Lista de obras - Akira Shimada - Dominio Público Uruguay

ABL kinase mutation and relapse in 4 pediatric Philadelphia chromosome-positive acute lymphoblastic leukemia cases

artículo científico publicado en 2014

AML1 mutation and FLT3-internal tandem duplication in leukemia transformed from myelodysplastic syndrome

artículo científico publicado en 2007

Aberrant phosphorylation of STAT5 by granulocyte-macrophage colony-stimulating factor in infant cytomegalovirus infection mimicking juvenile myelomonocytic leukemia

artículo científico publicado en 2011

Adults with germline CBL mutation complicated with juvenile myelomonocytic leukemia at infancy

artículo científico publicado en 2016

Advanced-stage gastrointestinal stromal tumor treated with imatinib in a 12-year-old girl with a unique mutation of PDGFRA.

artículo científico publicado en 2005

Adverse prognostic impact of KIT mutations in childhood CBF-AML: the results of the Japanese Pediatric Leukemia/Lymphoma Study Group AML-05 trial.

artículo científico publicado en 2015

Age-associated difference in gene expression of paediatric acute myelomonocytic lineage leukaemia (FAB M4 and M5 subtypes) and its correlation with prognosis.

artículo científico publicado en 2008

Appropriate dose reduction in induction therapy is essential for the treatment of infants with acute myeloid leukemia: a report from the Japanese Pediatric Leukemia/Lymphoma Study Group

artículo científico publicado en 2013

Attempts to optimize postinduction treatment in childhood acute myeloid leukemia without core-binding factors: A report from the Japanese Pediatric Leukemia/Lymphoma Study Group (JPLSG)

artículo científico publicado en 2020

Autoimmune-like hepatitis following unrelated BMT successfully treated with rituximab

artículo científico publicado en 2011

CD20-negative Epstein-Barr virus-associated post-transplant lymphoproliferative disease refractory to rituximab in a patient with severe aplastic anemia.

artículo científico publicado en 2011

Childhood acute myeloid leukemia with bone marrow eosinophilia caused by t(16;21)(q24;q22) ⬇️

artículo científico publicado el 9 de marzo de 2012

Childhood cancer survivors: Anxieties felt after treatment and the need for continued support

scientific article published on 01 November 2017

Congenital Glioblastoma with Distinct Clinical and Molecular Characteristics: Case Reports and a Literature Review

artículo científico publicado en 2017

Congenital pancreatoblastoma associated with β-catenin mutation

scientific article published on 23 September 2011

Copy number abnormality of acute lymphoblastic leukemia cell lines based on their genetic subtypes

artículo científico publicado en 2018

Correlation of CYP2C19 phenotype with voriconazole plasma concentration in children.

artículo científico publicado en 2013

Cytomegalovirus retinitis during maintenance therapy for T-cell acute lymphoblastic leukemia.

artículo científico publicado en 2013

DNMT3A mutations are rare in childhood acute myeloid leukaemia, myelodysplastic syndromes and juvenile myelomonocytic leukaemia.

artículo científico publicado en 2011

De novo childhood myelodysplastic/myeloproliferative disease with unique molecular characteristics.

artículo científico publicado en 2012

Desmoid-type fibromatosis in a boy with Down syndrome

scientific article published on 18 April 2017

Detection of ATM gene mutation in human glioma cell line M059J by a rapid frameshift/stop codon assay in yeast.

artículo científico publicado en 2002

Detection ofAPC mutations by a yeast-based protein truncation test (YPTT) ⬇️

artículo científico publicado el 1 de abril de 1998

Down syndrome and GATA1 mutations in transient abnormal myeloproliferative disorder: mutation classes correlate with progression to myeloid leukemia

scientific article published on 20 August 2010

EVI1 overexpression is a poor prognostic factor in pediatric patients with mixed lineage leukemia-AF9 rearranged acute myeloid leukemia.

artículo científico publicado en 2014

Enhanced AKT Phosphorylation of Circulating B Cells in Patients With Activated PI3Kδ Syndrome

artículo científico publicado en 2018

Everolimus for Treatment of Pseudomyogenic Hemangioendothelioma.

