-
1
-
-
77953952024
-
The inherited diseases of hemoglobin are an emerging global health burden
-
Weatherall DJ. The inherited diseases of hemoglobin are an emerging global health burden. Blood. 2010;115(22):4331-6.
-
(2010)
Blood
, vol.115
, Issue.22
, pp. 4331-4336
-
-
Weatherall, D.J.1
-
2
-
-
0020395177
-
Molecular and cellular pathogenesis of hemoglobin SC disease
-
Bunn HF, Noguchi CT, Hofrichter J, Schechter GP, Schechter AN, Eaton WA. Molecular and cellular pathogenesis of hemoglobin SC disease. Proc Natl Acad Sci. 1982;79(23):527-31.
-
(1982)
Proc Natl Acad Sci
, vol.79
, Issue.23
, pp. 527-531
-
-
Bunn, H.F.1
Noguchi, C.T.2
Hofrichter, J.3
Schechter, G.P.4
Schechter, A.N.5
Eaton, W.A.6
-
3
-
-
0019995787
-
Clinical, Hematological, and Biochemical Features of Hb SC Disease
-
Ballas SK, Lewis CN, Noone AM, Krasnow SH, Kamarulzaman E, Burka ER. Clinical, Hematological, and Biochemical Features of Hb SC Disease. Am J Hematol 1982; 13(1):37-51.
-
(1982)
Am J Hematol
, vol.13
, Issue.1
, pp. 37-51
-
-
Ballas, S.K.1
Lewis, C.N.2
Noone, A.M.3
Krasnow, S.H.4
Kamarulzaman, E.5
Burka, E.R.6
-
4
-
-
77952304543
-
Glomerular hyperfiltration in adult sickle cell anemia: A frequent hemolysis associated feature
-
Haymann JP, Stankovic K, Levy P, Avellino V, Tharaux PL, Letavernier E, et al. Glomerular hyperfiltration in adult sickle cell anemia: a frequent hemolysis associated feature. Clin J Am Soc Nephrol. 2010; 5(5):756-61.
-
(2010)
Clin J Am Soc Nephrol
, vol.5
, Issue.5
, pp. 756-761
-
-
Haymann, J.P.1
Stankovic, K.2
Levy, P.3
Avellino, V.4
Tharaux, P.L.5
Letavernier, E.6
-
5
-
-
10744233940
-
Pulmonary hypertension as a risk factor for death in patients with sickle cell disease
-
Gladwin MT, Sachdev V, Jison ML, Shizukuda Y, Plehn JF, Minter K, et al. Pulmonary hypertension as a risk factor for death in patients with sickle cell disease. N Engl J Med. 2004;350(9):886-95.
-
(2004)
N Engl J Med
, vol.350
, Issue.9
, pp. 886-895
-
-
Gladwin, M.T.1
Sachdev, V.2
Jison, M.L.3
Shizukuda, Y.4
Plehn, J.F.5
Minter, K.6
-
6
-
-
0036085773
-
Outcome in hemoglobin SC disease: A four-decade observational study of clinical, hematologic, and genetic factors
-
Powars DR, Hiti A, Ramicone E, Johnson C, Chan L. Outcome in hemoglobin SC disease: a four-decade observational study of clinical, hematologic, and genetic factors. Am J Hematol. 2002; 70(3):206-15.
-
(2002)
Am J Hematol
, vol.70
, Issue.3
, pp. 206-215
-
-
Powars, D.R.1
Hiti, A.2
Ramicone, E.3
Johnson, C.4
Chan, L.5
-
8
-
-
0035200111
-
Hemoglobin S-C disease revisited: Clinical study of 106 adults
-
Koduri PR, Agbemadzo B, Nathan S. Hemoglobin S-C disease revisited: clinical study of 106 adults. Am J Hematol. 2001; 68(4):298-300.
-
(2001)
Am J Hematol
, vol.68
, Issue.4
, pp. 298-300
-
-
Koduri, P.R.1
Agbemadzo, B.2
Nathan, S.3
-
10
-
-
77953661132
-
Guidelines for the Echocardiographic Assessment of the Right Heart in Adults: A Report from the American Society of Echocardiography: Endorsed by the European Association of Echocardiography, a registered branch of the European Society of Cardiology, and the Canadian Society of Echocardiography
-
Rudski LG, Lai WW, Afilalo J, Hua L, Handschumacher MD, Chandrasekaran K, et al. Guidelines for the Echocardiographic Assessment of the Right Heart in Adults: A Report from the American Society of Echocardiography: endorsed by the European Association of Echocardiography, a registered branch of the European Society of Cardiology, and the Canadian Society of Echocardiography. J Am Soc Echocardiogr. 2010;23(7):685-713.
