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Laboratory monitoring of P2Y12 inhibitors: communication from the SSC of the ISTH

Journal of thrombosis and haemostasis, 2018-11, Vol.16 (11), p.2341-2346

2018

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Innovation in the field of thrombocytopenias: achievements since the beginning of the century and promises for the future

Haematologica (Roma), 2016-01, Vol.101 (1), p.2-4

2016

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Clinical and genetic aspects of Bernard-Soulier syndrome: searching for genotype/phenotype correlations

Haematologica (Roma), 2011-03, Vol.96 (3), p.417-423

2011

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Proplatelet formation in heterozygous Bernard‐Soulier syndrome type Bolzano

Journal of thrombosis and haemostasis, 2009-03, Vol.7 (3), p.478-484

2009

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β‐1 tubulin R307H SNP alters microtubule dynamics and affects severity of a hereditary thrombocytopenia

Journal of thrombosis and haemostasis, 2015-04, Vol.13 (4), p.651-659

2015

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Platelet size distinguishes between inherited macrothrombocytopenias and immune thrombocytopenia

Journal of thrombosis and haemostasis, 2009-12, Vol.7 (12), p.2131-2136

2009

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Inherited thrombocytopenias: the evolving spectrum

Hämostaseologie, 2012, Vol.32 (4), p.259-270

2012

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International collaboration as a tool for diagnosis of patients with inherited thrombocytopenia in the setting of a developing country

Journal of thrombosis and haemostasis, 2012-08, Vol.10 (8), p.1653-1661

2012

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Platelet count and aging

Haematologica (Roma), 2014-06, Vol.99 (6), p.953-955

2014

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Congenital amegakaryocytic thrombocytopenia: clinical and biological consequences of five novel mutations

Haematologica (Roma), 2007-09, Vol.92 (9), p.1186-1193

2007

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Safety and efficacy of low‐dose fondaparinux (1.5 mg) for the prevention of venous thromboembolism in acutely ill medical patients with renal impairment: the FONDAIR study

Journal of thrombosis and haemostasis, 2012-11, Vol.10 (11), p.2291-2297

2012

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Lipid levels in the second year of life among HIV-infected and HIV-exposed uninfected Latin American children

AIDS (London), 2012-01, Vol.26 (2), p.235-240

2012

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Altered cytoskeleton organization in platelets from patients with MYH9‐related disease

Journal of thrombosis and haemostasis, 2005-05, Vol.3 (5), p.1026-1035

2005

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Inherited thrombocytopenias in the era of personalized medicine

Haematologica (Roma), 2015-02, Vol.100 (2), p.145-148

2015

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Personalized reference intervals for platelet count reduce the number of subjects with unexplained thrombocytopenia

Haematologica (Roma), 2015-09, Vol.100 (9), p.e338-e340

2015

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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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Relationship between size and thiazole orange fluorescence of platelets in patients undergoing high‐dose chemotherapy

British journal of haematology, 1999-07, Vol.106 (1), p.202-207

1999

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Factors influencing post-transfusional platelet increment in pediatric patients given hematopoietic stem cell transplantation

Leukemia, 2001-12, Vol.15 (12), p.1885-1891

2001

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Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes

Nature genetics, 2000-09, Vol.26 (1), p.103-105

Syndrome Consortium, The May-Hegglin/Fechtner

2000

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Donor–recipient incompatibility at CD31‐codon 563 is a major risk factor for acute graft‐versus‐host disease after allogeneic bone marrow transplantation from a human leucocyte antigen‐matched donor

British journal of haematology, 2001-09, Vol.114 (4), p.951-953

2001

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Autosomal dominant macrothrombocytopenia in Italy is most frequently a type of heterozygous Bernard-Soulier syndrome

Blood, 2001-03, Vol.97 (5), p.1330-1335

2001

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Platelet-Independent defect in hemostasis associated with sirolimus use

Transplantation proceedings, 2004-04, Vol.36 (3), p.700-702

2004

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Max(a), a new low-frequency platelet-specific antigen localized on glycoprotein IIb, is associated with neonatal alloimmune thrombocytopenia

Blood, 1995-08, Vol.86 (3), p.1019-1026

1995

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Incompatibility for CD31 and human platelet antigens and acute graft‐versus‐host disease after bone marrow transplantation

British journal of haematology, 1999-09, Vol.106 (3), p.723-729

1999

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Genetics, clinical and pathological features of glomerulonephrites associated with mutations of nonmuscle myosin IIA (Fechtner syndrome)

American journal of kidney diseases, 2003-01, Vol.41 (1), p.95-104

2003

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Laboratory monitoring of P2Y12 inhibitors: communication from the SSC of the ISTH

Innovation in the field of thrombocytopenias: achievements since the beginning of the century and promises for the future

Clinical and genetic aspects of Bernard-Soulier syndrome: searching for genotype/phenotype correlations

Proplatelet formation in heterozygous Bernard‐Soulier syndrome type Bolzano

β‐1 tubulin R307H SNP alters microtubule dynamics and affects severity of a hereditary thrombocytopenia

Platelet size distinguishes between inherited macrothrombocytopenias and immune thrombocytopenia

Inherited thrombocytopenias: the evolving spectrum

International collaboration as a tool for diagnosis of patients with inherited thrombocytopenia in the setting of a developing country

Platelet count and aging

Congenital amegakaryocytic thrombocytopenia: clinical and biological consequences of five novel mutations

Safety and efficacy of low‐dose fondaparinux (1.5 mg) for the prevention of venous thromboembolism in acutely ill medical patients with renal impairment: the FONDAIR study

Lipid levels in the second year of life among HIV-infected and HIV-exposed uninfected Latin American children

Altered cytoskeleton organization in platelets from patients with MYH9‐related disease

Inherited thrombocytopenias in the era of personalized medicine

Personalized reference intervals for platelet count reduce the number of subjects with unexplained thrombocytopenia

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

Relationship between size and thiazole orange fluorescence of platelets in patients undergoing high‐dose chemotherapy

Factors influencing post-transfusional platelet increment in pediatric patients given hematopoietic stem cell transplantation

Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes

Donor–recipient incompatibility at CD31‐codon 563 is a major risk factor for acute graft‐versus‐host disease after allogeneic bone marrow transplantation from a human leucocyte antigen‐matched donor

Autosomal dominant macrothrombocytopenia in Italy is most frequently a type of heterozygous Bernard-Soulier syndrome

Platelet-Independent defect in hemostasis associated with sirolimus use

Max(a), a new low-frequency platelet-specific antigen localized on glycoprotein IIb, is associated with neonatal alloimmune thrombocytopenia

Incompatibility for CD31 and human platelet antigens and acute graft‐versus‐host disease after bone marrow transplantation

Genetics, clinical and pathological features of glomerulonephrites associated with mutations of nonmuscle myosin IIA (Fechtner syndrome)

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