(Q37203609)

English

Rapidly progressive autosomal dominant Parkinsonism and dementia with Pallido-Ponto-Nigral Gegeneration (PPND) and Disinhibition-Dementia-Parkinsonism-Amyotrophy Complex (DDPAC) are clinically distinct conditions that are both linked to 17q21-22.

scientific article published on April 1997

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scholarly article

1 reference

Europe PubMed Central

PubMed publication ID

18 August 2017

Rapidly progressive autosomal dominant Parkinsonism and dementia with Pallido-Ponto-Nigral Gegeneration (PPND) and Disinhibition-Dementia-Parkinsonism-Amyotrophy Complex (DDPAC) are clinically distinct conditions that are both linked to 17q21-22. (English)

1 reference

Europe PubMed Central

PubMed publication ID

18 August 2017

0 references

Parkinson's disease

1 reference

based on heuristic

inferred from title

parkinsonian syndrome

1 reference

based on heuristic

inferred from title

Kirk Wilhelmsen

3

object named as

Wilhelmsen KC

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Europe PubMed Central

PubMed publication ID

18 August 2017

author name string

Wszolek ZK

1

1 reference

Europe PubMed Central

PubMed publication ID

18 August 2017

Lynch T

2

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Europe PubMed Central

PubMed publication ID

18 August 2017

publication date

1 April 1997

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Europe PubMed Central

PubMed publication ID

18 August 2017

number of pages

10

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inferred from page(s)

Parkinsonism and Related Disorders

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Europe PubMed Central

PubMed publication ID

18 August 2017

3

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Europe PubMed Central

PubMed publication ID

18 August 2017

2

1 reference

Europe PubMed Central

PubMed publication ID

18 August 2017

67-76

1 reference

Europe PubMed Central

PubMed publication ID

18 August 2017

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

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Localization of the gene for rapidly progressive autosomal dominant parkinsonism and dementia with pallido-ponto-nigral degeneration to chromosome 17q21

1 reference

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7 January 2021

based on heuristic

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

1 reference

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7 January 2021

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The neuropathology of chromosome 17-linked dementia

1 reference

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7 January 2021

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Frontal-subcortical circuits and human behavior

1 reference

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7 January 2021

based on heuristic

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Report of familial cases of parkinsonism. Evidence of a dominant trait in a patient's family.

1 reference

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Juvenile amyotrophic lateral sclerosis-dementia complex in a Dutch family

1 reference

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Sporadic and familial parkinsonism and motor neuron disease.

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Cerebral lesions in familial amyotrophic lateral sclerosis and dementia

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Hereditary Mental Depression and Parkinsonism With Taurine Deficiency

1 reference

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Dominantly inherited apathy, central hypoventilation, and Parkinson's syndrome: clinical, biochemical, and neuropathologic studies of 2 new cases.

1 reference

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Familial amyotrophic lateral sclerosis with dementia: A second Canadian family

1 reference

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7 January 2021

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A family with amyotrophic lateral sclerosis and Parkinsonism

1 reference

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Hereditary Amyotrophic Lateral Sclerosis. A report of two families.

1 reference

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Familial fatal parkinsonism with alveolar hypoventilation and mental depression

1 reference

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7 January 2021

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Familial amyotrophic lateral sclerosis, dementia, and psychosis

1 reference

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7 January 2021

based on heuristic

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Amyotrophic lateral sclerosis and its association with dementia, parkinsonism and other neurological disorders: a review

1 reference

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7 January 2021

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Familial dementia of adult onset with pathological findings of a 'non-specific' nature

1 reference

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7 January 2021

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New form of familial Parkinson-dementia syndrome: clinical and pathologic findings.

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2897%2900006-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Familial levodopa-responsive parkinsonian-pyramidal syndrome

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2897%2900006-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Familial occurrence of amyotrophic lateral sclerosis, parkinsonism, and dementia

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2897%2900006-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Familial tic disorder, parkinsonism, motor neuron disease, and acanthocytosis: a new syndrome

1 reference

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7 January 2021

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Thalamic and subcortical gliosis with dementia

1 reference

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7 January 2021

based on heuristic

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Familial parkinsonism, apathy, weight loss, and central hypoventilation: Successful long-term management

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2897%2900006-0

7 January 2021

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inferred from DOI database lookup

A parkinsonian kindred

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Dominantly inherited dementia and parkinsonism, with non-Alzheimer amyloid plaques: a new neurogenetic disorder.

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2897%2900006-0

7 January 2021

based on heuristic

inferred from DOI database lookup

A large kindred with autosomal dominant Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2897%2900006-0

7 January 2021

based on heuristic

inferred from DOI database lookup

A clinical and genetic study of familial Parkinson's disease

1 reference

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7 January 2021

based on heuristic

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Comparison of striatal 18F-dopa uptake in adult-onset dystonia-parkinsonism, Parkinson's disease, and dopa-responsive dystonia.

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2897%2900006-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Rapidly progressive aphasic dementia and motor neuron disease.

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2897%2900006-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Genetic linkage studies in autosomal dominant parkinsonism: evaluation of seven candidate genes

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2897%2900006-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Anticipation of onset age in familial Parkinson's disease

1 reference

https://api.crossref.org/works/10.1016%2FS1353-8020%2897%2900006-0

7 January 2021

based on heuristic

inferred from DOI database lookup

Familial progressive subcortical gliosis.

1 reference

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7 January 2021

based on heuristic

inferred from DOI database lookup

Autosomal dominant Lewy body parkinsonism in a four-generation family

1 reference

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inferred from DOI database lookup

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1 reference

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Identifiers

10.1016/S1353-8020(97)00006-0

1 reference

Europe PubMed Central

PubMed publication ID

18 August 2017

PubMed publication ID

1 reference

Europe PubMed Central

PubMed publication ID

18 August 2017

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