Pediatric myelodysplastic syndrome with inflammatory manifestations: Diagnosis, genetics, treatment, and outcome
暂无分享,去创建一个
S. Izraeli | H. Tamary | I. Geron | O. Dgany | T. Krasnov | Y. Birger | J. Stein | J. Yacobovich | G. Avrahami | Y. Kodman | O. Steinberg-Shemer | A. Krauss | Tamar Feuerstein | O. Gilad | A. Yanir | Jacques Mardoukh | S. Lotan | H. Fishman | Shlomit Barzilai Birenboim
[1] S. Miyano,et al. Clinical significance of RAS pathway alterations in pediatric acute myeloid leukemia , 2021, Haematologica.
[2] S. Izraeli,et al. Incorporation of somatic panels for the detection of haematopoietic transformation in children and young adults with leukaemia predisposition syndromes and with acquired cytopenias , 2020, British journal of haematology.
[3] J. Mullikin,et al. Somatic Mutations in UBA1 and Severe Adult-Onset Autoinflammatory Disease. , 2020, The New England journal of medicine.
[4] H. Kantarjian,et al. The Clinical impact of PTPN11 mutations in adults with acute myeloid leukemia , 2020, Leukemia.
[5] G. Garcia-Manero,et al. Adaptive response to inflammation contributes to sustained myelopoiesis and confers a competitive advantage in myelodysplastic syndrome HSCs , 2020, Nature Immunology.
[6] K. Ono,et al. The acquisition of trisomy 8 associated with Behçet's-like disease in myelodysplastic syndrome , 2020, Leukemia research reports.
[7] Y. Erzin,et al. How to treat myelodysplastic syndrome with clinical features resembling Behçet syndrome: a case-based systematic review , 2020, Annals of Hematology.
[8] F. Rieux-Laucat,et al. After 95 years, it's time to eRASe JMML. , 2020, Blood reviews.
[9] Supat Thongjuea,et al. Heterogeneous disease-propagating stem cells in juvenile myelomonocytic leukemia , 2019, bioRxiv.
[10] A. List,et al. The central role of inflammatory signaling in the pathogenesis of myelodysplastic syndromes. , 2019, Blood.
[11] M. Raaijmakers,et al. The mesenchymal niche in MDS. , 2019, Blood.
[12] A. Shimamura,et al. Genetic predisposition to MDS: clinical features and clonal evolution. , 2019, Blood.
[13] F. Carrat,et al. Gastrointestinal Behcet’s-like disease with myelodysplastic neoplasms with trisomy 8: a French case series and literature review , 2018, Leukemia & lymphoma.
[14] F. Carrat,et al. Inflammatory disorders associated with trisomy 8‐myelodysplastic syndromes: French retrospective case‐control study , 2018, European journal of haematology.
[15] P. Fenaux,et al. Autoimmune manifestations associated with myelodysplastic syndromes , 2018, Annals of Hematology.
[16] M. Wlodarski,et al. Monosomy 7 in Pediatric Myelodysplastic Syndromes. , 2018, Hematology/oncology clinics of North America.
[17] H. Tamary,et al. Targeted next generation sequencing for the diagnosis of patients with rare congenital anemias , 2018, European journal of haematology.
[18] F. Locatelli,et al. How I treat myelodysplastic syndromes of childhood. , 2018, Blood.
[19] J. Piette,et al. Biologics in myelodysplastic syndrome-related systemic inflammatory and autoimmune diseases: French multicenter retrospective study of 29 patients. , 2017, Autoimmunity reviews.
[20] C. Mecucci,et al. Practical considerations for diagnosis and management of patients and carriers. , 2017, Seminars in hematology.
[21] M. Wlodarski,et al. Mutational landscape in children with myelodysplastic syndromes is distinct from adults: specific somatic drivers and novel germline variants , 2017, Leukemia.
[22] H. Tsukahara,et al. Pediatric intestinal Behçet disease complicated by myeloid malignancies , 2017, International Journal of Hematology.
[23] J. Klco,et al. The genomic landscape of pediatric myelodysplastic syndromes , 2016, Nature Communications.
[24] R. Stone,et al. Autoimmunity and Inflammation in Myelodysplastic Syndromes , 2016, Acta Haematologica.
[25] Nicola D. Roberts,et al. Genomic Classification and Prognosis in Acute Myeloid Leukemia. , 2016, The New England journal of medicine.
