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...

Minimal detectable change and minimal clinically important difference in spinal muscular atrophy patients

European journal of neurology, 2021-06, Vol.28 (6), p.e40-e41

2021

Volltextzugriff (PDF)

Risdiplam in non‐sitter patients aged 16 years and older with 5q spinal muscular atrophy

Muscle & nerve, 2023-05, Vol.67 (5), p.407-411

2023

Volltextzugriff (PDF)

Nusinersen in adult patients with 5q spinal muscular atrophy: A multicenter observational cohorts' study

European journal of neurology, 2022-11, Vol.29 (11), p.3337-3346

2022

Volltextzugriff (PDF)

Validation of motor and functional scales for the evaluation of adult patients with 5q spinal muscular atrophy

European journal of neurology, 2022-12, Vol.29 (12), p.3666-3675

2022

Volltextzugriff (PDF)

Natural history data in adults with SMA

Lancet neurology, 2020-07, Vol.19 (7), p.564-565

Vázquez-Costa, Juan F

2020

Volltextzugriff (PDF)

Estimation of the prevalence and incidence of motor neuron diseases in two Spanish regions: Catalonia and Valencia

Scientific reports, 2021-03, Vol.11 (1), p.6207-15, Article 6207

2021

Volltextzugriff (PDF)

Distal hereditary motor neuropathies: Mutation spectrum and genotype–phenotype correlation

European journal of neurology, 2021-04, Vol.28 (4), p.1334-1343

2021

Volltextzugriff (PDF)

Insights into phenotypic variability caused by GARS1 pathogenic variants

European journal of neurology, 2024-10, Vol.31 (10), p.e16416-n/a

2024

Volltextzugriff (PDF)

Do we really need to calculate a minimal important difference for ALSFRS-R?: A letter in response to 'Clinically meaningful change: evaluation of the Rasch-built Overall Amyotrophic Lateral Sclerosis Disability Scale (ROADS) and the ALSFRS-R' published in Vol. 24(3-4), pp. 311-316

Amyotrophic lateral sclerosis and frontotemporal degeneration, 2024-02, Vol.25 (1-2), p.214-215

Vázquez-Costa, Juan Francisco

2024

Volltextzugriff (PDF)

Inhibition of autophagy rescues muscle atrophy in a LGMDD2 Drosophila model

The FASEB journal, 2021-10, Vol.35 (10), p.e21914-n/a

2021

Volltextzugriff (PDF)

A novel TRMT5 mutation causes a complex inherited neuropathy syndrome: The role of nerve pathology in defining a demyelinating neuropathy

Neuropathology and applied neurobiology, 2022-08, Vol.48 (5), p.e12817-n/a

2022

Volltextzugriff (PDF)

Analysis of the Importance of Oxides and Clays in Cd, Cr, Cu, Ni, Pb and Zn Adsorption and Retention with Regression Trees

PloS one, 2017-01, Vol.12 (1), p.e0168523

2017

Volltextzugriff (PDF)

Bioengineered in vitro 3D model of myotonic dystrophy type 1 human skeletal muscle

Biofabrication, 2021-07, Vol.13 (3), p.35035

2021

Volltextzugriff (PDF)

Primary lateral sclerosis and hereditary spastic paraplegia in sporadic patients. An important distinction in descriptive studies

Annals of neurology, 2016-07, Vol.80 (1), p.169-170

2016

Volltextzugriff (PDF)

Brain signal intensity changes as biomarkers in amyotrophic lateral sclerosis

Acta neurologica Scandinavica, 2018-02, Vol.137 (2), p.262-271

2018

Volltextzugriff (PDF)

Taurine activates the AKT-mTOR axis to restore muscle mass and contractile strength in human 3D in vitro models of steroid myopathy

Disease models & mechanisms, 2024-04, Vol.17 (4)

2024

Volltextzugriff (PDF)

Muscle-on-a-chip devices: a new era for in vitro modelling of muscular dystrophies

Disease models & mechanisms, 2023-06, Vol.16 (6)

2023

Volltextzugriff (PDF)

Integrated Bioluminescent Immunoassays for High-Throughput Sampling and Continuous Monitoring of Cytokines

Analytical chemistry (Washington), 2023-06, Vol.95 (23), p.8922-8931

2023

Volltextzugriff (PDF)

A study of the phenotypic variability and disease progression in Laing myopathy through the evaluation of muscle imaging

European journal of neurology, 2021-04, Vol.28 (4), p.1356-1365

2021

Volltextzugriff (PDF)

Bacillus subtilis biofilm extends Caenorhabditis elegans longevity through downregulation of the insulin-like signalling pathway

Nature communications, 2017-01, Vol.8 (1), p.14332-14332, Article 14332

2017

Volltextzugriff (PDF)

