메뉴 건너뛰기




Volumn 10, Issue 1, 1997, Pages 149-162

Megakaryocytes and inherited thrombocytopenias

Author keywords

Dysmegakaryocytopoiesis; Inherited thrombocytopathies; Inherited thrombocytopenias; Megakaryocyte; Megakaryocytopoiesis

Indexed keywords

THROMBOCYTE FACTOR 5; VON WILLEBRAND FACTOR;

EID: 0030945437     PISSN: 09503536     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0950-3536(97)80055-8     Document Type: Article
Times cited : (13)

References (91)
  • 1
    • 0015526142 scopus 로고
    • Nature of the platelet defect in the Wiskott-Aldrich syndrome
    • Baldini MG Nature of the platelet defect in the Wiskott-Aldrich syndrome Annals of the New York Academy of Sciences 201 1972 437 444
    • (1972) Annals of the New York Academy of Sciences , vol.201 , pp. 437-444
    • Baldini, MG1
  • 2
    • 0028343099 scopus 로고
    • Identification and cloning of a megakaryocyte growth and development factor that is a ligand for the cytokine receptor Mpl
    • Bartley TD Bogenberger J Hunt P Identification and cloning of a megakaryocyte growth and development factor that is a ligand for the cytokine receptor Mpl Cell 77 1994 1117 1124
    • (1994) Cell , vol.77 , pp. 1117-1124
    • Bartley, TD1    Bogenberger, J2    Hunt, P3
  • 3
    • 0021022146 scopus 로고
    • History of congenital hemorrhagic thrombocytopathic dystrophy
    • Bernard J History of congenital hemorrhagic thrombocytopathic dystrophy Blood Cells 9 1983 179 193
    • (1983) Blood Cells , vol.9 , pp. 179-193
    • Bernard, J1
  • 4
    • 84957409544 scopus 로고
    • Sur une nouvelle variété de dystrophie thrombocytaire hémorragipare congénitale
    • Bernard J Soulier JP Sur une nouvelle variété de dystrophie thrombocytaire hémorragipare congénitale Semaine des Hôpitaux de Paris 24 1948 3217 3223
    • (1948) Semaine des Hôpitaux de Paris , vol.24 , pp. 3217-3223
    • Bernard, J1    Soulier, JP2
  • 5
    • 84886611159 scopus 로고
    • Thrombocytopenia, macrothrombocytopathia, nephritis and deafness
    • Bernheim J Dechavanne M Bryon PA Thrombocytopenia, macrothrombocytopathia, nephritis and deafness American Journal of Medicine 61 1976 145 150
    • (1976) American Journal of Medicine , vol.61 , pp. 145-150
    • Bernheim, J1    Dechavanne, M2    Bryon, PA3
  • 7
    • 0001724681 scopus 로고
    • Thrombocytopenia inherited as an autosomal dominant trait
    • Bithell TC Didisheim P Cartwright GE Thrombocytopenia inherited as an autosomal dominant trait Blood 25 1965 231 240
    • (1965) Blood , vol.25 , pp. 231-240
    • Bithell, TC1    Didisheim, P2    Cartwright, GE3
  • 8
    • 0028952956 scopus 로고
    • A new congenital dysmegakaryopoietic thrombocytopenia (Paris-Trousseau) associated with giant platelet α-granules and chromosome 11 deletion at 11q23
    • Breton-Gorius J Favier R Guichard J A new congenital dysmegakaryopoietic thrombocytopenia (Paris-Trousseau) associated with giant platelet α-granules and chromosome 11 deletion at 11q23 Blood 85 1995 1805 1814
    • (1995) Blood , vol.85 , pp. 1805-1814
    • Breton-Gorius, J1    Favier, R2    Guichard, J3
  • 9
    • 46549093940 scopus 로고
    • Abnormality of glycoprotein Ib in two cases of ‘pseudo’ von Willebrand disease
    • Bryckaert MC Pietu G Ruan C Abnormality of glycoprotein Ib in two cases of ‘pseudo’ von Willebrand disease Journal of Laboratory and Clinical Medicine 106 1985 393 400
    • (1985) Journal of Laboratory and Clinical Medicine , vol.106 , pp. 393-400