-
(2010)
J Am Soc Echocardiogr
, vol.23
, Issue.7
, pp. 685-713
-
-
Rudski, L.G.1
Lai, W.W.2
Afilalo, J.3
Hua, L.4
Handschumacher, M.D.5
Chandrasekaran, K.6
-
11
-
-
0024467330
-
Leg ulcers in patients with sickle cell disease
-
Koshy M, Entsuah R, Koranda A, Kraus AP, Johnson R, Bellvue R, et al. Leg ulcers in patients with sickle cell disease. Blood. 1989;74(4):1403-8.
-
(1989)
Blood
, vol.74
, Issue.4
, pp. 1403-1408
-
-
Koshy, M.1
Entsuah, R.2
Koranda, A.3
Kraus, A.P.4
Johnson, R.5
Bellvue, R.6
-
12
-
-
0026076686
-
Sickle cell disease as a cause of osteonecrosis of the femoral head
-
Milner PF, Kraus AP, Sebes JI, Sleeper LA, Dukes KA, Embury SH, et al. Sickle cell disease as a cause of osteonecrosis of the femoral head. N Engl J Med. 1991;325(21): 1476-81.
-
(1991)
N Engl J Med
, vol.325
, Issue.21
, pp. 1476-1481
-
-
Milner, P.F.1
Kraus, A.P.2
Sebes, J.I.3
Sleeper, L.A.4
Dukes, K.A.5
Embury, S.H.6
-
13
-
-
27644445541
-
Incidence and natural history of proliferative sickle cell retinopathy
-
Downes SM, Hambleton IR, Chuang EL, Lois N, Serjeant GR, Bird AC. Incidence and natural history of proliferative sickle cell retinopathy. Ophthalmology. 2005; 112(11):1869-75.
-
(2005)
Ophthalmology
, vol.112
, Issue.11
, pp. 1869-1875
-
-
Downes, S.M.1
Hambleton, I.R.2
Chuang, E.L.3
Lois, N.4
Serjeant, G.R.5
Bird, A.C.6
-
14
-
-
18144390228
-
Hearing loss and auditory function in sickle cell disease
-
Burch-Sims GP, Matlock VR. Hearing loss and auditory function in sickle cell disease. J Commun Disord. 2005;38(4):321-9.
-
(2005)
J Commun Disord
, vol.38
, Issue.4
, pp. 321-329
-
-
Burch-Sims, G.P.1
Matlock, V.R.2
-
15
-
-
0025950655
-
Hearing disorders in sickle cell disease: Cochlear and retrocochlear findings
-
Gould HJ, Crawford MR, Smith WR, Beckford N, Gibson, WR, Pettit L, et al. Hearing disorders in sickle cell disease: Cochlear and retrocochlear findings. Ear Hear. 1991;12(5):352-4.
-
(1991)
Ear Hear
, vol.12
, Issue.5
, pp. 352-354
-
-
Gould, H.J.1
Crawford, M.R.2
Smith, W.R.3
Beckford, N.4
Gibson, W.R.5
Pettit, L.6
-
16
-
-
77957265003
-
Hearing impairment in persons with the hemoglobin SC genotype
-
Onakoya PA, Nwaorgu OG, Shokunbi WA. Hearing impairment in persons with the hemoglobin SC genotype. Ear Nose Throat J. 2010;89(7):306-10.
-
(2010)
Ear Nose Throat J
, vol.89
, Issue.7
, pp. 306-310
-
-
Onakoya, P.A.1
Nwaorgu, O.G.2
Shokunbi, W.A.3
-
17
-
-
0026232084
-
Prevalence of hearing loss in adults with sickle cell disease
-
Crawford MR, Gould HJ, Smith WR, Beckford N, Gibson WR, Bobo L. Prevalence of hearing loss in adults with sickle cell disease. Ear Hear. 1991;12(5): 349-51.
