(Q45856242)

17 December 2017

title

Hemophilia B+ or BM. first case reported in Italy (English)

1 reference

22 February 2023

0 references

0 references

0 references

A. Girolami

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4700225

22 February 2023

G. Cella

series ordinal

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4700225

22 February 2023

G. Bareggi

series ordinal

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4700225

22 February 2023

language of work or name

English

1 reference

National Center for Biotechnology Information

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/esummary.fcgi?db=pubmed&retmode=json&id=4700225

22 February 2023

publication date

1 April 1973

1 reference

17 December 2017

full work available at URL

http://link.springer.com/content/pdf/10.1007/BF01631791.pdf

file format

Portable Document Format

1 reference

http://link.springer.com/article/10.1007/BF01631791/fulltext.html

22 February 2023

1 reference

http://link.springer.com/content/pdf/10.1007/BF01631791

22 February 2023

1 reference

22 February 2023

1 reference

17 December 2017

volume

26

1 reference

17 December 2017

issue

4

1 reference

17 December 2017

page(s)

268-279

1 reference

17 December 2017

1 reference

12 December 2020

An investigation of three patients with Christmas disease due to an abnormal type of factor IX.

1 reference

12 December 2020

Variant of factor IX deficiency in female with 45, X Turner's syndrome

1 reference

12 December 2020

A study of the carrier state for plasma thromboplastin component (PTC, Christmas factor) deficiency, utilizing a new assay procedure.

1 reference

12 December 2020

The Genetic Heterogeneity of Hemophilia B

1 reference

12 December 2020

Genetic variants of hemophilia B: detection by means of a specific PTC inhibitor

1 reference

12 December 2020

Investigation of a haemorrhagic disease due to beta-prothromboplastin deficiency complicated by a specific inhibitor of thromboplastin formation

1 reference

12 December 2020

Another Genetic Variant of Haemophilia B: Haemophilia B Leyden

1 reference

12 December 2020

A ‘New’ Congenital Haemorrhagic Condition due to the Presence of an Abnormal Factor X (Factor X Friuli): Study of a Large Kindred

1 reference

12 December 2020

Haemophilia Bm: a new type of factor-IX deficiency

1 reference

12 December 2020

Congenital hypoprothrombinemia. Case report

1 reference

12 December 2020

Identifiers

DOI

10.1007/BF01631791

1 reference

17 December 2017

1 reference

17 December 2017