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...

Association of autoantibodies to muscarinic acetylcholine receptors with gastrointestinal symptoms and disease severity in patients with postural orthostatic tachycardia syndrome

Immunologic research, 2022-04, Vol.70 (2), p.197-207

2022

Volltextzugriff (PDF)

Acute Reversible Encephalopathy with Neuronal Intranuclear Inclusion Disease Diagnosed by a Brain Biopsy: Inferring the Mechanism of Encephalopathy from Radiological and Histological Findings

Internal Medicine, 2023/06/15, Vol.62(12), pp.1821-1825

2023

Volltextzugriff (PDF)

G protein-coupled receptors related to autoimmunity in postural orthostatic tachycardia syndrome

Immunological medicine, 2024-06, p.1-8

2024

Volltextzugriff (PDF)

Case report: MRI-negative myelitis following COVID-19 with SEP abnormalities: a case series and literature review

Frontiers in neurology, 2023-10, Vol.14

2023

Volltextzugriff (PDF)

Longitudinally extensive transverse myelitis as neurosarcoidosis accompanying duropathy

Neurology and clinical neuroscience, 2023-05, Vol.11 (3), p.173-175

2023

Volltextzugriff (PDF)

Coexistence of Hereditary Spastic Paraplegia Type 4 and Narcolepsy: A Case Report

Case reports in neurology, 2021-01, Vol.13 (1), p.84-91

2021

Volltextzugriff (PDF)

Deep brain stimulation for patients with dystonia in Machado–Joseph disease: three case reports

Journal of neurology, 2023-06, Vol.270 (6), p.3261-3265

2023

Volltextzugriff (PDF)

A case of non-fluent/agrammatic variant of primary progressive aphasia with logoclonia

Rinshō shinkeigaku, 2023, Vol.63 (1), p.7-14, Article cn-001628

2023

Volltextzugriff (PDF)

A Case of Acute Reversible Encephalopathy with Neuronal Intranuclear Inclusion Disease Diagnosed by a Brain Biopsy: Inferring the Mechanism of Encephalopathy from Radiological and Histological Findings

Internal Medicine, 2023, pp.0156-22

2023

Volltextzugriff (PDF)

Central nervous system involvement in patients with critical illness polyneuropathy

Journal of the neurological sciences, 2019-01, Vol.396, p.216-218

2019

Volltextzugriff (PDF)

A case of chronic postural tachycardia syndrome with positive anti-ganglionic acetylcholine receptor (gAChR) antibody

Rinshō shinkeigaku, 2021, Vol.61 (8), p.547-551, Article cn-001598

2021

Volltextzugriff (PDF)

Progressive supranuclear palsy-Richardson syndrome with visual attention disturbance (Holmes and Horrax) and ataxie optique (Garcin): a case report

Rinshō shinkeigaku, 2019, Vol.59 (11), p.730-735

2019

Volltextzugriff (PDF)

Clinical and genetic features of Charcot‐Marie‐Tooth disease 2F and hereditary motor neuropathy 2B in Japan

Journal of the peripheral nervous system, 2018-03, Vol.23 (1), p.40-48

2018

Volltextzugriff (PDF)

Dopa-responsive acute disseminated encephalomyelitis with marked atrophy of the striate body

BMJ case reports, 2016-06, Vol.2016, p.bcr2016215859

2016

Volltextzugriff (PDF)

Variable phenotypes in a family with mitochondrial encephalomyopathy harboring a 3291T > C mutation in mitochondrial DNA

Neurological sciences, 2011-10, Vol.32 (5), p.861-864

2011

Volltextzugriff (PDF)

Deep brain stimulation for patients with dystonia in Machado-Joseph disease: three case reports

Journal of neurology, 2023, Vol.270 (6), p.3261-3265

2023

Volltextzugriff (PDF)

Case report: MRI-negative myelitis following COVID-19 with SEP abnormalities: a case series and literature review

Frontiers in neurology, 2023, Vol.14, p.1275696-1275696

2023

Volltextzugriff (PDF)

Coexistence of Hereditary Spastic Paraplegia Type 4 and Narcolepsy: A Case Report

Case reports in neurology, 2021, Vol.13 (1), p.84-91

2021

Volltextzugriff (PDF)

Activation of the thrombopoietin receptor by mutant calreticulin in CALR-mutant myeloproliferative neoplasms

Blood, 2016-03, Vol.127 (10), p.1307-1316

2016

Volltextzugriff (PDF)

Distribution of genetic alterations in high-risk early-stage cervical cancer patients treated with postoperative radiation therapy

Scientific reports, 2021-05, Vol.11 (1), p.10567-10567, Article 10567

2021

Volltextzugriff (PDF)

