The rarer inherited coagulation disorders: A review (Q40426151)

20 September 2017

1 reference

title

The rarer inherited coagulation disorders: a review (English)

1 reference

20 September 2017

The rarer inherited coagulation disorders: A review (English)

1 reference

https://api.crossref.org/works/10.1016/S0268-960X(95)90027-6

21 May 2024

author name string

P. H. Bolton-Maggs

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7580392

21 May 2024

F. G. Hill

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?resulttype=core&format=json&query=SRC%3AMED%20AND%20EXT_ID%3A7580392

21 May 2024

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=7580392

21 May 2024

publication date

1 June 1995

1 reference

20 September 2017

number of pages

12

1 reference

full work available at URL

inferred from page(s)

https://api.elsevier.com/content/article/PII:S0268960X95900276?httpAccept=text/xml

1 reference

https://api.crossref.org/works/10.1016/S0268-960X(95)90027-6

https://api.elsevier.com/content/article/PII:S0268960X95900276?httpAccept=text/plain

21 May 2024

1 reference

https://api.crossref.org/works/10.1016/S0268-960X(95)90027-6

21 May 2024

1 reference

20 September 2017

volume

9

1 reference

20 September 2017

issue

2

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20 September 2017

page(s)

65-76

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Another Genetic Variant of Haemophilia B: Haemophilia B Leyden

20 September 2017

cites work

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7 January 2021

Hemophilia B Leyden: a sex-linked hereditary disorder that improves after puberty

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7 January 2021

Haemophilia B: database of point mutations and short additions and deletions--third edition, 1992

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7 January 2021

Haemophilia B Liverpool: a new British family with mild haemophilia B associated with a -6 G to A mutation in the factor IX promoter

1 reference

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7 January 2021

The high frequency of the -6G-->A factor IX promoter mutation is the result both of a founder effect and recurrent mutation at a CpG dinucleotide

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7 January 2021

Plasma thromboplastin antecedent (PTA) deficiency

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7 January 2021

Spontaneous hemorrhages caused by plasma-thromboplastin-antecedent deficiency; report of a case

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7 January 2021

Plasma thromboplastin antecedent deficiency and subarachnoid hemorrhage

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7 January 2021

Spontaneous spinal epidural hematoma, Brown-Séquard syndrome, and factor XI deficiency

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7 January 2021

Inheritance and bleeding in factor XI deficiency

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7 January 2021

Heredity and Coagulation Studies in Ten Families with Factor XI (Plasma Thromboplastin Antecedent) Deficiency

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7 January 2021

Factor XI deficiency in Ashkenazi Jews in Israel

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7 January 2021

Thrombogenic potential of factor XI concentrate

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7 January 2021

Factor XII activity and antigen concentrations in patients suffering from recurrent thrombosis

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7 January 2021

The Prevalence of Moderate and Severe FXII (Hageman Factor) Deficiency among the Normal Population: Evaluation of the Incidence of FXII Deficiency among 300 Healthy Blood Donors

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7 January 2021

John Hageman's factor and deep-vein thrombosis: Leiden thrombophilia Study

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7 January 2021

Heterogeneity of hereditary and acquired factor X deficiencies by combined immunochemical and functional analyses

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7 January 2021

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

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7 January 2021

Use of DDAVP in inherited and acquired platelet dysfunction

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7 January 2021

Bernard-Soulier syndrome in two Swedish families: effect of DDAVP on bleeding time.

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7 January 2021

Bernard-Soulier syndrome in pregnancy; a report of four pregnancies in one patient, and review of the literature

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7 January 2021

The Wiskott-Aldrich syndrome in the United States and Canada (1892-1979).

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7 January 2021

The UDP-galactose translocator gene is mapped to band Xp11.23-p11.22 containing the Wiskott-Aldrich syndrome locus

1 reference

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7 January 2021

Factor X.

38

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Variation in surface platelet glycoprotein Ib expression in Bernard-Soulier syndrome

21 May 2024

Molecular abnormalities in Glanzmann's thrombasthenia, Bernard-Soulier syndrome, and platelet-type von Willebrand's disease

43

0 references

53

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Sialophorin (CD43) and the Wiskott-Aldrich syndrome

21 May 2024

61

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21 May 2024

Identifiers

1 reference

20 September 2017

1 reference