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...

Neurological Manifestations of Influenza Infection in Children and Adults: Results of a National British Surveillance Study

Clinical infectious diseases, 2014-03, Vol.58 (6), p.775-784

2014

Volltextzugriff (PDF)

Laser-induced surface acoustic waves: An alternative method to nanoindentation for the mechanical characterization of porous nanostructured thin film electrode media

Mechanics of materials, 2015-12, Vol.91, p.333-342

2015

Volltextzugriff (PDF)

Longitudinal analysis of the neurological features of ataxia‐telangiectasia

Developmental medicine and child neurology, 2016-07, Vol.58 (7), p.690-697

2016

Volltextzugriff (PDF)

The clinical spectrum of the congenital myasthenic syndrome resulting from COL13A1 mutations

Brain (London, England : 1878), 2019-06, Vol.142 (6), p.1547-1560

2019

Volltextzugriff (PDF)

Congenital Myasthenic Syndrome Type 19 Is Caused by Mutations in COL13A1, Encoding the Atypical Non-fibrillar Collagen Type XIII α1 Chain

American journal of human genetics, 2015-12, Vol.97 (6), p.878-885

2015

Volltextzugriff (PDF)

Evaluation of an internet-based animated preparatory video for children undergoing non-sedated MRI

British journal of radiology, 2018-07, Vol.91 (1087), p.20170719-20170719

2018

Volltextzugriff (PDF)

Multiparametric cerebellar imaging and clinical phenotype in childhood ataxia telangiectasia

NeuroImage clinical, 2020-01, Vol.25, p.102110-102110, Article 102110

2020

Volltextzugriff (PDF)

Dual Diagnosis of Dihydropyrimidine Dehydrogenase Deficiency and GM1 Gangliosidosis

Pediatric neurology, 2012-03, Vol.46 (3), p.178-181

2012

Volltextzugriff (PDF)

Solitary Cervical Osteochondroma in a 9-Year-Old Child

Pediatric neurology, 2013-09, Vol.49 (3), p.218-219

2013

Volltextzugriff (PDF)

Neurologic Presentation of Triple A Syndrome

Pediatric neurology, 2011-11, Vol.45 (5), p.347-349

2011

Volltextzugriff (PDF)

Clinical features, course, and outcomes of a UK cohort of pediatric moyamoya

Neurology, 2018-02, Vol.90 (9), p.e763

2018

Volltextzugriff (PDF)

Trismus in the paediatric population

Developmental medicine and child neurology, 2015-04, Vol.57 (4), p.339-343

2015

Volltextzugriff (PDF)

Quality of life and neurological disability in children and young people with ataxia telangiectasia

European journal of paediatric neurology, 2022-09, Vol.40, p.34-39

2022

Volltextzugriff (PDF)

Zeolite as a wear-resistant coating

Microporous and mesoporous materials, 2012-03, Vol.151, p.346-351

2012

Volltextzugriff (PDF)

Genotype–phenotype correlation in a large population of muscular dystrophy patients with LAMA2 mutations

Neuromuscular disorders : NMD, 2010-04, Vol.20 (4), p.241-250

2010

Volltextzugriff (PDF)

Bioactive Materials for Regenerative Medicine: Zeolite-Hydroxyapatite Bone Mimetic Coatings

Advanced engineering materials, 2012-03, Vol.14 (3), p.200-206

2012

Volltextzugriff (PDF)

Early discharge and rehabilitation in paediatric acquired brain and neurological injury: a transferable model

Archives of disease in childhood. Education and practice edition, 2020-02, p.edpract-2018-315096

2020

Volltextzugriff (PDF)

Risdiplam in Spinal Muscular Atrophy: Safety Profile and Use Through The Early Access to Medicine Scheme for the Paediatric Cohort in Great Britain

Journal of neuromuscular diseases, 2024-01, Vol.11 (2), p.361-368

2024

Volltextzugriff (PDF)