-
(1991)
Ear Hear
, vol.12
, Issue.5
, pp. 349-351
-
-
Crawford, M.R.1
Gould, H.J.2
Smith, W.R.3
Beckford, N.4
Gibson, W.R.5
Bobo, L.6
-
18
-
-
33846279380
-
Deconstructing sickle cell disease: Reappraisal of the role of hemolysis in the development of clinical subphenotypes
-
Kato GJ, Gladwin MT, Steinberg MH. Deconstructing sickle cell disease: reappraisal of the role of hemolysis in the development of clinical subphenotypes. Blood Reviews. 2007;21(1):37-47.
-
(2007)
Blood Reviews
, vol.21
, Issue.1
, pp. 37-47
-
-
Kato, G.J.1
Gladwin, M.T.2
Steinberg, M.H.3
-
19
-
-
33746530641
-
Glomerular involvement in adults with sickle cell hemoglobinopathies. Prevalence and clinical correlates of progressive renal failure
-
Guasch A, Navarrete J, Nass K, Zayas CF. Glomerular involvement in adults with sickle cell hemoglobinopathies. Prevalence and clinical correlates of progressive renal failure. J Am Soc Nephrol. 2006;17(8):2228-35.
-
(2006)
J Am Soc Nephrol
, vol.17
, Issue.8
, pp. 2228-2235
-
-
Guasch, A.1
Navarrete, J.2
Nass, K.3
Zayas, C.F.4
-
20
-
-
13144267714
-
Early glomerular dysfunction in patients with sickle cell anemia
-
Schmitt F, Martinez F, Brillet G, Giatras I, Choukroun G, Girot R, et al. Early glomerular dysfunction in patients with sickle cell anemia. Am J Kidney Dis. 1998;32(2):208-14.
-
(1998)
Am J Kidney Dis
, vol.32
, Issue.2
, pp. 208-214
-
-
Schmitt, F.1
Martinez, F.2
Brillet, G.3
Giatras, I.4
Choukroun, G.5
Girot, R.6
-
21
-
-
34247173365
-
Albuminuria and renal function in homozygous sickle cell disease
-
Thompson J, Reid M, Hambleton I, Serjeant GR. Albuminuria and renal function in homozygous sickle cell disease. Arch Intern Med. 2007;167(7):701-8.
-
(2007)
Arch Intern Med
, vol.167
, Issue.7
, pp. 701-708
-
-
Thompson, J.1
Reid, M.2
Hambleton, I.3
Serjeant, G.R.4
-
22
-
-
77949887515
-
High prevalence of sickle cell trait in African Americans with ESRD
-
Derebail VK, Nachman PH, Key NS, Ansede H, Falk RJ, Kshirsagar AV. High prevalence of sickle cell trait in African Americans with ESRD. J Am Soc Nephrol. 2010;21(3):413-7.
-
(2010)
J Am Soc Nephrol
, vol.21
, Issue.3
, pp. 413-417
-
-
Derebail, V.K.1
Nachman, P.H.2
Key, N.S.3
Ansede, H.4
Falk, R.J.5
Kshirsagar, A.V.6
-
23
-
-
38349036151
-
Relative systemic hypertension in patients with sickle cell disease is associated with risk of pulmonary hypertension and renal insufficiency
-
Gordeuk VR, Sachdev V, Taylor JG, Gladwin MT, Kato G, Castro OL. Relative systemic hypertension in patients with sickle cell disease is associated with risk of pulmonary hypertension and renal insufficiency. Am J Hematol. 2007;83(1):15-8.
-
(2007)
Am J Hematol
, vol.83
, Issue.1
, pp. 15-18
-
-
Gordeuk, V.R.1
Sachdev, V.2
Taylor, J.G.3
Gladwin, M.T.4
Kato, G.5
Castro, O.L.6
-
24
-
-
26444560502
-
Arterial blood pressure and hyperviscosity in sickle cell disease
-
Johnson CS. Arterial blood pressure and hyperviscosity in sickle cell disease. Hematol Oncol Clin N Am. 2005;19(5):827-37.
-
(2005)
Hematol Oncol Clin N Am
, vol.19
, Issue.5
, pp. 827-837
-
-
Johnson, C.S.1
-
25
-
-
79960101398
-
A hemodynamic study of pulmonary hypertension in sickle cell disease
-
Parent F, Bachir D, Inamo J, Lionnet F, Driss F, Loko G, et al. A hemodynamic study of pulmonary hypertension in sickle cell disease. N Engl J Med. 2011;365(1):44-53.
