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Kenichi Sakamoto

Showing results (51-60 of 102) with videos related to

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Brain & Development|May 9, 2021
Mucolipidosis Ⅱ and III with neurological symptoms due to spinal cord compressionSachiko Nakaoka, Hidehito Kondo, Keiko Matsuoka, et al.
International Journal of Hematology|January 19, 2026
Hearing loss in Langerhans cell histiocytosis: close association with central nervous system consequencesAkira Kaino, Kenichi Sakamoto, Kunihiko Moriya, et al.
Veterinary Microbiology|January 24, 2017
Genome variability of foot-and-mouth disease virus during the short period of the 2010 epidemic in JapanTatsuya Nishi, Manabu Yamada, Katsuhiko Fukai, et al.
International Journal of Hematology|July 14, 2020
Functional analysis of a novel fusion protein PAX5-KIDINS220 identified in a pediatric Ph-like ALL patientTakuyo Kanayama, Toshihiko Imamura, Azusa Mayumi, et al.
The Journal of Veterinary Medical Science|October 25, 2016
Experimental infections using the foot-and-mouth disease virus O/JPN/2010 in animals administered a vaccine preserved for emergency use in JapanKatsuhiko Fukai, Tatsuya Nishi, Nobuaki Shimada, et al.
International Journal of Hematology|May 6, 2022
A retrospective survey of patients who discontinued participation in the JPLSG HLH-2004 clinical trialRintaro Ono, Kenichi Sakamoto, Takehiko Doi, et al.
Aging|July 25, 2017
Werner syndrome: a model for sarcopenia due to accelerated agingMasaya Yamaga, Minoru Takemoto, Mayumi Shoji, et al.
International Journal of Hematology|August 22, 2016
Development of acute lymphoblastic leukemia with IgH-EPOR in a patient with secondary erythrocytosisKenichi Sakamoto, Seiji Tanaka, Chihiro Tomoyasu, et al.
Journal of the American Geriatrics Society|April 11, 2017
Recent Trends in WRN Gene Mutation Patterns in Individuals with Werner SyndromeMasaya Yamaga, Minoru Takemoto, Aki Takada-Watanabe, et al.
Journal of Pediatric Hematology/Oncology|September 28, 2013
Acute lymphoblastic leukemia developing in a patient with Noonan syndrome harboring a PTPN11 germline mutationKenichi Sakamoto, Toshihiko Imamura, Daisuke Asai, et al.
Pageof 11

Showing results (51-60 of 102) with videos related to

Sort By:
Pageof 11
Brain & Development|May 9, 2021
Mucolipidosis Ⅱ and III with neurological symptoms due to spinal cord compressionSachiko Nakaoka, Hidehito Kondo, Keiko Matsuoka, et al.
International Journal of Hematology|January 19, 2026
Hearing loss in Langerhans cell histiocytosis: close association with central nervous system consequencesAkira Kaino, Kenichi Sakamoto, Kunihiko Moriya, et al.
Veterinary Microbiology|January 24, 2017
Genome variability of foot-and-mouth disease virus during the short period of the 2010 epidemic in JapanTatsuya Nishi, Manabu Yamada, Katsuhiko Fukai, et al.
International Journal of Hematology|July 14, 2020
Functional analysis of a novel fusion protein PAX5-KIDINS220 identified in a pediatric Ph-like ALL patientTakuyo Kanayama, Toshihiko Imamura, Azusa Mayumi, et al.
The Journal of Veterinary Medical Science|October 25, 2016
Experimental infections using the foot-and-mouth disease virus O/JPN/2010 in animals administered a vaccine preserved for emergency use in JapanKatsuhiko Fukai, Tatsuya Nishi, Nobuaki Shimada, et al.
International Journal of Hematology|May 6, 2022
A retrospective survey of patients who discontinued participation in the JPLSG HLH-2004 clinical trialRintaro Ono, Kenichi Sakamoto, Takehiko Doi, et al.
Aging|July 25, 2017
Werner syndrome: a model for sarcopenia due to accelerated agingMasaya Yamaga, Minoru Takemoto, Mayumi Shoji, et al.
International Journal of Hematology|August 22, 2016
Development of acute lymphoblastic leukemia with IgH-EPOR in a patient with secondary erythrocytosisKenichi Sakamoto, Seiji Tanaka, Chihiro Tomoyasu, et al.
Journal of the American Geriatrics Society|April 11, 2017
Recent Trends in WRN Gene Mutation Patterns in Individuals with Werner SyndromeMasaya Yamaga, Minoru Takemoto, Aki Takada-Watanabe, et al.
Journal of Pediatric Hematology/Oncology|September 28, 2013
Acute lymphoblastic leukemia developing in a patient with Noonan syndrome harboring a PTPN11 germline mutationKenichi Sakamoto, Toshihiko Imamura, Daisuke Asai, et al.
Pageof 11