| Publication |
Sentence |
Publish Date |
Extraction Date |
Species |
| Banu Aygun, Jennifer Parker, Molly B Freeman, Alexis L Stephens, Matthew P Smeltzer, Song Wu, Jane S Hankins, Winfred C Wan. Neurocognitive screening with the Brigance preschool screen-II in 3-year-old children with sickle cell disease. Pediatric blood & cancer. vol 56. issue 4. 2011-03-24. PMID:21298749. |
neurocognitive deficits have been described in school age children with sickle cell disease (scd), even in the absence of stroke or silent infarcts. |
2011-03-24 |
2023-08-12 |
Not clear |
| Elsie Gyang, Kristen Yeom, Carolyn Hoppe, Sonia Partap, Michael Jen. Effect of chronic red cell transfusion therapy on vasculopathies and silent infarcts in patients with sickle cell disease. American journal of hematology. vol 86. issue 1. 2011-02-11. PMID:21117059. |
regular, chronic red cell transfusions (ctx) have been shown to be effective prophylaxis against stroke in sickle cell disease (scd) in those at risk. |
2011-02-11 |
2023-08-12 |
Not clear |
| Elsie Gyang, Kristen Yeom, Carolyn Hoppe, Sonia Partap, Michael Jen. Effect of chronic red cell transfusion therapy on vasculopathies and silent infarcts in patients with sickle cell disease. American journal of hematology. vol 86. issue 1. 2011-02-11. PMID:21117059. |
thus, we retrospectively evaluated the magnetic resonance imaging reports of a cohort of scd patients who were prescribed ctx for either primary or secondary stroke prophylaxis. |
2011-02-11 |
2023-08-12 |
Not clear |
| Zhou Zhou, Hyojeong Han, Miguel A Cruz, José A López, Jing-Fei Dong, Prasenjit Guchhai. Haemoglobin blocks von Willebrand factor proteolysis by ADAMTS-13: a mechanism associated with sickle cell disease. Thrombosis and haemostasis. vol 101. issue 6. 2010-09-17. PMID:19492149. |
vascular occlusion, thromboembolism and strokes are hallmark events in sickle cell disease (scd). |
2010-09-17 |
2023-08-12 |
Not clear |
| Ariel Koren, Daniel Fink, Osnat Admoni, Yardena Tennenbaum-Rakover, Carina Levi. Non-transferrin-bound labile plasma iron and iron overload in sickle-cell disease: a comparative study between sickle-cell disease and beta-thalassemic patients. European journal of haematology. vol 84. issue 1. 2010-05-14. PMID:19732137. |
blood transfusions are the standard of care in b thalassemia and transfusions are also indicated in sickle cell disease (scd) patients with hypersplenism, recurrent vaso-occlusive crises and for stroke prevention. |
2010-05-14 |
2023-08-12 |
Not clear |
| Michael M Dowling, Nancy Lee, Charles T Quinn, Zora R Rogers, Deborah Boger, Naveed Ahmad, Claudio Ramaciotti, George R Buchana. Prevalence of intracardiac shunting in children with sickle cell disease and stroke. The Journal of pediatrics. vol 156. issue 4. 2010-04-29. PMID:20022343. |
to determine the prevalence of potential intracardiac shunts, including patent foramen ovale (pfo), in children with sickle cell disease (scd) and stroke. |
2010-04-29 |
2023-08-12 |
Not clear |
| Heba Mourad, Wael Fadel, Manal El Batch, Mohamed Rowish. Heamostatic and genetic predisposing factors for stroke in children with sickle cell anemia. The Egyptian journal of immunology. vol 15. issue 1. 2010-04-21. PMID:20306667. |
sickle cell anemia (sca) is the most common type of scd and represents the homozygous form, in which the individual inherits a double dose of the abnormal gene that codes for hemoglobin s. this study was done to detect cases of silent and clinically overt strokes in children with sickle cell anemia (sca) and examine predisposing factors for stroke development. |
2010-04-21 |
2023-08-12 |
human |
| Elsa Mirre, Valentine Brousse, Laureline Berteloot, Karen Lambot-Juhan, Suzanne Verlhac, Claire Boulat, Marie-Dominique Dumont, Gérard Lenoir, Mariane de Montalember. Feasibility and efficacy of chronic transfusion for stroke prevention in children with sickle cell disease. European journal of haematology. vol 84. issue 3. 2010-03-26. PMID:19912310. |
in children with sickle cell disease (scd), chronic transfusion to maintain haemoglobin s (hbs) below 30% markedly decreases both the risk of a first stroke when transcranial doppler (tcd) ultrasonography shows abnormal cerebral blood flow velocities and the risk of recurrent stroke. |
2010-03-26 |
2023-08-12 |
Not clear |
| A Elira Dokekias, L Ngolet Ossini, F O Atipo Tsiba, F Malanda, I Koko, M De Montalember. [Blood transfusion assessment to 112 homozygous sickle-cell disease patients in university hospital of Brazzaville]. Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine. vol 16. issue 5-6. 2010-02-08. PMID:19369104. |
