From genotype to phenotype: a clinical pathological, and biochemical investigation of frontotemporal dementia and parkinsonism (FTDP-17) caused by the P301L tau mutation (Q48192068)

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From genotype to phenotype: A clinical, pathological, and biochemical investigation of frontotemporal dementia and parkinsonism (FTDP-17) caused by the P301L tau mutation

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English	From genotype to phenotype: a clinical pathological, and biochemical investigation of frontotemporal dementia and parkinsonism (FTDP-17) caused by the P301L tau mutation	scientific article	From genotype to phenotype: A clinical, pathological, and biochemical investigation of frontotemporal dementia and parkinsonism (FTDP-17) caused by the P301L tau mutation

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10360762

From genotype to phenotype: a clinical pathological, and biochemical investigation of frontotemporal dementia and parkinsonism (FTDP-17) caused by the P301L tau mutation (English)

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10360762

0 references

Parkinson's disease

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based on heuristic

inferred from title

frontotemporal dementia

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based on heuristic

inferred from title

parkinsonian syndrome

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based on heuristic

inferred from title

1 reference

based on heuristic

inferred from title

Kirk Wilhelmsen

9

object named as

Wilhelmsen KC

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10360762

author name string

Nasreddine ZS

1

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10360762

Loginov M

2

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10360762

Clark LN

3

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Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10360762

Lamarche J

4

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Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10360762

Miller BL

5

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Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10360762

Lamontagne A

6

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Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10360762

Zhukareva V

7

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10360762

Lee VM

8

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10360762

Geschwind DH

10

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10360762

publication date

1 June 1999

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10360762

Annals of Neurology

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PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10360762

45

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Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10360762

6

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Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10360762

704-715

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10360762

Frontotemporal dementia and parkinsonism linked to chromosome 17: a consensus conference. Conference Participants

1 reference

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Hereditary Pick's disease: second re-examination of the large family and discussion of other hereditary cases, with particular reference to electroencephalography, a computerized tomography

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Rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration

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Clinical characteristics of a family with chromosome 17-linked disinhibition-dementia-parkinsonism-amyotrophy complex.

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21 January 2018

Slowly progressive aphasia without generalized dementia

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21 January 2018

Hereditary dysphasic disinhibition dementia: a frontotemporal dementia linked to 17q21-22.

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Frontal lobe degeneration of non-Alzheimer type. II. Clinical picture and differential diagnosis

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21 January 2018

The neuropathology of chromosome 17-linked dementia

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21 January 2018

Familial presenile dementia with psychosis associated with cortical neurofibrillary tangles and degeneration of the amygdala

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21 January 2018

Localization of frontotemporal dementia with parkinsonism in an Australian kindred to chromosome 17q21-22.

1 reference

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21 January 2018

Re-examination of a family with Pick's disease

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%28199906%2945%3A6%3C704%3A%3AAID-ANA4%3E3.0.CO%3B2-X

21 January 2018

Familial progressive subcortical gliosis.

1 reference

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21 January 2018

Tau is a candidate gene for chromosome 17 frontotemporal dementia

1 reference

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21 January 2018

Association of missense and 5'-splice-site mutations in tau with the inherited dementia FTDP-17

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%28199906%2945%3A6%3C704%3A%3AAID-ANA4%3E3.0.CO%3B2-X

21 January 2018

Pathogenic implications of mutations in the tau gene in pallido-ponto-nigral degeneration and related neurodegenerative disorders linked to chromosome 17

1 reference

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21 January 2018

A study of the Lund-Manchester research criteria for frontotemporal dementia: clinical and single-photon emission CT correlations

1 reference

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21 January 2018

Strategies for multilocus linkage analysis in humans

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21 January 2018

Genetic dissection of complex traits: guidelines for interpreting and reporting linkage results

1 reference

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21 January 2018

The neuropathology of a chromosome 17-linked autosomal dominant parkinsonism and dementia ("pallido-ponto-nigral degeneration").

1 reference

https://api.crossref.org/works/10.1002%2F1531-8249%28199906%2945%3A6%3C704%3A%3AAID-ANA4%3E3.0.CO%3B2-X

21 January 2018

“Mini-mental state”

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21 January 2018

Biopsy-derived adult human brain tau is phosphorylated at many of the same sites as Alzheimer's disease paired helical filament tau.

1 reference

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21 January 2018

Mutation-specific functional impairments in distinct tau isoforms of hereditary FTDP-17.

1 reference

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21 January 2018

Tau protein pathology in neurodegenerative diseases

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21 January 2018

Selective expression of Ser 199/202 phosphorylated tau in a case of frontotemporal dementia

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Hereditary frontotemporal dementia is linked to chromosome 17q21?q22: A genetic and clinicopathological study of three dutch families

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21 January 2018

Identifiers

10.1002/1531-8249(199906)45:6<704::AID-ANA4>3.0.CO;2-X

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10360762

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

9 February 2018

http://europepmc.org/abstract/MED/10360762

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