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1.
Brain-derived neurotrophic factor levels in pediatric sickle cell disease.
Pediatr Blood Cancer;
67(2): e28076, 2020 02.
Artículo
en Inglés
| MEDLINE | ID: mdl-31736231
2.
Genome-wide association study to identify variants associated with acute severe vaso-occlusive pain in sickle cell anemia.
Blood;
130(5): 686-688, 2017 08 03.
Artículo
en Inglés
| MEDLINE | ID: mdl-28584135
3.
Heme oxygenase-1 gene promoter polymorphism is associated with reduced incidence of acute chest syndrome among children with sickle cell disease.
Blood;
120(18): 3822-8, 2012 Nov 01.
Artículo
en Inglés
| MEDLINE | ID: mdl-22966170
4.
Acute chest syndrome is associated with single nucleotide polymorphism-defined beta globin cluster haplotype in children with sickle cell anaemia.
Br J Haematol;
163(2): 268-76, 2013 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-23952145
5.
Association between baseline fetal hemoglobin levels and incidence of severe vaso-occlusive pain episodes in children with sickle cell anemia.
Pediatr Blood Cancer;
60(10): E125-7, 2013 Oct.
Artículo
en Inglés
| MEDLINE | ID: mdl-23677903
6.
Magnetic resonance angiography-defined intracranial vasculopathy is associated with silent cerebral infarcts and glucose-6-phosphate dehydrogenase mutation in children with sickle cell anaemia.
Br J Haematol;
159(3): 352-9, 2012 Nov.
Artículo
en Inglés
| MEDLINE | ID: mdl-22958163
7.
Elevation of IgE in children with sickle cell disease is associated with doctor diagnosis of asthma and increased morbidity.
J Allergy Clin Immunol;
127(6): 1440-6, 2011 Jun.
Artículo
en Inglés
| MEDLINE | ID: mdl-21388662
8.
Genome-wide association study identifies genetic variants influencing F-cell levels in sickle-cell patients.
J Hum Genet;
56(4): 316-23, 2011 Apr.
Artículo
en Inglés
| MEDLINE | ID: mdl-21326311
9.
Plasma glial fibrillary acidic protein levels in children with sickle cell disease.
Am J Hematol;
86(5): 427-9, 2011 May.
Artículo
en Inglés
| MEDLINE | ID: mdl-21523806
10.
Proteomic discovery in sickle cell disease: Elevated neurogranin levels in children with sickle cell disease.
Proteomics Clin Appl;
15(5): e2100003, 2021 09.
Artículo
en Inglés
| MEDLINE | ID: mdl-33915030
11.
Meta-analysis of 2040 sickle cell anemia patients: BCL11A and HBS1L-MYB are the major modifiers of HbF in African Americans.
Blood;
120(9): 1961-2, 2012 Aug 30.
Artículo
en Inglés
| MEDLINE | ID: mdl-22936743
12.
Thrombospondin-1 and L-selectin are associated with silent cerebral infarct in children with sickle cell anaemia.
Br J Haematol;
162(3): 421-4, 2013 Aug.
Artículo
en Inglés
| MEDLINE | ID: mdl-23672305
13.
Identification of Aptamers That Bind to Sickle Hemoglobin and Inhibit Its Polymerization.
Nucleic Acid Ther;
27(6): 354-364, 2017 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-29039727
14.
Proteomic and biomarker studies and neurological complications of pediatric sickle cell disease.
Proteomics Clin Appl;
8(11-12): 813-27, 2014 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-25290359
15.
Genome-wide meta-analysis of systolic blood pressure in children with sickle cell disease.
PLoS One;
8(9): e74193, 2013.
Artículo
en Inglés
| MEDLINE | ID: mdl-24058526
16.
A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia.
PLoS One;
7(4): e34741, 2012.
Artículo
en Inglés
| MEDLINE | ID: mdl-22558097
17.
Hemoglobin depletion from plasma: considerations for proteomic discovery in sickle cell disease and other hemolytic processes.
Proteomics Clin Appl;
4(12): 926-30, 2010 Dec.
Artículo
en Inglés
| MEDLINE | ID: mdl-21179892
18.
The role of peroxisomal ABC transporters in the mouse adrenal gland: the loss of Abcd2 (ALDR), Not Abcd1 (ALD), causes oxidative damage.
Lab Invest;
87(3): 261-72, 2007 Mar.
Artículo
en Inglés
| MEDLINE | ID: mdl-17260006
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