(Q48253951)

English

De novo FTL mutation: a clinical, neuroimaging, and molecular study.

scientific article published on 12 December 2012

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/23239021

De novo FTL mutation: a clinical, neuroimaging, and molecular study. (English)

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/23239021

0 references

Filippo Maria Santorelli

9

object named as

Filippo M Santorelli

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/23239021

author name string

Eugenia Storti

1

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/23239021

Francesca Cortese

2

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/23239021

Roberto Di Fabio

3

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/23239021

Chiara Fiorillo

4

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/23239021

Alberto Pierallini

5

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/23239021

Alessandra Tessa

6

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/23239021

Annamaria Valleriani

7

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/23239021

Francesco Pierelli

8

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/23239021

Carlo Casali

10

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/23239021

language of work or name

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publication date

12 December 2012

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/23239021

Movement Disorders

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/23239021

28

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/23239021

2

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/23239021

252-253

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/23239021

Oxidative stress and cell death in cells expressing L-ferritin variants causing neuroferritinopathy

1 reference

https://api.crossref.org/works/10.1002%2FMDS.25275

21 January 2018

Neuroferritinopathy: a new inborn error of iron metabolism

1 reference

https://api.crossref.org/works/10.1002%2FMDS.25275

21 January 2018

Neuroferritinopathy in a Japanese family with a duplication in the ferritin light chain gene

1 reference

https://api.crossref.org/works/10.1002%2FMDS.25275

21 January 2018

Neurodegeneration caused by proteins with an aberrant carboxyl-terminus

1 reference

https://api.crossref.org/works/10.1002%2FMDS.25275

21 January 2018

Mutant ferritin L-chains that cause neurodegeneration act in a dominant-negative manner to reduce ferritin iron incorporation

1 reference

https://api.crossref.org/works/10.1002%2FMDS.25275

21 January 2018

Identifiers

10.1002/MDS.25275

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/23239021

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

10 February 2018

http://europepmc.org/abstract/MED/23239021

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