(Q33396732)

26 July 2017

title

Thrombotic events in MYH9 gene-related autosomal macrothrombocytopenias (old May-Hegglin, Sebastian, Fechtner and Epstein syndromes). (English)

1 reference

26 July 2017

1

Antonio Girolami

1 reference

26 July 2017

Silvia Vettore

2

1 reference

26 July 2017

Emanuela Bonamigo

series ordinal

3

1 reference

26 July 2017

Fabrizio Fabris

series ordinal

4

1 reference

26 July 2017

publication date

1 November 2011

1 reference

Journal of Thrombosis and Thrombolysis

26 July 2017

published in

1 reference

26 July 2017

volume

32

1 reference

26 July 2017

issue

4

1 reference

26 July 2017

page(s)

474-477

1 reference

Myocardial infarction and other arterial occlusions in hemophilia a patients. A cardiological evaluation of all 42 cases reported in the literature

26 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1007%2FS11239-011-0623-4

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11239-011-0623-4

Arterial and venous thrombosis in patients with von Willebrand's disease: a critical review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11239-011-0623-4

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11239-011-0623-4

Coronary Thrombosis in a Patient with May-Hegglin Anomaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11239-011-0623-4

Functional compensation of the low platelet count by increased individual platelet size in a patient with May-Hegglin anomaly presenting with acute myocardial infarction

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11239-011-0623-4

Coronary bypass surgery in May-Hegglin anomaly

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11239-011-0623-4

Cerebral infarction in a patient with macrothrombocytopenia with leukocyte inclusions (MTCP, May-Hegglin anomaly/Sebastian syndrome).

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11239-011-0623-4

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11239-011-0623-4

Haematological characteristics of MYH9 disorders due to MYH9 R702 mutations

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11239-011-0623-4

Hereditary macrothrombocytopathia, nephritis and deafness

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11239-011-0623-4

Sebastian platelet syndrome: a new variant of hereditary macrothrombocytopenia with leukocyte inclusions

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11239-011-0623-4

Sebastian syndrome: case report and review of the literature

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11239-011-0623-4

Regulation of platelet biogenesis: insights from the May-Hegglin anomaly and other MYH9-related disorders

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11239-011-0623-4

Recurrent ischemic stroke in a patient with idiopathic thrombocytopenic purpura

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11239-011-0623-4

Primary percutaneous transluminal coronary angioplasty performed for acute myocardial infarction in a patient with idiopathic thrombocytopenic purpura

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11239-011-0623-4

A case report of recurrent vascular access thrombosis in a hemodialysis patient reveals combined acquired and inherited thrombophilia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11239-011-0623-4

Autosomal dominant Alport syndrome caused by a COL4A3 splice site mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11239-011-0623-4

Alport syndrome: a review

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11239-011-0623-4

Recent advances in the understanding and management of MYH9-related inherited thrombocytopenias

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11239-011-0623-4

Venous thrombosis in Glanzmann's thrombasthenia

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11239-011-0623-4

Unexplained recurrent venous thrombosis in a patient withMYH9-related disease

21 January 2018

1 reference

https://api.crossref.org/works/10.1007%2FS11239-011-0623-4

Thrombosis in inherited factor VII deficiency

21 January 2018

1 reference

12 December 2020

Thrombotic complications in patients with hereditary bleeding disorders

1 reference

12 December 2020

Sebastian syndrome: report of the first case in a South American family.

1 reference

12 December 2020

Primary angioplasty in a patient with the May-Hegglin anomaly, a rare heredity thrombocytopenia. A case report and review of the literature

1 reference

12 December 2020

Fechtner syndrome--a variant of Alport's syndrome with leukocyte inclusions and macrothrombocytopenia

1 reference

12 December 2020

Congenital disorders associated with platelet dysfunctions

1 reference

12 December 2020

1 reference

12 December 2020

1 reference

12 December 2020

10.1007/S11239-011-0623-4

Identifiers

DOI

1 reference

26 July 2017

1 reference