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Volumn 91, Issue 6, 2012, Pages 917-921

Erratum: A novel ELISA for diagnosis of Glanzmann’s thrombasthenia and the heterozygote carriers [Annals of Hematology, 91, 6, (2015), (917-921), DOI 10.1007/s00277-011-1390-1];A novel ELISA for diagnosis of Glanzmann's thrombasthenia and the heterozygote carriers

Author keywords

Diagnosis; ELISA; Glanzmann's thrombasthenia; Heterozygote carriers

Indexed keywords

ALKALINE PHOSPHATASE; ANTIBODY; CD36 ANTIBODY; DISINTEGRIN; FIBRINOGEN RECEPTOR; HYBRID PROTEIN; UNCLASSIFIED DRUG;

EID: 84862688177     PISSN: 09395555     EISSN: 14320584     Source Type: Journal    
DOI: 10.1007/s00277-015-2382-3     Document Type: Erratum
Times cited : (4)

References (19)
  • 1
    • 0026621177 scopus 로고
    • Biochemical and molecular basis of Glanzmann's thrombasthenia
    • Perutelli P, Mori PG (1992) Biochemical and molecular basis of Glanzmann's thrombasthenia. Haematologica 77:421-426 (Pubitemid 23012089)
    • (1992) Haematologica , vol.77 , Issue.5 , pp. 421-426
    • Perutelli, P.1    Mori, P.G.2
  • 2
    • 0031929048 scopus 로고    scopus 로고
    • The molecular genetics of Glanzmann's thrombasthenia
    • French DL (1998) The molecular genetics of Glanzmann's thrombasthenia. Platelets 9:5-20
    • (1998) Platelets , vol.9 , pp. 5-20
    • French, D.L.1
  • 3
    • 0025253068 scopus 로고
    • Glanzmann's thrombasthenia: The spectrum of clinical disease
    • George JN, Caen JP, Nurden AT (1990) Glanzmann's thrombasthenia: the spectrum of clinical disease. Blood 75:1383-1395 (Pubitemid 20114873)
    • (1990) Blood , vol.75 , Issue.7 , pp. 1383-1395
    • George, J.N.1    Caen, J.P.2    Nurden, A.T.3
  • 4
    • 0025821346 scopus 로고
    • Detection of the Glanzmann's thrombasthenia mutations in Arab and Iraqi-Jewish patients by polymerase chain reaction and restriction analysis of blood or urine samples
    • Peretz H, Seligsohn U, Zwang CBS, Newman PJ (1991) Detection of the Glanzmann's thrombasthenia mutations in Arab and Iraqi-Jewish patients by polymerase chain reaction and restriction analysis of blood or urine samples. Thromb Haemost 66:500-504
    • (1991) Thromb Haemost , vol.66 , pp. 500-504
    • Peretz, H.1    Seligsohn, U.2    Zwang, C.B.S.3    Newman, P.J.4
  • 6
    • 0346786500 scopus 로고    scopus 로고
    • Platelet function tests using platelet aggregometry: Need for repetition of the test for diagnosis of defective platelet function
    • DOI 10.1080/09537100310001598792
    • Ghosh K, Nair S, Kulkarni B, Khare A, Shetty S, Mohanty D (2003) Platelet function tests using platelet aggregometry: need for repetition of the test for diagnosis of defective platelet function. Platelets 14:351-354 (Pubitemid 38037256)
    • (2003) Platelets , vol.14 , Issue.6 , pp. 351-354
    • Ghosh, K.1    Nair, S.2    Kulkarni, B.3    Khare, A.4    Shetty, S.5    Mohanty, D.6
  • 7
    • 0031959217 scopus 로고    scopus 로고
    • Rapid heterozygote detection in Glanzmann's thrombasthenia
    • DOI 10.1046/j.1365-2141.1998.00655.x
    • Sharp WJ, Khanduri UD, Christie BS (1998) Rapid heterozygote detection in Glanzmann's thrombasthenia. Br J Haematol 101:66-69 (Pubitemid 28197776)
    • (1998) British Journal of Haematology , vol.101 , Issue.1 , pp. 66-69
    • Sharp, W.J.1    Khanduri, U.D.2    Christie, B.S.3
  • 8
    • 61649089278 scopus 로고    scopus 로고
