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...

Pediatric tumefactive multiple sclerosis case (with baló-like lesions), diagnostic and treatment challenges

Neurological sciences, 2023-01, Vol.44 (1), p.343-345

2023

Volltextzugriff (PDF)

SCN1A Channels a Wide Range of Epileptic Phenotypes: Report of Novel and Known Variants with Variable Presentations

International journal of molecular sciences, 2024-06, Vol.25 (11), p.5644

2024

Volltextzugriff (PDF)

Case Report: Intracranial Hypertension Secondary to Guillain-Barre Syndrome

Frontiers in pediatrics, 2021-01, Vol.8, p.608695

2021

Volltextzugriff (PDF)

Genetic cause of epilepsy in a Greek cohort of children and young adults with heterogeneous epilepsy syndromes

Epilepsy & behavior reports, 2021-01, Vol.16, p.100477-100477, Article 100477

2021

Volltextzugriff (PDF)

Focal epileptic seizures anticipation based on patterns of heart rate variability parameters

Computer methods and programs in biomedicine, 2019-09, Vol.178, p.123-133

2019

Volltextzugriff (PDF)

Tolosa-Hunt Syndrome: Clinical Manifestations in Children

Pediatric neurology, 2019-10, Vol.99, p.60-63

2019

Volltextzugriff (PDF)

Correction to: Pediatric tumefactive multiple sclerosis case (with baló‑like lesions), diagnostic and treatment challenges

Neurological sciences, 2023-03, Vol.44 (3), p.1137-1137

2023

Volltextzugriff (PDF)

Frontal lobe epilepsy and mild malformation with oligodendroglial hyperplasia: Further observations on electroclinical and imaging phenotypes, and surgical perspectives

Epileptic disorders, 2023-06, Vol.25 (3), p.343-359

2023

Volltextzugriff (PDF)

Screening for TSC1 and TSC2 mutations using NGS in Greek children with tuberous sclerosis syndrome

European journal of paediatric neurology, 2018-05, Vol.22 (3), p.419-426

2018

Volltextzugriff (PDF)

Validation and Translation of the Greek Version of the “DCDDaily-Q-GR” Questionnaire

Health (Irvine, Calif.), 2021, Vol.13 (11), p.1222-1241

2021

Volltextzugriff (PDF)

A dynamic trinucleotide repeat (TNR) expansion in the DMD gene

Molecular and cellular probes, 2016-08, Vol.30 (4), p.254-260

2016

Volltextzugriff (PDF)

A computational platform for continuous seizure anticipation, monitoring and clinical evaluation

Studies in health technology and informatics, 2016, Vol.224, p.108

2016

Volltextzugriff (PDF)

A Short Proximal Promoter and the Distal Hepatic Control Region-1 (HCR-1) Contribute to the Liver Specificity of the Human Apolipoprotein C-II Gene

The Journal of biological chemistry, 1998-02, Vol.273 (7), p.4188-4196

1998

Volltextzugriff (PDF)

A8344G tRNALys mutation associated with recurrent brain stem stroke-like episodes

Journal of neurology, 2009-02, Vol.256 (2), p.271-273

2009

Volltextzugriff (PDF)

Absence seizure detection classifying matching pursuit features of EEG signals

EAI endorsed transactions on bioengineering and bioinformatics, 2021-02, Vol.1 (1), p.166556

2021

Volltextzugriff (PDF)

The impact of mode of delivery and gestational age on cord blood hematopoietic stem/progenitor cells

Annals of hematology, 2006-06, Vol.85 (6), p.381-385

2006

Volltextzugriff (PDF)

Absence seizure epilepsy detection using linear and nonlinear eeg analysis methods

2013 35th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC), 2013, Vol.2013, p.6333-6336

2013

Volltextzugriff (PDF)

Automatic Absence Seizure Detection Evaluating Matching Pursuit Features of EEG Signals

2019 IEEE 19th International Conference on Bioinformatics and Bioengineering (BIBE), 2019, p.886-889

2019

Volltextzugriff (PDF)

