(Q84862270)

English

Amyotrophic lateral sclerosis/frontotemporal dementia with predominant manifestations of obsessive-compulsive disorder associated to GGGGCC expansion of the c9orf72 gene

scientific article published on 24 August 2012

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scholarly article

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22918453%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

Amyotrophic lateral sclerosis/frontotemporal dementia with predominant manifestations of obsessive-compulsive disorder associated to GGGGCC expansion of the c9orf72 gene (English)

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22918453%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

amyotrophic lateral sclerosis

1 reference

based on heuristic

inferred from title

frontotemporal dementia

1 reference

based on heuristic

inferred from title

obsessive-compulsive disorder

1 reference

based on heuristic

inferred from title

1

1 reference

Europe PubMed Central

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:22918453%20AND%20SRC:MED&resulttype=core&format=json

11 February 2020

Cristina Moglia

2

1 reference

Europe PubMed Central

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11 February 2020

Angelina Cistaro

4

1 reference

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11 February 2020

8

1 reference

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11 February 2020

14

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11 February 2020

author name string

Antonio Canosa

3

1 reference

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11 February 2020

Consuelo Valentini

5

1 reference

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11 February 2020

Giovanna Carrara

6

1 reference

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11 February 2020

Enzo Soldano

7

1 reference

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11 February 2020

Enrica Bersano

9

1 reference

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11 February 2020

Davide Bertuzzo

10

1 reference

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11 February 2020

Maura Brunetti

11

1 reference

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11 February 2020

Irene Ossola

12

1 reference

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11 February 2020

Gabriella Restagno

13

1 reference

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11 February 2020

publication date

24 August 2012

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11 February 2020

Journal of Neurology

1 reference

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11 February 2020

259

1 reference

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11 February 2020

12

1 reference

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11 February 2020

2723-2725

1 reference

Europe PubMed Central

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11 February 2020

https://scigraph.springernature.com/pub.10.1007/s00415-012-6640-1

0 references

Left prefrontal glucose hypometabolism in the depressed state: a confirmation.

1 reference

https://pubmed.ncbi.nlm.nih.gov/22918453

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Local cerebral glucose metabolic rates in obsessive-compulsive disorder. Patients treated with clomipramine.

1 reference

https://pubmed.ncbi.nlm.nih.gov/22918453

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

[18F]FDG PET study in obsessive-compulsive disorder. A clinical/metabolic correlation study after treatment

1 reference

https://pubmed.ncbi.nlm.nih.gov/22918453

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cerebral glucose metabolism in childhood-onset obsessive-compulsive disorder.

1 reference

https://pubmed.ncbi.nlm.nih.gov/22918453

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Expanded GGGGCC hexanucleotide repeat in noncoding region of C9ORF72 causes chromosome 9p-linked FTD and ALS

1 reference

https://pubmed.ncbi.nlm.nih.gov/22918453

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cerebral glucose metabolic rates in nondepressed patients with obsessive-compulsive disorder

1 reference

https://pubmed.ncbi.nlm.nih.gov/22918453

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Frequency of the C9orf72 hexanucleotide repeat expansion in patients with amyotrophic lateral sclerosis and frontotemporal dementia: a cross-sectional study

1 reference

https://pubmed.ncbi.nlm.nih.gov/22918453

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72.

1 reference

https://pubmed.ncbi.nlm.nih.gov/22918453

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

A hexanucleotide repeat expansion in C9ORF72 is the cause of chromosome 9p21-linked ALS-FTD

1 reference

https://pubmed.ncbi.nlm.nih.gov/22918453

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

The syndrome of cognitive impairment in amyotrophic lateral sclerosis: a population-based study

1 reference

https://pubmed.ncbi.nlm.nih.gov/22918453

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Obsessional slowness. Functional studies with positron emission tomography.

1 reference

https://pubmed.ncbi.nlm.nih.gov/22918453

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Cognitive and clinical characteristics of patients with amyotrophic lateral sclerosis carrying a C9orf72 repeat expansion: a population-based cohort study

1 reference

https://pubmed.ncbi.nlm.nih.gov/22918453

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Distinct clinical and pathological characteristics of frontotemporal dementia associated with C9ORF72 mutations

1 reference

https://pubmed.ncbi.nlm.nih.gov/22918453

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population

1 reference

https://pubmed.ncbi.nlm.nih.gov/22918453

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

Clinical and pathological features of familial frontotemporal dementia caused by C9ORF72 mutation on chromosome 9p

1 reference

https://pubmed.ncbi.nlm.nih.gov/22918453

12 December 2020

based on heuristic

inferred from PubMed ID database lookup

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