-
1
-
-
0023179188
-
Development of the human coagulation system in the full-term infant
-
Andrew M, Paes B, Milner R, et al. Development of the human coagulation system in the full-term infant. Blood 1987; 70: 165-72.
-
(1987)
Blood
, vol.70
, pp. 165-172
-
-
Andrew, M.1
Paes, B.2
Milner, R.3
-
2
-
-
0023787137
-
Development of the human coagulation system in the healthy premature infant
-
Andrew M, Paes B, Milner R, et al. Development of the human coagulation system in the healthy premature infant. Blood 1988; 72: 1651-7.
-
(1988)
Blood
, vol.72
, pp. 1651-1657
-
-
Andrew, M.1
Paes, B.2
Milner, R.3
-
3
-
-
0026792857
-
Maturation of the hemostatic system during childhood
-
Andrew M, Vegh P, Johnston M, et al. Maturation of the hemostatic system during childhood. Blood 1992; 80: 1998-2005.
-
(1992)
Blood
, vol.80
, pp. 1998-2005
-
-
Andrew, M.1
Vegh, P.2
Johnston, M.3
-
4
-
-
50449098285
-
Mechanisms of thrombus formation
-
Furie B, Furie BC. Mechanisms of thrombus formation. N Engl J Med 2008; 359: 938-49.
-
(2008)
N Engl J Med
, vol.359
, pp. 938-949
-
-
Furie, B.1
Furie, B.C.2
-
5
-
-
0018662189
-
Clinical and laboratory diagnosis of hemostatic disorders in newborn infants
-
Zipursky A, deSa D, Hsu E, et al. Clinical and laboratory diagnosis of hemostatic disorders in newborn infants. Am J Pediatr Hematol Oncol 1979; 1: 217-26.
-
(1979)
Am J Pediatr Hematol Oncol
, vol.1
, pp. 217-226
-
-
Zipursky, A.1
deSa, D.2
Hsu, E.3
-
6
-
-
33748260015
-
Disseminated intravascular coagulation
-
Levi M, Ten Cate H. Disseminated intravascular coagulation. N Engl J Med 1999; 341: 586-92.
-
(1999)
N Engl J Med
, vol.341
, pp. 586-592
-
-
Levi, M.1
Ten Cate, H.2
-
7
-
-
0036022849
-
Haemostatic abnormalities in patients with liver disease
-
Lisman T, Leebeek FW, de Groot PG. Haemostatic abnormalities in patients with liver disease. J Hepatol 2002; 37: 280-7.
-
(2002)
J Hepatol
, vol.37
, pp. 280-287
-
-
Lisman, T.1
Leebeek, F.W.2
de Groot, P.G.3
-
8
-
-
41149105360
-
Acquired disorders of hemostasis
-
In: Nathan DG, Orkin SH, Ginsburg D, Look AT (eds) 6th edn. Philadelphia: WB Saunders
-
Monagle P, Andrew M. Acquired disorders of hemostasis. In: Nathan DG, Orkin SH, Ginsburg D, Look AT (eds). Nathan and Oski ' s Hematology of Infancy and Childhood, Vol. 2, 6th edn. Philadelphia: WB Saunders; 2003: 1631-67.
-
(2003)
Nathan and Oski's Hematology of Infancy and Childhood, Vol. 2
, pp. 1631-1667
-
-
Monagle, P.1
Andrew, M.2
-
9
-
-
56049098385
-
Rare inherited disorders of fibrinogen
-
Acharya SS, DiMichele DM. Rare inherited disorders of fibrinogen. Haemophilia 2008; 14: 1151-8.
-
(2008)
Haemophilia
, vol.14
, pp. 1151-1158
-
-
Acharya, S.S.1
DiMichele, D.M.2
-
11
-
-
0033828195
-
Von Willebrand disease in a pediatric-based population - Comparison of type 1 diagnostic criteria and use of the PFA-100 and a von Willebrand factor/ collagen-binding assay
-
Dean JA, Blanchette VS, Carcao MD, et al. von Willebrand disease in a pediatric-based population - Comparison of type 1 diagnostic criteria and use of the PFA-100 and a von Willebrand factor/ collagen-binding assay. Thromb Haemost 2000; 84: 401-9.