Familial idiopathic intracranial hypertension with variable phenotype

European journal of paediatric neurology, 2011-01, Vol.15 (1), p.81-83

2011

Volltextzugriff (PDF)

Late-Onset GM2 gangliosidosis presenting as burning dysesthesias

Pediatric neurology, 2001-07, Vol.25 (1), p.59-61

2001

Volltextzugriff (PDF)

LBSL: Case Series and DARS2 Variant Analysis in Early Severe Forms With Unexpected Presentations

Neurology. Genetics, 2021-04, Vol.7 (2), p.e559-e559

2021

Volltextzugriff (PDF)

Congenital Myasthenic Syndrome Type 19 Is Caused by Mutations in COL13A1, Encoding the Atypical Non-fibrillar Collagen Type XIII [Alpha]1 Chain

American journal of human genetics, 2015-12, Vol.97 (6), p.878

2015

Volltextzugriff (PDF)

Visual obscurations in children

Paediatrics and child health, 2014-11, Vol.24 (11), p.525-526

2014

Volltextzugriff (PDF)

Mechanical Characterization of Nanoporous Thin Films by Nanoindentation and Laser-induced Surface Acoustic Waves

Chow, Gabriel

2014

Volltextzugriff (PDF)

1 – 25 von 180

Suche als RSS-Feed

Aktive Filter

SpracheDeutsch

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(160)
Mit Volltextzugriff
(160)

Publikationsform

Sprache

Englisch
(179)
Japanisch
(20)

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(2)

Menü

Weitere Dienste

Einstellungen

Neurological Manifestations of Influenza Infection in Children and Adults: Results of a National British Surveillance Study

Laser-induced surface acoustic waves: An alternative method to nanoindentation for the mechanical characterization of porous nanostructured thin film electrode media

Longitudinal analysis of the neurological features of ataxia‐telangiectasia

The clinical spectrum of the congenital myasthenic syndrome resulting from COL13A1 mutations

Congenital Myasthenic Syndrome Type 19 Is Caused by Mutations in COL13A1, Encoding the Atypical Non-fibrillar Collagen Type XIII α1 Chain

Evaluation of an internet-based animated preparatory video for children undergoing non-sedated MRI

Multiparametric cerebellar imaging and clinical phenotype in childhood ataxia telangiectasia

Dual Diagnosis of Dihydropyrimidine Dehydrogenase Deficiency and GM1 Gangliosidosis

Solitary Cervical Osteochondroma in a 9-Year-Old Child

Neurologic Presentation of Triple A Syndrome

Respiratory Trajectories in Type 2 and 3 Spinal Muscular Atrophy in the iSMAC Cohort Study

Clinical features, course, and outcomes of a UK cohort of pediatric moyamoya

Trismus in the paediatric population

Quality of life and neurological disability in children and young people with ataxia telangiectasia

Zeolite as a wear-resistant coating

Genotype–phenotype correlation in a large population of muscular dystrophy patients with LAMA2 mutations

Bioactive Materials for Regenerative Medicine: Zeolite-Hydroxyapatite Bone Mimetic Coatings

Early discharge and rehabilitation in paediatric acquired brain and neurological injury: a transferable model

Risdiplam in Spinal Muscular Atrophy: Safety Profile and Use Through The Early Access to Medicine Scheme for the Paediatric Cohort in Great Britain

Familial idiopathic intracranial hypertension with variable phenotype

Late-Onset GM2 gangliosidosis presenting as burning dysesthesias

LBSL: Case Series and DARS2 Variant Analysis in Early Severe Forms With Unexpected Presentations

Congenital Myasthenic Syndrome Type 19 Is Caused by Mutations in COL13A1, Encoding the Atypical Non-fibrillar Collagen Type XIII [Alpha]1 Chain

Visual obscurations in children

Mechanical Characterization of Nanoporous Thin Films by Nanoindentation and Laser-induced Surface Acoustic Waves

Aktive Filter

Suchergebnisse filtern