-
1
-
-
0002978048
-
Hyaline thrombosis of the terminal arterioles and capillaries: A hitherto undescribed disease
-
Moschcowitz E. Hyaline thrombosis of the terminal arterioles and capillaries: a hitherto undescribed disease. Proc NY Pathol Soc 24: 21-24, 1924.
-
(1924)
Proc NY Pathol Soc
, vol.24
, pp. 21-24
-
-
Moschcowitz, E.1
-
2
-
-
0037158606
-
Thrombotic microangiopathies
-
Moake JL. Thrombotic microangiopathies. N Engl J Med 347: 589-600, 2002.
-
(2002)
N Engl J Med
, vol.347
, pp. 589-600
-
-
Moake, J.L.1
-
3
-
-
44949185826
-
Hemolytic uremic syndrome, thrombotic thrombocytopenia purpula, and other thrombotic microangiopathies and coagulopathies
-
6th ed. Jennett J, et al, Eds. Lippincott Williams & Wilkins, Philadelphia
-
Laszik ZG, Silva FG. Hemolytic uremic syndrome, thrombotic thrombocytopenia purpula, and other thrombotic microangiopathies and coagulopathies. In: Heptinstall’s Pathology of the Kidney. 6th ed. Jennett J, et al, Eds. Lippincott Williams & Wilkins, Philadelphia, 2007: 699-762.
-
(2007)
Heptinstall’s Pathology of the Kidney
, pp. 699-762
-
-
Laszik, Z.G.1
Silva, F.G.2
-
4
-
-
73049157744
-
Syndrome of hemolysis, thrombopenia and nephropathy in infancy
-
Javett SN, Senior B. Syndrome of hemolysis, thrombopenia and nephropathy in infancy. Pediatrics 29: 209-223, 1962.
-
(1962)
Pediatrics
, vol.29
, pp. 209-223
-
-
Javett, S.N.1
Senior, B.2
-
5
-
-
7244239052
-
Proportion of drugrelated serious rare blood dyscrasias: Estimates from the Berlin Case-Control Surveillance Study
-
Andersohn F, Bronder E, Klimpel A, Garbe E. Proportion of drugrelated serious rare blood dyscrasias: estimates from the Berlin Case-Control Surveillance Study. Am J Hematol 77: 316-318, 2004.
-
(2004)
Am J Hematol
, vol.77
, pp. 316-318
-
-
Andersohn, F.1
Bronder, E.2
Klimpel, A.3
Garbe, E.4
-
6
-
-
10744224391
-
Clopidogrelassociated TTP: An update of pharmacovigilance efforts conducted by independent researchers, pharmaceutical suppliers, and the Food and Drug Administration
-
Zakarija A, Bandarenko N, Pandey DK, et al. Clopidogrelassociated TTP: an update of pharmacovigilance efforts conducted by independent researchers, pharmaceutical suppliers, and the Food and Drug Administration. Stroke 35: 533-537, 2004.
-
(2004)
Stroke
, vol.35
, pp. 533-537
-
-
Zakarija, A.1
Bandarenko, N.2
Pandey, D.K.3
-
7
-
-
0032569461
-
Thrombotic thrombocytopenic purpura after stenting and ticlopidine
-
Bennett CL, Kiss JE, Weinberg PD, et al. Thrombotic thrombocytopenic purpura after stenting and ticlopidine. Lancet 352: 1036-1037, 1998.
-
(1998)
Lancet
, vol.352
, pp. 1036-1037
-
-
Bennett, C.L.1
Kiss, J.E.2
Weinberg, P.D.3
-
8
-
-
0033518847
-
Incidence and clinical course of thrombotic thrombocytopenic purpura due to ticlopidine following coronary stenting. EPISTENT Investigators. Evaluation of Platelet IIb/IIIa Inhibitor for Stenting
-
Steinhubl SR, Tan WA, Foody JM, Topol EJ. Incidence and clinical course of thrombotic thrombocytopenic purpura due to ticlopidine following coronary stenting. EPISTENT Investigators. Evaluation of Platelet IIb/IIIa Inhibitor for Stenting. JAMA 281: 806-810, 1999.
-
(1999)
JAMA
, vol.281
, pp. 806-810
-
-
Steinhubl, S.R.1
Tan, W.A.2
Foody, J.M.3
Topol, E.J.4
-
9
-
-
0033454749
-
Clopidogrel versus ti clopidine after intracoronary stent placement
-
Berger PB, Bell MR, Rihal CS, et al. Clopidogrel versus ti clopidine after intracoronary stent placement. J Am Coll Cardiol 34: 1891-1894, 1999.
