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...

Genetic Testing for Dilated Cardiomyopathy in Clinical Practice

Journal of cardiac failure, 2012-04, Vol.18 (4), p.296-303

2012

Volltextzugriff (PDF)

eP219: Genome Sequencing (GS) as a first test in the clinic

Genetics in medicine, 2022-03, Vol.24 (3), p.S136-S136

2022

Volltextzugriff (PDF)

P273: Adjusted polygenic score: Translation of a new concept for cardiovascular disease prevention and management

Genetics in Medicine Open, 2023, Vol.1 (1), p.100301, Article 100301

2023

Volltextzugriff (PDF)

A Rare Case of Congenital Myasthenia Syndrome 11 Caused by a Novel Mutation in RAPSN Diagnosed with Rapid Whole Genome Sequencing (rWGS). (P18-5.004)

Neurology, 2022-05, Vol.98 (18_supplement)

2022

Volltextzugriff (PDF)

POLYGENIC RISK SCORES AND THEIR PHENOTYPIC ADJUSTMENT: NOVEL BIOMARKERS IN CARDIOVASCULAR DISEASE PREVENTION

Journal of hypertension, 2023-06, Vol.41 (Suppl 3), p.e149-e150

2023

Volltextzugriff (PDF)

One stone, two birds: how a WGS-enabled diagnostic journey transforms into a precision population health service for the 21st century

Molecular genetics and metabolism, 2021-04, Vol.132, p.S77-S78

2021

Volltextzugriff (PDF)

eP344 - A novel deleterious NOTCH2 mutation (c.5422dup) on a female with premature ovarian insufficiency without symptoms of Alagille syndrome 2

Molecular genetics and metabolism, 2021-04, Vol.132, p.S220-S221

2021

Volltextzugriff (PDF)

eP114 - One stone, two birds: how a WGS-enabled diagnostic journey transforms into a precision population health service for the 21st century

Molecular genetics and metabolism, 2021-04, Vol.132, p.S77-S78

2021

Volltextzugriff (PDF)

A novel deleterious NOTCH2 mutation (c.5422dup) on a female with premature ovarian insufficiency without symptoms of Alagille syndrome 2

Molecular genetics and metabolism, 2021-04, Vol.132, p.S220-S221

2021

Volltextzugriff (PDF)

Primary appendiceal mucinous adenocarcinoma in two first-degree relatives: case report and review

Hereditary cancer in clinical practice, 2011-05, Vol.9 (1), p.1-1, Article 1

2011

Volltextzugriff (PDF)

Hereditary disorders of connective tissue: A guide to the emerging differential diagnosis

Genetics in medicine, 2010-06, Vol.12 (6), p.344-354

2010

Volltextzugriff (PDF)

De novo missense variants in MEIS2 recapitulate the microdeletion phenotype of cardiac and palate abnormalities, developmental delay, intellectual disability and dysmorphic features

American journal of medical genetics. Part A, 2018-09, Vol.176 (9), p.1845-1851

2018

Volltextzugriff (PDF)

POGZ truncating alleles cause syndromic intellectual disability

Genome medicine, 2016-01, Vol.8 (1), p.3, Article 3

2016

Volltextzugriff (PDF)

Mitral Annular Disjunction in Heritable Thoracic Aortic Disease: Insights From the Montalcino Aortic Consortium

Journal of the American Heart Association, 2024-10, p.e036274

2024

Volltextzugriff (PDF)

Overview of systematic reviews comparing endovascular to best medical treatment for large-vessel occlusion acute ischaemic stroke: an umbrella review

Therapeutic advances in neurological disorders, 2024-01, Vol.17, p.17562864241246938-17562864241246938

2024

Volltextzugriff (PDF)

Floating Carotid Thrombus in a Patient With Essential Thrombocytemia due to Calreticulin Mutation

Stroke (1970), 2023-05, Vol.54 (5), p.e207-e208

2023

Volltextzugriff (PDF)

Expanding indications for endovascular thrombectomy-how to leave no patient behind

Therapeutic Advances in Neurological Disorders, 2021, Vol.14, p.1756286421998905

2021

Volltextzugriff (PDF)

Off-label use of intravenous thrombolysis for acute ischemic stroke: a critical appraisal of randomized and real-world evidence

Therapeutic Advances in Neurological Disorders, 2021, Vol.14, p.1756286421997368

2021

Volltextzugriff (PDF)

Endovascular treatment for anterior circulation large-vessel occlusion ischemic stroke with low ASPECTS: a systematic review and meta-analysis

Therapeutic advances in neurological disorders, 2022-01, Vol.15, p.17562864221139632

