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Hiwatari

Showing results (101-110 of 231) with videos related to

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Pediatric Hematology and Oncology|November 5, 2020
<i>KMT2A</i>-rearranged diffuse large B-cell lymphoma in a child: a case report and molecular characterizationShota Kato, Yasuo Kubota, Masahiro Sekiguchi, et al.
Pediatric Neurology|September 21, 2020
Zonisamide Therapy for Patients With Paroxysmal Kinesigenic DyskinesiaRyuki Matsuura, Shin-Ichiro Hamano, Erika Hiwatari, et al.
Brain & Development|May 8, 2018
Treatment of infantile spasms by pediatric neurologists in JapanShin-Ichiro Hamano, Toshisaburo Nagai, Ryuki Matsuura, et al.
Radiology Case Reports|June 13, 2020
The potential for early diagnosis of pulmonary arterial hypertension using lung iodine-123-metaiodobenzylguanidine (<sup>123</sup>I-MIBG) uptake: A case reportKenjuro Higo, Kayoko Kubota, Sawako Hiwatari Takeshita, et al.
Pediatric Transplantation|June 17, 2020
Tandem high-dose chemotherapy with autologous stem cell rescue for stage M high-risk neuroblastoma: Experience using melphalan/etoposide/carboplatin and busulfan/melphalan regimensShota Kato, Yasuo Kubota, Kentaro Watanabe, et al.
World Neurosurgery|August 23, 2021
The Incidence of Depressed Skull Fractures Due to the Use of Pin-Type Head Frame Systems in the Adult Population: 10-year Experience of a Single Neurosurgical CenterTakaaki Hiwatari, Hitoshi Yamahata, Masanori Yonenaga, et al.
Leukemia|June 13, 2008
Novel gain-of-function mutation in the extracellular domain of the PDGFRA gene in infant acute lymphoblastic leukemia with t(4;11)(q21;q23)M Hiwatari, R Ono, T Taki, et al.
American Journal of Medical Genetics. Part A|March 26, 2019
A Japanese patient with RAD51-associated Fanconi anemiaSatoshi Takenaka, Yukiko Kuroda, Sayaka Ohta, et al.
Marine Pollution Bulletin|June 6, 2003
Crude oil bioremediation field experiment in the Sea of JapanHideaki Maki, Noriko Hirayama, Takehiko Hiwatari, et al.
European Journal of Neurology|November 29, 2013
A clinical variance in familial amyotrophic lateral sclerosis with a point mutation in Cu/Zn superoxide dismutase geneR Sakuma, K Abe, M Aoki, et al.
Pageof 24

Showing results (101-110 of 231) with videos related to

Sort By:
Pageof 24
Pediatric Hematology and Oncology|November 5, 2020
<i>KMT2A</i>-rearranged diffuse large B-cell lymphoma in a child: a case report and molecular characterizationShota Kato, Yasuo Kubota, Masahiro Sekiguchi, et al.
Pediatric Neurology|September 21, 2020
Zonisamide Therapy for Patients With Paroxysmal Kinesigenic DyskinesiaRyuki Matsuura, Shin-Ichiro Hamano, Erika Hiwatari, et al.
Brain & Development|May 8, 2018
Treatment of infantile spasms by pediatric neurologists in JapanShin-Ichiro Hamano, Toshisaburo Nagai, Ryuki Matsuura, et al.
Radiology Case Reports|June 13, 2020
The potential for early diagnosis of pulmonary arterial hypertension using lung iodine-123-metaiodobenzylguanidine (<sup>123</sup>I-MIBG) uptake: A case reportKenjuro Higo, Kayoko Kubota, Sawako Hiwatari Takeshita, et al.
Pediatric Transplantation|June 17, 2020
Tandem high-dose chemotherapy with autologous stem cell rescue for stage M high-risk neuroblastoma: Experience using melphalan/etoposide/carboplatin and busulfan/melphalan regimensShota Kato, Yasuo Kubota, Kentaro Watanabe, et al.
World Neurosurgery|August 23, 2021
The Incidence of Depressed Skull Fractures Due to the Use of Pin-Type Head Frame Systems in the Adult Population: 10-year Experience of a Single Neurosurgical CenterTakaaki Hiwatari, Hitoshi Yamahata, Masanori Yonenaga, et al.
Leukemia|June 13, 2008
Novel gain-of-function mutation in the extracellular domain of the PDGFRA gene in infant acute lymphoblastic leukemia with t(4;11)(q21;q23)M Hiwatari, R Ono, T Taki, et al.
American Journal of Medical Genetics. Part A|March 26, 2019
A Japanese patient with RAD51-associated Fanconi anemiaSatoshi Takenaka, Yukiko Kuroda, Sayaka Ohta, et al.
Marine Pollution Bulletin|June 6, 2003
Crude oil bioremediation field experiment in the Sea of JapanHideaki Maki, Noriko Hirayama, Takehiko Hiwatari, et al.
European Journal of Neurology|November 29, 2013
A clinical variance in familial amyotrophic lateral sclerosis with a point mutation in Cu/Zn superoxide dismutase geneR Sakuma, K Abe, M Aoki, et al.
Pageof 24