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Journal Abstract Search

222 related items for PubMed ID: 29540887

  • 21. 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; 64(11):. PubMed ID: 28485122
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  • 22. 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. Long-term subcutaneous protein C replacement in neonatal severe protein C deficiency.
    de Kort EH, Vrancken SL, van Heijst AF, Binkhorst M, Cuppen MP, Brons PP.
    Pediatrics; 2011 May 01; 127(5):e1338-42. PubMed ID: 21482600
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  • 30. Streptococcus pyogenes-purpura fulminans as an invasive form of group A streptococcal infection.
    Okuzono S, Ishimura M, Kanno S, Sonoda M, Kaku N, Motomura Y, Nishio H, Oba U, Hanada M, Fukushi JI, Urata M, Kang D, Takada H, Ohga S.
    Ann Clin Microbiol Antimicrob; 2018 Jul 09; 17(1):31. PubMed ID: 29986727
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  • 31. Fetal hydrocephalus and neonatal stroke as the first presentation of protein C deficiency.
    Ichiyama M, Ohga S, Ochiai M, Fukushima K, Ishimura M, Torio M, Urata M, Hotta T, Kang D, Hara T.
    Brain Dev; 2016 Feb 09; 38(2):253-6. PubMed ID: 26250584
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  • 32. Postinfectious purpura fulminans: A case report.
    Pombar RF, Tellería RL, Bianco B, Centeno MDV, Cervini AB.
    Arch Argent Pediatr; 2024 Aug 01; 122(4):e202310137. PubMed ID: 38231644
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  • 35. Neonatal purpura fulminans secondary to group B streptococcal infection.
    Zenciroglu A, Karagol BS, Ipek MS, Okumus N, Yarali N, Aydin M.
    Pediatr Hematol Oncol; 2010 Nov 01; 27(8):620-5. PubMed ID: 20795772
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  • 37. [Purpura fulminans, venous thrombosis and constitutional thrombophilia in an infant].
    Fadil F, Elfatoiki F, Mortaji K, Lasry F, Itri M, Khadir K, Benchikhi H, Sarbati N, Nadifi S.
    Arch Pediatr; 2013 May 01; 20(5):499-502. PubMed ID: 23566584
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  • 38. Prenatal diagnosis in a family with purfura fulminans.
    Shanbhag S, Pai N, Ghosh K, Shetty S.
    Blood Coagul Fibrinolysis; 2015 Apr 01; 26(3):350. PubMed ID: 25803516
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  • 39. 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 01; 4(5):1152-3. PubMed ID: 16689776
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  • 40. Clinical and genetic features of Chinese pediatric patients with severe congenital protein C deficiency who first presented with purpura fulminans: A case series study and literature review.
    Tang X, Zhang Z, Yang H, Xiao J, Wen X, Dou Y, Yu J, Hu Y.
    Thromb Res; 2022 Feb 01; 210():70-77. PubMed ID: 35026611
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