The NOS3 G894T (Glu298Asp) polymorphism is a risk factor for frontotemporal lobar degeneration (Q46195686)

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English	The NOS3 G894T (Glu298Asp) polymorphism is a risk factor for frontotemporal lobar degeneration	scientific article

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scholarly article

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Europe PubMed Central

PubMed publication ID

19087148

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20 December 2017

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http://europepmc.org/abstract/MED/19087148

title

The NOS3 G894T (Glu298Asp) polymorphism is a risk factor for frontotemporal lobar degeneration (English)

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Europe PubMed Central

PubMed publication ID

19087148

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20 December 2017

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http://europepmc.org/abstract/MED/19087148

main subject

risk factor

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author

Roberta Ghidoni

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6

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Europe PubMed Central

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19087148

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20 December 2017

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Elio Scarpini

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18

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Europe PubMed Central

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19087148

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20 December 2017

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http://europepmc.org/abstract/MED/19087148

Daniela Galimberti

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19087148

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20 December 2017

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Chiara Villa

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C Villa

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2

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Nereo Bresolin

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N Bresolin

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17

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E Venturelli

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1

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Europe PubMed Central

PubMed publication ID

19087148

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20 December 2017

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http://europepmc.org/abstract/MED/19087148

C Fenoglio

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3

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19087148

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http://europepmc.org/abstract/MED/19087148

F Clerici

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4

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19087148

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A Marcone

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5

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19087148

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F Cortini

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7

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19087148

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http://europepmc.org/abstract/MED/19087148

D Scalabrini

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8

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19087148

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S Gallone

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9

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19087148

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20 December 2017

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I Rainero

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10

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19087148

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20 December 2017

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A Mandelli

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11

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19087148

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20 December 2017

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http://europepmc.org/abstract/MED/19087148

I Restelli

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12

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Europe PubMed Central

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19087148

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20 December 2017

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http://europepmc.org/abstract/MED/19087148

G Binetti

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13

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19087148

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20 December 2017

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S Cappa

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14

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PubMed publication ID

19087148

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20 December 2017

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http://europepmc.org/abstract/MED/19087148

C Mariani

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15

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Europe PubMed Central

PubMed publication ID

19087148

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20 December 2017

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http://europepmc.org/abstract/MED/19087148

M T Giordana

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16

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Europe PubMed Central

PubMed publication ID

19087148

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20 December 2017

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http://europepmc.org/abstract/MED/19087148

publication date

1 January 2009

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Europe PubMed Central

PubMed publication ID

19087148

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20 December 2017

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http://europepmc.org/abstract/MED/19087148

published in

European Journal of Neurology

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Europe PubMed Central

PubMed publication ID

19087148

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20 December 2017

reference URL

http://europepmc.org/abstract/MED/19087148

volume

16

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Europe PubMed Central

PubMed publication ID

19087148

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20 December 2017

reference URL

http://europepmc.org/abstract/MED/19087148

issue

1

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Europe PubMed Central

PubMed publication ID

19087148

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20 December 2017

reference URL

http://europepmc.org/abstract/MED/19087148

page(s)

37-42

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PubMed publication ID

19087148

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http://europepmc.org/abstract/MED/19087148

cites work

Frontotemporal lobar degeneration: a consensus on clinical diagnostic criteria

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2008.02335.X

retrieved

21 January 2018

T-786-->C mutation in the 5'-flanking region of the endothelial nitric oxide synthase gene is associated with coronary spasm

1 reference

stated in

Crossref

reference URL

https://api.crossref.org/works/10.1111%2FJ.1468-1331.2008.02335.X

retrieved

21 January 2018

Identifiers

DOI

10.1111/J.1468-1331.2008.02335.X

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19087148

retrieved

20 December 2017

reference URL

http://europepmc.org/abstract/MED/19087148

PubMed publication ID

19087148

1 reference

stated in

Europe PubMed Central

PubMed publication ID

19087148

retrieved

20 December 2017

reference URL

http://europepmc.org/abstract/MED/19087148

ResearchGate publication ID

23668126

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