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Items: 1 to 20 of 125

1.
Early Diagnosis and Management of Congenital Afibrinogenemia: A Case Report of Umbilical Stump Bleeding
Qais M Salah, Rami R AlRashayda, Mohammad J Heresh, Aya Abulehya, Leena W Salah Al-deen
Cureus. 2023 Jul; 15(7): e42542. Published online 2023 Jul 27. doi: 10.7759/cureus.42542
PMCID:
PMC10460120
ArticlePDF–96K
2.
Treatment of Congenital Afibrinogenemia in a Neonate With Critical Pulmonary Stenosis
Priya Parikh, Kimvi Diep, Vinod Balasa, Tiffany L. Lucas
J Pediatr Pharmacol Ther. 2023; 28(3): 268–271. Published online 2023 Jun 2. doi: 10.5863/1551-6776-28.3.268
PMCID:
PMC10249975
ArticlePDF–655K
3.
A Case Report of Congenital Afibrinogenemia and Literature Review of Management of Post-circumcision Bleeding
Imteyaz Khan, Matthew Chow, Shakuntala Chandra, Mark Hiatt
Cureus. 2023 Mar; 15(3): e36459. Published online 2023 Mar 21. doi: 10.7759/cureus.36459
PMCID:
PMC10029106
ArticlePDF–256K
4.
A case of congenital afibrinogenemia with multiple thrombotic and hemorrhagic disorders
Lijian Wei, Yuting Tang, Zhuohua Wu, Pingyi Xu, Mingshu Mo
Clin Case Rep. 2022 Oct; 10(10): e6395. Published online 2022 Oct 20. doi: 10.1002/ccr3.6395
PMCID:
PMC9582684
ArticlePDF–919K
5.
A homozygous duplication of the FGG exon 8-intron 8 junction causes congenital afibrinogenemia. Lessons learned from the study of a large consanguineous Turkish family
Michel Guipponi, Frédéric Masclaux, Frédérique Sloan-Béna, Corinne Di Sanza, Namik Özbek, Flora Peyvandi, Marzia Menegatti, Alessandro Casini, Baris Malbora, Marguerite Neerman-Arbez
Haematologica. 2022 May 1; 107(5): 1064–1071. Published online 2021 Jul 1. doi: 10.3324/haematol.2021.278945
PMCID:
PMC9052919
ArticlePDF–3.6M
6.
Endovascular Treatment for Lower-extremity Arterial Thrombosis in a Patient with Congenital Afibrinogenemia and a History of Bleeding Complications
Daisuke Hiramatsu, Yoshito Ogihara, Takeshi Matsumoto, Kei Sato, Akihiro Takasaki, Tairo Kurita, Ryuji Okamoto, Hideo Wada, Kaoru Dohi
Intern Med. 2022 Feb 1; 61(3): 361–364. Published online 2021 Jul 30. doi: 10.2169/internalmedicine.7542-21
PMCID:
PMC8866793
ArticlePDF–573K
7.
Congenital Afibrinogenemia and Hypofibrinogenemia: Laboratory and Genetic Testing in Rare Bleeding Disorders with Life-Threatening Clinical Manifestations and Challenging Management
Tomas Simurda, Rosanna Asselta, Jana Zolkova, Monika Brunclikova, Miroslava Dobrotova, Zuzana Kolkova, Dusan Loderer, Ingrid Skornova, Jan Hudecek, Zora Lasabova, Jan Stasko, Peter Kubisz
Diagnostics (Basel) 2021 Nov; 11(11): 2140. Published online 2021 Nov 19. doi: 10.3390/diagnostics11112140
PMCID:
PMC8622093
ArticlePDF–1.3M
8.
Liver transplantation as a novel strategy for resolution of congenital afibrinogenemia in a pediatric patient
Fernando F. Corrales‐Medina, Tamir Miloh, Candelaria O’Farrell, David M. Andrews, Akin Tekin, Guillermo De Angulo
J Thromb Haemost. 2020 Dec; 18(12): 3232–3235. Published online 2020 Oct 6. doi: 10.1111/jth.15090
PMCID:
PMC7756576
ArticlePDF–422K
9.
Correction to: Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population
Arshi Naz, Arijit Biswas, Tehmina Nafees Khan, Anne Goodeve, Nisar Ahmed, Nazish Saqlain, Shariq Ahmed, Ikram Din Ujjan, Tahir S. Shamsi, Johannes Oldenburg
Thromb J. 2019; 17: 5. Published online 2019 Apr 4. doi: 10.1186/s12959-019-0193-9
Corrects:
Thromb J. 2017; 15: 24.
PMCID:
PMC6448250
CorrectionPDF–309K
10.
Identification of novel mutations in congenital afibrinogenemia patients and molecular modeling of missense mutations in Pakistani population
Arshi Naz, Arijit Biswas, Tehmina Nafees Khan, Anne Goodeve, Nisar Ahmed, Nazish Saqlain, Shariq Ahmed, Ikram Din Ujjan, Tahir S Shamsi, Johannes Oldenburg
Thromb J. 2017; 15: 24. Published online 2017 Sep 12. doi: 10.1186/s12959-017-0143-3
Correction in:
Thromb J. 2019; 17: 5.
