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Journal Abstract Search

249 related items for PubMed ID: 29270858

  • 21. 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; 41(1):24-31. PubMed ID: 1503096
    [Abstract] [Full Text] [Related]

  • 22. Treatment of homozygous protein C deficiency and neonatal purpura fulminans with a purified protein C concentrate.
    Dreyfus M, Magny JF, Bridey F, Schwarz HP, Planché C, Dehan M, Tchernia G.
    N Engl J Med; 1991 Nov 28; 325(22):1565-8. PubMed ID: 1944440
    [No Abstract] [Full Text] [Related]

  • 23. Neonatal purpura fulminans due to homozygous protein C or protein S deficiencies.
    Marlar RA, Neumann A.
    Semin Thromb Hemost; 1990 Oct 28; 16(4):299-309. PubMed ID: 2149204
    [Abstract] [Full Text] [Related]

  • 24. Replacement therapy with protein C concentrate in infants and adolescents with meningococcal sepsis and purpura fulminans.
    Ettingshausen CE, Veldmann A, Beeg T, Schneider W, Jäger G, Kreuz W.
    Semin Thromb Hemost; 1999 Oct 28; 25(6):537-41. PubMed ID: 10632475
    [Abstract] [Full Text] [Related]

  • 25. Diffuse Intracerebral Hemorrhage in an Infant With a Novel Homozygous Variant Leading to Severe Protein C Deficiency.
    Martin G, Thomas MA, Wei XC, Le D.
    J Pediatr Hematol Oncol; 2021 Aug 01; 43(6):e763-e765. PubMed ID: 33165188
    [Abstract] [Full Text] [Related]

  • 26. 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 01; 81(2):272-6. PubMed ID: 3340476
    [Abstract] [Full Text] [Related]

  • 27. Long-term management of homozygous protein C deficiency: replacement therapy with subcutaneous purified protein C concentrate.
    Sanz-Rodriguez C, Gil-Fernández JJ, Zapater P, Pinilla I, Granados E, Gómez-G de Soria V, Cano J, Sala N, Fernández-Rañada JM, Gómez-Gómez N.
    Thromb Haemost; 1999 Jun 01; 81(6):887-90. PubMed ID: 10404762
    [Abstract] [Full Text] [Related]

  • 28. 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 01; 24(8):890-2. PubMed ID: 24158118
    [Abstract] [Full Text] [Related]

  • 29. A Novel Protein C Mutation Causing Neonatal Purpura Fulminans.
    Devi R U, Bharathi S M, Kawankar N.
    Indian Pediatr; 2016 Nov 15; 53(11):1019-1021. PubMed ID: 27889735
    [Abstract] [Full Text] [Related]

  • 30. 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 15; 68(3):463-465. PubMed ID: 29540887
    [Abstract] [Full Text] [Related]

  • 31. Human protein C concentrates for replacement therapy in congenital and acquired protein C deficiency.
    Knoebl PN.
    Drugs Today (Barc); 2008 Jun 15; 44(6):429-41. PubMed ID: 18596997
    [Abstract] [Full Text] [Related]

  • 32. Protein C deficiency.
    Goldenberg NA, Manco-Johnson MJ.
    Haemophilia; 2008 Nov 15; 14(6):1214-21. PubMed ID: 19141162
    [Abstract] [Full Text] [Related]

  • 33. Homozygous protein C deficiency--management with protein C concentrate.
    Baliga V, Thwaites R, Tillyer ML, Minford A, Parapia L, Allgrove J.
    Eur J Pediatr; 1995 Jul 15; 154(7):534-8. PubMed ID: 7556318
    [Abstract] [Full Text] [Related]

  • 34. Modern concepts of the diagnosis and treatment of purpura fulminans.
    Edlich RF, Cross CL, Dahlstrom JJ, Long WB.
    J Environ Pathol Toxicol Oncol; 2008 Jul 15; 27(3):191-6. PubMed ID: 18652566
    [Abstract] [Full Text] [Related]

  • 35. [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]

  • 36. Severe acquired protein C deficiency in purpura fulminans associated with disseminated intravascular coagulation: treatment with protein C concentrate.
    Gerson WT, Dickerman JD, Bovill EG, Golden E.
    Pediatrics; 1993 Feb 02; 91(2):418-22. PubMed ID: 8424021
    [No Abstract] [Full Text] [Related]

  • 37. Purpura fulminans in congenital protein C deficiency successfully treated with fresh frozen plasma and thrombomodulin.
    Hayami T, Yamaguchi A, Kato T, Tanaka T, Nishizawa Y, Yanagi T, Taga T, Matsumoto S, Uchiumi T, Fujimoto N.
    J Dermatol; 2018 Jun 02; 45(6):e165-e166. PubMed ID: 29265490
    [No Abstract] [Full Text] [Related]

  • 38. Diagnosis and treatment of homozygous protein C deficiency. Report of the Working Party on Homozygous Protein C Deficiency of the Subcommittee on Protein C and Protein S, International Committee on Thrombosis and Haemostasis.
    Marlar RA, Montgomery RR, Broekmans AW.
    J Pediatr; 1989 Apr 02; 114(4 Pt 1):528-34. PubMed ID: 2647943
    [Abstract] [Full Text] [Related]

  • 39. Replacement therapy with a monoclonal antibody purified protein C concentrate in newborns with severe congenital protein C deficiency.
    Dreyfus M, Masterson M, David M, Rivard GE, Müller FM, Kreuz W, Beeg T, Minford A, Allgrove J, Cohen JD.
    Semin Thromb Hemost; 1995 Apr 02; 21(4):371-81. PubMed ID: 8747700
    [Abstract] [Full Text] [Related]

  • 40. 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
    [Abstract] [Full Text] [Related]

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