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List of works by Akira Shimada

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

scientific article published on 21 March 2014

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

scientific article published on 01 September 2007

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

scientific article published on 14 May 2011

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

scientific article published on 25 February 2016

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

scientific article

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

scientific article

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

scientific article

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

scientific article published on 26 September 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)

scientific article published on 04 September 2020

Autoimmune-like hepatitis following unrelated BMT successfully treated with rituximab

scientific article published on 13 June 2011

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

scientific article published on 11 May 2011

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

scientific article published on March 9, 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

scientific article published on 15 February 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

scientific article published on 21 May 2018

Correlation of CYP2C19 phenotype with voriconazole plasma concentration in children.

scientific article published in July 2013

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

scientific article published in March 2013

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

scientific article published on 8 October 2011

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

scientific article

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.

scientific article

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

scientific article published on April 1, 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.

scientific article published on 11 July 2014

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

scientific article

Everolimus for Treatment of Pseudomyogenic Hemangioendothelioma.

scientific article published on 24 January 2017

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

scientific article published on 22 April 2012

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

scientific article published on 14 January 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.

scientific article published on 3 August 2017

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

scientific article published on 03 April 2017

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

scientific article published on 18 January 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.

scientific article

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

scientific article published on 18 December 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.

scientific article

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.

scientific article

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

scientific article published on 27 June 2013

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

scientific article published on 15 September 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

scientific article published on 18 May 2006

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

scientific article published on 21 May 2016

Japanese family with congenital factor VII deficiency

scientific article published on 26 August 2015

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

scientific article published on January 2014

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

scientific article published on 07 August 2019

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

scientific article published on 30 August 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

scientific article published on 01 January 2018

Multiplex fusion gene testing in pediatric acute myeloid leukemia.

scientific article

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

scientific article published on 12 June 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

scientific article published on 01 January 2008

Mutations profile of polycythemia vera and essential thrombocythemia among Japanese children.

scientific article

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

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

scientific article published on 22 February 2007

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

scientific article published on 21 April 2005

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

scientific article published on June 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

scientific article

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

scientific article

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.

scientific article published on 24 February 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.

scientific article published on 15 November 2016

Persistent clonal chromosomal abnormalities in a chronic myeloid leukemia patient

scientific article published on 05 November 2015

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

scientific article published on 16 February 2018

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

scientific article published on 20 October 2015

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

scientific article published on 19 October 2006

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

scientific article published on 7 January 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.

scientific article

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

scientific article

Proinflammatory cytokinemia associated with transient myeloproliferative disorder in down syndrome

scientific article published on 10 December 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

scientific article published on 15 April 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 ⬇️

scientific article published on March 10, 2012

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

scientific article published on 28 December 2013

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

scientific article published on 22 December 2010

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

scientific article published on 27 July 2016

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

scientific article

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

scientific article published on 12 January 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.

scientific article

Somatic mosaicism for oncogenic NRAS mutations in juvenile myelomonocytic leukemia

scientific article published on 02 July 2012

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

scientific article published on 21 November 2017

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

scientific article published on 01 March 2007

Successful clinical response to irinotecan in relapsed neuroblastoma.

scientific article published in February 2003

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

scientific article published on August 1, 1997

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

scientific article published on 25 March 2015

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

scientific article published on 24 April 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

scientific article published on 26 December 2019

Transient myeloproliferative disorder with partial trisomy 21.

scientific article published in July 2015

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

scientific article

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.

scientific article published on 29 July 2016

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