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Select item 109273001.

Diagnostic value of clot formation parameters determined by rotational thromboelastometry in 63 patients with congenital dysfibrinogenemia

Tomas Simurda, Rita Marchi, Alessandro Casini, Marguerite Neerman-Arbez, Miroslava Drotarova, Ingrid Skornova, Jana Zolkova, Zuzana Kolkova, Dusan Loderer, Monika Brunclikova, Kristina Maria Belakova, Jan Stasko

Blood Coagul Fibrinolysis. 2024 Mar; 35(2): 56–61. Published online 2024 Jan 19. doi: 10.1097/MBC.0000000000001274

PMCID:: PMC10927300

Abstract Article PDF–152K

Select item 108481472.

The FGG c.952G>A variant causes congenital dysfibrinogenemia characterized by recurrent cerebral infarction: a case report

Anna Ying, Yuanlin Zhou, Chunyue Wang, Tao Wang, Xuan Zhang, Shanshan Wang, Shaofa Ke, Yuyan Bao, Yang Liu, Feng Wang

Front Neurol. 2024; 15: 1272802. Published online 2024 Jan 24. doi: 10.3389/fneur.2024.1272802

PMCID:: PMC10848147

Abstract Article PDF–437K

Select item 107522253.

Investigation of acquired dysfibrinogenaemia in adult patients with sepsis using fibrinogen function vs. concentration ratios: a cross-sectional study

Rosa Toenges, Michael Steiner, Christian Friedrich Weber, Wolfgang Miesbach

Front Med (Lausanne) 2023; 10: 1294301. Published online 2023 Dec 13. doi: 10.3389/fmed.2023.1294301

PMCID:: PMC10752225

Abstract Article PDF–322K

Select item 107067904.

Absence of Missense Variant Detection in Inherited Dysfibrinogenemia May Result from a Poor Raw Data Analysis Algorithm or Mosaicism

Philippe De Mazancourt, Elisabeth Mazoyer, Myriam Hormi, Michel Hanss

Int J Mol Sci. 2023 Dec; 24(23): 16551. Published online 2023 Nov 21. doi: 10.3390/ijms242316551

PMCID:: PMC10706790

Abstract Article PDF–900K

Select item 104394455.

Fibrinogen BOE II: dysfibrinogenemia with bleeding and defective thrombin binding

Yang Li, Qian Liang, Wenman Wu, Xiaobo Hu, Hualiang Wang, Xuefeng Wang, Qiulan Ding

Res Pract Thromb Haemost. 2023 Jul; 7(5): 102145. Published online 2023 Jul 7. doi: 10.1016/j.rpth.2023.102145

PMCID:: PMC10439445

Abstract Article PDF–3.0M

Select item 104088596.

1例遗传性异常纤维蛋白原血症的家系分析和诊断报告

娟骆, 苏容段, 华王

Sichuan Da Xue Xue Bao Yi Xue Ban. 2022 Jan 20; 53(1): 171–174. Chinese. doi: 10.12182/20220160201

PMCID:: PMC10408859

Abstract Article PDF–1.0M

Select item 97829307.

Congenital dysfibrinogenemia misdiagnosed and inappropriately treated as acute fatty liver in pregnancy: A case report and review of literature

Yan Jia, Xi-Wen Zhang, Yi-Shi Wu, Qing-Yu Wang, Shu-Li Yang

World J Clin Cases. 2022 Dec 16; 10(35): 12996–13005. Published online 2022 Dec 16. doi: 10.12998/wjcc.v10.i35.12996

PMCID:: PMC9782930

Abstract Article PDF–1009K

Select item 96785368.

A low-dose therapy of fibrinogen supplement during perioperative period of total knee arthroplasty in an asymptomatic man with congenital dysfibrinogenemia: A case report

Decheng Meng, Runzi Zhang, Chenni Ji, Shijun Gao, Juan Wang

Medicine (Baltimore) 2022 Nov 18; 101(46): e31644. Published online 2022 Nov 18. doi: 10.1097/MD.0000000000031644

PMCID:: PMC9678536

Abstract Article PDF–518K

Select item 94592809.

Misdiagnosis of a patient with congenital dysfibrinogenemia: A case report and literature review

Xinyan Chen, Jie Yan, Liqun Xiang, Faquan Lin

J Clin Lab Anal. 2022 Sep; 36(9): e24624. Published online 2022 Aug 10. doi: 10.1002/jcla.24624

PMCID:: PMC9459280

Abstract Article PDF–929K

Select item 859596410.

Management of congenital dysfibrinogenemia in pregnancy: A challenging patient case

Megan Langer, Meredith Manire, Matthew Clarkson, Yazan Samhouri, Deep Shah, Rama Bhagavatula

Res Pract Thromb Haemost. 2021 Dec; 5(8): e12619. Published online 2021 Nov 16. doi: 10.1002/rth2.12619

PMCID:: PMC8595964

Abstract Article PDF–554K

Select item 838007911.

