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...

Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study

The Lancet (British edition), 2008-05, Vol.371 (9623), p.1505-1512

2008

Volltextzugriff (PDF)

Citrulline and muscle protein homeostasis in three different models of hypercatabolism

Clinical nutrition (Edinburgh, Scotland), 2020-03, Vol.39 (3), p.917-927

2020

Volltextzugriff (PDF)

PT01.5: Citrulline and Muscle Protein in Hypercatabolic Situations

Clinical nutrition (Edinburgh, Scotland), 2016-09, Vol.35, p.S22-S23

2016

Volltextzugriff (PDF)

Cerebral cavernous malformations: mutations in Krit1

Neurology, 2002-03, Vol.58 (6), p.853-857

2002

Volltextzugriff (PDF)

CCM3 mutations are uncommon in cerebral cavernous malformations

Neurology, 2005-12, Vol.65 (12), p.1982-1983

2005

Volltextzugriff (PDF)

CCM1 mutation screen of sporadic cases with cerebral cavernous malformations

Neurology, 2004-04, Vol.62 (7), p.1213-1215

2004

Volltextzugriff (PDF)

A new locus for autosomal dominant intracranial aneurysm, ANIB4, maps to chromosome 5p15.2-14.3

Journal of medical genetics, 2006-06, Vol.43 (6), p.e31-e31

2006

Volltextzugriff (PDF)

Large germline deletions and duplication in isolated cerebral cavernous malformation patients

Neurogenetics, 2007-04, Vol.8 (2), p.149-153

2007

Volltextzugriff (PDF)

No CCM2 mutations in a cohort of 31 sporadic cases

Neurology, 2004-11, Vol.63 (10), p.1979-1979

2004

Volltextzugriff (PDF)

Inherited cavernous malformations of the central nervous system: clinical and genetic features in 19 Swiss families

Neurosurgical review, 2010, Vol.33 (1), p.47-51

2010

Volltextzugriff (PDF)

Mutations in a Gene Encoding a Novel Protein Containing a Phosphotyrosine-Binding Domain Cause Type 2 Cerebral Cavernous Malformations

American journal of human genetics, 2003-12, Vol.73 (6), p.1459-1464

2003

Volltextzugriff (PDF)

Clinical outcome after traumatic spinal fractures in patients with ankylosing spinal disorders compared with control patients

The spine journal, 2014-05, Vol.14 (5), p.729-740

2014

Volltextzugriff (PDF)

Linkage to the CCM2 locus and genetic heterogeneity in familial cerebral cavernous malformation

Canadian journal of neurological sciences, 2003-05, Vol.30 (2), p.122-128

2003

Volltextzugriff (PDF)

Endoscopic closure of acute perforations of the GI tract: a systematic review of the literature

Gastrointestinal endoscopy, 2015-10, Vol.82 (4), p.618-628.e5

2015

Volltextzugriff (PDF)

Bankart repair with remplissage vs. Latarjet procedure on recurrence, postoperative pain scores, external rotation, and Rowe score in patients with a Hill-Sachs lesion. A systematic review

JSES reviews, reports, and techniques, 2023-11, Vol.3 (4), p.461-468

2023

Volltextzugriff (PDF)

Effect of peroral endoscopic myotomy on esophagogastric junction physiology in patients with achalasia

Gastrointestinal endoscopy, 2013-07, Vol.78 (1), p.39-44

2013

Volltextzugriff (PDF)

The prevalence of vertebral fractures in diffuse idiopathic skeletal hyperostosis and ankylosing spondylitis: A systematic review and meta-analysis

North American Spine Society journal (NASSJ), 2024-03, Vol.17, p.100312-100312, Article 100312

2024

Volltextzugriff (PDF)

Familial cavernous malformations of the central nervous system. A clinical and genetic study of 15 German families

Nervenarzt, 2005-02, Vol.76 (2), p.175-180

2005

Volltextzugriff (PDF)

Stabilizing osteoporotic thoracolumbar fractures through an anterior or posterior approach: what works best?

