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Journal Abstract Search

151 related items for PubMed ID: 7841324

  • 1. A novel homozygous missense mutation (Val 325-->Ala) in the protein C gene causing neonatal purpura fulminans.
    Witt I, Beck S, Seydewitz HH, Tasangil C, Schenck W.
    Blood Coagul Fibrinolysis; 1994 Aug; 5(4):651-3. PubMed ID: 7841324
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  • 2. A homozygous 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.
    Blood Coagul Fibrinolysis; 1994 Aug; 5(4):647-9. PubMed ID: 7841323
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  • 3. Homozygous type I protein C deficiency in two unrelated families exhibiting thrombophilia related to Ala136-->Pro or Arg286-->His mutations.
    Long GL, Tomczak JA, Rainville IR, Dreyfus M, Schramm W, Schwarz HP.
    Thromb Haemost; 1994 Oct; 72(4):526-33. PubMed ID: 7878626
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  • 4. 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; 72(1):65-9. PubMed ID: 7974377
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  • 6. Neonatal purpura fulminans due to homozygous protein C or protein S deficiencies.
    Marlar RA, Neumann A.
    Semin Thromb Hemost; 1990 Oct; 16(4):299-309. PubMed ID: 2149204
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  • 7. Purpura fulminans in a patient homozygous for a mutation in the protein C gene--prenatal diagnosis in a subsequent pregnancy.
    Alessi MC, Aillaud MF, Paut O, Roquelaure B, Alhenc-Gelas M, Pellissier MC, Ghanen N, Juhan-Vague I.
    Thromb Haemost; 1996 Mar; 75(3):525-6. PubMed ID: 8701425
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  • 9. A novel mutation c.1048A>T at codon 350(Lys>Stop) in PROC gene causing neonatal purpura fulminans.
    Jain R, T L, Chandran J, Jayandharan GR, Palle A, Moses PD.
    Blood Coagul Fibrinolysis; 2013 Dec; 24(8):890-2. PubMed ID: 24158118
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  • 11. Three missense mutations in the protein C heavy chain causing type I and type II protein C deficiency.
    Miyata T, Zheng YZ, Sakata T, Tsushima N, Kato H.
    Thromb Haemost; 1994 Jan; 71(1):32-7. PubMed ID: 8165644
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  • 13. Application of two neutral MspI DNA polymorphisms in the analysis of hereditary protein C deficiency.
    Reitsma PH, te Lintel Hekkert W, Koenhen E, van der Velden PA, Allaart CF, Deutz-Terlouw PP, Poort SR, Bertina RM.
    Thromb Haemost; 1990 Oct 22; 64(2):239-44. PubMed ID: 1702905
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  • 15. 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 22; 30(8):608-11. PubMed ID: 18799939
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  • 16. Protein C (PROC) gene mutations in two Indian families with purpura fulminans.
    Pai N, Shetty S, Ghosh K.
    Ann Hematol; 2010 Aug 22; 89(8):835-6. PubMed ID: 20077116
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  • 18. [A point mutation of protein C gene in a congenital protein C deficiency pedigree].
    Liu L, Guo WR, He LS, Mu H, Jiang Y, Huang FQ, Li JZ.
    Zhonghua Xue Ye Xue Za Zhi; 2003 Mar 22; 24(3):115-8. PubMed ID: 12697119
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