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/vufind/Search/Results?lookfor=%22Coratti%2C+Giorgia%22&type=Person&sort=year
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PubPharm (106)
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
Bulbar function in spinal muscular atrophy (SMA) : State of art and new challenges. 21st July 2023, Rome, Italy
enthalten in:
Neuromuscular disorders : NMD
| 2024
von
McGrattan, K.
|
Cerchiari, A.
|
Conway, E.
| +41
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6
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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7
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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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
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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10
Clinical Phenotype of Pediatric and Adult Patients With Spinal Muscular Atrophy With Four SMN2 Copies : Are They Really All Stable?
enthalten in:
Annals of neurology
| 2023
von
Ricci, M.
|
Cicala, G.
|
Capasso, A.
| +72
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Neuromuscular disorders : NMD
10
PloS one
9
European journal of pediatrics
6
Journal of neuromuscular diseases
5
Muscle & nerve
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Orphanet journal of rare diseases
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Journal of clinical medicine
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Thema
78
Journal Article
40
Research Support, Non-U.S. Gov't
31
Spinal muscular atrophy
12
Multicenter Study
12
Oligonucleotides
10
5Z9SP3X666
10
Neuromuscular disorders
10
nusinersen
9
spinal muscular atrophy
7
Observational Study
6
Neonate
6
Nusinersen
6
Outcome measures
6
Review
5
Duchenne muscular dystrophy
5
Natural history
5
Quality of life
5
SMN2 protein, human
5
Survival of Motor Neuron 2 Protein
4
CHOP INTEND
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Erscheinungszeitraum
75
2020-
31
2010-2019
Erscheinungsjahr(e)
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Sprache
97
Englisch
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