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Items: 1 to 20 of 105

1.

Quantitative detection of target cells using unghosted cells (UGCs) of DxH 800 (Beckman Coulter).

Lee W, Kim JH, Sung IK, Park SK, Oh ST, Park HH, Park YJ, Kim Y, Oh EJ, Kim M, Park HI, Han K.

Clin Chem Lab Med. 2014 May;52(5):693-9. doi: 10.1515/cclm-2013-0676.

PMID:
24310771
2.

Evaluation of the new red cell parameters on Beckman Coulter DxH800 in distinguishing iron deficiency anaemia from thalassaemia trait.

Ng EH, Leung JH, Lau YS, Ma ES.

Int J Lab Hematol. 2015 Apr;37(2):199-207. doi: 10.1111/ijlh.12262. Epub 2014 May 28.

PMID:
24867505
3.

Red blood cell distribution width index in some hematologic diseases.

Roberts GT, El Badawi SB.

Am J Clin Pathol. 1985 Feb;83(2):222-6.

PMID:
3969961
4.

Reference values and hematologic changes from birth to 5 years in patients with sickle cell disease. Cooperative Study of Sickle Cell Disease.

Brown AK, Sleeper LA, Miller ST, Pegelow CH, Gill FM, Waclawiw MA.

Arch Pediatr Adolesc Med. 1994 Aug;148(8):796-804.

PMID:
7519102
5.

Reticulocyte counting in thalassemic and other conditions with the R-1000 Sysmex analyzer.

Paterakis GS, Voskaridou E, Loutradi A, Rombos J, Loukopoulos D.

Ann Hematol. 1991 Oct;63(4):218-22.

PMID:
1932302
6.

[Automated hematology analysers and spurious counts Part 3. Haemoglobin, red blood cells, cell count and indices, reticulocytes].

Godon A, Genevieve F, Marteau-Tessier A, Zandecki M.

Ann Biol Clin (Paris). 2012 Mar-Apr;70(2):155-68. doi: 10.1684/abc.2012.0685. Review. French.

7.

Discrimination of various thalassemia syndromes and iron deficiency and utilization of reticulocyte measurements in monitoring response to iron therapy.

Winichagoon P, Kumbunlue R, Sirankapracha P, Boonmongkol P, Fucharoen S.

Blood Cells Mol Dis. 2015 Apr;54(4):336-41. doi: 10.1016/j.bcmd.2015.01.010. Epub 2015 Jan 20.

PMID:
25633854
8.

Automated reticulocyte counting and immature reticulocyte fraction measurement. Comparison of ABX PENTRA 120 Retic, Sysmex R-2000, flow cytometry, and manual counts.

Lacombe F, Lacoste L, Vial JP, Briais A, Reiffers J, Boisseau MR, Bernard P.

Am J Clin Pathol. 1999 Nov;112(5):677-86.

PMID:
10549255
9.
10.

Simultaneous measurement of reticulocyte and red blood cell indices in healthy subjects and patients with microcytic and macrocytic anemia.

d'Onofrio G, Chirillo R, Zini G, Caenaro G, Tommasi M, Micciulli G.

Blood. 1995 Feb 1;85(3):818-23.

11.
12.

Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle-cell disease and sickle-cell thalassemia.

Sahli CA, Bibi A, Ouali F, Fredj SH, Dakhlaoui B, Othmani R, Laouini N, Jouini L, Ouenniche F, Siala H, Touhami I, Becher M, Fattoum S, Toumi Nel H, Messaoud T.

Clin Chem Lab Med. 2013 Nov;51(11):2115-24. doi: 10.1515/cclm-2013-0354.

PMID:
23800659
13.

CD36-positive stress reticulocytosis in sickle cell anemia.

Browne PV, Hebbel RP.

J Lab Clin Med. 1996 Apr;127(4):340-7.

PMID:
8656036
14.

Pitted red cell counts in sickle cell disease. Relationship to age, hemoglobin genotype, and splenic size.

Fatunde OJ, Scott RB.

Am J Pediatr Hematol Oncol. 1986 Winter;8(4):329-33.

PMID:
3799933
15.
16.

Reticulocyte hemoglobin: an integrated parameter for evaluation of erythropoietic activity.

Brugnara C, Zelmanovic D, Sorette M, Ballas SK, Platt O.

Am J Clin Pathol. 1997 Aug;108(2):133-42.

PMID:
9260753
17.

Comparison of automated differential blood cell counts from Abbott Sapphire, Siemens Advia 120, Beckman Coulter DxH 800, and Sysmex XE-2100 in normal and pathologic samples.

Meintker L, Ringwald J, Rauh M, Krause SW.

Am J Clin Pathol. 2013 May;139(5):641-50. doi: 10.1309/AJCP7D8ECZRXGWCG.

PMID:
23596116
18.

Red cell indices: differentiation between β-thalassemia trait and iron deficiency anemia and application to sickle cell disease and sickle cell thalassemia.

Sahli CA, Bibi A, Ouali F, Fredj SH, Dakhlaoui B, Othmani R, Laaouini N, Jouini L, Ouenniche F, Siala H, Touhami I, Becher M, Fattoum S, El Houda Toumi N, Messaoud T.

Clin Chem Lab Med. 2013 Aug;51(8):1595-603. doi: 10.1515/cclm-2012-0842.

PMID:
23492565
19.

Sickle cell syndromes. II. The sickle cell anemia-alpha-thalassemia syndrome.

Honig GR, Koshy M, Mason RG, Vida LN.

J Pediatr. 1978 Apr;92(4):556-61.

PMID:
633012
20.

Process to evaluate hematological parameters that reflex to manual differential cell counts in a pediatric institution.

Guarner J, Atuan MA, Nix B, Mishak C, Vejjajiva C, Curtis C, Park S, Mullins R.

Clin Lab. 2010;56(1-2):21-7.

PMID:
20380356

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