Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My NCBI Filters

Results by year

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

Year Number of Results
1978 3
1979 1
1980 1
1982 1
1983 3
1985 1
1989 2
1990 2
1991 3
1993 2
1994 3
1995 1
1997 2
2000 2
2001 1
2002 3
2003 3
2005 2
2006 1
2007 6
2008 2
2009 1
2010 3
2011 2
2012 2
2013 4
2014 4
2015 4
2016 7
2017 4
2018 3
2019 5
2020 1
2021 1
2022 5
2023 1
2024 0

Text availability

Article attribute

Article type

Publication date

Search Results

86 results

Results by year

Filters applied: . Clear all
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 …
Secondary Immune Deficiency and Primary Immune Deficiency Crossovers: Hematological Malignancies and Autoimmune Diseases.
Ballow M, Sánchez-Ramón S, Walter JE. Ballow M, et al. Front Immunol. 2022 Jul 18;13:928062. doi: 10.3389/fimmu.2022.928062. eCollection 2022. Front Immunol. 2022. PMID: 35924244 Free PMC article. Review.
The risk of hematological cancer is increased in PID: for example, lymphomas in PID may be driven by infections such as Epstein-Barr virus, and germline mutations associated with PID are enriched among patients with diffuse large B-cell lymphoma. Clues suggesting an …
The risk of hematological cancer is increased in PID: for example, lymphomas in PID may be driven by infections such as Epstein-Barr virus, …
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 …
B- and T-Cell Subset Abnormalities in Monogenic Common Variable Immunodeficiency.
Fekrvand S, Khanmohammadi S, Abolhassani H, Yazdani R. Fekrvand S, et al. Front Immunol. 2022 Jun 15;13:912826. doi: 10.3389/fimmu.2022.912826. eCollection 2022. Front Immunol. 2022. PMID: 35784324 Free PMC article. Review.
Monogenic defects account for the pathogenesis of about 20-50% of CVID patients, while a variety of cases do not have a defined genetic background. Deficiencies in molecules of B cell receptor signaling or other pathways involving B-cell development, a …
Monogenic defects account for the pathogenesis of about 20-50% of CVID patients, while a variety of cases do not have a defined genetic back …
[Chronic lymphocytic leukemia].
Jacque N, Leblond V. Jacque N, et al. Presse Med. 2019 Jul-Aug;48(7-8 Pt 1):807-815. doi: 10.1016/j.lpm.2019.07.019. Epub 2019 Aug 22. Presse Med. 2019. PMID: 31447332 Review. French.
The first line option is immunochemotherapy in 90% of the patients without genetic abnormalities associated with chemo resistance. The use of new compounds targeting different pathways is more frequent especially in relapsing patients and could be an alternative to the che …
The first line option is immunochemotherapy in 90% of the patients without genetic abnormalities associated with chemo resistance. Th …
Dyskeratosis congenita.
Gupta V, Kumar A. Gupta V, et al. Adv Exp Med Biol. 2010;685:215-9. doi: 10.1007/978-1-4419-6448-9_20. Adv Exp Med Biol. 2010. PMID: 20687509 Free article. Review.
Early childhood variants (Hoyeraal-Hreidarsson syndrome) are associated with immunological abnormalities in the form of low T- and B-cell numbers. Four genes, namely DKC1 (codes for dyskerin), TERC and TERT (code for telomerase) and NOP10, have been implicate …
Early childhood variants (Hoyeraal-Hreidarsson syndrome) are associated with immunological abnormalities in the form of low T- and …
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 …
Immunodeficiency in CHARGE syndrome.
Mehr S, Hsu P, Campbell D. Mehr S, et al. Am J Med Genet C Semin Med Genet. 2017 Dec;175(4):516-523. doi: 10.1002/ajmg.c.31594. Epub 2017 Nov 21. Am J Med Genet C Semin Med Genet. 2017. PMID: 29159871 Review.
Immunodeficiency can occur in CHARGE syndrome, with immunophenotypes including reduction in T-cell counts, combined T-B cell defects rarely requiring antibiotic prophylaxis or immunoglobulin replacement, and severe combined immunodeficiency, which is fatal wi …
Immunodeficiency can occur in CHARGE syndrome, with immunophenotypes including reduction in T-cell counts, combined T-B cel
T-Cell Abnormalities in Common Variable Immunodeficiency.
Azizi G, Rezaei N, Kiaee F, Tavakolinia N, Yazdani R, Mirshafiey A, Aghamohammadi A. Azizi G, et al. J Investig Allergol Clin Immunol. 2016;26(4):233-43. doi: 10.18176/jiaci.0069. Epub 2016 Apr 15. J Investig Allergol Clin Immunol. 2016. PMID: 27374799 Free article. Review.
Common variable immunodeficiency (CVID) is the most common clinical primary immunodeficiency. It is characterized by a defect in B-cell differentiation to plasma and memory B cells. Moreover, numerous T-cell abnormalities have been reported and include decrea …
Common variable immunodeficiency (CVID) is the most common clinical primary immunodeficiency. It is characterized by a defect in B- …
Abnormal T-cell function in B-cell chronic lymphocytic leukaemia.
Scrivener S, Goddard RV, Kaminski ER, Prentice AG. Scrivener S, et al. Leuk Lymphoma. 2003 Mar;44(3):383-9. doi: 10.1080/1042819021000029993. Leuk Lymphoma. 2003. PMID: 12688308 Review.
There is increasing evidence of T cell dysfunction in B cell chronic lymphocytic leukaemia (B-CLL) which may contribute to the aetiology and progress of the disease. ...Other abnormalities of cytokine secretion are described. These findings suggest that the T …
There is increasing evidence of T cell dysfunction in B cell chronic lymphocytic leukaemia (B-CLL) which may contribute to the …
86 results