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...

How to manage obsessive-compulsive disorder (OCD) under COVID-19: A clinician's guide from the International College of Obsessive Compulsive Spectrum Disorders (ICOCS) and the Obsessive-Compulsive and Related Disorders Research Network (OCRN) of the European College of Neuropsychopharmacology

Comprehensive psychiatry, 2020-07, Vol.100, p.152174-152174, Article 152174

2020

Volltextzugriff (PDF)

A comparison between print vs. internet methods for a clinical trial recruitment—A pan European OCD study

European neuropsychopharmacology, 2014-06, Vol.24 (6), p.874-878

2014

Volltextzugriff (PDF)

A Psychophysiological Examination of the Mutability of Type D Personality in a Therapeutic Trial

Journal of psychophysiology, 2021-04, Vol.35 (2), p.116-128

2021

Volltextzugriff (PDF)

Crossover interference and sex-specific genetic maps shape identical by descent sharing in close relatives

PLoS genetics, 2019-12, Vol.15 (12), p.e1007979-e1007979

2019

Volltextzugriff (PDF)

Quantifying center bias of observers in free viewing of dynamic natural scenes

Journal of vision (Charlottesville, Va.), 2009-07, Vol.9 (7), p.4-4

2009

Volltextzugriff (PDF)

Bbs2-Null Mice Have Neurosensory Deficits, a Defect in Social Dominance, and Retinopathy Associated with Mislocalization of Rhodopsin

Proceedings of the National Academy of Sciences - PNAS, 2004-11, Vol.101 (47), p.16588-16593

2004

Volltextzugriff (PDF)

Expanding the phenotype of CRB2 mutations - A new ciliopathy syndrome?

Clinical genetics, 2016-12, Vol.90 (6), p.540-544

2016

Volltextzugriff (PDF)

The Effect of Consanguinity on Between-Individual Identity-by-Descent Sharing

Genetics (Austin), 2019-05, Vol.212 (1), p.305-316

2019

Volltextzugriff (PDF)

Allogeneic IgG combined with dendritic cell stimuli induce antitumour T-cell immunity

Nature (London), 2015-05, Vol.521 (7550), p.99-104

2015

Volltextzugriff (PDF)

Limiting distribution of X-chromosomal coalescence times under first-cousin consanguineous mating

Theoretical population biology, 2022-10, Vol.147, p.1-15

2022

Volltextzugriff (PDF)

The Reciprocal Effects of Leisure Time Activities and Intellectual Functioning in Older People: A Longitudinal Analysis

Psychology and aging, 2001-09, Vol.16 (3), p.466-482

2001

Volltextzugriff (PDF)

Rare GABRA3 variants are associated with epileptic seizures, encephalopathy and dysmorphic features

Brain (London, England : 1878), 2017-11, Vol.140 (11), p.2879-2894

2017

Volltextzugriff (PDF)

Searching for the Favorable Donor Site for Fat Injection: In Vivo Study Using the Nude Mice Model

Dermatologic surgery, 2005-10, Vol.31 (10), p.1304-1307

2005

Volltextzugriff (PDF)

Mutation of a nuclear receptor gene, NR2E3 , causes enhanced S cone syndrome, a disorder of retinal cell fate

Nature genetics, 2000-02, Vol.24 (2), p.127-131

2000

Volltextzugriff (PDF)

Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2)

Human molecular genetics, 2001-04, Vol.10 (8), p.865-874

2001

Volltextzugriff (PDF)

Serum ferritin level as a predictor of impaired growth and puberty in thalassemia major patients

European journal of haematology, 2005-02, Vol.74 (2), p.93-100

2005

Volltextzugriff (PDF)

Ocular phenotypes of three genetic variants of Bardet-Biedl syndrome

American journal of medical genetics, 2005-01, Vol.132A (3), p.283-287

2005

Volltextzugriff (PDF)

Adrenocortical Suppression Blocks the Memory-Enhancing Effects of Amphetamine and Epinephrine

Proceedings of the National Academy of Sciences - PNAS, 1996-02, Vol.93 (4), p.1429-1433

1996

Volltextzugriff (PDF)

Mutational spectrum of the oral-facial-digital type I syndrome: a study on a large collection of patients

Human mutation, 2008-10, Vol.29 (10), p.1237-1246

2008

Volltextzugriff (PDF)

The Roles of Fatalism, Self-Confidence, and Intellectual Resources in the Disablement Process in Older Adults

