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Journal Abstract Search

147 related items for PubMed ID: 32980846

  • 21. 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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  • 22. Definite diagnosis in Japanese patients with protein C deficiency by identification of causative PROC mutations.
    Takagi A, Tanaka R, Nakashima D, Fujimori Y, Yamada T, Okumura K, Murate T, Yamada M, Horikoshi Y, Yamamoto K, Katsumi A, Matsushita T, Naoe T, Kojima T.
    Int J Hematol; 2009 May; 89(4):555-557. PubMed ID: 19373522
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  • 23. Isolated Protein C Deficiency in a Newborn.
    Bencharef H, Hidki F, Lahmoudi A, Pongo C, Chemsi M, Lehlimi M, Habzi A, Benomar S, Oukkache B.
    Clin Lab; 2023 May 01; 69(5):. PubMed ID: 37145086
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  • 24. Clinical and laboratory characteristics of children with venous thromboembolism and protein C-deficiency: an observational Israeli-German cohort study.
    Limperger V, Klostermeier UC, Kenet G, Holzhauer S, Alhenc Gelas M, Finckh U, Junker R, Heller C, Zieger B, Kurnik K, Knöfler R, Mesters R, Halimeh S, Nowak-Göttl U.
    Br J Haematol; 2014 Nov 01; 167(3):385-93. PubMed ID: 25039884
    [Abstract] [Full Text] [Related]

  • 25. Severe Congenital Protein C Deficiency: Practical Aspects of Management.
    Shah R, Ferreira P, Karmali S, Le D.
    Pediatr Blood Cancer; 2016 Aug 01; 63(8):1488-90. PubMed ID: 27138381
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  • 27. 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 01; 26(8):597-600. PubMed ID: 19954370
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  • 28. Neonatal Purpura Fulminans, a rare genetic disorder due to protein C deficiency: A case report.
    Irfan Kazi SG, Siddiqui E, Habib I, Tabassum S, Afzal B, Khan IQ.
    J Pak Med Assoc; 2018 Mar 01; 68(3):463-465. PubMed ID: 29540887
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  • 29. Protein C deficiency.
    Goldenberg NA, Manco-Johnson MJ.
    Haemophilia; 2008 Nov 01; 14(6):1214-21. PubMed ID: 19141162
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  • 31. 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 01; 30(2):166-71. PubMed ID: 18376272
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  • 37. Neonatal purpura fulminans due to homozygous protein C deficiency.
    Ezer U, Misirlioglu ED, Colba V, Ogoz E, Kurt C.
    Pediatr Hematol Oncol; 2001 Feb 01; 18(7):453-8. PubMed ID: 11594708
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  • 38. A case of purpura fulminans is caused by homozygous delta8857 mutation (protein C-nagoya) and successfully treated with activated protein C concentrate.
    Nakayama T, Matsushita T, Hidano H, Suzuki C, Hamaguchi M, Kojima T, Saito H.
    Br J Haematol; 2000 Sep 01; 110(3):727-30. PubMed ID: 10997987
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  • 39. 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 01; 5(4):651-3. PubMed ID: 7841324
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