artículo científico publicado en 2017

Excellent outcome of allogeneic bone marrow transplantation for Fanconi anemia using fludarabine-based reduced-intensity conditioning regimen.

artículo científico publicado en 2012

Excellent outcomes of children with CML treated with imatinib mesylate compared to that in pre-imatinib era.

artículo científico publicado en 2011

Excess treatment reduction including anthracyclines results in higher incidence of relapse in core binding factor acute myeloid leukemia in children

scientific article published on 16 May 2013

FLT3-internal tandem duplication in a pediatric patient with t(8;21) acute myeloid leukemia

scientific article published on 01 December 2010

Fludarabine, cytarabine, granulocyte colony-stimulating factor and idarubicin for relapsed childhood acute myeloid leukemia.

artículo científico publicado en 2017

Gene expression analysis of hypersensitivity to mosquito bite, chronic active EBV infection and NK/T-lymphoma/leukemia.

artículo científico

Germline IKAROS mutation associated with primary immunodeficiency that progressed to T-cell acute lymphoblastic leukemia

artículo científico publicado en 2017

Hemophagocytic lymphohistiocytosis associated with uncontrolled inflammatory cytokinemia and chemokinemia was caused by systemic anaplastic large cell lymphoma: a case report and review of the literature.

artículo científico publicado en 2008

High PRDM16 expression identifies a prognostic subgroup of pediatric acute myeloid leukaemia correlated to FLT3-ITD, KMT2A-PTD, and NUP98-NSD1: the results of the Japanese Paediatric Leukaemia/Lymphoma Study Group AML-05 trial

artículo científico publicado en 2015

High WT1 mRNA expression after induction chemotherapy and FLT3-ITD have prognostic impact in pediatric acute myeloid leukemia: a study of the Japanese Childhood AML Cooperative Study Group.

artículo científico publicado en 2012

High event-free survival rate with minimum-dose-anthracycline treatment in childhood acute promyelocytic leukaemia: a nationwide prospective study by the Japanese Paediatric Leukaemia/Lymphoma Study Group.

artículo científico publicado en 2016

IKZF1 and CRLF2 gene alterations correlate with poor prognosis in Japanese BCR-ABL1-negative high-risk B-cell precursor acute lymphoblastic leukemia.

artículo científico publicado en 2013

Incidence, clinical features, and risk factors of idiopathic pneumonia syndrome following hematopoietic stem cell transplantation in children.

artículo científico publicado en 2011

Irinotecan for children with relapsed solid tumors

scientific article published on 01 March 2006

JAK2 mutation in a boy with polycythemia vera, but not in other pediatric hematologic Disorders

artículo científico publicado en 2006

JAK2, MPL, and CALR mutations in children with essential thrombocythemia

artículo científico publicado en 2016

Japanese family with congenital factor VII deficiency

artículo científico publicado en 2015

Long-term parvovirus B19 infections with genetic drift after cord blood transplantation complicated by persistent CD4+ lymphocytopenia.

artículo científico publicado en 2014

Lupus anticoagulant-hypoprothrombinemia syndrome and immunoglobulin-A vasculitis: a report of Japanese sibling cases and review of the literature

artículo científico publicado en 2019

MSH2 deletion with CREBBP and KRAS mutations in pediatric high-hyperdiploid acute lymphoblastic leukemia

artículo científico publicado en 2017

Molecular lesions in childhood and adult acute megakaryoblastic leukaemia

scientific article published on 28 November 2011

Monitoring of fusion gene transcripts to predict relapse in pediatric acute myeloid leukemia

artículo científico publicado en 2018

Multiplex fusion gene testing in pediatric acute myeloid leukemia

artículo científico publicado en 2018

Mutation in the THPO gene is not associated with aplastic anaemia in Japanese children

artículo científico publicado en 2012

Mutations of GATA1, FLT3, MLL-partial tandem duplication, NRAS, and RUNX1 genes are not found in a 7-year-old Down syndrome patient with acute myeloid leukemia (FAB-M2) having a good prognosis

artículo científico publicado en 2008

Mutations profile of polycythemia vera and essential thrombocythemia among Japanese children

