrophy in a multiplex highly consanguineous kindredBen Pode-Shakked, Dina Marek-Yagel, Shoshana Greenberger, et al.
Pageof 9