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...

Diffusion MRI-based cortical connectome reconstruction: dependency on tractography procedures and neuroanatomical characteristics

Brain Structure and Function, 2018-06, Vol.223 (5), p.2269-2285

2018

Volltextzugriff (PDF)

Statistical power of clinical trials increased while effect size remained stable: an empirical analysis of 136,212 clinical trials between 1975 and 2014

Journal of clinical epidemiology, 2018-10, Vol.102, p.123-128

2018

Volltextzugriff (PDF)

Re-emergence of acute myeloid leukemia in donor cells following allogeneic transplantation in a family with a germline DDX41 mutation

Leukemia, 2017-02, Vol.31 (2), p.520-522

2017

Volltextzugriff (PDF)

Bayesian exponential random graph modeling of whole-brain structural networks across lifespan

NeuroImage (Orlando, Fla.), 2016-07, Vol.135, p.79-91

2016

Volltextzugriff (PDF)

An association screen of myelin-related genes implicates the chromosome 22q11 PIK4CA gene in schizophrenia

Molecular psychiatry, 2008-11, Vol.13 (11), p.1060-1068

2008

Volltextzugriff (PDF)

Distinct structure-function relationships across cortical regions and connectivity scales in the rat brain

Scientific reports, 2020-01, Vol.10 (1), p.56-56, Article 56

2020

Volltextzugriff (PDF)

Imaging Markers for the Characterization of Gray and White Matter Changes from Acute to Chronic Stages after Experimental Traumatic Brain Injury

Journal of neurotrauma, 2021-06, Vol.38 (12), p.1642-1653

2021

Volltextzugriff (PDF)

A Whole-Genome Scan in 164 Dutch Sib Pairs with Attention-Deficit/Hyperactivity Disorder: Suggestive Evidence for Linkage on Chromosomes 7p and 15q

American journal of human genetics, 2003-05, Vol.72 (5), p.1251-1260

2003

Volltextzugriff (PDF)

Evolution of genome diagnostics in epidermolysis bullosa: Unveiling the power of next-generation sequencing

Journal of the European Academy of Dermatology and Venereology, 2024-03

2024

Volltextzugriff (PDF)

Cardiomyopathy in patients with epidermolysis bullosa simplex with mutations in KLHL24

British journal of dermatology (1951), 2018-11, Vol.179 (5), p.1181-1183

2018

Volltextzugriff (PDF)

“Duodenal Adenocarcinoma Giving Rise to Rectal Metastasis” a Rare Disease with an Extremely Rare Metastatic Pattern

Journal of gastrointestinal cancer, 2019-09, Vol.50 (3), p.586-588

2019

Volltextzugriff (PDF)

Herlitz junctional epidermolysis bullosa: diagnostic features, mutational profile, incidence and population carrier frequency in the Netherlands

British journal of dermatology (1951), 2011-12, Vol.165 (6), p.1314-1322

2011

Volltextzugriff (PDF)

Spinocerebellar ataxias in the Netherlands: prevalence and age at onset variance analysis

Neurology, 2002-03, Vol.58 (5), p.702-708

2002

Volltextzugriff (PDF)

Novel Algorithms for Improved Sensitivity in Non-Invasive Prenatal Testing

Scientific reports, 2017-05, Vol.7 (1), p.1838-11, Article 1838

2017

Volltextzugriff (PDF)

ITGB4-associated non-Herlitz junctional epidermolysis bullosa: report of two new cases carrying two novel ITGB4 mutations

British journal of dermatology (1951), 2013-02, Vol.168 (2), p.432-434

2013

Volltextzugriff (PDF)

Junctional epidermolysis bullosa of late onset explained by mutations in COL17A1

British journal of dermatology (1951), 2011-06, Vol.164 (6), p.1280-1284

2011

Volltextzugriff (PDF)

Identification of a novel SCA14 mutation in a Dutch autosomal dominant cerebellar ataxia family

Neurology, 2003-12, Vol.61 (12), p.1760-1765

2003

Volltextzugriff (PDF)

Association between an agouti-related protein gene polymorphism and anorexia nervosa

Molecular psychiatry, 2001-05, Vol.6 (3), p.325-328

2001

Volltextzugriff (PDF)

The association of alcohol intake with gamma-glutamyl transferase (GGT) levels: Evidence for correlated genetic effects

Drug and alcohol dependence, 2014-01, Vol.134, p.99-105

2014

Volltextzugriff (PDF)

Regulation of HDL-c levels via ABCA1 : A role for Lrp1

Atherosclerosis, 2016-09, Vol.252, p.e264-e264

2016

Volltextzugriff (PDF)

