UB Paderborn / Katalog / Suche / in CDI

26 – 50 von 62

Sortiert nach

Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management

Lancet neurology, 2010, Vol.9 (1), p.77-93

2010

Volltextzugriff (PDF)

Genomic and Functional Variation of the Chlorophyll d -Producing Cyanobacterium Acaryochloris marina

Microorganisms (Basel), 2022-03, Vol.10 (3), p.569

2022

Volltextzugriff (PDF)

The Most Important Skills Required by Local Public Health Departments for Responding to Community Needs and Improving Health Outcomes

Journal of community health, 2022-02, Vol.47 (1), p.79-86

2022

Volltextzugriff (PDF)

SPP1 genotype is a determinant of disease severity in Duchenne muscular dystrophy

Neurology, 2011-01, Vol.76 (3), p.219

2011

Volltextzugriff (PDF)

Interleukin 1 Receptor-Like 1 Protein (ST2) is a Potential Biomarker for Cardiomyopathy in Duchenne Muscular Dystrophy

Pediatric cardiology, 2017-12, Vol.38 (8), p.1606-1612

2017

Volltextzugriff (PDF)

Light-induced structural changes in photosynthetic reaction center: implications for mechanism of electron-proton transfer

Science (American Association for the Advancement of Science), 1997-05, Vol.276 (5313), p.812-816

1997

Volltextzugriff (PDF)

Safety and effectiveness of ataluren: comparison of results from the STRIDE Registry and CINRG DMD Natural History Study

Journal of comparative effectiveness research, 2020-04, Vol.9 (5), p.341-360

2020

Volltextzugriff (PDF)

Association Study of Exon Variants in the NF-κB and TGFβ Pathways Identifies CD40 as a Modifier of Duchenne Muscular Dystrophy

American journal of human genetics, 2016-11, Vol.99 (5), p.1163-1171

2016

Volltextzugriff (PDF)

Using Palliative Care in Progressive Neuromuscular Disease to Maximize Quality of Life

Physical medicine and rehabilitation clinics of North America, 2012-11, Vol.23 (4), p.903-909

2012

Volltextzugriff (PDF)

Rasch Analysis of the Pediatric Quality of Life Inventory 4.0 Generic Core Scales Administered to Patients With Duchenne Muscular Dystrophy

Value in health, 2021-10, Vol.24 (10), p.1490-1498

2021

Volltextzugriff (PDF)

P.2.9 The 6-min walk test and other endpoints in Duchenne MD: Multi center longitudinal natural history observations over 48 weeks

Neuromuscular disorders : NMD, 2013-10, Vol.23 (9), p.751-751

2013

Volltextzugriff (PDF)

P.2.6 Comparison of 6MWD and person-reported functional measures in boys with Duchenne muscular dystrophy aged 4–12 years

Neuromuscular disorders : NMD, 2013-10, Vol.23 (9), p.750-750

2013

Volltextzugriff (PDF)

P.2.8 The 6-min walk test and clinical endpoints in Duchenne MD: Reliability, validity, and clinically-important differences

Neuromuscular disorders : NMD, 2013-10, Vol.23 (9), p.751-751

2013

Volltextzugriff (PDF)

P.2.4 Upper extremity reachable workspace evaluation in DMD using Kinect

Neuromuscular disorders : NMD, 2013-10, Vol.23 (9), p.749-750

2013

Volltextzugriff (PDF)

Efficacy and Safety of Vamorolone in Duchenne Muscular Dystrophy: A 30-Month Nonrandomized Controlled Open-Label Extension Trial

JAMA network open, 2022-01, Vol.5 (1), p.e2144178-e2144178

2022

Volltextzugriff (PDF)

Randomized Controlled Trial Comparing Acupuncture With Placebo Acupuncture for the Treatment of Carpal Tunnel Syndrome

PM & R, 2012-05, Vol.4 (5), p.367-373

2012

Volltextzugriff (PDF)

Efficacy of Integrated Social Cognitive Remediation vs. Neurocognitive Remediation in Improving Functional Outcome in Schizophrenia: Concept and Design of a Multicenter, Single-Blind RCT (The ISST Study)

Frontiers in psychiatry, 2022-06, Vol.13, p.909370-909370

2022

Volltextzugriff (PDF)

Socially Constructing Library as Place and Space

The Future of Library Space, 2016, Vol.36, p.103-129

2016

Volltextzugriff (PDF)

Meta-analyses of deflazacort versus prednisone/prednisolone in patients with nonsense mutation Duchenne muscular dystrophy

Journal of comparative effectiveness research, 2021-12, Vol.10 (18), p.1337-1347

2021

Volltextzugriff (PDF)

Modafinil to treat fatigue in amyotrophic lateral sclerosis: An open label pilot study

American journal of hospice & palliative medicine, 2005-01, Vol.22 (1), p.55-59

2005

Volltextzugriff (PDF)

