-
1
-
-
80053329221
-
TNF-alpha and IL-8: Serum levels and gene polymorphisms (-308G>A and -251A>T) are associated with classical biomarkers and medical history in children with sickle cell anemia
-
Cajado C, Cerqueira BA, Couto FD, Moura-Neto JP, Vilas-Boas W, Dorea MJ et al (2011) TNF-alpha and IL-8: serum levels and gene polymorphisms (-308G>A and -251A>T) are associated with classical biomarkers and medical history in children with sickle cell anemia. Cytokine 56:312-317
-
(2011)
Cytokine
, vol.56
, pp. 312-317
-
-
Cajado, C.1
Cerqueira, B.A.2
Couto, F.D.3
Moura-Neto, J.P.4
Vilas-Boas, W.5
Dorea, M.J.6
-
2
-
-
65549111723
-
Genetic etiologies for phenotypic diversity in sickle cell anemia
-
Steinberg MH (2009) Genetic etiologies for phenotypic diversity in sickle cell anemia. Sci World J 9:46-67
-
(2009)
Sci World J
, vol.9
, pp. 46-67
-
-
Steinberg, M.H.1
-
3
-
-
5044239523
-
Sickle-cell disease
-
DOI 10.1016/S0140-6736(04)17192-4, PII S0140673604171924
-
Stuart MJ, Nagel RL (2004) Sickle-cell disease. Lancet 364:1343-1360 (Pubitemid 39335827)
-
(2004)
Lancet
, vol.364
, Issue.9442
, pp. 1343-1360
-
-
Stuart, M.J.1
Nagel, R.L.2
-
4
-
-
0031965089
-
Cerebrovascular accidents in sickle cell disease: Rates and risk factors
-
Ohene-Frempong K, Weiner SJ, Sleeper LA, Miller ST, Embury S, Moohr JW et al (1998) Cerebrovascular accidents in sickle cell disease: rates and risk factors. Blood 91:288-294 (Pubitemid 28018756)
-
(1998)
Blood
, vol.91
, Issue.1
, pp. 288-294
-
-
Ohene-Frempong, K.1
Weiner, S.J.2
Sleeper, L.A.3
Miller, S.T.4
Embury, S.5
Moohr, J.W.6
Wethers, D.L.7
Pegelow, C.H.8
Gill, F.M.9
-
5
-
-
0028291736
-
Mortality in sickle cell disease. Life expectancy and risk factors for early death
-
Platt OS, Brambilla DJ, Rosse WF, Milner PF, Castro O, Steinberg MH et al (1994) Mortality in sickle cell disease. Life expectancy and risk factors for early death. N Engl J Med 330:1639-1644
-
(1994)
N Engl J Med
, vol.330
, pp. 1639-1644
-
-
Platt, O.S.1
Brambilla, D.J.2
Rosse, W.F.3
Milner, P.F.4
Castro, O.5
Steinberg, M.H.6
-
6
-
-
47749090563
-
Chronic hyper-hemolysis in sickle cell anemia: Association of vascular complications andmortalitywith less frequent vasoocclusive pain
-
Taylor JG, Nolan VG, Mendelsohn L, Kato GJ, Gladwin MT, SteinbergMH (2008) Chronic hyper-hemolysis in sickle cell anemia: association of vascular complications andmortalitywith less frequent vasoocclusive pain. PLoS One 3:e2095
-
(2008)
PLoS One
, vol.3
-
-
Taylor, J.G.1
Nolan, V.G.2
Mendelsohn, L.3
Kato, G.J.4
Gladwin, M.T.5
Steinberg, M.H.6
-
7
-
-
0030703240
-
Circulating activated endothelial cells in sickle cell anemia
-
DOI 10.1056/NEJM199711273372203
-
Solovey A, Lin Y, Browne P, Choong S, Wayner E, Hebbel RP (1997) Circulating activated endothelial cells in sickle cell anemia. N Engl J Med 337:1584-1590 (Pubitemid 27509761)
-
(1997)
New England Journal of Medicine
, vol.337
, Issue.22
, pp. 1584-1590
-
-
Solovey, A.1
Lin, Y.2
Browne, P.3
Choong, S.4
Wayner, E.5
Hebbel, R.P.6
