메뉴 건너뛰기




Volumn 103, Issue 1, 2000, Pages 41-48

Paroxysmal nocturnal haemoglobinuria: A replacement of haematopoietic tissue?

Author keywords

Aplastic anaemia; Glycosylphosphatidyl inositol anchor; Paroxysmal nocturnal haemoglobinuria; Pathophysiology; PIG A gene

Indexed keywords

CYCLOSPORIN A; GLYCOSYLPHOSPHATIDYLINOSITOL; GLYCOSYLPHOSPHATIDYLINOSITOL ANCHORED PROTEIN; GRANULOCYTE COLONY STIMULATING FACTOR; IMMUNOSUPPRESSIVE AGENT; INTERLEUKIN 3; LYMPHOCYTE ANTIBODY; METHYLPREDNISOLONE; PROTEIN; UNCLASSIFIED DRUG;

EID: 0034096753     PISSN: 00015792     EISSN: None     Source Type: Journal    
DOI: 10.1159/000041003     Document Type: Article
Times cited : (24)

References (45)
  • 1
    • 0023789856 scopus 로고
    • Late haematological complications in severe aplastic anaemia
    • Tichelli A, Gratwohl A, Wursch A, et al: Late haematological complications in severe aplastic anaemia. Br J Haematol 1988;69:413-418.
    • (1988) Br J Haematol , vol.69 , pp. 413-418
    • Tichelli, A.1    Gratwohl, A.2    Wursch, A.3
  • 2
    • 0028296371 scopus 로고
    • Late clonal complications in severe aplastic anemia
    • Tichelli A, Gratwohl A, Nissen C, et al: Late clonal complications in severe aplastic anemia. Leuk Lymphoma 1994;12:167-175.
    • (1994) Leuk Lymphoma , vol.12 , pp. 167-175
    • Tichelli, A.1    Gratwohl, A.2    Nissen, C.3
  • 3
    • 0028884057 scopus 로고
    • The molecular basis of paroxysmal nocturnal hemoglobinuria
    • Rosse WF, Ware RE: The molecular basis of paroxysmal nocturnal hemoglobinuria. Blood 1995;86:3277-3286.
    • (1995) Blood , vol.86 , pp. 3277-3286
    • Rosse, W.F.1    Ware, R.E.2
  • 4
    • 0029887115 scopus 로고    scopus 로고
    • The dual pathogenesis of paroxysmal nocturnal hemoglobinuria
    • Luzzatto L, Bessler M: The dual pathogenesis of paroxysmal nocturnal hemoglobinuria. Curr Opin Hematol 1996;3:101-110.
    • (1996) Curr Opin Hematol , vol.3 , pp. 101-110
    • Luzzatto, L.1    Bessler, M.2
  • 5
    • 0028897137 scopus 로고
    • A pathogenetic link between aplastic anemia and paroxysmal nocturnal hemoglobinuria is suggested by a high frequency of aplastic anemia patients with a deficiency of phosphatidylinositol glycan anchored proteins
    • Schrezenmeier H, Hertenstein B, Wagner B, et al: A pathogenetic link between aplastic anemia and paroxysmal nocturnal hemoglobinuria is suggested by a high frequency of aplastic anemia patients with a deficiency of phosphatidylinositol glycan anchored proteins. Exp Hematol 1995;23:81-87.
    • (1995) Exp Hematol , vol.23 , pp. 81-87
    • Schrezenmeier, H.1    Hertenstein, B.2    Wagner, B.3
  • 6
    • 0033592318 scopus 로고    scopus 로고
    • Paroxysmal nocturnal hemoglobinuria cells in patients with bone marrow failure syndromes
    • Dunn DE, Tanawattanacharoen P, Boccuni P, et al: Paroxysmal nocturnal hemoglobinuria cells in patients with bone marrow failure syndromes (sec comments). Ann Intern Med 1999; 131:401-408.
    • (1999) Ann Intern Med , vol.131 , pp. 401-408
    • Dunn, D.E.1    Tanawattanacharoen, P.2    Boccuni, P.3
  • 7
    • 0029032667 scopus 로고
    • Flow cytometric analysis of decay-accelerating factor (CD55) on neutrophils from aplastic anaemia patients
    • Fores R, Alcocer M, Diez Martin JL, et al: Flow cytometric analysis of decay-accelerating factor (CD55) on neutrophils from aplastic anaemia patients. Br J Haematol 1995;90:728-730.
