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 *

126 related articles for article (PubMed ID: 3341937)

  • 1. Homozygous protein C deficiency in a newborn. Clinicopathologic correlation.
    Tarras S; Gadia C; Meister L; Roldan E; Gregorios JB
    Arch Neurol; 1988 Feb; 45(2):214-6. PubMed ID: 3341937
    [TBL] [Abstract][Full Text] [Related]  

  • 2. 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
    [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. Activation-resistant homozygous protein C R229W mutation causing familial perinatal intracranial hemorrhage and delayed onset of thrombosis.
    Alsultan A; Gale AJ; Kurban K; Khalifah M; Albadr FB; Griffin JH
    Thromb Res; 2016 Jul; 143():17-21. PubMed ID: 27172833
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Severe inherited "homozygous" protein C deficiency in a newborn infant.
    Estellés A; Garcia-Plaza I; Dasí A; Aznar J; Duart M; Sanz G; Pérez-Requejo JL; España F; Jimenez C; Abeledo G
    Thromb Haemost; 1984 Aug; 52(1):53-6. PubMed ID: 6548587
    [TBL] [Abstract][Full Text] [Related]  

  • 6. 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; 11(4):395-401. PubMed ID: 2618972
    [TBL] [Abstract][Full Text] [Related]  

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

  • 8. 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]  

  • 9. Successful treatment of homozygous protein C deficiency by hepatic transplantation.
    Casella JF; Lewis JH; Bontempo FA; Zitelli BJ; Markel H; Starzl TE
    Lancet; 1988 Feb; 1(8583):435-8. PubMed ID: 2893866
    [TBL] [Abstract][Full Text] [Related]  

  • 10. 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]  

  • 11. Cerebral venous congestion as indication for thrombolytic treatment.
    Tsai FY; Kostanian V; Rivera M; Lee KW; Chen CC; Nguyen TH
    Cardiovasc Intervent Radiol; 2007; 30(4):675-87. PubMed ID: 17573553
    [TBL] [Abstract][Full Text] [Related]  

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

  • 13. 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; 38(2):253-6. PubMed ID: 26250584
    [TBL] [Abstract][Full Text] [Related]  

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

  • 15. [Sinus thrombosis caused by hereditary coagulation defects].
    Kristensen B
    Lakartidningen; 1991 May; 88(18):1691-4. PubMed ID: 2041417
    [No Abstract]   [Full Text] [Related]  

  • 16. Severe protein C deficiency in a newborn caused by a homozygous pathogenic variant in the PROC gene: a case report.
    Song U; Ryu YH; Hong K; Shim SY; Park S; Lee JS; Ju YS; Shin SH; Lee S
    BMC Pediatr; 2021 Oct; 21(1):453. PubMed ID: 34654403
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Late-onset homozygous protein C deficiency manifesting cerebral infarction as the first symptom at age 27.
    Deguchi K; Tsukada T; Iwasaki E; Wada H; Murashima S; Miyazaki M; Shirakawa S
    Intern Med; 1992 Jul; 31(7):922-5. PubMed ID: 1333307
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Tumefaction of the dural sinuses associated with a coagulopathy following treatment of hydrocephalus in a perinate: case report.
    Hanigan WC; Fraser K; Tarantino M; Wang H
    J Neurosurg; 2005 May; 102(4 Suppl):426-30. PubMed ID: 15926397
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Hereditary protein C deficiency.
    Broekmans AW
    Haemostasis; 1985; 15(4):233-40. PubMed ID: 3840112
    [TBL] [Abstract][Full Text] [Related]  

  • 20. [Activated protein C resistance and mutation of coagulation factor V].
    Samama MM
    Arch Mal Coeur Vaiss; 1996 Jun; 89(6):669-70. PubMed ID: 8760650
    [No Abstract]   [Full Text] [Related]  

    [Next]    [New Search]
    of 7.