2022

Volltextzugriff (PDF)

Endovascular treatment for large-core ischaemic stroke: a meta-analysis of randomised controlled clinical trials

Journal of neurology, neurosurgery and psychiatry, 2023-10, Vol.94 (10), p.781-785

2023

Volltextzugriff (PDF)

Computed Tomography Perfusion Imaging in Acute Ischemic Stroke: Accurate Interpretation Matters

Stroke (1970), 2023-03, Vol.54 (3), p.e104-e108

2023

Volltextzugriff (PDF)

Diagnosis and treatment of acute isolated proximal internal carotid artery occlusions: a narrative review

Therapeutic Advances in Neurological Disorders, 2022-01, Vol.15, p.17562864221136335-17562864221136335

2022

Volltextzugriff (PDF)

Heart failure and stroke: The underrepresentation of the heart failure with preserved ejection fraction subtype in randomized clinical trials of therapeutic anticoagulation

Journal of the neurological sciences, 2024-11, Vol.466, p.123231, Article 123231

2024

Volltextzugriff (PDF)

Endovascular treatment for basilar artery occlusion: A systematic review and meta‐analysis

European journal of neurology, 2021-06, Vol.28 (6), p.2106-2110

2021

Volltextzugriff (PDF)

Acute reperfusion therapies for acute ischemic stroke patients with unknown time of symptom onset or in extended time windows: an individualized approach

Therapeutic Advances in Neurological Disorders, 2021, Vol.14, p.17562864211021182

2021

Volltextzugriff (PDF)

1 – 25 von 57

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(51)
Mit Volltextzugriff
(46)

Publikationsform

Artikel
(55)
Berichte
(2)

Sprache

Englisch
(57)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

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

Menü

Weitere Dienste

Einstellungen

Genetic Testing for Dilated Cardiomyopathy in Clinical Practice

eP219: Genome Sequencing (GS) as a first test in the clinic

P273: Adjusted polygenic score: Translation of a new concept for cardiovascular disease prevention and management

A Rare Case of Congenital Myasthenia Syndrome 11 Caused by a Novel Mutation in RAPSN Diagnosed with Rapid Whole Genome Sequencing (rWGS). (P18-5.004)

POLYGENIC RISK SCORES AND THEIR PHENOTYPIC ADJUSTMENT: NOVEL BIOMARKERS IN CARDIOVASCULAR DISEASE PREVENTION

One stone, two birds: how a WGS-enabled diagnostic journey transforms into a precision population health service for the 21st century

eP344 - A novel deleterious NOTCH2 mutation (c.5422dup) on a female with premature ovarian insufficiency without symptoms of Alagille syndrome 2

eP114 - One stone, two birds: how a WGS-enabled diagnostic journey transforms into a precision population health service for the 21st century

A novel deleterious NOTCH2 mutation (c.5422dup) on a female with premature ovarian insufficiency without symptoms of Alagille syndrome 2

Primary appendiceal mucinous adenocarcinoma in two first-degree relatives: case report and review

Hereditary disorders of connective tissue: A guide to the emerging differential diagnosis

De novo missense variants in MEIS2 recapitulate the microdeletion phenotype of cardiac and palate abnormalities, developmental delay, intellectual disability and dysmorphic features

POGZ truncating alleles cause syndromic intellectual disability

Mitral Annular Disjunction in Heritable Thoracic Aortic Disease: Insights From the Montalcino Aortic Consortium

Overview of systematic reviews comparing endovascular to best medical treatment for large-vessel occlusion acute ischaemic stroke: an umbrella review

Floating Carotid Thrombus in a Patient With Essential Thrombocytemia due to Calreticulin Mutation

Expanding indications for endovascular thrombectomy-how to leave no patient behind

Off-label use of intravenous thrombolysis for acute ischemic stroke: a critical appraisal of randomized and real-world evidence

Endovascular treatment for anterior circulation large-vessel occlusion ischemic stroke with low ASPECTS: a systematic review and meta-analysis

Endovascular treatment for large-core ischaemic stroke: a meta-analysis of randomised controlled clinical trials

Computed Tomography Perfusion Imaging in Acute Ischemic Stroke: Accurate Interpretation Matters

Diagnosis and treatment of acute isolated proximal internal carotid artery occlusions: a narrative review

Heart failure and stroke: The underrepresentation of the heart failure with preserved ejection fraction subtype in randomized clinical trials of therapeutic anticoagulation

Endovascular treatment for basilar artery occlusion: A systematic review and meta‐analysis

Acute reperfusion therapies for acute ischemic stroke patients with unknown time of symptom onset or in extended time windows: an individualized approach

Suchergebnisse filtern