    • (1995) Br J Haematol , vol.90 , pp. 728-730
    • Fores, R.1    Alcocer, M.2    Diez Martin, J.L.3
  • 8
    • 0028962569 scopus 로고
    • Aplastic anemia and paroxysmal nocturnal hemoglobinuria: Search for a pathogenetic link
    • Griscelli Bennaceur A, Gluckman E, Scrobohaci ML, et al: Aplastic anemia and paroxysmal nocturnal hemoglobinuria: Search for a pathogenetic link. Blood 1995;85:1354-1363.
    • (1995) Blood , vol.85 , pp. 1354-1363
    • Griscelli Bennaceur, A.1    Gluckman, E.2    Scrobohaci, M.L.3
  • 9
    • 0028295447 scopus 로고
    • Development of the glycosylphosphatitylinositol-anchoring defect characteristic for paroxysmal nocturnal hemoglobinuria in patients with aplastic anemia
    • Schubert J, Vogt HG, Ziclinska Skowronek M, et al: Development of the glycosylphosphatitylinositol-anchoring defect characteristic for paroxysmal nocturnal hemoglobinuria in patients with aplastic anemia. Blood 1994;83:2323-2328.
    • (1994) Blood , vol.83 , pp. 2323-2328
    • Schubert, J.1    Vogt, H.G.2    Ziclinska Skowronek, M.3
  • 10
    • 0029617630 scopus 로고
    • The novel monoclonal antibody By114 helps detect the early emergence of a paroxysmal nocturnal hemoglobinuria clone in aplastic anemia
    • Tooze JA, Saso R, Marsh JC, et al: The novel monoclonal antibody By114 helps detect the early emergence of a paroxysmal nocturnal hemoglobinuria clone in aplastic anemia. Exp Hematol 1995;23:1484-1491.
    • (1995) Exp Hematol , vol.23 , pp. 1484-1491
    • Tooze, J.A.1    Saso, R.2    Marsh, J.C.3
  • 11
    • 0032794311 scopus 로고    scopus 로고
    • High incidence of transiently appearing complement-sensitive bone marrow precursor cells in patients with severe aplastic anemia: A possible role of high endogenous IL-2 in their suppression
    • Nissen C, Tichelli A, Gratwohl A, et al: High incidence of transiently appearing complement-sensitive bone marrow precursor cells in patients with severe aplastic anemia: A possible role of high endogenous IL-2 in their suppression. Acta Haematol 1999;101:165-172.
    • (1999) Acta Haematol , vol.101 , pp. 165-172
    • Nissen, C.1    Tichelli, A.2    Gratwohl, A.3
  • 13
    • 0027323293 scopus 로고
    • Membrane proteins in paroxysmal nocturnal haemoglobinuria
    • Rotoli B, Bessler M. Alfinito F, et al: Membrane proteins in paroxysmal nocturnal haemoglobinuria. Blood Rev 1993;7:75-86.
    • (1993) Blood Rev , vol.7 , pp. 75-86
    • Rotoli, B.1    Bessler, M.2    Alfinito, F.3
  • 14
    • 0026596863 scopus 로고
    • The problem of clonality in aplastic anemia: Dr Dameshek's riddle, restated
    • Young NS: The problem of clonality in aplastic anemia: Dr Dameshek's riddle, restated. Blood 1992;79:1385-1392.
    • (1992) Blood , vol.79 , pp. 1385-1392
    • Young, N.S.1
  • 15
    • 0025865140 scopus 로고
    • Treatment of aplastic anemia with antilymphocyte globulin and methylprednisolone with or without cyclosporine
    • Frickhofen N, Kaltwasser JP, Schrezenmeier H, et al: Treatment of aplastic anemia with antilymphocyte globulin and methylprednisolone with or without cyclosporine. N Engl J Med 1991;324:1297-1304.