Seizure Detection using Common Spatial Patterns and Classification Techniques

2019 IEEE 19th International Conference on Bioinformatics and Bioengineering (BIBE), 2019, p.890-893

2019

Volltextzugriff (PDF)

In vitro proliferative and differentiating characteristics of CD133 + and CD34 + cord blood cells in the presence of thrombopoietin (TPO) or erythropoietin (EPO) : Potential implications for hematopoietic cell transplantation

Leukemia research, 2003-12, Vol.27 (12), p.1143-1151

2003

Volltextzugriff (PDF)

An approach to absence epileptic seizures detection using Approximate Entropy

2013 35th Annual International Conference of the IEEE Engineering in Medicine and Biology Society (EMBC), 2013, Vol.2013, p.413-416

2013

Volltextzugriff (PDF)

A short proximal promoter and the distal hepatic control region-1 (HCR-1) contribute to the liver specificity of the human apolipoprotein C-II gene. Hepatic enhancement by HCR-1 requires two proximal hormone response elements which have different binding specificities for orphan receptors HNF-4, ARP-1, and EAR-2

The Journal of biological chemistry, 1998-02, Vol.273 (7), p.4188-4196

1998

Volltextzugriff (PDF)

1 – 25 von 28

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(20)
Mit Volltextzugriff
(25)

Publikationsform

Sprache

Englisch
(28)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Pediatric tumefactive multiple sclerosis case (with baló-like lesions), diagnostic and treatment challenges

SCN1A Channels a Wide Range of Epileptic Phenotypes: Report of Novel and Known Variants with Variable Presentations

Case Report: Intracranial Hypertension Secondary to Guillain-Barre Syndrome

Genetic cause of epilepsy in a Greek cohort of children and young adults with heterogeneous epilepsy syndromes

Focal epileptic seizures anticipation based on patterns of heart rate variability parameters

Evaluation of Genotypes and Epidemiology of Spinal Muscular Atrophy in Greece: A Nationwide Study Spanning 24 Years

Tolosa-Hunt Syndrome: Clinical Manifestations in Children

Correction to: Pediatric tumefactive multiple sclerosis case (with baló‑like lesions), diagnostic and treatment challenges

Frontal lobe epilepsy and mild malformation with oligodendroglial hyperplasia: Further observations on electroclinical and imaging phenotypes, and surgical perspectives

Screening for TSC1 and TSC2 mutations using NGS in Greek children with tuberous sclerosis syndrome

Combined exome analysis and exome depth assessment achieve a high diagnostic yield in an epilepsy case series, revealing significant genomic heterogeneity and novel mechanisms

Validation and Translation of the Greek Version of the “DCDDaily-Q-GR” Questionnaire

A dynamic trinucleotide repeat (TNR) expansion in the DMD gene

Diagnostic Whole Exome Sequencing to Study a Cohort of Greek Patients with Heterogeneous Neurological and Other Disorders (P5.134)

A computational platform for continuous seizure anticipation, monitoring and clinical evaluation

A Short Proximal Promoter and the Distal Hepatic Control Region-1 (HCR-1) Contribute to the Liver Specificity of the Human Apolipoprotein C-II Gene

A8344G tRNALys mutation associated with recurrent brain stem stroke-like episodes

Absence seizure detection classifying matching pursuit features of EEG signals

The impact of mode of delivery and gestational age on cord blood hematopoietic stem/progenitor cells

Absence seizure epilepsy detection using linear and nonlinear eeg analysis methods

Automatic Absence Seizure Detection Evaluating Matching Pursuit Features of EEG Signals

Seizure Detection using Common Spatial Patterns and Classification Techniques

In vitro proliferative and differentiating characteristics of CD133 + and CD34 + cord blood cells in the presence of thrombopoietin (TPO) or erythropoietin (EPO) : Potential implications for hematopoietic cell transplantation

An approach to absence epileptic seizures detection using Approximate Entropy

Suchergebnisse filtern