BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

260 related articles for article (PubMed ID: 10666208)

  • 21. Liver histology of an afibrinogenemic patient with the Bbeta-L353R mutation showing no evidence of hepatic endoplasmic reticulum storage disease (ERSD); comparative study in COS-1 cells of the intracellular processing of the Bbeta-L353R fibrinogen vs. the ERSD-associated gamma-G284R mutant.
    Duga S; Braidotti P; Asselta R; Maggioni M; Santagostino E; Pellegrini C; Coggi G; Malcovati M; Tenchini ML
    J Thromb Haemost; 2005 Apr; 3(4):724-32. PubMed ID: 15842357
    [TBL] [Abstract][Full Text] [Related]  

  • 22. Mutations in the fibrinogen aalpha gene account for the majority of cases of congenital afibrinogenemia.
    Neerman-Arbez M; de Moerloose P; Bridel C; Honsberger A; Schönbörner A; Rossier C; Peerlinck K; Claeyssens S; Di Michele D; d'Oiron R; Dreyfus M; Laubriat-Bianchin M; Dieval J; Antonarakis SE; Morris MA
    Blood; 2000 Jul; 96(1):149-52. PubMed ID: 10891444
    [TBL] [Abstract][Full Text] [Related]  

  • 23. Congenital afibrinogenaemia caused by uniparental isodisomy of chromosome 4 containing a novel 15-kb deletion involving fibrinogen Aalpha-chain gene.
    Spena S; Duga S; Asselta R; Peyvandi F; Mahasandana C; Malcovati M; Tenchini ML
    Eur J Hum Genet; 2004 Nov; 12(11):891-8. PubMed ID: 15489905
    [TBL] [Abstract][Full Text] [Related]  

  • 24. Fibrinogen gene mutations accounting for congenital afibrinogenemia.
    Neerman-Arbez M
    Ann N Y Acad Sci; 2001; 936():496-508. PubMed ID: 11460507
    [TBL] [Abstract][Full Text] [Related]  

  • 25. A novel frameshift mutation in FGA (c.1846 del A) leading to congenital afibrinogenemia in a consanguineous Syrian family.
    Levrat E; Aboukhamis I; de Moerloose P; Farho J; Chamaa S; Reber G; Fort A; Neerman-Arbez M
    Blood Coagul Fibrinolysis; 2011 Mar; 22(2):148-50. PubMed ID: 21245743
    [TBL] [Abstract][Full Text] [Related]  

  • 26. Congenital hypofibrinogenemia associated with novel homozygous fibrinogen Aα and heterozygous Bβ chain mutations.
    Castaman G; Rimoldi V; Giacomelli SH; Duga S
    Thromb Res; 2015 Jul; 136(1):144-7. PubMed ID: 25981141
    [TBL] [Abstract][Full Text] [Related]  

  • 27. Hepatic fibrinogen storage disease: identification of two novel mutations (p.Asp316Asn, fibrinogen Pisa and p.Gly366Ser, fibrinogen Beograd) impacting on the fibrinogen γ-module.
    Asselta R; Robusto M; Braidotti P; Peyvandi F; Nastasio S; D'Antiga L; Perisic VN; Maggiore G; Caccia S; Duga S
    J Thromb Haemost; 2015 Aug; 13(8):1459-67. PubMed ID: 26039544
    [TBL] [Abstract][Full Text] [Related]  

  • 28. Prenatal diagnosis for congenital afibrinogenemia caused by a novel nonsense mutation in the FGB gene in a Palestinian family.
    Neerman-Arbez M; Vu D; Abu-Libdeh B; Bouchardy I; Morris MA
    Blood; 2003 May; 101(9):3492-4. PubMed ID: 12511408
    [TBL] [Abstract][Full Text] [Related]  

  • 29. The molecular basis of quantitative fibrinogen disorders.
    Asselta R; Duga S; Tenchini ML
    J Thromb Haemost; 2006 Oct; 4(10):2115-29. PubMed ID: 16999847
    [TBL] [Abstract][Full Text] [Related]  

  • 30. Genetic and clinical characterization of congenital fibrinogen disorders in Polish patients: Identification of three novel fibrinogen gamma chain mutations.
    Wypasek E; Klukowska A; Zdziarska J; Zawilska K; Treliński J; Iwaniec T; Mital A; Pietrys D; Sydor W; Neerman-Arbez M; Undas A
    Thromb Res; 2019 Oct; 182():133-140. PubMed ID: 31479941
    [TBL] [Abstract][Full Text] [Related]  

