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...

Recessive PIEZO2 stop mutation causes distal arthrogryposis with distal muscle weakness, scoliosis and proprioception defects

Journal of human genetics, 2017-04, Vol.62 (4), p.497-501

2017

Volltextzugriff (PDF)

Isolated spinal cord granulomatous angiitis: a case report and review of the literature

Journal of neurology, 2022-06, Vol.269 (6), p.3175-3179

2022

Volltextzugriff (PDF)

Electrodiagnostic features of sciatic neuropathy: Six-year referral center experience

Neurological sciences and neurophysiology, 2023-07, Vol.40 (3), p.145-151

2023

Volltextzugriff (PDF)

Vincristine-induced neurotoxicity: electrophysiological features in children

Neurological research (New York), 2016-02, Vol.38 (2), p.124-129

2016

Volltextzugriff (PDF)

Adult mouse basal forebrain harbors two distinct cholinergic populations defined by their electrophysiology

Frontiers in behavioral neuroscience, 2012-05, Vol.6, p.21-21

2012

Volltextzugriff (PDF)

A study on the modeling and simulation for the motor unit action potential

Communications Series A1 Mathematics & Statistics, 2021-01, Vol.70 (1), p.290-299

2021

Volltextzugriff (PDF)

Alteration of the affective modulation of the startle reflex during antidepressant treatment

Psychophysiology, 2019-02, Vol.56 (2), p.e13286-n/a

2019

Volltextzugriff (PDF)

Concentric needle jitter analysis of the genioglossus muscle in patients with motor neuron disease

Neurological research (New York), 2024-06, Vol.46 (6), p.578-582

2024

Volltextzugriff (PDF)

Expanding the genotype-phenotype spectrum of autosomal recessive Charcot-Marie-Tooth disease: A novel PLEKHG5 gene mutation: A novel PLEKHG5 gene mutation

Neurology Asia, 2021-09, Vol.26 (3), p.607-612

2021

Volltextzugriff (PDF)

Electrophysiologic evaluation of facial nerve functions after oxaliplatin treatment

Cancer chemotherapy and pharmacology, 2019-09, Vol.84 (3), p.513-520

2019

Volltextzugriff (PDF)

Modulation of Cerebellar‐Cortical Connections in Multiple System Atrophy Type C by Cerebellar Repetitive Transcranial Magnetic Stimulation

Neuromodulation (Malden, Mass.), 2018-06, Vol.21 (4), p.402-408

2018

Volltextzugriff (PDF)

Brachial Diparesis due to Motor Neuronopathy as One of the Predominant Presenting Signs of Occult Small Cell Lung Carcinoma

Internal Medicine, 2016/06/15, Vol.55(12), pp.1641-1643

2016

Volltextzugriff (PDF)

Identification of a Novel Twinkle Mutation in a Family With Infantile Onset Spinocerebellar Ataxia by Whole Exome Sequencing

Pediatric neurology, 2012-03, Vol.46 (3), p.172-177

2012

Volltextzugriff (PDF)

A rare case of longitudinal Brucella myelitis

The spine journal, 2015-07, Vol.15 (7), p.1689-1690

2015

Volltextzugriff (PDF)

Sclerotherapy with bleomycin does not adversely affect facial nerve function in children with cervicofacial cystic lymphatic malformation

Journal of pediatric surgery, 2010-08, Vol.45 (8), p.1627-1632

2010

Volltextzugriff (PDF)

The effect of poly(3-hydroxybutyrate-co-3- hydroxyhexanoate) (PHBHHx) and human mesenchymal stem cell (hMSC) on axonal regeneration in experimental sciatic nerve damage

International journal of neuroscience, 2014-09, Vol.124 (9), p.685-696

2014

Volltextzugriff (PDF)

New Measurement in the Diagnosis of Critical Illness Myopathy: Stimulus Intensity and Compound Muscle Action Potential Duration Relationship (P1-11.013)

Neurology, 2024-04, Vol.102 (17_supplement_1)

2024

Volltextzugriff (PDF)

‘Jaw clenching’ in anti-Ri – Antibody-associated paraneoplastic syndrome

Parkinsonism & related disorders, 2013-01, Vol.19 (1), p.132-133

2013

Volltextzugriff (PDF)

Fulminant Central Plus Peripheral Nervous System Demyelination without Antibodies to Neurofascin