-
(2000)
Thromb Haemost
, vol.84
, pp. 401-409
-
-
Dean, J.A.1
Blanchette, V.S.2
Carcao, M.D.3
-
12
-
-
29244439008
-
The discriminant power of bleeding history for the diagnosis of type 1 von Willebrand disease: An international, multicenter study
-
Rodeghiero F, Castaman G, Tosetto A, et al. The discriminant power of bleeding history for the diagnosis of type 1 von Willebrand disease: An international, multicenter study. J Thromb Haemost 2005; 3: 2619-26.
-
(2005)
J Thromb Haemost
, vol.3
, pp. 2619-2626
-
-
Rodeghiero, F.1
Castaman, G.2
Tosetto, A.3
-
13
-
-
43149083497
-
Bleeding scores in inherited bleeding disorders: Clinical or research tools?
-
Tosetto A, Castaman G, Rodeghiero F. Bleeding scores in inherited bleeding disorders: Clinical or research tools? Haemophilia 2008; 14: 415-22.
-
(2008)
Haemophilia
, vol.14
, pp. 415-422
-
-
Tosetto, A.1
Castaman, G.2
Rodeghiero, F.3
-
14
-
-
44249116406
-
Relevance of quantitative assessment of bleeding in haemorrhagic disorders
-
Rodeghiero F, Kadir RA, Tosetto A, James PD. Relevance of quantitative assessment of bleeding in haemorrhagic disorders. Haemophilia 2008; 14 ( Suppl. 3 ): 68-75.
-
(2008)
Haemophilia
, vol.14
, Issue.SUPPL. 3
, pp. 68-75
-
-
Rodeghiero, F.1
Kadir, R.A.2
Tosetto, A.3
James, P.D.4
-
15
-
-
0023951722
-
Prevalence and significance of mild bleeding disorders in children with recurrent epistaxis
-
Katsanis E, Luke KH, Hsu E, Li M, Lillicrap D. Prevalence and significance of mild bleeding disorders in children with recurrent epistaxis. J Pediatr 1988; 113: 73-6.
-
(1988)
J Pediatr
, vol.113
, pp. 73-76
-
-
Katsanis, E.1
Luke, K.H.2
Hsu, E.3
Li, M.4
Lillicrap, D.5
-
16
-
-
0025183484
-
Assessment of menstrual blood loss using a pictorial chart
-
Higham JM, O ' Brien PM, Shaw RW. Assessment of menstrual blood loss using a pictorial chart. Br J Obstet Gynaecol 1990; 97: 734-9.
-
(1990)
Br J Obstet Gynaecol
, vol.97
, pp. 734-739
-
-
Higham, J.M.1
O'Brien, P.M.2
Shaw, R.W.3
-
17
-
-
0036843499
-
Grading of hemorrhage in children with idiopathic thrombocytopenic purpura
-
Buchanan GR, Adix L. Grading of hemorrhage in children with idiopathic thrombocytopenic purpura. J Pediatr 2002; 141: 683-8.
-
(2002)
J Pediatr
, vol.141
, pp. 683-688
-
-
Buchanan, G.R.1
Adix, L.2
-
18
-
-
0024425034
-
New variant of von Willebrand disease with defective binding to factor VIII
-
Nishino M, Girma JP, Rothschild C, et al. New variant of von Willebrand disease with defective binding to factor VIII. Blood 1989; 74: 1591-9.
-
(1989)
Blood
, vol.74
, pp. 1591-1599
-
-
Nishino, M.1
Girma, J.P.2
Rothschild, C.3
-
19
-
-
0029813966
-
Factor VIII binding assay of von Willebrand factor and the diagnosis of type 2N von Willebrand disease - Results of an international survey On behalf of the Subcommittee on von Willebrand Factor of the Scientific and Standardization Committee of the ISTH
-
Mazurier C, Meyer D. Factor VIII binding assay of von Willebrand factor and the diagnosis of type 2N von Willebrand disease - Results of an international survey. On behalf of the Subcommittee on von Willebrand Factor of the Scientific and Standardization Committee of the ISTH. Thromb Haemost 1996; 76: 270-4.
-
(1996)
Thromb Haemost
, vol.76
, pp. 270-274
-
-
Mazurier, C.1
Meyer, D.2
-
20
-
-
0029842964
-
Results of a screening for von Willebrand disease type 2N in patients with suspected haemophilia A or von Willebrand disease type 1
-
Schneppenheim R, Budde U, Krey S, et al. Results of a screening for von Willebrand disease type 2N in patients with suspected haemophilia A or von Willebrand disease type 1. Thromb Haemost 1996; 76: 598-602.
