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Journal Abstract Search

132 related items for PubMed ID: 9766136

  • 1. [Homozygous protein C deficiency can be detected by prenatal diagnosis].
    Jerkeman A, Henriksson P, Jonsson NO, Berntorp E.
    Lakartidningen; 1998 Sep 02; 95(36):3772, 3775-7. PubMed ID: 9766136
    [Abstract] [Full Text] [Related]

  • 2. Neonatal purpura fulminans due to homozygous protein C deficiency.
    Ezer U, Misirlioglu ED, Colba V, Ogoz E, Kurt C.
    Pediatr Hematol Oncol; 2001 Sep 02; 18(7):453-8. PubMed ID: 11594708
    [Abstract] [Full Text] [Related]

  • 3. Neonatal purpura fulminans due to homozygous protein C deficiency.
    Kafali G, Tanzer F, Yildiz E.
    J Trop Pediatr; 1998 Apr 02; 44(2):122-3. PubMed ID: 9604607
    [No Abstract] [Full Text] [Related]

  • 4. Diagnosis and treatment of a newborn with homozygous protein C deficiency.
    Salonvaara M, Kuismanen K, Mononen T, Riikonen P.
    Acta Paediatr; 2004 Jan 02; 93(1):137-9. PubMed ID: 14989454
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  • 5. 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 02; 110(3):727-30. PubMed ID: 10997987
    [Abstract] [Full Text] [Related]

  • 6. 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 02; 72(1):65-9. PubMed ID: 7974377
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  • 8. Homozygous protein C deficiency presenting as neonatal purpura fulminans: management with fresh frozen plasma, low molecular weight heparin and protein C concentrate.
    Kizilocak H, Ozdemir N, Dikme G, Koc B, Celkan T.
    J Thromb Thrombolysis; 2018 Feb 02; 45(2):315-318. PubMed ID: 29270858
    [Abstract] [Full Text] [Related]

  • 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 02; 24(8):890-2. PubMed ID: 24158118
    [Abstract] [Full Text] [Related]

  • 10. 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 02; 75(3):525-6. PubMed ID: 8701425
    [No Abstract] [Full Text] [Related]

  • 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 02; 30(8):608-11. PubMed ID: 18799939
    [Abstract] [Full Text] [Related]

  • 12. Protein C survival during replacement therapy in homozygous protein C deficiency.
    Marlar RA, Sills RH, Groncy PK, Montgomery RR, Madden RM.
    Am J Hematol; 1992 Sep 02; 41(1):24-31. PubMed ID: 1503096
    [Abstract] [Full Text] [Related]

  • 13. Homozygous protein C deficiency: observations on the nature of the molecular abnormality and the effectiveness of warfarin therapy.
    Peters C, Casella JF, Marlar RA, Montgomery RR, Zinkham WH.
    Pediatrics; 1988 Feb 02; 81(2):272-6. PubMed ID: 3340476
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  • 14. Homozygous protein C deficiency with purpura fulminans: report of a new case and a description of a novel mutation.
    Abu-Amero KK, Al-Hamed MH, Al-Batniji FS.
    Blood Coagul Fibrinolysis; 2003 Apr 02; 14(3):303-6. PubMed ID: 12695756
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  • 16. Homozygous protein C deficiency: early treatment with warfarin.
    Hartman KR, Manco-Johnson M, Rawlings JS, Bower DJ, Marlar RA.
    Am J Pediatr Hematol Oncol; 1989 Apr 02; 11(4):395-401. PubMed ID: 2618972
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  • 17. [Neonatal purpura fulminans without sepsis due to a severe congenital protein C deficiency].
    Hmami F, Cherrabi H, Oulmaati A, Bouabdallah Y, Bouharrou A.
    Arch Pediatr; 2015 Oct 02; 22(10):1027-31. PubMed ID: 26228809
    [Abstract] [Full Text] [Related]

  • 18. Bilateral leukocoria in a patient with homozygous protein C deficiency.
    Khan NM, Al-Dohayan ND, Al-Batiniji FS.
    Saudi Med J; 2007 Jul 02; 28(7):1129-32. PubMed ID: 17603727
    [Abstract] [Full Text] [Related]

  • 19. 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 02; 36(7):e452-5. PubMed ID: 24136027
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