-
1
-
-
0034508220
-
Stroke in children: Recognition, treatment, and future directions
-
deVeber G., Roach E.S., Riela A.R., and Wiznitzer M. Stroke in children: Recognition, treatment, and future directions. Semin Pediatr Neurol 7 (2000) 309-317
-
(2000)
Semin Pediatr Neurol
, vol.7
, pp. 309-317
-
-
deVeber, G.1
Roach, E.S.2
Riela, A.R.3
Wiznitzer, M.4
-
2
-
-
0037121249
-
Prospective assessment of risk factors for recurrent stroke during childhood-A 5-year follow-up study
-
Strater R., Becker S., von Eckardstein A., et al. Prospective assessment of risk factors for recurrent stroke during childhood-A 5-year follow-up study. Lancet 360 (2002) 1540-1545
-
(2002)
Lancet
, vol.360
, pp. 1540-1545
-
-
Strater, R.1
Becker, S.2
von Eckardstein, A.3
-
3
-
-
38149034173
-
Hemoglobin Fairfax, a tandem duplication of β90-94 inserted between β94-β95 (proved by DNA sequence analysis): A previously undescribed unstable hemoglobin variant associated with severe hemolytic anemia and stroke during early childhood
-
[Abstract]
-
Greenberg J., Fairbanks V.F., Hoyer J., Thibodeau S.N., and Fairfax V.A. Hemoglobin Fairfax, a tandem duplication of β90-94 inserted between β94-β95 (proved by DNA sequence analysis): A previously undescribed unstable hemoglobin variant associated with severe hemolytic anemia and stroke during early childhood. Blood 90 Suppl. 1 (1997) 27B [Abstract]
-
(1997)
Blood
, vol.90
, Issue.SUPPL. 1
-
-
Greenberg, J.1
Fairbanks, V.F.2
Hoyer, J.3
Thibodeau, S.N.4
Fairfax, V.A.5
-
5
-
-
0031935430
-
Moyamoya disease in a patient with hereditary spherocytosis
-
Holz A., Woldenberg R., Miller D., Kalina P., Black K., and Lane E. Moyamoya disease in a patient with hereditary spherocytosis. Pediatr Radiol 28 (1998) 95-97
-
(1998)
Pediatr Radiol
, vol.28
, pp. 95-97
-
-
Holz, A.1
Woldenberg, R.2
Miller, D.3
Kalina, P.4
Black, K.5
Lane, E.6
-
6
-
-
0029042362
-
Fanconi anemia and moyamoya: Evidence for an association
-
Paylakis S.G., Verlander P.C., Gould R.J., Strimling B.C., and Auerbach A.D. Fanconi anemia and moyamoya: Evidence for an association. Neurology 45 (1995) 998-1000
-
(1995)
Neurology
, vol.45
, pp. 998-1000
-
-
Paylakis, S.G.1
Verlander, P.C.2
Gould, R.J.3
Strimling, B.C.4
Auerbach, A.D.5
-
7
-
-
0033955246
-
Cytoskeleton alterations of erythrocytes from patients with Fanconi's anemia
-
Malorni W., Straface E., Pagano G., et al. Cytoskeleton alterations of erythrocytes from patients with Fanconi's anemia. FEBS Lett 468 (2000) 125-128
-
(2000)
FEBS Lett
, vol.468
, pp. 125-128
-
-
Malorni, W.1
Straface, E.2
Pagano, G.3
-
8
-
-
0029382825
-
Moyamoya disease and beta-thalassemia
-
Mukherjee A. Moyamoya disease and beta-thalassemia. J Assoc Physicians India 43 (1995) 710-711
-
(1995)
J Assoc Physicians India
, vol.43
, pp. 710-711
-
-
Mukherjee, A.1
-
9
-
-
24144436910
-
Moyamoya syndrome associated with hemolytic anemia due to Hb Alesha
-
