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Associated prothrombotic conditions are probably responsible for the occurrence of thrombosis in almost all patients with congenital FVII deficiency. Critical review of the literature

Journal of thrombosis and thrombolysis, 2010-08, Vol.30 (2), p.172-178

2010

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Arterial and venous thrombosis in rare congenital bleeding disorders: a critical review

Haemophilia : the official journal of the World Federation of Hemophilia, 2006-07, Vol.12 (4), p.345-351

2006

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Rectus muscle sheath haematoma in a patient with congenital FX deficiency and in another with congenital FVII deficiency

Haemophilia : the official journal of the World Federation of Hemophilia, 2010-01, Vol.16 (1), p.182-185

2010

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About the rarity of haemoptysis in congenital bleeding disorders. A report of five cases

Haemophilia : the official journal of the World Federation of Hemophilia, 2009-05, Vol.15 (3), p.825-827

2009

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Congenital FX deficiency combined with other clotting defects or with other abnormalities: a critical evaluation of the literature

Haemophilia : the official journal of the World Federation of Hemophilia, 2008-03, Vol.14 (2), p.323-328

2008

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Pregnancy and oral contraceptives in factor V deficiency: a study of 22 patients (five homozygotes and 17 heterozygotes) and review of the literature

Haemophilia : the official journal of the World Federation of Hemophilia, 2005-01, Vol.11 (1), p.26-30

2005

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Risk factors for thrombosis in patients with immune mediated heparin‐induced thrombocytopenia

Journal of internal medicine, 2002-08, Vol.252 (2), p.149-154

2002

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Unexplained Discrepancies in the Activity—Antigen Ratio in Congenital FX Deficiencies With Defects in the Catalytic Domain

Clinical and applied thrombosis/hemostasis, 2009-12, Vol.15 (6), p.621-627

2009

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Congenital Bleeding Disorders of the Vitamin K‐Dependent Clotting Factors

Vitamin K, 2008, Vol.78, p.281-374

2008

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Previous thrombosis-free pregnancies are no guarantee that subsequent oral contraception may also remain asymptomatic

Journal of thrombosis and thrombolysis, 2008-08, Vol.26 (1), p.62-63

2008

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Hemospermia in Patients with Congenital Coagulation Disorders: A Study of Three Cases

Acta haematologica, 2009-01, Vol.121 (1), p.42-46

2009

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Novel point mutation in a leucine-rich repeat of the GPIb{alpha} chain of the platelet von Willebrand factor receptor, GPIb/IX/V, resulting in an inherited dominant form of Bernard-Soulier syndrome affecting two unrelated families: the N41H variant

Haematologica (Roma), 2008-09, Vol.93 (11), p.1743-1747

2008

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Heavy chain myosin 9-related disease (MYH9 -RD): neutrophil inclusions of myosin-9 as a pathognomonic sign of the disorder

Thrombosis and haemostasis, 2010-04, Vol.103 (4), p.826-832

2010

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The management of feto-maternal alloimmune thrombocytopenia: Report of three cases

The journal of maternal-fetal & neonatal medicine, 2006-08, Vol.19 (8), p.517-520

2006

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Non-catheter associated venous thrombosis in hemophilia A and B. A critical review of all reported cases

Journal of thrombosis and thrombolysis, 2006-06, Vol.21 (3), p.279-284

2006

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Indirect study of thrombopoiesis(TPO, reticulated platelets, glycocalicin)in patients with hereditary macrothrombocytopenia

European journal of haematology, 2000-03, Vol.64 (3), p.151-156

2000

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Platelet-associated autoantibodies as detected by a solid-phase modified antigen capture ELISA test (MACE) are a useful prognostic factor in idiopathic thrombocytopenic purpura

Blood, 2004-06, Vol.103 (12), p.4562-4564

2004

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Intriguing outcome of JAK2V617F mutation seen in a patient with MYH9-related hereditary macrothrombocytopenia

Thrombosis and haemostasis, 2010-10, Vol.104 (4), p.858-859

2010

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A A386G biallelic GPIb gene mutation with anomalous behavior: a new mechanism suggested for Bernard-Soulier syndrome pathogenesis