-
9
-
-
60749094795
-
Newer aspects of the pathophysiology of sickle cell disease vaso-occlusion
-
Conran N, Franco-Penteado CF, Costa FF (2009) Newer aspects of the pathophysiology of sickle cell disease vaso-occlusion. Hemoglobin 33:1-16
-
(2009)
Hemoglobin
, vol.33
, pp. 1-16
-
-
Conran, N.1
Franco-Penteado, C.F.2
Costa, F.F.3
-
10
-
-
0026541648
-
Stroke in a cohort of patients with homozygous sickle cell disease
-
Balkaran B, Char G, Morris JS, Thomas PW, Serjeant BE, Serjeant GR (1992) Stroke in a cohort of patients with homozygous sickle cell disease. J Pediatr 120:360-366
-
(1992)
J Pediatr
, vol.120
, pp. 360-366
-
-
Balkaran, B.1
Char, G.2
Morris, J.S.3
Thomas, P.W.4
Serjeant, B.E.5
Serjeant, G.R.6
-
11
-
-
0031814431
-
Abnormalities of the central nervous system in very young children with sickle cell anemia
-
DOI 10.1016/S0022-3476(98)70397-X
-
Wang WC, Langston JW, Steen RG, Wynn LW, Mulhern RK, Wilimas JA et al (1998) Abnormalities of the central nervous system in very young children with sickle cell anemia. J Pediatr 132:994-998 (Pubitemid 28280412)
-
(1998)
Journal of Pediatrics
, vol.132
, Issue.6
, pp. 994-998
-
-
Wang, W.C.1
Langston, J.W.2
Steen, R.G.3
Wynn, L.W.4
Mulbern, R.K.5
Wilimas, J.A.6
Kim, F.M.7
Figueroa, R.E.8
-
12
-
-
0024446352
-
Mortality in children and adolescents with sickle cell disease
-
Leikin SL, Gallagher D, Kinney TR, Sloane D, Klug P, Rida W (1989) Mortality in children and adolescents with sickle cell disease. Cooperative study of sickle cell disease. Pediatrics 84:500-508 (Pubitemid 19216350)
-
(1989)
Pediatrics
, vol.84
, Issue.3
, pp. 500-508
-
-
Leikin, S.L.1
Gallagher, D.2
Kinney, T.R.3
Sloane, D.4
Klug, P.5
Rida, W.6
-
14
-
-
34548269532
-
Confirmation of an association between the TNF(-308) promoter polymorphism and stroke risk in children with sickle cell anemia
-
DOI 10.1161/STROKEAHA.107.483115, PII 0000767020070800000020
-
Hoppe C, KlitzW, D'Harlingue K, Cheng S, Grow M, Steiner L et al (2007) Confirmation of an association between the TNF(-308) promoter polymorphism and stroke risk in children with sickle cell anemia. Stroke 38:2241-2246 (Pubitemid 47457562)
-
(2007)
Stroke
, vol.38
, Issue.8
, pp. 2241-2246
-
-
Hoppe, C.1
Klitz, W.2
D'Harlingue, K.3
Cheng, S.4
Grow, M.5
Steiner, L.6
Noble, J.7
Adams, R.8
Styles, L.9
-
15
-
-
15844431322
-
TCD in sickle cell disease: An important and useful test
-
Adams RJ (2005) TCD in sickle cell disease: an important and useful test. Pediatr Radiol 35:229-234
-
(2005)
Pediatr Radiol
, vol.35
, pp. 229-234
-
-
Adams, R.J.1
-
16
-
-
1542283710
-
Gene interactions and stroke risk in children with sickle cell anemia
-
DOI 10.1182/blood-2003-09-3015
-
Hoppe C, Klitz W, Cheng S, Apple R, Steiner L, Robles L et al (2004) Gene interactions and stroke risk in children with sickle cell anemia. Blood 103:2391-2396 (Pubitemid 38326263)
-
(2004)
Blood
, vol.103
, Issue.6
, pp. 2391-2396
-
-
Hoppe, C.1
Klitz, W.2
Cheng, S.3
Apple, R.4
Steiner, L.5
Robles, L.6
Girard, T.7
Vichinsky, E.8
