Preserving eye function in prematurely born children with severe protein C deficiency
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| Published in: | Journal of thrombosis and haemostasis Vol. 1; no. 8; pp. 1858 - 1859 |
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| Main Authors: | , , , , |
| Format: | Journal Article |
| Language: | English |
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Oxford, UK
Blackwell Science Inc
01-08-2003
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| Author | Hongeng, S. Chuansumrit, A. Hanutsaha, P. Pakakasama, S. Sirachainan, N. |
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| Author_xml | – sequence: 1 givenname: N. surname: Sirachainan fullname: Sirachainan, N. – sequence: 2 givenname: A. surname: Chuansumrit fullname: Chuansumrit, A. – sequence: 3 givenname: P. surname: Hanutsaha fullname: Hanutsaha, P. – sequence: 4 givenname: S. surname: Pakakasama fullname: Pakakasama, S. – sequence: 5 givenname: S. surname: Hongeng fullname: Hongeng, S. |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/12911612$$D View this record in MEDLINE/PubMed |
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| CitedBy_id | crossref_primary_10_1016_j_thromres_2009_10_016 crossref_primary_10_1111_j_1538_7836_2007_02463_x crossref_primary_10_1186_s12886_020_01424_x |
| Cites_doi | 10.1055/s-0037-1614593 10.1056/NEJM198403013100904 10.1055/s-0038-1653885 10.1136/bjo.84.1.117d 10.1136/bjo.85.2.238d 10.1002/1097-0223(200009)20:9<746::AID-PD901>3.0.CO;2-8 10.1097/00003246-200009001-00010 10.1055/s-0038-1646629 10.1055/s-0037-1613219 |
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| References | 2000; 84 1995; 73 1989; 61 2000; 28 1999; 81 1984; 310 1994; 5 2001; 85 2000; 20 2002; 88 Reitsma (10.1046/j.1538-7836.2003.00296.x_bb0055) 1995; 73 Kirkinen (10.1046/j.1538-7836.2003.00296.x_bb0015) 2000; 20 Ergenekon (10.1046/j.1538-7836.2003.00296.x_bb0030) 2000; 84 Seligsohn (10.1046/j.1538-7836.2003.00296.x_bb0020) 1984; 310 Marlar (10.1046/j.1538-7836.2003.00296.x_bb0045) 1989; 61 Churchill (10.1046/j.1538-7836.2003.00296.x_bb0010) 2001; 85 Charles (10.1046/j.1538-7836.2003.00296.x_bb0035) 2000; 28 Sanz-Rodriguez (10.1046/j.1538-7836.2003.00296.x_bb0040) 1999; 81 Millar (10.1046/j.1538-7836.2003.00296.x_bb0050) 1994; 5 Barnes (10.1046/j.1538-7836.2003.00296.x_bb0025) 2002; 88 |
| References_xml | – volume: 28 start-page: 44 year: 2000 end-page: 8 article-title: The protein C pathway publication-title: Crit Care Med – volume: 81 start-page: 887 year: 1999 end-page: 90 article-title: Long term management of homozygous protein C deficiency: Replacement therapy with subcutaneous purified protein C concentrate publication-title: Thromb Haemost – volume: 20 start-page: 746 year: 2000 end-page: 9 article-title: Antepartum findings in fetal protein C deficiency publication-title: Prenat Diagn – volume: 84 start-page: 120 year: 2000 end-page: 1 article-title: Can leucocoria be the first manifestation of protein C deficiency? publication-title: Br J Ophthalmol – volume: 73 start-page: 876 year: 1995 end-page: 89 article-title: Protein C deficiency: a database of mutations, 1995 update publication-title: Thromb Haemost – volume: 5 start-page: 647 year: 1994 end-page: 9 article-title: A homozygous deletion/insertion mutation in the protein C (PROC) gene causing neonatal purpura fulminans: prenatal diagnosis in an at‐risk pregnancy publication-title: Blood Coagul Fibrinolysis – volume: 88 start-page: 370 year: 2002 end-page: 1 article-title: Perinatal management of patients at high risk of homozygous protein C deficiency publication-title: Thromb Haemost – volume: 85 start-page: 241 year: 2001 end-page: 