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/vufind/Search/Results?lookfor=%22Pane%2C+Marika%22&type=Person&sort=year
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PubPharm (294)
1
Determining minimal clinically important differences in the Hammersmith Functional Motor Scale Expanded for untreated spinal muscular atrophy patients : An international study
enthalten in:
European journal of neurology
| 2024
von
Coratti, G.
|
Bovis, F.
|
Pera, M.
| +44
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2
2-year Change in Revised Hammersmith Scale scores in a large cohort of untreated paediatric type 2 and 3 SMA participants
enthalten in:
bioRxiv.org
| 2024
von
Stimpson, G.
|
Ramsey, D.
|
Wolfe, A.
| +29
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3
Communicative development inventory in type 1 and presymptomatic infants with spinal muscular atrophy : a cohort study
enthalten in:
Archives of disease in childhood
| 2024
von
Buchignani, B.
|
Cicala, G.
|
Cumbo, F.
| +21
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4
Early neurological signs in infants identified through neonatal screening for SMA : do they predict outcome?
enthalten in:
European journal of pediatrics
| 2024
von
Pane, M.
|
Stanca, G.
|
Ticci, C.
| +25
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5
Disease Trajectories in the Revised Hammersmith Scale in a Cohort of Untreated Patients with Spinal Muscular Atrophy types 2 and 3
enthalten in:
Journal of neuromuscular diseases
| 2024
von
Wolfe, A.
|
Stimpson, G.
|
Ramsey, D.
| +32
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6
Early treatment of type II SMA slows rate of progression of scoliosis
enthalten in:
Journal of neurology, neurosurgery, and psychiatry
| 2024
von
Coratti, G.
|
Lenkowicz, J.
|
Pera, M.
| +23
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7
The emerging spectrum of neurodevelopmental comorbidities in early-onset Spinal Muscular Atrophy
enthalten in:
European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society
| 2024
von
Baranello, G.
|
Neurodevelopment in SMA Working Group
|
Roy, S.
| +55
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8
Can the CHOP-INTEND be used as An Outcome Measure in the First Months of Age? Implications for Clinical Trials and Real World Data
enthalten in:
Journal of neuromuscular diseases
| 2024
von
Cutrona, C.
|
de Sanctis, R.
|
Coratti, G.
| +14
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9
The IAAM LTBP4 Haplotype is Protective Against Dystrophin-Deficient Cardiomyopathy
enthalten in:
Journal of neuromuscular diseases
| 2024
von
Bello, L.
|
Sabbatini, D.
|
Fusto, A.
| +36
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10
Gain and loss of upper limb abilities in Duchenne muscular dystrophy patients : A 24-month study
enthalten in:
Neuromuscular disorders : NMD
| 2024
von
Coratti, G.
|
Pane, M.
|
Brogna, C.
| +42
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294
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Neuromuscular disorders : NMD
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PloS one
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European journal of pediatrics
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Acta myologica : myopathies and cardiomyopathie...
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Annals of Clinical and Translational Neurology
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4
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4
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3
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Thema
176
Journal Article
93
Research Support, Non-U.S. Gov't
39
Spinal muscular atrophy
36
Multicenter Study
24
Duchenne muscular dystrophy
18
Dystrophin
17
Oligonucleotides
17
spinal muscular atrophy
15
Review
14
5Z9SP3X666
14
nusinersen
12
Neuromuscular disorders
9
Survival of Motor Neuron 2 Protein
8
Case Reports
8
Observational Study
8
Survival of Motor Neuron 1 Protein
7
Comparative Study
7
Outcome measures
7
SMN2 protein, human
6
Clinical Trial, Phase II
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2020-
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2010-2019
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