    • Bryckaert, MC1    Pietu, G2    Ruan, C3
  • 10
    • 0008978943 scopus 로고
    • Interaction between platelets and von Willebrand factor provides a new scheme for primary haemostasis
    • Caen J Levy-Toledano S Interaction between platelets and von Willebrand factor provides a new scheme for primary haemostasis Nature New Biology 244 1973 159 160
    • (1973) Nature New Biology , vol.244 , pp. 159-160
    • Caen, J1    Levy-Toledano, S2
  • 12
    • 0019442921 scopus 로고
    • Platelet membrane studies in the May-Hegglin anomaly
    • Coller BS Zarrabi MH Platelet membrane studies in the May-Hegglin anomaly Blood 58 1981 279 284
    • (1981) Blood , vol.58 , pp. 279-284
    • Coller, BS1    Zarrabi, MH2
  • 13
    • 0022377796 scopus 로고
    • Gray-platelet syndrome: immunoelectron microscopic localization of fibrinogen and von Willebrand factor in platelets and megakaryocytes
    • Cramer EM Vainchenker W Vinci G Gray-platelet syndrome: immunoelectron microscopic localization of fibrinogen and von Willebrand factor in platelets and megakaryocytes Blood 66 1985 1309 1316
    • (1985) Blood , vol.66 , pp. 1309-1316
    • Cramer, EM1    Vainchenker, W2    Vinci, G3
  • 16
    • 0027937223 scopus 로고
    • Isolation of a novel gene mutated in Wiskott-Aldrich syndrome
    • Derry JMJ Ochs HJ Francke U Isolation of a novel gene mutated in Wiskott-Aldrich syndrome Cell 78 1994 635 644
    • (1994) Cell , vol.78 , pp. 635-644
    • Derry, JMJ1    Ochs, HJ2    Francke, U3
  • 17
    • 0014074461 scopus 로고
    • Phocomelia with congenital hypoplastic thrombocytopenia and myeloid leukemoid reactions
    • Dignan PJ Mauer AM Frantz C Phocomelia with congenital hypoplastic thrombocytopenia and myeloid leukemoid reactions Journal of Pediatrics 70 1967 561 573
    • (1967) Journal of Pediatrics , vol.70 , pp. 561-573
    • Dignan, PJ1    Mauer, AM2    Frantz, C3
  • 18
    • 0021998315 scopus 로고
    • Studies of a familial platelet disorder
    • Dowton SB Beardsley D Jamielson D Studies of a familial platelet disorder Blood 65 1985 557 563
    • (1985) Blood , vol.65 , pp. 557-563
    • Dowton, SB1    Beardsley, D2    Jamielson, D3
  • 19
    • 0016506243 scopus 로고
    • Hereditary thrombocytopenia, deafness, and renal disease
    • Eckstein J Filip DJ Watts JC Hereditary thrombocytopenia, deafness, and renal disease Annals of Internal Medicine 82 1975 639 645
    • (1975) Annals of Internal Medicine , vol.82 , pp. 639-645
    • Eckstein, J1    Filip, DJ2    Watts, JC3
  • 20
    • 0015304377 scopus 로고
    • Hereditary macrothrombocytopathia, nephritis, and deafness
    • Epstein CJ Sahud MA Piel CF Hereditary macrothrombocytopathia, nephritis, and deafness American Journal of Medicine 52 1972 299 310
    • (1972) American Journal of Medicine , vol.52 , pp. 299-310
    • Epstein, CJ1    Sahud, MA2    Piel, CF3
  • 21
    • 0018922538 scopus 로고
    • Plasma and platelet beta-thromboglobulin levels in patients with May-Hegglin anomaly
    • Fabris F Casonato A Randi ML Girolami A Plasma and platelet beta-thromboglobulin levels in patients with May-Hegglin anomaly Haemostasis 9 1980 126 130
    • (1980) Haemostasis , vol.9 , pp. 126-130
    • Fabris, F1    Casonato, A2    Randi, ML3    Girolami, A4
  • 22
    • 0025347106 scopus 로고
    • Simultaneous occurrence of grey platelet syndrome and idiopathic pulmonary fibrosis: a role for abnormal megakaryocyte in the pathogenesis of pulmonary fibrosis?
