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Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1969 3
1970 1
1972 1
1973 1
1974 4
1975 11
1976 15
1977 12
1978 14
1979 14
1980 18
1981 23
1982 17
1983 22
1984 30
1985 25
1986 36
1987 32
1988 26
1989 20
1990 35
1991 31
1992 33
1993 39
1994 35
1995 40
1996 51
1997 49
1998 53
1999 65
2000 61
2001 53
2002 58
2003 70
2004 54
2005 45
2006 61
2007 58
2008 65
2009 59
2010 61
2011 58
2012 64
2013 67
2014 76
2015 103
2016 71
2017 74
2018 62
2019 87
2020 86
2021 68
2022 32
2023 34
2024 11

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2,099 results

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Quoted phrase not found in phrase index: "Abnormal bone marrow cell morphology"
Page 1
Updated Diagnostic Criteria and Staging System for Multiple Myeloma.
Rajkumar SV. Rajkumar SV. Am Soc Clin Oncol Educ Book. 2016;35:e418-23. doi: 10.1200/EDBK_159009. Am Soc Clin Oncol Educ Book. 2016. PMID: 27249749 Free article. Review.
In 2014, the International Myeloma Working Group (IMWG) updated the diagnostic criteria for MM to add three specific biomarkers that can be used to diagnose the disease in patients who did not have CRAB features: clonal bone marrow plasma cells greater than o …
In 2014, the International Myeloma Working Group (IMWG) updated the diagnostic criteria for MM to add three specific biomarkers that can be …
Clinical evolution, genetic landscape and trajectories of clonal hematopoiesis in SAMD9/SAMD9L syndromes.
Sahoo SS, Pastor VB, Goodings C, Voss RK, Kozyra EJ, Szvetnik A, Noellke P, Dworzak M, Starý J, Locatelli F, Masetti R, Schmugge M, De Moerloose B, Catala A, Kállay K, Turkiewicz D, Hasle H, Buechner J, Jahnukainen K, Ussowicz M, Polychronopoulou S, Smith OP, Fabri O, Barzilai S, de Haas V, Baumann I, Schwarz-Furlan S; European Working Group of MDS in Children (EWOG-MDS); Niewisch MR, Sauer MG, Burkhardt B, Lang P, Bader P, Beier R, Müller I, Albert MH, Meisel R, Schulz A, Cario G, Panda PK, Wehrle J, Hirabayashi S, Derecka M, Durruthy-Durruthy R, Göhring G, Yoshimi-Noellke A, Ku M, Lebrecht D, Erlacher M, Flotho C, Strahm B, Niemeyer CM, Wlodarski MW. Sahoo SS, et al. Nat Med. 2021 Oct;27(10):1806-1817. doi: 10.1038/s41591-021-01511-6. Epub 2021 Oct 7. Nat Med. 2021. PMID: 34621053 Free PMC article.
In total, 67 patients had 58 distinct germline SAMD9/9L(mut) clustering to protein middle regions. Despite inconclusive in silico prediction, 94% of SAMD9/9L(mut) suppressed HEK293 cell growth, and mutations expressed in CD34(+) cells induced overt cell …
In total, 67 patients had 58 distinct germline SAMD9/9L(mut) clustering to protein middle regions. Despite inconclusive in silico predict …
Myelodysplastic syndromes with ring sideroblasts (MDS-RS) and MDS/myeloproliferative neoplasm with RS and thrombocytosis (MDS/MPN-RS-T) - "2021 update on diagnosis, risk-stratification, and management".
Patnaik MM, Tefferi A. Patnaik MM, et al. Am J Hematol. 2021 Mar 1;96(3):379-394. doi: 10.1002/ajh.26090. Epub 2021 Jan 28. Am J Hematol. 2021. PMID: 33428785 Free article. Review.
DISEASE OVERVIEW: Ring sideroblasts (RS) are erythroid precursors with abnormal perinuclear mitochondrial iron accumulation. Two myeloid neoplasms defined by the presence of RS, include myelodysplastic syndromes with RS (MDS-RS) and MDS/myeloproliferative neoplasm with RS …
DISEASE OVERVIEW: Ring sideroblasts (RS) are erythroid precursors with abnormal perinuclear mitochondrial iron accumulation. Two myel …
Idiopathic myelofibrosis.
Barosi G, Hoffman R. Barosi G, et al. Semin Hematol. 2005 Oct;42(4):248-58. doi: 10.1053/j.seminhematol.2005.05.018. Semin Hematol. 2005. PMID: 16210038 Review.
