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...

Jellification of medicine after simple suspension method for muscular dystrophy patients with dysphagia

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S147-S147

2016

Volltextzugriff (PDF)

G.P.7

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9), p.796-796

2014

Volltextzugriff (PDF)

EP.68Carnitine deficiency in patients with Duchenne muscular dystrophy requiring long-term tube feeding and heart function improvement by carnitine replacement

Neuromuscular disorders : NMD, 2019-10, Vol.29, p.S172-S172

2019

Volltextzugriff (PDF)

P.21.6 A case of familial Rippling muscle disease showing decreased of caveolin-3 in muscle biopsy suggesting an immunologic mechanism

Neuromuscular disorders : NMD, 2013-10, Vol.23 (9), p.845-845

2013

Volltextzugriff (PDF)

P.10.12 Difference of the mechanism of dysphagia between Duchenne muscular dystrophy and myotonic dystrophy type 1

Neuromuscular disorders : NMD, 2013-10, Vol.23 (9), p.792-792

2013

Volltextzugriff (PDF)

Life prognostic factor of patients with Duchenne muscular dystrophy

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S122-S122

2016

Volltextzugriff (PDF)

P1.08 Clinical features and swallowing test in two very mild Fukuyama type congenital muscular dystrophy (FCMD)

Neuromuscular disorders : NMD, 2010-10, Vol.20 (9), p.601-602

2010

Volltextzugriff (PDF)

P110 A multicenter retrospective study of the impact of COVID-19 on patients with muscular dystrophies

Neuromuscular disorders : NMD, 2023-10, Vol.33, p.S172-S172

2023

Volltextzugriff (PDF)

P.282Relationship between verbal IQ and gene mutation in patients with Duchenne muscular dystrophy (longitudinal study)

Neuromuscular disorders : NMD, 2019-10, Vol.29, p.S149-S149

2019

Volltextzugriff (PDF)

G.P.9.10 A case of fibro-dysplasia ossificans progressiva with a novel mutation (G356D) of the activin receptor type 1 gene (ACVR1(ALK2))

Neuromuscular disorders : NMD, 2008-10, Vol.18 (9), p.788-788

2008

Volltextzugriff (PDF)

P.203 - Jellification of medicine after simple suspension method for muscular dystrophy patients with dysphagia

Neuromuscular disorders : NMD, 2016-10, Vol.26, p.S147-S147

2016

Volltextzugriff (PDF)

DUCHENNE MUSCULAR DYSTROPHY – CLINICAL: P.21Changes over years in the verbal IQ of patients with Duchenne muscular dystrophy

Neuromuscular disorders : NMD, 2018-10, Vol.28, p.S37-S38

2018

Volltextzugriff (PDF)

DUCHENNE MUSCULAR DYSTROPHY – CLINICAL

Neuromuscular disorders : NMD, 2018-10, Vol.28, p.S37-S38

2018

Volltextzugriff (PDF)

G.P.7: Longitudinal studies of dysphagia in oculopharyngeal muscular dystrophies

Neuromuscular disorders : NMD, 2014-10, Vol.24 (9-10), p.796-796

2014

Volltextzugriff (PDF)

Percutaneous endoscopic gastrostomy in patients with duchenne muscular dystrophy compare with amyotrophic lateral sclerosis: a retrospective study

Journal of the neurological sciences, 2017-10, Vol.381, p.267-268

2017

Volltextzugriff (PDF)

Period of communication after the commencement of respiratory or nutritional support in neurodegenerative diseases

Journal of the neurological sciences, 2017-10, Vol.381, p.559-559

2017

Volltextzugriff (PDF)

Percutaneous endoscopic gastrostomy in patients with Duchenne muscular dystrophy compared with amyotrophic lateral sclerosis and Parkinson syndrome

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S102

2017

Volltextzugriff (PDF)

P.11 - Percutaneous endoscopic gastrostomy in patients with Duchenne muscular dystrophy compared with amyotrophic lateral sclerosis and Parkinson syndrome

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S102-S102

2017

Volltextzugriff (PDF)

P.87Carnitine deficiency in patients with neuromuscular diseases on long-term tube feeding

Neuromuscular disorders : NMD, 2019-10, Vol.29, p.S66-S66

2019

Volltextzugriff (PDF)

Study on factor related to general condition and prognosis of patients with duchenne muscular dystrophy

Journal of the neurological sciences, 2017-10, Vol.381, p.831-831

2017

Volltextzugriff (PDF)

METABOLIC MYOPATHIES II: P.348Identification of late-onset Pompe disease with nationwide high-risk screening study in Japan

