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Journal Abstract Search

312 related items for PubMed ID: 23379934

  • 21. Protein C and protein S deficiency - practical diagnostic issues.
    Wypasek E, Undas A.
    Adv Clin Exp Med; 2013; 22(4):459-67. PubMed ID: 23986205
    [Abstract] [Full Text] [Related]

  • 22. Successful protein C concentrate administration during initiation of oral anticoagulation in adult patients with severe congenital protein C deficiency: report of two cases.
    Imberti D, Pierfranceschi MG.
    Pathophysiol Haemost Thromb; 2008; 36(2):53-7. PubMed ID: 19127082
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  • 23. Fulminant sepsis/meningitis due to Haemophilus influenzae in a protein C-deficient heterozygote treated with activated protein C therapy.
    Ishimura M, Saito M, Ohga S, Hoshina T, Baba H, Urata M, Kira R, Takada H, Kusuhara K, Kang D, Hara T.
    Eur J Pediatr; 2009 Jun; 168(6):673-7. PubMed ID: 18751723
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  • 24. A novel mutation in protein C gene (PROC) causing severe phenotype in neonatal period.
    Unal S, Gumruk F, Yigit S, Tuncer M, Tavil B, Cil O, Takci S, Urata M, Hotta T, Kang D, Cetin M.
    Pediatr Blood Cancer; 2014 Apr; 61(4):763-4. PubMed ID: 24115609
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  • 25. Purpura fulminans: recognition, diagnosis and management.
    Chalmers E, Cooper P, Forman K, Grimley C, Khair K, Minford A, Morgan M, Mumford AD.
    Arch Dis Child; 2011 Nov; 96(11):1066-71. PubMed ID: 21233082
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  • 28. 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; 36(7):e452-5. PubMed ID: 24136027
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  • 29. Management of neonatal purpura fulminans with severe protein C deficiency.
    Sen K, Roy A.
    Indian Pediatr; 2006 Jun; 43(6):542-5. PubMed ID: 16820665
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  • 31. [Hereditary deficiency of antithrombin III, protein C, protein S and factor XII in 121 patients with venous or arterial thrombosis].
    Miljić P, Rolović Z, Elezović I, Antunović P, Stanojević M, Colović M.
    Srp Arh Celok Lek; 1999 Jun; 127(1-2):21-7. PubMed ID: 10377836
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  • 32. Activated protein C concentrate treatment for skin necrosis under warfarin treatment in severe genetic protein C deficiency combined with prothrombin mutation and factor V Leiden.
    Rosenzweig N, Strauss T, Rubinstein M, Paret G, Kenet G.
    Thromb Haemost; 2009 Feb; 101(2):405-7. PubMed ID: 19190829
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  • 34. The clinical and genetic landscape of early-onset thrombophilia in Japan.
    Egami N, Ishimura M, Ochiai M, Ichiyama M, Inoue H, Suenobu S, Nishikubo T, Nogami K, Ishiguro A, Hotta T, Uchiumi T, Kang D, Ohga S.
    Pediatr Blood Cancer; 2024 Mar; 71(3):e30824. PubMed ID: 38155150
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  • 36. Severe congenital protein C deficiency: description of a new mutation and prophylactic protein C therapy and in vivo pharmacokinetics.
    Tcheng WY, Dovat S, Gurel Z, Donkin J, Wong WY.
    J Pediatr Hematol Oncol; 2008 Feb; 30(2):166-71. PubMed ID: 18376272
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  • 37. [A pedigree analysis of pulmonary embolism caused by compound heterozygous mutations of protein C].
    Ye X, Liu X, Feng Y, Ding Q, Zhou X, Wang X.
    Nan Fang Yi Ke Da Xue Xue Bao; 2012 Jan; 32(1):109-12. PubMed ID: 22366017
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  • 38. 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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  • 40. Protein C and protein S assessment in hospital laboratories: which strategy and what role for DNA sequencing?
    Labrouche S, Reboul MP, Guérin V, Vergnes C, Freyburger G.
    Blood Coagul Fibrinolysis; 2003 Sep; 14(6):531-8. PubMed ID: 12960605
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