(Q42663078)

4 November 2017

title

Catechol-O-methyltransferase Val158Met polymorphism in schizophrenia: associations with cognitive and motor impairment (English)

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4 November 2017

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13

Maria Del Zompo

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Armida Mucci

Armida Mucci

5

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Stefano Pini

Stefano Pini

8

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Paolo Stratta

Paolo Stratta

11

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Silvana Galderisi

Silvana Galderisi

1

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Alessandro Rossi

Alessandro Rossi

7

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Brian Kirkpatrick

3

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Giordano Invernizzi

6

Giordano Invernizzi

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4 November 2017

10

Paolo Cassano

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4

Paola Piccardi

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4 November 2017

12

Giovanni Severino

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4 November 2017

Mario Maj

2

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4 November 2017

Antonio Vita

9

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4 November 2017

publication date

19 July 2005

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4 November 2017

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4 November 2017

volume

52

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4 November 2017

issue

2

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4 November 2017

page(s)

83-89

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IQ and risk for schizophrenia: a population-based cohort study

4 November 2017

cites work

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Attention, memory, and motor skills as childhood predictors of schizophrenia-related psychoses: the New York High-Risk Project.

21 January 2018

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Childhood neuromotor dysfunction in schizophrenia patients and their unaffected siblings: a prospective cohort study

21 January 2018

1 reference

Effect of COMT Val108/158 Met genotype on frontal lobe function and risk for schizophrenia

21 January 2018

1 reference

Children at risk for schizophrenia: the Jerusalem Infant Development Study. II. Neurobehavioral deficits at school age.

21 January 2018

1 reference

Neurological soft signs in schizophrenic patients and their nonpsychotic siblings.

21 January 2018

1 reference

Neurocognitive correlates of the COMT Val(158)Met polymorphism in chronic schizophrenia.

21 January 2018

1 reference

No evidence for phenotypic variation between probands in case-control versus family-based association studies of schizophrenia.

21 January 2018

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Eye movement disturbances in schizophrenia and a polymorphism of catechol-O-methyltransferase gene

21 January 2018

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COMT Val(158)Met and BDNF C(270)T polymorphisms in schizophrenia: a case-control study.

21 January 2018

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Neuropsychological impairments in deficit vs nondeficit forms of schizophrenia.

21 January 2018

1 reference

A separate disease within the syndrome of schizophrenia

21 January 2018

1 reference

Historical, psychopathological, neurological, and neuropsychological aspects of deficit schizophrenia: a multicenter study

21 January 2018

1 reference

Sibling correlation of deficit syndrome in the Irish study of high-density schizophrenia families

21 January 2018

1 reference

The Schedule for the Deficit syndrome: an instrument for research in schizophrenia.

21 January 2018

1 reference

Association study of a functional catechol-O-methyltransferase genetic polymorphism with age of onset, cognitive function, symptomatology and prognosis in chronic schizophrenia

21 January 2018

1 reference

The molecular genetics of schizophrenia: new findings promise new insights

21 January 2018

1 reference

Neurological Signs and the Heterogeneity of Schizophrenia

21 January 2018

1 reference

21 January 2018

Identifiers

DOI

10.1159/000087096

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4 November 2017

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