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Items: 1 to 20 of 365

1.

Is Hb A2 elevated in adults with sickle-alpha-thalassemia (beta(S)/beta(S); -alpha/-alpha)?

Ballas SK, Gay RN, Chehab FF.

Hemoglobin. 1997 Sep;21(5):405-50.

PMID:
9322076
2.

Beta-cluster haplotypes, alpha-gene status, and hematological data from SS, SC, and S-beta-thalassemia patients in southern California.

Schroeder WA, Powars DR, Kay LM, Chan LS, Huynh V, Shelton JB, Shelton JR.

Hemoglobin. 1989;13(4):325-53.

PMID:
2473969
3.

alpha-thalassemia-2 and the variability of hematological values in children with sickle cell anemia.

Altay C, Gravely ME, Joseph BR, Williams DF.

Pediatr Res. 1981 Aug;15(8):1093-6.

PMID:
7267182
4.

The effect of Hb F and alpha-thalassemia on the red cell indices in sickle cell anemia.

Milner PF, Garbutt GJ, Nolan-Davis LV, Jonah F, Wilson LB, Wilson JT.

Am J Hematol. 1986 Apr;21(4):383-95.

PMID:
2420172
5.

Sickle cell anemia associated with alpha-thalassemia in Malaysian Indians.

Lie-Injo LE, Hassan K, Joishy SK, Lim ML.

Am J Hematol. 1986 Jul;22(3):265-74.

PMID:
2424302
6.

Effects of alpha-thalassemia-2 on the developmental changes of hematological values in children with sickle cell disease from Georgia.

Felice AE, McKie KM, Cleek MP, Marino EM, Kutlar A, McKie VC.

Am J Hematol. 1987 Aug;25(4):389-400.

PMID:
2441597
7.

Gender and haplotype effects upon hematological manifestations of adult sickle cell anemia.

Steinberg MH, Hsu H, Nagel RL, Milner PF, Adams JG, Benjamin L, Fryd S, Gillette P, Gilman J, Josifovska O, et al.

Am J Hematol. 1995 Mar;48(3):175-81.

PMID:
7532353
8.

[Use of capillary electrophoresis to determine hemoglobin A2 in healthy adults and alpha- and beta-thalassemia carriers].

Hua L, Li J, Liu ZY, Zhong HZ, Liao C, Xu XM.

Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2003 Oct;20(5):421-4. Chinese.

PMID:
14556197
9.

Chromatographic measurements of hemoglobin A2 in blood samples that contain sickle hemoglobin.

Shokrani M, Terrell F, Turner EA, Aguinaga MD.

Ann Clin Lab Sci. 2000 Apr;30(2):191-4.

PMID:
10807164
10.

Molecular characteristics of pediatric patients with sickle cell anemia and stroke.

Sarnaik SA, Ballas SK.

Am J Hematol. 2001 Jul;67(3):179-82.

11.

Hemoglobinopathies among the Gond tribal groups of central India; interaction of alpha- and beta-thalassemia with beta chain variants.

Gupta RB, Tiwary RS, Pande PL, Kutlar F, Oner C, Oner R, Huisman TH.

Hemoglobin. 1991;15(5):441-58. Review.

PMID:
1802886
12.

Alpha thalassemia and stroke risk in sickle cell anemia.

Adams RJ, Kutlar A, McKie V, Carl E, Nichols FT, Liu JC, McKie K, Clary A.

Am J Hematol. 1994 Apr;45(4):279-82.

PMID:
8178798
13.

Modification of hemoglobin H disease by sickle trait.

Matthay KK, Mentzer WC Jr, Dozy AM, Kan YW, Bainton DF.

J Clin Invest. 1979 Oct;64(4):1024-32.

14.

Observations on the levels of Hb A2 in patients with different beta-thalassemia mutations and a delta chain variant.

Codrington JF, Li HW, Kutlar F, Gu LH, Ramachandran M, Huisman TH.

Blood. 1990 Sep 15;76(6):1246-9.

15.
16.

Compound heterozygosity for a mild beta (+) and a rare beta(0)-thalassemia allele.

Codrington J, Anijs J, Wisse JH, Codrington FA, Li HW, Kutlar F, Ramachandran M, Huisman TH.

Acta Haematol. 1990;84(3):135-8.

PMID:
2123063
19.

Silent thalassemias: genotypes and phenotypes.

Bianco I, Cappabianca MP, Foglietta E, Lerone M, Deidda G, Morlupi L, Grisanti P, Ponzini D, Rinaldi S, Graziani B.

Haematologica. 1997 May-Jun;82(3):269-80.

20.

beta S haplotypes, alpha-globin gene status, and hematological data of sickle cell disease patients in Guadeloupe (F.W.I.).

Kéclard L, Ollendorf V, Berchel C, Loret H, Mérault G.

Hemoglobin. 1996 Feb;20(1):63-74.

PMID:
8745433

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