UB Paderborn / Katalog / Suche / in CDI

1 – 25 von 119

Sortiert nach

Healthy environments for athleTes (HEAT): environmental conditions along a 90 km ultra-marathon event, South Africa

International journal of biometeorology, 2024-06

2024

Volltextzugriff (PDF)

Trends in time‐loss injuries during the 2011‐2016 South African Rugby Youth Weeks

Scandinavian journal of medicine & science in sports, 2018-09, Vol.28 (9), p.2066-2073

2018

Volltextzugriff (PDF)

The efficacy of the BokSmart Safe Six exercise-based intervention on injury risk profiles in healthy active adults: A feasibility study

Journal of science and medicine in sport, 2017-11, Vol.20, p.61-61

2017

Volltextzugriff (PDF)

Prevalence of lower airway dysfunction in athletes: a systematic review and meta-analysis by a subgroup of the IOC consensus group on ‘acute respiratory illness in the athlete’

British journal of sports medicine, 2022-02, Vol.56 (4), p.213-222

2022

Volltextzugriff (PDF)

Diagnostic approach to lower airway dysfunction in athletes: a systematic review and meta-analysis by a subgroup of the IOC consensus on ‘acute respiratory illness in the athlete’

British journal of sports medicine, 2023-04, Vol.57 (8), p.481-489

2023

Volltextzugriff (PDF)

Pre‐race screening and stratification predicts adverse events—A 4‐year study in 29585 ultra‐marathon entrants, SAFER X

Scandinavian journal of medicine & science in sports, 2020-07, Vol.30 (7), p.1205-1211

2020

Volltextzugriff (PDF)

Risk factors for not finishing an ultramarathon: 4-year study in 23,996 race starters, SAFER XXI

The Journal of sports medicine and physical fitness, 2022-05, Vol.62 (5), p.710

2022

Volltextzugriff (PDF)

The Currie Cup Premiership Competition Injury Surveillance Report 2014–2017

South African journal of sports medicine, 2018-01, Vol.30 (1), p.1-42

2018

Volltextzugriff (PDF)

Diagnostic approach to the congenital muscular dystrophies

Neuromuscular disorders : NMD, 2014-04, Vol.24 (4), p.289-311

2014

Volltextzugriff (PDF)

The histopathological spectrum of malignant hyperthermia and rhabdomyolysis due to RYR1 mutations

Journal of neurology, 2019-04, Vol.266 (4), p.876-887

2019

Volltextzugriff (PDF)

Mutations in MYH7 cause Multi-minicore Disease (MmD) with variable cardiac involvement

Neuromuscular disorders : NMD, 2012-12, Vol.22 (12), p.1096-1104

2012

Volltextzugriff (PDF)

Nemaline myopathy with stiffness and hypertonia associated with an ACTA1 mutation

Neurology, 2012-04, Vol.78 (14), p.1100

2012

Volltextzugriff (PDF)

Phenotypic and molecular insights into spinal muscular atrophy due to mutations in BICD2

Brain (London, England : 1878), 2015-02, Vol.138 (Pt 2), p.293-310

2015

Volltextzugriff (PDF)

Mutations in KLHL40 Are a Frequent Cause of Severe Autosomal-Recessive Nemaline Myopathy

American journal of human genetics, 2013-07, Vol.93 (1), p.6-18

2013

Volltextzugriff (PDF)

Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of α-dystroglycan

Human molecular genetics, 2003-11, Vol.12 (21), p.2853-2861

2003

Volltextzugriff (PDF)

Next generation sequencing in a large cohort of patients presenting with neuromuscular disease before or at birth

Orphanet journal of rare diseases, 2015-11, Vol.10 (148), p.148-148, Article 148

2015

Volltextzugriff (PDF)

Central core disease: clinical, pathological, and genetic features

Archives of disease in childhood, 2003-12, Vol.88 (12), p.1051-1055

2003

Volltextzugriff (PDF)

Mutations in the Fukutin-Related Protein Gene ( FKRP) Cause a Form of Congenital Muscular Dystrophy with Secondary Laminin α2 Deficiency and Abnormal Glycosylation of α-Dystroglycan

American journal of human genetics, 2001, Vol.69 (6), p.1198-1209

2001

Volltextzugriff (PDF)

