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

Year Number of Results
1904 1
1905 1
1907 2
1908 2
1909 4
1910 1
1912 2
1913 3
1914 2
1915 1
1916 1
1918 2
1919 2
1920 2
1921 1
1923 4
1925 3
1926 3
1927 3
1928 3
1929 2
1930 3
1931 7
1932 5
1933 4
1934 2
1935 2
1936 4
1938 2
1939 2
1940 2
1941 1
1942 5
1944 1
1945 11
1946 12
1947 26
1948 40
1949 48
1950 63
1951 82
1952 93
1953 86
1954 80
1955 86
1956 67
1957 89
1958 86
1959 95
1960 103
1961 139
1962 120
1963 192
1964 278
1965 203
1966 174
1967 218
1968 265
1969 228
1970 192
1971 241
1972 248
1973 226
1974 217
1975 236
1976 193
1977 188
1978 197
1979 200
1980 191
1981 231
1982 191
1983 223
1984 202
1985 189
1986 207
1987 186
1988 194
1989 228
1990 198
1991 203
1992 201
1993 188
1994 223
1995 160
1996 170
1997 202
1998 173
1999 153
2000 167
2001 157
2002 191
2003 199
2004 227
2005 238
2006 298
2007 339
2008 313
2009 280
2010 300
2011 360
2012 349
2013 405
2014 404
2015 432
2016 459
2017 391
2018 365
2019 395
2020 501
2021 544
2022 514
2023 455
2024 225

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16,536 results

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Page 1
Polycythemia and chorea.
Marvi MM, Lew MF. Marvi MM, et al. Handb Clin Neurol. 2011;100:271-6. doi: 10.1016/B978-0-444-52014-2.00019-7. Handb Clin Neurol. 2011. PMID: 21496586 Review.
Polycythemia vera is a sporadic myeloproliferative disorder of increased red blood cell mass affecting multiple organ systems. ...Chorea has also been uncommonly reported as arising from secondary causes of polycythemia; however, the underlying pathophysiology has n …
Polycythemia vera is a sporadic myeloproliferative disorder of increased red blood cell mass affecting multiple organ systems. ...Cho …
Polycythemia: evaluation and management.
Hocking WG, Golde DW. Hocking WG, et al. Blood Rev. 1989 Mar;3(1):59-65. doi: 10.1016/0268-960x(89)90026-x. Blood Rev. 1989. PMID: 2650777 Review.
The approach to diagnosis and classification of patients with polycythemia is reviewed with presentation of general and specific guidelines for the management of patients with polycythemia vera, secondary polycythemia and relative polycythemia....
The approach to diagnosis and classification of patients with polycythemia is reviewed with presentation of general and specific guid …
Polycythemia and oxygen sensing.
Maran J, Prchal J. Maran J, et al. Pathol Biol (Paris). 2004 Jun;52(5):280-4. doi: 10.1016/j.patbio.2004.02.006. Pathol Biol (Paris). 2004. PMID: 15217714 Review.
Polycythemia vera (PV) is the most common primary polycythemia. PV bone marrow progenitors cells can form erythroid colonies in the absence of exogenous erythropoietin in vitro. These endogenous erythroid colonies (EEC) are useful in differentiating PV and secondary …
Polycythemia vera (PV) is the most common primary polycythemia. PV bone marrow progenitors cells can form erythroid colonies i …
Polycythemia in the newborn.
Upadhyay A, Aggarwal R, Deorari AK, Paul VK. Upadhyay A, et al. Indian J Pediatr. 2002 Jan;69(1):79-82. doi: 10.1007/BF02723782. Indian J Pediatr. 2002. PMID: 11876126 Review.
Polycythemia is defined as a venous hematocrit above 65%. The relationship between viscosity and hematocrit is almost linear till 65% and exponential thereafter. ...The hematocrit in a newborn peaks at 2 hours of age and decreases gradually after that. The etiology of p …
Polycythemia is defined as a venous hematocrit above 65%. The relationship between viscosity and hematocrit is almost linear till 65% …
Neonatal polycythemia and hyperviscosity.
Sarkar S, Rosenkrantz TS. Sarkar S, et al. Semin Fetal Neonatal Med. 2008 Aug;13(4):248-55. doi: 10.1016/j.siny.2008.02.003. Semin Fetal Neonatal Med. 2008. PMID: 18424246 Review.
Although polycythemia can reflect normal fetal adaptation, it has been thought to be responsible for abnormalities in the neonate. Polycythemia and hyperviscosity are associated with blood-flow changes in some organs, which alter their function. ...
Although polycythemia can reflect normal fetal adaptation, it has been thought to be responsible for abnormalities in the neonate. …
Polycythemia vera and other primary polycythemias.
Prchal JT. Prchal JT. Curr Opin Hematol. 2005 Mar;12(2):112-6. doi: 10.1097/01.moh.0000154029.05396.d2. Curr Opin Hematol. 2005. PMID: 15725900 Review.
PURPOSE OF REVIEW: Diagnosis and therapy of polycythemia vera are controversial since the molecular basis of polycythemia vera remains unknown. ...Our knowledge of cellular responses to hypoxia has recently exploded and led to the elucidation of the molecular basis …
PURPOSE OF REVIEW: Diagnosis and therapy of polycythemia vera are controversial since the molecular basis of polycythemia vera …
[Inherited primitive and secondary polycythemia].
Barba T, Boileau JC, Pasquet F, Hot A, Pavic M. Barba T, et al. Rev Med Interne. 2016 Jul;37(7):460-5. doi: 10.1016/j.revmed.2015.12.022. Epub 2016 Jan 27. Rev Med Interne. 2016. PMID: 26827274 Review. French.
Myeloproliferative disorders and secondary polycythemia cover most of the polycythemia cases encountered in daily practice. Inherited polycythemias are rare entities that have to be suspected when the classical causes of acquired polycythemia have been …
Myeloproliferative disorders and secondary polycythemia cover most of the polycythemia cases encountered in daily practice. In …
Secondary erythrocytosis.
Babakhanlou R, Verstovsek S, Pemmaraju N, Rojas-Hernandez CM. Babakhanlou R, et al. Expert Rev Hematol. 2023 Apr;16(4):245-251. doi: 10.1080/17474086.2023.2192475. Epub 2023 Mar 23. Expert Rev Hematol. 2023. PMID: 36927204 Review.
[Inherited polycythemia].
Pavic M, Rousset H. Pavic M, et al. Rev Med Interne. 2003 Aug;24(8):514-21. doi: 10.1016/s0248-8663(03)00059-6. Rev Med Interne. 2003. PMID: 12888172 Review. French.
PURPOSE: The majority of polycythemias occurs sporadically without any other familial case. Very occasionally polycythemia finds a familial support. ...FUTURE PROSPECTS AND PROJECTS: Progressively, the part of really idiopathic polycythemias is smaller and sm …
PURPOSE: The majority of polycythemias occurs sporadically without any other familial case. Very occasionally polycythemia fin …
Molecular basis for polycythemia.
Prchal JF, Prchal JT. Prchal JF, et al. Curr Opin Hematol. 1999 Mar;6(2):100-9. doi: 10.1097/00062752-199903000-00008. Curr Opin Hematol. 1999. PMID: 10088640 Review.
This overview concentrates on familial and congenital polycythemias in the context of other polycythemic disorders, with emphasis on those with established molecular lesions. ...The most common primary polycythemia, polycythemia vera, as well as the only like …
This overview concentrates on familial and congenital polycythemias in the context of other polycythemic disorders, with emphasis on …
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