homozygous, sickle-cell disease (scd) is responsible for acute complication, especially anaemic crisis and special situation such as acute chest syndrome, stroke and acute priapism. |
2010-02-08 |
2023-08-12 |
Not clear |
| A Elira Dokekias, L Ngolet Ossini, F O Atipo Tsiba, F Malanda, I Koko, M De Montalember. [Blood transfusion assessment to 112 homozygous sickle-cell disease patients in university hospital of Brazzaville]. Transfusion clinique et biologique : journal de la Societe francaise de transfusion sanguine. vol 16. issue 5-6. 2010-02-08. PMID:19369104. |
in the second group (20 cases), scd patients have particularly situations: pregnancy (10 cases); stroke (six cases); cardiac failure (two cases) and priapism (two cases). |
2010-02-08 |
2023-08-12 |
Not clear |
| Luis A Verduzco, David G Natha. Sickle cell disease and stroke. Blood. vol 114. issue 25. 2010-01-08. PMID:19797523. |
twenty-four percent of sickle cell disease (scd) patients have a stroke by the age of 45 years. |
2010-01-08 |
2023-08-12 |
Not clear |
| Luis A Verduzco, David G Natha. Sickle cell disease and stroke. Blood. vol 114. issue 25. 2010-01-08. PMID:19797523. |
although viscosity is of importance in the noncerebral manifestations of scd, inflammation may play a larger role than viscosity in the development of large-vessel stroke. |
2010-01-08 |
2023-08-12 |
Not clear |
| Luis A Verduzco, David G Natha. Sickle cell disease and stroke. Blood. vol 114. issue 25. 2010-01-08. PMID:19797523. |
the future of scd stroke management lies in the avoidance of transfusion. |
2010-01-08 |
2023-08-12 |
Not clear |
| Luis A Verduzco, David G Natha. Sickle cell disease and stroke. Blood. vol 114. issue 25. 2010-01-08. PMID:19797523. |
recent genome-wide association studies may provide methods for modulating fetal hemoglobin production enough to attenuate stroke risk and other complications of scd. |
2010-01-08 |
2023-08-12 |
Not clear |
| Erfan Nur, Yu-Sok Kim, Jasper Truijen, Eduard J van Beers, Shyrin C A T Davis, Dees P Brandjes, Bart J Biemond, Johannes J van Lieshou. Cerebrovascular reserve capacity is impaired in patients with sickle cell disease. Blood. vol 114. issue 16. 2009-11-06. PMID:19700663. |
in scd patients, impaired cerebrovascular co2 responsiveness reflects reduced cerebrovascular reserve capacity, which may play a role in pathophysiology of stroke. |
2009-11-06 |
2023-08-12 |
human |
| John J Strouse, Lori C Jordan, Sophie Lanzkron, James F Casell. The excess burden of stroke in hospitalized adults with sickle cell disease. American journal of hematology. vol 84. issue 9. 2009-10-08. PMID:19623672. |
this report compares the relative rates and risk factors associated with stroke in adults versus children with sickle cell disease (scd) in the united states over the last decade. |
2009-10-08 |
2023-08-12 |
Not clear |
| John J Strouse, Lori C Jordan, Sophie Lanzkron, James F Casell. The excess burden of stroke in hospitalized adults with sickle cell disease. American journal of hematology. vol 84. issue 9. 2009-10-08. PMID:19623672. |
we identified incident strokes in patients with scd using icd-9 codes for acute stroke and scd and the california patient discharge databases. |
2009-10-08 |
2023-08-12 |
Not clear |
| John J Strouse, Lori C Jordan, Sophie Lanzkron, James F Casell. The excess burden of stroke in hospitalized adults with sickle cell disease. American journal of hematology. vol 84. issue 9. 2009-10-08. PMID:19623672. |
our results suggest that the rate of stroke in scd peaks in older adults and is three-fold higher than rates previously reported in african-americans of similar age (35-64 years) without scd. |
2009-10-08 |
2023-08-12 |
Not clear |
| John J Strouse, Lori C Jordan, Sophie Lanzkron, James F Casell. The excess burden of stroke in hospitalized adults with sickle cell disease. American journal of hematology. vol 84. issue 9. 2009-10-08. PMID:19623672. |
stroke in scd is associated with several known adult risk factors for ischemic and hemorrhagic stroke. |
2009-10-08 |
2023-08-12 |
Not clear |
| John J Strouse, Lori C Jordan, Sophie Lanzkron, James F Casell. The excess burden of stroke in hospitalized adults with sickle cell disease. American journal of hematology. vol 84. issue 9. 2009-10-08. PMID:19623672. |
studies for the primary and secondary prevention of stroke in adults with scd are urgently needed. |
2009-10-08 |
2023-08-12 |
Not clear |