    • Facon T Goudeman J Caron C Simultaneous occurrence of grey platelet syndrome and idiopathic pulmonary fibrosis: a role for abnormal megakaryocyte in the pathogenesis of pulmonary fibrosis? British Journal of Haematology 74 1990 542 543
    • (1990) British Journal of Haematology , vol.74 , pp. 542-543
    • Facon, T1    Goudeman, J2    Caron, C3
  • 23
    • 0029129034 scopus 로고
    • Mutations in the gene for granulocyte-colony stimulating factor receptor in patients with acute myeloid leukemia preceded by severe congenital neutropenia
    • Fan D Brynes FK Tidow N Mutations in the gene for granulocyte-colony stimulating factor receptor in patients with acute myeloid leukemia preceded by severe congenital neutropenia New England Journal of Medicine 333 1995 487 493
    • (1995) New England Journal of Medicine , vol.333 , pp. 487-493
    • Fan, D1    Brynes, FK2    Tidow, N3
  • 24
    • 0027365480 scopus 로고
    • Defective adhesion of blood platelets to vascular microfibrils in the Bernard-Soulier syndrome
    • Fauvel-Lafeve F Tabaka V Caen JP Legrand Y Defective adhesion of blood platelets to vascular microfibrils in the Bernard-Soulier syndrome Blood 82 1993 1985 1988
    • (1993) Blood , vol.82 , pp. 1985-1988
    • Fauvel-Lafeve, F1    Tabaka, V2    Caen, JP3    Legrand, Y4
  • 25
    • 0028557354 scopus 로고
    • Human thrombopoietin: gene structure, cDNA sequence, expression and chromosomal localization
    • Foster DC Sprecher CA Grant FJ Human thrombopoietin: gene structure, cDNA sequence, expression and chromosomal localization Proceedings of the National Academy of Sciences of the USA 91 1994 13023 13027
    • (1994) , pp. 13023-13027
    • Foster, DC1    Sprecher, CA2    Grant, FJ3
  • 26
    • 0015978724 scopus 로고
    • May-Hegglin anomaly: defect in megakaryocyte fragmentation?
    • Godwin HA Ginsburg AD May-Hegglin anomaly: defect in megakaryocyte fragmentation? British Journal of Haematology 26 1974 117 128
    • (1974) British Journal of Haematology , vol.26 , pp. 117-128
    • Godwin, HA1    Ginsburg, AD2
  • 28
    • 0019960145 scopus 로고
    • Factor VIII/Von Willebrand factor binding to von Willebrand's disease platelets
    • Gralnick HR Williams SB Shafer BC Corash L Factor VIII/Von Willebrand factor binding to von Willebrand's disease platelets Blood 60 1982 328 332
    • (1982) Blood , vol.60 , pp. 328-332
    • Gralnick, HR1    Williams, SB2    Shafer, BC3    Corash, L4
  • 29
    • 0023226894 scopus 로고
    • A new familial giant platelet syndrome with structural, metabolic, and functional abnormalities of platelets due to a primary megakaryocyte defect
    • Greaves M Pickering C Martin J A new familial giant platelet syndrome with structural, metabolic, and functional abnormalities of platelets due to a primary megakaryocyte defect British Journal of Haematology 65 1987 429 435
    • (1987) British Journal of Haematology , vol.65 , pp. 429-435
    • Greaves, M1    Pickering, C2    Martin, J3
  • 30
    • 0025008774 scopus 로고
    • Hereditary types of thrombocytopenia with giant platelets and inclusion bodies in the leukocytes
    • Greinacher A Mueller-Eckhardt C Hereditary types of thrombocytopenia with giant platelets and inclusion bodies in the leukocytes Blut 60 1990 53 60
    • (1990) Blut , vol.60 , pp. 53-60
    • Greinacher, A1    Mueller-Eckhardt, C2
  • 31
    • 0025606519 scopus 로고
    • Sebastian platelet syndrome: a new variant of hereditary macrothrombocytopenia with leukocyte inclusions
    • Greinacher A Nieuwenhuis HK White JG Sebastian platelet syndrome: a new variant of hereditary macrothrombocytopenia with leukocyte inclusions Blut 61 1990 282 288
    • (1990) Blut , vol.61 , pp. 282-288
    • Greinacher, A1    Nieuwenhuis, HK2    White, JG3
  • 32
    • 0014489806 scopus 로고
    • Congenital thrombocytopenia with giant platelets: a defect in the platelet membrane
    • Gröttum KA Solum NO Congenital thrombocytopenia with giant platelets: a defect in the platelet membrane British Journal of Haematology 16 1969 277 290
    • (1969) British Journal of Haematology , vol.16 , pp. 277-290
