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Gideon Eshel

Showing results (21-30 of 26) with videos related to

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Journal of Pediatric Orthopedics. Part B|September 1, 2007
Superior mesenteric artery syndrome after scoliosis repair surgery: a case study and reassessment of the syndrome's pathogenesisRoei Hod-Feins, Leonel Copeliovitch, Ibrahim Abu-Kishk, et al.
Surgery Today|July 13, 2011
Blunt pancreatic trauma in childrenBaruch Klin, Ibrahim Abu-Kishk, Igor Jeroukhimov, et al.
AJNR. American Journal of Neuroradiology|August 11, 2005
Thiamine deficiency in infants: MR findings in the brainLiora Kornreich, Efrat Bron-Harlev, Chen Hoffmann, et al.
Pediatrics|February 3, 2005
Outbreak of life-threatening thiamine deficiency in infants in Israel caused by a defective soy-based formulaAviva Fattal-Valevski, Anat Kesler, Ben-Ami Sela, et al.
American Journal of Human Genetics|September 27, 2008
Mutations in LPIN1 cause recurrent acute myoglobinuria in childhoodAvraham Zeharia, Avraham Shaag, Riekelt H Houtkooper, et al.
American Journal of Human Genetics|March 2, 2002
A PEX6-defective peroxisomal biogenesis disorder with severe phenotype in an infant, versus mild phenotype resembling Usher syndrome in the affected parentsAnnick Raas-Rothschild, Ronald J A Wanders, Petra A W Mooijer, et al.
Pageof 3

Showing results (21-30 of 26) with videos related to

Sort By:
Pageof 3
You have reached the last page of results.This site can display upto 26 results.
Journal of Pediatric Orthopedics. Part B|September 1, 2007
Superior mesenteric artery syndrome after scoliosis repair surgery: a case study and reassessment of the syndrome's pathogenesisRoei Hod-Feins, Leonel Copeliovitch, Ibrahim Abu-Kishk, et al.
Surgery Today|July 13, 2011
Blunt pancreatic trauma in childrenBaruch Klin, Ibrahim Abu-Kishk, Igor Jeroukhimov, et al.
AJNR. American Journal of Neuroradiology|August 11, 2005
Thiamine deficiency in infants: MR findings in the brainLiora Kornreich, Efrat Bron-Harlev, Chen Hoffmann, et al.
Pediatrics|February 3, 2005
Outbreak of life-threatening thiamine deficiency in infants in Israel caused by a defective soy-based formulaAviva Fattal-Valevski, Anat Kesler, Ben-Ami Sela, et al.
American Journal of Human Genetics|September 27, 2008
Mutations in LPIN1 cause recurrent acute myoglobinuria in childhoodAvraham Zeharia, Avraham Shaag, Riekelt H Houtkooper, et al.
American Journal of Human Genetics|March 2, 2002
A PEX6-defective peroxisomal biogenesis disorder with severe phenotype in an infant, versus mild phenotype resembling Usher syndrome in the affected parentsAnnick Raas-Rothschild, Ronald J A Wanders, Petra A W Mooijer, et al.
Pageof 3