Styles, L.9
-
17
-
-
16844366938
-
Genetic dissection and prognostic modeling of overt stroke in sickle cell anemia
-
Sebastiani P, Ramoni MF, Nolan V, Baldwin CT, Steinberg MH (2005) Genetic dissection and prognostic modeling of overt stroke in sickle cell anemia. Nat Genet 37:435-440
-
(2005)
Nat Genet
, vol.37
, pp. 435-440
-
-
Sebastiani, P.1
Ramoni, M.F.2
Nolan, V.3
Baldwin, C.T.4
Steinberg, M.H.5
-
18
-
-
33845956434
-
Promoter polymorphisms in the plasma glutathione peroxidase (GPx-3) gene: A novel risk factor for arterial ischemic stroke among young adults and children
-
DOI 10.1161/01.STR.0000252027.53766.2b, PII 0000767020070100000015
-
Voetsch B, Jin RC, Bierl C, Benke KS, Kenet G, Simioni P et al (2007) Promoter polymorphisms in the plasma glutathione peroxidase (GPx-3) gene: a novel risk factor for arterial ischemic stroke among young adults and children. Stroke 38:41-49 (Pubitemid 46035604)
-
(2007)
Stroke
, vol.38
, Issue.1
, pp. 41-49
-
-
Voetsch, B.1
Jin, R.C.2
Bierl, C.3
Benke, K.S.4
Kenet, G.5
Simioni, P.6
Ottaviano, F.7
Damasceno, B.P.8
Annichino-Bizacchi, J.M.9
Handy, D.E.10
Loscalzo, J.11
-
19
-
-
79959278268
-
Genetic predictors for stroke in children with sickle cell anemia
-
Flanagan JM, Frohlich DM, Howard TA, Schultz WH, Driscoll C, Nagasubramanian R et al (2011) Genetic predictors for stroke in children with sickle cell anemia. Blood 117:6681-6684
-
(2011)
Blood
, vol.117
, pp. 6681-6684
-
-
Flanagan, J.M.1
Frohlich, D.M.2
Howard, T.A.3
Schultz, W.H.4
Driscoll, C.5
Nagasubramanian, R.6
-
20
-
-
0037443399
-
Stroke risk in siblings with sickle cell anemia
-
DOI 10.1182/blood.V101.6.2401
-
Driscoll MC, Hurlet A, Styles L, McKie V, Files B, Olivieri N et al (2003) Stroke risk in siblings with sickle cell anemia. Blood 101:2401-2404 (Pubitemid 36302088)
-
(2003)
Blood
, vol.101
, Issue.6
, pp. 2401-2404
-
-
Driscoll, M.C.1
Hurlet, A.2
Styles, L.3
McKie, V.4
Files, B.5
Olivieri, N.6
Pegelow, C.7
Berman, B.8
Drachtman, R.9
Patel, K.10
Brambilla, D.11
-
21
-
-
0038607018
-
Transcranial Doppler ultrasonography in siblings with sickle cell disease
-
DOI 10.1046/j.1365-2141.2003.04276.x
-
Kwiatkowski JL, Hunter JV, Smith-Whitley K, Katz ML, Shults J, Ohene-Frempong K (2003) Transcranial Doppler ultrasonography in siblings with sickle cell disease. Br J Haematol 121:932-937 (Pubitemid 36760314)
-
(2003)
British Journal of Haematology
, vol.121
, Issue.6
, pp. 932-937
-
-
Kwiatkowski, J.L.1
Hunter, J.V.2
Smith-Whitley, K.3
Katz, M.L.4
Shults, J.5
Ohene-Frempong, K.6
-
22
-
-
0025165882
-
Identification of a single base change in a new human mutant glucose-6-phosphate dehydrogenase gene by polymerase-chain-reaction amplification of the entire coding region from genomic DNA
-
Poggi V, Town M, Foulkes NS, Luzzatto L (1990) Identification of a single base change in a new human mutant glucose-6-phosphate dehydrogenase gene by polymerase-chain-reaction amplification of the entire coding region from genomic DNA. Biochem J 271:157-160 (Pubitemid 20331211)