    • Gröttum, KA1    Solum, NO2
  • 33
    • 0014589953 scopus 로고
    • Wiskott-Aldrich syndrome: qualitative defects and short platelet survival
    • Gröttum KA Hovig T Holmsen H Wiskott-Aldrich syndrome: qualitative defects and short platelet survival British Journal of Haematology 17 1969 373 388
    • (1969) British Journal of Haematology , vol.17 , pp. 373-388
    • Gröttum, KA1    Hovig, T2    Holmsen, H3
  • 34
    • 0028899548 scopus 로고
    • Genomic structure, chromosomal localization and conserved alternative splice forms of thrombopoietin
    • Gurney AL Kuang WJ Xie MH Genomic structure, chromosomal localization and conserved alternative splice forms of thrombopoietin Blood 85 1995 981 988
    • (1995) Blood , vol.85 , pp. 981-988
    • Gurney, AL1    Kuang, WJ2    Xie, MH3
  • 35
    • 0014605655 scopus 로고
    • Thrombocytopenia with absent radius (tar)
    • Hall JG Levin J Kuhn JP Thrombocytopenia with absent radius (tar) Medicine (Baltimore) 48 1969 411 439
    • (1969) Medicine (Baltimore) , vol.48 , pp. 411-439
    • Hall, JG1    Levin, J2    Kuhn, JP3
  • 36
    • 0024560203 scopus 로고
    • Amergakaryocytic thrombocytopenia with duplication of part of the long arm of chromosome 3
    • Hallett JM Martell RW Sher C Jacobs P Amergakaryocytic thrombocytopenia with duplication of part of the long arm of chromosome 3 British Journal of Haematology 71 1989 291 292
    • (1989) British Journal of Haematology , vol.71 , pp. 291-292
    • Hallett, JM1    Martell, RW2    Sher, C3    Jacobs, P4
  • 37
  • 38
    • 0025248229 scopus 로고
    • Platelet factor 4 inhibits human megakaryocytopoiesis in vitro
    • Han ZC Sensebe L Abgrall JF Platelet factor 4 inhibits human megakaryocytopoiesis in vitro Blood 75 1990 1234 1239
    • (1990) Blood , vol.75 , pp. 1234-1239
    • Han, ZC1    Sensebe, L2    Abgrall, JF3
  • 39
    • 9244248429 scopus 로고
    • Identification of an autosomal dominant bleeding disorder that is associated with a deficiency of platelet multimerin and a defect in platelet factor V
    • abstract. Hayward CPM Rivard GE Moore JC Kelton JG Identification of an autosomal dominant bleeding disorder that is associated with a deficiency of platelet multimerin and a defect in platelet factor V Blood 84 1994 428 441
    • (1994) Blood , vol.84 , pp. 428-441
    • Hayward, CPM1    Rivard, GE2    Moore, JC3    Kelton, JG4
  • 40
    • 0029094499 scopus 로고
    • Factor V is complexed with multimerin in resting platelet lysates and colocalizes with multimerin within platelet alpha granules
    • Hayward CPM Furmaniak-Kazmierczak E Cieutat AM Factor V is complexed with multimerin in resting platelet lysates and colocalizes with multimerin within platelet alpha granules Journal of Biological Chemistry 270 1995 19217 19224
    • (1995) Journal of Biological Chemistry , vol.270 , pp. 19217-19224
    • Hayward, CPM1    Furmaniak-Kazmierczak, E2    Cieutat, AM3
  • 41
    • 0024232175 scopus 로고
    • Congenital macrothrombocytopenia, leucocyte inclusions, deafness and proteinuria: functional and electron microscopic observations on platelets and megakaryocytes
    • Heynen MJ Blockmans D Verwilghen RL Vermylen J Congenital macrothrombocytopenia, leucocyte inclusions, deafness and proteinuria: functional and electron microscopic observations on platelets and megakaryocytes British Journal of Haematology 70 1988 441 448
    • (1988) British Journal of Haematology , vol.70 , pp. 441-448
    • Heynen, MJ1    Blockmans, D2    Verwilghen, RL3    Vermylen, J4
  • 42
    • 0025817137 scopus 로고
    • Aberrant O-linked oligosaccharide biosynthesis in lymphocytes and platelets from patients with the Wiskott-Aldrich syndrome
    • Higgins EA Siminovitch KA Zhuang D Aberrant O-linked oligosaccharide biosynthesis in lymphocytes and platelets from patients with the Wiskott-Aldrich syndrome Journal of Biological Chemistry 266 1991 6280 6290
    • (1991) Journal of Biological Chemistry , vol.266 , pp. 6280-6290
    • Higgins, EA1    Siminovitch, KA2    Zhuang, D3
  • 43
    • 0023720268 scopus 로고