Canadian journal of neurological sciences, 2016-01, Vol.43 (1), p.149-156

2016

Volltextzugriff (PDF)

Multimodal integration and modulation of visual and somatosensory inputs on the corticospinal excitability

Neurophysiologie clinique, 2023-06, Vol.53 (3), p.102842-102842, Article 102842

2023

Volltextzugriff (PDF)

Tracking Pain in Resting State Networks in Patients with Hereditary and Diabetic Neuropathy

Noro Psikiyatri Arsivi, 2019-06, Vol.56 (2), p.92-98

2019

Volltextzugriff (PDF)

Cystinosis beyond kidneys: gastrointestinal system and muscle involvement

BMC gastroenterology, 2020-07, Vol.20 (1), p.242-242, Article 242

2020

Volltextzugriff (PDF)

Winged Scapula: Clinical and Electrophysiological Features and Common Causes Based on 20 Years of Experience in a Referral Center in Turkey

Journal of clinical neurophysiology, 2023-05, Vol.40 (4), p.286-292

2023

Volltextzugriff (PDF)

Medial plantar and dorsal sural nerve conduction studies increase the sensitivity in the detection of neuropathy in diabetic patients

Clinical neurophysiology, 2008-04, Vol.119 (4), p.880-885

2008

Volltextzugriff (PDF)

Propriospinal Myoclonus in a Child

Journal of child neurology, 2010-07, Vol.25 (7), p.912-915

2010

Volltextzugriff (PDF)

1 – 25 von 83

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(70)
Mit Volltextzugriff
(57)

Publikationsform

Sprache

Englisch
(81)
Türkisch
(2)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

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

Menü

Weitere Dienste

Einstellungen

Recessive PIEZO2 stop mutation causes distal arthrogryposis with distal muscle weakness, scoliosis and proprioception defects

Isolated spinal cord granulomatous angiitis: a case report and review of the literature

Electrodiagnostic features of sciatic neuropathy: Six-year referral center experience

Vincristine-induced neurotoxicity: electrophysiological features in children

Adult mouse basal forebrain harbors two distinct cholinergic populations defined by their electrophysiology

A study on the modeling and simulation for the motor unit action potential

Alteration of the affective modulation of the startle reflex during antidepressant treatment

Concentric needle jitter analysis of the genioglossus muscle in patients with motor neuron disease

Expanding the genotype-phenotype spectrum of autosomal recessive Charcot-Marie-Tooth disease: A novel PLEKHG5 gene mutation: A novel PLEKHG5 gene mutation

Electrophysiologic evaluation of facial nerve functions after oxaliplatin treatment

Modulation of Cerebellar‐Cortical Connections in Multiple System Atrophy Type C by Cerebellar Repetitive Transcranial Magnetic Stimulation

Brachial Diparesis due to Motor Neuronopathy as One of the Predominant Presenting Signs of Occult Small Cell Lung Carcinoma

Identification of a Novel Twinkle Mutation in a Family With Infantile Onset Spinocerebellar Ataxia by Whole Exome Sequencing

A rare case of longitudinal Brucella myelitis

Sclerotherapy with bleomycin does not adversely affect facial nerve function in children with cervicofacial cystic lymphatic malformation

The effect of poly(3-hydroxybutyrate-co-3- hydroxyhexanoate) (PHBHHx) and human mesenchymal stem cell (hMSC) on axonal regeneration in experimental sciatic nerve damage

New Measurement in the Diagnosis of Critical Illness Myopathy: Stimulus Intensity and Compound Muscle Action Potential Duration Relationship (P1-11.013)

‘Jaw clenching’ in anti-Ri – Antibody-associated paraneoplastic syndrome

Fulminant Central Plus Peripheral Nervous System Demyelination without Antibodies to Neurofascin

Multimodal integration and modulation of visual and somatosensory inputs on the corticospinal excitability

Tracking Pain in Resting State Networks in Patients with Hereditary and Diabetic Neuropathy

Cystinosis beyond kidneys: gastrointestinal system and muscle involvement

Winged Scapula: Clinical and Electrophysiological Features and Common Causes Based on 20 Years of Experience in a Referral Center in Turkey

Medial plantar and dorsal sural nerve conduction studies increase the sensitivity in the detection of neuropathy in diabetic patients

Propriospinal Myoclonus in a Child

Suchergebnisse filtern