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...

SEPN1-related myopathies: clinical course in a large cohort of patients

Neurology, 2011-06, Vol.76 (24), p.2073-2078

2011

Volltextzugriff (PDF)

Reporting of paediatric osteoporotic vertebral fractures in Duchenne muscular dystrophy and potential impact on clinical management: the need for standardised and structured reporting

Pediatric radiology, 2024-01, Vol.54 (1), p.117-126

2024

Volltextzugriff (PDF)

Intralabyrinthine Schwannomas: Imaging Diagnosis and Classification

American journal of neuroradiology : AJNR, 2012-01, Vol.33 (1), p.104-109

2012

Volltextzugriff (PDF)

Subdural haematoma and effusion in infancy: an epidemiological study

Archives of disease in childhood, 2005-09, Vol.90 (9), p.952-955

2005

Volltextzugriff (PDF)

Severe childhood SMA and axonal CMT due to anticodon binding domain mutations in the GARS gene

Neurology, 2006-11, Vol.67 (9), p.1710-1712

2006

Volltextzugriff (PDF)

Variable phenotype including Leigh syndrome with a 9185T>C mutation in the MTATP6 gene

Neuropediatrics, 2007-12, Vol.38 (6), p.313-316

2007

Volltextzugriff (PDF)

Magnetic resonance imaging of the infant brain: anatomical characteristics and clinical significance of punctate lesions

Archives of disease in childhood. Fetal and neonatal edition, 2002-05, Vol.86 (3), p.F171-177

2002

Volltextzugriff (PDF)

On the receiving end V: Patient perceptions of the side effects of cancer chemotherapy in 1993

Annals of oncology, 1996-02, Vol.7 (2), p.189-195

1996

Volltextzugriff (PDF)

PLA2G6-associated neurodegeneration (PLAN): Further expansion of the clinical, radiological and mutation spectrum associated with infantile and atypical childhood-onset disease

Molecular genetics and metabolism, 2014-06, Vol.112 (2), p.183-189

2014

Volltextzugriff (PDF)

Differential induction of PPAR-gamma by luminal glutamine and iNOS by luminal arginine in the rodent postischemic small bowel

American journal of physiology: Gastrointestinal and liver physiology, 2006-04, Vol.290 (4), p.G616-G623

2006

Volltextzugriff (PDF)

Neurovascular compression of the trigeminal and glossopharyngeal nerve: three case reports

Archives of disease in childhood, 2000-04, Vol.82 (4), p.311-315

2000

Volltextzugriff (PDF)

Surface Morphology of Poly(caprolactone)-b-poly(dimethylsiloxane)-b-poly(caprolactone) Copolymers: Effects on Protein Adsorption

Biomacromolecules, 2001, Vol.2 (2), p.526-537

2001

Volltextzugriff (PDF)

Endocrine and Bone Monitoring in Boys with Duchenne Muscular Dystrophy; Do we adhere to the standards of care?

Journal of neuromuscular diseases, 2023-01, Vol.10 (6), p.1143-1144

2023

Volltextzugriff (PDF)

Cerebral Maturation in Premature Infants: Quantitative Assessment Using MR Imaging

American journal of neuroradiology : AJNR, 2001-09, Vol.22 (8), p.1577-1582

2001

Volltextzugriff (PDF)

Small particle growth in silane radio-frequency discharges

Journal of applied physics, 2000-02, Vol.87 (3), p.1076-1085

2000

Volltextzugriff (PDF)

MR features of developing periventricular white matter in preterm infants: evidence of glial cell migration

American journal of neuroradiology : AJNR, 1998-05, Vol.19 (5), p.971-976

1998

Volltextzugriff (PDF)

MANNA: Just Enough for the Day

The American journal of geriatric psychiatry, 2024-05, Vol.32 (5), p.653-653

Childs, Jeanne

2024

Volltextzugriff (PDF)

Assessment of face validity of a disease model of nonsense mutation Duchenne muscular dystrophy: a multi-national Delphi panel study

Journal of medical economics, 2022, Vol.25 (1), p.808-816

2022

Volltextzugriff (PDF)

Hospice provision and usage amongst young people with neuromuscular disease in the United Kingdom

European journal of paediatric neurology, 2011-07, Vol.15 (4), p.326-330

2011

Volltextzugriff (PDF)

P24 Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signalling

Neuromuscular disorders : NMD, 2014-03, Vol.24, p.S13-S13

2014

Volltextzugriff (PDF)

P67 SEPN1 related myopathies: Clinical course in a large cohort of patients

Neuromuscular disorders : NMD, 2011, Vol.21, p.S26-S26

2011

Volltextzugriff (PDF)