-
(1996)
Thromb Haemost
, vol.76
, pp. 598-602
-
-
Schneppenheim, R.1
Budde, U.2
Krey, S.3
-
21
-
-
0030755267
-
The two common mutations causing factor XI deficiency in Jews stem from distinct founders: One of ancient Middle Eastern origin and another of more recent European origin
-
Peretz H, Mulai A, Usher S, et al. The two common mutations causing factor XI deficiency in Jews stem from distinct founders: One of ancient Middle Eastern origin and another of more recent European origin. Blood 1997; 90: 2654-9.
-
(1997)
Blood
, vol.90
, pp. 2654-2659
-
-
Peretz, H.1
Mulai, A.2
Usher, S.3
-
22
-
-
0032521229
-
A common genetic polymorphism (46 C to T substitution) in the 5 '-untranslated region of the coagulation factor XII gene is associated with low translation efficiency and decrease in plasma factor XII level
-
Kanaji T, Okamura T, Osaki K, et al. A common genetic polymorphism (46 C to T substitution) in the 5 '-untranslated region of the coagulation factor XII gene is associated with low translation efficiency and decrease in plasma factor XII level. Blood 1998; 91: 2010-14.
-
(1998)
Blood
, vol.91
, pp. 2010-2014
-
-
Kanaji, T.1
Okamura, T.2
Osaki, K.3
-
23
-
-
0019845596
-
Reduced titers of Hageman factor (Factor XII) in Orientals
-
Gordon EM, Donaldson VH, Saito H, Su E, Ratnoff OD. Reduced titers of Hageman factor (Factor XII) in Orientals. Ann Intern Med 2001; 95: 697.
-
(2001)
Ann Intern Med
, vol.95
, pp. 697
-
-
Gordon, E.M.1
Donaldson, V.H.2
Saito, H.3
Su, E.4
Ratnoff, O.D.5
-
24
-
-
0037910378
-
MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single illness
-
Seri M, Pecci A, Di Bari F, et al. MYH9-related disease: May-Hegglin anomaly, Sebastian syndrome, Fechtner syndrome, and Epstein syndrome are not distinct entities but represent a variable expression of a single illness. Medicine (Baltimore) 2003; 82: 203-15.
-
(2003)
Medicine (Baltimore)
, vol.82
, pp. 203-215
-
-
Seri, M.1
Pecci, A.2
Di Bari, F.3
-
25
-
-
22144455398
-
The role of PFA-100 testing in the investigation and management of haemostatic defects in children and adults
-
Harrison P. The role of PFA-100 testing in the investigation and management of haemostatic defects in children and adults. Br J Haematol 2005; 130: 3-10.
-
(2005)
Br J Haematol
, vol.130
, pp. 3-10
-
-
Harrison, P.1
-
26
-
-
0029951954
-
Estimation of the lower limits of manual and automated platelet counting
-
Hanseler E, Fehr J, Keller H. Estimation of the lower limits of manual and automated platelet counting. Am J Clin Pathol 1996; 105: 782-7.
-
(1996)
Am J Clin Pathol
, vol.105
, pp. 782-787
-
-
Hanseler, E.1
Fehr, J.2
Keller, H.3
-
27
-
-
0029131921
-
EDTA-dependent pseudothrombocytopenia: A clinical and epidemiological study of 112 cases, with 10-year follow-up
-
Bizzaro N. EDTA-dependent pseudothrombocytopenia: A clinical and epidemiological study of 112 cases, with 10-year follow-up. Am J Hematol 1995; 50: 103-9.
-
(1995)
Am J Hematol
, vol.50
, pp. 103-109
-
-
Bizzaro, N.1
-
28
-
-
0019401772
-
The platelet count and mean platelet volume
-
Giles C. The platelet count and mean platelet volume. Br J Haematol 1981; 48: 31-7.
-
(1981)
Br J Haematol
, vol.48
, pp. 31-37
-
-
Giles, C.1
-
29
-
-
33947325827
-
Identification of inherited macrothrombocytopenias based on mean platelet volume among patients diagnosed with idiopathic thrombocytopenia
-
Gohda F, Uchiumi H, Handa H, et al. Identification of inherited macrothrombocytopenias based on mean platelet volume among patients diagnosed with idiopathic thrombocytopenia. Thromb Res 2007; 119: 741-6.
