메뉴 건너뛰기




Volumn 106, Issue 8, 1999, Pages 1525-1530

Vitreoretinal findings similar to retinopathy of prematurity in infants with compound heterozygous protein S deficiency

Author keywords

[No Author keywords available]

Indexed keywords

PROTEIN S;

EID: 0033490961     PISSN: 01616420     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0161-6420(99)90448-7     Document Type: Article
Times cited : (20)

References (32)
  • 1
    • 0030870825 scopus 로고    scopus 로고
    • Factor V Leiden and other coagulation factor mutations affecting thrombotic risk
    • Bertina RM. Factor V Leiden and other coagulation factor mutations affecting thrombotic risk. Clin Chem 1997;43: 1678-83.
    • (1997) Clin Chem , vol.43 , pp. 1678-1683
    • Bertina, R.M.1
  • 2
    • 0030915871 scopus 로고    scopus 로고
    • Location on the human genetic linkage map of 26 genes involved in blood coagulation
    • Koeleman BPC, Reitsma PH, Bakker E, Bertina RM. Location on the human genetic linkage map of 26 genes involved in blood coagulation. Thromb Haemost 1997;77:873-8.
    • (1997) Thromb Haemost , vol.77 , pp. 873-878
    • Koeleman, B.P.C.1    Reitsma, P.H.2    Bakker, E.3    Bertina, R.M.4
  • 3
    • 0028083284 scopus 로고
    • Homozygous anti-thrombin deficiency: Report of two new cases (99Leu to Phe) associated with arterial and venous thrombosis
    • Chowdhury V, Lane DA, Mille B, et al. Homozygous anti-thrombin deficiency: report of two new cases (99Leu to Phe) associated with arterial and venous thrombosis. Thromb Haemost 1994;72:198-202.
    • (1994) Thromb Haemost , vol.72 , pp. 198-202
    • Chowdhury, V.1    Lane, D.A.2    Mille, B.3
  • 4
    • 0021086761 scopus 로고
    • Inherited protein C deficiency and coumarin-responsive chronic relapsing purpura fulminans in a newborn infant
    • Branson HE, Katz J, Marble R, Griffin JH. Inherited protein C deficiency and coumarin-responsive chronic relapsing purpura fulminans in a newborn infant. Lancet 1983;2:1165-8.
    • (1983) Lancet , vol.2 , pp. 1165-1168
    • Branson, H.E.1    Katz, J.2    Marble, R.3    Griffin, J.H.4
  • 5
    • 0021124825 scopus 로고
    • Severe inherited "homozygous" protein C deficiency in a newborn infant
    • Estellés A, Garcia-Plaza I, Dasi A, et al. Severe inherited "homozygous" protein C deficiency in a newborn infant. Thromb Haemost 1984;52:53-6.
    • (1984) Thromb Haemost , vol.52 , pp. 53-56
    • Estellés, A.1    Garcia-Plaza, I.2    Dasi, A.3
  • 6
    • 0021930913 scopus 로고
    • Neonatal purpura fulminans: A genetic disorder related to the absence of protein C in blood
    • Marciniak E, Wilson HD, Marlar RA. Neonatal purpura fulminans: a genetic disorder related to the absence of protein C in blood. Blood 1985;65:15-20.
    • (1985) Blood , vol.65 , pp. 15-20
    • Marciniak, E.1    Wilson, H.D.2    Marlar, R.A.3
  • 7
    • 0022656222 scopus 로고
    • Purpura fulminans in a Chinese boy with congenital protein C deficiency
    • Yuen P, Cheung A, Lin HJ, et al. Purpura fulminans in a Chinese boy with congenital protein C deficiency. Pediatrics 1986;77:670-6.
    • (1986) Pediatrics , vol.77 , pp. 670-676
    • Yuen, P.1    Cheung, A.2    Lin, H.J.3
  • 9
    • 0023656942 scopus 로고
    • Protein C deficiency associated with vitreous hemorrhage in a neonate
    • Pulido JS, Lingua RW, Cristol S, Byrne SF. Protein C deficiency associated with vitreous hemorrhage in a neonate. Am J Ophthalmol 1987;104:546-7.
    • (1987) Am J Ophthalmol , vol.104 , pp. 546-547