    • (1991) N Engl J Med , vol.324 , pp. 1297-1304
    • Frickhofen, N.1    Kaltwasser, J.P.2    Schrezenmeier, H.3
  • 16
    • 0023794546 scopus 로고
    • Bone marrow transplantation (BMT) versus immunosuppression for the treatment of severe aplastic anaemia (SAA): A report of the EBMT SAA working party
    • Bacigalupo A, Hows J, Gluckman E, et al: Bone marrow transplantation (BMT) versus immunosuppression for the treatment of severe aplastic anaemia (SAA): A report of the EBMT SAA working party. Br J Haematol 1988;70: 177-182.
    • (1988) Br J Haematol , vol.70 , pp. 177-182
    • Bacigalupo, A.1    Hows, J.2    Gluckman, E.3
  • 17
    • 0030502943 scopus 로고    scopus 로고
    • Long-term interleukin-3 and intensive immunosuppression in the treatment of aplastic anemia
    • Raghavachar A, Ganser A, Freund M, et al: Long-term interleukin-3 and intensive immunosuppression in the treatment of aplastic anemia. Cytokincs Mol Ther 1996;215-223.
    • (1996) Cytokincs Mol Ther , pp. 215-223
    • Raghavachar, A.1    Ganser, A.2    Freund, M.3
  • 18
    • 0028057807 scopus 로고
    • Paroxysmal nocturnal haemoglobinuria (PNH) is caused by somatic mutations in the PIG-A gene
    • Bessler M, Mason PJ, Hillmen P, et al: Paroxysmal nocturnal haemoglobinuria (PNH) is caused by somatic mutations in the PIG-A gene. EMBO J 1994;13:110-117.
    • (1994) EMBO J , vol.13 , pp. 110-117
    • Bessler, M.1    Mason, P.J.2    Hillmen, P.3
  • 19
    • 0028299834 scopus 로고
    • Somatic mutations and cellular selection in paroxysmal nocturnal haemoglobinuria
    • Bessler M, Mason P, Hillmen P, et al: Somatic mutations and cellular selection in paroxysmal nocturnal haemoglobinuria. Lancet 1994;343: 951-953.
    • (1994) Lancet , vol.343 , pp. 951-953
    • Bessler, M.1    Mason, P.2    Hillmen, P.3
  • 20
    • 0028110863 scopus 로고
    • Mutations in the PIG-A gene causing partial deficiency of GPI-linked surface proteins (PNH II) in patients with paroxysmal nocturnal haemoglobinuria
    • Bessler M, Mason PJ, Hillmen P, et al: Mutations in the PIG-A gene causing partial deficiency of GPI-linked surface proteins (PNH II) in patients with paroxysmal nocturnal haemoglobinuria. Br J Haematol 1994;87:863-866.
    • (1994) Br J Haematol , vol.87 , pp. 863-866
    • Bessler, M.1    Mason, P.J.2    Hillmen, P.3
  • 21
    • 0027412627 scopus 로고
    • The cloning of PIG-A, a component in the early step of GPI-anchor biosynthesis
    • Miyata T, Takeda J, Iida Y, et al: The cloning of PIG-A, a component in the early step of GPI-anchor biosynthesis. Science 1993;259: 1318-1320.
    • (1993) Science , vol.259 , pp. 1318-1320
    • Miyata, T.1    Takeda, J.2    Iida, Y.3
  • 22
    • 0028907854 scopus 로고
    • Heterogeneous PIG-A mutations in different cell lineages in paroxysmal nocturnal hemoglobinuria heterogeneous PIG-A mutations in different cell lineages in paroxysmal nocturnal hemoglobinuria
    • Ostendorf T, Nischan C, Schubert J, et al: Heterogeneous PIG-A mutations in different cell lineages in paroxysmal nocturnal hemoglobinuria heterogeneous PIG-A mutations in different cell lineages in paroxysmal nocturnal hemoglobinuria. Blood 1995;85:1640-1646.
    • (1995) Blood , vol.85 , pp. 1640-1646
    • Ostendorf, T.1    Nischan, C.2    Schubert, J.3
  • 23
    • 0027310539 scopus 로고
    • Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria
    • Takeda J, Miyata T, Kawagoe K, et al: Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria. Cell 1993;73:703-711.
