Sudden hearing loss and MTHFR 677C>T/1298A>C gene polymorphisms (Q46388221)

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Language	Label	Description	Also known as
English	Sudden hearing loss and MTHFR 677C>T/1298A>C gene polymorphisms	scientific article

Statements

instance of

scholarly article

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15775757

retrieved

21 December 2017

reference URL

http://europepmc.org/abstract/MED/15775757

title

Sudden hearing loss and MTHFR 677C>T/1298A>C gene polymorphisms (English)

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15775757

retrieved

21 December 2017

reference URL

http://europepmc.org/abstract/MED/15775757

main subject

hearing loss

1 reference

based on heuristic

inferred from title

author

Francesco Ottaviani

series ordinal

2

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15775757

retrieved

21 December 2017

reference URL

http://europepmc.org/abstract/MED/15775757

Umberto Ambrosetti

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4

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stated in

Europe PubMed Central

PubMed publication ID

15775757

retrieved

21 December 2017

reference URL

http://europepmc.org/abstract/MED/15775757

author name string

Capaccio P

series ordinal

1

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15775757

retrieved

21 December 2017

reference URL

http://europepmc.org/abstract/MED/15775757

Cuccarini V

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3

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stated in

Europe PubMed Central

PubMed publication ID

15775757

retrieved

21 December 2017

reference URL

http://europepmc.org/abstract/MED/15775757

Fagnani E

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5

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stated in

Europe PubMed Central

PubMed publication ID

15775757

retrieved

21 December 2017

reference URL

http://europepmc.org/abstract/MED/15775757

Bottero A

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6

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15775757

retrieved

21 December 2017

reference URL

http://europepmc.org/abstract/MED/15775757

Cenzuales S

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7

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15775757

retrieved

21 December 2017

reference URL

http://europepmc.org/abstract/MED/15775757

Cesana BM

series ordinal

8

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15775757

retrieved

21 December 2017

reference URL

http://europepmc.org/abstract/MED/15775757

Pignataro L

series ordinal

9

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15775757

retrieved

21 December 2017

reference URL

http://europepmc.org/abstract/MED/15775757

language of work or name

English

0 references

publication date

1 March 2005

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15775757

retrieved

21 December 2017

reference URL

http://europepmc.org/abstract/MED/15775757

published in

Genetics in Medicine

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15775757

retrieved

21 December 2017

reference URL

http://europepmc.org/abstract/MED/15775757

volume

7

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15775757

retrieved

21 December 2017

reference URL

http://europepmc.org/abstract/MED/15775757

issue

3

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15775757

retrieved

21 December 2017

reference URL

http://europepmc.org/abstract/MED/15775757

page(s)

206-208

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stated in

Europe PubMed Central

PubMed publication ID

15775757

retrieved

21 December 2017

reference URL

http://europepmc.org/abstract/MED/15775757

cites work

Anti-endothelial autoantibodies in patients with sudden hearing loss

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1097%2F01.GIM.0000157817.92509.45

retrieved

21 January 2018

Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1097%2F01.GIM.0000157817.92509.45

retrieved

21 January 2018

Genetic Variations Observed in Arterial and Venous Thromboembolism – Relevance for Therapy, Risk Prevention and Prognosis

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https://api.crossref.org/works/10.1097%2F01.GIM.0000157817.92509.45

retrieved

21 January 2018

A second common variant in the methylenetetrahydrofolate reductase (MTHFR) gene and its relationship to MTHFR enzyme activity, homocysteine, and cardiovascular disease risk

1 reference

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Crossref

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https://api.crossref.org/works/10.1097%2F01.GIM.0000157817.92509.45

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21 January 2018

Folate, homocysteine, endothelial function and cardiovascular disease. What is the link?

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https://api.crossref.org/works/10.1097%2F01.GIM.0000157817.92509.45

retrieved

21 January 2018

Association between factor V Leiden, prothrombin G20210A, and methylenetetrahydrofolate reductase C677T mutations and events of the arterial circulatory system: a meta-analysis of published studies

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https://api.crossref.org/works/10.1097%2F01.GIM.0000157817.92509.45

retrieved

21 January 2018

Plasma homocysteine levels correlated to interactions between folate status and methylene tetrahydrofolate reductase gene mutation in women with unexplained recurrent pregnancy loss

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https://api.crossref.org/works/10.1097%2F01.GIM.0000157817.92509.45

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21 January 2018

Methylenetetrahydrofolate reductase and transcobalamin genetic polymorphisms in human spontaneous abortion: biological and clinical implications

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Crossref

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https://api.crossref.org/works/10.1097%2F01.GIM.0000157817.92509.45

retrieved

21 January 2018

Platelet GPIaC807T polymorphism is associated with negative outcome of sudden hearing loss

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1097%2F01.GIM.0000157817.92509.45

retrieved

21 January 2018

Folic acid and homocysteine in age-related disease

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1097%2F01.GIM.0000157817.92509.45

retrieved

21 January 2018

Prognosis of sudden deafness with special reference to risk factors of microvascular pathology

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1097%2F01.GIM.0000157817.92509.45

retrieved

21 January 2018

Low serum folate levels: a risk factor for sudden sensorineural hearing loss?

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1097%2F01.GIM.0000157817.92509.45

retrieved

21 January 2018

Identifiers

DOI

10.1097/01.GIM.0000157817.92509.45

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15775757

retrieved

21 December 2017

reference URL

http://europepmc.org/abstract/MED/15775757

Dimensions Publication ID

1024103178

0 references

PubMed publication ID

15775757

1 reference

stated in

Europe PubMed Central

PubMed publication ID

15775757

retrieved

21 December 2017

reference URL

http://europepmc.org/abstract/MED/15775757

ResearchGate publication ID

7958750

0 references

 

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