artículo científico publicado en 2011

N822 mutation of KIT gene was frequent in pediatric acute myeloid leukemia patients with t(8;21) in Japan: a study of the Japanese childhood AML cooperative study group

scientific article published on 24 May 2007

NUP98‐NSD1 gene fusion and its related gene expression signature are strongly associated with a poor prognosis in pediatric acute myeloid leukemia ⬇️

artículo científico publicado el 30 de abril de 2013

No nucleophosmin mutations in pediatric acute myeloid leukemia with normal karyotype: a study of the Japanese Childhood AML Cooperative Study Group

artículo científico publicado en 2007

Oligoclonal expansion of T lymphocytes with multiple second-site mutations leads to Omenn syndrome in a patient with RAG1-deficient severe combined immunodeficiency

artículo científico publicado en 2005

Omenn syndrome--review of several phenotypes of Omenn syndrome and RAG1/RAG2 mutations in Japan.

artículo científico publicado en 2006

Outcome in 146 patients with paediatric acute myeloid leukaemia treated according to the AML99 protocol in the period 2003-06 from the Japan Association of Childhood Leukaemia Study

scientific article published on 28 August 2012

Outcome of adolescent patients with acute myeloid leukemia treated with pediatric protocols

artículo científico publicado en 2015

Outcome of children with relapsed acute myeloid leukemia following initial therapy under the AML99 protocol.

artículo científico publicado en 2014

Outcome of relapsed core binding factor acute myeloid leukemia in children: A result from the Japanese Pediatric Leukemia/Lymphoma Study Group (JPLSG) AML-05R study.

artículo científico publicado en 2017

Panel-based next-generation sequencing identifies prognostic and actionable genes in childhood acute lymphoblastic leukemia and is suitable for clinical sequencing

scientific article published on 17 November 2018

Pediatric intestinal Behçet disease complicated by myeloid malignancies.

artículo científico publicado en 2016

Persistent clonal chromosomal abnormalities in a chronic myeloid leukemia patient

artículo científico publicado en 2015

Pharmacological inhibition of JAK3 enhances the antitumor activity of imatinib in human chronic myeloid leukemia

artículo científico publicado en 2018

Preserved High Probability of Overall Survival with Significant Reduction of Chemotherapy for Myeloid Leukemia in Down Syndrome: A Nationwide Prospective Study in Japan.

artículo científico publicado en 2015

Pro-inflammatory cytokinemia is frequently found in Down syndrome patients with hematological disorders.

artículo científico publicado en 2006

Prognostic impact of specific molecular profiles in pediatric acute megakaryoblastic leukemia in non-Down syndrome

artículo científico publicado en 2017

Prognostic significance of the BAALC isoform pattern and CEBPA mutations in pediatric acute myeloid leukemia with normal karyotype: a study by the Japanese Childhood AML Cooperative Study Group.

artículo científico publicado en 2010

Prognostic value of genetic mutations in adolescent and young adults with acute myeloid leukemia

artículo científico publicado en 2017

Proinflammatory cytokinemia associated with transient myeloproliferative disorder in down syndrome

artículo científico publicado en 2003

Prominent eosinophilia but less eosinophil activation in a patient with Omenn syndrome

scientific article published on 01 August 2010

Pulmonary metastases after nephrectomy only for small, stage I/favorable-histology Wilms' tumor

artículo científico publicado en 2005

RAS mutations are frequent in FAB type M4 and M5 of acute myeloid leukemia, and related to late relapse: a study of the Japanese Childhood AML Cooperative Study Group ⬇️

artículo científico publicado el 10 de marzo de 2012

RUNX1 mutation associated with clonal evolution in relapsed pediatric acute myeloid leukemia with t(16;21)(p11;q22).

artículo científico publicado en 2013

Reduced-intensity conditioning for alternative donor hematopoietic stem cell transplantation in patients with dyskeratosis congenita

artículo científico publicado en 2010

Relapsed childhood acute myeloid leukemia patient with inversion of chromosome 16 harboring a low FLT3 internal tandem duplication allelic burden and KIT mutations

artículo científico publicado en 2016

Relapsed infant MLL-rearranged acute lymphoblastic leukemia with additional genetic alterations.