[26] Mario Cazzola,et al. The 2016 revision to the World Health Organization classification of myeloid neoplasms and acute leukemia. , 2016, Blood.
[27] B. Williamson,et al. Autoimmune Syndromes Presenting as a Paraneoplastic Manifestation of Myelodysplastic Syndromes: Clinical Features, Course, Treatment and Outcome , 2016, Hematology reports.
[28] O. Ohara,et al. Autoimmunity Including Intestinal Behçet Disease Bearing the KRAS Mutation in Lymphocytes: A Case Report , 2016, Pediatrics.
[29] J. Piette,et al. Systemic inflammatory and autoimmune manifestations associated with myelodysplastic syndromes and chronic myelomonocytic leukaemia: a French multicentre retrospective study. , 2016, Rheumatology.
[30] Sheng Wei,et al. The inflammatory microenvironment in MDS , 2015, Cellular and Molecular Life Sciences.
[31] S. Scholl,et al. Paraneoplastic inflammation in myelodysplastic syndrome or bone marrow failure: case series with focus on 5‐azacytidine and literature review , 2014, European journal of haematology.
[32] D. Inokuma,et al. Behçet's disease-like symptoms associated with myelodysplastic syndrome with trisomy 8: a case report and review of the literature. , 2014, Acta dermato-venereologica.
[33] C. Kim,et al. Autoimmune disease and multiple autoantibodies in 42 patients with RASopathies , 2012, American journal of medical genetics. Part A.
[34] C. Niemeyer,et al. Advances in the prognostication and management of advanced MDS in children , 2011, British journal of haematology.
[35] J. B. Oliveira,et al. Somatic KRAS mutations associated with a human nonmalignant syndrome of autoimmunity and abnormal leukocyte homeostasis. , 2011, Blood.
[36] T. Morio,et al. Autoimmune lymphoproliferative syndrome-like disease with somatic KRAS mutation. , 2011, Blood.
[37] J. Harbott,et al. Complex karyotype newly defined: the strongest prognostic factor in advanced childhood myelodysplastic syndrome. , 2010, Blood.
[38] A. Green,et al. Constitutional trisomy 8 and Behçet syndrome , 2009, American journal of medical genetics. Part A.
[39] Rainer Haas,et al. Epidemiology, classification and prognosis of adults and children with myelodysplastic syndromes , 2008, Annals of Hematology.
[40] R. Moots,et al. Myelodysplastic syndrome with trisomy 8 associated with Behçet syndrome: An immunologic link to a karyotypic abnormality , 2008, Pediatric blood & cancer.
[41] V. Tonk,et al. Juvenile myelomonocytic leukemia in a child with Crohn disease. , 2006, Cancer genetics and cytogenetics.
[42] N. Hatta,et al. BehÇet’s disease associated with myelodysplastic syndrome with elevated levels of inflammatory cytokines , 2003, Modern rheumatology.
[43] J. Licht,et al. Somatic mutations in PTPN11 in juvenile myelomonocytic leukemia, myelodysplastic syndromes and acute myeloid leukemia , 2003, Nature Genetics.
[44] J. Maciejewski,et al. Application of the Molecular Analysis of the T-Cell Receptor Repertoire in the Study of Immune-Mediated Hematologic Diseases , 2003, Hematology.
[45] I. Baumann,et al. A pediatric approach to the WHO classification of myelodysplastic and myeloproliferative diseases , 2003, Leukemia.
[46] Michael A. Patton,et al. Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome , 2001, Nature Genetics.
[47] K. Koike,et al. Lupus nephritis in juvenile myelomonocytic leukemia. , 1999, Clinical nephrology.
[48] A Orfao,et al. Revisiting guidelines for integration of flow cytometry results in the WHO classification of myelodysplastic syndromes—proposal from the International/European LeukemiaNet Working Group for Flow Cytometry in MDS , 2014, Leukemia.
[49] S. Bicciato,et al. PTPN11 mutations in childhood acute lymphoblastic leukemia occur as a secondary event associated with high hyperdiploidy , 2010, Leukemia.
[50] S. Nagataki,et al. Behçet's disease complicated with myelodysplastic syndrome a report of two cases and review of the literature , 2005, Clinical Rheumatology.
[51] A. Brice,et al. Mutations in PTPN11, encoding the protein tyrosine phosphatase SHP-2, cause Noonan syndrome , 2002, Nature Genetics.