-
(1990)
Biochemical Journal
, vol.271
, Issue.1
, pp. 157-160
-
-
Poggi, V.1
Town, M.2
Foulkes, N.S.3
Luzzatto, L.4
-
23
-
-
0025756644
-
Beta s-gene-cluster haplotypes in sickle cell anemia. Clinical and hematologic features
-
Powars DR (1991) Beta s-gene-cluster haplotypes in sickle cell anemia. Clinical and hematologic features. Hematol Oncol Clin North Am 5:475-493
-
(1991)
Hematol Oncol Clin North Am
, vol.5
, pp. 475-493
-
-
Powars, D.R.1
-
26
-
-
0344235471
-
eNOS T-786C Genotype, Physical Activity, and Peak Forearm Blood Flow in Females
-
DOI 10.1249/01.MSS.0000099105.99682.8B
-
Data SA, Roltsch MH, Hand B, Ferrell RE, Park JJ, Brown MD (2003) eNOS T-786C genotype, physical activity, and peak forearm blood flow in females. Med Sci Sports Exerc 35:1991-1997 (Pubitemid 37509697)
-
(2003)
Medicine and Science in Sports and Exercise
, vol.35
, Issue.12
, pp. 1991-1997
-
-
Data, S.A.1
Roltsch, M.H.2
Hand, B.3
Ferrell, R.E.4
Park, J.-J.5
Brown, M.D.6
-
27
-
-
0029049553
-
A candidate genetic risk factor for vascular disease: A commonmutation in methylenetetrahydrofolate reductase
-
Frosst P, Blom HJ, Milos R, Goyette P, Sheppard CA, Matthews RG et al (1995) A candidate genetic risk factor for vascular disease: a commonmutation in methylenetetrahydrofolate reductase. Nat Genet 10:111-113
-
(1995)
Nat Genet
, vol.10
, pp. 111-113
-
-
Frosst, P.1
Blom, H.J.2
Milos, R.3
Goyette, P.4
Sheppard, C.A.5
Matthews, R.G.6
-
28
-
-
0029850530
-
A common genetic variation in the 3'-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis
-
Poort SR, Rosendaal FR, Reitsma PH, Bertina RM (1996) A common genetic variation in the 3′-untranslated region of the prothrombin gene is associated with elevated plasma prothrombin levels and an increase in venous thrombosis. Blood 88:3698-3703 (Pubitemid 26383091)
-
(1996)
Blood
, vol.88
, Issue.10
, pp. 3698-3703
-
-
Poort, S.R.1
Rosendaal, F.R.2
Reitsma, P.H.3
Bertina, R.M.4
-
29
-
-
42449097982
-
Family screening for HBB*S gene and detection of new cases of sickle cell trait in Northeastern Brazil
-
Bandeira FM, Santos MN, Bezerra MA, Gomes YM, Araujo AS, Braga MC et al (2008) Family screening for HBB*S gene and detection of new cases of sickle cell trait in Northeastern Brazil. Rev Saude Publica 42:234-241
-
(2008)
Rev Saude Publica
, vol.42
, pp. 234-241
-
-
Bandeira, F.M.1
Santos, M.N.2
Bezerra, M.A.3
Gomes, Y.M.4
Araujo, A.S.5
Braga, M.C.6
-
30
-
-
33847015229
-
Molecular variations linked to the grouping of beta- and alpha-globin genes in neonatal patients with sickle cell disease in the state of Pernambuco, Brazil
-
Bezerra MA, Santos MN, Araujo AS, Gomes YM, Abath FG, Bandeira FM (2007) Molecular variations linked to the grouping of beta- and alpha-globin genes in neonatal patients with sickle cell disease in the state of Pernambuco, Brazil. Hemoglobin 31:83-88
-
(2007)
Hemoglobin
, vol.31
, pp. 83-88
-
-
Bezerra, M.A.1
Santos, M.N.2
Araujo, A.S.3
Gomes, Y.M.4
Abath, F.G.5
Bandeira, F.M.6
-
31
-
-
33644828167
-