-
(2007)
Thromb Res
, vol.119
, pp. 741-746
-
-
Gohda, F.1
Uchiumi, H.2
Handa, H.3
-
30
-
-
0035127878
-
Megathrombocytes and spurious thrombocytopenia
-
Racchi O, Rapezzi D. Megathrombocytes and spurious thrombocytopenia. Eur J Haematol 2001; 66: 140-1.
-
(2001)
Eur J Haematol
, vol.66
, pp. 140-141
-
-
Racchi, O.1
Rapezzi, D.2
-
31
-
-
21644478439
-
Giant platelet syndromes and the MYH9 mutations
-
Balduini CL. Giant platelet syndromes and the MYH9 mutations. Lab Hematol 2004; 10: 187-8.
-
(2004)
Lab Hematol
, vol.10
, pp. 187-188
-
-
Balduini, C.L.1
-
33
-
-
0025166288
-
A critical reappraisal of the bleeding time
-
Rodgers RP, Levin J. A critical reappraisal of the bleeding time. Semin Thromb Haemost 1990; 16: 1-20.
-
(1990)
Semin Thromb Haemost
, vol.16
, pp. 1-20
-
-
Rodgers, R.P.1
Levin, J.2
-
34
-
-
0034867946
-
Platelet function analyzer (PFA-100): A tool to quantify congenital or acquired platelet dysfunction
-
Jilma B. Platelet function analyzer (PFA-100): A tool to quantify congenital or acquired platelet dysfunction. J Lab Clin Med 2001; 138: 152-63.
-
(2001)
J Lab Clin Med
, vol.138
, pp. 152-163
-
-
Jilma, B.1
-
35
-
-
7144227947
-
The Platelet Function Analyzer (PFA-100): A novel in-vitro system for evaluation of primary hemostasis in children
-
Carcao MD, Blanchette VS, Dean JA, et al. The Platelet Function Analyzer (PFA-100): A novel in-vitro system for evaluation of primary hemostasis in children. Br J Haematol 1998; 101: 70-3.
-
(1998)
Br J Haematol
, vol.101
, pp. 70-73
-
-
Carcao, M.D.1
Blanchette, V.S.2
Dean, J.A.3
-
36
-
-
0036344893
-
Clinical application of the PFA-100
-
Favaloro EJ. Clinical application of the PFA-100. Curr Opin Hematol 2002; 9: 407-15.
-
(2002)
Curr Opin Hematol
, vol.9
, pp. 407-415
-
-
Favaloro, E.J.1
-
37
-
-
13244279572
-
Template bleeding time and PFA-100 have low sensitivity to screen patients with hereditary mucocutaneous hemorrhages: Comparative study in 148 patients
-
Quiroga T, Goycoolea M, Mu ñ oz B, et al. Template bleeding time and PFA-100 have low sensitivity to screen patients with hereditary mucocutaneous hemorrhages: Comparative study in 148 patients. J Thromb Haemost 2004; 2: 892-8.
-
(2004)
J Thromb Haemost
, vol.2
, pp. 892-898
-
-
Quiroga, T.1
Goycoolea, M.2
Muñoz, B.3
-
38
-
-
33645557848
-
The Platelet Physiology Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis Platelet function analyzer (PFA)-100 closure time in the evaluation of platelet disorders and platelet function
-
Hayward CP, Harrison P, Cattaneo M, et al. The Platelet Physiology Subcommittee of the Scientific and Standardization Committee of the International Society on Thrombosis and Haemostasis. Platelet function analyzer (PFA)-100 closure time in the evaluation of platelet disorders and platelet function. J Thromb Haemost 2006; 4: 312-19.
-
(2006)
J Thromb Haemost
, vol.4
, pp. 312-319
-
-
Hayward, C.P.1
Harrison, P.2
Cattaneo, M.3
-
39
-
-
33646868601
-
Evaluation of prolonged aPTT values in the pediatric population
-
Shah MD, O ' Riordan MA, Alexander SW. Evaluation of prolonged aPTT values in the pediatric population. Clin Pediatr 2006; 45: 347-53.
