Detalhe da pesquisa
1.
[Sickle cell disease, a genetic haemoglobin disease]. / La drépanocytose, une maladie génétique de l'hémoglobine.
Rev Infirm
; 71(277): 16-17, 2022 Jan.
Artigo
em Francês
| MEDLINE | ID: mdl-35090621
2.
A Toll-like receptor 2 genetic variant modulates occurrence of bacterial infections in patients with sickle cell disease.
Br J Haematol
; 185(5): 918-924, 2019 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-30908604
3.
Renin-angiotensin system blockade promotes a cardio-renal protection in albuminuric homozygous sickle cell patients.
Br J Haematol
; 179(5): 820-828, 2017 12.
Artigo
em Inglês
| MEDLINE | ID: mdl-29048108
4.
Family cord blood banking for sickle cell disease: a twenty-year experience in two dedicated public cord blood banks.
Haematologica
; 102(6): 976-983, 2017 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-28302713
5.
Transfusion independence and HMGA2 activation after gene therapy of human ß-thalassaemia.
Nature
; 467(7313): 318-22, 2010 Sep 16.
Artigo
em Inglês
| MEDLINE | ID: mdl-20844535
6.
A hemodynamic study of pulmonary hypertension in sickle cell disease.
N Engl J Med
; 365(1): 44-53, 2011 Jul 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-21732836
7.
Outcomes of adult patients with sickle cell disease admitted to the ICU: a case series*.
Crit Care Med
; 42(7): 1629-39, 2014 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-24674925
8.
Sickle-cell disease stroke throughout life: a retrospective study in an adult referral center.
Am J Hematol
; 89(3): 267-72, 2014 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-24779035
9.
The association of CD81 polymorphisms with alloimmunization in sickle cell disease.
Clin Dev Immunol
; 2013: 937846, 2013.
Artigo
em Inglês
| MEDLINE | ID: mdl-23762099
10.
Hemoglobin sickle cell disease complications: a clinical study of 179 cases.
Haematologica
; 97(8): 1136-41, 2012 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-22315500
11.
Sideroblastic anemia: molecular analysis of the ALAS2 gene in a series of 29 probands and functional studies of 10 missense mutations.
Hum Mutat
; 32(6): 590-7, 2011 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-21309041
12.
Endothelin receptor antagonism prevents hypoxia-induced mortality and morbidity in a mouse model of sickle-cell disease.
J Clin Invest
; 118(5): 1924-33, 2008 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-18382768
13.
Iron restriction is an important treatment of hemoglobin SC disease.
Am J Hematol
; 91(7): E320, 2016 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-27059108
14.
Clinical follow-up of hydroxyurea-treated adults with sickle cell disease.
Acta Haematol
; 125(3): 145-52, 2011.
Artigo
em Inglês
| MEDLINE | ID: mdl-21196716
15.
Strong association between a new marker of hemolysis and glomerulopathy in sickle cell anemia.
Blood Cells Mol Dis
; 45(4): 289-92, 2010 Dec 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-20833087
16.
Complications and treatment of patients with ß-thalassemia in France: results of the National Registry.
Haematologica
; 95(5): 724-9, 2010 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-20007138
17.
An Evaluation of Three Ways of Communicating Carrier Status Results to the Parents of Children in a Neonatal Sickle Cell Screening Programme.
Front Pediatr
; 8: 300, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-32637386
18.
Polymorphisms in Inflammatory Genes Modulate Clinical Complications in Patients With Sickle Cell Disease.
Front Immunol
; 11: 2041, 2020.
Artigo
em Inglês
| MEDLINE | ID: mdl-33013863
19.
Does regular blood transfusion prevent progression of cerebrovascular lesions in children with sickle cell disease?
Ann Hematol
; 88(8): 785-8, 2009 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-19107481
20.
Influence of sickle cell disease and treatment with hydroxyurea on sperm parameters and fertility of human males.
Haematologica
; 93(7): 988-93, 2008 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-18508803