artículo científico publicado en 2016

Risk-stratified therapy for children with FLT3-ITD-positive acute myeloid leukemia: results from the JPLSG AML-05 study.

artículo científico publicado en 2018

Selective laser trabeculoplasty for steroid glaucoma in a child with leukemia

scientific article published on 07 February 2019

Simultaneous detection of ABL1 mutation and IKZF1 deletion in Philadelphia chromosome-positive acute lymphoblastic leukemia using a customized target enrichment system panel.

artículo científico publicado en 2018

Somatic mosaicism for oncogenic NRAS mutations in juvenile myelomonocytic leukemia

artículo científico publicado en 2012

Sorafenib treatment for papillary thyroid carcinoma with diffuse lung metastases in a child with autism spectrum disorder: a case report.

artículo científico publicado en 2017

Spontaneous improvement of hematologic abnormalities in patients having juvenile myelomonocytic leukemia with specific RAS mutations

artículo científico publicado en 2007

Successful clinical response to irinotecan in relapsed neuroblastoma.

artículo científico publicado en 2003

Suspected acute encephalopathy with symmetrical abnormal signal areas in the basal ganglia, thalamus, midbrain and pons diagnosed by magnetic resonance imaging ⬇️

artículo científico publicado el 1 de agosto de 1997

Suspected early onset of congenital Langerhans cell histiocytosis involving ectopic cervical thymus and mediastinal thymus, simultaneously.

artículo científico publicado en 2015

Sustained cytokinemia and chemokinemia concomitant with juvenile myelomonocytic leukemia in an infant with Noonan syndrome

artículo científico publicado en 2010

Tandem duplications of MLL and FLT3 are correlated with poor prognoses in pediatric acute myeloid leukemia: a study of the Japanese childhood AML Cooperative Study Group

scientific article published on 01 February 2008

The effect of graft-versus-host disease on outcomes after allogeneic stem cell transplantation for refractory lymphoblastic lymphoma in children and young adults

artículo científico publicado en 2019

Transient myeloproliferative disorder with partial trisomy 21.

artículo científico publicado en 2015

Verification of risk scores to predict i.v. immunoglobulin resistance in incomplete Kawasaki disease

artículo científico publicado en 2015

Wernicke's encephalopathy in a child with autism during chemotherapy for T-cell acute leukemia

scientific article published on 01 August 2018

Whole-exome sequencing reveals the spectrum of gene mutations and the clonal evolution patterns in paediatric acute myeloid leukaemia.

artículo científico publicado en 2016

Lista de obras de Akira Shimada

ABL kinase mutation and relapse in 4 pediatric Philadelphia chromosome-positive acute lymphoblastic leukemia cases

AML1 mutation and FLT3-internal tandem duplication in leukemia transformed from myelodysplastic syndrome

Aberrant phosphorylation of STAT5 by granulocyte-macrophage colony-stimulating factor in infant cytomegalovirus infection mimicking juvenile myelomonocytic leukemia

Adults with germline CBL mutation complicated with juvenile myelomonocytic leukemia at infancy

Advanced-stage gastrointestinal stromal tumor treated with imatinib in a 12-year-old girl with a unique mutation of PDGFRA.

Adverse prognostic impact of KIT mutations in childhood CBF-AML: the results of the Japanese Pediatric Leukemia/Lymphoma Study Group AML-05 trial.

Age-associated difference in gene expression of paediatric acute myelomonocytic lineage leukaemia (FAB M4 and M5 subtypes) and its correlation with prognosis.

Appropriate dose reduction in induction therapy is essential for the treatment of infants with acute myeloid leukemia: a report from the Japanese Pediatric Leukemia/Lymphoma Study Group

Attempts to optimize postinduction treatment in childhood acute myeloid leukemia without core-binding factors: A report from the Japanese Pediatric Leukemia/Lymphoma Study Group (JPLSG)

Autoimmune-like hepatitis following unrelated BMT successfully treated with rituximab

CD20-negative Epstein-Barr virus-associated post-transplant lymphoproliferative disease refractory to rituximab in a patient with severe aplastic anemia.

