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Tokinari Abe

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

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Journal of Child Neurology|August 2, 2002
Normally developed infant with a suppression burst pattern on electroencephalography in the neonatal periodHideto Yoshikawa, Takeshige Honma, Sawako Yamazaki, et al.
Brain & Development|April 12, 2003
Hypouricemia in severely disabled children: influence of valproic acid and bed-ridden stateHideto Yoshikawa, Sawako Yamazaki, Toru Watanabe, et al.
Journal of Child Neurology|April 16, 2003
Vitamin K deficiency in severely disabled childrenHideto Yoshikawa, Sawako Yamazaki, Toru Watanabe, et al.
Pediatric Nephrology (Berlin, Germany)|March 24, 2005
Secondary renal Fanconi syndrome caused by valproate therapyToru Watanabe, Hideto Yoshikawa, Sawako Yamazaki, et al.
Hormone Research in Paediatrics|June 14, 2014
Association between compound heterozygous mutations of SLC34A3 and hypercalciuriaYuki Abe, Keisuke Nagasaki, Toru Watanabe, et al.
Pediatric Neurology|August 10, 2011
Hemiconvulsion-hemiplegia-epilepsy syndrome associated with CACNA1A S218L mutationSawako Yamazaki, Kanju Ikeno, Tokinari Abe, et al.
Pediatric Nephrology (Berlin, Germany)|April 17, 2003
Renal involvement in children with influenza A virus infectionToru Watanabe, Hideto Yoshikawa, Yuki Abe, et al.
Pediatric Nephrology (Berlin, Germany)|February 27, 2007
Sterile pyuria in patients with Kawasaki disease originates from both the urethra and the kidneyToru Watanabe, Yuki Abe, Seiichi Sato, et al.
Pediatric Nephrology (Berlin, Germany)|March 28, 2006
Hyponatremia in Kawasaki diseaseToru Watanabe, Yuki Abe, Seiichi Sato, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 11, 2012
A case of Rabson-Mendenhall syndrome with a novel mutation in the tyrosine kinase domain of the insulin receptor gene complicated by medullary sponge kidneyYuki Abe, Takashi Sato, Masaki Takagi, et al.
Pageof 2

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

Sort By:
Pageof 2
You have reached the last page of results.This site can display upto 20 results.
Journal of Child Neurology|August 2, 2002
Normally developed infant with a suppression burst pattern on electroencephalography in the neonatal periodHideto Yoshikawa, Takeshige Honma, Sawako Yamazaki, et al.
Brain & Development|April 12, 2003
Hypouricemia in severely disabled children: influence of valproic acid and bed-ridden stateHideto Yoshikawa, Sawako Yamazaki, Toru Watanabe, et al.
Journal of Child Neurology|April 16, 2003
Vitamin K deficiency in severely disabled childrenHideto Yoshikawa, Sawako Yamazaki, Toru Watanabe, et al.
Pediatric Nephrology (Berlin, Germany)|March 24, 2005
Secondary renal Fanconi syndrome caused by valproate therapyToru Watanabe, Hideto Yoshikawa, Sawako Yamazaki, et al.
Hormone Research in Paediatrics|June 14, 2014
Association between compound heterozygous mutations of SLC34A3 and hypercalciuriaYuki Abe, Keisuke Nagasaki, Toru Watanabe, et al.
Pediatric Neurology|August 10, 2011
Hemiconvulsion-hemiplegia-epilepsy syndrome associated with CACNA1A S218L mutationSawako Yamazaki, Kanju Ikeno, Tokinari Abe, et al.
Pediatric Nephrology (Berlin, Germany)|April 17, 2003
Renal involvement in children with influenza A virus infectionToru Watanabe, Hideto Yoshikawa, Yuki Abe, et al.
Pediatric Nephrology (Berlin, Germany)|February 27, 2007
Sterile pyuria in patients with Kawasaki disease originates from both the urethra and the kidneyToru Watanabe, Yuki Abe, Seiichi Sato, et al.
Pediatric Nephrology (Berlin, Germany)|March 28, 2006
Hyponatremia in Kawasaki diseaseToru Watanabe, Yuki Abe, Seiichi Sato, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM|August 11, 2012
A case of Rabson-Mendenhall syndrome with a novel mutation in the tyrosine kinase domain of the insulin receptor gene complicated by medullary sponge kidneyYuki Abe, Takashi Sato, Masaki Takagi, et al.
Pageof 2