(Q64865143)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19208384%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

title

The co-occurrence of early onset Parkinson disease and 22q11.2 deletion syndrome (English)

1 reference

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21 January 2020

1 reference

4

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21 January 2020

author name string

Christina Zaleski

1

1 reference

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21 January 2020

Anne S Bassett

2

1 reference

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21 January 2020

Karen Tam

3

1 reference

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21 January 2020

Eva W C Chow

5

1 reference

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21 January 2020

Elizabeth McPherson

6

1 reference

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21 January 2020

publication date

1 March 2009

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19208384%20AND%20SRC:MED&resulttype=core&format=json

American Journal of Medical Genetics

21 January 2020

published in

1 reference

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21 January 2020

volume

149A

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21 January 2020

issue

3

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21 January 2020

page(s)

525-528

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Incidence of Parkinson's disease: variation by age, gender, and race/ethnicity

21 January 2020

cites work

1 reference

12 December 2020

A population-based study of the 22q11.2 deletion: phenotype, incidence, and contribution to major birth defects in the population

1 reference

12 December 2020

Neuropsychological and perceptual defects in Parkinson's disease

1 reference

12 December 2020

Incidence and prevalence of the 22q11 deletion syndrome: a population-based study in Western Sweden

1 reference

12 December 2020

Planning ability in Parkinson's disease is influenced by the COMT val158met polymorphism

1 reference

12 December 2020

The effect of monoamine oxidase B (MAOB) and catechol-O-methyltransferase (COMT) polymorphisms on levodopa therapy in patients with sporadic Parkinson's disease

1 reference

12 December 2020

Effect of 6-hydroxydopamine lesions of the medial prefrontal cortex on neurotransmitter systems in subcortical sites in the rat

1 reference

12 December 2020

Cerebellar atrophy in a patient with velocardiofacial syndrome

1 reference

12 December 2020

Childhood-onset schizophrenia associated with parkinsonism in a patient with a microdeletion of chromosome 22.

1 reference

12 December 2020

Frontal, midbrain and striatal dopaminergic function in early and advanced Parkinson's disease A 3D [(18)F]dopa-PET study

1 reference

12 December 2020

Catechol-O-methyltransferase and monoamine oxidase B genes and susceptibility to sporadic Parkinson's disease in a Polish population.

1 reference

12 December 2020

Clinical features of 78 adults with 22q11 Deletion Syndrome.

1 reference

12 December 2020

What is the evidence for a premorbid parkinsonian personality: a systematic review

1 reference

12 December 2020

Neurocognitive profile in 22q11 deletion syndrome and schizophrenia

1 reference

12 December 2020

Catechol O-methyltransferase Val158Met genotype influences frontoparietal activity during planning in patients with Parkinson's disease

1 reference

12 December 2020

Catechol-O-methyl transferase and expression of schizophrenia in 73 adults with 22q11 deletion syndrome

1 reference

12 December 2020

Schizophrenia and 22q11.2 deletion syndrome

1 reference

12 December 2020

Increased frontal [(18)F]fluorodopa uptake in early Parkinson's disease: sex differences in the prefrontal cortex

1 reference

12 December 2020

Risk tables for parkinsonism and Parkinson's disease.

1 reference

12 December 2020

Prevalence of Parkinson's disease in Estonia

1 reference

12 December 2020

Identifiers

DOI

10.1002/AJMG.A.32650

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:19208384%20AND%20SRC:MED&resulttype=core&format=json

21 January 2020

1 reference

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21 January 2020

PubMed publication ID

19208384

1 reference