Pseudohomozygous dysfibrinogenemia

Rachel C. Peck, Lucy Fitzgibbon, Christopher Reilly‐Stitt, Christopher Doherty, Emma Phillips, Andrew D. Mumford

Res Pract Thromb Haemost. 2021 Aug; 5(6): e12568. Published online 2021 Aug 21. doi: 10.1002/rth2.12568

PMCID:: PMC8380079

Abstract Article PDF–469K

Select item 772906212.

Case Report: Unmasked Inherited Dysfibrinogenemia After Everolimus Therapy

Alona A. Merkulova, Steven C. Mitchell, Sergei Merkulov, Alisa S. Wolberg, Marguerite Neerman-Arbez, Alvin H. Schmaier

Front Med (Lausanne) 2020; 7: 591546. Published online 2020 Nov 27. doi: 10.3389/fmed.2020.591546

PMCID:: PMC7729062

Abstract Article PDF–660K

Select item 771228413.

A family study of congenital dysfibrinogenemia caused by a novel mutation in the FGA gene: A case report

Yingli Qiao, Qisi Zhang, Poshi Xu, Yuhui Deng

Open Med (Wars) 2020; 15(1): 769–773. Published online 2020 Aug 3. doi: 10.1515/med-2020-0214

PMCID:: PMC7712284

Abstract Article PDF–528K

Select item 751161314.

Congenital dysfibrinogenaemia presented with preterm premature rupture of the membranes and vaginal bleeding

Zaker I Schwabkey, Farrell C Sheehan, Courtney Bellomo, Mihir Raval

BMJ Case Rep. 2020; 13(9): e235961. Published online 2020 Sep 18. doi: 10.1136/bcr-2020-235961

PMCID:: PMC7511613

Abstract Article PDF–187K

Select item 681687615.

Combined use of Clauss and prothrombin time‐derived methods for determining fibrinogen concentrations: Screening for congenital dysfibrinogenemia

Liqun Xiang, Meiling Luo, Jie Yan, Lin Liao, Weijie Zhou, Xuelian Deng, Donghong Deng, Peng Cheng, Faquan Lin

J Clin Lab Anal. 2018 May; 32(4): e22322. Published online 2017 Sep 18. doi: 10.1002/jcla.22322

PMCID:: PMC6816876

Abstract Article PDF–345K

Select item 681685216.

Management of dysfibrinogenemia in pregnancy: A case report

Jie Yan, Donghong Deng, Peng Cheng, Lin Liao, Meiling Luo, Faquan Lin

J Clin Lab Anal. 2018 Mar; 32(3): e22319. Published online 2017 Sep 26. doi: 10.1002/jcla.22319

PMCID:: PMC6816852

Abstract Article PDF–372K

Select item 666332017.

Bleeding due to acquired dysfibrinogenemia as the initial presentation of multiple myeloma

Namrah Siddiq, Colin Bergstrom, Larry D Anderson, Jr, Srikanth Nagalla

BMJ Case Rep. 2019; 12(7): e229312. Published online 2019 Jul 17. doi: 10.1136/bcr-2019-229312

PMCID:: PMC6663320

Abstract Article PDF–359K

Select item 652491518.

Interference of Monoclonal Gammopathy with Fibrinogen Assay Producing Spurious Dysfibrinogenemia

Francesca Martini, Nadia Cecconi, Aldo Paolicchi, Sara Galimberti, Giulia Cervetti, Gabriele Buda, Mario Petrini

TH Open. 2019 Jan; 3(1): e64–e66. Published online 2019 Mar 19. doi: 10.1055/s-0039-1683969

PMCID:: PMC6524915

Abstract Article PDF–131K

Select item 620048019.

A novel fibrinogen variant in a Chinese pedigree with congenital dysfibrinogenemia caused by FGA P. Arg38Thr mutation: A case report

Ruimin Cai, Yi Li, Wenyang Wang, Xue Gao, Meirong Liu, Youxiang Diao, Yi Tang, Qiang Feng

Medicine (Baltimore) 2018 Oct; 97(40): e12697. Published online 2018 Oct 5. doi: 10.1097/MD.0000000000012697

PMCID:: PMC6200480

Abstract Article PDF–628K

Select item 599701920.

Dysfibrinogenemia and multiple sclerosis: spuriously associated or causally linked?

VK Kimiskidis, E Papadakis, V Papaliagkas, S Papagiannopoulos, DK Galanakis

Hippokratia. 2017 Jan-Mar; 21(1): 49–51.

PMCID:: PMC5997019

Abstract Article PDF–417K

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PMC Articles for MedGen (Select 226778) (88)
PMC
anthranilate/para-aminobenzoate synthase component I [Anaerobaculum mobile DSM 1...
anthranilate/para-aminobenzoate synthase component I [Anaerobaculum mobile DSM 13181]
gi|392408109|ref|YP_006444717.1|

Protein
LysR family transcriptional regulator [Rhizobium leguminosarum]
LysR family transcriptional regulator [Rhizobium leguminosarum]
gi|501555243|ref|WP_012559753.1|

Protein
anthranilate synthase component I family protein [Acetomicrobium mobile]
anthranilate synthase component I family protein [Acetomicrobium mobile]
gi|504620514|ref|WP_014807616.1|

Protein
Hereditary factor I deficiency disease
Hereditary factor I deficiency disease

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