313 related articles for article (PubMed ID: 16819336)
61. The molecular basis of inherited afibrinogenaemia.
Neerman-Arbez M
Thromb Haemost; 2001 Jul; 86(1):154-63. PubMed ID: 11487003
[TBL] [Abstract][Full Text] [Related]
62. Clinical and biological features of 3 cases of hypofibrinogenemia associated with three different mutations (gamma Ala341Thr, Bbeta Tyr326Cys and Aalpha Asp496Asn).
Hanss M; Chevreaud C; French P; Négrier C; de Mazancourt P
Thromb Haemost; 2007 Sep; 98(3):689-91. PubMed ID: 17849064
[No Abstract] [Full Text] [Related]
63. The fibrous form of intracellular inclusion bodies in recombinant variant fibrinogen-producing cells is specific to the hepatic fibrinogen storage disease-inducible variant fibrinogen.
Arai S; Ogiwara N; Mukai S; Takezawa Y; Sugano M; Honda T; Okumura N
Int J Hematol; 2017 Jun; 105(6):758-768. PubMed ID: 28161763
[TBL] [Abstract][Full Text] [Related]
64. [Analysis of a family with congenital dysfibrinogenemia caused by an Arg275His mutation in the gamma chain of fibrinogen].
Yan J; Deng D; Deng X; Luo M; Cheng P; Liao L; Lin F
Zhonghua Yi Xue Yi Chuan Xue Za Zhi; 2016 Apr; 33(2):160-3. PubMed ID: 27060305
[TBL] [Abstract][Full Text] [Related]
65. Protein Misfolding and Aggregation: The Relatedness between Parkinson's Disease and Hepatic Endoplasmic Reticulum Storage Disorders.
Padilla-Godínez FJ; Ramos-Acevedo R; Martínez-Becerril HA; Bernal-Conde LD; Garrido-Figueroa JF; Hiriart M; Hernández-López A; Argüero-Sánchez R; Callea F; Guerra-Crespo M
Int J Mol Sci; 2021 Nov; 22(22):. PubMed ID: 34830348
[TBL] [Abstract][Full Text] [Related]
66. Hereditary hypofibrinogenemia with fibrinogen storage in the liver.
Wehinger H; Klinge O; Alexandrakis E; Schürmann J; Witt J; Seydewitz HH
Eur J Pediatr; 1983 Dec; 141(2):109-12. PubMed ID: 6662138
[TBL] [Abstract][Full Text] [Related]
67. Molecular characterization of 7 patients affected by dys- or hypo-dysfibrinogenemia: Identification of a novel mutation in the fibrinogen Bbeta chain causing a gain of glycosylation.
Asselta R; Robusto M; Platé M; Santoro C; Peyvandi F; Duga S
Thromb Res; 2015 Jul; 136(1):168-74. PubMed ID: 26006300
[TBL] [Abstract][Full Text] [Related]
68. Fibrinogen Nový Jicín and Praha II: cases of hereditary Aalpha 16 Arg-->Cys and Aalpha 16 Arg-->His dysfibrinogenemia.
Kotlín R; Chytilová M; Suttnar J; Riedel T; Salaj P; Blatný J; Santrůcek J; Klener P; Dyr JE
Thromb Res; 2007; 121(1):75-84. PubMed ID: 17408725
[TBL] [Abstract][Full Text] [Related]
69. A novel mutation in the FGB: c.1105C>T turns the codon for amino acid Bβ Q339 into a stop codon causing hypofibrinogenemia.
Marchi R; Brennan S; Meyer M; Rojas H; Kanzler D; De Agrela M; Ruiz-Saez A
Blood Cells Mol Dis; 2013 Mar; 50(3):177-81. PubMed ID: 23266225
[TBL] [Abstract][Full Text] [Related]
70. Hypofibrinogenaemia resulting from novel single nucleotide deletion at codon Bbeta58 (3404del A) associated with thrombotic stroke in infancy.
Brennan SO; Mosesson MW; Lowen R; Siebenlist KR; Matsunaga A
Thromb Haemost; 2006 Apr; 95(4):738-9. PubMed ID: 16601848
[No Abstract] [Full Text] [Related]
71. 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]
72. Hypofibrinogenemia associated with a heterozygous missense mutation gamma153Cys to arg (Matsumoto IV): in vitro expression demonstrates defective secretion of the variant fibrinogen.
Terasawa F; Okumura N; Kitano K; Hayashida N; Shimosaka M; Okazaki M; Lord ST
Blood; 1999 Dec; 94(12):4122-31. PubMed ID: 10590057
[TBL] [Abstract][Full Text] [Related]
73. Unique de-novo mutation of fibrinogen gene in a Chinese girl with hypofibrinogenemia.
Wang Y; Zhu L; Hao X; Xie Y; Jin Y; Wang M
Blood Coagul Fibrinolysis; 2014 Oct; 25(7):780-2. PubMed ID: 24717425
[TBL] [Abstract][Full Text] [Related]
74. Inherited dysfibrinogenemia: clinical phenotypes associated with five different fibrinogen structure defects.
Miesbach W; Scharrer I; Henschen A; Neerman-Arbez M; Spitzer S; Galanakis D
Blood Coagul Fibrinolysis; 2010 Jan; 21(1):35-40. PubMed ID: 19923982
[TBL] [Abstract][Full Text] [Related]
75. 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]
76. A novel mutation in exon 2 of FGB caused by c.221G>T
Shlebak AA; Katsarou AD; Adams G; Fernando F
J Thromb Thrombolysis; 2017 Feb; 43(2):263-270. PubMed ID: 27812779
[TBL] [Abstract][Full Text] [Related]
77. Laboratory and Genetic Investigation of Mutations Accounting for Congenital Fibrinogen Disorders.
Neerman-Arbez M; de Moerloose P; Casini A
Semin Thromb Hemost; 2016 Jun; 42(4):356-65. PubMed ID: 27019463
[TBL] [Abstract][Full Text] [Related]
78. 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]
79. Fibrinogen Poissy I: a new case of the A alpha Arg 16His fibrinogen variant.
Mathonnet F; Guillon L; Detruit H; Van Amerongen G; Denninger MH; Giudicelli Y; de Mazancourt P
Blood Coagul Fibrinolysis; 1997 Oct; 8(7):441-4. PubMed ID: 9391726
[TBL] [Abstract][Full Text] [Related]
80. Fibrinogen Seoul (FGG Ala341Asp): a novel mutation associated with hypodysfibrinogenemia.
Song KS; Park NJ; Choi JR; Doh HJ; Chung KH
Clin Appl Thromb Hemost; 2006 Jul; 12(3):338-43. PubMed ID: 16959688
[TBL] [Abstract][Full Text] [Related]
[Previous] [Next] [New Search]
