Splicing mutations: making sense with antisense therapy [PDF]
Tese de mestrado. Biologia (Biologia Molecular e Genética). Universidade de Lisboa, Faculdade de Ciências, 2012Galactose-1-phosphate uridylyltransferase (GALT) transfers a UMP group from UDP-glucose to Gal1P in the second step of the Leloir pathway for ...
Lourenço, Sílvia Pires, 1990-
core
PO07 | Liver transplant in a case of congenital afibrinogenemia
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.
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Frequency of Adverse Maternal and Neonatal Outcomes in Patients with Low Serum Fibrinogen Level and Placental Abruption [PDF]
Objective: To assess frequency of adverse maternal and neonatal outcomes in patients with low serum fibrinogen level and placental abruption.Place and duration: It was held in Gynecology Department Nishtar Hospital Multan from 12 November 2017 to 25 July
Bhatti, Hina Javaid +2 more
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Severe elbow arthropathy in a patient with congenital afibrinogenemia: a case report [PDF]
Brand, B, Jost, B, Reidy, K
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Afibrinogénémie congénitale et contrôle de qualité de la sécrétion du fibrinogène [PDF]
Neerman-Arbez, Marguerite, Vu, Dung
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Liver transplantation as a novel strategy for resolution of congenital afibrinogenemia in a pediatric patient. [PDF]
Corrales-Medina FF +5 more
europepmc +1 more source
P130 | LIVER TRANSPLANT IN CONGENITAL AFIBRINOGENEMIA: A CASE REPORT
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 +12 more
doaj
The role of nucleotide composition in premature termination codon recognition [PDF]
core +1 more source
[Congenital afibrinogenemia: about a case]. [PDF]
Assani K, Karboubi L, Dakhama BS.
europepmc +1 more source

