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Saori Katayama

Showing results (1-10 of 23) with videos related to

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IUBMB Life|December 11, 2019
Two effects of GATA2 enhancer repositioning by 3q chromosomal rearrangementsMikiko Suzuki, Saori Katayama, Masayuki Yamamoto
Cureus|June 23, 2025
Epileptic Encephalopathy After Human Herpes Virus 6-Related Post-Transplant Acute Limbic Encephalitis in Children: A Case Report and Review of the LiteratureYusuke Goto, Yusuke Takezawa, Saori Katayama, et al.
Blood Advances|April 25, 2020
EVI1 and GATA2 misexpression induced by inv(3)(q21q26) contribute to megakaryocyte-lineage skewing and leukemogenesisAyaka Yamaoka, Mikiko Suzuki, Saori Katayama, et al.
Journal of Pediatric Hematology/Oncology|September 26, 2022
Stage M Infantile Neuroblastoma With Involvement of Falx Cerebri: Case Report and Literature ReviewMiyu Sai, Kunihiko Moriya, Akira Kaino, et al.
Journal of Child Neurology|March 1, 2013
Lower back pain as a symptom of migrainous corpalgiaYosuke Kakisaka, Tomoichiro Ohara, Saori Katayama, et al.
The Tohoku Journal of Experimental Medicine|November 10, 2012
Human herpes virus type 6 can cause skin lesions at the BCG inoculation site similar to Kawasaki DiseaseYosuke Kakisaka, Tomoichiro Ohara, Saori Katayama, et al.
International Journal of Hematology|August 23, 2021
Refractory T-cell/histiocyte-rich large B-cell lymphoma in a patient with ataxia-telangiectasia caused by novel compound heterozygous variants in ATMDaichi Sato, Kunihiko Moriya, Tomohiro Nakano, et al.
The Tohoku Journal of Experimental Medicine|September 26, 2012
Panax ginseng: a newly identified cause of gynecomastiaYosuke Kakisaka, Tomoichiro Ohara, Hideo Tozawa, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|October 23, 2014
Mesenchymal chondrosarcoma diagnosed on FISH for HEY1-NCOA2 fusion geneKunihiko Moriya, Saori Katayama, Masaei Onuma, et al.
Pediatric Hematology and Oncology|September 25, 2024
Comprehensive genetic analysis for identification of monogenic disorders and selection of appropriate treatments in pediatric patients with persistent thrombocytopeniaDaichi Sato, Hinako Kirikae, Tomohiro Nakano, et al.
Pageof 3

Showing results (1-10 of 23) with videos related to

Sort By:
Pageof 3
IUBMB Life|December 11, 2019
Two effects of GATA2 enhancer repositioning by 3q chromosomal rearrangementsMikiko Suzuki, Saori Katayama, Masayuki Yamamoto
Cureus|June 23, 2025
Epileptic Encephalopathy After Human Herpes Virus 6-Related Post-Transplant Acute Limbic Encephalitis in Children: A Case Report and Review of the LiteratureYusuke Goto, Yusuke Takezawa, Saori Katayama, et al.
Blood Advances|April 25, 2020
EVI1 and GATA2 misexpression induced by inv(3)(q21q26) contribute to megakaryocyte-lineage skewing and leukemogenesisAyaka Yamaoka, Mikiko Suzuki, Saori Katayama, et al.
Journal of Pediatric Hematology/Oncology|September 26, 2022
Stage M Infantile Neuroblastoma With Involvement of Falx Cerebri: Case Report and Literature ReviewMiyu Sai, Kunihiko Moriya, Akira Kaino, et al.
Journal of Child Neurology|March 1, 2013
Lower back pain as a symptom of migrainous corpalgiaYosuke Kakisaka, Tomoichiro Ohara, Saori Katayama, et al.
The Tohoku Journal of Experimental Medicine|November 10, 2012
Human herpes virus type 6 can cause skin lesions at the BCG inoculation site similar to Kawasaki DiseaseYosuke Kakisaka, Tomoichiro Ohara, Saori Katayama, et al.
International Journal of Hematology|August 23, 2021
Refractory T-cell/histiocyte-rich large B-cell lymphoma in a patient with ataxia-telangiectasia caused by novel compound heterozygous variants in ATMDaichi Sato, Kunihiko Moriya, Tomohiro Nakano, et al.
The Tohoku Journal of Experimental Medicine|September 26, 2012
Panax ginseng: a newly identified cause of gynecomastiaYosuke Kakisaka, Tomoichiro Ohara, Hideo Tozawa, et al.
Pediatrics International : Official Journal of the Japan Pediatric Society|October 23, 2014
Mesenchymal chondrosarcoma diagnosed on FISH for HEY1-NCOA2 fusion geneKunihiko Moriya, Saori Katayama, Masaei Onuma, et al.
Pediatric Hematology and Oncology|September 25, 2024
Comprehensive genetic analysis for identification of monogenic disorders and selection of appropriate treatments in pediatric patients with persistent thrombocytopeniaDaichi Sato, Hinako Kirikae, Tomohiro Nakano, et al.
Pageof 3