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Shimon W Moses

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

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European Journal of Pediatrics|October 10, 2002
Historical highlights and unsolved problems in glycogen storage disease type 1Shimon W Moses
Current Molecular Medicine|April 13, 2002
The variable presentations of glycogen storage disease type IV: a review of clinical, enzymatic and molecular studiesShimon W Moses, Ruti Parvari
International Journal of Dermatology|October 4, 2007
The percentage of patients achieving PASI 75 after 1 month and remission time after climatotherapy at the Dead SeaMarco Harari, Lena Novack, Joachim Barth, et al.
The Israel Medical Association Journal : IMAJ|August 16, 2011
Impact of descent and stay at a Dead Sea resort (low altitude) on patients with systolic congestive heart failure and an implantable cardioverter defibrillatorIsack Gabizon, Arthur Shiyovich, Victor Novack, et al.
European Journal of Human Genetics : EJHG|June 26, 2003
Muscle glycogenosis with low phosphorylase kinase activity: mutations in PHKA1, PHKG1 or six other candidate genes explain only a minority of casesBarbara Burwinkel, Bin Hu, Anja Schroers, et al.
Pageof 1

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

Sort By:
Pageof 1
European Journal of Pediatrics|October 10, 2002
Historical highlights and unsolved problems in glycogen storage disease type 1Shimon W Moses
Current Molecular Medicine|April 13, 2002
The variable presentations of glycogen storage disease type IV: a review of clinical, enzymatic and molecular studiesShimon W Moses, Ruti Parvari
International Journal of Dermatology|October 4, 2007
The percentage of patients achieving PASI 75 after 1 month and remission time after climatotherapy at the Dead SeaMarco Harari, Lena Novack, Joachim Barth, et al.
The Israel Medical Association Journal : IMAJ|August 16, 2011
Impact of descent and stay at a Dead Sea resort (low altitude) on patients with systolic congestive heart failure and an implantable cardioverter defibrillatorIsack Gabizon, Arthur Shiyovich, Victor Novack, et al.
European Journal of Human Genetics : EJHG|June 26, 2003
Muscle glycogenosis with low phosphorylase kinase activity: mutations in PHKA1, PHKG1 or six other candidate genes explain only a minority of casesBarbara Burwinkel, Bin Hu, Anja Schroers, et al.
Pageof 1