Brockmann K., Stolpe S., Fels C., Khan N., Kulozik A.E., and Pekrun A. Moyamoya syndrome associated with hemolytic anemia due to Hb Alesha. J Pediatr Hematol Oncol 27 (2005) 436-440
-
(2005)
J Pediatr Hematol Oncol
, vol.27
, pp. 436-440
-
-
Brockmann, K.1
Stolpe, S.2
Fels, C.3
Khan, N.4
Kulozik, A.E.5
Pekrun, A.6
-
10
-
-
33646894306
-
Moyamoya syndrome in a splenectomized patient with beta-thalassemia intermedia
-
Sanefuji M., Ohga S., Kira R., Yoshiura T., Torisu H., and Hara T. Moyamoya syndrome in a splenectomized patient with beta-thalassemia intermedia. J Child Neurol 21 (2006) 75-77
-
(2006)
J Child Neurol
, vol.21
, pp. 75-77
-
-
Sanefuji, M.1
Ohga, S.2
Kira, R.3
Yoshiura, T.4
Torisu, H.5
Hara, T.6
-
11
-
-
33750828453
-
Enhanced aggregability of red blood cells of β-thalassemia major patients
-
Chen S., Eldor A., Barshtein G., et al. Enhanced aggregability of red blood cells of β-thalassemia major patients. Am J Physiol 270 (1996) H1951-H1956
-
(1996)
Am J Physiol
, vol.270
-
-
Chen, S.1
Eldor, A.2
Barshtein, G.3
-
12
-
-
0036092892
-
The hypercoagulable state in thalassemia
-
Eldor A., and Rachmilewitz E. The hypercoagulable state in thalassemia. Blood 99 (2002) 36-44
-
(2002)
Blood
, vol.99
, pp. 36-44
-
-
Eldor, A.1
Rachmilewitz, E.2
-
13
-
-
0027102386
-
Hypoxia-mediated induction of endothelial cell interleukin-1α: An autocrine mechanism promoting expression of leukocyte adhesion molecules on the vessel surface
-
Shreeniwas R., Koga S., Karakurum M., et al. Hypoxia-mediated induction of endothelial cell interleukin-1α: An autocrine mechanism promoting expression of leukocyte adhesion molecules on the vessel surface. J Clin Invest 90 (1992) 2333-2339
-
(1992)
J Clin Invest
, vol.90
, pp. 2333-2339
-
-
Shreeniwas, R.1
Koga, S.2
Karakurum, M.3
-
14
-
-
0032474692
-
Prevention of a first stroke by transfusions in children with sickle cell anemia and abnormal results on transcranial Doppler ultrasonography
-
Adams R.J., McKie V.C., Hsu L., et al. Prevention of a first stroke by transfusions in children with sickle cell anemia and abnormal results on transcranial Doppler ultrasonography. N Engl J Med 339 (1998) 5-11
-
(1998)
N Engl J Med
, vol.339
, pp. 5-11
-
-
Adams, R.J.1
McKie, V.C.2
Hsu, L.3
-
15
-
-
0019967483
-
Marrow transplantation for thalassaemia
-
Thomas E.D., Buckner C.D., Sanders J.E., et al. Marrow transplantation for thalassaemia. Lancet 2 (1982) 227-229
-
(1982)
Lancet
, vol.2
, pp. 227-229
-
-
Thomas, E.D.1
Buckner, C.D.2
Sanders, J.E.3
-
16
-
-
0036566530
-
Moyamoya syndrome in childhood sickle cell disease: A predictive factor for recurrent cerebrovascular events
-
Dobson S.R., Holden K.R., Nietert P.J., et al. Moyamoya syndrome in childhood sickle cell disease: A predictive factor for recurrent cerebrovascular events. Blood 99 (2002) 3144-3150
-
(2002)
Blood
, vol.99
, pp. 3144-3150
-
-
Dobson, S.R.1
Holden, K.R.2
Nietert, P.J.3
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