메뉴 건너뛰기




Volumn 1, Issue 8, 2003, Pages 1858-1859

Preserving eye function in prematurely born children with severe protein C deficiency

Author keywords

[No Author keywords available]

Indexed keywords

PROTEIN C; WARFARIN;

EID: 2142712987     PISSN: 15387933     EISSN: 15387836     Source Type: Journal    
DOI: 10.1046/j.1538-7836.2003.00296.x     Document Type: Letter
Times cited : (3)

References (10)
  • 4
    • 0036339163 scopus 로고    scopus 로고
    • Perinatal manage ment of patients at high risk of homozygous protein C deficiency
    • Barnes C, Newall F, Higgins S, Carden S, Monagle P. Perinatal manage ment of patients at high risk of homozygous protein C deficiency. Thromb Haemost 2002; 88: 370-1.
    • (2002) Thromb Haemost , vol.88 , pp. 370-371
    • Barnes, C.1    Newall, F.2    Higgins, S.3    Carden, S.4    Monagle, P.5
  • 5
    • 0033628141 scopus 로고    scopus 로고
    • Can leucocoria be the first manifestation of protein C deficiency?
    • Ergenekon E, Solak B, Ozturk G, Atalay Y, Koc E. Can leucocoria be the first manifestation of protein C deficiency? Br J Ophthalmol 2000; 84: 120-1.
    • (2000) Br J Ophthalmol , vol.84 , pp. 120-121
    • Ergenekon, E.1    Solak, B.2    Ozturk, G.3    Atalay, Y.4    Koc, E.5
  • 6
    • 0033815369 scopus 로고    scopus 로고
    • The protein C pathway
    • Charles E. The protein C pathway. Crit Care Med 2000; 28: 44-8.
    • (2000) Crit Care Med , vol.28 , pp. 44-48
    • Charles, E.1
  • 8
    • 0024399901 scopus 로고
    • Report on the diagnosis and treatment of homozygous protein C deficiency Report of the working party on homozygous protein C deficiency of the ICTH-Subcommittee on protein C and protein S
    • Marlar RA, Montgomery RR, Broekmans AW. Report on the diagnosis and treatment of homozygous protein C deficiency. Report of the working party on homozygous protein C deficiency of the ICTH-Subcommittee on protein C and protein S. Thromb Haemost 1989; 61: 529-31.
    • (1989) Thromb Haemost , vol.61 , pp. 529-531
    • Marlar, R.A.1    Montgomery, R.R.2    Broekmans, A.W.3
  • 9
    • 0027931513 scopus 로고
    • A homo zygous deletion/insertion mutation in the protein C (PROC) gene causing neonatal purpura fulminans: prenatal diagnosis in an at-risk pregnancy
    • Millar DS, Allgrove J, Rodeck C, Kakkar VV, Cooper DN. A homo zygous deletion/insertion mutation in the protein C (PROC) gene causing neonatal purpura fulminans: prenatal diagnosis in an at-risk pregnancy. Blood Coagul Fibrinolysis 1994; 5: 647-9.
    • (1994) Blood Coagul Fibrinolysis , vol.5 , pp. 647-649
    • Millar, D.S.1    Allgrove, J.2    Rodeck, C.3    Kakkar, V.V.4    Cooper, D.N.5


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.