    • Defective megakaryocytopoiesis in the syndrome of thrombocytopenia with absent radii
    • Homans AC Cohen LJ Mazur EM Defective megakaryocytopoiesis in the syndrome of thrombocytopenia with absent radii British Journal of Haematology 70 1988 205 210
    • (1988) British Journal of Haematology , vol.70 , pp. 205-210
    • Homans, AC1    Cohen, LJ2    Mazur, EM3
  • 44
    • 0025646605 scopus 로고
    • Studies on the megakaryocytes of a patient with the Bernard-Soulier syndrome
    • Hourdillé P Pico M Jandrot-Perrus M Studies on the megakaryocytes of a patient with the Bernard-Soulier syndrome British Journal of Haematology 76 1990 521 530
    • (1990) British Journal of Haematology , vol.76 , pp. 521-530
    • Hourdillé, P1    Pico, M2    Jandrot-Perrus, M3
  • 45
    • 0015918491 scopus 로고
    • Hereditary giant platelets syndrome, a disorder of a new aspect of platelets function
    • Howard MA Hutton RA Hardisty RP Hereditary giant platelets syndrome, a disorder of a new aspect of platelets function British Medical Journal 2 1973 586 588
    • (1973) British Medical Journal , vol.2 , pp. 586-588
    • Howard, MA1    Hutton, RA2    Hardisty, RP3
  • 46
    • 0028304622 scopus 로고
    • Gray platelet syndrome with splenomegaly and signs of extramedullary hematopoiesis: a case report with review of the literature
    • Jantunen E Hanninen A Naukkarinen A Gray platelet syndrome with splenomegaly and signs of extramedullary hematopoiesis: a case report with review of the literature American Journal of Hematology 46 1994 218 224
    • (1994) American Journal of Hematology , vol.46 , pp. 218-224
    • Jantunen, E1    Hanninen, A2    Naukkarinen, A3
  • 47
    • 0017666917 scopus 로고
    • Megakaryocytes in the giant platelet syndrome. A cytochemical and ultrastructural study
    • Kass L Leichtman DA Beals TF Schnitzer B Megakaryocytes in the giant platelet syndrome. A cytochemical and ultrastructural study Thrombosis and Haemostasis 38 1977 652 659
    • (1977) Thrombosis and Haemostasis , vol.38 , pp. 652-659
    • Kass, L1    Leichtman, DA2    Beals, TF3    Schnitzer, B4
  • 52
    • 0028199208 scopus 로고
    • Murine thrombopoietin: expression cloning, cDNA sequence and stimulation of platelet production in vivo
    • Lok S Kaushansky K Holly RD Murine thrombopoietin: expression cloning, cDNA sequence and stimulation of platelet production in vivo Nature 369 1994 565 568
    • (1994) Nature , vol.369 , pp. 565-568
    • Lok, S1    Kaushansky, K2    Holly, RD3
  • 54
    • 0016529194 scopus 로고
    • Ultrastructure of platelets in Bernard-Soulier syndrome
    • Maldonado JE Gilchrist GS Bridgen LP Bowie EJ Ultrastructure of platelets in Bernard-Soulier syndrome Mayo Clinic Proceedings 50 1975 402 406
    • (1975) , pp. 402-406
    • Maldonado, JE1    Gilchrist, GS2    Bridgen, LP3    Bowie, EJ4
  • 56
    • 0023553383 scopus 로고
    • Unique interactions of asialo von Willebrand factor with platelets in platelet-type von Willebrand disease
    • Miller JL Ruggeri ZM Lyle VA Unique interactions of asialo von Willebrand factor with platelets in platelet-type von Willebrand disease Blood 70 1987 1804 1809
    • (1987) Blood , vol.70 , pp. 1804-1809
    • Miller, JL1    Ruggeri, ZM2    Lyle, VA3
  • 57
    • 0025896722 scopus 로고
    • Mutation in the gene encoding the α chain of platelet glycoprotein Ib in platelet-type von Willebrand disease
    • Miller JL Cunningham D Lyle VA Finch CH Mutation in the gene encoding the α chain of platelet glycoprotein Ib in platelet-type von Willebrand disease Proceedings of the National Academy of Sciences of the USA 88 1991 4761 4765
    • (1991) , pp. 4761-4765
    • Miller, JL1    Cunningham, D2    Lyle, VA3    Finch, CH4
  • 58
    • 0018341219 scopus 로고
    • Shape-changing agents produce abnormally large platelets in a hereditary ‘giant platelets syndrome’ (MPS)
    • Milton JG Frojmovic MM Shape-changing agents produce abnormally large platelets in a hereditary ‘giant platelets syndrome’ (MPS) Journal of Laboratory and Clinical Medicine 93 1979 154 161
    • (1979) Journal of Laboratory and Clinical Medicine , vol.93 , pp. 154-161
