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PubPharm (101)
71
Assessing the influence of age and gender on the phenotype of myotonic dystrophy type 2
enthalten in:
Journal of neurology
| 2017
von
Montagnese, F.
|
Mondello, S.
|
Wenninger, S.
| +2
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72
Two patients with GMPPB mutation : The overlapping phenotypes of limb-girdle myasthenic syndrome and limb-girdle muscular dystrophy dystroglycanopathy
enthalten in:
Muscle & nerve
| 2017
von
Montagnese, F.
|
Klupp, E.
|
Karampinos, D.
| +4
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73
Two patients with GMPPB mutation: The overlapping phenotypes of limb-girdle myasthenic syndrome and limb-girdle muscular dystrophy dystroglycanopathy
enthalten in:
Muscle & nerve
| 2017
von
Montagnese, F.
|
Klupp, E.
|
Karampinos, D.
| +4
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74
Two patients with GMPPB mutation: The overlapping phenotypes of limb‐girdle myasthenic syndrome and limb‐girdle muscular dystrophy dystroglycanopathy
enthalten in:
Muscle & nerve
| 2017
von
Montagnese, F.
|
Klupp, E.
|
Karampinos, D.
| +4
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75
Long-term whole-body vibration training in two late-onset Pompe disease patients
enthalten in:
Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology
| 2016
von
Montagnese, F.
|
Thiele, S.
|
Wenninger, S.
| +1
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76
Long-term whole-body vibration training in two late-onset Pompe disease patients
enthalten in:
Neurological sciences
| 2016
von
Montagnese, F.
|
Thiele, S.
|
Wenninger, S.
| +1
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77
Long-term whole-body vibration training in two late-onset Pompe disease patients
enthalten in:
Neurological sciences
| 2016
von
Montagnese, F.
|
Thiele, S.
|
Wenninger, S.
| +1
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78
Long-term whole-body vibration training in two late-onset Pompe disease patients
enthalten in:
Neurological sciences
| 2016
von
Montagnese, F.
|
Thiele, S.
|
Wenninger, S.
| +1
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79
Intracranial arterial abnormalities in patients with late onset Pompe disease (LOPD)
enthalten in:
Journal of inherited metabolic disease
| 2016
von
Montagnese, F.
|
Granata, F.
|
Musumeci, O.
| +7
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80
Intracranial arterial abnormalities in patients with late onset Pompe disease (LOPD)
enthalten in:
Journal of inherited metabolic disease
| 2016
von
Montagnese, F.
|
Granata, F.
|
Musumeci, O.
| +7
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Journal of neurology
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