Childhood acute myeloid leukemia with bone marrow eosinophilia caused by t(16;21)(q24;q22) ⬇️

Childhood cancer survivors: Anxieties felt after treatment and the need for continued support

Congenital Glioblastoma with Distinct Clinical and Molecular Characteristics: Case Reports and a Literature Review

Congenital pancreatoblastoma associated with β-catenin mutation

Copy number abnormality of acute lymphoblastic leukemia cell lines based on their genetic subtypes

Correlation of CYP2C19 phenotype with voriconazole plasma concentration in children.

Cytomegalovirus retinitis during maintenance therapy for T-cell acute lymphoblastic leukemia.

DNMT3A mutations are rare in childhood acute myeloid leukaemia, myelodysplastic syndromes and juvenile myelomonocytic leukaemia.

De novo childhood myelodysplastic/myeloproliferative disease with unique molecular characteristics.

Desmoid-type fibromatosis in a boy with Down syndrome

Detection of ATM gene mutation in human glioma cell line M059J by a rapid frameshift/stop codon assay in yeast.

Detection ofAPC mutations by a yeast-based protein truncation test (YPTT) ⬇️

Down syndrome and GATA1 mutations in transient abnormal myeloproliferative disorder: mutation classes correlate with progression to myeloid leukemia

EVI1 overexpression is a poor prognostic factor in pediatric patients with mixed lineage leukemia-AF9 rearranged acute myeloid leukemia.

Enhanced AKT Phosphorylation of Circulating B Cells in Patients With Activated PI3Kδ Syndrome

Everolimus for Treatment of Pseudomyogenic Hemangioendothelioma.

Excellent outcome of allogeneic bone marrow transplantation for Fanconi anemia using fludarabine-based reduced-intensity conditioning regimen.

Excellent outcomes of children with CML treated with imatinib mesylate compared to that in pre-imatinib era.

Excess treatment reduction including anthracyclines results in higher incidence of relapse in core binding factor acute myeloid leukemia in children

FLT3-internal tandem duplication in a pediatric patient with t(8;21) acute myeloid leukemia

Fludarabine, cytarabine, granulocyte colony-stimulating factor and idarubicin for relapsed childhood acute myeloid leukemia.

Gene expression analysis of hypersensitivity to mosquito bite, chronic active EBV infection and NK/T-lymphoma/leukemia.

Germline IKAROS mutation associated with primary immunodeficiency that progressed to T-cell acute lymphoblastic leukemia

Hemophagocytic lymphohistiocytosis associated with uncontrolled inflammatory cytokinemia and chemokinemia was caused by systemic anaplastic large cell lymphoma: a case report and review of the literature.

High PRDM16 expression identifies a prognostic subgroup of pediatric acute myeloid leukaemia correlated to FLT3-ITD, KMT2A-PTD, and NUP98-NSD1: the results of the Japanese Paediatric Leukaemia/Lymphoma Study Group AML-05 trial

High WT1 mRNA expression after induction chemotherapy and FLT3-ITD have prognostic impact in pediatric acute myeloid leukemia: a study of the Japanese Childhood AML Cooperative Study Group.

High event-free survival rate with minimum-dose-anthracycline treatment in childhood acute promyelocytic leukaemia: a nationwide prospective study by the Japanese Paediatric Leukaemia/Lymphoma Study Group.

IKZF1 and CRLF2 gene alterations correlate with poor prognosis in Japanese BCR-ABL1-negative high-risk B-cell precursor acute lymphoblastic leukemia.

Incidence, clinical features, and risk factors of idiopathic pneumonia syndrome following hematopoietic stem cell transplantation in children.

Irinotecan for children with relapsed solid tumors

JAK2 mutation in a boy with polycythemia vera, but not in other pediatric hematologic Disorders

JAK2, MPL, and CALR mutations in children with essential thrombocythemia

Japanese family with congenital factor VII deficiency

Long-term parvovirus B19 infections with genetic drift after cord blood transplantation complicated by persistent CD4+ lymphocytopenia.

