UB Paderborn / Katalog / Suche / in CDI

Sortiert nach

Einfacher Volltextzugriff von (fast) überall

Installieren Sie die LibKey Nomad-Browsererweiterung und erhalten Sie von vielen Webseiten einfachen Zugriff auf lizenzierte Volltexte oder Open Access Publikationen. Mehr erfahren...

The influence of biomimetic topographical features and the extracellular matrix peptide RGD on human corneal epithelial contact guidance

Acta biomaterialia, 2013-02, Vol.9 (2), p.5040-5051

2013

Volltextzugriff (PDF)

Anatomy and aging of the amygdala and hippocampus in autism spectrum disorder: an in vivo magnetic resonance imaging study of Asperger syndrome

Autism research, 2012-02, Vol.5 (1), p.3-12

2012

Volltextzugriff (PDF)

Clinical symptomatology and the psychosis risk gene ZNF804A

Schizophrenia research, 2010-09, Vol.122 (1), p.273-275

2010

Volltextzugriff (PDF)

The Letter-Number Sequencing Test and its association with potential to work among people with psychotic illness

European psychiatry, 2010-03, Vol.25 (2), p.101-104

2010

Volltextzugriff (PDF)

Expanded CAG repeats in schizophrenia and bipolar disorder

Nature genetics, 1995-08, Vol.10 (4), p.380-381

1995

Volltextzugriff (PDF)

Neuropsychiatric manifestations in a patient with prolonged COVID-19 encephalopathy: case report and literature review

Irish journal of psychological medicine, 2023-09, Vol.40 (3), p.487-490

2023

Volltextzugriff (PDF)

Mood congruent psychotic symptoms and specific cognitive deficits in carriers of the novel schizophrenia risk variant at MIR-137

Neuroscience letters, 2013-01, Vol.532, p.33-38

2013

Volltextzugriff (PDF)

Remission and recovery from first-episode psychosis in adults: A systematic review and meta-analysis of long-term outcome studies

European psychiatry, 2017-04, Vol.41 (S1), p.S819-S819

2017

Volltextzugriff (PDF)

Annotation: Velo-cardio-facial syndrome

Journal of child psychology and psychiatry, 2005-06, Vol.46 (6), p.563-571

Murphy, K.C.

2005

Volltextzugriff (PDF)

The influence of biomimetic topographic features and the extracellular matrix peptide RGD on human corneal epithelial contact guidance

Acta biomaterialia, 2012-10, Vol.9 (2), p.5040-5051

2012

Volltextzugriff (PDF)

Genotype and psychological phenotype in tuberous sclerosis

Journal of medical genetics, 2004-03, Vol.41 (3), p.203-207

2004

Volltextzugriff (PDF)

Velo-cardio-facial syndrome: a model for understanding the genetics and pathogenesis of schizophrenia

British journal of psychiatry, 2001-11, Vol.179 (5), p.397-402

2001

Volltextzugriff (PDF)

An investigation of the neuropsychological profile in adults with velo-cardio-facial syndrome (VCFS)

Neuropsychologia, 2002, Vol.40 (5), p.471-478

2002

Volltextzugriff (PDF)

A Systematic Genomewide Linkage Study in 353 Sib Pairs with Schizophrenia

American journal of human genetics, 2003-12, Vol.73 (6), p.1355-1367

2003

Volltextzugriff (PDF)

No association between polymorphisms of catechol-o-methyltransferase (COMT) or monoamine oxidase (MAO) genes and schizophrenia in adults with velo-cardio-facial syndrome

Schizophrenia research, 2000, Vol.41 (1), p.96-96

2000

Volltextzugriff (PDF)

The behavioural phenotype in velo-cardio-facial syndrome

Schizophrenia research, 1998, Vol.29 (1), p.132-132

1998

Volltextzugriff (PDF)

Cognitive deficits associated with schizophrenia in adults with velocardio-facial syndrome

Schizophrenia research, 2003-03, Vol.60 (1), p.91-91

2003

Volltextzugriff (PDF)

High rates of schizophrenia in adults with velo-cardio-facial syndrome (VCFS)

Schizophrenia research, 2000, Vol.41 (1), p.29-29

2000

Volltextzugriff (PDF)

Effects of estrogen replacement therapy on human brain aging: An in vivo 1 H MRS study