-
(2011)
N Engl J Med
, vol.365
, Issue.1
, pp. 44-53
-
-
Parent, F.1
Bachir, D.2
Inamo, J.3
Lionnet, F.4
Driss, F.5
Loko, G.6
-
26
-
-
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. Mortality in sickle cell disease. Life expectancy and risk factors for early death. N Engl J Med. 1994; 330(23):1639-44.
-
(1994)
N Engl J Med
, vol.330
, Issue.23
, 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
-
27
-
-
0142215534
-
Causes of death in sickle cell disease: An autopsy study
-
Manci EA, Culberson DE, Yang YM, Gardner TM, Powell R, Haynes J, et al. Causes of death in sickle cell disease: an autopsy study. Br J Haematol. 2003;123(2): 359-65.
-
(2003)
Br J Haematol
, vol.123
, Issue.2
, pp. 359-365
-
-
Manci, E.A.1
Culberson, D.E.2
Yang, Y.M.3
Gardner, T.M.4
Powell, R.5
Haynes, J.6
-
28
-
-
0028345470
-
Acute multiorgan failure syndrome: A potentially catastrophic complication of severe sickle cell pain episodes
-
Hassell KL, Eckman JR, Lane PA. Acute multiorgan failure syndrome: a potentially catastrophic complication of severe sickle cell pain episodes. Am J Med. 1994;96(2): 155-62.
-
(1994)
Am J Med
, vol.96
, Issue.2
, pp. 155-162
-
-
Hassell, K.L.1
Eckman, J.R.2
Lane, P.A.3
-
29
-
-
0037404579
-
Iron in sickle cell disease: A review why less is better
-
Koduri PR. Iron in sickle cell disease: a review why less is better. Am J Hematol. 2003;73(1):59-63.
-
(2003)
Am J Hematol
, vol.73
, Issue.1
, pp. 59-63
-
-
Koduri, P.R.1
-
30
-
-
0019914185
-
Overt iron deficiency in sickle cell disease
-
Haddy TB, Castro O. Overt iron deficiency in sickle cell disease. Arch Intern Med. 1982;142(9):1621-4.
-
(1982)
Arch Intern Med
, vol.142
, Issue.9
, pp. 1621-1624
-
-
Haddy, T.B.1
Castro, O.2
-
31
-
-
0017855570
-
Irreversibly Sickled Cells and Red Cell Survival in Sickle Cell Anemia. A Study with Both DF3P and 51CR
-
McCurdy PR, Sherman AS. Irreversibly Sickled Cells and Red Cell Survival in Sickle Cell Anemia. A Study with Both DF3P and 51CR. Am J Med. 1978;64(2):253-8.
-
(1978)
Am J Med
, vol.64
, Issue.2
, pp. 253-258
-
-
McCurdy, P.R.1
Sherman, A.S.2
-
32
-
-
0016669440
-
Red cell life span in sickle cell-hemoglobin C disease with a note about sickle cellhemoglobin O ARAB
-
McCurdy PR, Mahmood L, Sherman AS. Red cell life span in sickle cell-hemoglobin C disease with a note about sickle cellhemoglobin O ARAB. Blood. 1975;45(2): 273-9.
-
(1975)
Blood
, vol.45
, Issue.2
, pp. 273-279
-
-
McCurdy, P.R.1
Mahmood, L.2
Sherman, A.S.3
-
33
-
-
33644775612
-
Lactate dehydrogenase as a biomarker of hemolysis-associated nitric oxide resistance, priapism, leg ulceration, pulmonary hypertension, and death in patients with sickle cell disease
-
Kato GJ, McGowan V, Machado RF, Little JA, Taylor J 6th, Morris CR, et al. Lactate dehydrogenase as a biomarker of hemolysis-associated nitric oxide resistance, priapism, leg ulceration, pulmonary hypertension, and death in patients with sickle cell disease. Blood. 2006;107(6):2279-85.
