Results 101 to 110 of about 7,240 (211)

Heterozygous Hemoglobin Sherwood Forest Causing Polycythemia

Case Reports in Hematology, 2017
Hemoglobin (Hb) Sherwood Forest is a rare high-affinity hemoglobin first described in 1977, arising from an Arg to Thr substitution at codon 104 of the beta chain.
Vikram M. Raghunathan, James N. Butera, Diana O. Treaba   +2 more
doaj   +1 more source

Is altitude‐induced polycythaemia an unintended evolutionary mistake?

Experimental Physiology, Volume 111, Issue 7, Page 3117-3121, 1 July 2026.
Peter D. Wagner, Tatum S. Simonson
wiley   +1 more source

Cyanotic congenital heart disease (CCHD) with symptomatic erythrocytosis. [PDF]

, 2007
Secondary erythrocytosis of cyanotic congenital heart disease (CCHD) is pathologically different from primary erythrocytosis of polycythemia vera (PV).
Hoover, Donald R, Rose, Shelonitda S, Saidi, Parvin, Shah, Ashish A   +3 more
core  

Cllinical and laboratory profiles of blood donors with erythrocytosis [PDF]

, 2016
In blood banking setting, every blood donors are mandatory to have their haemoglobin (Hb) values tested before blood donation procedure. In current practice, donors with high Hb will be deferred from blood donation.
Kamaruzzaman, Siti Fatimah Mohamed
core  

Relative Erythrocytosis [PDF]

British Journal of Haematology, 2002
openaire   +2 more sources

Pediatric Familial Erythrocytosis Type 2 due to a Homozygous von Hippel–Lindau Variant Presenting with Cerebral Infarcts

Journal of Applied Hematology
Familial erythrocytosis type 2 (ECYT2), also known as Chuvash polycythemia, is a rare autosomal recessive disorder caused by pathogenic variants in the von Hippel–Lindau (VHL) gene, resulting in dysregulated oxygen sensing and increased erythropoietin ...
Sagar Venkatesh, Usha Bangalore Kantharajanna, Dhanalakshmi Kumble, Swathi Govind Naik, Pratibha Gopalakrishna   +4 more
doaj   +1 more source

Elevated and Unexplained: Navigating Erythrocytosis and Thrombocytosis [PDF]

Elevated and Unexplained: Navigating Erythrocytosis and Thrombocytosis. Dr. Aniket Vijay Rao, Internal Medicine Resident Program, PGY2, Rochester General Hospital; Dr. Peter Kouides, Hematology/Oncology Department, Rochester General Hospital Objectives:
Kouides, Peter A, Rao, Aniket-Vijay
core  

Case report: Childhood erythrocytosis due to hypermanganesemia caused by homozygous SLC30A10 mutation

Frontiers in Hematology
We present a rare case of erythrocytosis due to a homozygous SLC30A10 mutation, causative of Hypermanganesemia with Dystonia, Polycythemia, and Cirrhosis (HMDPC).
Tiziana Coppola, Hannah Hughes, Paul T. Finch, Joshua A. Hess, Steve Wu, Steve Wu, Carlos E. Prada, Carlos E. Prada, Alexander G. Miethke, Alexander G. Miethke, Wenying Zhang, Wenying Zhang, Theodosia A. Kalfa, Theodosia A. Kalfa   +13 more
doaj   +1 more source

A case of renal cell carcinoma with erythrocytosis [PDF]

, 1992
A case of renal cell carcinoma with erythrocytosis is presented. A 51-year-old man was referred to us for evaluation of left renal mass. Laboratory data revealed marked erythrocytosis and elevated serum erythropoietin level.
白波瀬, 敏明, 諸井, 誠司, 金丸, 洋史, 木原, 裕次   +3 more
core  

Utility of next-generation sequencing in identifying congenital erythrocytosis in patients with idiopathic erythrocytosis [PDF]

Background: Congenital erythrocytosis (CE) is increasingly recognized as the cause of erythrocytosis in patients in whom polycythemia vera and secondary acquired causes have been excluded. The aim of our study was to determine possible genetic background
Kristan, Aleša, Maver, Aleš, Pajič, Tadej, Kraljić, Nika, Debeljak, Nataša, Anžej Doma, Saša, Preložnik Zupan, Irena   +6 more
core   +1 more source