(Q54671242)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15825549%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

title

Neurofilament M gene in a French-Canadian population with Parkinson's disease (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15825549%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

author name string

F Han

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15825549%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

D E Bulman

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15825549%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

M Panisset

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15825549%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

D A Grimes

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15825549%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

publication date

1 February 2005

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15825549%20AND%20SRC:MED&resulttype=core&format=json

Canadian Journal of Neurological Sciences

10 January 2020

published in

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15825549%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

volume

32

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15825549%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

issue

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15825549%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

page(s)

68-70

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15825549%20AND%20SRC:MED&resulttype=core&format=json

Complete genomic screen in Parkinson disease: evidence for multiple genes.

10 January 2020

cites work

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100016905

7 January 2021

Transgenic mice carrying a human mutant superoxide dismutase transgene develop neuronal cytoskeletal pathology resembling human amyotrophic lateral sclerosis lesions

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100016905

7 January 2021

Aggregation of neurofilament and alpha-synuclein proteins in Lewy bodies: implications for the pathogenesis of Parkinson disease and Lewy body dementia

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100016905

7 January 2021

The prevalence of Parkinson's disease in British Columbia, Canada, estimated by using drug tracer methodology

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100016905

7 January 2021

Improved accuracy of clinical diagnosis of Lewy body Parkinson's disease

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100016905

7 January 2021

Mutation analysis of the neurofilament M gene in Parkinson's disease

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100016905

7 January 2021

Mutations in NR4A2 associated with familial Parkinson disease

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100016905

7 January 2021

Parkinson's genetics--creating exciting new insights

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100016905

7 January 2021

Biomedicine. Parkinson's--divergent causes, convergent mechanisms.

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100016905

7 January 2021

Mutations in the DJ-1 gene associated with autosomal recessive early-onset parkinsonism

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100016905

7 January 2021

Hereditary early-onset Parkinson's disease caused by mutations in PINK1

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100016905

7 January 2021

A mutation in the human neurofilament M gene in Parkinson's disease that suggests a role for the cytoskeleton in neuronal degeneration

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100016905

7 January 2021

Increased expression of neurofilament subunit NF-L produces morphological alterations that resemble the pathology of human motor neuron disease

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100016905

7 January 2021

A structural scaffolding of intermediate filaments in health and disease

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100016905

7 January 2021

Diagnostic criteria for Parkinson disease

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100016905

7 January 2021

Neurofilament deficiency in quail caused by nonsense mutation in neurofilament-L gene

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100016905

7 January 2021

A novel NF-L mutation Pro22Ser is associated with CMT2 in a large Slovenian family

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100016905

7 January 2021

A new variant of Charcot-Marie-Tooth disease type 2 is probably the result of a mutation in the neurofilament-light gene

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100016905

7 January 2021

Deletions of the heavy neurofilament subunit tail in amyotrophic lateral sclerosis

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100016905

7 January 2021

Novel insertion in the KSP region of the neurofilament heavy gene in amyotrophic lateral sclerosis (ALS)

1 reference

https://api.crossref.org/works/10.1017%2FS0317167100016905

7 January 2021

10.1017/S0317167100016905

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:15825549%20AND%20SRC:MED&resulttype=core&format=json

10 January 2020

1 reference