Neurology, 2001-12, Vol.57 (11), p.2114-2117

2001

Volltextzugriff (PDF)

Premutation expansion of CGG triplet repeats affects brain; a study of male carriers of fragile X syndrome

NeuroImage (Orlando, Fla.), 2001, Vol.13 (6), p.1076-1076

2001

Volltextzugriff (PDF)

The Kings Schizotypy Questionnaire as a quantitative measure of schizophrenia liability

Schizophrenia research, 2000-10, Vol.45 (3), p.213-221

2000

Volltextzugriff (PDF)

The role of chromosome 22q11 in the aetiology of schizophrenia

Murphy, K.C

2000

Volltextzugriff (PDF)

No evidence for allelic association between schizophrenia and a functional variant of the human dopamine β-hydroxylase gene (DBH)

American journal of medical genetics, 1999-10, Vol.88 (5), p.557-559

1999

Volltextzugriff (PDF)

Chromosome 22gl1 deletions—An under-recognized cause of idiopathic learning disability?

Schizophrenia research, 1998, Vol.29 (1), p.132-132

1998

Volltextzugriff (PDF)

4 - Financing and economics of nuclear facility decommissioning

Nuclear decommissioning, 2012, p.49-86

2012

Volltextzugriff (PDF)

1 – 25 von 95

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(87)
Mit Volltextzugriff
(78)

Publikationsform

Sprache

Englisch
(95)

Erscheinungsjahr

n.n

Thema

Science & Technology
(60)
Life Sciences & Biomedicine
(49)
Humans
(29)
Female
(24)
Male
(23)
Biological And Medical Sciences
(19)
Animals
(14)
Medical Sciences
(14)
Adult
(13)
Middle Aged
(11)
Schizophrenia - Genetics
(9)
Psychiatry
(8)
Psychology. Psychoanalysis. Psychiatry
(8)
Psychopathology. Psychiatry
(8)
Genetics & Heredity
(7)
Risk Factors
(7)
Social Sciences
(7)
Adolescent
(6)
Genotype
(6)
Schizophrenia
(6)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

The influence of biomimetic topographical features and the extracellular matrix peptide RGD on human corneal epithelial contact guidance

Anatomy and aging of the amygdala and hippocampus in autism spectrum disorder: an in vivo magnetic resonance imaging study of Asperger syndrome

Clinical symptomatology and the psychosis risk gene ZNF804A

The Letter-Number Sequencing Test and its association with potential to work among people with psychotic illness

Expanded CAG repeats in schizophrenia and bipolar disorder

Neuropsychiatric manifestations in a patient with prolonged COVID-19 encephalopathy: case report and literature review

Mood congruent psychotic symptoms and specific cognitive deficits in carriers of the novel schizophrenia risk variant at MIR-137

Remission and recovery from first-episode psychosis in adults: A systematic review and meta-analysis of long-term outcome studies

Annotation: Velo-cardio-facial syndrome

The influence of biomimetic topographic features and the extracellular matrix peptide RGD on human corneal epithelial contact guidance

Genotype and psychological phenotype in tuberous sclerosis

Velo-cardio-facial syndrome: a model for understanding the genetics and pathogenesis of schizophrenia

An investigation of the neuropsychological profile in adults with velo-cardio-facial syndrome (VCFS)

A Systematic Genomewide Linkage Study in 353 Sib Pairs with Schizophrenia

No association between polymorphisms of catechol-o-methyltransferase (COMT) or monoamine oxidase (MAO) genes and schizophrenia in adults with velo-cardio-facial syndrome

The behavioural phenotype in velo-cardio-facial syndrome

Cognitive deficits associated with schizophrenia in adults with velocardio-facial syndrome

High rates of schizophrenia in adults with velo-cardio-facial syndrome (VCFS)

Effects of estrogen replacement therapy on human brain aging: An in vivo 1 H MRS study

Premutation expansion of CGG triplet repeats affects brain; a study of male carriers of fragile X syndrome

The Kings Schizotypy Questionnaire as a quantitative measure of schizophrenia liability

The role of chromosome 22q11 in the aetiology of schizophrenia

No evidence for allelic association between schizophrenia and a functional variant of the human dopamine β-hydroxylase gene (DBH)

Chromosome 22gl1 deletions—An under-recognized cause of idiopathic learning disability?

4 - Financing and economics of nuclear facility decommissioning

Suchergebnisse filtern