Clinical, hematological, and molecular characterization of sickle cell anemia pediatric patients fromtwo different cities in Brazil
-
Lyra IM, GoncalvesMS, Braga JA,GesteiraMF, CarvalhoMH, Saad ST et al (2005) Clinical, hematological, and molecular characterization of sickle cell anemia pediatric patients fromtwo different cities in Brazil. Cad Saude Publica 21:1287-1290
-
(2005)
Cad Saude Publica
, vol.21
, pp. 1287-1290
-
-
Lyra, I.M.1
Goncalves, M.S.2
Braga, J.A.3
Gesteira, M.F.4
Carvalho, M.H.5
Saad, S.T.6
-
32
-
-
0034969365
-
Molecular characteristics of pediatric patients with sickle cell anemia and stroke
-
DOI 10.1002/ajh.1103
-
Sarnaik SA, Ballas SK (2001) Molecular characteristics of pediatric patients with sickle cell anemia and stroke. Am J Hematol 67:179-182 (Pubitemid 32538616)
-
(2001)
American Journal of Hematology
, vol.67
, Issue.3
, pp. 179-182
-
-
Sarnaik, S.A.1
Ballas, S.K.2
-
33
-
-
74049109698
-
Geneticmodifiers of the severity of sickle cell anemia identified through a genome-wide association study
-
Sebastiani P, Solovieff N, Hartley SW, Milton JN, Riva A, Dworkis DA et al (2010) Geneticmodifiers of the severity of sickle cell anemia identified through a genome-wide association study. Am J Hematol 85:29-35
-
(2010)
Am J Hematol
, vol.85
, pp. 29-35
-
-
Sebastiani, P.1
Solovieff, N.2
Hartley, S.W.3
Milton, J.N.4
Riva, A.5
Dworkis, D.A.6
-
34
-
-
0028231790
-
Alpha thalassemia and stroke risk in sickle cell anemia
-
Adams RJ, Kutlar A, McKie V, Carl E, Nichols FT, Liu JC et al (1994) Alpha thalassemia and stroke risk in sickle cell anemia. Am J Hematol 45:279-282 (Pubitemid 24109901)
-
(1994)
American Journal of Hematology
, vol.45
, Issue.4
, pp. 279-282
-
-
Adams, R.J.1
Kutlar, A.2
McKie, V.3
Carl, E.4
Nichols, F.T.5
Jin, C.L.6
McKie, K.7
Clary, A.8
-
35
-
-
79952158856
-
Coinheritance of alpha-thalassemia decreases the risk of cerebrovascular disease in a cohort of children with sickle cell anemia
-
Belisario AR, Rodrigues CV, Martins ML, Silva CM, Viana MB (2010) Coinheritance of alpha-thalassemia decreases the risk of cerebrovascular disease in a cohort of children with sickle cell anemia. Hemoglobin 34:516-529
-
(2010)
Hemoglobin
, vol.34
, pp. 516-529
-
-
Belisario, A.R.1
Rodrigues, C.V.2
Martins, M.L.3
Silva, C.M.4
Viana, M.B.5
-
36
-
-
0042570486
-
Alpha thalassemia is associated with decreased risk of abnormal transcranial Doppler ultrasonography in children with sickle cell anemia
-
DOI 10.1097/00043426-200308000-00007
-
Hsu LL, Miller ST, Wright E, Kutlar A, McKie V, Wang W et al (2003) Alpha thalassemia is associated with decreased risk of abnormal transcranial Doppler ultrasonography in children with sickle cell anemia. J Pediatr Hematol Oncol 25:622-628 (Pubitemid 36959423)
-
(2003)
Journal of Pediatric Hematology/Oncology
, vol.25
, Issue.8
, pp. 622-628
-
-
Hsu, L.L.1
Miller, S.T.2
Wright, E.3
Kutlar, A.4
McKie, V.5
Wang, W.6
Pegelow, C.H.7
Driscoll, C.8
Hurlet, A.9
Woods, G.10
Elsas, L.11
Embury, S.12
Adams, R.J.13
-
37
-