2 article-title: Clinical manifestations of protein C deficiency: a spectrum within one family publication-title: Br J Ophthalmol – volume: 61 start-page: 529 year: 1989 end-page: 31 article-title: 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 publication-title: Thromb Haemost – volume: 310 start-page: 559 year: 1984 end-page: 62 article-title: Homozygous protein C deficiency manifested by massive venous thrombosis in the newborn publication-title: N Engl J Med – volume: 81 start-page: 887 year: 1999 ident: 10.1046/j.1538-7836.2003.00296.x_bb0040 article-title: Long term management of homozygous protein C deficiency: Replacement therapy with subcutaneous purified protein C concentrate publication-title: Thromb Haemost doi: 10.1055/s-0037-1614593 contributor: fullname: Sanz-Rodriguez – volume: 310 start-page: 559 year: 1984 ident: 10.1046/j.1538-7836.2003.00296.x_bb0020 article-title: Homozygous protein C deficiency manifested by massive venous thrombosis in the newborn publication-title: N Engl J Med doi: 10.1056/NEJM198403013100904 contributor: fullname: Seligsohn – volume: 5 start-page: 647 year: 1994 ident: 10.1046/j.1538-7836.2003.00296.x_bb0050 article-title: A homozygous deletion/insertion mutation in the protein C (PROC) gene causing neonatal purpura fulminans: prenatal diagnosis in an at-risk pregnancy publication-title: Blood Coagul Fibrinolysis contributor: fullname: Millar – volume: 73 start-page: 876 year: 1995 ident: 10.1046/j.1538-7836.2003.00296.x_bb0055 article-title: Protein C deficiency: a database of mutations, 1995 update publication-title: Thromb Haemost doi: 10.1055/s-0038-1653885 contributor: fullname: Reitsma – volume: 84 start-page: 120 year: 2000 ident: 10.1046/j.1538-7836.2003.00296.x_bb0030 article-title: Can leucocoria be the first manifestation of protein C deficiency? publication-title: Br J Ophthalmol doi: 10.1136/bjo.84.1.117d contributor: fullname: Ergenekon – volume: 85 start-page: 241 year: 2001 ident: 10.1046/j.1538-7836.2003.00296.x_bb0010 article-title: Clinical manifestations of protein C deficiency: a spectrum within one family publication-title: Br J Ophthalmol doi: 10.1136/bjo.85.2.238d contributor: fullname: Churchill – volume: 20 start-page: 746 year: 2000 ident: 10.1046/j.1538-7836.2003.00296.x_bb0015 article-title: Antepartum findings in fetal protein C deficiency publication-title: Prenat Diagn doi: 10.1002/1097-0223(200009)20:9<746::AID-PD901>3.0.CO;2-8 contributor: fullname: Kirkinen – volume: 28 start-page: 44 year: 2000 ident: 10.1046/j.1538-7836.2003.00296.x_bb0035 article-title: The protein C pathway publication-title: Crit Care Med doi: 10.1097/00003246-200009001-00010 contributor: fullname: Charles – volume: 61 start-page: 529 year: 1989 ident: 10.1046/j.1538-7836.2003.00296.x_bb0045 article-title: 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 publication-title: Thromb Haemost doi: 10.1055/s-0038-1646629 contributor: fullname: Marlar – volume: 88 start-page: 370 year: 2002 ident: 10.1046/j.1538-7836.2003.00296.x_bb0025 article-title: Perinatal management of patients at high risk of homozygous protein C deficiency publication-title: Thromb Haemost doi: 10.1055/s-0037-1613219 contributor: fullname: Barnes |
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| SubjectTerms | Diseases in Twins Eye Diseases - prevention & control Heterozygote Homozygote Humans Infant, Newborn Infant, Premature Male Ocular Physiological Phenomena Protein C - biosynthesis Protein C Deficiency - genetics Time Factors Warfarin - therapeutic use |
| Title | Preserving eye function in prematurely born children with severe protein C deficiency |
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