136 related articles for article (PubMed ID: 19551918)
21. A novel nonsense mutation in the FGA gene in a Chinese family with congenital afibrinogenaemia.
Wu S; Wang Z; Dong N; Bai X; Ruan C
Blood Coagul Fibrinolysis; 2005 Apr; 16(3):221-6. PubMed ID: 15795544
[TBL] [Abstract][Full Text] [Related]
22. Analysis of Iranian patients allowed the identification of the first truncating mutation in the fibrinogen Bbeta-chain gene causing afibrinogenemia.
Asselta R; Spena S; Duga S; Peyvandi F; Malcovati M; Mannucci PM; Tenchini ML
Haematologica; 2002 Aug; 87(8):855-9. PubMed ID: 12161363
[TBL] [Abstract][Full Text] [Related]
23. Genetic Analysis of Afibrinogenemia and Hypofibrinogenemia: Novel Mutations in the FGB Gene in the Turkish Population.
Özkan DT; Sarper N; Akar N
Acta Haematol; 2020; 143(6):529-532. PubMed ID: 32289806
[TBL] [Abstract][Full Text] [Related]
24. Mutational screening of six afibrinogenemic patients: identification and characterization of four novel molecular defects.
Monaldini L; Asselta R; Duga S; Peyvandi F; Karimi M; Malcovati M; Tenchini ML
Thromb Haemost; 2007 Apr; 97(4):546-51. PubMed ID: 17393016
[TBL] [Abstract][Full Text] [Related]
25. 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]
26. A novel missense mutation in the FGB gene (p.Gly302Arg) leading to afibrinogenemia. Predicted structure and function consequences.
Ivaškevičius V; Rühl H; Detarsio G; Biswas A; Gupta S; Davoli M; Quartara A; Pérez S; Raviola M; Oldenburg J
Hamostaseologie; 2016 Nov; 36(Suppl. 2):S34-S38. PubMed ID: 27824214
[TBL] [Abstract][Full Text] [Related]
27. Mutations in the fibrinogen gene cluster accounting for congenital afibrinogenemia: an update and report of 10 novel mutations.
Neerman-Arbez M; de Moerloose P
Hum Mutat; 2007 Jun; 28(6):540-53. PubMed ID: 17295221
[TBL] [Abstract][Full Text] [Related]
28. Mutational Epidemiology of Congenital Fibrinogen Disorders.
Casini A; Blondon M; Tintillier V; Goodyer M; Sezgin ME; Gunes AM; Hanss M; de Moerloose P; Neerman-Arbez M
Thromb Haemost; 2018 Nov; 118(11):1867-1874. PubMed ID: 30332696
[TBL] [Abstract][Full Text] [Related]
29. Congenital afibrinogenemia: identification and expression of a missense mutation in FGB impairing fibrinogen secretion.
Vu D; Bolton-Maggs PH; Parr JR; Morris MA; de Moerloose P; Neerman-Arbez M
Blood; 2003 Dec; 102(13):4413-5. PubMed ID: 12893758
[TBL] [Abstract][Full Text] [Related]
30. A nonsense mutation in FGA g.3807C-->T (p.R159X) causes afibrinogenaemia in the homozygous form.
Marchi Cappelletti R; Tersek Y; Ruiz-Sáez A; Meyer M
Acta Haematol; 2009; 121(4):216-7. PubMed ID: 19468208
[No Abstract] [Full Text] [Related]
31. A case of congenital afibrinogenemia: fibrinogen Hakata, a novel nonsense mutation of the fibrinogen gamma-chain gene.
Iida H; Ishii E; Nakahara M; Urata M; Wakiyama M; Kurihara M; Watanabe K; Kai T; Ihara K; Kinoshita S; Hamasaki N
Thromb Haemost; 2000 Jul; 84(1):49-53. PubMed ID: 10928469
[TBL] [Abstract][Full Text] [Related]
32. Identification of a novel mutation in congenital afibrinogenemia in Iranian patients.
Nojehdeh ST; Mojbafan M; Masoodifard M; Amini M; Zeinali S
Blood Coagul Fibrinolysis; 2021 Jul; 32(5):323-327. PubMed ID: 33901106
[TBL] [Abstract][Full Text] [Related]
33. Fibrinogen Martin: A Novel Mutation in FGB (Gln180Stop) Causing Congenital Afibrinogenemia.
Simurda T; Snahnicanova Z; Loderer D; Sokol J; Stasko J; Lasabova Z; Kubisz P
Semin Thromb Hemost; 2016 Jun; 42(4):455-8. PubMed ID: 27148845
[No Abstract] [Full Text] [Related]
34. 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]
35. A rare heterozygous variant in FGB (Fibrinogen Merivale) causing hypofibrinogenemia in a Swedish family.
Fager Ferrari M; Leinoe E; Rossing M; Norström E; Zetterberg E
Blood Coagul Fibrinolysis; 2020 Oct; 31(7):481-484. PubMed ID: 32852326
[TBL] [Abstract][Full Text] [Related]
36. Expression and analysis of a split premature termination codon in FGG responsible for congenital afibrinogenemia: escape from RNA surveillance mechanisms in transfected cells.
Neerman-Arbez M; Germanos-Haddad M; Tzanidakis K; Vu D; Deutsch S; David A; Morris MA; de Moerloose P
Blood; 2004 Dec; 104(12):3618-23. PubMed ID: 15284111
[TBL] [Abstract][Full Text] [Related]
37. 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]
38. Rare inherited disorders of fibrinogen.
Acharya SS; Dimichele DM
Haemophilia; 2008 Nov; 14(6):1151-8. PubMed ID: 19141154
[TBL] [Abstract][Full Text] [Related]
39. 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]
40. 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]
[Previous] [Next] [New Search]
