(Q51331719)

English

A proportion of hereditary upper urinary tract urothelial carcinomas are misclassified as sporadic according to a multi-institutional database analysis: proposal of patient-specific risk identification tool.

scientific article published on 15 June 2012

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

3 April 2018

http://europepmc.org/abstract/MED/22703159

A proportion of hereditary upper urinary tract urothelial carcinomas are misclassified as sporadic according to a multi-institutional database analysis: proposal of patient-specific risk identification tool. (English)

1 reference

Europe PubMed Central

PubMed publication ID

3 April 2018

http://europepmc.org/abstract/MED/22703159

0 references

misclassification

1 reference

based on heuristic

inferred from title

Olivier Cussenot

object named as

Olivier Cussenot

19

0 references

Morgan Rouprêt

20

object named as

Morgan Rouprêt

1 reference

Europe PubMed Central

PubMed publication ID

3 April 2018

http://europepmc.org/abstract/MED/22703159

4

object named as

Adil Ouzzane

1 reference

Europe PubMed Central

PubMed publication ID

3 April 2018

http://europepmc.org/abstract/MED/22703159

author name string

François Audenet

1

1 reference

Europe PubMed Central

PubMed publication ID

3 April 2018

http://europepmc.org/abstract/MED/22703159

Pierre Colin

2

1 reference

Europe PubMed Central

PubMed publication ID

3 April 2018

http://europepmc.org/abstract/MED/22703159

David R Yates

3

1 reference

Europe PubMed Central

PubMed publication ID

3 April 2018

http://europepmc.org/abstract/MED/22703159

Géraldine Pignot

5

1 reference

Europe PubMed Central

PubMed publication ID

3 April 2018

http://europepmc.org/abstract/MED/22703159

Jean-Alexandre Long

6

1 reference

Europe PubMed Central

PubMed publication ID

3 April 2018

http://europepmc.org/abstract/MED/22703159

Michel Soulie

7

1 reference

Europe PubMed Central

PubMed publication ID

3 April 2018

http://europepmc.org/abstract/MED/22703159

Véronique Phé

8

1 reference

Europe PubMed Central

PubMed publication ID

3 April 2018

http://europepmc.org/abstract/MED/22703159

Henri Bensadoun

9

1 reference

Europe PubMed Central

PubMed publication ID

3 April 2018

http://europepmc.org/abstract/MED/22703159

Laurent Guy

10

1 reference

Europe PubMed Central

PubMed publication ID

3 April 2018

http://europepmc.org/abstract/MED/22703159

Alain Ruffion

11

1 reference

Europe PubMed Central

PubMed publication ID

3 April 2018

http://europepmc.org/abstract/MED/22703159

Antoine Valeri

12

1 reference

Europe PubMed Central

PubMed publication ID

3 April 2018

http://europepmc.org/abstract/MED/22703159

Luc Cormier

13

1 reference

Europe PubMed Central

PubMed publication ID

3 April 2018

http://europepmc.org/abstract/MED/22703159

Stéphane Droupy

14

1 reference

Europe PubMed Central

PubMed publication ID

3 April 2018

http://europepmc.org/abstract/MED/22703159

Alexandre de La Taille

15

1 reference

Europe PubMed Central

PubMed publication ID

3 April 2018

http://europepmc.org/abstract/MED/22703159

Fabien Saint

16

1 reference

Europe PubMed Central

PubMed publication ID

3 April 2018

http://europepmc.org/abstract/MED/22703159

Pierre-Olivier Faïs

17

1 reference

Europe PubMed Central

PubMed publication ID

3 April 2018

http://europepmc.org/abstract/MED/22703159

Alain Houlgatte

18

1 reference

Europe PubMed Central

PubMed publication ID

3 April 2018

http://europepmc.org/abstract/MED/22703159

French Collaborative National Database on UUT-UC

21

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Europe PubMed Central

PubMed publication ID

3 April 2018

http://europepmc.org/abstract/MED/22703159

publication date

15 June 2012

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Europe PubMed Central

PubMed publication ID

3 April 2018

http://europepmc.org/abstract/MED/22703159

BJU International

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3 April 2018

http://europepmc.org/abstract/MED/22703159

110

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Europe PubMed Central

PubMed publication ID

3 April 2018

http://europepmc.org/abstract/MED/22703159

11 Pt B

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Europe PubMed Central

PubMed publication ID

3 April 2018

http://europepmc.org/abstract/MED/22703159

E583-9

1 reference

Europe PubMed Central

PubMed publication ID

3 April 2018

http://europepmc.org/abstract/MED/22703159

Management of extracolonic tumours in patients with Lynch syndrome

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2012.11298.X

21 January 2018

The risk of extra-colonic, extra-endometrial cancer in the Lynch syndrome.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2012.11298.X

21 January 2018

Upper urinary tract urothelial cell carcinomas and other urological malignancies involved in the hereditary nonpolyposis colorectal cancer (lynch syndrome) tumor spectrum

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2012.11298.X

21 January 2018

New clinical criteria for hereditary nonpolyposis colorectal cancer (HNPCC, Lynch syndrome) proposed by the International Collaborative group on HNPCC.

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2012.11298.X

21 January 2018

Who should be sent for genetic testing in hereditary colorectal cancer syndromes?

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2012.11298.X

21 January 2018

Microsatellite instability as indicator of MSH2 gene mutation in patients with upper urinary tract transitional cell carcinoma

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2012.11298.X

21 January 2018

Revised Bethesda Guidelines for hereditary nonpolyposis colorectal cancer (Lynch syndrome) and microsatellite instability

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2012.11298.X

21 January 2018

European guidelines for the diagnosis and management of upper urinary tract urothelial cell carcinomas: 2011 update

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2012.11298.X

21 January 2018

Upper urinary tract carcinoma in Lynch syndrome cases

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2012.11298.X

21 January 2018

Quasimonomorphic mononucleotide repeats for high-level microsatellite instability analysis

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2012.11298.X

21 January 2018

Family information service and hereditary cancer

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2012.11298.X

21 January 2018

Accuracy of the routine detection of mutation in mismatch repair genes in patients with susceptibility to hereditary upper urinary tract transitional cell carcinoma

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2012.11298.X

21 January 2018

Distinct patterns of microsatellite instability are seen in tumours of the urinary tract

1 reference

https://api.crossref.org/works/10.1111%2FJ.1464-410X.2012.11298.X

21 January 2018

Identifiers

10.1111/J.1464-410X.2012.11298.X

1 reference

Europe PubMed Central

PubMed publication ID

3 April 2018

http://europepmc.org/abstract/MED/22703159

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

3 April 2018

http://europepmc.org/abstract/MED/22703159

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