    • Milton, JG1    Frojmovic, MM2
  • 59
    • 0027217332 scopus 로고
    • Expression of the phenotypic abnormality of platelet-type von Willebrand disease in a recombinant glycoprotein Ib α fragment
    • Murata M Russel SR Ruggeri ZM Ware J Expression of the phenotypic abnormality of platelet-type von Willebrand disease in a recombinant glycoprotein Ib α fragment Journal of Clinical Investigation 91 1993 2133 2137
    • (1993) Journal of Clinical Investigation , vol.91 , pp. 2133-2137
    • Murata, M1    Russel, SR2    Ruggeri, ZM3    Ware, J4
  • 60
    • 0015498851 scopus 로고
    • Platelet size and kinetics in hereditary and acquired thrombocytopenia
    • Murphy S Osiki FA Naiman JL Platelet size and kinetics in hereditary and acquired thrombocytopenia New England Journal of Medicine 286 1972 499 504
    • (1972) New England Journal of Medicine , vol.286 , pp. 499-504
    • Murphy, S1    Osiki, FA2    Naiman, JL3
  • 62
    • 0029897340 scopus 로고    scopus 로고
    • Thrombocytopenies pures sans excès de destruction: un syndrome mal classé
    • Najean Y Thrombocytopenies pures sans excès de destruction: un syndrome mal classé Hématologie 2 1996 224 232
    • (1996) Hématologie , vol.2 , pp. 224-232
    • Najean, Y1
  • 63
    • 0025141664 scopus 로고
    • Genetic thrombocytopenia with autosomal dominant transmission: a review of 54 cases
    • Najean Y Lecompte T Genetic thrombocytopenia with autosomal dominant transmission: a review of 54 cases British Journal of Haematology 74 1990 203 208
    • (1990) British Journal of Haematology , vol.74 , pp. 203-208
    • Najean, Y1    Lecompte, T2
  • 65
    • 0014624947 scopus 로고
    • Abnormalities of platelet function and ultrastructure in macrothrombocytic thrombopathia
    • Niewiarowski S Poplawski A Prokopowicz J Abnormalities of platelet function and ultrastructure in macrothrombocytic thrombopathia Scandinavian Journal of Haematology 6 1969 377 385
    • (1969) Scandinavian Journal of Haematology , vol.6 , pp. 377-385
    • Niewiarowski, S1    Poplawski, A2    Prokopowicz, J3
  • 66
    • 0016862422 scopus 로고
    • Specific roles for platelet surface glycoproteins in platelet function
    • Nurden AT Caen JP Specific roles for platelet surface glycoproteins in platelet function Nature 225 1975 720 722
    • (1975) Nature , vol.225 , pp. 720-722
    • Nurden, AT1    Caen, JP2
  • 67
    • 0018751193 scopus 로고
    • The different glycoprotein abnormalities in thrombasthenic and Bernard-Soulier platelets
    • Nurden AT Caen JP The different glycoprotein abnormalities in thrombasthenic and Bernard-Soulier platelets Seminars in Hematology 16 1979 234 250
    • (1979) Seminars in Hematology , vol.16 , pp. 234-250
    • Nurden, AT1    Caen, JP2
  • 68
    • 0024402639 scopus 로고
    • Montreal platelet syndrome: a defect in calcium activated neutral proteinase (calpain)
    • Okita JR Frojmovic MM Kristopeit S Montreal platelet syndrome: a defect in calcium activated neutral proteinase (calpain) Blood 74 1989 715 721
    • (1989) Blood , vol.74 , pp. 715-721
    • Okita, JR1    Frojmovic, MM2    Kristopeit, S3
  • 70
    • 0021956321 scopus 로고
    • Fechtner syndrome: a variant of Alport's syndrome with leukocyte inclusions and macrothrombocytopenia
    • Peterson LC Rao KV Crosson JT White JA Fechtner syndrome: a variant of Alport's syndrome with leukocyte inclusions and macrothrombocytopenia Blood 65 1985 397 406
    • (1985) Blood , vol.65 , pp. 397-406
    • Peterson, LC1    Rao, KV2    Crosson, JT3    White, JA4
  • 71
    • 0023774148 scopus 로고
    • Analysis of the membrane glycoproteins of platelets in the Wiskott-Aldrich syndrome
    • Pidard D Didry D Le Deist F Analysis of the membrane glycoproteins of platelets in the Wiskott-Aldrich syndrome British Journal of Haematology 69 1988 529 535
    • (1988) British Journal of Haematology , vol.69 , pp. 529-535
    • Pidard, D1    Didry, D2    Le Deist, F3
  • 72
    • 0022342923 scopus 로고
    • Acute megakaryoblastic leukemia with 3q inversion and elevated thrombopoetin (TSF): an autocrine role for TSF?