Homomultimerization of mutant calreticulin is a prerequisite for MPL binding and activation

Leukemia, 2019-01, Vol.33 (1), p.122-131

2019

Volltextzugriff (PDF)

Angioimmunoblastic T-cell Lymphoma Presenting as a Methotrexate-associated Lymphoproliferative Disorder with Extreme Peripheral Blood Plasmacytosis

Internal Medicine, 2022/09/01, Vol.61(17), pp.2655-2660

2022

Volltextzugriff (PDF)

Frequent BRAF or EGFR Mutations in Ciliated Muconodular Papillary Tumors of the Lung

Journal of thoracic oncology, 2016-02, Vol.11 (2), p.261-265

2016

Volltextzugriff (PDF)

Genomic alterations in STK11 can predict clinical outcomes in cervical cancer patients

Gynecologic oncology, 2020-01, Vol.156 (1), p.203-210

2020

Volltextzugriff (PDF)

JAK2, CALR, and MPL mutation spectrum in Japanese patients with myeloproliferative neoplasms

Haematologica (Roma), 2015-02, Vol.100 (2), p.e46-e48

2015

Volltextzugriff (PDF)

1 – 25 von 69

Suche als RSS-Feed

Aktive Filter

SpracheEnglisch

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(61)
Mit Volltextzugriff
(63)

Publikationsform

Artikel
(65)
Berichte
(4)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

Plos One
(7)
Blood
(5)
Internal Medicine
(4)
Journal Of Thoracic Oncology
(4)
Anticancer Research
(3)
Anticancer Research/anticancer Research
(3)
Circulation
(3)
Rinshō Shinkeigaku
(3)
International Journal Of Hematology
(2)
Oncotarget
(2)

5 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Association of autoantibodies to muscarinic acetylcholine receptors with gastrointestinal symptoms and disease severity in patients with postural orthostatic tachycardia syndrome

Acute Reversible Encephalopathy with Neuronal Intranuclear Inclusion Disease Diagnosed by a Brain Biopsy: Inferring the Mechanism of Encephalopathy from Radiological and Histological Findings

G protein-coupled receptors related to autoimmunity in postural orthostatic tachycardia syndrome

Case report: MRI-negative myelitis following COVID-19 with SEP abnormalities: a case series and literature review

Longitudinally extensive transverse myelitis as neurosarcoidosis accompanying duropathy

Coexistence of Hereditary Spastic Paraplegia Type 4 and Narcolepsy: A Case Report

Deep brain stimulation for patients with dystonia in Machado–Joseph disease: three case reports

A case of non-fluent/agrammatic variant of primary progressive aphasia with logoclonia

A Case of Acute Reversible Encephalopathy with Neuronal Intranuclear Inclusion Disease Diagnosed by a Brain Biopsy: Inferring the Mechanism of Encephalopathy from Radiological and Histological Findings

Central nervous system involvement in patients with critical illness polyneuropathy

A case of chronic postural tachycardia syndrome with positive anti-ganglionic acetylcholine receptor (gAChR) antibody

Progressive supranuclear palsy-Richardson syndrome with visual attention disturbance (Holmes and Horrax) and ataxie optique (Garcin): a case report

Clinical and genetic features of Charcot‐Marie‐Tooth disease 2F and hereditary motor neuropathy 2B in Japan

Dopa-responsive acute disseminated encephalomyelitis with marked atrophy of the striate body

Variable phenotypes in a family with mitochondrial encephalomyopathy harboring a 3291T > C mutation in mitochondrial DNA

Deep brain stimulation for patients with dystonia in Machado-Joseph disease: three case reports

Case report: MRI-negative myelitis following COVID-19 with SEP abnormalities: a case series and literature review

Coexistence of Hereditary Spastic Paraplegia Type 4 and Narcolepsy: A Case Report

Activation of the thrombopoietin receptor by mutant calreticulin in CALR-mutant myeloproliferative neoplasms

Distribution of genetic alterations in high-risk early-stage cervical cancer patients treated with postoperative radiation therapy

Homomultimerization of mutant calreticulin is a prerequisite for MPL binding and activation

Angioimmunoblastic T-cell Lymphoma Presenting as a Methotrexate-associated Lymphoproliferative Disorder with Extreme Peripheral Blood Plasmacytosis

Frequent BRAF or EGFR Mutations in Ciliated Muconodular Papillary Tumors of the Lung

Genomic alterations in STK11 can predict clinical outcomes in cervical cancer patients

JAK2, CALR, and MPL mutation spectrum in Japanese patients with myeloproliferative neoplasms

Aktive Filter

Suchergebnisse filtern