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Journal Abstract Search

132 related items for PubMed ID: 16689776

  • 1. Severe type I protein C deficiency with neonatal purpura fulminans due to a novel homozygous mutation in exon 6 of the protein C gene.
    Abu-Amero KK, Owaidah TM, Al-Mahed M.
    J Thromb Haemost; 2006 May; 4(5):1152-3. PubMed ID: 16689776
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  • 3. Diffuse Intracerebral Hemorrhage in an Infant With a Novel Homozygous Variant Leading to Severe Protein C Deficiency.
    Martin G, Thomas MA, Wei XC, Le D.
    J Pediatr Hematol Oncol; 2021 Aug 01; 43(6):e763-e765. PubMed ID: 33165188
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  • 5. Protein C (PROC) gene mutations in two Indian families with purpura fulminans.
    Pai N, Shetty S, Ghosh K.
    Ann Hematol; 2010 Aug 01; 89(8):835-6. PubMed ID: 20077116
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  • 6. Severe Protein C Deficiency due to Novel Biallelic Variants in PROC and Their Phenotype Correlation.
    Barg AA, Dardik R, Levin C, Koren A, Levy-Mendelovich S, Pode-Shakked B, Kenet G.
    Acta Haematol; 2021 Aug 01; 144(3):327-331. PubMed ID: 32980846
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  • 7. Neonatal purpura fulminans due to homozygous protein C deficiency.
    Ezer U, Misirlioglu ED, Colba V, Ogoz E, Kurt C.
    Pediatr Hematol Oncol; 2001 Aug 01; 18(7):453-8. PubMed ID: 11594708
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  • 8. Long-term follow-up of homozygote protein C deficiency after multimodal therapy.
    Monagle K, Ignjatovic V, Hardikar W, Newall F, Monagle P.
    J Pediatr Hematol Oncol; 2014 Oct 01; 36(7):e452-5. PubMed ID: 24136027
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  • 10. A novel compound heterozygous form of severe protein C deficiency causing bleeding without purpura fulminans.
    Herrick NL, Geddis AE, Lovejoy AE, Kim J, Schiff D, Thornburg CD.
    Pediatr Blood Cancer; 2017 Nov 01; 64(11):. PubMed ID: 28485122
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  • 11. A neonate with homozygous protein C deficiency with a homozygous Arg178Trp mutation.
    Ozlu F, Kyotani M, Taskin E, Ozcan K, Kojima T, Matsushita T, Yapicioğlu H, Takagi A, Saşmaz I, Satar M, Narli N.
    J Pediatr Hematol Oncol; 2008 Aug 01; 30(8):608-11. PubMed ID: 18799939
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  • 12. Management of neonatal purpura fulminans with severe protein C deficiency.
    Sen K, Roy A.
    Indian Pediatr; 2006 Jun 01; 43(6):542-5. PubMed ID: 16820665
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  • 13. A Novel Protein C Mutation Causing Neonatal Purpura Fulminans.
    Devi R U, Bharathi S M, Kawankar N.
    Indian Pediatr; 2016 Nov 15; 53(11):1019-1021. PubMed ID: 27889735
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  • 14. Severe purpura fulminans due to coexistence of homozygous protein C deficiency and homozygous methylenetetrahydrofolate reductase mutation.
    Demirel N, Bas AY, Okumus N, Zenciroglu A, Yarali N.
    Pediatr Hematol Oncol; 2009 Nov 15; 26(8):597-600. PubMed ID: 19954370
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  • 16. Neonatal purpura fulminans due to homozygous protein C or protein S deficiencies.
    Marlar RA, Neumann A.
    Semin Thromb Hemost; 1990 Oct 15; 16(4):299-309. PubMed ID: 2149204
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  • 20. Severe homozygous protein C deficiency: identification of a splice site missense mutation (184, Q-->H) in exon 7 of the protein C gene.
    Soria JM, Brito D, Barceló J, Fontcuberta J, Botero L, Maldonado J, Estivill X, Sala N.
    Thromb Haemost; 1994 Jul 15; 72(1):65-9. PubMed ID: 7974377
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