(Q45876213)

17 December 2017

title

Correlating clinical manifestations with factor levels in rare bleeding disorders: a report from Southern India (English)

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17 December 2017

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4

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author name string

A Viswabandya

1

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17 December 2017

S Baidya

2

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17 December 2017

S C Nair

3

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17 December 2017

B George

5

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17 December 2017

V Mathews

6

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17 December 2017

M Chandy

7

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17 December 2017

A Srivastava

8

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17 December 2017

publication date

4 January 2012

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17 December 2017

published in

Haemophilia

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17 December 2017

volume

18

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17 December 2017

issue

3

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17 December 2017

page(s)

e195-200

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17 December 2017

Rare coagulation deficiencies.

cites work

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.2011.02730.X

Recessively inherited coagulation disorders.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.2011.02730.X

Rare Bleeding Disorder Registry: deficiencies of factors II, V, VII, X, XIII, fibrinogen and dysfibrinogenemias

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.2011.02730.X

The rare coagulation disorders--review with guidelines for management from the United Kingdom Haemophilia Centre Doctors' Organisation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.2011.02730.X

Bleeding symptoms in 27 Iranian patients with the combined deficiency of factor V and factor VIII.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.2011.02730.X

Bleeding and thrombosis in 55 patients with inherited afibrinogenaemia

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.2011.02730.X

Symptoms of inherited factor V deficiency in 35 Iranian patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.2011.02730.X

Haemorrhagic manifestations and prevalence of factor V deficiency in north-eastern Iran

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.2011.02730.X

Clinical picture and management of congenital factor VII deficiency

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.2011.02730.X

Factor VII deficiency: clinical manifestation of 717 subjects from Europe and Latin America with mutations in the factor 7 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.2011.02730.X

Factor X deficiency: clinical manifestation of 102 subjects from Europe and Latin America with mutations in the factor 10 gene

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.2011.02730.X

Congenital factor X deficiency: spectrum of bleeding symptoms in 32 Iranian patients

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.2011.02730.X

Combined factor V and factor VIII deficiency among non-Ashkenazi Jews

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.2011.02730.X

Haemorrhagic symptoms in patients with combined factors V and VIII deficiency in north-eastern Iran

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.2011.02730.X

21 January 2018

Factor XIII deficiency

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.2011.02730.X

Mutations in the MCFD2 gene are predominant among patients with hereditary combined FV and FVIII deficiency (F5F8D) in India

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.2011.02730.X

Six novel mutations including triple heterozygosity for Phe31Ser, 514delT and 516T-->G factor X gene mutations are responsible for congenital factor X deficiency in patients of Nepali and Indian origin

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.2011.02730.X

Molecular genetics of hereditary prothrombin deficiency in Indian patients: identification of a novel Ala362 --> Thr (Prothrombin Vellore 1) mutation

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.2011.02730.X

Novel missense mutations in two patients with factor XI deficiency (Val271Leu and Tyr351Ser) and one patient with combined factor XI and factor IX deficiency (Phe349Val).

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FJ.1365-2516.2011.02730.X

10.1111/J.1365-2516.2011.02730.X

21 January 2018

Identifiers

DOI

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17 December 2017

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17 December 2017