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 *

147 related articles for article (PubMed ID: 34654403)

  • 21. 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]  

  • 22. 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; 45(2):315-318. PubMed ID: 29270858
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Clinical and genetic features of Chinese pediatric patients with severe congenital protein C deficiency who first presented with purpura fulminans: A case series study and literature review.
    Tang X; Zhang Z; Yang H; Xiao J; Wen X; Dou Y; Yu J; Hu Y
    Thromb Res; 2022 Feb; 210():70-77. PubMed ID: 35026611
    [TBL] [Abstract][Full Text] [Related]  

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

  • 25. Diagnosis and treatment of a newborn with homozygous protein C deficiency.
    Salonvaara M; Kuismanen K; Mononen T; Riikonen P
    Acta Paediatr; 2004 Jan; 93(1):137-9. PubMed ID: 14989454
    [TBL] [Abstract][Full Text] [Related]  

  • 26. The clinical presentation and genotype of protein C deficiency with double mutations of the protein C gene.
    Inoue H; Terachi SI; Uchiumi T; Sato T; Urata M; Ishimura M; Koga Y; Hotta T; Hara T; Kang D; Ohga S
    Pediatr Blood Cancer; 2017 Jul; 64(7):. PubMed ID: 28111891
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Homozygous type I Protein C deficiency in neonatal purpura fulminans with a novel frame-shift deletion of 10 base pairs in exon 8 of PROC gene.
    Park HJ; Song KS; Nah BM; Choi JR; Kim MJ
    J Thromb Haemost; 2005 Mar; 3(3):593-5. PubMed ID: 15748260
    [No Abstract]   [Full Text] [Related]  

  • 28. 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]  

  • 29. Protein C deficiency; PROC gene variants in a Danish population.
    Winther-Larsen A; Kjaergaard AD; Larsen OH; Hvas AM; Nissen PH
    Thromb Res; 2020 Jan; 185():153-159. PubMed ID: 31821907
    [TBL] [Abstract][Full Text] [Related]  

  • 30. 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]  

  • 31. Protein C deficiency as the major cause of thrombophilias in childhood.
    Ohga S; Ishiguro A; Takahashi Y; Shima M; Taki M; Kaneko M; Fukushima K; Kang D; Hara T;
    Pediatr Int; 2013 Jun; 55(3):267-71. PubMed ID: 23521084
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Neonatal arterial iliac thrombosis in type-I protein C deficiency: a case report.
    Tridapalli E; Stella M; Capretti MG; Faldella G
    Ital J Pediatr; 2010 Mar; 36():23. PubMed ID: 20211026
    [TBL] [Abstract][Full Text] [Related]  

  • 33. 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]  

  • 34. [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]  

  • 35. 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; 114(4 Pt 1):528-34. PubMed ID: 2647943
    [TBL] [Abstract][Full Text] [Related]  

  • 36. Acroangiodermatitis of Mali in protein C deficiency due to a novel PROC gene mutation.
    Wei-Min Tan A; Lee JS; Pramono ZA; Chong WS
    Am J Dermatopathol; 2012 Apr; 34(2):e19-21. PubMed ID: 22441373
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Neonatal asphyxia and renal failure as the presentation of non-inherited protein C deficiency.
    Matsunaga Y; Ohga S; Kinjo T; Ochiai M; Ito N; Doi T; Kang D; Hara T
    J Perinatol; 2013 Mar; 33(3):239-41. PubMed ID: 23443294
    [TBL] [Abstract][Full Text] [Related]  

  • 38. 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; 14(3):303-6. PubMed ID: 12695756
    [TBL] [Abstract][Full Text] [Related]  

  • 39. 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]  

  • 40. 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]  

    [Previous]   [Next]    [New Search]
    of 8.