Idiopathic myelofibrosis (IMF) is characterized by anemia, progressive splenomegaly, bone marrow fibrosis, and extramedullary hematopoiesis. However, patients with a transitional myeloproliferative disorder (MPD), a prefibrotic form of myelofibrosis, or myelofibrosi …
Idiopathic myelofibrosis (IMF) is characterized by anemia, progressive splenomegaly, bone marrow fibrosis, and extramedullary …
Childhood myelodysplastic syndrome.
Chatterjee T, Choudhry VP. Chatterjee T, et al. Indian J Pediatr. 2013 Sep;80(9):764-71. doi: 10.1007/s12098-013-1130-8. Epub 2013 Aug 3. Indian J Pediatr. 2013. PMID: 23912822 Review.
Myelodysplastic syndrome (MDS) comprises of a heterogeneous group of bone marrow disorders resulting from a clonal stem cell defect characterised by cytopenias despite a relatively hypercellular marrow, ineffective hematopoiesis, morphological dysplasi …
Myelodysplastic syndrome (MDS) comprises of a heterogeneous group of bone marrow disorders resulting from a clonal stem cel …
Human preleukemia.
Koeffler HP, Golde DW. Koeffler HP, et al. Ann Intern Med. 1980 Aug;93(2):347-53. doi: 10.7326/0003-4819-93-2-347. Ann Intern Med. 1980. PMID: 6931507
Clinically, preleukemia is characterized by variable degrees of pancytopenia, with associated symptoms due to decreased circulating blood elements. The bone marrow is usually hypercellular, and there are prominent morphologic abnormalities in erythroid precur …
Clinically, preleukemia is characterized by variable degrees of pancytopenia, with associated symptoms due to decreased circulating blood el …
Concise Review: Perspectives and Clinical Implications of Bone Marrow and Circulating Stem Cell Defects in Diabetes.
Fadini GP, Ciciliot S, Albiero M. Fadini GP, et al. Stem Cells. 2017 Jan;35(1):106-116. doi: 10.1002/stem.2445. Epub 2016 Jul 11. Stem Cells. 2017. PMID: 27401837 Review.
From a clinical perspective, pauperization of circulating stem cells predicts adverse outcomes and death. Furthermore, studies in murine models and humans have identified the bone marrow (BM) as a previously neglected site of diabetic end-organ damage, …
From a clinical perspective, pauperization of circulating stem cells predicts adverse outcomes and death. Furthermore, studies …
The bone marrow microenvironment - Home of the leukemic blasts.
Shafat MS, Gnaneswaran B, Bowles KM, Rushworth SA. Shafat MS, et al. Blood Rev. 2017 Sep;31(5):277-286. doi: 10.1016/j.blre.2017.03.004. Epub 2017 Mar 12. Blood Rev. 2017. PMID: 28318761 Review.
Acute Myeloid Leukaemia (AML) is a genetically, biologically and clinically heterogeneous set of diseases, which are characterised by an increased growth of abnormal myeloid progenitor cells within the bone marrow (BM). Ex-vivo AML exhibits a high leve …
Acute Myeloid Leukaemia (AML) is a genetically, biologically and clinically heterogeneous set of diseases, which are characterised by an inc …
Erythroblastemia.
Tavassoli M. Tavassoli M. West J Med. 1975 Mar;122(3):194-8. West J Med. 1975. PMID: 1096474 Free PMC article.
Interpretation should take into account the number and spectrum of maturity of the nucleated red cells; the presence or absence of reticulocytosis and other red cell abnormalities (for example, poikilocytosis); the presence or absence of anemia; the presence …
Interpretation should take into account the number and spectrum of maturity of the nucleated red cells; the presence or absence of re …
Fibrogenesis in Primary Myelofibrosis: Diagnostic, Clinical, and Therapeutic Implications.
Nazha A, Khoury JD, Rampal RK, Daver N. Nazha A, et al. Oncologist. 2015 Oct;20(10):1154-60. doi: 10.1634/theoncologist.2015-0094. Epub 2015 Aug 24. Oncologist. 2015. PMID: 26304912 Free PMC article. Review.
Primary myelofibrosis is a stem cell-derived clonal malignancy characterized by unchecked proliferation of myeloid cells, resulting in bone marrow fibrosis, osteosclerosis, and pathologic angiogenesis. Bone marrow fibrosis (BMF) plays a c …
Primary myelofibrosis is a stem cell-derived clonal malignancy characterized by unchecked proliferation of myeloid cells, resu …
2,099 results