-
79953859114
-
β-Globin gene cluster haplotypes in sickle cell patients from Panama
-
Rusanova I, Cossio G,Moreno B, Javier PF, De Borace RG, PereaM et al (2011) β-Globin gene cluster haplotypes in sickle cell patients from Panama. Am J Hum Biol 23:377-380
-
(2011)
Am J Hum Biol
, vol.23
, pp. 377-380
-
-
Rusanova, I.1
Cossio, G.2
Moreno, B.3
Javier, P.F.4
De Borace, R.G.5
Perea, M.6
-
38
-
-
84865387516
-
Reply: Genetic polymorphisms and cerebrovascular disease in children with sickle cell anemia from Rio de Janeiro
-
da Silva Filho IL, Leite AC,Moura PG, Ribeiro GS, Cavalcante AC, de Azevedo FC et al (2012) Reply: genetic polymorphisms and cerebrovascular disease in children with sickle cell anemia from Rio de Janeiro. Brazil Arq Neuropsiquiatr 70:648-649
-
(2012)
Brazil Arq Neuropsiquiatr
, vol.70
, pp. 648-649
-
-
Da Silva Filho, I.L.1
Leite, A.C.2
Moura, P.G.3
Ribeiro, G.S.4
Cavalcante, A.C.5
De Azevedo, F.C.6
-
39
-
-
45549101008
-
National Institutes of Health Consensus Development Conference statement: Hydroxyurea treatment for sickle cell disease
-
Brawley OW, Cornelius LJ, Edwards LR, Gamble VN, Green BL, Inturrisi C et al (2008) National Institutes of Health Consensus Development Conference statement: hydroxyurea treatment for sickle cell disease. Ann Intern Med 148:932-938 (Pubitemid 351860825)
-
(2008)
Annals of Internal Medicine
, vol.148
, Issue.12
, pp. 932-938
-
-
Brawley, O.W.1
Cornelius, L.J.2
Edwards, L.R.3
Northington, G.V.4
Green, B.L.5
Inturrisi, C.6
James, A.H.7
Laraque, D.8
Mendez, M.9
Montoya, C.J.10
Pollock, B.H.11
Robinson, L.12
Scholnik, A.P.13
Schori, M.14
-
40
-
-
45549105597
-
Systematic review: Hydroxyurea for the treatment of adults with sickle cell disease
-
Lanzkron S, Strouse JJ, Wilson R, Beach MC, Haywood C, Park H et al (2008) Systematic review: hydroxyurea for the treatment of adults with sickle cell disease. Ann Intern Med 148:939-955 (Pubitemid 351860826)
-
(2008)
Annals of Internal Medicine
, vol.148
, Issue.12
, pp. 939-955
-
-
Lanzkron, S.1
Strouse, J.J.2
Wilson, R.3
Beach, M.C.4
Haywood, C.5
Park, H.6
Witkop, C.7
Bass, E.B.8
Segal, J.B.9
-
41
-
-
0037414164
-
Effect of Hydroxyurea on Mortality and Morbidity in Adult Sickle Cell Anemia: Risks and Benefits Up to 9 Years of Treatment
-
DOI 10.1001/jama.289.13.1645
-
SteinbergMH, Barton F, Castro O, Pegelow CH, Ballas SK, Kutlar A et al (2003) Effect of hydroxyurea onmortality andmorbidity in adult sickle cell anemia: risks and benefits up to 9 years of treatment. JAMA 289:1645-1651 (Pubitemid 37430269)
-
(2003)
Journal of the American Medical Association
, vol.289
, Issue.13
, pp. 1645-1651
-
-
Steinberg, M.H.1
Barton, F.2
Castro, O.3
Pegelow, C.H.4
Ballas, S.K.5
Kutlar, A.6
Orringer, E.7
Bellevue, R.8
Olivieri, N.9
Eckman, J.10
Varma, M.11
Ramirez, G.12
Adler, B.13
Smith, W.14
Carlos, T.15
Ataga, K.16
DeCastro, L.17
Bigelow, C.18
Saunthararajah, Y.19
Telfer, M.20
Vichinsky, E.21
Claster, S.22
Shurin, S.23
Bridges, K.24
Waclawiw, M.25
Bonds, D.26
Terrin, M.27
more..
