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Essam A Ismail

Showing results (1-10 of 5) with videos related to

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Acta Paediatrica (Oslo, Norway : 1992)|August 30, 2006
Allgrove syndrome with features of familial dysautonomia: a novel mutation in the AAAS geneEssam A Ismail, Anna Tulliot-Pelet, Ameer M Mohsen, et al.
Neurosciences (Riyadh, Saudi Arabia)|November 5, 2010
Ethylmalonic encephalopathy. Another patient from KuwaitEssam A Ismail, Tarek M Seoudi, Eman A Morsi, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|October 9, 2012
Neonatal suppurative parotitis over the last 4 decades: report of three new cases and reviewEssam A Ismail, Tarek M Seoudi, Mohamad Al-Amir, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 2, 2005
Hereditary juvenile cobalamin deficiency caused by mutations in the intrinsic factor geneStephan M Tanner, Zhongyuan Li, James D Perko, et al.
Human Mutation|March 17, 2004
Genetically heterogeneous selective intestinal malabsorption of vitamin B12: founder effects, consanguinity, and high clinical awareness explain aggregations in Scandinavia and the Middle EastStephan M Tanner, Zhongyuan Li, Ryan Bisson, et al.
Pageof 1

Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
Acta Paediatrica (Oslo, Norway : 1992)|August 30, 2006
Allgrove syndrome with features of familial dysautonomia: a novel mutation in the AAAS geneEssam A Ismail, Anna Tulliot-Pelet, Ameer M Mohsen, et al.
Neurosciences (Riyadh, Saudi Arabia)|November 5, 2010
Ethylmalonic encephalopathy. Another patient from KuwaitEssam A Ismail, Tarek M Seoudi, Eman A Morsi, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|October 9, 2012
Neonatal suppurative parotitis over the last 4 decades: report of three new cases and reviewEssam A Ismail, Tarek M Seoudi, Mohamad Al-Amir, et al.
Proceedings of the National Academy of Sciences of the United States of America|March 2, 2005
Hereditary juvenile cobalamin deficiency caused by mutations in the intrinsic factor geneStephan M Tanner, Zhongyuan Li, James D Perko, et al.
Human Mutation|March 17, 2004
Genetically heterogeneous selective intestinal malabsorption of vitamin B12: founder effects, consanguinity, and high clinical awareness explain aggregations in Scandinavia and the Middle EastStephan M Tanner, Zhongyuan Li, Ryan Bisson, et al.
Pageof 1