Congenital macrothrombocytopenia is a heterogeneous disorder in India (Q33432986)

26 July 2017

title

Congenital macrothrombocytopenia is a heterogeneous disorder in India (English)

1 reference

26 July 2017

0 references

Giant platelet disorder

1 reference

based on heuristic

inferred from title

author

Maitreyee Bhattacharyya

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27291889 AND SRC:MED&resulttype=core&format=json

8 June 2020

author name string

S Ali

1

1 reference

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8 June 2020

K Ghosh

2

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8 June 2020

M E Daly

3

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8 June 2020

D J Hampshire

4

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8 June 2020

M Makris

5

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8 June 2020

M Ghosh

6

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8 June 2020

L Mukherjee

7

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8 June 2020

S Shetty

9

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8 June 2020

publication date

13 June 2016

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26 July 2017

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8 June 2020

volume

22

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8 June 2020

issue

4

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8 June 2020

page(s)

570-582

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8 June 2020

1 reference

Stomatocytic haemolysis and macrothrombocytopenia (Mediterranean stomatocytosis/macrothrombocytopenia) is the haematological presentation of phytosterolaemia

21 January 2018

1 reference

Familial dyserythropoietic anaemia and thrombocytopenia due to an inherited mutation in GATA1

21 January 2018

1 reference

Asymptomatic constitutional macrothrombocytopenia among West Bengal blood donors.

21 January 2018

1 reference

Harris syndrome - a geographic perspective.

21 January 2018

1 reference

Role of antiidiotypic antibodies on the clinical course of idiopathic thrombocytopenic purpura.

21 January 2018

1 reference

Prediction of missense mutation functionality depends on both the algorithm and sequence alignment employed

21 January 2018

1 reference

I-Mutant2.0: predicting stability changes upon mutation from the protein sequence or structure

21 January 2018

1 reference

Prediction of protein stability changes for single-site mutations using support vector machines

21 January 2018

1 reference

Thrombolysis in acute ischemic stroke: Experience from a tertiary care centre in India

21 January 2018

1 reference

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

21 January 2018

1 reference

R1933X mutation in the MYH9 gene in May-Hegglin anomaly mimicking idiopathic thrombocytopenic purpura

21 January 2018

1 reference

Clinical and laboratory features of 103 patients from 42 Italian families with inherited thrombocytopenia derived from the monoallelic Ala156Val mutation of GPIbα (Bolzano mutation)

21 January 2018

1 reference

Novel point mutation in a leucine-rich repeat of the GPIbalpha 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

21 January 2018

1 reference

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

21 January 2018

1 reference

Point mutation in a leucine-rich repeat of platelet glycoprotein Ib alpha resulting in the Bernard-Soulier syndrome

21 January 2018

1 reference

Novel heterozygous missense mutation in the platelet glycoprotein Ib beta gene associated with isolated giant platelet disorder

21 January 2018

1 reference

Macrothrombocytopenia in north India: role of automated platelet data in the detection of an under diagnosed entity

21 January 2018

1 reference

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1111/HAE.12917

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:27291889 AND SRC:MED&resulttype=core&format=json

release_35w2wa5xmnbutomvhmybvdkk5e

8 June 2020

Fatcat ID

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Fatcat

https://api.fatcat.wiki/v0/release/35w2wa5xmnbutomvhmybvdkk5e

mapped directly with Wikidata item

24 November 2022

based on heuristic

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