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PubPharm (35)
1
Myoclonus : Differential diagnosis and current management
enthalten in:
Epilepsia open
| 2024
von
Riva, A.
|
D'Onofrio, G.
|
Ferlazzo, E.
| +16
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2
Fostering education in epilepsy : a Canadian League Against Epilepsy teaching initiative
enthalten in:
The Canadian journal of neurological sciences. Le journal canadien des sciences neurologiques
| 2024
von
D'Onofrio, G.
|
RamachandranNair, R.
|
Reid, A.
| +5
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3
Pharmacodynamic rationale for the choice of antiseizure medications in the paediatric population
enthalten in:
Neurotherapeutics : the journal of the American Society for Experimental NeuroTherapeutics
| 2024
von
D'Onofrio, G.
|
Roberti, R.
|
Riva, A.
| +4
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4
A European pilot study in Dravet Syndrome to delineate what really matters for the patients and families
enthalten in:
Epilepsia open
| 2024
von
Chemaly, N.
|
Kuchenbuch, M.
|
Teng, T.
| +7
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5
Myoclonus : Differential diagnosis and current management
enthalten in:
Epilepsia Open
| 2024
von
Riva, A.
|
D'Onofrio, G.
|
Ferlazzo, E.
| +16
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6
A proposal for a shared therapeutic algorithm in children with prolonged convulsive seizures and status epilepticus
enthalten in:
Expert review of neurotherapeutics
| 2024
von
Roberti, R.
|
Riva, A.
|
D'Onofrio, G.
| +16
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7
A PAK1 mutational hotspot within the regulatory CRIPaK domain is associated with severe neurodevelopmental disorders in children
enthalten in:
Pediatric neurology
| December 2023
von
Scorrano, G.
|
D'Onofrio, G.
|
Accogli, A.
| +23
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8
A PAK1 Mutational Hotspot Within the Regulatory CRIPaK Domain is Associated With Severe Neurodevelopmental Disorders in Children
enthalten in:
Pediatric neurology
| 2023
von
Scorrano, G.
|
D'Onofrio, G.
|
Accogli, A.
| +23
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9
Treatment of Refractory Epilepsy With MEK Inhibitor in Patients With RASopathy
enthalten in:
Pediatric neurology
| 2023
von
D'Onofrio, G.
|
Delrue, M.
|
Lortie, A.
| +5
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10
Novel biallelic variants expand the phenotype of NAA20-related syndrome
enthalten in:
Clinical genetics
| 2023
von
D'Onofrio, G.
|
Cuccurullo, C.
|
Larsen, S.
| +18
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Epilepsia open
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Frontiers in neurology
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PEX13; mitochondrial dysfunction
3
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3
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3
Zellweger spectrum disorder
3
epilepsy
2
6158TKW0C5
2
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epileptic encephalopathy
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2MRO291B4U
1
44YRR34555
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2024
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2020
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