The long-term outcome of liver disease-related fibrinogen Aguadilla storage disease in a child is reported
Background & AimsLiver disease in Alagille syndrome is highly variable. Many of the patients pre...
Background & AimsLiver disease in Alagille syndrome is highly variable. Many of the patients pre...
Background & AimsLiver disease in Alagille syndrome is highly variable. Many of the patients pre...
We report hypofibrinogenemia and massive hepatic storage of fibrinogen in a child with cryptogenic c...
We report hypofibrinogenemia and massive hepatic storage of fibrinogen in a child with cryptogenic c...
INTRODUCTION Fibrinogen storage disease (FSD) is characterized by hypofibrinogenemia and hepatic ...
The mutation γ375Arg → Trp (fibrinogen Aguadilla) is one of four mutations (Brescia, Aguadilla, Ange...
p.R375W (Fibrinogen Aguadilla) is one out of seven identified mutations (Brescia, Aguadilla, Angers,...
Hepatic fibrinogen storage disease is a rare autosomal dominant genetic disorder characterized by hy...
p.R375W (Fibrinogen Aguadilla) is one out of seven identified mutations (Brescia, Aguadilla, Angers,...
SUMMARY A total of 123 patients with neonatal liver disease without extrahepatic bile duct obstructi...
Background & AimsLiver disease in Alagille syndrome is highly variable. Many of the patients pre...
Objective: to report two cases of children with type Ia glycogen storage disease compatible with Von...
Background & AimsLiver disease in Alagille syndrome is highly variable. Many of the patients present...
Background & AimsLiver disease in Alagille syndrome is highly variable. Many of the patients pre...
Background & AimsLiver disease in Alagille syndrome is highly variable. Many of the patients pre...
Background & AimsLiver disease in Alagille syndrome is highly variable. Many of the patients pre...
Background & AimsLiver disease in Alagille syndrome is highly variable. Many of the patients pre...
We report hypofibrinogenemia and massive hepatic storage of fibrinogen in a child with cryptogenic c...
We report hypofibrinogenemia and massive hepatic storage of fibrinogen in a child with cryptogenic c...
INTRODUCTION Fibrinogen storage disease (FSD) is characterized by hypofibrinogenemia and hepatic ...
The mutation γ375Arg → Trp (fibrinogen Aguadilla) is one of four mutations (Brescia, Aguadilla, Ange...
p.R375W (Fibrinogen Aguadilla) is one out of seven identified mutations (Brescia, Aguadilla, Angers,...
Hepatic fibrinogen storage disease is a rare autosomal dominant genetic disorder characterized by hy...
p.R375W (Fibrinogen Aguadilla) is one out of seven identified mutations (Brescia, Aguadilla, Angers,...
SUMMARY A total of 123 patients with neonatal liver disease without extrahepatic bile duct obstructi...
Background & AimsLiver disease in Alagille syndrome is highly variable. Many of the patients pre...
Objective: to report two cases of children with type Ia glycogen storage disease compatible with Von...
Background & AimsLiver disease in Alagille syndrome is highly variable. Many of the patients present...
Background & AimsLiver disease in Alagille syndrome is highly variable. Many of the patients pre...
Background & AimsLiver disease in Alagille syndrome is highly variable. Many of the patients pre...
Background & AimsLiver disease in Alagille syndrome is highly variable. Many of the patients pre...
Background & AimsLiver disease in Alagille syndrome is highly variable. Many of the patients pre...
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