    • (1993) Cell , vol.73 , pp. 703-711
    • Takeda, J.1    Miyata, T.2    Kawagoe, K.3
  • 24
    • 0028353422 scopus 로고
    • Mutations within the Piga gene in patients with paroxysmal nocturnal hemoglobinuria
    • Ware RE, Rosse WF, Howard TA: Mutations within the Piga gene in patients with paroxysmal nocturnal hemoglobinuria. Blood 1994;83: 2418-2422.
    • (1994) Blood , vol.83 , pp. 2418-2422
    • Ware, R.E.1    Rosse, W.F.2    Howard, T.A.3
  • 25
    • 0028897279 scopus 로고
    • Somatic mutations of the PIG-A gene found in Japanese patients with paroxysmal nocturnal hemoglobinuria
    • Yamada N, Miyata T, Maeda K, et al: Somatic mutations of the PIG-A gene found in Japanese patients with paroxysmal nocturnal hemoglobinuria. Blood 1995;85:885-892.
    • (1995) Blood , vol.85 , pp. 885-892
    • Yamada, N.1    Miyata, T.2    Maeda, K.3
  • 26
    • 0029871217 scopus 로고    scopus 로고
    • Molecular basis of the heterogeneity of expression of glycosyl phosphatidylinositol anchored proteins in paroxysmal nocturnal hemoglobinuria
    • Endo M, Ware RE, Vreeke TM, et al: Molecular basis of the heterogeneity of expression of glycosyl phosphatidylinositol anchored proteins in paroxysmal nocturnal hemoglobinuria. Blood 1996;87:2546-2557.
    • (1996) Blood , vol.87 , pp. 2546-2557
    • Endo, M.1    Ware, R.E.2    Vreeke, T.M.3
  • 27
    • 0031007363 scopus 로고    scopus 로고
    • PIG-A gene mutations in four Taiwanese patients with paroxysmal nocturnal haemoglobinuria following aplastic anaemia
    • Lin LI, Liu CH, Chen YC, et al: PIG-A gene mutations in four Taiwanese patients with paroxysmal nocturnal haemoglobinuria following aplastic anaemia. Br J Haematol 1997;97:286-292.
    • (1997) Br J Haematol , vol.97 , pp. 286-292
    • Lin, L.I.1    Liu, C.H.2    Chen, Y.C.3
  • 28
    • 0028885951 scopus 로고
    • Mutations in the PIG-A gene causing paroxysmal nocturnal hemoglobinuria are mainly of the frame-shift type
    • Nafa K, Mason PJ, Hillmen P, et al: Mutations in the PIG-A gene causing paroxysmal nocturnal hemoglobinuria are mainly of the frame-shift type. Blood 1995;86:4650-4655.
    • (1995) Blood , vol.86 , pp. 4650-4655
    • Nafa, K.1    Mason, P.J.2    Hillmen, P.3
  • 29
    • 0028802885 scopus 로고
    • Genetic defects underlying paroxysmal nocturnal hemoglobinuria that arises out of aplastic anemia
    • Nagarajan S, Brodsky RA, Young NS, et al: Genetic defects underlying paroxysmal nocturnal hemoglobinuria that arises out of aplastic anemia. Blood 1995;86:4656-4661.
    • (1995) Blood , vol.86 , pp. 4656-4661
    • Nagarajan, S.1    Brodsky, R.A.2    Young, N.S.3
  • 30
    • 0030942613 scopus 로고    scopus 로고
    • A patient with paroxysmal nocturnal hemoglobinuria bearing four independent PIG-A mutant clones
    • Nishimura J, Inoue N, Wada H, et al: A patient with paroxysmal nocturnal hemoglobinuria bearing four independent PIG-A mutant clones. Blood 1997;89:3470-3476.
    • (1997) Blood , vol.89 , pp. 3470-3476
    • Nishimura, J.1    Inoue, N.2    Wada, H.3
  • 31
    • 0030050851 scopus 로고    scopus 로고
    • Identification of three novel mutations in the PIG-A gene in paroxysmal nocturnal haemoglobinuria (PNH) patients
    • Savoia A, Ianzano L, Lunardi C. et al: Identification of three novel mutations in the PIG-A gene in paroxysmal nocturnal haemoglobinuria (PNH) patients. Hum Genet 1996;97:45-48.
