(Q33341716)

25 July 2017

title

Immunocytochemistry for the heavy chain of the non-muscle myosin IIA as a diagnostic tool for MYH9-related disorders (English)

1 reference

25 July 2017

Alessandro Pecci

1

0 references

Anna Savoia

Anna Savoia

4

0 references

Marco Seri

Marco Seri

5

0 references

Gian Marco Ghiggeri

Gian Marco Ghiggeri

6

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Nicola Bizzaro

9

Nicola Bizzaro

1 reference

25 July 2017

Patrizia Noris

2

1 reference

25 July 2017

Rosangela Invernizzi

3

1 reference

25 July 2017

Saverio Sartore

7

1 reference

25 July 2017

Simone Gangarossa

8

1 reference

25 July 2017

Carlo L Balduini

10

1 reference

25 July 2017

language of work or name

English

0 references

publication date

1 April 2002

1 reference

British Journal of Haematology

25 July 2017

number of pages

4

1 reference

based on heuristic

inferred from page(s)

published in

1 reference

25 July 2017

volume

117

1 reference

25 July 2017

issue

1

1 reference

25 July 2017

page(s)

164-167

1 reference

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

25 July 2017

cites work

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2002.03385.X

Mutations in the NMMHC-A gene cause autosomal dominant macrothrombocytopenia with leukocyte inclusions (May-Hegglin anomaly/Sebastian syndrome).

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2002.03385.X

The gene for May-Hegglin anomaly localizes to a <1-Mb region on chromosome 22q12.3-13.1.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2002.03385.X

Inherited giant platelet disorders. Classification and literature review

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2002.03385.X

Thrombocytopenia, giant platelets, and leukocyte inclusion bodies (May-Hegglin anomaly): clinical and laboratory findings.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2002.03385.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2002.03385.X

Myosins: a diverse superfamily

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2002.03385.X

Mutations in MYH9 result in the May-Hegglin anomaly, and Fechtner and Sebastian syndromes. The May-Heggllin/Fechtner Syndrome Consortium

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2002.03385.X

Genetic linkage of autosomal-dominant Alport syndrome with leukocyte inclusions and macrothrombocytopenia (Fechtner syndrome) to chromosome 22q11-13

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.2002.03385.X

10.1046/J.1365-2141.2002.03385.X

21 January 2018

Identifiers

DOI

1 reference

25 July 2017

1 reference