-
(2006)
Clin Pediatr
, vol.45
, pp. 347-353
-
-
Shah, M.D.1
O'Riordan, M.A.2
Alexander, S.W.3
-
40
-
-
0027960173
-
Transient lupus anticoagulant associated with prothrombin deficiency: Unusual cause of bleeding in a 5-year-old girl
-
Humphries JE, Acker MN, Pinkston JE, Ruddy S. Transient lupus anticoagulant associated with prothrombin deficiency: Unusual cause of bleeding in a 5-year-old girl. Am J Pediatr Hematol Oncol 1994; 16: 372-6.
-
(1994)
Am J Pediatr Hematol Oncol
, vol.16
, pp. 372-376
-
-
Humphries, J.E.1
Acker, M.N.2
Pinkston, J.E.3
Ruddy, S.4
-
41
-
-
34250191847
-
Evidence of a U-shaped association between factor XII activity and overall survival
-
Endler G, Marsik C, Jilma B, et al. Evidence of a U-shaped association between factor XII activity and overall survival. J Thromb Haemost 2007; 5: 1143-8.
-
(2007)
J Thromb Haemost
, vol.5
, pp. 1143-1148
-
-
Endler, G.1
Marsik, C.2
Jilma, B.3
-
42
-
-
0022629982
-
In vitro neutralization of heparin in plasma prior to the activated partial thromboplastin time test: An assessment of four heparin antagonists and two anion exchange resins
-
Cumming AM, Jones GR, Wensley RT, Cundall RB. In vitro neutralization of heparin in plasma prior to the activated partial thromboplastin time test: An assessment of four heparin antagonists and two anion exchange resins. Thromb Res 1986; 41: 43-56.
-
(1986)
Thromb Res
, vol.41
, pp. 43-56
-
-
Cumming, A.M.1
Jones, G.R.2
Wensley, R.T.3
Cundall, R.B.4
-
44
-
-
0017056002
-
Removal of heparin and protamine from plasma
-
Thompson AR, Counts RB. Removal of heparin and protamine from plasma. J Lab Clin Med 1976; 88: 922-9.
-
(1976)
J Lab Clin Med
, vol.88
, pp. 922-929
-
-
Thompson, A.R.1
Counts, R.B.2
-
45
-
-
33748802581
-
Update on the pathophysiology and classification of von Willebrand disease: A report of the Subcommittee on von Willebrand Factor
-
Working Party on von Willebrand Disease Classification
-
Sadler JE, Budde U, Eikenboom JC, et al.; Working Party on von Willebrand Disease Classification. Update on the pathophysiology and classification of von Willebrand disease: A report of the Subcommittee on von Willebrand Factor. J Thromb Haemost 2006; 4: 2103-14.
-
(2006)
J Thromb Haemost
, vol.4
, pp. 2103-2114
-
-
Sadler, J.E.1
Budde, U.2
Eikenboom, J.C.3
-
46
-
-
33646146198
-
Laboratory issues in bleeding disorders
-
Lillicrap D, Nair SC, Srivastava A, et al. Laboratory issues in bleeding disorders. Haemophilia 2006; 12 ( Suppl. 3 ): 68-75.
-
(2006)
Haemophilia
, vol.12
, Issue.SUPPL. 3
, pp. 68-75
-
-
Lillicrap, D.1
Nair, S.C.2
Srivastava, A.3
-
47
-
-
0023257218
-
The effect of ABO blood group on the diagnosis of von Willebrand disease
-
Gill JC, Endres-Brooks J, Bauer PJ, et al. The effect of ABO blood group on the diagnosis of von Willebrand disease. Blood 1987; 69: 1691-5.
-
(1987)
Blood
, vol.69
, pp. 1691-1695
-
-
Gill, J.C.1
Endres-Brooks, J.2
Bauer, P.J.3
-
48
-
-
0019998246
-
Platelet-type von Willebrand ' s disease: Characterization of a new bleeding disorder
-
Miller JL, Castella A. Platelet-type von Willebrand ' s disease: Characterization of a new bleeding disorder. Blood 1982; 60: 790-4.
-
(1982)
Blood
, vol.60
, pp. 790-794
-
-
Miller, J.L.1
Castella, A.2
-
50
-
-
0033502512
-
Laboratory assessment as a critical component of the appropriate diagnosis and sub-classification of von Willebrand ' s disease
-
Favaloro EJ. Laboratory assessment as a critical component of the appropriate diagnosis and sub-classification of von Willebrand ' s disease. Blood Rev 1999; 13: 185-204.