Mapping of the SCA23 locus involved in autosomal dominant cerebellar ataxia to chromosome region 20p13-12.3

Brain (London, England : 1878), 2004-11, Vol.127 (11), p.2551-2557

2004

Volltextzugriff (PDF)

Natural fibre reinforced sheet moulding compound

Composites. Part A, Applied science and manufacturing, 2001-01, Vol.32 (9), p.1271-1279

2001

Volltextzugriff (PDF)

Differences in structural and functional networks between young adult and aged rat brains before and after stroke lesion simulations

Neurobiology of disease, 2019-06, Vol.126, p.23-35

2019

Volltextzugriff (PDF)

Is there an influence of X-chromosomal imprinting on the phenotype in Klinefelter syndrome? A clinical and molecular genetic study of 61 cases

Clinical genetics, 2006-07, Vol.70 (1), p.43-48

2006

Volltextzugriff (PDF)

A systematic review on the quantitative relationship between structural and functional network connectivity strength in mammalian brains

Journal of Cerebral Blood Flow & Metabolism, 2019-02, Vol.39 (2), p.189-209

2019

Volltextzugriff (PDF)

1 – 25 von 262

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(224)
Mit Volltextzugriff
(229)

Publikationsform

2 weitere anzeigen...

Weniger anzeigen...

Sprache

Erscheinungsjahr

n.n

Thema

Science & Technology
(189)
Life Sciences & Biomedicine
(124)
Humans
(97)
Biological And Medical Sciences
(60)
Male
(57)
Female
(53)
Technology
(44)
Neurosciences & Neurology
(41)
Genetics & Heredity
(40)
Medical Sciences
(40)
Physical Sciences
(39)
Materials Science
(37)
Neurosciences
(33)
Adult
(31)
Middle Aged
(25)
Fundamental And Applied Biological Sciences. Psychology
(24)
Physics
(24)
Mutation
(22)
Exact Sciences And Technology
(20)
Neurology
(20)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Diffusion MRI-based cortical connectome reconstruction: dependency on tractography procedures and neuroanatomical characteristics

Statistical power of clinical trials increased while effect size remained stable: an empirical analysis of 136,212 clinical trials between 1975 and 2014

Re-emergence of acute myeloid leukemia in donor cells following allogeneic transplantation in a family with a germline DDX41 mutation

Bayesian exponential random graph modeling of whole-brain structural networks across lifespan

An association screen of myelin-related genes implicates the chromosome 22q11 PIK4CA gene in schizophrenia

Distinct structure-function relationships across cortical regions and connectivity scales in the rat brain

Imaging Markers for the Characterization of Gray and White Matter Changes from Acute to Chronic Stages after Experimental Traumatic Brain Injury

A Whole-Genome Scan in 164 Dutch Sib Pairs with Attention-Deficit/Hyperactivity Disorder: Suggestive Evidence for Linkage on Chromosomes 7p and 15q

Evolution of genome diagnostics in epidermolysis bullosa: Unveiling the power of next-generation sequencing

Cardiomyopathy in patients with epidermolysis bullosa simplex with mutations in KLHL24

“Duodenal Adenocarcinoma Giving Rise to Rectal Metastasis” a Rare Disease with an Extremely Rare Metastatic Pattern

Herlitz junctional epidermolysis bullosa: diagnostic features, mutational profile, incidence and population carrier frequency in the Netherlands

Spinocerebellar ataxias in the Netherlands: prevalence and age at onset variance analysis

Novel Algorithms for Improved Sensitivity in Non-Invasive Prenatal Testing

ITGB4-associated non-Herlitz junctional epidermolysis bullosa: report of two new cases carrying two novel ITGB4 mutations

Junctional epidermolysis bullosa of late onset explained by mutations in COL17A1

Identification of a novel SCA14 mutation in a Dutch autosomal dominant cerebellar ataxia family

Association between an agouti-related protein gene polymorphism and anorexia nervosa

The association of alcohol intake with gamma-glutamyl transferase (GGT) levels: Evidence for correlated genetic effects

Regulation of HDL-c levels via ABCA1 : A role for Lrp1

Mapping of the SCA23 locus involved in autosomal dominant cerebellar ataxia to chromosome region 20p13-12.3

Natural fibre reinforced sheet moulding compound

Differences in structural and functional networks between young adult and aged rat brains before and after stroke lesion simulations

Is there an influence of X-chromosomal imprinting on the phenotype in Klinefelter syndrome? A clinical and molecular genetic study of 61 cases

A systematic review on the quantitative relationship between structural and functional network connectivity strength in mammalian brains

Suchergebnisse filtern