    • (1996) Hum Genet , vol.97 , pp. 45-48
    • Savoia, A.1    Ianzano, L.2    Lunardi, C.3
  • 32
    • 0026614934 scopus 로고
    • Expansion of a paroxysmal nocturnal hemoglobinuria (PNH) clone after cyclosporine therapy for aplastic anemia/PNH syndrome
    • Nakao S, Yamaguchi M, Takamatsu H, et al: Expansion of a paroxysmal nocturnal hemoglobinuria (PNH) clone after cyclosporine therapy for aplastic anemia/PNH syndrome (letter; comment). Blood 1992;80:2943-2944.
    • (1992) Blood , vol.80 , pp. 2943-2944
    • Nakao, S.1    Yamaguchi, M.2    Takamatsu, H.3
  • 33
    • 0026537310 scopus 로고
    • Two distinct patterns of glycosylphosphatidylinositol (GPI) linked protein deficiency in the red cells of patients with paroxysmal nocturnal haemoglobinuria
    • Hillmen P, Hows JM, Luzzatto L: Two distinct patterns of glycosylphosphatidylinositol (GPI) linked protein deficiency in the red cells of patients with paroxysmal nocturnal haemoglobinuria. Br J Haematol 1992;80:399-405.
    • (1992) Br J Haematol , vol.80 , pp. 399-405
    • Hillmen, P.1    Hows, J.M.2    Luzzatto, L.3
  • 34
    • 0028920152 scopus 로고
    • The effect of cyclosporine on haematological parameters in patients with paroxysmal nocturnal haemoglobinuria
    • van Kamp H, van Imhoff GW, de Wolf JT, et al: The effect of cyclosporine on haematological parameters in patients with paroxysmal nocturnal haemoglobinuria. Br J Haematol 1995; 89:79-82.
    • (1995) Br J Haematol , vol.89 , pp. 79-82
    • Van Kamp, H.1    Van Imhoff, G.W.2    De Wolf, J.T.3
  • 35
    • 0019268572 scopus 로고
    • Paroxysmal nocturnal haemoglobinuria
    • Dacie J: Paroxysmal nocturnal haemoglobinuria. Sangre 1980;25:890-895.
    • (1980) Sangre , vol.25 , pp. 890-895
    • Dacie, J.1
  • 36
    • 85038047421 scopus 로고
    • Long-term follow-up of 80 patients with PNH: 11 of 32 patients surviving 10 years achieve spontaneous remission
    • Hillmen P, Bessler M, Luzzatto L, et al: Long-term follow-up of 80 patients with PNH: 11 of 32 patients surviving 10 years achieve spontaneous remission (abstract). Blood 1993;82 (suppl 1):310a.
    • (1993) Blood , vol.82 , Issue.SUPPL. 1
    • Hillmen, P.1    Bessler, M.2    Luzzatto, L.3
  • 37
    • 0028802443 scopus 로고
    • Natural history of paroxysmal nocturnal hemoglobinuria
    • Hillmen P, Lewis SM, Bessler M, et al: Natural history of paroxysmal nocturnal hemoglobinuria. N Engl J Med 1995;333:1253-1258.
    • (1995) N Engl J Med , vol.333 , pp. 1253-1258
    • Hillmen, P.1    Lewis, S.M.2    Bessler, M.3
  • 38
    • 0023738967 scopus 로고
    • Complete response to antilymphocyte globulin in a case of aplastic anemia-paroxysmal nocturnal hemoglobinuria syndrome
    • Kusminsky GD, Barazzutti L, Korin JD, et al: Complete response to antilymphocyte globulin in a case of aplastic anemia-paroxysmal nocturnal hemoglobinuria syndrome (letter). Am J Hematol 1988;29:123.
    • (1988) Am J Hematol , vol.29 , pp. 123
    • Kusminsky, G.D.1    Barazzutti, L.2    Korin, J.D.3
  • 39
    • 0028131848 scopus 로고
    • Persistence of affected T lymphoctes in long-term clinical remission in paroxysmal nocturnal hemoglobinuria
    • Nakakuma H, Nagakura S, Kawaguchi T, et al: Persistence of affected T lymphoctes in long-term clinical remission in paroxysmal nocturnal hemoglobinuria. Blood 1994;84:3925-3928.