Neuromuscular disorders : NMD, 2018-10, Vol.28, p.S135-S135

2018

Volltextzugriff (PDF)

METABOLIC MYOPATHIES II

Neuromuscular disorders : NMD, 2018-10, Vol.28, p.S135

2018

Volltextzugriff (PDF)

High-risk screening for late-onset Pompe disease in Japan

Journal of the neurological sciences, 2017-10, Vol.381, p.826-826

2017

Volltextzugriff (PDF)

P.13 - Study on factors related to general condition and prognosis of patients with Duchenne muscular dystrophy

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S102-S102

2017

Volltextzugriff (PDF)

Study on factors related to general condition and prognosis of patients with Duchenne muscular dystrophy

Neuromuscular disorders : NMD, 2017-10, Vol.27, p.S102

2017

Volltextzugriff (PDF)

1 – 25 von 181

Suche als RSS-Feed

Suchergebnisse filtern

Filter anzeigen

Nur zeigen

Geprüft (Peer-Review)
(162)
Mit Volltextzugriff
(138)

Publikationsform

Sprache

Englisch
(163)
Japanisch
(56)

Erscheinungsjahr

n.n

Thema

Humans
(108)
Science & Technology
(101)
Life Sciences & Biomedicine
(87)
Male
(55)
Biological And Medical Sciences
(51)
Muscular Dystrophies - Genetics
(44)
Neurology
(44)
Medical Sciences
(42)
Neurosciences & Neurology
(40)
Adult
(38)
Female
(37)
Clinical Neurology
(36)
Diseases Of Striated Muscles. Neuromuscular Diseases
(32)
Dystrophin
(29)
Neurosciences
(29)
Immunohistochemistry
(25)
Middle Aged
(25)
Adolescent
(24)
Animals
(22)
Child
(20)

15 weitere anzeigen...

Weniger anzeigen...

Menü

Weitere Dienste

Einstellungen

Jellification of medicine after simple suspension method for muscular dystrophy patients with dysphagia

G.P.7

EP.68Carnitine deficiency in patients with Duchenne muscular dystrophy requiring long-term tube feeding and heart function improvement by carnitine replacement

P.21.6 A case of familial Rippling muscle disease showing decreased of caveolin-3 in muscle biopsy suggesting an immunologic mechanism

P.10.12 Difference of the mechanism of dysphagia between Duchenne muscular dystrophy and myotonic dystrophy type 1

Life prognostic factor of patients with Duchenne muscular dystrophy

P1.08 Clinical features and swallowing test in two very mild Fukuyama type congenital muscular dystrophy (FCMD)

P110 A multicenter retrospective study of the impact of COVID-19 on patients with muscular dystrophies

P.282Relationship between verbal IQ and gene mutation in patients with Duchenne muscular dystrophy (longitudinal study)

G.P.9.10 A case of fibro-dysplasia ossificans progressiva with a novel mutation (G356D) of the activin receptor type 1 gene (ACVR1(ALK2))

P.203 - Jellification of medicine after simple suspension method for muscular dystrophy patients with dysphagia

DUCHENNE MUSCULAR DYSTROPHY – CLINICAL: P.21Changes over years in the verbal IQ of patients with Duchenne muscular dystrophy

DUCHENNE MUSCULAR DYSTROPHY – CLINICAL

G.P.7: Longitudinal studies of dysphagia in oculopharyngeal muscular dystrophies

Percutaneous endoscopic gastrostomy in patients with duchenne muscular dystrophy compare with amyotrophic lateral sclerosis: a retrospective study

Period of communication after the commencement of respiratory or nutritional support in neurodegenerative diseases

Percutaneous endoscopic gastrostomy in patients with Duchenne muscular dystrophy compared with amyotrophic lateral sclerosis and Parkinson syndrome

P.11 - Percutaneous endoscopic gastrostomy in patients with Duchenne muscular dystrophy compared with amyotrophic lateral sclerosis and Parkinson syndrome

P.87Carnitine deficiency in patients with neuromuscular diseases on long-term tube feeding

Study on factor related to general condition and prognosis of patients with duchenne muscular dystrophy

METABOLIC MYOPATHIES II: P.348Identification of late-onset Pompe disease with nationwide high-risk screening study in Japan

METABOLIC MYOPATHIES II

High-risk screening for late-onset Pompe disease in Japan

P.13 - Study on factors related to general condition and prognosis of patients with Duchenne muscular dystrophy

Study on factors related to general condition and prognosis of patients with Duchenne muscular dystrophy

Suchergebnisse filtern