-
(1999)
J am Coll Cardiol
, vol.34
, pp. 1891-1894
-
-
Berger, P.B.1
Bell, M.R.2
Rihal, C.S.3
-
10
-
-
84901739636
-
ACCF/AHA/ SCAI guideline for percutaneous coronary intervention: A report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines and the Society for Cardiovascular Angiography and Interventions
-
2013
-
Levine GN, Bates ER, Blankenship JC, et al. 2011 ACCF/AHA/ SCAI guideline for percutaneous coronary intervention: a report of the American College of Cardiology Foundation/American Heart Association Task Force on Practice Guidelines and the Society for Cardiovascular Angiography and Interventions. Catheter Cardiovasc Interv 82: E266-E355, 2013.
-
(2011)
Catheter Cardiovasc Interv
, vol.82
, pp. E266-E355
-
-
Levine, G.N.1
Bates, E.R.2
Blankenship, J.C.3
-
11
-
-
84868544027
-
Ticlopidine-, clopidogrel-, and prasugrel-associated thrombotic thrombocytopenic purpura: A 20-year review from the Southern Network on Adverse Reactions (SONAR)
-
Jacob S, Dunn BL, Qureshi ZP, et al. Ticlopidine-, clopidogrel-, and prasugrel-associated thrombotic thrombocytopenic purpura: a 20-year review from the Southern Network on Adverse Reactions (SONAR). Semin Thromb Hemost 38: 845-853, 2012.
-
(2012)
Semin Thromb Hemost
, vol.38
, pp. 845-853
-
-
Jacob, S.1
Dunn, B.L.2
Qureshi, Z.P.3
-
12
-
-
0034660472
-
Thrombotic thrombocytopenic purpura associated with clopidogrel
-
Bennett CL, Connors JM, Carwile JM, et al. Thrombotic thrombocytopenic purpura associated with clopidogrel. N Engl J Med 342: 1773-1777, 2000.
-
(2000)
N Engl J Med
, vol.342
, pp. 1773-1777
-
-
Bennett, C.L.1
Connors, J.M.2
Carwile, J.M.3
-
13
-
-
84963531140
-
-
[cited 2014 Jan. 30]
-
Pharmaceuticals and Medical Devices Agency [Internet]. [cited 2014 Jan. 30]. Available from: http://www.info.pmda.go.jp/fsearch new/jsp/menu_fukusayou_base.jsp
-
-
-
-
14
-
-
34548542028
-
Two mechanistic pathways for thienopyridine-associated thrombotic thrombocytopenic purpura: A report from the SERF-TTP Research Group and the RADAR Project
-
Bennett CL, Kim B, Zakarija A, et al. Two mechanistic pathways for thienopyridine-associated thrombotic thrombocytopenic purpura: a report from the SERF-TTP Research Group and the RADAR Project. J Am Coll Cardiol 50: 1138-1143, 2007.
-
(2007)
J am Coll Cardiol
, vol.50
, pp. 1138-1143
-
-
Bennett, C.L.1
Kim, B.2
Zakarija, A.3
-
15
-
-
0032569884
-
Von Willebrand factorcleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome
-
Furlan M, Robles R, Galbusera M, et al. von Willebrand factorcleaving protease in thrombotic thrombocytopenic purpura and the hemolytic-uremic syndrome. N Engl J Med 339: 1578-1584, 1998.
-
(1998)
N Engl J Med
, vol.339
, pp. 1578-1584
-
-
Furlan, M.1
Robles, R.2
Galbusera, M.3
-
16
-
-
2542490269
-
Effect of plasma exchange on plasma ADAMTS13 metalloprotease activity, inhibitor level, and clinical outcome in patients with idiopathic and nonidiopathic thrombotic thrombocytopenic purpura
-
Zheng XL, Kaufman RM, Goodnough LT, Sadler JE. Effect of plasma exchange on plasma ADAMTS13 metalloprotease activity, inhibitor level, and clinical outcome in patients with idiopathic and nonidiopathic thrombotic thrombocytopenic purpura. Blood 103: 4043-4049, 2004.
-
(2004)
Blood
, vol.103
, pp. 4043-4049
-
-
Zheng, X.L.1
Kaufman, R.M.2
Goodnough, L.T.3
Sadler, J.E.4
-
17
-
-
33644830187
-
Clinical aspects and molecular basis of primary deficiencies of complement component C3 and its regulatory proteins factor I and factor H
-
Reis ES, Falcao DA, Isaac L. Clinical aspects and molecular basis of primary deficiencies of complement component C3 and its regulatory proteins factor I and factor H. Scand J Immunol 63: 155-168, 2006.
