(Q36227376)

12 August 2017

0 references

Co-occurrence of affective and schizophrenia spectrum disorders with PINK1 mutations (English)

1 reference

12 August 2017

1 reference

Inke König

8

0 references

Christine Klein

9

object named as

Christine Klein

1 reference

12 August 2017

10

Rebekka Lencer

1 reference

12 August 2017

Susanne Steinlechner

1

1 reference

12 August 2017

Jessica Stahlberg

2

1 reference

12 August 2017

Birgit Völkel

3

1 reference

12 August 2017

Ana Djarmati

4

1 reference

12 August 2017

Johann Hagenah

5

1 reference

12 August 2017

Anja Hiller

6

1 reference

12 August 2017

Katja Hedrich

7

1 reference

12 August 2017

language of work or name

English

0 references

publication date

3 January 2007

1 reference

Journal of Neurology, Neurosurgery and Psychiatry

12 August 2017

1 reference

12 August 2017

78

1 reference

12 August 2017

5

1 reference

12 August 2017

532-535

1 reference

The genetics of Parkinson disease: Implications for neurological care

12 August 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2117826

PINK1 protein in normal human brain and Parkinson's disease

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2117826

Expanded motor and psychiatric phenotype in autosomal dominant Segawa syndrome due to GTP cyclohydrolase deficiency.

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2117826

Novel PINK1 mutations in early-onset parkinsonism

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2117826

PINK1 mutations are associated with sporadic early-onset parkinsonism

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2117826

Depression in Parkinson's disease. An update

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2117826

Range of neuropsychiatric disturbances in patients with Parkinson's disease

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2117826

Homozygous PINK1 C-terminus mutation causing early-onset parkinsonism.

1 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2117826

Parkin disease: a phenotypic study of a large case series

22 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2117826

Phenotypic features of myoclonus-dystonia in three kindreds

22 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2117826

Does treatment with dopamine agonists affect utilization of exogenous levodopa in the parkinsonian striatum?

22 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2117826

The Roscommon Family Study. I. Methods, diagnosis of probands, and risk of schizophrenia in relatives

22 September 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=2117826

Hallucinations in Parkinson's disease. prevalence, phenomenology and risk factors. Fenelon G* mahieux F, huon R, Ziegler M. Brain 2000;123:733-745

22 September 2018

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17202228

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

A heterozygous effect for PINK1 mutations in Parkinson's disease?

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17202228

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Clinical Spectrum of Homozygous and Heterozygous PINK1 Mutations in a Large German Family With Parkinson Disease

1 reference

PubMed

https://pubmed.ncbi.nlm.nih.gov/17202228

inferred from PubMed ID database lookup

12 December 2020

based on heuristic

Identifiers

DOI

10.1136/JNNP.2006.105676

1 reference

12 August 2017

1 reference

12 August 2017

1 reference