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

Year Number of Results
1968 1
1970 1
1971 3
1972 3
1973 2
1974 4
1975 13
1976 8
1977 4
1978 6
1979 7
1980 2
1981 6
1982 5
1983 7
1984 3
1985 12
1986 9
1987 9
1988 4
1989 3
1990 10
1991 8
1992 15
1993 11
1994 5
1995 8
1996 14
1997 10
1998 13
1999 14
2000 12
2001 17
2002 10
2003 13
2004 17
2005 12
2006 12
2007 17
2008 16
2009 8
2010 17
2011 21
2012 20
2013 23
2014 19
2015 14
2016 13
2017 19
2018 13
2019 24
2020 17
2021 23
2022 12
2023 12
2024 8

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572 results

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Quoted phrase not found in phrase index: "Abnormal spleen physiology"
Page 1
Primary myelofibrosis: 2023 update on diagnosis, risk-stratification, and management.
Tefferi A. Tefferi A. Am J Hematol. 2023 May;98(5):801-821. doi: 10.1002/ajh.26857. Epub 2023 Feb 6. Am J Hematol. 2023. PMID: 36680511 Free article. Review.
Type 1/like CALR mutation is associated with superior survival. KARYOTYPE: Very high-risk abnormalities include -7, inv (3), i(17q), +21, +19, 12p- and 11q-. Favorable risk abnormalities include normal karyotype or isolated +9, 13q-, 20q-, 1q abnormalities an …
Type 1/like CALR mutation is associated with superior survival. KARYOTYPE: Very high-risk abnormalities include -7, inv (3), i(17q), …
Post-splenectomy and hyposplenic states.
Di Sabatino A, Carsetti R, Corazza GR. Di Sabatino A, et al. Lancet. 2011 Jul 2;378(9785):86-97. doi: 10.1016/S0140-6736(10)61493-6. Epub 2011 Apr 5. Lancet. 2011. PMID: 21474172 Review.
The spleen is crucial in regulating immune homoeostasis through its ability to link innate and adaptive immunity and in protecting against infections. The impairment of splenic function is defined as hyposplenism, an acquired disorder caused by several haematological and i …
The spleen is crucial in regulating immune homoeostasis through its ability to link innate and adaptive immunity and in protecting ag …
Genetic and phenotypic attributes of splenic marginal zone lymphoma.
Bonfiglio F, Bruscaggin A, Guidetti F, Terzi di Bergamo L, Faderl M, Spina V, Condoluci A, Bonomini L, Forestieri G, Koch R, Piffaretti D, Pini K, Pirosa MC, Cittone MG, Arribas A, Lucioni M, Ghilardi G, Wu W, Arcaini L, Baptista MJ, Bastidas G, Bea S, Boldorini R, Broccoli A, Buehler MM, Canzonieri V, Cascione L, Ceriani L, Cogliatti S, Corradini P, Derenzini E, Devizzi L, Dietrich S, Elia AR, Facchetti F, Gaidano G, Garcia JF, Gerber B, Ghia P, Gomes da Silva M, Gritti G, Guidetti A, Hitz F, Inghirami G, Ladetto M, Lopez-Guillermo A, Lucchini E, Maiorana A, Marasca R, Matutes E, Meignin V, Merli M, Moccia A, Mollejo M, Montalban C, Novak U, Oscier DG, Passamonti F, Piazza F, Pizzolitto S, Rambaldi A, Sabattini E, Salles G, Santambrogio E, Scarfò L, Stathis A, Stüssi G, Geyer JT, Tapia G, Tarella C, Thieblemont C, Tousseyn T, Tucci A, Vanini G, Visco C, Vitolo U, Walewska R, Zaja F, Zenz T, Zinzani PL, Khiabanian H, Calcinotto A, Bertoni F, Bhagat G, Campo E, De Leval L, Dirnhofer S, Pileri SA, Piris MA, Traverse-Glehen A, Tzankov A, Paulli M, Ponzoni M, Mazzucchelli L, Cavalli F, Zucca E, Rossi D. Bonfiglio F, et al. Blood. 2022 Feb 3;139(5):732-747. doi: 10.1182/blood.2021012386. Blood. 2022. PMID: 34653238 Free article.
We sought to clarify the heterogeneity of SMZL by resolving different subgroups and their underlying genomic abnormalities, pathway signatures, and microenvironment compositions to uncover biomarkers and therapeutic vulnerabilities. We studied 303 SMZL spleen sample …
We sought to clarify the heterogeneity of SMZL by resolving different subgroups and their underlying genomic abnormalities, pathway s …