    • Pulido, J.S.1    Lingua, R.W.2    Cristol, S.3    Byrne, S.F.4
  • 10
    • 0023911084 scopus 로고
    • Homozygous protein C deficiency: Observations on the nature of the molecular abnormality and the effectiveness of warfarin therapy
    • Peters C, Casella JF, Marlar RA, et al. Homozygous protein C deficiency: observations on the nature of the molecular abnormality and the effectiveness of warfarin therapy. Pediatrics 1988;81:272-6.
    • (1988) Pediatrics , vol.81 , pp. 272-276
    • Peters, C.1    Casella, J.F.2    Marlar, R.A.3
  • 11
    • 0023707069 scopus 로고
    • Purpura fulminans: A cutaneous manifestation of severe protein C deficiency
    • Auletta MJ, Headington JT. Purpura fulminans: a cutaneous manifestation of severe protein C deficiency. Arch Dermatol 1988;124:1387-91.
    • (1988) Arch Dermatol , vol.124 , pp. 1387-1391
    • Auletta, M.J.1    Headington, J.T.2
  • 12
    • 0042905221 scopus 로고    scopus 로고
    • Protein C and protein S deficiencies
    • Schafer AJ, ed. Austin, TX: Landes Bioscience and Chapman & Hall, chap. 3
    • Marlar RA, Hassell KL. Protein C and protein S deficiencies. In: Schafer AJ, ed. Molecular Mechanisms of Hypercoagulable States. Austin, TX: Landes Bioscience and Chapman & Hall, 1997; chap. 3.
    • (1997) Molecular Mechanisms of Hypercoagulable States
    • Marlar, R.A.1    Hassell, K.L.2
  • 13
    • 0025064295 scopus 로고
    • Neonatal purpura fulminans associated with homozygous protein S deficiency
    • Mahasandana C, Suvatte V, Marlar RA, et al. Neonatal purpura fulminans associated with homozygous protein S deficiency [letter]. Lancet 1990;335:61-2.
    • (1990) Lancet , vol.335 , pp. 61-62
    • Mahasandana, C.1    Suvatte, V.2    Marlar, R.A.3
  • 14
    • 0025155588 scopus 로고
    • Homozygous protein S deficiency in an infant with purpura fulminans
    • Mahasandana C, Suvatte V, Chuansumrit A, et al. Homozygous protein S deficiency in an infant with purpura fulminans. J Pediatr 1990;117:750-3.
    • (1990) J Pediatr , vol.117 , pp. 750-753
    • Mahasandana, C.1    Suvatte, V.2    Chuansumrit, A.3
  • 17
    • 0028175686 scopus 로고
    • Homozygous protein S deficiency due to a one base pair deletion that leads to a stop codon in exon III of the protein S gene
    • Gomez E, Ledford MR, Pegelow CH, et al. Homozygous protein S deficiency due to a one base pair deletion that leads to a stop codon in exon III of the protein S gene. Thromb Haemost 1994;71:723-6.
    • (1994) Thromb Haemost , vol.71 , pp. 723-726
    • Gomez, E.1    Ledford, M.R.2    Pegelow, C.H.3
  • 18
    • 0021741550 scopus 로고
    • Familial protein S deficiency is associated with recurrent thrombosis
    • Comp PC, Nixon RR, Cooper MR, Esmon CT. Familial protein S deficiency is associated with recurrent thrombosis. J Clin Invest 1984;74:2082-8.
    • (1984) J Clin Invest , vol.74 , pp. 2082-2088
    • Comp, P.C.1    Nixon, R.R.2    Cooper, M.R.3    Esmon, C.T.4
  • 19
    • 0023851558 scopus 로고
    • The gene for protein S maps near the centromere of human chromosome 3
    • Watkins PC, Eddy R, Fukushima Y, et al. The gene for protein S maps near the centromere of human chromosome 3. Blood 1988;71:238-41.
    • (1988) Blood , vol.71 , pp. 238-241
    • Watkins, P.C.1    Eddy, R.2    Fukushima, Y.3
  • 20
    • 0030897765 scopus 로고    scopus 로고
    • Long-term form identification vision after early, closed, lensectomy-vitrectomy for stage 5 retinopathy of prematurity
