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Items: 1 to 20 of 117

1.

Asymptomatic elevation of the hyperchromic red blood cell subpopulation is associated with decreased red cell deformability.

Deuel JW, Lutz HU, Misselwitz B, Goede JS.

Ann Hematol. 2012 Sep;91(9):1427-34. doi: 10.1007/s00277-012-1467-5. Epub 2012 Apr 18.

PMID:
22526368
2.

Temporal differences in membrane loss lead to distinct reticulocyte features in hereditary spherocytosis and in immune hemolytic anemia.

Da Costa L, Mohandas N, Sorette M, Grange MJ, Tchernia G, Cynober T.

Blood. 2001 Nov 15;98(10):2894-9.

4.

Experience with eosin-5'-maleimide as a diagnostic tool for red cell membrane cytoskeleton disorders.

Kedar PS, Colah RB, Kulkarni S, Ghosh K, Mohanty D.

Clin Lab Haematol. 2003 Dec;25(6):373-6.

PMID:
14641141
5.
6.

Additional erythrocytic and reticulocytic parameters helpful for diagnosis of hereditary spherocytosis: results of a multicentre study.

Mullier F, Lainey E, Fenneteau O, Da Costa L, Schillinger F, Bailly N, Cornet Y, Chatelain C, Dogne JM, Chatelain B.

Ann Hematol. 2011 Jul;90(7):759-68. doi: 10.1007/s00277-010-1138-3. Epub 2010 Dec 22.

PMID:
21181161
7.
9.
10.

[Silent forms of hereditary spherocytosis].

Brabec V, Cermák J, Jarolím P.

Vnitr Lek. 1999 Oct;45(10):594-7. Czech.

PMID:
10951867
12.

Diagnostic tool for red blood cell membrane disorders: Assessment of a new generation ektacytometer.

Da Costa L, Suner L, Galimand J, Bonnel A, Pascreau T, Couque N, Fenneteau O, Mohandas N; Society of Hematology and Pediatric Immunology (SHIP) group; French Society of Hematology (SFH).

Blood Cells Mol Dis. 2016 Jan;56(1):9-22. doi: 10.1016/j.bcmd.2015.09.001. Epub 2015 Sep 16.

13.

Screening and confirmation of hereditary spherocytosis in children using a CELL-DYN Sapphire haematology analyser.

Rooney S, Hoffmann JJ, Cormack OM, McMahon C.

Int J Lab Hematol. 2015 Feb;37(1):98-104. doi: 10.1111/ijlh.12245. Epub 2014 Apr 17.

PMID:
24739214
14.

Using the eosin-5-maleimide binding test in the differential diagnosis of hereditary spherocytosis and hereditary pyropoikilocytosis.

King MJ, Telfer P, MacKinnon H, Langabeer L, McMahon C, Darbyshire P, Dhermy D.

Cytometry B Clin Cytom. 2008 Jul;74(4):244-50. doi: 10.1002/cyto.b.20413.

15.

The differential diagnosis of hemolytic anemias.

Costea N.

Med Clin North Am. 1973 Mar;57(2):289-302. Review. No abstract available.

PMID:
4570931
16.

Analyzing red blood cell-deformability distributions.

Dobbe JG, Hardeman MR, Streekstra GJ, Strackee J, Ince C, Grimbergen CA.

Blood Cells Mol Dis. 2002 May-Jun;28(3):373-84.

PMID:
12367581
17.

Flow cytometric detection of erythrocyte osmotic fragility.

Won DI, Suh JS.

Cytometry B Clin Cytom. 2009 Mar;76(2):135-41. doi: 10.1002/cyto.b.20448.

18.

The xerocytosis of Hb SC disease.

Ballas SK, Larner J, Smith ED, Surrey S, Schwartz E, Rappaport EF.

Blood. 1987 Jan;69(1):124-30.

19.
20.

Does higher red blood cell (RBC) lactate transporter activity explain impaired RBC deformability in sickle cell trait?

Connes P, Sara F, Hardy-Dessources MD, Etienne-Julan M, Hue O.

Jpn J Physiol. 2005 Dec;55(6):385-7. Epub 2006 Jan 31.

PMID:
16441976

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