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
1964 1
1966 2
1968 2
1969 1
1971 4
1972 6
1973 2
1974 8
1975 3
1976 5
1977 5
1978 3
1979 10
1980 4
1981 8
1982 13
1983 11
1984 14
1985 11
1986 21
1987 25
1988 17
1989 19
1990 21
1991 11
1992 20
1993 17
1994 16
1995 17
1996 29
1997 23
1998 35
1999 23
2000 45
2001 32
2002 39
2003 41
2004 37
2005 34
2006 42
2007 31
2008 40
2009 46
2010 47
2011 53
2012 55
2013 62
2014 69
2015 69
2016 54
2017 40
2018 45
2019 46
2020 62
2021 62
2022 46
2023 43
2024 24

Text availability

Article attribute

Article type

Publication date

Search Results

1,429 results

Results by year

Filters applied: . Clear all
Quoted phrase not found in phrase index: "Genetic anomaly of leukocyte"
Page 1
Update on Lymphoblastic Leukemia/Lymphoma.
Luca DC. Luca DC. Clin Lab Med. 2021 Sep;41(3):405-416. doi: 10.1016/j.cll.2021.04.003. Clin Lab Med. 2021. PMID: 34304772 Review.
The classification of B-lymphoblastic neoplasms relies predominantly on genetic and molecular findings, whereas the same is not true for those of T-lymphoid origin. Many of these recurrent cytogenetic abnormalities have important prognostic and therapeutic implicati …
The classification of B-lymphoblastic neoplasms relies predominantly on genetic and molecular findings, whereas the same is not true …
Myelodysplastic syndromes.
Adès L, Itzykson R, Fenaux P. Adès L, et al. Lancet. 2014 Jun 28;383(9936):2239-52. doi: 10.1016/S0140-6736(13)61901-7. Epub 2014 Mar 21. Lancet. 2014. PMID: 24656536 Review.
Prognosis depends largely on the marrow blast percentage, number and extent of cytopenias, and cytogenetic abnormalities. Treatment of patients with lower-risk myelodysplastic syndromes, especially for anaemia, includes growth factors, lenalidomide, and transfusions. ...
Prognosis depends largely on the marrow blast percentage, number and extent of cytopenias, and cytogenetic abnormalities. Treatment o …
Monogenic autoinflammatory diseases.
Russo RA, Brogan PA. Russo RA, et al. Rheumatology (Oxford). 2014 Nov;53(11):1927-39. doi: 10.1093/rheumatology/keu170. Epub 2014 May 15. Rheumatology (Oxford). 2014. PMID: 24831056 Review.
The proteins encoded by these genes are involved in the regulatory pathways of inflammation and are mostly expressed in cells of the innate immune system. Diagnosis remains clinical, with genetic confirmation where feasible. Although a group of patients exhibit episodic sy …
The proteins encoded by these genes are involved in the regulatory pathways of inflammation and are mostly expressed in cells of the innate …
Alpha-mannosidosis.
Malm D, Nilssen Ø. Malm D, et al. Orphanet J Rare Dis. 2008 Jul 23;3:21. doi: 10.1186/1750-1172-3-21. Orphanet J Rare Dis. 2008. PMID: 18651971 Free PMC article. Review.
Diagnosis is made by measuring acid alpha-mannosidase activity in leukocytes or other nucleated cells and can be confirmed by genetic testing. ...Antenatal diagnosis is possible, based on both biochemical and genetic methods. The management should be pro-acti …
Diagnosis is made by measuring acid alpha-mannosidase activity in leukocytes or other nucleated cells and can be confirmed by gene …
Genetic Abnormalities in Extramedullary Multiple Myeloma.
McAvera R, Quinn J, Murphy P, Glavey S. McAvera R, et al. Int J Mol Sci. 2023 Jul 9;24(14):11259. doi: 10.3390/ijms241411259. Int J Mol Sci. 2023. PMID: 37511018 Free PMC article. Review.
Generally, high-risk cytogenetic abnormalities and gene signatures are associated with EMD, alongside mutations in RAS signalling pathways. ...Therefore, the focus of this review is to summarize and discuss what is currently known about the genetic background of EMD …
Generally, high-risk cytogenetic abnormalities and gene signatures are associated with EMD, alongside mutations in RAS signalling pat …
Heavy-chain diseases.
Fermand JP, Brouet JC. Fermand JP, et al. Hematol Oncol Clin North Am. 1999 Dec;13(6):1281-94. doi: 10.1016/s0889-8588(05)70127-1. Hematol Oncol Clin North Am. 1999. PMID: 10626151 Review.
This review underscores the diversity of the structural and genetic abnormalities of HCD proteins and of the clinicopathologic features of the underlying lymphoproliferative disorders. ...
This review underscores the diversity of the structural and genetic abnormalities of HCD proteins and of the clinicopathologic …
Genetic immunodeficiency diseases.
Abrams M, Paller A. Abrams M, et al. Adv Dermatol. 2007;23:197-229. doi: 10.1016/j.yadr.2007.08.001. Adv Dermatol. 2007. PMID: 18159903 Review.
The approach to the patient with genetic immunodeficiency is multidisciplinary, and requires close interaction between the primary care physician, immunologist, and other specialists. ...The underlying genetic basis is now known for most forms of immunodeficiency, w …
The approach to the patient with genetic immunodeficiency is multidisciplinary, and requires close interaction between the primary ca …
Neutropenia and leukemia development: genetic risk factors and prognosis.
Shahrabi S, Maleknia M, Tavakolifar Y, D Zayeri Z, Saki N. Shahrabi S, et al. Leuk Lymphoma. 2019 Dec;60(14):3363-3374. doi: 10.1080/10428194.2019.1630622. Epub 2019 Jun 19. Leuk Lymphoma. 2019. PMID: 31213100 Review.
Neutropenia is known as a clinical consequence in various genetic disorders and other neutropenia-inducing mutations (NIM) nonmalignant diseases. ...We searched the PubMed database and Google Scholar engine using English-language article (1980-2019) using the terms 'Neutro …
Neutropenia is known as a clinical consequence in various genetic disorders and other neutropenia-inducing mutations (NIM) nonmaligna …
Hereditary myopathies associated with hematological abnormalities.
Beecher G, Fleming MD, Liewluck T. Beecher G, et al. Muscle Nerve. 2022 Apr;65(4):374-390. doi: 10.1002/mus.27474. Epub 2022 Jan 5. Muscle Nerve. 2022. PMID: 34985130 Review.
A diverse spectrum of hematological abnormalities is associated with hereditary myopathies, including anemias, leukocyte abnormalities, and thrombocytopenia. ...Peripheral eosinophilia may accompany eosinophilic inflammation in recessive calpainopathy. Lipid …
A diverse spectrum of hematological abnormalities is associated with hereditary myopathies, including anemias, leukocyte ab …
T- and NK-cell lymphoproliferative disorders of the gastrointestinal tract: review and update.
van Vliet C, Spagnolo DV. van Vliet C, et al. Pathology. 2020 Jan;52(1):128-141. doi: 10.1016/j.pathol.2019.10.001. Epub 2019 Nov 11. Pathology. 2020. PMID: 31727264 Review.
This review covers the aforementioned lymphoid proliferations, emphasising their salient clinicopathological features and genetic abnormalities. It also provides practical insights into resolving difficult differential diagnoses in daily surgical pathology practice. …
This review covers the aforementioned lymphoid proliferations, emphasising their salient clinicopathological features and genetic …
1,429 results