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Akira Shimada

Showing results (201-210 of 360) with videos related to

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Pediatrics International : Official Journal of the Japan Pediatric Society|October 21, 2010
Prominent eosinophilia but less eosinophil activation in a patient with Omenn syndromeMitsuru Seki, Hirokazu Kimura, Akio Mori, et al.
The Journal of Clinical Endocrinology and Metabolism|April 10, 2008
Insulin intervention in slowly progressive insulin-dependent (type 1) diabetes mellitusTaro Maruyama, Shoichiro Tanaka, Akira Shimada, et al.
Journal of Human Genetics|March 8, 2003
Evaluation of the diagnostic accuracy of the stop codon (SC) assay for identifying protein-truncating mutations in the BRCA1and BRCA2genes in familial breast cancerMasato Sakayori, Masanori Kawahara, Kazuko Shiraishi, et al.
International Journal of Hematology|December 31, 2013
RUNX1 mutation associated with clonal evolution in relapsed pediatric acute myeloid leukemia with t(16;21)(p11;q22)Olfat Ismael, Akira Shimada, Shaimaa Elmahdi, et al.
Genes, Chromosomes & Cancer|March 7, 2006
Mutations of the PTPN11 and RAS genes in rhabdomyosarcoma and pediatric hematological malignanciesYuyan Chen, Junko Takita, Mitsuteru Hiwatari, et al.
Pancreas|September 8, 2018
Distinct Inflammatory Changes of the Pancreas of Slowly Progressive Insulin-dependent (Type 1) DiabetesKaoru Aida, Tomoyasu Fukui, Erika Jimbo, et al.
International Journal of Hematology|May 12, 2011
CD20-negative Epstein-Barr virus-associated post-transplant lymphoproliferative disease refractory to rituximab in a patient with severe aplastic anemiaHideki Muramatsu, Yoshiyuki Takahashi, Yoshie Shimoyama, et al.
BMC Cancer|November 23, 2017
Sorafenib treatment for papillary thyroid carcinoma with diffuse lung metastases in a child with autism spectrum disorder: a case reportYousuke Higuchi, Takayuki Motoki, Hisashi Ishida, et al.
Blood|April 23, 2005
Oligoclonal expansion of T lymphocytes with multiple second-site mutations leads to Omenn syndrome in a patient with RAG1-deficient severe combined immunodeficiencyTaizo Wada, Tomoko Toma, Hiroyuki Okamoto, et al.
Leukemia Research|April 27, 2010
Sustained cytokinemia and chemokinemia concomitant with juvenile myelomonocytic leukemia in an infant with Noonan syndromeKaoru Okazaki, Jun Unemoto, Masatoshi Kondo, et al.
Pageof 36

Showing results (201-210 of 360) with videos related to

Sort By:
Pageof 36
Pediatrics International : Official Journal of the Japan Pediatric Society|October 21, 2010
Prominent eosinophilia but less eosinophil activation in a patient with Omenn syndromeMitsuru Seki, Hirokazu Kimura, Akio Mori, et al.
The Journal of Clinical Endocrinology and Metabolism|April 10, 2008
Insulin intervention in slowly progressive insulin-dependent (type 1) diabetes mellitusTaro Maruyama, Shoichiro Tanaka, Akira Shimada, et al.
Journal of Human Genetics|March 8, 2003
Evaluation of the diagnostic accuracy of the stop codon (SC) assay for identifying protein-truncating mutations in the BRCA1and BRCA2genes in familial breast cancerMasato Sakayori, Masanori Kawahara, Kazuko Shiraishi, et al.
International Journal of Hematology|December 31, 2013
RUNX1 mutation associated with clonal evolution in relapsed pediatric acute myeloid leukemia with t(16;21)(p11;q22)Olfat Ismael, Akira Shimada, Shaimaa Elmahdi, et al.
Genes, Chromosomes & Cancer|March 7, 2006
Mutations of the PTPN11 and RAS genes in rhabdomyosarcoma and pediatric hematological malignanciesYuyan Chen, Junko Takita, Mitsuteru Hiwatari, et al.
Pancreas|September 8, 2018
Distinct Inflammatory Changes of the Pancreas of Slowly Progressive Insulin-dependent (Type 1) DiabetesKaoru Aida, Tomoyasu Fukui, Erika Jimbo, et al.
International Journal of Hematology|May 12, 2011
CD20-negative Epstein-Barr virus-associated post-transplant lymphoproliferative disease refractory to rituximab in a patient with severe aplastic anemiaHideki Muramatsu, Yoshiyuki Takahashi, Yoshie Shimoyama, et al.
BMC Cancer|November 23, 2017
Sorafenib treatment for papillary thyroid carcinoma with diffuse lung metastases in a child with autism spectrum disorder: a case reportYousuke Higuchi, Takayuki Motoki, Hisashi Ishida, et al.
Blood|April 23, 2005
Oligoclonal expansion of T lymphocytes with multiple second-site mutations leads to Omenn syndrome in a patient with RAG1-deficient severe combined immunodeficiencyTaizo Wada, Tomoko Toma, Hiroyuki Okamoto, et al.
Leukemia Research|April 27, 2010
Sustained cytokinemia and chemokinemia concomitant with juvenile myelomonocytic leukemia in an infant with Noonan syndromeKaoru Okazaki, Jun Unemoto, Masatoshi Kondo, et al.
Pageof 36