    • (1994) Blood , vol.84 , pp. 3925-3928
    • Nakakuma, H.1    Nagakura, S.2    Kawaguchi, T.3
  • 40
    • 0029895043 scopus 로고    scopus 로고
    • Preferential hematopoiesis by paroxysmal nocturnal hemoglobinuria clone engrafted in SCID mice
    • Iwamoto N, Kawaguchi T, Horikawa K, et al: Preferential hematopoiesis by paroxysmal nocturnal hemoglobinuria clone engrafted in SCID mice. Blood 1996;87:4944-4948.
    • (1996) Blood , vol.87 , pp. 4944-4948
    • Iwamoto, N.1    Kawaguchi, T.2    Horikawa, K.3
  • 41
    • 0029873584 scopus 로고    scopus 로고
    • Glycosylphosphalidylinositol-anchor-deficient mice: Implications for clonal dominance of mutant cells in paroxysmal nocturnal hemoglobinuria
    • Kawagoe K, Kitamura D, Okabe M, et al: Glycosylphosphalidylinositol-anchor-deficient mice: Implications for clonal dominance of mutant cells in paroxysmal nocturnal hemoglobinuria. Blood 1996;87:3600-3606.
    • (1996) Blood , vol.87 , pp. 3600-3606
    • Kawagoe, K.1    Kitamura, D.2    Okabe, M.3
  • 42
    • 0033594885 scopus 로고    scopus 로고
    • X inactivation and somatic cell selection rescue female mice carrying a Piga-null mutation
    • Keller P, Tremml G, Rosti V, et al: X inactivation and somatic cell selection rescue female mice carrying a Piga-null mutation. Proc Natl Acad Sci USA 1999;96:7479-7483.
    • (1999) Proc Natl Acad Sci USA , vol.96 , pp. 7479-7483
    • Keller, P.1    Tremml, G.2    Rosti, V.3
  • 43
    • 0031042052 scopus 로고    scopus 로고
    • Impaired hematopoiesis in paroxysmal nocturnal hemoglobinuria / aplastic anemia is not associated with a selective proliferative defect in the glycosylphosphatidylinositol-anchored protein-deficient clone
    • Maciejewski JP, Sloand EM, Sato T, et al: Impaired hematopoiesis in paroxysmal nocturnal hemoglobinuria / aplastic anemia is not associated with a selective proliferative defect in the glycosylphosphatidylinositol-anchored protein-deficient clone. Blood 1997;89:1173-1181.
    • (1997) Blood , vol.89 , pp. 1173-1181
    • Maciejewski, J.P.1    Sloand, E.M.2    Sato, T.3
  • 44
    • 0029670929 scopus 로고    scopus 로고
    • Emergence of CD52-, glycosylphosphatidylinositol-anchor-deficient lymphocytes in rheumatoid arthritis patients following Campath-1 treatment
    • Brett SJ, Baxter G, Cooper H, et al: Emergence of CD52-, glycosylphosphatidylinositol-anchor-deficient lymphocytes in rheumatoid arthritis patients following Campath-1 treatment. Int Immunol 1996;8:325-334.
    • (1996) Int Immunol , vol.8 , pp. 325-334
    • Brett, S.J.1    Baxter, G.2    Cooper, H.3
  • 45
    • 0028978684 scopus 로고
    • Emergence of CD52-, phosphatidylinositolglycan-anchor-deficient T lymphocytes after in vivo application of Campath-1H for refractory B-cell Non-Hodgkin Lymphoma Emergence of CD52-, phosphatidylinositolglycan-anchor-deficient T lymphocytes after in vivo application of Campath-1H for refractory B-cell non-Hodgkin lymphoma
    • Hertenstein B, Wagner B, Bunjes D, et al: Emergence of CD52-, phosphatidylinositolglycan-anchor-deficient T lymphocytes after in vivo application of Campath-1H for refractory B-cell Non-Hodgkin Lymphoma Emergence of CD52-, phosphatidylinositolglycan-anchor-deficient T lymphocytes after in vivo application of Campath-1H for refractory B-cell non-Hodgkin lymphoma. Blood 1995;86:1487-1492.
    • (1995) Blood , vol.86 , pp. 1487-1492
    • Hertenstein, B.1    Wagner, B.2    Bunjes, D.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.