Results 91 to 100 of about 239,927 (172)

P130 | LIVER TRANSPLANT IN CONGENITAL AFIBRINOGENEMIA: A CASE REPORT

Haematologica
Background: Fibrinogen (FBG) is involved in the final steps of coagulation as a precursor of fibrin monomers. Inherited FBG disorders are generally classified as quantitative or qualitative. Quantitative disorders include afibrinogenemia (aFBG), which is
G. Murante, S. Bergonzi, C. Sella, F. Valeri, C. Dainese, A. Valpreda, R. Pastorino, R. Romagnoli, D. Patrono, D. Cussa, S. Martini, B. Bruno, and A. Borchiellini   +12 more
doaj  

Congenital Hypofibrinogenemia or Afibrinogenemia? A Diagnostic Dilemma in Neonatal Period/ Konjenital Hipofibrinojenemi veya Afibrinojenemi? Yenidog an Do neminde Tanısal Bir İ kilem

, 2020
Congenital Afibrinogenemia/Hypofibrinogenemia (OMIM, 202400) (CA/CH) is one of the rare causes of hereditary hemostasis and is inherited in an autosomal-recessive.
Tekin, Ayşe Neslihan, Sürmeli Onay, Özge, Özdemir, Zeynep Canan, Yücel, Mehmet, Ceylaner, Serdar, Bör, Özcan   +5 more
core  

Congenital Afibrinogenaemia [PDF]

BMJ, 1951
C C, DE SILVA, R S, THANABALASUNDARAM
openaire   +2 more sources

Perianal Crohn Disease in a Patient With Congenital Afibrinogenemia: A Multidisciplinary Therapeutic Management Challenge. [PDF]

Cureus
Bouziane A, Elmqaddam O, Koulali H, Zazour A, Ismaili Z, Kharrasse G.   +5 more
europepmc   +1 more source

[Congenital afibrinogenemia: about a case]. [PDF]

Pan Afr Med J, 2016
Assani K, Karboubi L, Dakhama BS.
europepmc   +1 more source

Congenital Afibrinogenemia With Coexisting Factor V Leiden Mutation Complicated by Budd-Chiari Syndrome: A Case Report. [PDF]

Cureus
Boutari RA, Hsayan FI, Mallah F, Diab M.
europepmc   +1 more source

Spontaneous splenic rupture in a patient with congenital afibrinogenemia. [PDF]

Turk Pediatri Ars, 2014
Arcagök BC, Özdemir N, Tekin A, Özcan R, Eliçevik M, Şenyüz OF, Çam H, Celkan T.   +7 more
europepmc   +1 more source

Recurrent massive haemoperitoneum associated with ruptured corpus luteum in women with congenital afibrinogenemia; case report. [PDF]

Turk J Obstet Gynecol, 2014
Özdemir Ö, Sarı ME, Kurt A, Şen E, Atalay CR.   +4 more
europepmc   +1 more source

Quantitative fibrinogen disorders: A retrospective study from a tertiary care centre in India. [PDF]

Indian J Med Res
Jain M, Shukla H, Kushwaha R, Mishra S, Yadav G, Verma N.   +5 more
europepmc   +1 more source

Thrombosis in rare bleeding disorders: a bleeding phenotype does not fully preclude thrombotic risk- frequency, clinical contexts, and management in a large Iranian cohort. [PDF]

Thromb J
Naderi M, Yaghoubi S, Rajaee S, Mirzaei I, Tabibian S.   +4 more
europepmc   +1 more source