    • Pinto MR King MA Goss GD Acute megakaryoblastic leukemia with 3q inversion and elevated thrombopoetin (TSF): an autocrine role for TSF? British Journal of Haematology 61 1985 687 694
    • (1985) British Journal of Haematology , vol.61 , pp. 687-694
    • Pinto, MR1    King, MA2    Goss, GD3
  • 73
    • 0015176866 scopus 로고
    • Gray platelet syndrome: a variety of qualitative platelet disorder
    • Raccuglia G Fac P Gray platelet syndrome: a variety of qualitative platelet disorder American Journal of Medicine 51 1971 818 828
    • (1971) American Journal of Medicine , vol.51 , pp. 818-828
    • Raccuglia, G1    Fac, P2
  • 74
    • 0026548070 scopus 로고
    • Effect of platelet calpain on normal T-lymphocyte CD43: hypothesis of events in the Wiskott-Aldrich syndrome
    • Remold-O'Donnell E Van Brocklyn J Kenney DM Effect of platelet calpain on normal T-lymphocyte CD43: hypothesis of events in the Wiskott-Aldrich syndrome Blood 79 1992 1754 1762
    • (1992) Blood , vol.79 , pp. 1754-1762
    • Remold-O'Donnell, E1    Van Brocklyn, J2    Kenney, DM3
  • 76
    • 0019786838 scopus 로고
    • Monoclonal antibody to human platelet glycoprotein I. Effects on human platelet function
    • Ruan C Tobelem G McMichael AJ Monoclonal antibody to human platelet glycoprotein I. Effects on human platelet function British Journal of Haematology 41 1981 511 519
    • (1981) British Journal of Haematology , vol.41 , pp. 511-519
    • Ruan, C1    Tobelem, G2    McMichael, AJ3
  • 77
    • 0027481159 scopus 로고
    • Pseudo-von Willebrand disease: a mutation in the platelet glycoprotein Ib α gene associated with a hyperactive surface receptor
    • Russel SD Roth GJ Pseudo-von Willebrand disease: a mutation in the platelet glycoprotein Ib α gene associated with a hyperactive surface receptor Blood 81 1993 1787 1791
    • (1993) Blood , vol.81 , pp. 1787-1791
    • Russel, SD1    Roth, GJ2
  • 78
    • 0021839268 scopus 로고
    • Type IIB Tampa: a variant of von Willebrand disease with chronic thrombocytopenia, circulating platelet aggregates, and spontaneous platelet aggregation
    • Sabah H Saba S Dent J Type IIB Tampa: a variant of von Willebrand disease with chronic thrombocytopenia, circulating platelet aggregates, and spontaneous platelet aggregation Blood 66 1985 282 286
    • (1985) Blood , vol.66 , pp. 282-286
    • Sabah, H1    Saba, S2    Dent, J3
  • 80
    • 0028302409 scopus 로고
    • Stimulation of megakaryocytopoiesis and thrombopoiesis by the c-Mpl ligand
    • de Sauvage FJ Hass PE Spencer SD Stimulation of megakaryocytopoiesis and thrombopoiesis by the c-Mpl ligand Nature 369 1994 533 538
    • (1994) Nature , vol.369 , pp. 533-538
    • de Sauvage, FJ1    Hass, PE2    Spencer, SD3
  • 81
    • 73649188803 scopus 로고
    • Hereditary hypoplastic thrombocytopenia
    • Seip M Hereditary hypoplastic thrombocytopenia Acta Paediatrica Scandinavica 52 1963 370 376
    • (1963) Acta Paediatrica Scandinavica , vol.52 , pp. 370-376
    • Seip, M1
  • 82
    • 0030006284 scopus 로고    scopus 로고
    • Wiskott-Aldrich syndrome protein, a novel effector for the GTPase CDC42Hs, is implicated in actin polymerization
    • Symons M Derry JMJ Karlak B Wiskott-Aldrich syndrome protein, a novel effector for the GTPase CDC42Hs, is implicated in actin polymerization Cell 84 1996 723 734
    • (1996) Cell , vol.84 , pp. 723-734
    • Symons, M1    Derry, JMJ2    Karlak, B3
  • 83
    • 0017318801 scopus 로고
    • New approach to determination of specific functions of platelet membrane sites
