BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

135 related articles for article (PubMed ID: 12439046)

  • 1. Chronic disseminated intravascular coagulation and childhood-onset skin necrosis resulting from homozygosity for a protein C Gla domain mutation, Arg15Trp.
    Steinkamp M; Geva A; Joffe S; Lapp CN; Neufeld EJ
    J Pediatr Hematol Oncol; 2002 Nov; 24(8):685-8. PubMed ID: 12439046
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 30(8):608-11. PubMed ID: 18799939
    [TBL] [Abstract][Full Text] [Related]  

  • 4. 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; 45(6):e165-e166. PubMed ID: 29265490
    [No Abstract]   [Full Text] [Related]  

  • 5. Homozygous type I protein C deficiency in two unrelated families exhibiting thrombophilia related to Ala136-->Pro or Arg286-->His mutations.
    Long GL; Tomczak JA; Rainville IR; Dreyfus M; Schramm W; Schwarz HP
    Thromb Haemost; 1994 Oct; 72(4):526-33. PubMed ID: 7878626
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Successful liver transplantation for homozygous protein C deficiency with a type II mutation using a heterozygous living related donor.
    Boucher AA; Luchtman-Jones L; Nathan JD; Palumbo JS
    Am J Hematol; 2018 Mar; 93(3):462-466. PubMed ID: 29218739
    [No Abstract]   [Full Text] [Related]  

  • 7. [Meningococcal meningitis in the adult complicated by cutaneous necrosis: description of a clinical case].
    Porro F; Cattaneo M
    Ann Ital Med Int; 2000; 15(4):291-5. PubMed ID: 11202631
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Perioperative management of a patient with purpura fulminans syndrome due to protein C deficiency.
    Kumagai K; Nishiwaki K; Sato K; Kitamura H; Yano K; Komatsu T; Shimada Y
    Can J Anaesth; 2001 Dec; 48(11):1070-4. PubMed ID: 11744581
    [TBL] [Abstract][Full Text] [Related]  

  • 9. 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; 21(4):371-81. PubMed ID: 8747700
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Protein C Sapporo (protein C Glu 25 --> Lys): a heterozygous missense mutation in the Gla domain provides new insight into the interaction between protein C and endothelial protein C receptor.
    Nakabayashi T; Mizukami K; Naitoh S; Takeda M; Shikamoto Y; Nakagawa T; Kaneko H; Tarumi T; Mizoguchi I; Mizuno H; Ieko M; Koike T
    Thromb Haemost; 2005 Nov; 94(5):942-50. PubMed ID: 16363234
    [TBL] [Abstract][Full Text] [Related]  

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

  • 12. 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; 110(3):727-30. PubMed ID: 10997987
    [TBL] [Abstract][Full Text] [Related]  

  • 13. [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; 22(10):1027-31. PubMed ID: 26228809
    [TBL] [Abstract][Full Text] [Related]  

  • 14. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 15. [Protein C in dermatology].
    Lazareth I
    Ann Dermatol Venereol; 1989; 116(8):591-3. PubMed ID: 2688519
    [No Abstract]   [Full Text] [Related]  

  • 16. 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; 4(5):1152-3. PubMed ID: 16689776
    [No Abstract]   [Full Text] [Related]  

  • 17. 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; 5(4):651-3. PubMed ID: 7841324
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Familial thrombotic risk based on the genetic background of Protein C Deficiency in a Portuguese Study.
    Fidalgo T; Martinho P; Salvado R; Manco L; Oliveira AC; Pinto CS; Gonçalves E; Marques D; Sevivas T; Martins N; Ribeiro ML
    Eur J Haematol; 2015 Oct; 95(4):294-307. PubMed ID: 25533856
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Purpura fulminans in an adult.
    Tishler M; Abramov AL; Seligsohn U; Kahn Y
    Isr J Med Sci; 1986 Nov; 22(11):820-2. PubMed ID: 3793438
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Homozygous protein C deficiency with delayed onset of symptoms at 7 to 10 months.
    Tuddenham EG; Takase T; Thomas AE; Awidi AS; Madanat FF; Abu Hajir MM; Kernoff PB; Hoffbrand AV
    Thromb Res; 1989 Mar; 53(5):475-84. PubMed ID: 2660320
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 7.