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Journal Abstract Search

195 related items for PubMed ID: 28111891

  • 1. 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
    [Abstract] [Full Text] [Related]

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

  • 3. Age-specific onset and distribution of the natural anticoagulant deficiency in pediatric thromboembolism.
    Ichiyama M, Ohga S, Ochiai M, Tanaka K, Matsunaga Y, Kusuda T, Inoue H, Ishimura M, Takimoto T, Koga Y, Hotta T, Kang D, Hara T.
    Pediatr Res; 2016 Jan; 79(1-1):81-6. PubMed ID: 26372516
    [Abstract] [Full Text] [Related]

  • 4. Clinical and laboratory characteristics of children with venous thromboembolism and protein C-deficiency: an observational Israeli-German cohort study.
    Limperger V, Klostermeier UC, Kenet G, Holzhauer S, Alhenc Gelas M, Finckh U, Junker R, Heller C, Zieger B, Kurnik K, Knöfler R, Mesters R, Halimeh S, Nowak-Göttl U.
    Br J Haematol; 2014 Nov; 167(3):385-93. PubMed ID: 25039884
    [Abstract] [Full Text] [Related]

  • 5. 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
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  • 7. 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
    [Abstract] [Full Text] [Related]

  • 8. Different impact of two mutations of a novel compound heterozygous protein C deficiency with late onset thrombosis.
    Yang LH, Wang MS, Zheng FX, Li J, Chen Y, Jin YH, Xie HX, Yang XL, Chen BC.
    Genet Mol Res; 2014 Apr 16; 13(2):2969-77. PubMed ID: 24782131
    [Abstract] [Full Text] [Related]

  • 9. The clinical and genetic landscape of early-onset thrombophilia in Japan.
    Egami N, Ishimura M, Ochiai M, Ichiyama M, Inoue H, Suenobu S, Nishikubo T, Nogami K, Ishiguro A, Hotta T, Uchiumi T, Kang D, Ohga S.
    Pediatr Blood Cancer; 2024 Mar 16; 71(3):e30824. PubMed ID: 38155150
    [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 16; 61(4):763-4. PubMed ID: 24115609
    [Abstract] [Full Text] [Related]

  • 11. Two novel compound heterozygous mutations associated with types I and II protein C deficiency with unusual phenotypes.
    Deng MY, Liu ZX, Huang HF, Chen YH, Luo YJ, Sun NN, Cheng Z, Yan WZ, Zhang GS.
    Thromb Res; 2016 Sep 16; 145():93-9. PubMed ID: 27517348
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  • 13. 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 16; 210():70-77. PubMed ID: 35026611
    [Abstract] [Full Text] [Related]

  • 14. A Series of 14 Polish Patients with Thrombotic Events and PC Deficiency-Novel c.401-1G>A PROC Gene Splice Site Mutation in a Patient with Aneurysms.
    Weronska A, Potaczek DP, Oto J, Medina P, Undas A, Wypasek E.
    Genes (Basel); 2022 Apr 22; 13(5):. PubMed ID: 35627118
    [Abstract] [Full Text] [Related]

  • 15. A novel compound heterozygous mutations in protein C gene causing neonatal purpura fulminans.
    Zhang H, Bi X, Su Z, Tu X, Wang L, Shen B.
    Blood Coagul Fibrinolysis; 2018 Mar 22; 29(2):216-219. PubMed ID: 29356699
    [Abstract] [Full Text] [Related]

  • 16. Protein C deficiency.
    Goldenberg NA, Manco-Johnson MJ.
    Haemophilia; 2008 Nov 22; 14(6):1214-21. PubMed ID: 19141162
    [Abstract] [Full Text] [Related]

  • 17. 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]

  • 18. Genotype-Phenotype Relationships in a Large French Cohort of Subjects with Inherited Protein C Deficiency.
    Alhenc-Gelas M, Plu-Bureau G, Mauge L, Gandrille S, Présot I, GFHT Study Group on Genetic Thrombophilia.
    Thromb Haemost; 2020 Sep 01; 120(9):1270-1281. PubMed ID: 32717757
    [Abstract] [Full Text] [Related]

  • 19. The significance of F139V mutation on thrombotic events in compound heterozygous and homozygous protein C deficiency.
    Yang LH, Zheng FX, Chen Y, Jin YH, Zhang Z, Xie HX, Yang XL, Wang MS, Chen BC.
    Blood Coagul Fibrinolysis; 2014 Dec 01; 25(8):824-30. PubMed ID: 24911457
    [Abstract] [Full Text] [Related]

  • 20. Clinical Impact of Heritable Thrombophilia on Neonatal-Onset Thromboembolism: A Nationwide Study in Japan.
    Egami N, Ochiai M, Ichiyama M, Inoue H, Sonoda M, Ishimura M, Suenobu S, Nishikubo T, Ishiguro A, Hotta T, Uchiumi T, Kang D, Ohga S.
    J Pediatr; 2021 Nov 01; 238():259-267.e2. PubMed ID: 34245770
    [Abstract] [Full Text] [Related]

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