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Items: 1 to 20 of 108

2.

Discontinuation of long-term transfusion therapy in patients with sickle cell disease and stroke.

Rana S, Houston PE, Surana N, Shalaby-Rana EI, Castro OL.

J Pediatr. 1997 Nov;131(5):757-60.

PMID:
9403661
3.

Rapid quantitation of hemoglobin S in sickle cell patients using the Variant II Turbo analyzer.

Edwards HD, Sabio H, Shihabi ZK.

Ann Clin Lab Sci. 2009 Winter;39(1):32-7.

PMID:
19201738
4.

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. doi: 10.1111/j.1537-2995.2008.01840.x. No abstract available.

PMID:
19054375
5.

Increased blood requirements during long-term transfusion therapy for sickle cell disease.

Cohen AR, Buchanan GR, Martin M, Ohene-Frempong K.

J Pediatr. 1991 Mar;118(3):405-7. No abstract available.

PMID:
1999779
6.
7.
8.

Chronic transfusion practice for children with sickle cell anaemia and stroke.

Aygun B, McMurray MA, Schultz WH, Kwiatkowski JL, Hilliard L, Alvarez O, Heeney M, Kalinyak K, Lee MT, Miller S, Helms RW, Ware RE; SWiTCH Trial Investigators..

Br J Haematol. 2009 May;145(4):524-8. doi: 10.1111/j.1365-2141.2009.07630.x.

PMID:
19344396
9.

Chronic transfusion practices for prevention of primary stroke in children with sickle cell anemia and abnormal TCD velocities.

Aygun B, Wruck LM, Schultz WH, Mueller BU, Brown C, Luchtman-Jones L, Jackson S, Iyer R, Rogers ZR, Sarnaik S, Thompson AA, Gauger C, Helms RW, Ware RE; TCD With Transfusions Changing to Hydroxyurea (TWiTCH) Trial Investigators..

Am J Hematol. 2012 Apr;87(4):428-30. doi: 10.1002/ajh.23105. No abstract available.

10.

Liquid chromatography used in diagnosis of a rare hemoglobin combination: hemoglobin S/LeporeBoston.

Wessels RA, Rogers BB, Ou CN, Alcorn R, Buffone GJ.

Clin Chem. 1986 May;32(5):903-6.

11.

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 27;333(4):206-13.

12.

Mass spectral analysis of asymmetric hemoglobin hybrids: demonstration of Hb FS (alpha2gammabetaS) in sickle cell disease.

Ofori-Acquah SF, Green BN, Davies SC, Nicolaides KH, Serjeant GR, Layton DM.

Anal Biochem. 2001 Nov 1;298(1):76-82.

PMID:
11673898
13.

Blood transfusion therapy is feasible in a clinical trial setting in children with sickle cell disease and silent cerebral infarcts.

King AA, Noetzel M, White DA, McKinstry RC, Debaun MR.

Pediatr Blood Cancer. 2008 Mar;50(3):599-602.

PMID:
17985350
14.

Blood transfusion in sickle cell disease.

Marouf R.

Hemoglobin. 2011;35(5-6):495-502. doi: 10.3109/03630269.2011.596984.

PMID:
21981466
15.

[Sickle cell disease: laboratory and hemoglobin study].

Wajcman H, Galacteros F.

Bull Soc Pathol Exot. 2001 May;94(2):80-4. Review. French.

PMID:
11475032
16.
17.

Moyamoya syndrome in childhood sickle cell disease: a predictive factor for recurrent cerebrovascular events.

Dobson SR, Holden KR, Nietert PJ, Cure JK, Laver JH, Disco D, Abboud MR.

Blood. 2002 May 1;99(9):3144-50.

18.

Blood transfusions leading to apparent hemoglobin C, S, and O-Arab hemoglobinopathies.

Kozarski TB, Howanitz PJ, Howanitz JH, Lilic N, Chauhan YS.

Arch Pathol Lab Med. 2006 Dec;130(12):1830-3.

PMID:
17149958
19.

Effect of long-term transfusion on growth in children with sickle cell anemia: results of the STOP trial.

Wang WC, Morales KH, Scher CD, Styles L, Olivieri N, Adams R, Brambilla D; STOP Investigators..

J Pediatr. 2005 Aug;147(2):244-7.

PMID:
16126058
20.

A modified transfusion program for prevention of stroke in sickle cell disease.

Cohen AR, Martin MB, Silber JH, Kim HC, Ohene-Frempong K, Schwartz E.

Blood. 1992 Apr 1;79(7):1657-61.

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