    • Tobelem G Levy-Toledano S Bredoux R New approach to determination of specific functions of platelet membrane sites Nature 263 1976 427 429
    • (1976) Nature , vol.263 , pp. 427-429
    • Tobelem, G1    Levy-Toledano, S2    Bredoux, R3
  • 84
    • 0023129457 scopus 로고
    • Proplatelets and stress platelets
    • Tong M Seth P Penington DG Proplatelets and stress platelets Blood 69 1987 522 528
    • (1987) Blood , vol.69 , pp. 522-528
    • Tong, M1    Seth, P2    Penington, DG3
  • 85
    • 0021745376 scopus 로고
    • Factor V (Quebec): a bleeding diathesis associated with a qualitative platelet factor V deficiency
    • Tracy PB Giles AR Mann KG Factor V (Quebec): a bleeding diathesis associated with a qualitative platelet factor V deficiency Journal of Clinical Investigation 74 1984 1221 1228
    • (1984) Journal of Clinical Investigation , vol.74 , pp. 1221-1228
    • Tracy, PB1    Giles, AR2    Mann, KG3
  • 86
    • 0020525540 scopus 로고
    • Thrombocytopenic purpura with giant platelets and ultrastructural platelet defects
    • Vizcaino GJ Diez-Ewald M Thrombocytopenic purpura with giant platelets and ultrastructural platelet defects American Journal of Hematology 15 1983 86 95
    • (1983) American Journal of Hematology , vol.15 , pp. 86-95
    • Vizcaino, GJ1    Diez-Ewald, M2
  • 87
    • 0020068005 scopus 로고
    • Pseudo von Willebrand's disease: an intrinsic platelet defect with aggregation by unmodified human factor VIII/von Willebrand factor and enhanced adsorption of its high molecular weight multimers
    • Weiss HJ Meyer D Rabinowitz R Pseudo von Willebrand's disease: an intrinsic platelet defect with aggregation by unmodified human factor VIII/von Willebrand factor and enhanced adsorption of its high molecular weight multimers New England Journal of Medicine 306 1982 326 333
    • (1982) New England Journal of Medicine , vol.306 , pp. 326-333
    • Weiss, HJ1    Meyer, D2    Rabinowitz, R3
  • 88
    • 0028176283 scopus 로고
    • The Mpl ligand is a humoral regulator of megakaryocytopoiesis
    • Wendling F Maraskovsky E Debili N The Mpl ligand is a humoral regulator of megakaryocytopoiesis Nature 369 1994 571 574
    • (1994) Nature , vol.369 , pp. 571-574
    • Wendling, F1    Maraskovsky, E2    Debili, N3
  • 89
    • 0017082701 scopus 로고
    • Ultrastructural features of abnormal blood platelets. A review
    • White JG Gerrard JM Ultrastructural features of abnormal blood platelets. A review American Journal of Pathology 83 1976 589 632
    • (1976) American Journal of Pathology , vol.83 , pp. 589-632
    • White, JG1    Gerrard, JM2
  • 90
    • 0025254049 scopus 로고
    • Familial macrothrombocytopenia associated with decreased glycosylation of platelet membrane glycoprotein IV
    • Yufu Y Ideguchi H Narishige T Familial macrothrombocytopenia associated with decreased glycosylation of platelet membrane glycoprotein IV American Journal of Hematology 33 1990 271 273
    • (1990) American Journal of Hematology , vol.33 , pp. 271-273
    • Yufu, Y1    Ideguchi, H2    Narishige, T3
  • 91
    • 0028786330 scopus 로고
    • The Wiskott-Aldrich syndrome and X-linked congenital thrombocytopenia are caused by mutation of the same gene
    • Zhu Q Zhang M Blaese RM The Wiskott-Aldrich syndrome and X-linked congenital thrombocytopenia are caused by mutation of the same gene Blood 86 1995 3797 3804
    • (1995) Blood , vol.86 , pp. 3797-3804
    • Zhu, Q1    Zhang, M2    Blaese, RM3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.