Accessory spleen.
Radu CC, Muţiu G, Pop O. Radu CC, et al. Rom J Morphol Embryol. 2014;55(3 Suppl):1243-6. Rom J Morphol Embryol. 2014. PMID: 25607414 Free article.
An accessory spleen (AS), or splenunculus, is a small nodule of splenic tissue found outside of the spleen. ...We present two incidental cases of splenunculi, one localized in greater omentum and a second one localized in the hilum of the spleen, diagnosed du …
An accessory spleen (AS), or splenunculus, is a small nodule of splenic tissue found outside of the spleen. ...We present two …
Gaucher disease.
Guggenbuhl P, Grosbois B, Chalès G. Guggenbuhl P, et al. Joint Bone Spine. 2008 Mar;75(2):116-24. doi: 10.1016/j.jbspin.2007.06.006. Epub 2007 Aug 31. Joint Bone Spine. 2008. PMID: 17996473 Review.
The enzyme substrate, glucocerebroside, accumulates in the body, predominantly in the liver, spleen, and bone marrow. Osteoarticular manifestations are often inaugural and contribute much of the morbidity and disability associated with Gaucher disease. ...The most common i …
The enzyme substrate, glucocerebroside, accumulates in the body, predominantly in the liver, spleen, and bone marrow. Osteoarticular …
Gaucher disease.
Beutler E. Beutler E. Blood Rev. 1988 Mar;2(1):59-70. doi: 10.1016/0268-960x(88)90009-4. Blood Rev. 1988. PMID: 3289655 Review.
Gaucher disease is a glycolipid storage disorder characterized by accumulation of glucocerebroside in the liver, spleen, and bones, and caused by a deficiency of glucocerebrosidase. ...On an experimental basis, splenectomy may be partial instead of total. Because the disea …
Gaucher disease is a glycolipid storage disorder characterized by accumulation of glucocerebroside in the liver, spleen, and bones, a …
Hereditary spherocytosis.
Iolascon A, Avvisati RA, Piscopo C. Iolascon A, et al. Transfus Clin Biol. 2010 Sep;17(3):138-42. doi: 10.1016/j.tracli.2010.05.006. Epub 2010 Jul 23. Transfus Clin Biol. 2010. PMID: 20655264
Hereditary spherocytosis is a common hemolytic disorder characterized by a defect or deficiency in one or more of the proteins composing red blood cell membrane. As a result, red blood cells have an abnormal shape, higher metabolic requirements, and are prematurely trapped …
Hereditary spherocytosis is a common hemolytic disorder characterized by a defect or deficiency in one or more of the proteins composing red …
Childhood visceral leishmaniasis.
Bhattacharya SK, Sur D, Karbwang J. Bhattacharya SK, et al. Indian J Med Res. 2006 Mar;123(3):353-6. Indian J Med Res. 2006. PMID: 16778316 Free article. Review.
Prolonged fever with anorexia and loss of appetite are the major presenting features. Marked enlargement of the spleen and liver (spleen larger than liver) with moderate to severe anaemia and changes in hair take place. Bacterial infection is a common coinfection an …
Prolonged fever with anorexia and loss of appetite are the major presenting features. Marked enlargement of the spleen and liver ( …
Acid phosphatase.
Henneberry MO, Engel G, Grayhack JT. Henneberry MO, et al. Urol Clin North Am. 1979 Oct;6(3):629-41. Urol Clin North Am. 1979. PMID: 388794 Review.
Although the postpuberteral prostatic epithelial cell contains a uniquely high concentration of acid phosphatase, cellular components of bone, spleen, kidney, liver, intestine, and blood also contain this enzyme. ...Judgment of their efficacy awaits further testing and eva …
Although the postpuberteral prostatic epithelial cell contains a uniquely high concentration of acid phosphatase, cellular components of bon …
572 results