(Q50864482)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9755361%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

title

No mitochondrial haplotype was found to increase risk for Alzheimer's disease (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9755361%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9755361%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

author name string

J Kálmán

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9755361%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

A Császár

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9755361%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

I Raskó

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9755361%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

Z Janka

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9755361%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

P Venetianer

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9755361%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

language of work or name

English

0 references

publication date

1 September 1998

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9755361%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

published in

Biological Psychiatry

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9755361%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

volume

44

1 reference

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5 December 2019

issue

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9755361%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

page(s)

371-373

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9755361%20AND%20SRC:MED&resulttype=core&format=json

Wolfram (DIDMOAD) syndrome and Leber hereditary optic neuropathy (LHON) are associated with distinct mitochondrial DNA haplotypes

5 December 2019

cites work

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900461-7

A mitochondrial DNA clone is associated with increased risk for Alzheimer disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900461-7

Alternative, simultaneous complex I mitochondrial DNA mutations in Leber's hereditary optic neuropathy

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900461-7

Apolipoprotein E allele frequencies in patients with late-onset sporadic Alzheimer's dementia in Hungary.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900461-7

Clinical diagnosis of Alzheimer's disease: report of the NINCDS-ADRDA Work Group under the auspices of Department of Health and Human Services Task Force on Alzheimer's Disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900461-7

Mitochondrial DNA variants observed in Alzheimer disease and Parkinson disease patients.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900461-7

Apolipoprotein E: high-avidity binding to beta-amyloid and increased frequency of type 4 allele in late-onset familial Alzheimer disease

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900461-7

The tRNA(Gln) 4336 mitochondrial DNA variant is not a high penetrance mutation which predisposes to dementia before the age of 75 years.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900461-7

No association found between Alzheimer's disease and a mitochondrial tRNA glutamine gene variant.

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900461-7

Mitochondrial mutation as a probable causative factor in familial progressive tubulointerstitial nephritis

7 January 2021

1 reference

https://api.crossref.org/works/10.1016%2FS0006-3223%2897%2900461-7

10.1016/S0006-3223(97)00461-7

7 January 2021

Identifiers

DOI

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:9755361%20AND%20SRC:MED&resulttype=core&format=json

5 December 2019

1 reference