These tools will no longer be maintained as of December 31, 2024. Archived website can be found here. PubMed4Hh GitHub repository can be found here. Contact NLM Customer Service if you have questions.


BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

163 related articles for article (PubMed ID: 28485122)

  • 1. 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
    [No Abstract]   [Full Text] [Related]  

  • 2. Fulminant sepsis/meningitis due to Haemophilus influenzae in a protein C-deficient heterozygote treated with activated protein C therapy.
    Ishimura M; Saito M; Ohga S; Hoshina T; Baba H; Urata M; Kira R; Takada H; Kusuhara K; Kang D; Hara T
    Eur J Pediatr; 2009 Jun; 168(6):673-7. PubMed ID: 18751723
    [TBL] [Abstract][Full Text] [Related]  

  • 3. 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; 43(6):e763-e765. PubMed ID: 33165188
    [TBL] [Abstract][Full Text] [Related]  

  • 4. Paediatric presentation and outcome of congenital protein C deficiency in Japan.
    Ohga S; Kang D; Kinjo T; Ochiai M; Doi T; Ishimura M; Kayamori Y; Urata M; Yamamoto J; Suenobu SI; Kanegane H; Ikenoue T; Shirahata A; Hara T
    Haemophilia; 2013 May; 19(3):378-84. PubMed ID: 23379934
    [TBL] [Abstract][Full Text] [Related]  

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

  • 6. 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]  

  • 7. 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]  

  • 8. Protein C (PROC) gene mutations in two Indian families with purpura fulminans.
    Pai N; Shetty S; Ghosh K
    Ann Hematol; 2010 Aug; 89(8):835-6. PubMed ID: 20077116
    [No Abstract]   [Full Text] [Related]  

  • 9. Efficacy and safety of protein C concentrate to treat purpura fulminans and thromboembolic events in severe congenital protein C deficiency.
    Manco-Johnson MJ; Bomgaars L; Palascak J; Shapiro A; Geil J; Fritsch S; Pavlova BG; Gelmont D
    Thromb Haemost; 2016 Jul; 116(1):58-68. PubMed ID: 27052576
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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
    [TBL] [Abstract][Full Text] [Related]  

  • 11. 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; 36(7):e452-5. PubMed ID: 24136027
    [TBL] [Abstract][Full Text] [Related]  

  • 12. 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]  

  • 13. 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; 68(3):463-465. PubMed ID: 29540887
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Activated protein C concentrate treatment for skin necrosis under warfarin treatment in severe genetic protein C deficiency combined with prothrombin mutation and factor V Leiden.
    Rosenzweig N; Strauss T; Rubinstein M; Paret G; Kenet G
    Thromb Haemost; 2009 Feb; 101(2):405-7. PubMed ID: 19190829
    [No Abstract]   [Full Text] [Related]  

  • 15. Long-term survival of a child with homozygous protein C deficiency successfully treated with living donor liver transplantation.
    Lee MJ; Kim KM; Kim JS; Kim YJ; Lee YJ; Ghim TT
    Pediatr Transplant; 2009 Mar; 13(2):251-4. PubMed ID: 18482214
    [TBL] [Abstract][Full Text] [Related]  

  • 16. 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; 127(5):e1338-42. PubMed ID: 21482600
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Use of protein C concentrate in neonatal period.
    De Carolis MP
    Minerva Pediatr; 2010 Jun; 62(3 Suppl 1):29-30. PubMed ID: 21089715
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Severe clinical presentation of protein C deficiency in a type I/II compound heterozygote newborn.
    Fernandez-Burriel M
    Thromb Haemost; 2005 Jul; 94(1):216-8. PubMed ID: 16113807
    [No Abstract]   [Full Text] [Related]  

  • 19. Purpura fulminans: recognition, diagnosis and management.
    Chalmers E; Cooper P; Forman K; Grimley C; Khair K; Minford A; Morgan M; Mumford AD
    Arch Dis Child; 2011 Nov; 96(11):1066-71. PubMed ID: 21233082
    [TBL] [Abstract][Full Text] [Related]  

  • 20. 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]  

    [Next]    [New Search]
    of 9.