  • 31. Hypodysfibrinogenemia: A novel abnormal fibrinogen associated with bleeding and thrombotic complications.
    Amri Y; Kallel C; Becheur M; Dabboubi R; Elloumi M; Belaaj H; Kammoun S; Messaoud T; de Moerloose P; Toumi Nel H
    Clin Chim Acta; 2016 Sep; 460():55-62. PubMed ID: 27343352
    [TBL] [Abstract][Full Text] [Related]  

  • 32. Hypofibrinogenaemia caused by a novel FGG missense mutation (W253C) in the gamma chain globular domain impairing fibrinogen secretion.
    Vu D; de Moerloose P; Batorova A; Lazur J; Palumbo L; Neerman-Arbez M
    J Med Genet; 2005 Sep; 42(9):e57. PubMed ID: 16141000
    [TBL] [Abstract][Full Text] [Related]  

  • 33. [Congenital afibrinogenemia caused by a novel insertion mutation in the FGB gene].
    Zhang J; Zhao XJ; Wang ZY; Yu ZQ; Cao LJ; Ma ZN; Zhang J; Zhang W; Bai X; Ruan CG
    Zhonghua Xue Ye Xue Za Zhi; 2013 Sep; 34(9):751-6. PubMed ID: 24103871
    [TBL] [Abstract][Full Text] [Related]  

  • 34. Clinical and molecular characterisation of 21 patients affected by quantitative fibrinogen deficiency.
    Asselta R; Platè M; Robusto M; Borhany M; Guella I; Soldà G; Afrasiabi A; Menegatti M; Shamsi T; Peyvandi F; Duga S
    Thromb Haemost; 2015 Mar; 113(3):567-76. PubMed ID: 25427968
    [TBL] [Abstract][Full Text] [Related]  

  • 35. Novel missense mutations affecting the structure of the conserved fibrinogen Bβ C-terminal domain cause congenital hypofibrinogenemia.
    Bártolo R; Arbez M; Vilar R; Szanto T; Lehtinen E; Trillot N; Rauch A; Casini A; Neerman-Arbez M
    Thromb Res; 2021 Oct; 206():5-8. PubMed ID: 34352655
    [TBL] [Abstract][Full Text] [Related]  

  • 36. [Fibrinogen beta chain gene mutation contributes to one congenital afibrinogenemia].
    Xu XC; Zhou RF; Wu JS; Fang Y; Wang XF; Zhai ZM; Wang HL
    Zhonghua Xue Ye Xue Za Zhi; 2005 Mar; 26(3):137-9. PubMed ID: 15946523
    [TBL] [Abstract][Full Text] [Related]  

  • 37. Afibrinogenemia resulting from homozygous nonsense mutation in A alpha chain gene associated with multiple thrombotic episodes.
    Simsek I; de Mazancourt P; Horellou MH; Erdem H; Pay S; Dinc A; Samama MM
    Blood Coagul Fibrinolysis; 2008 Apr; 19(3):247-53. PubMed ID: 18388508
    [TBL] [Abstract][Full Text] [Related]  

  • 38. A novel frameshift mutation in FGA accounting for congenital afibrinogenemia predicted to encode an aberrant peptide terminating 158 amino acids downstream.
    Robert-Ebadi H; de Moerloose P; El Khorassani M; El Khattab M; Neerman-Arbez M
    Blood Coagul Fibrinolysis; 2009 Jul; 20(5):385-7. PubMed ID: 19417632
    [TBL] [Abstract][Full Text] [Related]  

  • 39. Fibrinogen Aα gene genotyping in patients with inherited afibrinogenemia deficiency; a novel mutation in Iranian afibrinogenemia patients.
    Moazzeni A; Naderi M; Dorgalaleh A; Alizadeh S
    Blood Coagul Fibrinolysis; 2023 Dec; 34(8):517-522. PubMed ID: 37823427
    [TBL] [Abstract][Full Text] [Related]  

  • 40. Diagnosis of congenital fibrinogen disorders.
    Lebreton A; Casini A
    Ann Biol Clin (Paris); 2016 Aug; 74(4):405-12. PubMed ID: 27492693
    [TBL] [Abstract][Full Text] [Related]  

    [Previous]   [Next]    [New Search]
    of 13.