Cognitions, coping and social environment predict adjustment to pain in persons with myotonic and facioscapulohumeral muscular dystrophy

The journal of pain, 2009-04, Vol.10 (4), p.S67-S67

2009

Volltextzugriff (PDF)

Quality of Life: Issues for Persons with Neuromuscular Diseases

Physical medicine and rehabilitation clinics of North America, 1998-02, Vol.9 (1), p.233-248

1998

Volltextzugriff (PDF)

M.P.3.04 Assessment of StepWatch™ activity monitoring in phase 2b study of ataluren (PTC124™) in nmDMD/BMD

Neuromuscular disorders : NMD, 2009-09, Vol.19 (8), p.602-602

2009

Volltextzugriff (PDF)

Employment profiles in neuromuscular diseases

American journal of physical medicine & rehabilitation, 1997-01, Vol.76 (1), p.26

1997

Volltextzugriff (PDF)

Effect of hind-limb suspension on young and adult skeletal muscle: I. Normal mice

Experimental neurology, 1989, Vol.103 (1), p.68-76

1989

Volltextzugriff (PDF)

26 – 50 von 62

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(60)
Mit Volltextzugriff
(56)

Publikationsform

Artikel
(61)
Buchkapitel
(1)

Sprache

Englisch
(57)
Japanisch
(13)
Deutsch
(6)

Erscheinungsjahr

n.n

Thema

Science & Technology
(34)
Life Sciences & Biomedicine
(31)
Humans
(27)
Male
(24)
Neurology
(17)
Muscular Dystrophy
(16)
Biological And Medical Sciences
(13)
Clinical Neurology
(13)
Female
(13)
Neurosciences & Neurology
(13)
Child
(12)
Muscular Dystrophy, Duchenne - Drug Therapy
(12)
Adolescent
(11)
Neurosciences
(11)
Child, Preschool
(10)
Medical Sciences
(10)
Adult
(9)
Muscular Dystrophy, Duchenne - Physiopathology
(9)
Animals
(8)
Glucocorticoids - Therapeutic Use
(8)

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Diagnosis and management of Duchenne muscular dystrophy, part 1: diagnosis, and pharmacological and psychosocial management

Genomic and Functional Variation of the Chlorophyll d -Producing Cyanobacterium Acaryochloris marina

The Most Important Skills Required by Local Public Health Departments for Responding to Community Needs and Improving Health Outcomes

SPP1 genotype is a determinant of disease severity in Duchenne muscular dystrophy

Interleukin 1 Receptor-Like 1 Protein (ST2) is a Potential Biomarker for Cardiomyopathy in Duchenne Muscular Dystrophy

Light-induced structural changes in photosynthetic reaction center: implications for mechanism of electron-proton transfer

Safety and effectiveness of ataluren: comparison of results from the STRIDE Registry and CINRG DMD Natural History Study

Association Study of Exon Variants in the NF-κB and TGFβ Pathways Identifies CD40 as a Modifier of Duchenne Muscular Dystrophy

Using Palliative Care in Progressive Neuromuscular Disease to Maximize Quality of Life

Rasch Analysis of the Pediatric Quality of Life Inventory 4.0 Generic Core Scales Administered to Patients With Duchenne Muscular Dystrophy

P.2.9 The 6-min walk test and other endpoints in Duchenne MD: Multi center longitudinal natural history observations over 48 weeks

P.2.6 Comparison of 6MWD and person-reported functional measures in boys with Duchenne muscular dystrophy aged 4–12 years

P.2.8 The 6-min walk test and clinical endpoints in Duchenne MD: Reliability, validity, and clinically-important differences

P.2.4 Upper extremity reachable workspace evaluation in DMD using Kinect

Efficacy and Safety of Vamorolone in Duchenne Muscular Dystrophy: A 30-Month Nonrandomized Controlled Open-Label Extension Trial

Randomized Controlled Trial Comparing Acupuncture With Placebo Acupuncture for the Treatment of Carpal Tunnel Syndrome

Efficacy of Integrated Social Cognitive Remediation vs. Neurocognitive Remediation in Improving Functional Outcome in Schizophrenia: Concept and Design of a Multicenter, Single-Blind RCT (The ISST Study)

Socially Constructing Library as Place and Space

Meta-analyses of deflazacort versus prednisone/prednisolone in patients with nonsense mutation Duchenne muscular dystrophy

Modafinil to treat fatigue in amyotrophic lateral sclerosis: An open label pilot study

Cognitions, coping and social environment predict adjustment to pain in persons with myotonic and facioscapulohumeral muscular dystrophy

Quality of Life: Issues for Persons with Neuromuscular Diseases

M.P.3.04 Assessment of StepWatch™ activity monitoring in phase 2b study of ataluren (PTC124™) in nmDMD/BMD

Employment profiles in neuromuscular diseases

Effect of hind-limb suspension on young and adult skeletal muscle: I. Normal mice

Suchergebnisse filtern