Reversible simulation of bipartite product Hamiltonians

IEEE transactions on information theory, 2004-06, Vol.50 (6), p.1189-1197

2004

Volltextzugriff (PDF)

Any AND-OR Formula of Size N Can Be Evaluated in Time $N^{1/2+o(1)}$ on a Quantum Computer

SIAM journal on computing, 2010-01, Vol.39 (6), p.2513-2530

2010

Volltextzugriff (PDF)

Fractures and Linear Growth in a Nationwide Cohort of Boys With Duchenne Muscular Dystrophy With and Without Glucocorticoid Treatment: Results From the UK NorthStar Database

JAMA neurology, 2019-06, Vol.76 (6), p.701

2019

Volltextzugriff (PDF)

Magnetic Resonance and Cranial Ultrasound Characteristics of Periventricular White Matter Abnormalities in Newborn Infants

Clinical radiology, 2001-08, Vol.56 (8), p.647-655

2001

Volltextzugriff (PDF)

1 – 25 von 6.608

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(5.304)
Mit Volltextzugriff
(4.600)

Publikationsform

8 weitere anzeigen...

Weniger anzeigen...

Sprache

6 weitere anzeigen...

Weniger anzeigen...

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Kollektion

MEDLINE
(3.057)
EZB Electronic Journals Library
(2.664)
Journals@Ovid
(2.593)
Ingenta
(2.441)
Publisher website
(1.842)
Elsevier ScienceDirect Journals Complete
(1.161)
IngentaConnect Journals
(884)
Wiley-Blackwell Journals
(728)
Elsevier Journal Backfiles on ScienceDirect (DFG Nationallizenzen)
(617)
Wiley Online Library Full Collection 2018
(495)
Jstor Complete Legacy
(421)
Ebook Central Perpetual and DDA
(353)
eBooks on EBSCOhost
(347)
Oxford University Press Journals Current
(287)
ScienceDirect eBooks
(252)
SpringerLink
(252)
Nature Journals
(206)
Oxford Journals 2020 Medicine
(200)
ERIC
(189)
Nexis Uni
(189)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

Menü

Weitere Dienste

Einstellungen

SEPN1-related myopathies: clinical course in a large cohort of patients

Reporting of paediatric osteoporotic vertebral fractures in Duchenne muscular dystrophy and potential impact on clinical management: the need for standardised and structured reporting

Intralabyrinthine Schwannomas: Imaging Diagnosis and Classification

Subdural haematoma and effusion in infancy: an epidemiological study

Severe childhood SMA and axonal CMT due to anticodon binding domain mutations in the GARS gene

Variable phenotype including Leigh syndrome with a 9185T>C mutation in the MTATP6 gene

Magnetic resonance imaging of the infant brain: anatomical characteristics and clinical significance of punctate lesions

On the receiving end V: Patient perceptions of the side effects of cancer chemotherapy in 1993

PLA2G6-associated neurodegeneration (PLAN): Further expansion of the clinical, radiological and mutation spectrum associated with infantile and atypical childhood-onset disease

Differential induction of PPAR-gamma by luminal glutamine and iNOS by luminal arginine in the rodent postischemic small bowel

Neurovascular compression of the trigeminal and glossopharyngeal nerve: three case reports

Surface Morphology of Poly(caprolactone)-b-poly(dimethylsiloxane)-b-poly(caprolactone) Copolymers: Effects on Protein Adsorption

Endocrine and Bone Monitoring in Boys with Duchenne Muscular Dystrophy; Do we adhere to the standards of care?

Cerebral Maturation in Premature Infants: Quantitative Assessment Using MR Imaging

Small particle growth in silane radio-frequency discharges

MR features of developing periventricular white matter in preterm infants: evidence of glial cell migration

MANNA: Just Enough for the Day

Assessment of face validity of a disease model of nonsense mutation Duchenne muscular dystrophy: a multi-national Delphi panel study

Hospice provision and usage amongst young people with neuromuscular disease in the United Kingdom

P24 Loss-of-function mutations in MICU1 cause a brain and muscle disorder linked to primary alterations in mitochondrial calcium signalling

P67 SEPN1 related myopathies: Clinical course in a large cohort of patients

Reversible simulation of bipartite product Hamiltonians

Any AND-OR Formula of Size N Can Be Evaluated in Time $N^{1/2+o(1)}$ on a Quantum Computer

Fractures and Linear Growth in a Nationwide Cohort of Boys With Duchenne Muscular Dystrophy With and Without Glucocorticoid Treatment: Results From the UK NorthStar Database

Magnetic Resonance and Cranial Ultrasound Characteristics of Periventricular White Matter Abnormalities in Newborn Infants

Suchergebnisse filtern