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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 syndrome
Mitsuru 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 mellitus
Taro 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 cancer
Masato 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 malignancies
Yuyan Chen, Junko Takita, Mitsuteru Hiwatari, et al.
Pancreas
|
September 8, 2018
Distinct Inflammatory Changes of the Pancreas of Slowly Progressive Insulin-dependent (Type 1) Diabetes
Kaoru 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 anemia
Hideki 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 report
Yousuke 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 immunodeficiency
Taizo 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 syndrome
Kaoru Okazaki, Jun Unemoto, Masatoshi Kondo, et al.
Page
of 36
Search research articles
Search
Showing results (201-210 of 360) with videos related to
Sort By:
Page
of 36
Pediatrics International : Official Journal of the Japan Pediatric Society
|
October 21, 2010
Prominent eosinophilia but less eosinophil activation in a patient with Omenn syndrome
Mitsuru 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 mellitus
Taro 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 cancer
Masato 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 malignancies
Yuyan Chen, Junko Takita, Mitsuteru Hiwatari, et al.
Pancreas
|
September 8, 2018
Distinct Inflammatory Changes of the Pancreas of Slowly Progressive Insulin-dependent (Type 1) Diabetes
Kaoru 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 anemia
Hideki 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 report
Yousuke 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 immunodeficiency
Taizo 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 syndrome
Kaoru Okazaki, Jun Unemoto, Masatoshi Kondo, et al.
Page
of 36