Haematologica (Roma), 2011-12, Vol.96 (12), p.1878-1882

2011

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CONGENITAL BLEEDING DISORDERS OF THE VITAMIN K-DEPENDENT CLOTTING FACTORS: Vitamin K

Vitamins and hormones, 2008, Vol.78, p.281-374

2008

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Attempt to improve the diagnosis of immune thrombocytopenia by combined use of two different platelet autoantibodies assays (PAIgG and MACE)

Haematologica (Roma), 2002-10, Vol.87 (10), p.1046

2002

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Closed versus open technique in the management of labyrinthine fistulae

The American journal of otology (New York, N.Y.), 1988-11, Vol.9 (6), p.470

1988

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Management of the labyrinthine fistula in cholesteatoma surgery

O.R.L. Journal for oto-rhino-laryngology and its related specialties, 1984-01, Vol.46 (3), p.165-172

1984

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Residual and recurrent cholesteatoma in closed tympanoplasty

The American journal of otology (New York, N.Y.), 1984-04, Vol.5 (4), p.277

1984

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Autologous fitted incus versus Plastipore PORP in ossicular chain reconstruction

Journal of laryngology and otology, 1985-02, Vol.99 (2), p.137-141

1985

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Associated prothrombotic conditions are probably responsible for the occurrence of thrombosis in almost all patients with congenital FVII deficiency. Critical review of the literature

Arterial and venous thrombosis in rare congenital bleeding disorders: a critical review

Rectus muscle sheath haematoma in a patient with congenital FX deficiency and in another with congenital FVII deficiency

About the rarity of haemoptysis in congenital bleeding disorders. A report of five cases

Congenital FX deficiency combined with other clotting defects or with other abnormalities: a critical evaluation of the literature

Pregnancy and oral contraceptives in factor V deficiency: a study of 22 patients (five homozygotes and 17 heterozygotes) and review of the literature

Risk factors for thrombosis in patients with immune mediated heparin‐induced thrombocytopenia

Unexplained Discrepancies in the Activity—Antigen Ratio in Congenital FX Deficiencies With Defects in the Catalytic Domain

Congenital Bleeding Disorders of the Vitamin K‐Dependent Clotting Factors

Previous thrombosis-free pregnancies are no guarantee that subsequent oral contraception may also remain asymptomatic

Hemospermia in Patients with Congenital Coagulation Disorders: A Study of Three Cases

Novel point mutation in a leucine-rich repeat of the GPIb{alpha} chain of the platelet von Willebrand factor receptor, GPIb/IX/V, resulting in an inherited dominant form of Bernard-Soulier syndrome affecting two unrelated families: the N41H variant

Heavy chain myosin 9-related disease (MYH9 -RD): neutrophil inclusions of myosin-9 as a pathognomonic sign of the disorder

The management of feto-maternal alloimmune thrombocytopenia: Report of three cases

Non-catheter associated venous thrombosis in hemophilia A and B. A critical review of all reported cases

Indirect study of thrombopoiesis(TPO, reticulated platelets, glycocalicin)in patients with hereditary macrothrombocytopenia

Platelet-associated autoantibodies as detected by a solid-phase modified antigen capture ELISA test (MACE) are a useful prognostic factor in idiopathic thrombocytopenic purpura

Intriguing outcome of JAK2V617F mutation seen in a patient with MYH9-related hereditary macrothrombocytopenia

A A386G biallelic GPIb gene mutation with anomalous behavior: a new mechanism suggested for Bernard-Soulier syndrome pathogenesis

CONGENITAL BLEEDING DISORDERS OF THE VITAMIN K-DEPENDENT CLOTTING FACTORS: Vitamin K

Attempt to improve the diagnosis of immune thrombocytopenia by combined use of two different platelet autoantibodies assays (PAIgG and MACE)

Closed versus open technique in the management of labyrinthine fistulae

Management of the labyrinthine fistula in cholesteatoma surgery

Residual and recurrent cholesteatoma in closed tympanoplasty

Autologous fitted incus versus Plastipore PORP in ossicular chain reconstruction

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