The spine journal, 2013-12, Vol.13 (12), p.1733-1735

Verlaan, J.J., MD, PhD

2013

Volltextzugriff (PDF)

Diffuse idiopathic skeletal hyperostosis of the cervical spine: an underestimated cause of dysphagia and airway obstruction

The spine journal, 2011-11, Vol.11 (11), p.1058-1067

2011

Volltextzugriff (PDF)

Spinal instability as defined by the spinal instability neoplastic score is associated with radiotherapy failure in metastatic spinal disease

The spine journal, 2014-12, Vol.14 (12), p.2835-2840

2014

Volltextzugriff (PDF)

The 14q restless legs syndrome locus in the French Canadian population

Annals of neurology, 2004-06, Vol.55 (6), p.887-891

2004

Volltextzugriff (PDF)

Endoscopic gastric volume reduction with a novel articulating plication device is safe and effective in the treatment of obesity (with video)

Gastrointestinal endoscopy, 2015-02, Vol.81 (2), p.312-320

2015

Volltextzugriff (PDF)

A mutation in the HSN2 gene causes sensory neuropathy type II in a Lebanese family

Annals of neurology, 2004-10, Vol.56 (4), p.572-575

2004

Volltextzugriff (PDF)

1 – 25 von 229

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(204)
Mit Volltextzugriff
(195)

Publikationsform

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 30 Tagen
(1)
... seit 90 Tagen
(3)

Menü

Weitere Dienste

Einstellungen

Bone mineral density, osteoporosis, and osteoporotic fractures: a genome-wide association study

Citrulline and muscle protein homeostasis in three different models of hypercatabolism

PT01.5: Citrulline and Muscle Protein in Hypercatabolic Situations

Cerebral cavernous malformations: mutations in Krit1

CCM3 mutations are uncommon in cerebral cavernous malformations

CCM1 mutation screen of sporadic cases with cerebral cavernous malformations

A new locus for autosomal dominant intracranial aneurysm, ANIB4, maps to chromosome 5p15.2-14.3

Large germline deletions and duplication in isolated cerebral cavernous malformation patients

No CCM2 mutations in a cohort of 31 sporadic cases

Inherited cavernous malformations of the central nervous system: clinical and genetic features in 19 Swiss families

Mutations in a Gene Encoding a Novel Protein Containing a Phosphotyrosine-Binding Domain Cause Type 2 Cerebral Cavernous Malformations

Clinical outcome after traumatic spinal fractures in patients with ankylosing spinal disorders compared with control patients

Linkage to the CCM2 locus and genetic heterogeneity in familial cerebral cavernous malformation

Endoscopic closure of acute perforations of the GI tract: a systematic review of the literature

Surgery for metastatic spine tumors in the elderly. Advanced age is not a contraindication to surgery

Bankart repair with remplissage vs. Latarjet procedure on recurrence, postoperative pain scores, external rotation, and Rowe score in patients with a Hill-Sachs lesion. A systematic review

Effect of peroral endoscopic myotomy on esophagogastric junction physiology in patients with achalasia

The prevalence of vertebral fractures in diffuse idiopathic skeletal hyperostosis and ankylosing spondylitis: A systematic review and meta-analysis

Familial cavernous malformations of the central nervous system. A clinical and genetic study of 15 German families

Stabilizing osteoporotic thoracolumbar fractures through an anterior or posterior approach: what works best?

Diffuse idiopathic skeletal hyperostosis of the cervical spine: an underestimated cause of dysphagia and airway obstruction

Spinal instability as defined by the spinal instability neoplastic score is associated with radiotherapy failure in metastatic spinal disease

The 14q restless legs syndrome locus in the French Canadian population

Endoscopic gastric volume reduction with a novel articulating plication device is safe and effective in the treatment of obesity (with video)

A mutation in the HSN2 gene causes sensory neuropathy type II in a Lebanese family

Suchergebnisse filtern