    • Glanzmann's thrombasthenia in North Indians: Sub classification and carrier detection by flow cytometry
    • Kannan M, Ahmad F, Yadav BK, Anand M, Jain P, Kumar R, Saxena R (2009) Glanzmann's thrombasthenia in North Indians: sub classification and carrier detection by flow cytometry. Platelets 20:12-15
    • (2009) Platelets , vol.20 , pp. 12-15
    • Kannan, M.1    Ahmad, F.2    Yadav, B.K.3    Anand, M.4    Jain, P.5    Kumar, R.6    Saxena, R.7
  • 9
    • 23944442844 scopus 로고    scopus 로고
    • Mutations in GPIIIa molecule as a cause for Glanzmann thrombasthenia in Indian patients
    • DOI 10.1111/j.1538-7836.2005.01159.x
    • Nair S, Ghosh K, Shetty S, Mohanty D (2005) Mutations in GPIIIa molecule as a cause for Glanzmann thrombasthenia in Indian patients. J Thromb Haemost 3:482-488 (Pubitemid 41632873)
    • (2005) Journal of Thrombosis and Haemostasis , vol.3 , Issue.3 , pp. 482-488
    • Nair, S.1    Ghosh, K.2    Shetty, S.3    Mohanty, D.4
  • 10
    • 61649112977 scopus 로고    scopus 로고
    • Novel mutations in GP IIb gene in Glanzmann's thrombasthenia from India
    • Vijapurkar M, Ghosh K, Shetty S (2009) Novel mutations in GP IIb gene in Glanzmann's thrombasthenia from India. Platelets 20:35-40
    • (2009) Platelets , vol.20 , pp. 35-40
    • Vijapurkar, M.1    Ghosh, K.2    Shetty, S.3
  • 12
    • 0026024976 scopus 로고
    • Platelet vitronectin receptor expression differentiates Iraqi-Jewish from Arab patients with Glanzmann thrombasthenia in Israel
    • Coller BS, Cheresh DA, Asch E, Seligsohn U (1991) Platelet vitronectin receptor expression differentiates Iraqi-Jewish from Arab patients with Glanzmann thrombasthenia in Israel. Blood 77:75-83
    • (1991) Blood , vol.77 , pp. 75-83
    • Coller, B.S.1    Cheresh, D.A.2    Asch, E.3    Seligsohn, U.4
  • 13
    • 0023234277 scopus 로고
    • Type I Glanzmann thrombasthenia patients from the Iraqi-Jewish and Arab populations in Israel can be differentiated by platelet glycoprotein IIIa immunoblot analysis
    • Coller BS, Seligsohn U, Little PA (1987) Type I Glanzmann thrombasthenia patients from the Iraqi-Jewish and Arab populations in Israel can be differentiated by platelet glycoprotein IIIa immunoblot analysis. Blood 69:1696-1703 (Pubitemid 17091628)
    • (1987) Blood , vol.69 , Issue.6 , pp. 1696-1703
    • Coller, B.S.1    Seligsohn, U.2    Little, P.A.3
  • 14
    • 48249151202 scopus 로고    scopus 로고
    • Carrier detection in Glanzmann thrombasthenia: Comparison of flow cytometry and Western blot with respect to DNA mutation
    • Kannan M, Ahmad F, Yadav BK (2008) Carrier detection in Glanzmann thrombasthenia: comparison of flow cytometry and Western blot with respect to DNA mutation. Am J Clin Pathol 130:93-98
    • (2008) Am J Clin Pathol , vol.130 , pp. 93-98
    • Kannan, M.1    Ahmad, F.2    Yadav, B.K.3
  • 17
    • 70449399296 scopus 로고    scopus 로고
    • Molecular defects in ITGA2B and ITGB3 genes in patients with Glanzmann thrombasthenia
    • Kannan M, Ahmad F, Yadav BK, Kumar R, Choudhry VP, Saxena R (2009) Molecular defects in ITGA2B and ITGB3 genes in patients with Glanzmann thrombasthenia. J Thromb Haemost 7:1878-1885
    • (2009) J Thromb Haemost , vol.7 , pp. 1878-1885
    • Kannan, M.1    Ahmad, F.2    Yadav, B.K.3    Kumar, R.4    Choudhry, V.P.5    Saxena, R.6


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.