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Quoted phrase not found in phrase index: "Physiological polycythemia"
Page 1
Spurious polycythemia.
Weinreb NJ, Shih CF. Weinreb NJ, et al. Semin Hematol. 1975 Oct;12(4):397-407. Semin Hematol. 1975. PMID: 1198127
Spurious polycythemia is not a primary disease process. It sometimes may be nothing more than an unusual, but normal, physiologic state. ...Nonhematologic parameters, particularly hypertension, are the major factors of significance in the substantial cardiovascular …
Spurious polycythemia is not a primary disease process. It sometimes may be nothing more than an unusual, but normal, physiologic
Dysregulated iron metabolism in polycythemia vera: etiology and consequences.
Ginzburg YZ, Feola M, Zimran E, Varkonyi J, Ganz T, Hoffman R. Ginzburg YZ, et al. Leukemia. 2018 Oct;32(10):2105-2116. doi: 10.1038/s41375-018-0207-9. Epub 2018 Jul 24. Leukemia. 2018. PMID: 30042411 Free PMC article. Review.
Polycythemia vera (PV) is a chronic myeloproliferative neoplasm. Virtually all PV patients are iron deficient at presentation and/or during the course of their disease. The co-existence of iron deficiency and polycythemia presents a physiological disco
Polycythemia vera (PV) is a chronic myeloproliferative neoplasm. Virtually all PV patients are iron deficient at presentation and/or
Hematologic disorders in the elderly.
Walsh JR. Walsh JR. West J Med. 1981 Dec;135(6):446-54. West J Med. 1981. PMID: 6801866 Free PMC article. Review.
The most prevalent type of leukemia in the elderly is chronic lymphocytic leukemia. A benign asymptomatic course requires no therapy, but aggressive disease requires treatment. ...After definitive diagnosis, phlebotomy therapy should be considered for both polycythemia
The most prevalent type of leukemia in the elderly is chronic lymphocytic leukemia. A benign asymptomatic course requires no therapy, …
Chronic myeloproliferative disorders (CMPD).
Burkhardt R, Bartl R, Jäger K, Frisch B, Kettner G, Mahl G, Sund M. Burkhardt R, et al. Pathol Res Pract. 1984 Nov;179(2):131-86. doi: 10.1016/S0344-0338(84)80124-7. Pathol Res Pract. 1984. PMID: 6395125 Review.
The predominant proliferative cell line characterizes the classical entities of PV, PT and CML, and their different prognoses. Pure erythrocytic and megakaryocytic proliferations are more compatible with sustained physiologic bone marrow functions than granulocytic …
The predominant proliferative cell line characterizes the classical entities of PV, PT and CML, and their different prognoses. Pure e …
"Benign erythrocytosis" and other familial and congenital polycythemias.
Prchal JT, Sokol L. Prchal JT, et al. Eur J Haematol. 1996 Oct;57(4):263-8. Eur J Haematol. 1996. PMID: 8982288 Review.
The term familial and congenital polycythemia encompasses a heterogeneous group of disorders with the common characteristic of an absolute increased red cell mass since birth and/or similar phenotype also present in relatives. ...Various designations have been used in the …
The term familial and congenital polycythemia encompasses a heterogeneous group of disorders with the common characteristic of an abs …
Myeloproliferative neoplasms.
Publicover A, Medd P. Publicover A, et al. Clin Med (Lond). 2013 Apr;13(2):188-92. doi: 10.7861/clinmedicine.13-2-188. Clin Med (Lond). 2013. PMID: 23681871 Free PMC article.
As more than one mutation is involved, and as JAK2 has a necessary physiological role (unlike BCR-ABL), the development of targeted therapy remains a challenge. ...
As more than one mutation is involved, and as JAK2 has a necessary physiological role (unlike BCR-ABL), the development of targeted t …
The potential impact of anaemia of chronic disease in COPD.
Similowski T, Agustí A, MacNee W, Schönhofer B. Similowski T, et al. Eur Respir J. 2006 Feb;27(2):390-6. doi: 10.1183/09031936.06.00143704. Eur Respir J. 2006. PMID: 16452598 Free article. Review.
Although chronic obstructive pulmonary disease (COPD) is "traditionally" associated with polycythaemia, the systemic inflammation that is now recognised as a feature of COPD makes it a possible cause of ACD. ...These preliminary evidences point to the need to study the pre …
Although chronic obstructive pulmonary disease (COPD) is "traditionally" associated with polycythaemia, the systemic inflammation tha …
Neonatal polycythemia: prevalence, risk factors and predictors of severity.
Martins AS, Flor-DE-Lima F, Rocha G, Soares P, Machado AP, Guimarães MH. Martins AS, et al. Minerva Pediatr (Torino). 2024 Feb;76(1):64-71. doi: 10.23736/S2724-5276.21.05851-1. Minerva Pediatr (Torino). 2024. PMID: 38376233
BACKGROUND: Polycythemia is a disorder with several causes and risk factors. The clinical presentation is variable, ranging from asymptomatic newborns to cases with severe physiological changes. The aim of this study was to assess the prevalence, risk factors and …
BACKGROUND: Polycythemia is a disorder with several causes and risk factors. The clinical presentation is variable, ranging from asym …
Idiopathic erythrocytosis, diagnosis and clinical management.
Pearson TC, Messinezy M. Pearson TC, et al. Pathol Biol (Paris). 2001 Mar;49(2):170-7. doi: 10.1016/s0369-8114(00)00025-0. Pathol Biol (Paris). 2001. PMID: 11317965 Review.
By definition, idiopathic erythrocytosis (IE) applies to a group of patients characterised by having a measured RCM above their predicted normal range (an absolute erythrocytosis) and following investigation do not have a form of primary or secondary erythrocytosis. Patien …
By definition, idiopathic erythrocytosis (IE) applies to a group of patients characterised by having a measured RCM above their predicted
Rheology of the absolute polycythaemias.
Pearson TC. Pearson TC. Baillieres Clin Haematol. 1987 Sep;1(3):637-64. doi: 10.1016/s0950-3536(87)80019-7. Baillieres Clin Haematol. 1987. PMID: 3327560 Review.
The absolute polycythaemias include all patients who have a raised red cell mass. They may be divided by clinical and laboratory investigation into: primary proliferative polycythaemia (polycythaemia rubra vera), secondary polycythaemias, and idiopathi …
The absolute polycythaemias include all patients who have a raised red cell mass. They may be divided by clinical and laboratory inve …
42 results