Genetic contributions to changes of fiber tracts of ventral visual stream in 22q11.2 deletion syndrome.
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White matter abnormalities and cognitive impairment in early-onset schizophrenia-spectrum disorders.Altered white matter microstructure is associated with social cognition and psychotic symptoms in 22q11.2 microdeletion syndrome.White matter microstructural abnormalities of the cingulum bundle in youths with 22q11.2 deletion syndrome: associations with medication, neuropsychological function, and prodromal symptoms of psychosisVisual memory profile in 22q11.2 microdeletion syndrome: are there differences in performance and neurobiological substrates between tasks linked to ventral and dorsal visual brain structures? A cross-sectional and longitudinal study.Machine-learning classification of 22q11.2 deletion syndrome: A diffusion tensor imaging study.Long-range dysconnectivity in frontal and midline structures is associated to psychosis in 22q11.2 deletion syndrome.Visual perception skills: a comparison between patients with Noonan syndrome and 22q11.2 deletion syndrome.Abnormalities in brain white matter in adolescents with 22q11.2 deletion syndrome and psychotic symptoms.Patterns of white matter microstructure in individuals at ultra-high-risk for psychosis: associations to level of functioning and clinical symptoms.White matter microstructure abnormalities in pediatric migraine patients.
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Genetic contributions to changes of fiber tracts of ventral visual stream in 22q11.2 deletion syndrome.
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article científic
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article scientifique
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articolo scientifico
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artigo científico
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bilimsel makale
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scientific article published on September 2013
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vedecký článok
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vetenskaplig artikel
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videnskabelig artikel
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vědecký článek
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name
Genetic contributions to chang ...... in 22q11.2 deletion syndrome.
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Genetic contributions to chang ...... in 22q11.2 deletion syndrome.
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type
label
Genetic contributions to chang ...... in 22q11.2 deletion syndrome.
@en
Genetic contributions to chang ...... in 22q11.2 deletion syndrome.
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Genetic contributions to chang ...... in 22q11.2 deletion syndrome.
@en
Genetic contributions to chang ...... in 22q11.2 deletion syndrome.
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P2093
P2860
P50
P1476
Genetic contributions to chang ...... in 22q11.2 deletion syndrome.
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P2093
Christine T Finn
Diandra Lucia
Erica Tworog-Dube
Michael J Coleman
Nikos Makris
Raju Kucherlapati
Ron Kikinis
P2860
P2888
P304
P356
10.1007/S11682-013-9232-5
P577
2013-09-01T00:00:00Z