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Thromboembolism in patients with congenital afibrinogenaemia. Long-term observational data and systematic review

Thrombosis and haemostasis, 2016-10, Vol.116 (4), p.722

2016

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Efficacy and safety of fibrinogen concentrate for on‐demand treatment of bleeding and surgical prophylaxis in paediatric patients with congenital fibrinogen deficiency

Haemophilia : the official journal of the World Federation of Hemophilia, 2021-03, Vol.27 (2), p.283-292

2021

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Obstetrical and postpartum complications in women with hereditary fibrinogen disorders: A systematic literature review

Haemophilia : the official journal of the World Federation of Hemophilia, 2019-09, Vol.25 (5), p.747-754

2019

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Management of congenital quantitative fibrinogen disorders: a Delphi consensus

Haemophilia : the official journal of the World Federation of Hemophilia, 2016-11, Vol.22 (6), p.898-905

2016

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High incidence of intracranial haemorrhage in Egyptian children with congenital afibrinogenaemia

Haemophilia : the official journal of the World Federation of Hemophilia, 2023-03, Vol.29 (2), p.572-577

2023

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Can the phenotype of inherited fibrinogen disorders be predicted?

Haemophilia : the official journal of the World Federation of Hemophilia, 2016-09, Vol.22 (5), p.667-675

2016

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Clinical and molecular characterisation of 21 patients affected by quantitative fibrinogen deficiency

Thrombosis and haemostasis, 2015-03, Vol.113 (3), p.567

2015

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Acquired hypofibrinogenemia: current perspectives

Journal of Blood Medicine, 2016-01, Vol.7, p.217-225

2016

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Bone cysts in patients with afibrinogenaemia: a literature review and two new cases

Haemophilia : the official journal of the World Federation of Hemophilia, 2014-03, Vol.20 (2), p.244-248

2014

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Rare coagulation deficiencies

Haemophilia : the official journal of the World Federation of Hemophilia, 2002-05, Vol.8 (3), p.308-321

2002

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Bleeding and thrombosis in 55 patients with inherited afibrinogenaemia

British journal of haematology, 1999-10, Vol.107 (1), p.204-206

1999

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Efficacy and tolerability of a pasteurised human fibrinogen concentrate in patients with congenital fibrinogen deficiency

Transfusion and apheresis science, 2005-06, Vol.32 (3), p.247-253

2005

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A novel fibrinogen B beta chain frameshift mutation causes congenital afibrinogenaemia

Thrombosis and haemostasis, 2013-07, Vol.110 (1), p.76

2013

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The molecular mechanisms of congenital hypofibrinogenaemia

Cellular and molecular life sciences : CMLS, 2004-06, Vol.61 (12), p.1427-1438

2004

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Pharmacokinetic properties of a pasteurised fibrinogen concentrate

Transfusion and apheresis science, 2005-06, Vol.32 (3), p.239-246

2005

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Pseudo‐exon activation caused by a deep‐intronic mutation in the fibrinogen γ‐chain gene as a novel mechanism for congenital afibrinogenaemia

British journal of haematology, 2007-10, Vol.139 (1), p.128-132

2007

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Prenatal and peripartum management of congenital afibrinogenaemia

British journal of haematology, 2000-05, Vol.109 (2), p.364-366

2000

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Delayed inflammatory responses to endotoxin in fibrinogen-deficient mice

The Journal of pathology, 2006-11, Vol.210 (3), p.325-333

2006

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Management of acute bleeding in a patient with congenital afibrinogenaemia

Haemophilia : the official journal of the World Federation of Hemophilia, 2006-11, Vol.12 (6), p.676-678

2006

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Identification of three FGA mutations in two Chinese families with congenital afibrinogenaemia

Haemophilia : the official journal of the World Federation of Hemophilia, 2006-11, Vol.12 (6), p.615-620

2006

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Afibrinogenaemia: a rare cause of young myocardial infarct

Singapore medical journal, 2008-04, Vol.49 (4), p.e104-e106

2008

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Congenital afibrinogenaemia in a newborn infant due to a novel mutation in the fibrinogen aα gene

British journal of haematology, 2002-10, Vol.119 (1), p.282-283

2002

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Spontaneous intracranial bleeding in two patients with congenital afibrinogenaemia and the role of replacement therapy

Haemophilia : the official journal of the World Federation of Hemophilia, 2000-11, Vol.6 (6), p.705-708

2000

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A novel nonsense mutation in the FGA gene in a Chinese family with congenital afibrinogenaemia

Blood coagulation & fibrinolysis, 2005-04, Vol.16 (3), p.221-226

2005

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Digital skin necrosis in congenital afibrinogenaemia associated with hepatitis C virus infection, mixed cryoglobulinaemia and anticardiolipin antibodies

Acta dermato-venereologica, 2005, Vol.85 (1), p.56-59

2005

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Thromboembolism in patients with congenital afibrinogenaemia. Long-term observational data and systematic review

Efficacy and safety of fibrinogen concentrate for on‐demand treatment of bleeding and surgical prophylaxis in paediatric patients with congenital fibrinogen deficiency

Obstetrical and postpartum complications in women with hereditary fibrinogen disorders: A systematic literature review

Management of congenital quantitative fibrinogen disorders: a Delphi consensus

High incidence of intracranial haemorrhage in Egyptian children with congenital afibrinogenaemia

Can the phenotype of inherited fibrinogen disorders be predicted?

Clinical and molecular characterisation of 21 patients affected by quantitative fibrinogen deficiency

Acquired hypofibrinogenemia: current perspectives

Bone cysts in patients with afibrinogenaemia: a literature review and two new cases

Rare coagulation deficiencies

Bleeding and thrombosis in 55 patients with inherited afibrinogenaemia

Efficacy and tolerability of a pasteurised human fibrinogen concentrate in patients with congenital fibrinogen deficiency

A novel fibrinogen B beta chain frameshift mutation causes congenital afibrinogenaemia

The molecular mechanisms of congenital hypofibrinogenaemia

Pharmacokinetic properties of a pasteurised fibrinogen concentrate

Pseudo‐exon activation caused by a deep‐intronic mutation in the fibrinogen γ‐chain gene as a novel mechanism for congenital afibrinogenaemia

Prenatal and peripartum management of congenital afibrinogenaemia

Delayed inflammatory responses to endotoxin in fibrinogen-deficient mice

Management of acute bleeding in a patient with congenital afibrinogenaemia

Identification of three FGA mutations in two Chinese families with congenital afibrinogenaemia

Afibrinogenaemia: a rare cause of young myocardial infarct

Congenital afibrinogenaemia in a newborn infant due to a novel mutation in the fibrinogen aα gene

Spontaneous intracranial bleeding in two patients with congenital afibrinogenaemia and the role of replacement therapy

A novel nonsense mutation in the FGA gene in a Chinese family with congenital afibrinogenaemia

Digital skin necrosis in congenital afibrinogenaemia associated with hepatitis C virus infection, mixed cryoglobulinaemia and anticardiolipin antibodies

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