A two-site ELISA can quantify upregulation of SMN protein by drugs for spinal muscular atrophy

Neurology, 2008-11, Vol.71 (22), p.1757

2008

Volltextzugriff (PDF)

The spectrum of pathology in central core disease

Neuromuscular disorders : NMD, 2002-12, Vol.12 (10), p.930-938

2002

Volltextzugriff (PDF)

Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2i as a milder allelic variant of congenital muscular dystrophy MDC1C

Human molecular genetics, 2001-12, Vol.10 (25), p.2851-2859

2001

Volltextzugriff (PDF)

Approach to the diagnosis of congenital myopathies

Neuromuscular disorders : NMD, 2014-02, Vol.24 (2), p.97-116

2014

Volltextzugriff (PDF)

Phenotypic spectrum associated with mutations in the fukutin-related protein gene

Annals of neurology, 2003-04, Vol.53 (4), p.537-542

2003

Volltextzugriff (PDF)

Autosomal recessive inheritance of RYR1 mutations in a congenital myopathy with cores

Neurology, 2002-07, Vol.59 (2), p.284

2002

Volltextzugriff (PDF)

1 – 25 von 119

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(115)
Mit Volltextzugriff
(113)

Publikationsform

Artikel
(117)
Tagungsberichte
(2)

Sprache

Erscheinungsjahr

n.n

Thema

15 weitere anzeigen...

Weniger anzeigen...

Neu hinzugefügt

... seit 90 Tagen
(1)

Menü

Weitere Dienste

Einstellungen

Healthy environments for athleTes (HEAT): environmental conditions along a 90 km ultra-marathon event, South Africa

Trends in time‐loss injuries during the 2011‐2016 South African Rugby Youth Weeks

The efficacy of the BokSmart Safe Six exercise-based intervention on injury risk profiles in healthy active adults: A feasibility study

Prevalence of lower airway dysfunction in athletes: a systematic review and meta-analysis by a subgroup of the IOC consensus group on ‘acute respiratory illness in the athlete’

Diagnostic approach to lower airway dysfunction in athletes: a systematic review and meta-analysis by a subgroup of the IOC consensus on ‘acute respiratory illness in the athlete’

Pre‐race screening and stratification predicts adverse events—A 4‐year study in 29585 ultra‐marathon entrants, SAFER X

Risk factors for not finishing an ultramarathon: 4-year study in 23,996 race starters, SAFER XXI

The Currie Cup Premiership Competition Injury Surveillance Report 2014–2017

Diagnostic approach to the congenital muscular dystrophies

The histopathological spectrum of malignant hyperthermia and rhabdomyolysis due to RYR1 mutations

Mutations in MYH7 cause Multi-minicore Disease (MmD) with variable cardiac involvement

Nemaline myopathy with stiffness and hypertonia associated with an ACTA1 mutation

Phenotypic and molecular insights into spinal muscular atrophy due to mutations in BICD2

Mutations in KLHL40 Are a Frequent Cause of Severe Autosomal-Recessive Nemaline Myopathy

Identification of KLHL41 Mutations Implicates BTB-Kelch-Mediated Ubiquitination as an Alternate Pathway to Myofibrillar Disruption in Nemaline Myopathy

Mutations in the human LARGE gene cause MDC1D, a novel form of congenital muscular dystrophy with severe mental retardation and abnormal glycosylation of α-dystroglycan

Next generation sequencing in a large cohort of patients presenting with neuromuscular disease before or at birth

Central core disease: clinical, pathological, and genetic features

Mutations in the Fukutin-Related Protein Gene ( FKRP) Cause a Form of Congenital Muscular Dystrophy with Secondary Laminin α2 Deficiency and Abnormal Glycosylation of α-Dystroglycan

A two-site ELISA can quantify upregulation of SMN protein by drugs for spinal muscular atrophy

The spectrum of pathology in central core disease

Mutations in the fukutin-related protein gene (FKRP) identify limb girdle muscular dystrophy 2i as a milder allelic variant of congenital muscular dystrophy MDC1C

Approach to the diagnosis of congenital myopathies

Phenotypic spectrum associated with mutations in the fukutin-related protein gene

Autosomal recessive inheritance of RYR1 mutations in a congenital myopathy with cores

Suchergebnisse filtern