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

Year Number of Results
1947 2
1964 2
1965 2
1966 4
1967 2
1968 4
1969 2
1970 2
1971 1
1972 3
1973 3
1974 5
1975 13
1976 16
1977 17
1978 13
1979 22
1980 22
1981 26
1982 21
1983 23
1984 26
1985 27
1986 32
1987 25
1988 27
1989 25
1990 40
1991 43
1992 51
1993 44
1994 42
1995 48
1996 41
1997 55
1998 64
1999 53
2000 57
2001 66
2002 79
2003 79
2004 77
2005 64
2006 84
2007 81
2008 76
2009 81
2010 97
2011 117
2012 107
2013 119
2014 104
2015 110
2016 115
2017 115
2018 100
2019 111
2020 102
2021 120
2022 118
2023 108
2024 34

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2,948 results

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Page 1
Disseminated histoplasmosis.
Subramanian S, Abraham OC, Rupali P, Zachariah A, Mathews MS, Mathai D. Subramanian S, et al. J Assoc Physicians India. 2005 Mar;53:185-9. J Assoc Physicians India. 2005. PMID: 15926599
Weight loss, fever and oropharyngeal ulcers were the commonest symptoms. Physical signs included hepatosplenomegaly, oropharyngeal ulcers and lymphadenopathy. The diagnosis was confirmed by histopathology and/or culture from the following sites: bone marrow, adrenal gland, …
Weight loss, fever and oropharyngeal ulcers were the commonest symptoms. Physical signs included hepatosplenomegaly, oropharyngeal ul …
Schnitzler syndrome.
Soubrier M. Soubrier M. Joint Bone Spine. 2008 May;75(3):263-6. doi: 10.1016/j.jbspin.2007.07.014. Epub 2008 Feb 22. Joint Bone Spine. 2008. PMID: 18378180 Review.
Schnitzler syndrome is characterized by monoclonal IgM gammopathy, urticaria, recurrent fever, evidence of inflammation, bone pain, and arthralgia, occasionally in combination with lymphadenopathy and/or hepatosplenomegaly. Only about 80 cases have been reported to date. D …
Schnitzler syndrome is characterized by monoclonal IgM gammopathy, urticaria, recurrent fever, evidence of inflammation, bone pain, and arth …
Osteopetrosis.
Khan MN, Datta PK, Hasan MI, Hossain MA, Patwary KH, Ferdous J. Khan MN, et al. Mymensingh Med J. 2011 Oct;20(4):715-8. Mymensingh Med J. 2011. PMID: 22081195
A 15 years old Bangladeshi boy presented with hepatosplenomegaly, anaemia, multiple fractures (symptomatic and asymptomatic) without jaundice was investigated. ...
A 15 years old Bangladeshi boy presented with hepatosplenomegaly, anaemia, multiple fractures (symptomatic and asymptomatic) without …
Hemophagocytic Lymphohistiocytosis in Adults.
Campo M, Berliner N. Campo M, et al. Hematol Oncol Clin North Am. 2015 Oct;29(5):915-25. doi: 10.1016/j.hoc.2015.06.009. Epub 2015 Aug 14. Hematol Oncol Clin North Am. 2015. PMID: 26461151 Review.
Clinically the syndrome, whether genetic or acquired, is characterized by fever, hepatosplenomegaly, cytopenias, and activated macrophages in hematopoietic organs. ...
Clinically the syndrome, whether genetic or acquired, is characterized by fever, hepatosplenomegaly, cytopenias, and activated macrop …
Familial myelofibrosis.
Sieff CA, Malleson P. Sieff CA, et al. Arch Dis Child. 1980 Nov;55(11):888-93. doi: 10.1136/adc.55.11.888. Arch Dis Child. 1980. PMID: 7436463 Free PMC article.
The illness presented with pallor, haemorrhagic symptoms, and hepatosplenomegaly, and the blood picture was that of pancytopenia and leucoerythroblastosis. ...
The illness presented with pallor, haemorrhagic symptoms, and hepatosplenomegaly, and the blood picture was that of pancytopenia and …
Extramedullary haematopoiesis: radiological imaging features.
Roberts AS, Shetty AS, Mellnick VM, Pickhardt PJ, Bhalla S, Menias CO. Roberts AS, et al. Clin Radiol. 2016 Sep;71(9):807-14. doi: 10.1016/j.crad.2016.05.014. Epub 2016 Jul 1. Clin Radiol. 2016. PMID: 27377325 Review.
In the thorax, EMH most commonly presents as paravertebral fat-containing masses, and typically does not present a diagnostic dilemma; however, EMH in the abdomen most commonly manifests as hepatosplenomegaly with or without focal soft-tissue masses in the liver, spleen, p …
In the thorax, EMH most commonly presents as paravertebral fat-containing masses, and typically does not present a diagnostic dilemma; howev …
Budd-Chiari syndrome.
Sutradhar SR, Sarker CB, Rahman S, Debnath CR, Siddiqui NI, Huq HM, Barman TK, Khan GK, Miah MT. Sutradhar SR, et al. Mymensingh Med J. 2005 Jan;14(1):84-7. Mymensingh Med J. 2005. PMID: 15695963
Direction of venous flow was from below upward. There were mild hepatosplenomegaly, ascites and bilateral testicular atrophy. He was diagnosed as a case of Budd-Chiari Syndrome (BCS) on the basis of physical examination and it was confirmed by the findings of ultrasonograp …
Direction of venous flow was from below upward. There were mild hepatosplenomegaly, ascites and bilateral testicular atrophy. He was …
Omenn's disease.
Dyke MP, Marlow N, Berry PJ. Dyke MP, et al. Arch Dis Child. 1991 Oct;66(10):1247-8. doi: 10.1136/adc.66.10.1247. Arch Dis Child. 1991. PMID: 1835343 Free PMC article.
The importance of accurate pathological diagnosis is emphasised in the case of a newborn infant who presented with alopecia, a generalised erythrodermatous skin eruption, and hepatosplenomegaly. She subsequently developed generalised lymphadenopathy and recurrent septicaem …
The importance of accurate pathological diagnosis is emphasised in the case of a newborn infant who presented with alopecia, a generalised e …
Caroli's disease.
Gupta AK, Gupta A, Bhardwaj VK, Chansoria M. Gupta AK, et al. Indian J Pediatr. 2006 Mar;73(3):233-5. doi: 10.1007/BF02825490. Indian J Pediatr. 2006. PMID: 16567920
A case of caroli's disease in an 8-years-old boy with bilobar involvement of liver, (specially affecting right superior lobe) presenting with intermittent abdominal pain, fever and hepatosplenomegaly is reported here....
A case of caroli's disease in an 8-years-old boy with bilobar involvement of liver, (specially affecting right superior lobe) presenting wit …
Hereditary and acquired hemophagocytic lymphohistiocytosis.
Zhang L, Zhou J, Sokol L. Zhang L, et al. Cancer Control. 2014 Oct;21(4):301-12. doi: 10.1177/107327481402100406. Cancer Control. 2014. PMID: 25310211 Free article. Review.
BACKGROUND: Hemophagocytic lymphohistiocytosis (HLH) is a rare but life-threatening hyperinflammatory/hypercytokinemia syndrome clinicopathologically manifested by fever, hepatosplenomegaly, cytopenias, liver dysfunction, and hemophagocytosis. ...
BACKGROUND: Hemophagocytic lymphohistiocytosis (HLH) is a rare but life-threatening hyperinflammatory/hypercytokinemia syndrome clinicopatho …
2,948 results