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...

DHDDS related epilepsy––Report of familial cases and review of the literature

Seizure (London, England), 2021-10, Vol.91, p.189-191

2021

Volltextzugriff (PDF)

Perampanel and decanoic acid show synergistic action against AMPA receptors and seizures

Epilepsia (Copenhagen), 2018-11, Vol.59 (11), p.e172-e178

2018

Volltextzugriff (PDF)

Heterozygous truncation mutations of the SMC1A gene cause a severe early onset epilepsy with cluster seizures in females: Detailed phenotyping of 10 new cases

Epilepsia (Copenhagen), 2017-04, Vol.58 (4), p.565-575

2017

Volltextzugriff (PDF)

Suspected pheochromocytoma in a patient with Guillain-Barré syndrome

Pediatrics (Evanston), 2013-03, Vol.131 (3), p.e955-e958

2013

Volltextzugriff (PDF)

The p.M292T NDUFS2 mutation causes complex I-deficient Leigh syndrome in multiple families

Brain (London, England : 1878), 2010-10, Vol.133 (10), p.2952-2963

2010

Volltextzugriff (PDF)

Teaching NeuroImages: alternating ptosis and Marcus Gunn jaw-winking phenomenon with PHOX2B mutation

Neurology, 2012-10, Vol.79 (17), p.e153

2012

Volltextzugriff (PDF)

Speech and language delay in two children: an unusual presentation of hyperthyroidism

Journal of Pediatric Endocrinology and Metabolism, 2013-11, Vol.26 (11), p.1171-1174

2013

Volltextzugriff (PDF)

Levetiracetam in the treatment of infantile spasms

European journal of paediatric neurology, 2005, Vol.9 (1), p.19-22

2005

Volltextzugriff (PDF)

Cystic fibrosis presenting with bilateral facial palsy

European journal of paediatric neurology, 2007-07, Vol.11 (4), p.240-242

2007

Volltextzugriff (PDF)

Heterozygous truncation mutations of the SMC 1A gene cause a severe early onset epilepsy with cluster seizures in females: Detailed phenotyping of 10 new cases

Epilepsia (Copenhagen), 2017-04, Vol.58 (4), p.565-575

2017

Volltextzugriff (PDF)

Epilepsy with Myoclonic Absences

Handbook of Pediatric Epilepsy Case Studies, 2023, p.259-264

2, 2023

Volltextzugriff (PDF)

Bidirectional superior cavopulmonary anastomosis: how young is too young?

Heart (British Cardiac Society), 1996-01, Vol.75 (1), p.78-82

1996

Volltextzugriff (PDF)

Childhood Obesity and Cardiovascular Dysfunction

Journal of the American College of Cardiology, 2013-10, Vol.62 (15), p.1309-1319

2013

Volltextzugriff (PDF)

Tissue distribution of Coxiella burnetii and antibody responses in macropods co-grazing with livestock in Queensland, Australia

PloS one, 2024-05, Vol.19 (5), p.e0303877-e0303877

2024

Volltextzugriff (PDF)

Obesity and arterial stiffness in children: systematic review and meta-analysis

Arteriosclerosis, thrombosis, and vascular biology, 2015-04, Vol.35 (4), p.1038-1044

2015

Volltextzugriff (PDF)

Serological evidence for the presence of wobbly possum disease virus in Australia

PloS one, 2020-08, Vol.15 (8), p.e0237091-e0237091

2020

Volltextzugriff (PDF)

Validation of an Indirect Immunofluorescence Assay and Commercial Q Fever Enzyme-Linked Immunosorbent Assay for Use in Macropods

Journal of clinical microbiology, 2022-07, Vol.60 (7), p.e0023622-e0023622

2022

Volltextzugriff (PDF)

Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis

The Lancet (British edition), 2013-04, Vol.381 (9875), p.1371-1379

2013

Volltextzugriff (PDF)

Perioperative Safety in the Longitudinal Assessment of Bariatric Surgery

The New England journal of medicine, 2009-07, Vol.361 (5), p.445-454

2009

Volltextzugriff (PDF)

