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Year Number of Results
1970 1
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1982 2
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1984 4
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1988 2
1989 5
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1998 4
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2000 12
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2007 11
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2009 9
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307 results

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Quoted phrase not found in phrase index: "Abnormal B cell count"
Page 1
Acute lymphoblastic leukemia: a comprehensive review and 2017 update.
Terwilliger T, Abdul-Hay M. Terwilliger T, et al. Blood Cancer J. 2017 Jun 30;7(6):e577. doi: 10.1038/bcj.2017.53. Blood Cancer J. 2017. PMID: 28665419 Free PMC article. Review.
In adults, 75% of cases develop from precursors of the B-cell lineage, with the remainder of cases consisting of malignant T-cell precursors. Traditionally, risk stratification has been based on clinical factors such age, white blood cell count and response t …
In adults, 75% of cases develop from precursors of the B-cell lineage, with the remainder of cases consisting of malignant T-c …
Genomic aberrations and survival in chronic lymphocytic leukemia.
Döhner H, Stilgenbauer S, Benner A, Leupolt E, Kröber A, Bullinger L, Döhner K, Bentz M, Lichter P. Döhner H, et al. N Engl J Med. 2000 Dec 28;343(26):1910-6. doi: 10.1056/NEJM200012283432602. N Engl J Med. 2000. PMID: 11136261 Free article.
BACKGROUND: Fluorescence in situ hybridization has improved the detection of genomic aberrations in chronic lymphocytic leukemia. We used this method to identify chromosomal abnormalities in patients with chronic lymphocytic leukemia and assessed their prognostic im …
BACKGROUND: Fluorescence in situ hybridization has improved the detection of genomic aberrations in chronic lymphocytic leukemia. We used th …
Monoclonal B-cell lymphocytosis.
Rawstron AC. Rawstron AC. Hematology Am Soc Hematol Educ Program. 2009:430-9. doi: 10.1182/asheducation-2009.1.430. Hematology Am Soc Hematol Educ Program. 2009. PMID: 20008229 Review.
Routine diagnostic techniques can now detect very low levels of CLL phenotype cells. Monoclonal B-cell lymphocytosis (MBL) is a relatively recent diagnostic category encapsulating individuals with an abnormal B-cell population but not meeting th …
Routine diagnostic techniques can now detect very low levels of CLL phenotype cells. Monoclonal B-cell lymphocytosis (MBL) is …
Unexplained macrocytosis.
Younes M, Dagher GA, Dulanto JV, Njeim M, Kuriakose P. Younes M, et al. South Med J. 2013 Feb;106(2):121-5. doi: 10.1097/SMJ.0b013e3182824cdf. South Med J. 2013. PMID: 23380746
OBJECTIVES: Macrocytosis is a relatively common finding in adult patients undergoing blood cell counting. Approximately 10% of patients will have unexplained macrocytosis after laboratory evaluation. ...A total of 11.6% patients developed a primary bone marrow disorder (tw …
OBJECTIVES: Macrocytosis is a relatively common finding in adult patients undergoing blood cell counting. Approximately 10% of patien …
Involvement of B cells in the development of systemic sclerosis.
Yoshizaki A, Fukasawa T, Ebata S, Yoshizaki-Ogawa A, Sato S. Yoshizaki A, et al. Front Immunol. 2022 Jul 28;13:938785. doi: 10.3389/fimmu.2022.938785. eCollection 2022. Front Immunol. 2022. PMID: 35967355 Free PMC article. Review.
Systemic sclerosis (SSc) is a rare intractable systemic disease that causes fibrosis and vasculopathy against a background of autoimmune abnormalities. Although the etiology is not yet fully understood, the type of autoantibodies detected in SSc is closely associated with …
Systemic sclerosis (SSc) is a rare intractable systemic disease that causes fibrosis and vasculopathy against a background of autoimmune …
Differential prognosis of single and multiple TP53 abnormalities in high-count MBL and untreated CLL.
