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Journal Abstract Search

134 related items for PubMed ID: 19373522

  • 1. Definite diagnosis in Japanese patients with protein C deficiency by identification of causative PROC mutations.
    Takagi A, Tanaka R, Nakashima D, Fujimori Y, Yamada T, Okumura K, Murate T, Yamada M, Horikoshi Y, Yamamoto K, Katsumi A, Matsushita T, Naoe T, Kojima T.
    Int J Hematol; 2009 May; 89(4):555-557. PubMed ID: 19373522
    [No Abstract] [Full Text] [Related]

  • 2. Qualitative protein C deficiency due to PROC c.577_579delAAG mutation not detected by chromogenic assays: A case of intractable cerebral sinovenous thrombosis.
    Wang V, Vo KH, Mahajerin A.
    Pediatr Blood Cancer; 2019 Jan; 66(1):e27443. PubMed ID: 30255615
    [No Abstract] [Full Text] [Related]

  • 3. Severe Protein C Deficiency due to Novel Biallelic Variants in PROC and Their Phenotype Correlation.
    Barg AA, Dardik R, Levin C, Koren A, Levy-Mendelovich S, Pode-Shakked B, Kenet G.
    Acta Haematol; 2021 Jan; 144(3):327-331. PubMed ID: 32980846
    [Abstract] [Full Text] [Related]

  • 4. A novel frameshift mutation Gly239Serfs*8 in the PROC gene results in protein C deficiency in a Korean patient.
    Park SH, Jang S, Yang HK, Shim H, Park CJ, Chi HS, Oh YM.
    Ann Hematol; 2012 Nov; 91(11):1829-30. PubMed ID: 22588326
    [No Abstract] [Full Text] [Related]

  • 5. Novel human pathological mutations. Gene symbol: PROC. Disease: Protein C deficiency.
    Pathare A, Al Zadjali S, Shah W.
    Hum Genet; 2009 Aug; 126(2):336-7. PubMed ID: 19694010
    [No Abstract] [Full Text] [Related]

  • 6. Type I protein C deficiency in French Canadians: evidence of a founder effect and association of specific protein C gene mutations with plasma protein C levels.
    Couture P, Demers C, Morissette J, Delage R, Jomphe M, Couture L, Simard J.
    Thromb Haemost; 1998 Oct; 80(4):551-6. PubMed ID: 9798967
    [Abstract] [Full Text] [Related]

  • 7. 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; 25(8):824-30. PubMed ID: 24911457
    [Abstract] [Full Text] [Related]

  • 8. Analysis of PROC mutations and clinical features in 22 unrelated families with inherited protein C deficiency.
    Xu F, Zhang K, Xu Q, Ye L, Zeng M, Jin Y, Wang M, Yang L.
    Ann Hematol; 2024 Feb; 103(2):645-652. PubMed ID: 37950050
    [Abstract] [Full Text] [Related]

  • 9. 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; 145():93-9. PubMed ID: 27517348
    [Abstract] [Full Text] [Related]

  • 10. 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]

  • 11. 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]

  • 12. Three novel PROC gene lesions causing protein C deficiency.
    Hallam PJ, Mannucci P, Tripodi A, Bevan D, Laursen B, Tengborn L, Wacey A, Cooper DN.
    Clin Genet; 1998 Sep; 54(3):231-3. PubMed ID: 9788727
    [Abstract] [Full Text] [Related]

  • 13. 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]

  • 14. A missense mutation G109R in the PROC gene associated with type I protein C deficiency in a young Polish man with acute myocardial infarction.
    Wypasek E, Pankiw-Bembenek O, Potaczek DP, Alhenc-Gelas M, Trebacz J, Undas A.
    Int J Cardiol; 2013 Sep 01; 167(5):e146-8. PubMed ID: 23643436
    [No Abstract] [Full Text] [Related]

  • 15. [Analysis of phenotypes and genetic mutations in two pedigrees affected with hereditary protein C deficiency].
    Yang L, Jin Y, Yang T, Chen X, Zhu L, Wang M.
    Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2017 Feb 10; 34(1):10-14. PubMed ID: 28186585
    [Abstract] [Full Text] [Related]

  • 16. Compound heterozygous protein C deficiency with pulmonary embolism caused by a novel PROC gene mutation: Case report and literature review.
    Zhang Z, Yang Z, Chen M, Li Y.
    Medicine (Baltimore); 2022 Oct 21; 101(42):e31221. PubMed ID: 36281079
    [Abstract] [Full Text] [Related]

  • 17. Protein C (PROC) gene mutations in two Indian families with purpura fulminans.
    Pai N, Shetty S, Ghosh K.
    Ann Hematol; 2010 Aug 21; 89(8):835-6. PubMed ID: 20077116
    [No Abstract] [Full Text] [Related]

  • 18. Identification of mutations in 15 Hungarian families with hereditary protein C deficiency.
    Dávid M, Losonczy H, Sas G, Nagy A, Kutscher G, Meyer M.
    Br J Haematol; 2000 Oct 21; 111(1):129-35. PubMed ID: 11091192
    [Abstract] [Full Text] [Related]

  • 19. Colonic Perforation in a Term Newborn with Hereditary Protein C Deficiency.
    Mizumoto H, Kimura M, Hata D.
    Indian Pediatr; 2019 Dec 15; 56(12):1057-1059. PubMed ID: 31884442
    [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 15; 93(3):462-466. PubMed ID: 29218739
    [No Abstract] [Full Text] [Related]

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