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Items: 1 to 20 of 197

1.

Common α-globin variants modify hematologic and other clinical phenotypes in sickle cell trait and disease.

Raffield LM, Ulirsch JC, Naik RP, Lessard S, Handsaker RE, Jain D, Kang HM, Pankratz N, Auer PL, Bao EL, Smith JD, Lange LA, Lange EM, Li Y, Thornton TA, Young BA, Abecasis GR, Laurie CC, Nickerson DA, McCarroll SA, Correa A, Wilson JG; NHLBI Trans-Omics for Precision Medicine (TOPMed) Consortium, Hematology & Hemostasis, Diabetes, and Structural Variation TOPMed Working Groups, Lettre G, Sankaran VG, Reiner AP.

PLoS Genet. 2018 Mar 28;14(3):e1007293. doi: 10.1371/journal.pgen.1007293. eCollection 2018 Mar.

2.

The co-inheritance of alpha-thalassemia and sickle cell anemia is associated with better hematological indices and lower consultations rate in Cameroonian patients and could improve their survival.

Rumaney MB, Ngo Bitoungui VJ, Vorster AA, Ramesar R, Kengne AP, Ngogang J, Wonkam A.

PLoS One. 2014 Jun 30;9(6):e100516. doi: 10.1371/journal.pone.0100516. eCollection 2014.

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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.

6.

Sickle Cell Trait and Renal Function in Hispanics in the United States: The Northern Manhattan Study.

Dueker ND, Della-Morte D, Rundek T, Sacco RL, Blanton SH.

Ethn Dis. 2017 Jan 19;27(1):11-14. doi: 10.18865/ed.27.1.11.

7.

Fetal hemoglobin and alpha thalassemia modulate the phenotypic expression of HbSD-Punjab.

Patel DK, Purohit P, Dehury S, Das P, Dutta A, Meher S, Patel S, Bag S, Mashon RS, Das K.

Int J Lab Hematol. 2014 Aug;36(4):444-50. doi: 10.1111/ijlh.12165. Epub 2013 Nov 19.

PMID:
24245819
8.

Sickle cell anemia--molecular diagnosis and prenatal counseling: SGPGI experience.

Kumar R, Panigrahi I, Dalal A, Agarwal S.

Indian J Pediatr. 2012 Jan;79(1):68-74. doi: 10.1007/s12098-011-0510-1. Epub 2011 Jun 29.

PMID:
21713598
9.

Molecular analysis and association with clinical and laboratory manifestations in children with sickle cell anemia.

Camilo-Araújo RF, Amancio OM, Figueiredo MS, Cabanãs-Pedro AC, Braga JA.

Rev Bras Hematol Hemoter. 2014 Sep-Oct;36(5):334-9. doi: 10.1016/j.bjhh.2014.06.002. Epub 2014 Jul 9.

10.

Discordance between self-report and genetic confirmation of sickle cell disease status in African-American adults.

Bean CJ, Hooper WC, Ellingsen D, DeBaun MR, Sonderman J, Blot WJ.

Public Health Genomics. 2014;17(3):169-72. doi: 10.1159/000360260. Epub 2014 Mar 28.

11.

Genetic Modifiers of Sickle Cell Disease: A Genotype-Phenotype Relationship Study in a Cohort of 82 Children on Mayotte Island.

Muszlak M, Pissard S, Badens C, Chamouine A, Maillard O, Thuret I.

Hemoglobin. 2015;39(3):156-61. doi: 10.3109/03630269.2015.1023897. Epub 2015 Mar 25.

PMID:
25806420
12.

Sickle cell syndromes. I. Hemoglobin SC-alpha-thalassemia.

Honig GR, Gunay U, Mason RG, Vida LN, Ferenc C.

Pediatr Res. 1976 Jun;10(6):613-20.

PMID:
1272638
13.

The alpha-globin genotype does not influence sickle cell disease severity in a retrospective cross-validation study of the pediatric severity score.

Joly P, Pondarré C, Bardel C, Francina A, Martin C.

Eur J Haematol. 2012 Jan;88(1):61-7. doi: 10.1111/j.1600-0609.2011.01705.x. Epub 2011 Nov 15.

PMID:
21910753
14.
15.

Sickle hemoglobin (HbS) allele and sickle cell disease: a HuGE review.

Ashley-Koch A, Yang Q, Olney RS.

Am J Epidemiol. 2000 May 1;151(9):839-45. Review.

PMID:
10791557
16.

A second generation transgenic mouse model expressing both hemoglobin S (HbS) and HbS-Antilles results in increased phenotypic severity.

Fabry ME, Sengupta A, Suzuka SM, Costantini F, Rubin EM, Hofrichter J, Christoph G, Manci E, Culberson D, Factor SM, Nagel RL.

Blood. 1995 Sep 15;86(6):2419-28.

PMID:
7662990
17.

Association of classical markers and establishment of the dyslipidemic sub-phenotype of sickle cell anemia.

Aleluia MM, da Guarda CC, Santiago RP, Fonseca TC, Neves FI, de Souza RQ, Farias LA, Pimenta FA, Fiuza LM, Pitanga TN, Ferreira JR, Adorno EV, Cerqueira BA, Gonçalves MS.

Lipids Health Dis. 2017 Apr 11;16(1):74. doi: 10.1186/s12944-017-0454-1.

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Evidence that microdeletions in the alpha globin gene protect against the development of sickle cell glomerulopathy in humans.

Guasch A, Zayas CF, Eckman JR, Muralidharan K, Zhang W, Elsas LJ.

J Am Soc Nephrol. 1999 May;10(5):1014-9.

20.

[Beta globin haplotypes in hemoglobin S carriers in Colombia].

Durán CL, Morales OL, Echeverri SJ, Isaza M.

Biomedica. 2012 Jan-Mar;32(1):103-11. doi: 10.1590/S0120-41572012000100012. Spanish.

PMID:
23235792

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