Lupus anticoagulant-hypoprothrombinemia syndrome and immunoglobulin-A vasculitis: a report of Japanese sibling cases and review of the literature

MSH2 deletion with CREBBP and KRAS mutations in pediatric high-hyperdiploid acute lymphoblastic leukemia

Molecular lesions in childhood and adult acute megakaryoblastic leukaemia

Monitoring of fusion gene transcripts to predict relapse in pediatric acute myeloid leukemia

Multiplex fusion gene testing in pediatric acute myeloid leukemia

Mutation in the THPO gene is not associated with aplastic anaemia in Japanese children

Mutations of GATA1, FLT3, MLL-partial tandem duplication, NRAS, and RUNX1 genes are not found in a 7-year-old Down syndrome patient with acute myeloid leukemia (FAB-M2) having a good prognosis

Mutations profile of polycythemia vera and essential thrombocythemia among Japanese children

N822 mutation of KIT gene was frequent in pediatric acute myeloid leukemia patients with t(8;21) in Japan: a study of the Japanese childhood AML cooperative study group

NUP98‐NSD1 gene fusion and its related gene expression signature are strongly associated with a poor prognosis in pediatric acute myeloid leukemia ⬇️

No nucleophosmin mutations in pediatric acute myeloid leukemia with normal karyotype: a study of the Japanese Childhood AML Cooperative Study Group

Oligoclonal expansion of T lymphocytes with multiple second-site mutations leads to Omenn syndrome in a patient with RAG1-deficient severe combined immunodeficiency

Omenn syndrome--review of several phenotypes of Omenn syndrome and RAG1/RAG2 mutations in Japan.

Outcome in 146 patients with paediatric acute myeloid leukaemia treated according to the AML99 protocol in the period 2003-06 from the Japan Association of Childhood Leukaemia Study

Outcome of adolescent patients with acute myeloid leukemia treated with pediatric protocols

Outcome of children with relapsed acute myeloid leukemia following initial therapy under the AML99 protocol.

Outcome of relapsed core binding factor acute myeloid leukemia in children: A result from the Japanese Pediatric Leukemia/Lymphoma Study Group (JPLSG) AML-05R study.

Panel-based next-generation sequencing identifies prognostic and actionable genes in childhood acute lymphoblastic leukemia and is suitable for clinical sequencing

Pediatric intestinal Behçet disease complicated by myeloid malignancies.

Persistent clonal chromosomal abnormalities in a chronic myeloid leukemia patient

Pharmacological inhibition of JAK3 enhances the antitumor activity of imatinib in human chronic myeloid leukemia

Preserved High Probability of Overall Survival with Significant Reduction of Chemotherapy for Myeloid Leukemia in Down Syndrome: A Nationwide Prospective Study in Japan.

Pro-inflammatory cytokinemia is frequently found in Down syndrome patients with hematological disorders.

Prognostic impact of specific molecular profiles in pediatric acute megakaryoblastic leukemia in non-Down syndrome

Prognostic significance of the BAALC isoform pattern and CEBPA mutations in pediatric acute myeloid leukemia with normal karyotype: a study by the Japanese Childhood AML Cooperative Study Group.

Prognostic value of genetic mutations in adolescent and young adults with acute myeloid leukemia

Proinflammatory cytokinemia associated with transient myeloproliferative disorder in down syndrome

Prominent eosinophilia but less eosinophil activation in a patient with Omenn syndrome

Pulmonary metastases after nephrectomy only for small, stage I/favorable-histology Wilms' tumor

RAS mutations are frequent in FAB type M4 and M5 of acute myeloid leukemia, and related to late relapse: a study of the Japanese Childhood AML Cooperative Study Group ⬇️

RUNX1 mutation associated with clonal evolution in relapsed pediatric acute myeloid leukemia with t(16;21)(p11;q22).

Reduced-intensity conditioning for alternative donor hematopoietic stem cell transplantation in patients with dyskeratosis congenita

Relapsed childhood acute myeloid leukemia patient with inversion of chromosome 16 harboring a low FLT3 internal tandem duplication allelic burden and KIT mutations

Relapsed infant MLL-rearranged acute lymphoblastic leukemia with additional genetic alterations.