(Q47720691)

5 February 2018

title

Paroxysmal nocturnal haemoglobinuria clones in patients with myelodysplastic syndromes. (English)

1 reference

5 February 2018

author name string

Iwanaga M

1

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5 February 2018

Furukawa K

2

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5 February 2018

Amenomori T

3

1 reference

5 February 2018

Mori H

4

1 reference

5 February 2018

Nakamura H

5

1 reference

5 February 2018

Fuchigami K

6

1 reference

5 February 2018

Kamihira S

7

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5 February 2018

Nakakuma H

8

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5 February 2018

Tomonaga M

9

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5 February 2018

language of work or name

English

0 references

publication date

1 July 1998

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5 February 2018

British Journal of Haematology

published in

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5 February 2018

volume

102

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5 February 2018

page(s)

465-474

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issue

2

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Epidemiological and etiological aspects of myelodysplastic syndromes

cites work

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.1998.00794.X

Proposals for the classification of the myelodysplastic syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.1998.00794.X

Paroxysmal nocturnal haemoglobinuria (PNH) is caused by somatic mutations in the PIG-A gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.1998.00794.X

STUDIES ON DESTRUCTION OF RED BLOOD CELLS. II. CHRONIC HEMOLYTIC ANEMIA WITH PAROXYSMAL NOCTURNAL HEMOGLOBINURIA: CERTAIN IMMUNOLOGICAL ASPECTS OF THE HEMOLYTIC MECHANISM WITH SPECIAL REFERENCE TO SERUM COMPLEMENT.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.1998.00794.X

A point mutation at codon 13 of the N-ras oncogene in myelodysplastic syndrome

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.1998.00794.X

Polymerase chain reaction--single-strand conformation polymorphism analysis of polymorphism in DPA1 and DPB1 genes: a simple, economical, and rapid method for histocompatibility testing

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.1998.00794.X

Role of phosphatidylinositol-linked proteins in paroxysmal nocturnal hemoglobinuria pathogenesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.1998.00794.X

The cloning of PIG-A, a component in the early step of GPI-anchor biosynthesis

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.1998.00794.X

Abnormalities of PIG-A transcripts in granulocytes from patients with paroxysmal nocturnal hemoglobinuria

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.1998.00794.X

Mechanism of intravascular hemolysis in paroxysmal nocturnal hemoglobinuria (PNH).

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.1998.00794.X

Expression of cryptantigen Th on paroxysmal nocturnal hemoglobinuria erythrocytes in association with a hemolytic exacerbation

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.1998.00794.X

Karyotypic analysis in primary myelodysplastic syndromes

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.1998.00794.X

Trisomy 8 detection in granulomonocytic, erythrocytic and megakaryocytic lineages by chromosomal in situ suppression hybridization in a case of refractory anaemia with ringed sideroblasts complicating the course of paroxysmal nocturnal haemoglobinur

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.1998.00794.X

Evolution of clinical understanding: paroxysmal nocturnal hemoglobinuria as a paradigm.

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.1998.00794.X

Deficiency of the GPI anchor caused by a somatic mutation of the PIG-A gene in paroxysmal nocturnal hemoglobinuria

21 January 2018

1 reference

https://api.crossref.org/works/10.1046%2FJ.1365-2141.1998.00794.X

10.1046/J.1365-2141.1998.00794.X

21 January 2018

Identifiers

DOI

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5 February 2018

PubMed ID

9695961

1 reference

5 February 2018