Sebastian platelet syndrome: a new variant of hereditary macrothrombocytopenia with leukocyte inclusions (Q33396285)

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

Statements

scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

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

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

Giant platelet disorder

1 reference

based on heuristic

inferred from title

author name string

A Greinacher

1

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

H K Nieuwenhuis

2

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

J G White

3

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

publication date

1 November 1990

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

61

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

5

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

282-288

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

An improved method for the extraction of endogenous platelet serotonin

1 reference

https://pubmed.ncbi.nlm.nih.gov/2176899

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

ULTRASTRUCTURAL STUDIES OF THE MAY-HEGGLIN ANOMALY

1 reference

https://pubmed.ncbi.nlm.nih.gov/2176899

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Congenital macrothrombocytopenia, leucocyte inclusions, deafness and proteinuria: functional and electron microscopic observations on platelets and megakaryocytes

1 reference

https://pubmed.ncbi.nlm.nih.gov/2176899

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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

1 reference

https://pubmed.ncbi.nlm.nih.gov/2176899

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The inclusions of the May-Hegglin anomaly and Döhle bodies of infection: an ultrastructural comparison.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2176899

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Hereditary Nephritis Associated with May-Hegglin Anomaly

1 reference

https://pubmed.ncbi.nlm.nih.gov/2176899

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

1 reference

https://pubmed.ncbi.nlm.nih.gov/2176899

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Determination of ATP and ADP in blood platelets: a modification of the firefly luciferase assay for plasma

1 reference

https://pubmed.ncbi.nlm.nih.gov/2176899

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

HEREDITARY FAMILIAL CONGENITAL HAEMORRHAGIC NEPHRITIS.

1 reference

https://pubmed.ncbi.nlm.nih.gov/2176899

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Identifiers

10.1007/BF01732878

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

26 July 2017

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