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1.
Influence of UGT1A1 promoter polymorphism, α-thalassemia and ßs haplotype in bilirubin levels and cholelithiasis in a large sickle cell anemia cohort.
Ann Hematol
; 100(4): 903-911, 2021 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-33523291
2.
High levels of proinflammatory cytokines IL-6 and IL-8 are associated with a poor clinical outcome in sickle cell anemia.
Ann Hematol
; 99(5): 947-953, 2020 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-32140892
3.
Influence of alpha thalassemia on clinical and laboratory parameters among nigerian children with sickle cell anemia.
J Clin Lab Anal
; 33(2): e22656, 2019 Feb.
Artículo
en Inglés
| MEDLINE | ID: mdl-30129219
4.
Thalassemia major phenotype caused by HB Zürich-Albisrieden [α2 59(E8) Gly > Arg (HBA2:C.178G > C)] in a Brazilian child.
Pediatr Blood Cancer
; 65(12): e27413, 2018 12.
Artículo
en Inglés
| MEDLINE | ID: mdl-30151892
5.
Coinheritance of Hb Bristol-Alesha [ß67(E11)ValâMet; HBB: c.202G>A] and the α212 Patchwork Allele in a Brazilian Child with Severe Congenital Hemolytic Anemia.
Hemoglobin
; 41(3): 203-208, 2017 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-28670945
6.
Rare α0-thalassemia deletions detected by MLPA in five unrelated Brazilian patients.
Genet Mol Biol
; 40(4): 768-773, 2017.
Artículo
en Inglés
| MEDLINE | ID: mdl-28981562
7.
Reduced rate of sickle-related complications in Brazilian patients carrying HbF-promoting alleles at the BCL11A and HMIP-2 loci.
Br J Haematol
; 173(3): 456-60, 2016 05.
Artículo
en Inglés
| MEDLINE | ID: mdl-26888013
8.
Abnormal expression of inflammatory genes in placentas of women with sickle cell anemia and sickle hemoglobin C disease.
Ann Hematol
; 95(11): 1859-67, 2016 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-27546026
9.
An inherited mutation leading to production of only the short isoform of GATA-1 is associated with impaired erythropoiesis.
Nat Genet
; 38(7): 807-12, 2006 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-16783379
10.
Influence of the ßs haplotype and α-thalassemia on stroke development in a Brazilian population with sickle cell anaemia.
Ann Hematol
; 93(7): 1123-9, 2014 Jul.
Artículo
en Inglés
| MEDLINE | ID: mdl-24493127
11.
Cytomegalovirus (CMV) genotype in allogeneic hematopoietic stem cell transplantation.
BMC Infect Dis
; 13: 310, 2013 Jul 10.
Artículo
en Inglés
| MEDLINE | ID: mdl-23841715
12.
Functional characterization of compound heterozygosity Hb S/Hb Deer Lodge in Brazil.
Hematol Transfus Cell Ther
; 2023 Dec 07.
Artículo
en Inglés
| MEDLINE | ID: mdl-38307823
13.
Hb S-São Paulo: a new sickling hemoglobin with stable polymers and decreased oxygen affinity.
Arch Biochem Biophys
; 519(1): 23-31, 2012 Mar 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-22244832
14.
Surveillance of active human cytomegalovirus infection in hematopoietic stem cell transplantation (HLA sibling identical donor): search for optimal cutoff value by real-time PCR.
BMC Infect Dis
; 10: 147, 2010 Jun 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-20515464
15.
Angiogenesis-Related Genes in Endothelial Progenitor Cells May Be Involved in Sickle Cell Stroke.
J Am Heart Assoc
; 9(3): e014143, 2020 02 04.
Artículo
en Inglés
| MEDLINE | ID: mdl-32009522
16.
PIP4KIIA and beta-globin: transcripts differentially expressed in reticulocytes and associated with high levels of Hb H in two siblings with Hb H disease.
Eur J Haematol
; 83(5): 490-3, 2009 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-19656170
17.
Two new unstable haemoglobins leading to chronic haemolytic anaemia: Hb Caruaru [beta122 (GH5) Phe-->Ser], a probable case of germ line mutation, and Hb Olinda [beta22 (B4) - 25 (B7)], a deletion of a 12 base-pair sequence.
Eur J Haematol
; 83(4): 378-82, 2009 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-19527272
18.
Prevalence of HIV-1 subtypes in Brazilian children with perinatally acquired infection.
J Int Assoc Physicians AIDS Care (Chic)
; 8(2): 106-12, 2009.
Artículo
en Inglés
| MEDLINE | ID: mdl-19264724
19.
Thalassemia major phenotypes secondary to the association of ß 5'UTR +20(C â T) allele with ß 39(C â T).
Eur J Haematol
; 89(3): 273-5, 2012 Sep.
Artículo
en Inglés
| MEDLINE | ID: mdl-22672614
20.
Featured Article: Modulation of fetal hemoglobin in hereditary persistence of fetal hemoglobin deletion type-2, compared to Sicilian 뫧-thalassemia, by BCL11A and SOX6-targeting microRNAs.
Exp Biol Med (Maywood)
; 242(3): 267-274, 2017 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-27591578