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2014 1
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Page 1
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.
JAK2 unmutated erythrocytosis: current diagnostic approach and therapeutic views.
Gangat N, Szuber N, Pardanani A, Tefferi A. Gangat N, et al. Leukemia. 2021 Aug;35(8):2166-2181. doi: 10.1038/s41375-021-01290-6. Epub 2021 May 21. Leukemia. 2021. PMID: 34021251 Free PMC article. Review.
Further investigation in both categories is facilitated by determination of serum erythropoietin level (EPO). Workup for hereditary/congenital erythrocytosis requires documentation of family history and laboratory screening for high-oxygen affinity hemoglobin varian …
Further investigation in both categories is facilitated by determination of serum erythropoietin level (EPO). Workup for hereditary/conge …
Congenital erythrocytosis.
Mallik N, Das R, Malhotra P, Sharma P. Mallik N, et al. Eur J Haematol. 2021 Jul;107(1):29-37. doi: 10.1111/ejh.13632. Epub 2021 Apr 23. Eur J Haematol. 2021. PMID: 33840141 Review.
Erythrocytosis, or increased red cell mass, may be labeled as primary or secondary, depending on whether the molecular defect is intrinsic to the red blood cells/their precursors or extrinsic to them, the latter being typically associated with elevated erythropoietin (EPO) levels …
Erythrocytosis, or increased red cell mass, may be labeled as primary or secondary, depending on whether the molecular defect is intrinsic t …
Congenital erythrocytosis.
McMullin MF. McMullin MF. Int J Lab Hematol. 2016 May;38 Suppl 1:59-65. doi: 10.1111/ijlh.12506. Epub 2016 May 9. Int J Lab Hematol. 2016. PMID: 27161533 Review.
RESULTS: The finding of a known or new molecular variant confirms a diagnosis of congenital erythrocytosis. A congenital erythrocytosis may be an incidental finding but nonspecific symptoms are described. ...CONCLUSIONS: Rare individuals presenting oft …
RESULTS: The finding of a known or new molecular variant confirms a diagnosis of congenital erythrocytosis. A congenital …
Genetic Background of Congenital Erythrocytosis.
McMullin MF. McMullin MF. Genes (Basel). 2021 Jul 28;12(8):1151. doi: 10.3390/genes12081151. Genes (Basel). 2021. PMID: 34440325 Free PMC article. Review.
In many cases, a genetic variant cannot be identified, leaving a group of patients with the label idiopathic erythrocytosis who should be the subject of future investigations. The clinical course in congenital erythrocytosis is hard to evaluate as these are rare cas …
In many cases, a genetic variant cannot be identified, leaving a group of patients with the label idiopathic erythrocytosis who should be th …
Heritable disorders of oxygen sensing.
Semenza GL. Semenza GL. Am J Med Genet A. 2021 Nov;185(11):3334-3339. doi: 10.1002/ajmg.a.62521. Am J Med Genet A. 2021. PMID: 34655169 Review.
Genetic basis of congenital erythrocytosis.
Bento C. Bento C. Int J Lab Hematol. 2018 May;40 Suppl 1:62-67. doi: 10.1111/ijlh.12828. Int J Lab Hematol. 2018. PMID: 29741264 Review.
INTRODUCTION: Congenital Erythrocytosis (CE) represents a rare and heterogeneous clinical entity. ...
INTRODUCTION: Congenital Erythrocytosis (CE) represents a rare and heterogeneous clinical entity. ...
Erythrocytosis: genes and pathways involved in disease development.
Gašperšič J, Kristan A, Kunej T, Zupan IP, Debeljak N. Gašperšič J, et al. Blood Transfus. 2021 Nov;19(6):518-532. doi: 10.2450/2020.0197-20. Epub 2020 Dec 16. Blood Transfus. 2021. PMID: 33370224 Free PMC article. Review.
More rarely, erythrocytosis has a known genetic background, such as for polycythaemia vera and familial erythrocytosis. The majority of cases of polycythaemia vera are associated with acquired variants in JAK2, while familial erythrocytosis is a group …
More rarely, erythrocytosis has a known genetic background, such as for polycythaemia vera and familial erythrocytosis. The ma …
Genetic variants of erythropoietin (EPO) and EPO receptor genes in familial erythrocytosis.
Vočanec D, Prijatelj T, Debeljak N, Kunej T. Vočanec D, et al. Int J Lab Hematol. 2019 Apr;41(2):162-167. doi: 10.1111/ijlh.12949. Epub 2018 Dec 3. Int J Lab Hematol. 2019. PMID: 30507031 Free PMC article. Review.
OBJECTIVES: Erythrocytosis is characterized by the expansion of erythrocyte compartment including elevated red blood cell number, hematocrit, and hemoglobin content. Familial erythrocytosis (FE) is a congenital disorder with different genetic background. ...
OBJECTIVES: Erythrocytosis is characterized by the expansion of erythrocyte compartment including elevated red blood cell number, hematocrit …
49 results