-
(2006)
Scand J Immunol
, vol.63
, pp. 155-168
-
-
Reis, E.S.1
Falcao, D.A.2
Isaac, L.3
-
18
-
-
57649170093
-
Human C3 deficiency associated with impairments in dendritic cell differentiation, memory B cells, and regulatory T cells
-
Ghannam A, Pernollet M, Fauquert JL, et al. Human C3 deficiency associated with impairments in dendritic cell differentiation, memory B cells, and regulatory T cells. J Immunol 181: 5158-5166, 2008.
-
(2008)
J Immunol
, vol.181
, pp. 5158-5166
-
-
Ghannam, A.1
Pernollet, M.2
Fauquert, J.L.3
-
19
-
-
0035219868
-
Identification of a novel mutation (Tyr1081Ter) in sisters with hereditary component C3 deficiency and SLE-like symptoms
-
Matsuyama W, Nakagawa M, Takashima H, Muranaga F, Sano Y, Osame M. Identification of a novel mutation (Tyr1081Ter) in sisters with hereditary component C3 deficiency and SLE-like symptoms. Hum Mutat 17: 79, 2001.
-
(2001)
Hum Mutat
, vol.17
, pp. 79
-
-
Matsuyama, W.1
Nakagawa, M.2
Takashima, H.3
Muranaga, F.4
Sano, Y.5
Osame, M.6
-
20
-
-
70350279315
-
Atypical hemolytic-uremic syndrome
-
Noris M, Remuzzi G. Atypical hemolytic-uremic syndrome. N Engl J Med 361: 1676-1687, 2009.
-
(2009)
N Engl J Med
, vol.361
, pp. 1676-1687
-
-
Noris, M.1
Remuzzi, G.2
-
21
-
-
0035089983
-
Familial hemolytic uremic syndrome associated with complement factor H deficiency
-
Landau D, Shalev H, Levy-Finer G, Polonsky A, Segev Y, Katchko L. Familial hemolytic uremic syndrome associated with complement factor H deficiency. J Pediatr 138: 412-417, 2001.
-
(2001)
J Pediatr
, vol.138
, pp. 412-417
-
-
Landau, D.1
Shalev, H.2
Levy-Finer, G.3
Polonsky, A.4
Segev, Y.5
Katchko, L.6
-
22
-
-
38949155911
-
Factor H autoantibodies in atypical hemolytic uremic syndrome correlate with CFHR1/ CFHR3 deficiency
-
Jozsi M, Licht C, Strobel S, et al. Factor H autoantibodies in atypical hemolytic uremic syndrome correlate with CFHR1/ CFHR3 deficiency. Blood 111: 1512-1514, 2008.
-
(2008)
Blood
, vol.111
, pp. 1512-1514
-
-
Jozsi, M.1
Licht, C.2
Strobel, S.3
-
23
-
-
84876044818
-
Genetics and outcome of atypical hemolytic uremic syndrome: A nationwide French series comparing children and adults
-
Fremeaux-Bacchi V, Fakhouri F, Garnier A, et al. Genetics and outcome of atypical hemolytic uremic syndrome: a nationwide French series comparing children and adults. Clin J Am Soc Nephrol 8: 554-562, 2013.
-
(2013)
Clin J am Soc Nephrol
, vol.8
, pp. 554-562
-
-
Fremeaux-Bacchi, V.1
Fakhouri, F.2
Garnier, A.3
-
24
-
-
77958587405
-
Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype
-
Noris M, Caprioli J, Bresin E, et al. Relative role of genetic complement abnormalities in sporadic and familial aHUS and their impact on clinical phenotype. Clin J Am Soc Nephrol 5: 1844-1859, 2010.
-
(2010)
Clin J am Soc Nephrol
, vol.5
, pp. 1844-1859
-
-
Noris, M.1
Caprioli, J.2
Bresin, E.3
-
25
-
-
84880453521
-
Complement factor H mutations are present in ADAMTS13-deficient, ticlopidine-associated thrombotic microangiopathies
-
Chapin J, Eyler S, Smith R, Tsai HM, Laurence J. Complement factor H mutations are present in ADAMTS13-deficient, ticlopidine-associated thrombotic microangiopathies. Blood 121: 4012-4013, 2013.
-
(2013)
Blood
, vol.121
, pp. 4012-4013
-
-
Chapin, J.1
Eyler, S.2
Smith, R.3
Tsai, H.M.4
Laurence, J.5
-
26
-
-
84945437213
-
Thrombotic microangiopathy, cancer, and cancer drugs
-
Izzedine H, Perazella MA. Thrombotic microangiopathy, cancer, and cancer drugs. Am J Kidney Dis 66: 857-868, 2015.
-
(2015)
Am J Kidney Dis
, vol.66
, pp. 857-868
-
-
Izzedine, H.1
Perazella, M.A.2
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