Psychology and aging, 2003-09, Vol.18 (3), p.551-561

2003

Volltextzugriff (PDF)

Familial aggregation in the fibromyalgia syndrome

Seminars in arthritis and rheumatism, 1996-12, Vol.26 (3), p.605-611

1996

Volltextzugriff (PDF)

Complement Factor H Gene Mutation Associated with Autosomal Recessive Atypical Hemolytic Uremic Syndrome

American journal of human genetics, 1999-12, Vol.65 (6), p.1538-1546

1999

Volltextzugriff (PDF)

Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss

Human mutation, 1998, Vol.11 (5), p.387-394

1998

Volltextzugriff (PDF)

A side-by-side prospective study of intense pulsed light and Nd:YAG laser treatment for vascular lesions

Annals of plastic surgery, 2006-02, Vol.56 (2), p.164-170

2006

Volltextzugriff (PDF)

ALSUntangled No. 35: Hyperbaric Oxygen Therapy

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2016-11, Vol.17 (7-8), p.622-624

2016

Volltextzugriff (PDF)

1 – 25 von 56

Suche als RSS-Feed

Aktive Filter

ThemaMale

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(52)
Mit Volltextzugriff
(46)

Publikationsform

Artikel
(56)

Sprache

Erscheinungsjahr

n.n

Thema

Humans
(52)
Female
(49)
Science & Technology
(46)
Life Sciences & Biomedicine
(43)
Adult
(25)
Biological And Medical Sciences
(24)
Genetics & Heredity
(18)
Medical Sciences
(18)
Pedigree
(17)
Middle Aged
(14)
Social Sciences
(12)
Adolescent
(10)
Child
(10)
Psychology
(10)
Animals
(9)
Aged
(8)
Child, Preschool
(8)
Mice
(7)
Psychology. Psychoanalysis. Psychiatry
(7)

14 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

How to manage obsessive-compulsive disorder (OCD) under COVID-19: A clinician's guide from the International College of Obsessive Compulsive Spectrum Disorders (ICOCS) and the Obsessive-Compulsive and Related Disorders Research Network (OCRN) of the European College of Neuropsychopharmacology

A comparison between print vs. internet methods for a clinical trial recruitment—A pan European OCD study

A Psychophysiological Examination of the Mutability of Type D Personality in a Therapeutic Trial

Crossover interference and sex-specific genetic maps shape identical by descent sharing in close relatives

Quantifying center bias of observers in free viewing of dynamic natural scenes

Bbs2-Null Mice Have Neurosensory Deficits, a Defect in Social Dominance, and Retinopathy Associated with Mislocalization of Rhodopsin

Expanding the phenotype of CRB2 mutations - A new ciliopathy syndrome?

The Effect of Consanguinity on Between-Individual Identity-by-Descent Sharing

Allogeneic IgG combined with dendritic cell stimuli induce antitumour T-cell immunity

Limiting distribution of X-chromosomal coalescence times under first-cousin consanguineous mating

The Reciprocal Effects of Leisure Time Activities and Intellectual Functioning in Older People: A Longitudinal Analysis

Rare GABRA3 variants are associated with epileptic seizures, encephalopathy and dysmorphic features

Searching for the Favorable Donor Site for Fat Injection: In Vivo Study Using the Nude Mice Model

Mutation of a nuclear receptor gene, NR2E3 , causes enhanced S cone syndrome, a disorder of retinal cell fate

Positional cloning of a novel gene on chromosome 16q causing Bardet-Biedl syndrome (BBS2)

Serum ferritin level as a predictor of impaired growth and puberty in thalassemia major patients

Ocular phenotypes of three genetic variants of Bardet-Biedl syndrome

Adrenocortical Suppression Blocks the Memory-Enhancing Effects of Amphetamine and Epinephrine

Mutational spectrum of the oral-facial-digital type I syndrome: a study on a large collection of patients

The Roles of Fatalism, Self-Confidence, and Intellectual Resources in the Disablement Process in Older Adults

Familial aggregation in the fibromyalgia syndrome

Complement Factor H Gene Mutation Associated with Autosomal Recessive Atypical Hemolytic Uremic Syndrome

Identification of mutations in the connexin 26 gene that cause autosomal recessive nonsyndromic hearing loss

A side-by-side prospective study of intense pulsed light and Nd:YAG laser treatment for vascular lesions

ALSUntangled No. 35: Hyperbaric Oxygen Therapy

Aktive Filter

Suchergebnisse filtern