PMCID:
PMC5594472
ArticlePDF–1.0M
11.
Recurrent massive haemoperitoneum associated with ruptured corpus luteum in women with congenital afibrinogenemia; case report
Özhan Özdemir, Mustafa Erkan Sarı, Aslıhan Kurt, Ertuğrul Şen, Cemal Reşat Atalay
Turk J Obstet Gynecol. 2014 Dec; 11(4): 242–245. Published online 2014 Dec 15. doi: 10.4274/tjod.04935
PMCID:
PMC5558369
ArticlePDF–84K
12.
Afibrinogénémie congénitale: à propos d’une observation
Karim Assani, Lamya Karboubi, Badr Sououd Benjelloun Dakhama
Pan Afr Med J. 2016; 25: 233. French. Publication en ligne 2016 déc. 9. DOI : 10.11604/pamj.2016.25.233.10754
PMCID:
PMC5337292
ArticlePDF–363K
13.
Congenital afibrinogenemia: a case report of a spontaneous hepatic hematoma
Stephanie Malaquin, Lionel Rebibo, Cyril Chivot, Louise Badoux, Yazine Mahjoub, Herve Dupont
Medicine (Baltimore) 2016 Jul; 95(28): e4150. Published online 2016 Jul 18. doi: 10.1097/MD.0000000000004150
PMCID:
PMC4956798
ArticlePDF–387K
14.
Spontaneous splenic rupture in a patient with congenital afibrinogenemia
Baran Cengiz Arcagök, Nihal Özdemir, Ayşe Tekin, Rahşan Özcan, Mehmet Eliçevik, Osman Faruk Şenyüz, Halit Çam, Tiraje Celkan
Turk Pediatri Ars. 2014 Sep; 49(3): 247–249. Published online 2014 Sep 1. doi: 10.5152/tpa.2014.1070
PMCID:
PMC4462307
ArticlePDF–122K
15.
Recurrent Myocardial Infarction in a Case of Congenital Afibrinogenemia
Soumya Patra, Babu Reddy, C. M. Nagesh, B. C. Srinivas, C. N. Manjunath
Heart Views. 2014 Jan-Mar; 15(1): 16–18. doi: 10.4103/1995-705X.132141
PMCID:
PMC4062984
Article
16.
Anaesthetic management of a child with congenital afibrinogenemia - A rare inherited coagulation disorder
Sham Sunder Goyal, D Vimal Bhardwaj, UK Shenoy, Bhavya Reddy
Indian J Anaesth. 2011 Nov-Dec; 55(6): 605–607. doi: 10.4103/0019-5049.90617
PMCID:
PMC3249869
ArticlePDF–319K
17.
Congenital Afibrinogenemia presenting as antenatal intracranial bleed: a case report
Gopakumar Hariharan, Sivji Ramachandran, Rajiv Parapurath
Ital J Pediatr. 2010; 36: 1. Published online 2010 Jan 5. doi: 10.1186/1824-7288-36-1
PMCID:
PMC2841604
ArticlePDF–730K
18.
von Willebrand factor interaction with the glycoprotein IIb/IIa complex. Its role in platelet function as demonstrated in patients with congenital afibrinogenemia.
L De Marco, A Girolami, T S Zimmerman, Z M Ruggeri
J Clin Invest. 1986 Apr; 77(4): 1272–1277. doi: 10.1172/JCI112430
PMCID:
PMC424474
SummaryPage BrowsePDF–1.1M
19.
Delayed-Type Hypersensitivity Skin Reactions in Congenital Afibrinogenemia Lack Fibrin Deposition and Induration
Robert B. Colvin, Michael W. Mosesson, Harold F. Dvorak
J Clin Invest. 1979 Jun; 63(6): 1302–1306. doi: 10.1172/JCI109425
PMCID:
PMC372079
SummaryPage BrowsePDF–1.2M
20.
Congenital fibrinogen disorders: a retrospective clinical and genetic analysis of the Prospective Rare Bleeding Disorders Database
Samin Mohsenian, Roberta Palla, Marzia Menegatti, Andrea Cairo, Anna Lecchi, Alessandro Casini, Marguerite Neerman-Arbez, Rosanna Asselta, Sara Scardo, Simona Maria Siboni, Jan Blatny, Ondrej Zapletal, Jean-Francois Schved, Muriel Giansily-Blaizot, Susan Halimeh, Mohamad Ayman Daoud, Helen Platokouki, Helen Pergantou, Roger E. G. Schutgens, Monique Van Haaften-Spoor, Paul Brons, Britta Laros-van Gorkom, Elise Van Pinxten, Munira Borhany, Naveena Fatima, Danijela Mikovic, Marko Saracevic, Gül Nihal Özdemir, Yılmaz Ay, Michael Makris, Caryl Lockley, Andrew Mumford, Andrew Harvey, Steve Austin, Amy Shapiro, Adrianna Williamson, Catherine McGuinn, Ilene Goldberg, Philippe De Moerloose, Flora Peyvandi
Blood Adv. 2024 Mar 26; 8(6): 1392–1404. Published online 2024 Jan 30. doi: 10.1182/bloodadvances.2023012186
PMCID:
PMC10950829
ArticlePDF–1.2M

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