    • Mintz-Hittner HA, O'Malley RE, Kretzer FL. Long-term form identification vision after early, closed, lensectomy-vitrectomy for stage 5 retinopathy of prematurity. Ophthalmology 1997;104:454-9.
    • (1997) Ophthalmology , vol.104 , pp. 454-459
    • Mintz-Hittner, H.A.1    O'Malley, R.E.2    Kretzer, F.L.3
  • 21
  • 24
    • 0030785316 scopus 로고    scopus 로고
    • Persistent fetal vasculature (PFV): An integrated interpretation of signs and symptoms associated with persistent hyperplastic primary vitreous (PHPV). LIV Edward Jackson Memorial Lecture
    • Goldberg MF. Persistent fetal vasculature (PFV): an integrated interpretation of signs and symptoms associated with persistent hyperplastic primary vitreous (PHPV). LIV Edward Jackson Memorial Lecture. Am J Ophthalmol 1997;124:587-626.
    • (1997) Am J Ophthalmol , vol.124 , pp. 587-626
    • Goldberg, M.F.1
  • 25
    • 0028202180 scopus 로고
    • Postnatal retinal vascularization in former preterm infants with retinopathy of prematurity
    • Mintz-Hittner HA, Kretzer FL. Postnatal retinal vascularization in former preterm infants with retinopathy of prematurity. Ophthalmology 1994;101:548-58.
    • (1994) Ophthalmology , vol.101 , pp. 548-558
    • Mintz-Hittner, H.A.1    Kretzer, F.L.2
  • 26
    • 0029816808 scopus 로고    scopus 로고
    • Regulation of vascular endothelial growth factor by oxygen in a model of retinopathy of prematurity
    • Pierce EA, Foley ED, Smith LEH. Regulation of vascular endothelial growth factor by oxygen in a model of retinopathy of prematurity. Arch Ophthalmol 1996;114:1219-28.
    • (1996) Arch Ophthalmol , vol.114 , pp. 1219-1228
    • Pierce, E.A.1    Foley, E.D.2    Smith, L.E.H.3
  • 27
    • 0031896301 scopus 로고    scopus 로고
    • Factor V Leiden and genetic defects of thrombophilia in childhood porencephaly
    • Debus O, Koch HG, Kurlemann G, et al. Factor V Leiden and genetic defects of thrombophilia in childhood porencephaly. Arch Dis Child Fetal Neonatal Ed 1998;78:F121-4.
    • (1998) Arch Dis Child Fetal Neonatal Ed , vol.78
    • Debus, O.1    Koch, H.G.2    Kurlemann, G.3
  • 28
    • 0001328399 scopus 로고
    • Ocular signs associated with hydranencephaly
    • Hill K, Cogan DG, Dodge PR. Ocular signs associated with hydranencephaly. Am J Ophthalmol 1961;51:267-75.
    • (1961) Am J Ophthalmol , vol.51 , pp. 267-275
    • Hill, K.1    Cogan, D.G.2    Dodge, P.R.3
  • 29
    • 0014124670 scopus 로고
    • Anencephaly related to ocular development and malformation
    • Andersen SR, Bro-Rasmussen F, Tygstrup I. Anencephaly related to ocular development and malformation. Am J Ophthalmol 1967;64:559-66.
    • (1967) Am J Ophthalmol , vol.64 , pp. 559-566
    • Andersen, S.R.1    Bro-Rasmussen, F.2    Tygstrup, I.3
  • 30
    • 0014988909 scopus 로고
    • Eye findings in hydranencephaly
    • Manschot WA. Eye findings in hydranencephaly. Ophthalmologica 1971;162:151-9.
    • (1971) Ophthalmologica , vol.162 , pp. 151-159
    • Manschot, W.A.1
  • 32
    • 0030919857 scopus 로고    scopus 로고
    • Identification of missense mutations in the Norrie disease gene associated with advanced retinopathy of prematurity
    • Shastry BS, Pendergast SD, Hartzer MK, et al. Identification of missense mutations in the Norrie disease gene associated with advanced retinopathy of prematurity. Arch Ophthalmol 1997;115:651-5.
    • (1997) Arch Ophthalmol , vol.115 , pp. 651-655
    • Shastry, B.S.1    Pendergast, S.D.2    Hartzer, M.K.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.