Genetic and immunological characterization of fibrinogen inclusion bodies in patients with hepatic fibrinogen storage and liver disease

Annals of the New York Academy of Sciences

Volumn 936, Issue , 2001, Pages 522-525

  Medicina, Daniela ^a   Fabbretti, Giovanna ^a   Brennan, Stephen O ^b   George, Peter M ^b   Kudryk, B O ^c   Callea, Francesco ^a,d  

^a Spedali Civili Brescia   (Italy)

^b Christchurch University   (New Zealand)

^c Blood Transfusion Center   (United States)

^d SPEDALI CIVILI   (Italy)

Author keywords

Fibrinogen; Hypofibrinogenemia; Immunohistochemistry; Liver disease

Indexed keywords

FIBRINOGEN; MONOCLONAL ANTIBODY; POLYCLONAL ANTIBODY;

CELL INCLUSION; CONFERENCE PAPER; GENETIC ANALYSIS; HUMAN; HYPOFIBRINOGENEMIA; IMMUNOASSAY; IMMUNOHISTOCHEMISTRY; LIVER DISEASE; PATHOGENESIS; PHENOTYPE; POINT MUTATION; STORAGE DISEASE;

EID: 0034968658     PISSN: 00778923     EISSN: None     Source Type: Book Series    
DOI: 10.1111/j.1749-6632.2001.tb03538.x     Document Type: Conference Paper

References (6)

1. Hepatic endoplasmic reticulum storage diseases
2. Fibrinogen Brescia: Hepatic endoplasmic reticulum storage and hypofibrinogenemia due to a 284 Gly-Arg mutation
3. Himmunohistochemical characterization of fibrin(ogen)-related antigens in human tissues using monoclonal antibodies
4. Fibrinogen-fibrin: Preparation and use of monoclonal antibodies as diagnostics
5. Conformational disease
6. Hereditary hypofibrinogenaemia with hepatic storage of fibrinogen: A new endoplasmic reticulum storage disease