-
(1999)
Blood Rev
, vol.13
, pp. 185-204
-
-
Favaloro, E.J.1
-
51
-
-
0141609789
-
Inherited platelet-based bleeding disorders
-
Cattaneo M. Inherited platelet-based bleeding disorders. J Thromb Haemost 2003; 1: 1628-36.
-
(2003)
J Thromb Haemost
, vol.1
, pp. 1628-1636
-
-
Cattaneo, M.1
-
52
-
-
38949096839
-
Congenital disorders associated with platelet dysfunctions
-
Nurden P, Nurden A. Congenital disorders associated with platelet dysfunctions. Thromb Haemost 2008; 99: 253-63.
-
(2008)
Thromb Haemost
, vol.99
, pp. 253-263
-
-
Nurden, P.1
Nurden, A.2
-
53
-
-
0037187949
-
Immune thrombocytopenic purpura
-
Cines DB, Blanchette VS. Immune thrombocytopenic purpura. N Engl J Med 2002; 346: 995-1008.
-
(2002)
N Engl J Med
, vol.346
, pp. 995-1008
-
-
Cines, D.B.1
Blanchette, V.S.2
-
54
-
-
33646129692
-
Congenital platelet disorders: Overview of their mechanisms, diagnostic evaluation and treatment
-
Hayward CP, Rao AK, Cattaneo M. Congenital platelet disorders: Overview of their mechanisms, diagnostic evaluation and treatment. Haemophilia 2006; 12 ( Suppl. 3 ): 128-36.
-
(2006)
Haemophilia
, vol.12
, Issue.SUPPL. 3
, pp. 128-136
-
-
Hayward, C.P.1
Rao, A.K.2
Cattaneo, M.3
-
55
-
-
40849129940
-
Diagnostic approach to platelet function disorders
-
Hayward CP. Diagnostic approach to platelet function disorders. Transfus Apher Sci 2008; 38: 65-76.
-
(2008)
Transfus Apher Sci
, vol.38
, pp. 65-76
-
-
Hayward, C.P.1
-
56
-
-
0023485139
-
Reliability of absent platelet dense bodies as a diagnostic criterion for Hermansky-Pudlak syndrome
-
Witkop CJ, Krumwiede M, Sedano H, White JG. Reliability of absent platelet dense bodies as a diagnostic criterion for Hermansky-Pudlak syndrome. Am J Hematol 1987; 26: 305-11.
-
(1987)
Am J Hematol
, vol.26
, pp. 305-311
-
-
Witkop, C.J.1
Krumwiede, M.2
Sedano, H.3
White, J.G.4
-
57
-
-
0025262315
-
Platelet storage pool deficiency: Diagnosis in patients with prolonged bleeding times and normal platelet aggregation
-
Israels SJ, McNicol A, Robertson C, Gerrard JM. Platelet storage pool deficiency: Diagnosis in patients with prolonged bleeding times and normal platelet aggregation. Br J Haematol 1990; 75: 118-21.
-
(1990)
Br J Haematol
, vol.75
, pp. 118-121
-
-
Israels, S.J.1
McNicol, A.2
Robertson, C.3
Gerrard, J.M.4
-
58
-
-
0037245023
-
Immunofl uorescence analysis of neutrophil nonmuscle myosin heavy chain-A in MYH9 disorders: Association of subcellular localization with MYH9 mutations
-
Kunishima S, Matsushita T, Kojima T, et al. Immunofl uorescence analysis of neutrophil nonmuscle myosin heavy chain-A in MYH9 disorders: Association of subcellular localization with MYH9 mutations. Lab Invest 2003; 83: 115-22.
-
(2003)
Lab Invest
, vol.83
, pp. 115-122
-
-
Kunishima, S.1
Matsushita, T.2
Kojima, T.3
-
59
-
-
0035986783
-
Inherited thrombocytopenias: From genes to therapy
-
Balduini CL, Iolascon A, Savoia A. Inherited thrombocytopenias: From genes to therapy. Haematologica 2002; 87: 860-80.
-
(2002)
Haematologica
, vol.87
, pp. 860-880
-
-
Balduini, C.L.1
Iolascon, A.2
Savoia, A.3
|