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Journal Abstract Search

153 related items for PubMed ID: 31469059

  • 1. Expression and CpG island methylation pattern of MMP-2 and MMP-9 genes in patients with congenital factor XIII deficiency and intracranial hemorrhage.
    Noroozi-Aghideh A, Kashani Khatib Z, Naderi M, Dorgalaleh A, Yaghmaie M, Paryan M, Alizadeh S.
    Hematology; 2019 Dec; 24(1):601-605. PubMed ID: 31469059
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  • 6. The Role of Different Matrixin Gene Expressions on Cerebral Bleeding among Patients with Deficiency of Coagulation Factor XIII.
    Mao L, Huang Y, Jia W, Zhou Z, He X.
    Cell Mol Biol (Noisy-le-grand); 2022 Aug 31; 68(8):129-132. PubMed ID: 36800823
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  • 11. [An infant with umbilical cord and intracranial hemorrhage--severe factor XIII deficiency].
    von der Weid N, Furlan M, Siegenthaler I, Lämmle B.
    Ther Umsch; 1999 Sep 31; 56(9):544-6. PubMed ID: 10517131
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  • 12. Congenital factor XIII deficiency in Pakistan: characterization of seven families and identification of four novel mutations.
    Borhany M, Handrkova H, Cairo A, Schroeder V, Fatima N, Naz A, Amanat S, Shamsi T, Peyvandi F, Kohler HP.
    Haemophilia; 2014 Jul 31; 20(4):568-74. PubMed ID: 24329762
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  • 13. Efficacy and safety of prophylactic treatment with plasma-derived factor XIII concentrate (human) in patients with congenital factor XIII deficiency.
    Ashley C, Chang E, Davis J, Mangione A, Frame V, Nugent DJ.
    Haemophilia; 2015 Jan 31; 21(1):102-8. PubMed ID: 25377187
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  • 16. Comparison of F13A1 gene mutations in 73 patients treated with recombinant FXIII-A2.
    Ivaškevičius V, Biswas A, Garly ML, Oldenburg J.
    Haemophilia; 2017 May 31; 23(3):e194-e203. PubMed ID: 28520207
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  • 17. Congenital factor XIII deficiency in Switzerland: from the worldwide first case in 1960 to its molecular characterisation in 2005.
    Schroeder V, Durrer D, Meili E, Schubiger G, Kohler HP.
    Swiss Med Wkly; 2007 May 19; 137(19-20):272-8. PubMed ID: 17594539
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  • 19. Transient Platelet Dysfunction in Congenital Factor XIII Deficiency with Enhanced Thrombin Generation Potential.
    Oh I, Gu J, Kim HK, Choi JY.
    Clin Lab; 2022 Aug 01; 68(8):. PubMed ID: 35975501
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  • 20. Factor XIII deficiency: complete phenotypic characterization of two cases with novel causative mutations.
    Katona É, Muszbek L, Devreese K, Kovács KB, Bereczky Z, Jonkers M, Shemirani AH, Mondelaers V, Ermens AA.
    Haemophilia; 2014 Jan 01; 20(1):114-20. PubMed ID: 24118344
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