(Q53743719)

18 May 2018

reason for preferred rank

title

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

1 reference

https://api.crossref.org/works/10.1111/J.1365-2141.1970.TB01615.X

25 March 2023

A "new" congenital haemorrhagic condition due to the presence of an abnormal factor X (factor X Friuli): study of a large kindred (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4989292

coagulation factor x human

25 March 2023

main subject

1 reference

1

Girolami A

1 reference

18 May 2018

author name string

G. Molaro

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4989292

25 March 2023

M. Lazzarin

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4989292

25 March 2023

R. Scarpa

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4989292

25 March 2023

A. Brunetti

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A4989292

25 March 2023

language of work or name

English

0 references

publication date

1 August 1970

1 reference

18 May 2018

full work available at URL

https://api.wiley.com/onlinelibrary/tdm/v1/articles/10.1111%2Fj.1365-2141.1970.tb01615.x

1 reference

https://api.crossref.org/works/10.1111/J.1365-2141.1970.TB01615.X

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1365-2141.1970.tb01615.x/fullpdf

25 March 2023

1 reference

https://api.crossref.org/works/10.1111/J.1365-2141.1970.TB01615.X

British Journal of Haematology

25 March 2023

published in

1 reference

18 May 2018

volume

19

1 reference

18 May 2018

issue

2

1 reference

18 May 2018

page(s)

179-192

1 reference

18 May 2018

A new inherited coagulation disorder caused by an abnormal fibrinogen ('fibrinogen Baltimore').

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.1970.TB01615.X

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

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.1970.TB01615.X

Haemophilia Bm: a new type of factor-IX deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2141.1970.TB01615.X

21 January 2018

1

326

2873

Ascari R.

1964

1 reference

https://api.crossref.org/works/10.1111/J.1365-2141.1970.TB01615.X

Schweizerische medizinische Wochenschrift

25 March 2023

2

87

1221

Bachmann F.

1957

1 reference

https://api.crossref.org/works/10.1111/J.1365-2141.1970.TB01615.X

25 March 2023

3

2

24

Bachmann F.

1958

1 reference

https://api.crossref.org/works/10.1111/J.1365-2141.1970.TB01615.X

Morphology and enumeration of human blood platelets

25 March 2023

6

1 reference

https://api.crossref.org/works/10.1111/J.1365-2141.1970.TB01615.X

Fibrinolytic and proteolytic activity of a human plasminogen, prepared from fraction III of human plasma

25 March 2023

12

1 reference

https://api.crossref.org/works/10.1111/J.1365-2141.1970.TB01615.X

The specific assay of Prower-Stuart factor and factor VII

25 March 2023

13

1 reference

https://api.crossref.org/works/10.1111/J.1365-2141.1970.TB01615.X

Il Policlinico. Sezione medica

25 March 2023

16

72

93

Girolami A.

1965

1 reference

https://api.crossref.org/works/10.1111/J.1365-2141.1970.TB01615.X

Congenital haemorrhagic condition similar but not identical to factor X deficiency. A haemorrhagic state due to an abnormal factor X?

25 March 2023

17

1 reference

https://api.crossref.org/works/10.1111/J.1365-2141.1970.TB01615.X

Stuart clotting defect. II. Genetic aspects of a new hemorrhagic state

25 March 2023

20

1 reference

https://api.crossref.org/works/10.1111/J.1365-2141.1970.TB01615.X

25 March 2023

21

7

215

Hardisty R.M.

1962

1 reference

https://api.crossref.org/works/10.1111/J.1365-2141.1970.TB01615.X

A rapid screening test for disorders of thromboplastin generation

25 March 2023

22

1 reference

https://api.crossref.org/works/10.1111/J.1365-2141.1970.TB01615.X

Stuart clotting defect. I. Segregation of an hereditary hemorrhagic state from the heterogeneous group heretofore called stable factor (SPCA, proconvertin, factor VII) deficiency

25 March 2023

26

1 reference

https://api.crossref.org/works/10.1111/J.1365-2141.1970.TB01615.X

THE INHERITANCE OF STUART DISEASE: INVESTIGATION OF A FAMILY WITH FACTOR X DEFICIENCY

25 March 2023

30

1 reference

https://api.crossref.org/works/10.1111/J.1365-2141.1970.TB01615.X

25 March 2023

33

173

Menache D.

1964

1 reference

https://api.crossref.org/works/10.1111/J.1365-2141.1970.TB01615.X

[Familial deficiency of factor X]

25 March 2023

35

1 reference

https://api.crossref.org/works/10.1111/J.1365-2141.1970.TB01615.X

The control of dicumarol therapy and the quantitative determination of prothrombin and proconvertin

25 March 2023

36

1 reference

https://api.crossref.org/works/10.1111/J.1365-2141.1970.TB01615.X

25 March 2023

37

82

200

Pasero G.

1968

1 reference

https://api.crossref.org/works/10.1111/J.1365-2141.1970.TB01615.X

The Stuart-Prower factor: utilization of clotting factors obtained by starch-block electrophoresis for genetic evaluation

25 March 2023

39

1 reference

https://api.crossref.org/works/10.1111/J.1365-2141.1970.TB01615.X

25 March 2023

41

3

59

Roos J.

1959

1 reference

https://api.crossref.org/works/10.1111/J.1365-2141.1970.TB01615.X

25 March 2023

A new coagulation defect

42

1 reference

https://api.crossref.org/works/10.1111/J.1365-2141.1970.TB01615.X

An improved one-stage prothrombin method.

25 March 2023

44

1 reference

https://api.crossref.org/works/10.1111/J.1365-2141.1970.TB01615.X

25 March 2023

Identifiers

1 reference

18 May 2018

1 reference

18 May 2018