scholarly journals Agudização da afibrinogenemia congênita: um relato de caso / Acute worsening of congenital afibrinogenemia: a case report

2021 ◽  
Vol 4 (1) ◽  
pp. 3652-3655
Author(s):  
Yasmin Oliveira Santos ◽  
Ilca Pereira Prado ◽  
Yasmin Melo Toledo ◽  
Maria Eduarda Butarelli Nascimento ◽  
Michelle Rafaelle Andrade Gurgel ◽  
...  
Author(s):  
S. Evron ◽  
S.O. Anteby ◽  
A. Brzezinsky ◽  
A. Samueloff ◽  
A. Eldor

Angiology ◽  
1993 ◽  
Vol 44 (9) ◽  
pp. 745-749 ◽  
Author(s):  
Domenico De Mattia ◽  
Guido Regina ◽  
Paola Giordano ◽  
Giovanni Carlo Del Vecchio ◽  
Maria Altomare ◽  
...  

2001 ◽  
Vol 59 (8) ◽  
pp. 935-936 ◽  
Author(s):  
Joseph Cillo ◽  
Allen Pulsipher ◽  
Cynthia J. Rutherford ◽  
Edward Ellis

2020 ◽  
Vol 73 (4) ◽  
pp. 523-530
Author(s):  
G. Caimi ◽  
S. Raso ◽  
M. Napolitano ◽  
E. Hopps ◽  
R. Lo Presti ◽  
...  

2014 ◽  
Vol 1 (1) ◽  
pp. 27
Author(s):  
Aysen Turedi Yildirim ◽  
Gokmen Bilgili ◽  
Ozlem Buga ◽  
Ozen Tekin ◽  
Huseyin Gulen

2014 ◽  
Vol 11 (4) ◽  
pp. 242-245 ◽  
Author(s):  
Özhan Özdemir ◽  
Mustafa Erkan Sarı ◽  
Aslıhan Kurt ◽  
Ertuğrul Şen ◽  
Cemal Reşat Atalay

2010 ◽  
Vol 36 (1) ◽  
pp. 1 ◽  
Author(s):  
Gopakumar Hariharan ◽  
Sivji Ramachandran ◽  
Rajiv Parapurath

Haemophilia ◽  
2014 ◽  
Vol 21 (1) ◽  
pp. 88-94 ◽  
Author(s):  
S. M. Teresa ◽  
M. Marta ◽  
D. B. Emiliano ◽  
F. Mariangela ◽  
P. Raffaele ◽  
...  

2005 ◽  
Vol 38 (9) ◽  
pp. 1475-1479
Author(s):  
Tomoyuki Tagi ◽  
Shojiro Kikuchi ◽  
Tokunari Okayama ◽  
Toshiya Ochiai ◽  
Teruhisa Sonoyama ◽  
...  

2014 ◽  
Vol 1 (1) ◽  
pp. 27-30
Author(s):  
Aysen Turedi Yildirim ◽  
Gokmen Bilgili ◽  
Ozlem Buga ◽  
Ozen Tekin ◽  
Huseyin Gulen

Congenital afibrinogenemia is a rare bleeding disorder. It may be manifested as umblical, mucosal, intramuscular, intraarticular, or life-threatening intracranial bleeding. A third-day-old infant was admitted for umblical cord bleeding, and was found to have a prolonged prothrobin time [PT], and activated partial thromboplastin time [aPTT], and a very low fibrinogen level. He was diagnosed as congenital afibrinogenemia, and reported for the rarity of disease, and discussion of novel therapeutic approaches


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