196 related articles for article (PubMed ID: 10174684)
1. Unexpected hemoglobin electrophoresis results following red cell exchange in a sickle cell anemia patient with acute chest syndrome.
Robertson PB; Danielson CF; McCarthy LJ
Transfus Sci; 1997 Jun; 18(2):195-8. PubMed ID: 10174684
[TBL] [Abstract][Full Text] [Related]
2. Transfusion medicine illustrated. Hemoglobin D after a red-cell exchange for sickle-cell disease.
Brecher ME; Park YA; Whinna HC; McClannan LS; Afenyi-Annan A
Transfusion; 2008 Nov; 48(11):2277-8. PubMed ID: 19054375
[No Abstract] [Full Text] [Related]
3. Hemoglobin Variants Acquired Post-Exchange Transfusion in Pediatric Sickle Cell Disease (SCD) Patients.
Pandey S; Cottler-Fox M; Drobena G
Ann Clin Lab Sci; 2015; 45(6):627-30. PubMed ID: 26663791
[TBL] [Abstract][Full Text] [Related]
4. Effect of red cell exchange transfusion on plasma levels of inflammatory mediators in sickle cell patients with acute chest syndrome.
Liem RI; O'Gorman MR; Brown DL
Am J Hematol; 2004 May; 76(1):19-25. PubMed ID: 15114592
[TBL] [Abstract][Full Text] [Related]
5. [Acute pulmonary syndrome and cavernous pulmonary tuberculosis in a patient with sickle cell disease].
Riehl J; Schmitt H; Bergmann D; Fritz A; Sieberth HG
Dtsch Med Wochenschr; 1996 Nov; 121(44):1354, 1355-8. PubMed ID: 8964220
[TBL] [Abstract][Full Text] [Related]
6. Hemoglobin S monitoring on TOSOH G8 in hemoglobin A1c mode in case of urgent red blood cell exchange.
Van Aelst S; Claerhout H; Nackers E; Desmet K; Kieffer D
J Clin Lab Anal; 2018 Sep; 32(7):e22453. PubMed ID: 29667731
[TBL] [Abstract][Full Text] [Related]
7. Acquired hemoglobin variants and exposure to glucose-6-phosphate dehydrogenase deficient red blood cell units during exchange transfusion for sickle cell disease in a patient requiring antigen-matched blood.
Raciti PM; Francis RO; Spitalnik PF; Schwartz J; Jhang JS
J Clin Apher; 2013 Aug; 28(4):325-9. PubMed ID: 23450789
[TBL] [Abstract][Full Text] [Related]
8. Effects of total hemoglobin and hemoglobin S concentration on cerebral blood flow during transfusion therapy to prevent stroke in sickle cell disease.
Hurlet-Jensen AM; Prohovnik I; Pavlakis SG; Piomelli S
Stroke; 1994 Aug; 25(8):1688-92. PubMed ID: 8042222
[TBL] [Abstract][Full Text] [Related]
9. A comparison of conservative and aggressive transfusion regimens in the perioperative management of sickle cell disease. The Preoperative Transfusion in Sickle Cell Disease Study Group.
Vichinsky EP; Haberkern CM; Neumayr L; Earles AN; Black D; Koshy M; Pegelow C; Abboud M; Ohene-Frempong K; Iyer RV
N Engl J Med; 1995 Jul; 333(4):206-13. PubMed ID: 7791837
[TBL] [Abstract][Full Text] [Related]
10. Partial Red Blood Cell Exchange in Children and Young Patients with Sickle Cell Disease: Manual Versus Automated Procedure.
Escobar C; Moniz M; Nunes P; Abadesso C; Ferreira T; Barra A; Lichtner A; Loureiro H; Dias A; Almeida H
Acta Med Port; 2017 Oct; 30(10):727-733. PubMed ID: 29268067
[TBL] [Abstract][Full Text] [Related]
11. Transfusion support for patients with sickle cell disease.
Wallace LR; Thibodeaux SR
Transfus Apher Sci; 2022 Oct; 61(5):103556. PubMed ID: 36100552
[TBL] [Abstract][Full Text] [Related]
12. Low-shear red blood cell oxygen transport effectiveness is adversely affected by transfusion and further worsened by deoxygenation in sickle cell disease patients on chronic transfusion therapy.
Detterich J; Alexy T; Rabai M; Wenby R; Dongelyan A; Coates T; Wood J; Meiselman H
Transfusion; 2013 Feb; 53(2):297-305. PubMed ID: 22882132
[TBL] [Abstract][Full Text] [Related]
13. Improved method for automated red cell exchange in sickle cell disease.
Castro O; Finke-Castro H; Coats D
J Clin Apher; 1986; 3(2):93-9. PubMed ID: 3516980
[TBL] [Abstract][Full Text] [Related]
14. [Management of high risk pregnancy in sickle cell disease by a strategy of prophylactic red cell transfusion or automated red cell exchange].
Driss F; Tertian G; Becquemont L; Haddad B; Cynober T; Raphael M; Tchernia G
Transfus Clin Biol; 2007 Oct; 14(4):386-92. PubMed ID: 18035571
[TBL] [Abstract][Full Text] [Related]
15. Impact of chronic transfusion on incidence of pain and acute chest syndrome during the Stroke Prevention Trial (STOP) in sickle-cell anemia.
Miller ST; Wright E; Abboud M; Berman B; Files B; Scher CD; Styles L; Adams RJ;
J Pediatr; 2001 Dec; 139(6):785-9. PubMed ID: 11743502
[TBL] [Abstract][Full Text] [Related]
16. Determination of hemoglobin saturation in patients with acute sickle chest syndrome: a comparison of arterial blood gases and pulse oximetry.
Kress JP; Pohlman AS; Hall JB
Chest; 1999 May; 115(5):1316-20. PubMed ID: 10334146
[TBL] [Abstract][Full Text] [Related]
17. Variable degrees of suppression of hemoglobin S synthesis in subjects with hemoglobin SS disease on a long-term transfusion regimen.
Zinkham WH; Seidler AJ; Kickler TS
J Pediatr; 1994 Feb; 124(2):215-9. PubMed ID: 8301425
[TBL] [Abstract][Full Text] [Related]
18. How do we monitor hemoglobin S in patients who undergo red blood cell exchange and take voxelotor?
Godbey EA; Anderson MR; M Bachmann L; Sanford KW; Wieditz K; Roseff SD
Transfusion; 2021 Jun; 61(6):1680-1683. PubMed ID: 33880770
[No Abstract] [Full Text] [Related]
19. Oxygen saturation and hemoglobin A content in patients with sickle cell disease undergoing erythrocytapheresis.
Nifong TP; Domen RE
Ther Apher; 2002 Oct; 6(5):390-3. PubMed ID: 12423535
[TBL] [Abstract][Full Text] [Related]
20. Delayed hemolytic transfusion reaction/hyperhemolysis syndrome in children with sickle cell disease.
Talano JA; Hillery CA; Gottschall JL; Baylerian DM; Scott JP
Pediatrics; 2003 Jun; 111(6 Pt 1):e661-5. PubMed ID: 12777582
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]