-
42
-
-
20044367676
-
Predicting clinical severity in sickle cell anaemia
-
Steinberg MH (2005) Predicting clinical severity in sickle cell anaemia. Br J Haematol 129:465-481
-
(2005)
Br J Haematol
, vol.129
, pp. 465-481
-
-
Steinberg, M.H.1
-
43
-
-
33745141905
-
Regular transfusion lowers plasma free hemoglobin in children with sickle-cell disease at risk for stroke
-
DOI 10.1161/01.STR.0000221173.97108.01, PII 0000767020060600000026
-
Lezcano NE, Odo N, Kutlar A, Brambilla D, Adams RJ (2006) Regular transfusion lowers plasma free hemoglobin in children with sickle-cell disease at risk for stroke. Stroke 37:1424-1426 (Pubitemid 44305720)
-
(2006)
Stroke
, vol.37
, Issue.6
, pp. 1424-1426
-
-
Lezcano, N.E.1
Odo, N.2
Kutlar, A.3
Brambilla, D.4
Adams, R.J.5
-
44
-
-
77953057530
-
The risks and benefits of long-term use of hydroxyurea in sickle cell anemia: A 17.5-year follow-up
-
Steinberg MH, McCarthy WF, Castro O, Ballas SK, Armstrong FD, Smith W et al (2010) The risks and benefits of long-term use of hydroxyurea in sickle cell anemia: a 17.5-year follow-up. Am J Hematol 85:403-408
-
(2010)
Am J Hematol
, vol.85
, pp. 403-408
-
-
Steinberg, M.H.1
McCarthy, W.F.2
Castro, O.3
Ballas, S.K.4
Armstrong, F.D.5
Smith, W.6
-
45
-
-
34247480919
-
Genetics of ischaemic stroke among persons of non-European descent: A meta-analysis of eight genes involving approximately 32,500 individuals
-
Ariyaratnam R, Casas JP, Whittaker J, Smeeth L, Hingorani AD, Sharma P (2007) Genetics of ischaemic stroke among persons of non-European descent: a meta-analysis of eight genes involving approximately 32,500 individuals. PLoS Med 4:e131
-
(2007)
PLoS Med
, vol.4
-
-
Ariyaratnam, R.1
Casas, J.P.2
Whittaker, J.3
Smeeth, L.4
Hingorani, A.D.5
Sharma, P.6
-
46
-
-
33847335941
-
Association of gene polymorphism with genetic susceptibility to stroke in Asian populations: A meta-analysis
-
Banerjee I, Gupta V, Ganesh S (2007) Association of gene polymorphism with genetic susceptibility to stroke in Asian populations: a meta-analysis. J Hum Genet 52:205-219
-
(2007)
J Hum Genet
, vol.52
, pp. 205-219
-
-
Banerjee, I.1
Gupta, V.2
Ganesh, S.3
-
47
-
-
7744222619
-
Meta-analysis of genetic studies in ischemic stroke: Thirty-two genes involving approximately 18 000 cases and 58 000 controls
-
DOI 10.1001/archneur.61.11.1652
-
Casas JP, Hingorani AD, Bautista LE, Sharma P (2004) Meta-analysis of genetic studies in ischemic stroke: thirty-two genes involving approximately 18,000 cases and 58,000 controls. Arch Neurol 61:1652-1661 (Pubitemid 39463422)
-
(2004)
Archives of Neurology
, vol.61
, Issue.11
, pp. 1652-1661
-
-
Casas, J.P.1
Hingorani, A.D.2
Bautista, L.E.3
Sharma, P.4
-
48
-
-
58149143300
-
G6PD deficiency, absence of alpha-thalassemia, and hemolytic rate at baseline are significant independent risk factors for abnormally high cerebral velocities in patients with sickle cell anemia
-
Bernaudin F, Verlhac S, Chevret S, TorresM, Coic L, Arnaud C et al (2008) G6PD deficiency, absence of alpha-thalassemia, and hemolytic rate at baseline are significant independent risk factors for abnormally high cerebral velocities in patients with sickle cell anemia. Blood 112:4314-4317
-
(2008)
Blood