Muscular Echovariation: A New Biomarker in Amyotrophic Lateral Sclerosis

Ultrasound in medicine & biology, 2017-06, Vol.43 (6), p.1153-1162

2017

Volltextzugriff (PDF)

Remote DasaLAB: datacenter as a laboratory for remote learning

Interactive learning environments, 2024-02, p.1-21

2024

Volltextzugriff (PDF)

The hidden treasure of gestational diabetes-mediated myocardial function

Diabetes research and clinical practice, 2024-01, Vol.207, p.111049-111049, Article 111049

2024

Volltextzugriff (PDF)

Thermally and Photochemically Induced Dethreading of Fumaramide‐Based Kinetically Stable Pseudo[2]rotaxanes

European journal of organic chemistry, 2019-06, Vol.2019 (21), p.3480-3488

2019

Volltextzugriff (PDF)

Imaging Biomarkers for the Diagnosis and Prognosis of Neurodegenerative Diseases. The Example of Amyotrophic Lateral Sclerosis

Frontiers in neuroscience, 2018-10, Vol.12, p.784-784

2018

Volltextzugriff (PDF)

1 – 25 von 3.751

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(2.930)
Mit Volltextzugriff
(3.175)

Publikationsform

6 weitere anzeigen...

Weniger anzeigen...

Sprache

7 weitere anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

Science & Technology
(2.082)
Life Sciences & Biomedicine
(1.367)
Humans
(801)
Female
(480)
Male
(478)
Technology
(425)
Physical Sciences
(361)
Animals
(294)
Middle Aged
(284)
Adult
(272)
Aged
(232)
Neurosciences & Neurology
(206)
Science & Technology - Other Topics
(198)
Computer Science
(192)
Chemistry
(191)
Biological And Medical Sciences
(169)
Multidisciplinary Sciences
(152)
Neurosciences
(144)
Patients
(142)
Infectious Diseases
(129)

15 weitere anzeigen...

Weniger anzeigen...

Zeitschrift / Serie

5 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

Menü

Weitere Dienste

Einstellungen

Minimal detectable change and minimal clinically important difference in spinal muscular atrophy patients

Risdiplam in non‐sitter patients aged 16 years and older with 5q spinal muscular atrophy

Nusinersen in adult patients with 5q spinal muscular atrophy: A multicenter observational cohorts' study

Validation of motor and functional scales for the evaluation of adult patients with 5q spinal muscular atrophy

Natural history data in adults with SMA

Estimation of the prevalence and incidence of motor neuron diseases in two Spanish regions: Catalonia and Valencia

Distal hereditary motor neuropathies: Mutation spectrum and genotype–phenotype correlation

Insights into phenotypic variability caused by GARS1 pathogenic variants

Do we really need to calculate a minimal important difference for ALSFRS-R?: A letter in response to 'Clinically meaningful change: evaluation of the Rasch-built Overall Amyotrophic Lateral Sclerosis Disability Scale (ROADS) and the ALSFRS-R' published in Vol. 24(3-4), pp. 311-316

Inhibition of autophagy rescues muscle atrophy in a LGMDD2 Drosophila model

A novel TRMT5 mutation causes a complex inherited neuropathy syndrome: The role of nerve pathology in defining a demyelinating neuropathy

Analysis of the Importance of Oxides and Clays in Cd, Cr, Cu, Ni, Pb and Zn Adsorption and Retention with Regression Trees

Bioengineered in vitro 3D model of myotonic dystrophy type 1 human skeletal muscle

Primary lateral sclerosis and hereditary spastic paraplegia in sporadic patients. An important distinction in descriptive studies

Brain signal intensity changes as biomarkers in amyotrophic lateral sclerosis

Taurine activates the AKT-mTOR axis to restore muscle mass and contractile strength in human 3D in vitro models of steroid myopathy

Muscle-on-a-chip devices: a new era for in vitro modelling of muscular dystrophies

Integrated Bioluminescent Immunoassays for High-Throughput Sampling and Continuous Monitoring of Cytokines

A study of the phenotypic variability and disease progression in Laing myopathy through the evaluation of muscle imaging

Bacillus subtilis biofilm extends Caenorhabditis elegans longevity through downregulation of the insulin-like signalling pathway

Muscular Echovariation: A New Biomarker in Amyotrophic Lateral Sclerosis

Remote DasaLAB: datacenter as a laboratory for remote learning

The hidden treasure of gestational diabetes-mediated myocardial function

Thermally and Photochemically Induced Dethreading of Fumaramide‐Based Kinetically Stable Pseudo[2]rotaxanes

Imaging Biomarkers for the Diagnosis and Prognosis of Neurodegenerative Diseases. The Example of Amyotrophic Lateral Sclerosis

Suchergebnisse filtern