A phase 1 study of ibrutinib in combination with R-ICE in patients with relapsed or primary refractory DLBCL

Blood, 2018-04, Vol.131 (16), p.1805-1808

2018

Volltextzugriff (PDF)

Left ventricular mechanics and arterial-ventricular coupling following high-intensity interval exercise

Journal of applied physiology (1985), 2013-12, Vol.115 (11), p.1705-1713

2013

Volltextzugriff (PDF)

Characterising Eastern Grey Kangaroos (Macropus giganteus) as Hosts of Coxiella burnetii

Microorganisms (Basel), 2024-07, Vol.12 (7), p.1477

2024

Volltextzugriff (PDF)

Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease

American journal of human genetics, 2017-01, Vol.100 (1), p.75-90

2017

Volltextzugriff (PDF)

Radiotherapy Eradicates Malignant T Cells and Is Associated with Improved Survival in Early-Stage Mycosis Fungoides

Clinical cancer research, 2020-01, Vol.26 (2), p.408-418

2020

Volltextzugriff (PDF)

Disease Evolution and Response to Rapamycin in Activated Phosphoinositide 3-Kinase δ Syndrome: The European Society for Immunodeficiencies-Activated Phosphoinositide 3-Kinase δ Syndrome Registry

Frontiers in immunology, 2018-03, Vol.9, p.543-543

2018

Volltextzugriff (PDF)

1 – 25 von 46

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(45)
Mit Volltextzugriff
(40)

Publikationsform

Artikel
(45)
Buchkapitel
(1)

Sprache

Englisch
(46)
Japanisch
(4)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

DHDDS related epilepsy––Report of familial cases and review of the literature

Perampanel and decanoic acid show synergistic action against AMPA receptors and seizures

Heterozygous truncation mutations of the SMC1A gene cause a severe early onset epilepsy with cluster seizures in females: Detailed phenotyping of 10 new cases

Suspected pheochromocytoma in a patient with Guillain-Barré syndrome

The p.M292T NDUFS2 mutation causes complex I-deficient Leigh syndrome in multiple families

Teaching NeuroImages: alternating ptosis and Marcus Gunn jaw-winking phenomenon with PHOX2B mutation

Speech and language delay in two children: an unusual presentation of hyperthyroidism

Levetiracetam in the treatment of infantile spasms

Cystic fibrosis presenting with bilateral facial palsy

Heterozygous truncation mutations of the SMC 1A gene cause a severe early onset epilepsy with cluster seizures in females: Detailed phenotyping of 10 new cases

Epilepsy with Myoclonic Absences

Bidirectional superior cavopulmonary anastomosis: how young is too young?

Childhood Obesity and Cardiovascular Dysfunction

Tissue distribution of Coxiella burnetii and antibody responses in macropods co-grazing with livestock in Queensland, Australia

Obesity and arterial stiffness in children: systematic review and meta-analysis

Serological evidence for the presence of wobbly possum disease virus in Australia

Validation of an Indirect Immunofluorescence Assay and Commercial Q Fever Enzyme-Linked Immunosorbent Assay for Use in Macropods

Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis

Perioperative Safety in the Longitudinal Assessment of Bariatric Surgery

A phase 1 study of ibrutinib in combination with R-ICE in patients with relapsed or primary refractory DLBCL

Left ventricular mechanics and arterial-ventricular coupling following high-intensity interval exercise

Characterising Eastern Grey Kangaroos (Macropus giganteus) as Hosts of Coxiella burnetii

Comprehensive Rare Variant Analysis via Whole-Genome Sequencing to Determine the Molecular Pathology of Inherited Retinal Disease

Radiotherapy Eradicates Malignant T Cells and Is Associated with Improved Survival in Early-Stage Mycosis Fungoides

Disease Evolution and Response to Rapamycin in Activated Phosphoinositide 3-Kinase δ Syndrome: The European Society for Immunodeficiencies-Activated Phosphoinositide 3-Kinase δ Syndrome Registry

Suchergebnisse filtern