Griffin R, Wiedmeier-Nutor JE, Parikh SA, McCabe CE, O'Brien DR, Boddicker NJ, Kleinstern G, Rabe KG, Bruins L, Brown S, Bonolo de Campos C, Ding W, Leis JF, Hampel PJ, Call TG, Van Dyke DL, Kay NE, Cerhan JR, Yan H, Slager SL, Braggio E. Griffin R, et al. Blood Adv. 2023 Jul 11;7(13):3169-3179. doi: 10.1182/bloodadvances.2022009040. Blood Adv. 2023. PMID: 36877634 Free PMC article.
TP53 aberrations, including mutations and deletion of 17p13, are important adverse prognostic markers in chronic lymphocytic leukemia (CLL) but are less studied in high count monoclonal B-cell lymphocytosis (HCMBL), an asymptomatic pre-malignant stage …
TP53 aberrations, including mutations and deletion of 17p13, are important adverse prognostic markers in chronic lymphocytic leukemia …
Hematological manifestations and complications of Gaucher disease.
Linari S, Castaman G. Linari S, et al. Expert Rev Hematol. 2016 Jan;9(1):51-8. doi: 10.1586/17474086.2016.1112732. Epub 2015 Nov 13. Expert Rev Hematol. 2016. PMID: 26565753 Review.
Bleeding diathesis may not always be related to absolute platelet count but may be influenced by abnormal platelet function or coagulation factor deficiencies. A significant increased risk of severe hematological co-morbidities, including multiple myeloma and B …
Bleeding diathesis may not always be related to absolute platelet count but may be influenced by abnormal platelet function or …
Expression of CD markers' in immune thrombocytopenic purpura: prognostic approaches.
Behzad MM, Asnafi AA, Jaseb K, Jalali Far MA, Saki N. Behzad MM, et al. APMIS. 2017 Dec;125(12):1042-1055. doi: 10.1111/apm.12755. Epub 2017 Sep 28. APMIS. 2017. PMID: 28960510 Review.
T and B lymphocytes are the main immune cells in the body. Defective function causes disrupted balance of different subgroups of lymphocytes, and abnormal expression of surface markers of these cells results in self-tolerance dysfunction, as well as induction …
T and B lymphocytes are the main immune cells in the body. Defective function causes disrupted balance of different subgroups …
Evaluation of primary immunodeficiency disease in children.
Reust CE. Reust CE. Am Fam Physician. 2013 Jun 1;87(11):773-8. Am Fam Physician. 2013. PMID: 23939499 Free article. Review.
One in 2,000 children younger than 18 years is thought to have a primary immunodeficiency disease. Antibody, combined B-cell and T-cell, phagocytic, and complement disorders are the most common types. ...Abnormal serum immunoglobulin levels suggest a B …
One in 2,000 children younger than 18 years is thought to have a primary immunodeficiency disease. Antibody, combined B-cell a …
Expression of BCL11A in chronic lymphocytic leukaemia.
Tosic N, Ugrin M, Marjanovic I, Kostic T, Vukovic V, Tomic K, Otasevic V, Antic D, Mihaljevic B, Pavlovic S, Karan-Djurasevic T. Tosic N, et al. Int J Lab Hematol. 2023 Feb;45(1):64-71. doi: 10.1111/ijlh.13969. Epub 2022 Sep 19. Int J Lab Hematol. 2023. PMID: 36120992
INTRODUCTION: The B-cell lymphoma/leukaemia 11A (BCL11A) gene encodes a Kruppel-like transcription factor involved in lymphocyte development during normal haematopoiesis. ...However, its functions in the regulatory networks of malignant B lymphocytes a …
INTRODUCTION: The B-cell lymphoma/leukaemia 11A (BCL11A) gene encodes a Kruppel-like transcription factor involved in lymphocy …
307 results