, vol.112
, pp. 4314-4317
-
-
Bernaudin, F.1
Verlhac, S.2
Chevret, S.3
Torres, M.4
Coic, L.5
Arnaud, C.6
-
49
-
-
34247130850
-
Effect of the G-308A polymorphism of the tumor necrosis factor alpha gene on the risk of ischemic heart disease and ischemic stroke: A meta-analysis
-
DOI 10.1016/j.ahj.2007.02.031, PII S0002870307001664
-
Pereira TV, Rudnicki M, Franco RF, Pereira AC, Krieger JE (2007) Effect of the G-308A polymorphism of the tumor necrosis factor alpha gene on the risk of ischemic heart disease and ischemic stroke: a meta-analysis. Am Heart J 153:821-830 (Pubitemid 46602156)
-
(2007)
American Heart Journal
, vol.153
, Issue.5
, pp. 821-830
-
-
Pereira, T.V.1
Rudnicki, M.2
Franco, R.F.3
Pereira, A.C.4
Krieger, J.E.5
-
50
-
-
29244433512
-
A role of TNF-alpha gene variant on juvenile ischemic stroke: A case-control study
-
DOI 10.1111/j.1468-1331.2005.01136.x
-
Rubattu S, Speranza R, Ferrari M, Evangelista A, BecciaM, Stanzione R et al (2005) A role of TNF-alpha gene variant on juvenile ischemic stroke: a case-control study. Eur J Neurol 12:989-993 (Pubitemid 41820054)
-
(2005)
European Journal of Neurology
, vol.12
, Issue.12
, pp. 989-993
-
-
Rubattu, S.1
Speranza, R.2
Ferrari, M.3
Evangelista, A.4
Beccia, M.5
Stanzione, R.6
Assenza, G.E.7
Volpe, M.8
Rasura, M.9
-
51
-
-
84881664862
-
Relationship between endothelial nitric oxide synthase gene polymorphisms and ischemic stroke: A meta-analysis
-
Niu PP,YangG, Zheng BK,Guo ZN, Jin H,YangY(2013) Relationship between endothelial nitric oxide synthase gene polymorphisms and ischemic stroke: a meta-analysis. Acta Neurol Scand 128:202-212
-
(2013)
Acta Neurol Scand
, vol.128
, pp. 202-212
-
-
Niu, P.P.1
Yang, G.2
Zheng, B.K.3
Guo, Z.N.4
Jin, H.5
Yang, Y.6
-
52
-
-
84891049130
-
Methylenetetrahydrofolate reductase (MTHFR) gene polymorphisms and susceptibility to ischemic stroke: A meta-analysis
-
Li P, Qin C (2013) Methylenetetrahydrofolate reductase (MTHFR) gene polymorphisms and susceptibility to ischemic stroke: a meta-analysis. Gene 535:359-64
-
(2013)
Gene
, vol.535
, pp. 359-364
-
-
Li, P.1
Qin, C.2
-
53
-
-
84875447601
-
Endothelial NO synthase gene polymorphisms and risk of ischemic stroke in Asian population: A meta-analysis
-
Wang M, Jiang X,Wu W, Zhang D (2013) Endothelial NO synthase gene polymorphisms and risk of ischemic stroke in Asian population: a meta-analysis. PLoS One 8:e60472
-
(2013)
PLoS One
, vol.8
-
-
Wang, M.1
Jiang, X.2
Wu, W.3
Zhang, D.4
-
54
-
-
84898849858
-
Endothelial nitric oxide: Protector of a healthy mind
-
in press
-
Katusic ZS, Austin SA (2014) Endothelial nitric oxide: protector of a healthy mind. Eur Heart J (in press)
-
(2014)
Eur Heart J
-
-
Katusic, Z.S.1
Austin, S.A.2
-
55
-
-
33846279380
-
Deconstructing sickle cell disease: Reappraisal of the role of hemolysis in the development of clinical subphenotypes
-
DOI 10.1016/j.blre.2006.07.001, PII S0268960X06000415
-
Kato GJ, Gladwin MT, Steinberg MH (2007) Deconstructing sickle cell disease: reappraisal of the role of hemolysis in the development of clinical subphenotypes. Blood Rev 21:37-47 (Pubitemid 46110926)
-
(2007)
Blood Reviews
, vol.21
, Issue.1
, pp. 37-47
-
-
Kato, G.J.1
Gladwin, M.T.2
Steinberg, M.H.3
|