-
(2006)
Blood
, vol.107
, Issue.6
, pp. 2279-2285
-
-
Kato, G.J.1
McGowan, V.2
Machado, R.F.3
Little, J.A.4
Taylor VI, J.5
Morris, C.R.6
-
34
-
-
78851468762
-
Reconstructing sickle cell disease: A data-based analysis of the "hyperhemolysis paradigm" for pulmonary hypertension from the perspective of evidencebased medicine
-
Hebbel RP. Reconstructing sickle cell disease: A data-based analysis of the "hyperhemolysis paradigm" for pulmonary hypertension from the perspective of evidencebased medicine. Am J Hematol. 2011;86(2): 123-54.
-
(2011)
Am J Hematol
, vol.86
, Issue.2
, pp. 123-154
-
-
Hebbel, R.P.1
-
35
-
-
0029922667
-
Protein and energy metabolism in prepubertal children with sickle cell anemia
-
Salman EK, Haymond MW, Bayne E, Sager BK, Wiisanen A, Pitel P, et al. Protein and energy metabolism in prepubertal children with sickle cell anemia. Pediatr Res. 1996;40(1):34-40.
-
(1996)
Pediatr Res
, vol.40
, Issue.1
, pp. 34-40
-
-
Salman, E.K.1
Haymond, M.W.2
Bayne, E.3
Sager, B.K.4
Wiisanen, A.5
Pitel, P.6
-
36
-
-
0020355891
-
SC erythrocytes have an abnormally high intracellular hemoglobin concentration. Pathophysiological consequencies
-
Fabry ME, Kaul DK, Raventos-Suarez C, Chang H, Nagel RL. SC erythrocytes have an abnormally high intracellular hemoglobin concentration. Pathophysiological consequencies. J Clin Invest. 1982;70(6):1315-9.
-
(1982)
J Clin Invest
, vol.70
, Issue.6
, pp. 1315-1319
-
-
Fabry, M.E.1
Kaul, D.K.2
Raventos-Suarez, C.3
Chang, H.4
Nagel, R.L.5
-
37
-
-
0037609659
-
Role of phlebotomy in the management of hemoglobin SC disease: Case report and review of the literature
-
Markham MJ, Lottenberg R, Zumberg M. Role of phlebotomy in the management of hemoglobin SC disease: case report and review of the literature. Am J Hematol. 2003;73(2):121-5.
-
(2003)
Am J Hematol
, vol.73
, Issue.2
, pp. 121-125
-
-
Markham, M.J.1
Lottenberg, R.2
Zumberg, M.3
-
38
-
-
0034162841
-
Prevention of sickle cell crises with multiple phlebotomies
-
Bouchaïr N, Manigne P, Kanfer A, Raphalen P, de Montalembert M, Hagege I, et al. Prevention of sickle cell crises with multiple phlebotomies. Arch Pediatr. 2000;7(3):249-55.
-
(2000)
Arch Pediatr
, vol.7
, Issue.3
, pp. 249-255
-
-
Bouchaïr, N.1
Manigne, P.2
Kanfer, A.3
Raphalen, P.4
de Montalembert, M.5
Hagege, I.6
-
39
-
-
0036301616
-
Amelioration of painful crises in sickle cell disease by venesections
-
Rombos Y, Tzanetea R, Kalotychou V, Konstantopoulos K, Simitzis S, Tassiopoulos T, et al. Amelioration of painful crises in sickle cell disease by venesections. Blood Cells Mol Dis. 2002;28(2):283-7.
-
(2002)
Blood Cells Mol Dis
, vol.28
, Issue.2
, pp. 283-287
-
-
Rombos, Y.1
Tzanetea, R.2
Kalotychou, V.3
Konstantopoulos, K.4
Simitzis, S.5
Tassiopoulos, T.6
-
40
-
-
0027930702
-
Improvement of sickle cell anemia by iron-limited erythropoiesis
-
Castro O, Poillon WN, Finke H, Massac E, Kim BC. Improvement of sickle cell anemia by iron-limited erythropoiesis. Am J Hematol. 1994;47(2):74-81.
-
(1994)
Am J Hematol
, vol.47
, Issue.2
, pp. 74-81
-
-
Castro, O.1
Poillon, W.N.2
Finke, H.3
Massac, E.4
Kim, B.C.5
-
41
-
-
77955905049
-
How I use hydroxyurea to treat young patients with sickle cell anemia
-
Ware RE. How I use hydroxyurea to treat young patients with sickle cell anemia. Blood. 2010;115(26):5300-11.
-
(2010)
Blood
, vol.115
, Issue.26
, pp. 5300-5311
-
-
Ware, R.E.1
|