190 related articles for article (PubMed ID: 29244742)
1. Fibrinogen Gamma Chain Mutations Provoke Fibrinogen and Apolipoprotein B Plasma Deficiency and Liver Storage.
Callea F; Giovannoni I; Sari S; Guldal E; Dalgic B; Akyol G; Sogo T; Al-Hussaini A; Maggiore G; Bartuli A; Boldrini R; Francalanci P; Bellacchio E
Int J Mol Sci; 2017 Dec; 18(12):. PubMed ID: 29244742
[TBL] [Abstract][Full Text] [Related]
2. Hepatic fibrinogen storage disease due to the fibrinogen γ375 Arg → Trp mutation "fibrinogen Aguadilla" is present in Arabs.
Al-Hussaini A; Altalhi A; El Hag I; AlHussaini H; Francalanci P; Giovannoni I; Callea F
Saudi J Gastroenterol; 2014; 20(4):255-61. PubMed ID: 25038212
[TBL] [Abstract][Full Text] [Related]
3. 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]
4. Hypofibrinogenemia and liver disease: a new case of Aguadilla fibrinogen and review of the literature.
Casini A; Sokollik C; Lukowski SW; Lurz E; Rieubland C; de Moerloose P; Neerman-Arbez M
Haemophilia; 2015 Nov; 21(6):820-7. PubMed ID: 25990487
[TBL] [Abstract][Full Text] [Related]
5. Fibrinogen gamma375 arg-->trp mutation (fibrinogen aguadilla) causes hereditary hypofibrinogenemia, hepatic endoplasmic reticulum storage disease and cirrhosis.
Rubbia-Brandt L; Neerman-Arbez M; Rougemont AL; Malé PJ; Spahr L
Am J Surg Pathol; 2006 Jul; 30(7):906-11. PubMed ID: 16819336
[TBL] [Abstract][Full Text] [Related]
6. Novel fibrinogen gamma375 Arg-->Trp mutation (fibrinogen aguadilla) causes hepatic endoplasmic reticulum storage and hypofibrinogenemia.
Brennan SO; Maghzal G; Shneider BL; Gordon R; Magid MS; George PM
Hepatology; 2002 Sep; 36(3):652-8. PubMed ID: 12198657
[TBL] [Abstract][Full Text] [Related]
7. Novel fibrinogen mutation γ314Thr→Pro (fibrinogen AI duPont) associated with hepatic fibrinogen storage disease and hypofibrinogenaemia.
Brennan SO; Davis RL; Conard K; Savo A; Furuya KN
Liver Int; 2010 Nov; 30(10):1541-7. PubMed ID: 20666993
[TBL] [Abstract][Full Text] [Related]
8. Autophagy-enhancing drug carbamazepine diminishes hepatocellular death in fibrinogen storage disease.
Puls F; Goldschmidt I; Bantel H; Agne C; Bröcker V; Dämmrich M; Lehmann U; Berrang J; Pfister ED; Kreipe HH; Baumann U
J Hepatol; 2013 Sep; 59(3):626-30. PubMed ID: 23707368
[TBL] [Abstract][Full Text] [Related]
9. Hepatic fibrinogen storage disease and hypofibrinogenemia caused by fibrinogen Aguadilla mutation: a case report.
Gu L; Wang B; Liu L; Gan Q; Liu X; Chen L; Chen L
J Int Med Res; 2020 Jan; 48(1):300060519898033. PubMed ID: 31965886
[TBL] [Abstract][Full Text] [Related]
10. Mutant fibrinogen cleared from the endoplasmic reticulum via endoplasmic reticulum-associated protein degradation and autophagy: an explanation for liver disease.
Kruse KB; Dear A; Kaltenbrun ER; Crum BE; George PM; Brennan SO; McCracken AA
Am J Pathol; 2006 Apr; 168(4):1299-308; quiz 1404-5. PubMed ID: 16565503
[TBL] [Abstract][Full Text] [Related]
11. Structural Characteristics in the γ Chain Variants Associated with Fibrinogen Storage Disease Suggest the Underlying Pathogenic Mechanism.
Burcu G; Bellacchio E; Sag E; Cebi AH; Saygin I; Bahadir A; Yilmaz G; Corbeddu M; Cakir M; Callea F
Int J Mol Sci; 2020 Jul; 21(14):. PubMed ID: 32698516
[TBL] [Abstract][Full Text] [Related]
12. Fibrinogen storage disease and cirrhosis associated with hypobetalipoproteinemia owing to fibrinogen Aguadilla in a Turkish child.
Sari S; Yilmaz G; Gonul II; Dalgic B; Akyol G; Giovannoni I; Francalanci P; Callea F
Liver Int; 2015 Dec; 35(12):2501-5. PubMed ID: 26176881
[TBL] [Abstract][Full Text] [Related]
13. Fibrinogen brescia: hepatic endoplasmic reticulum storage and hypofibrinogenemia because of a gamma284 Gly-->Arg mutation.
Brennan SO; Wyatt J; Medicina D; Callea F; George PM
Am J Pathol; 2000 Jul; 157(1):189-96. PubMed ID: 10880389
[TBL] [Abstract][Full Text] [Related]
14. 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]
15. Severe liver disease in early childhood due to fibrinogen storage and de novo gamma375Arg-->Trp gene mutation.
Francalanci P; Santorelli FM; Talini I; Boldrini R; Devito R; Camassei FD; Maggiore G; Callea F
J Pediatr; 2006 Mar; 148(3):396-8. PubMed ID: 16615976
[TBL] [Abstract][Full Text] [Related]
16. Hereditary Hypofibrinogenemia with Hepatic Storage.
Asselta R; Paraboschi EM; Duga S
Int J Mol Sci; 2020 Oct; 21(21):. PubMed ID: 33105716
[TBL] [Abstract][Full Text] [Related]
17. Hepatic Fibrinogen Storage Disease in a Patient with Hypofibrinogenemia: Report of a Case with a Missense Mutation of the FGA Gene.
Lee MJ; Venick R; Bhuta S; Li X; Wang HL
Semin Liver Dis; 2015 Nov; 35(4):439-43. PubMed ID: 26676819
[TBL] [Abstract][Full Text] [Related]
18. γ375W fibrinogen-synthesizing CHO cells indicate the accumulation of variant fibrinogen within endoplasmic reticulum.
Kobayashi T; Arai S; Ogiwara N; Takezawa Y; Nanya M; Terasawa F; Okumura N
Thromb Res; 2014 Jan; 133(1):101-7. PubMed ID: 24210681
[TBL] [Abstract][Full Text] [Related]
19. The Recruitment-Secretory Block ("R-SB") Phenomenon and Endoplasmic Reticulum Storage Diseases.
Callea F; Tomà P; Bellacchio E
Int J Mol Sci; 2021 Jun; 22(13):. PubMed ID: 34202771
[TBL] [Abstract][Full Text] [Related]
20. Fibrinogen storage disease in a Chinese boy with de novo fibrinogen Aguadilla mutation: Incomplete response to carbamazepine and ursodeoxycholic acid.
Zhang MH; Knisely AS; Wang NL; Gong JY; Wang JS
BMC Gastroenterol; 2016 Aug; 16(1):92. PubMed ID: 27520927
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]