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Grazia G Salerno

Showing results (1-10 of 5) with videos related to

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American Journal of Medical Genetics. Part A|November 16, 2019
IRF2BPL gene variants: One new caseCarlotta Spagnoli, Susanna Rizzi, Grazia G Salerno, et al.
American Journal of Medical Genetics. Part A|July 26, 2022
Novel CTNNB1 variant leading to neurodevelopmental disorder with spastic diplegia and visual defects plus peripheral neuropathy: A case reportCarlotta Spagnoli, Grazia G Salerno, Susanna Rizzi, et al.
Journal of Pediatric Neurosciences|September 25, 2014
Neuropsychological implications of adjunctive levetiracetam in childhood epilepsyAnnio Posar, Grazia G Salerno, Morena Monti, et al.
Developmental Medicine and Child Neurology|April 12, 2020
Paediatric-onset hereditary spastic paraplegias: a retrospective cohort studySilvia Schiavoni, Carlotta Spagnoli, Susanna Rizzi, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|March 7, 2020
A Novel De Novo KIF21A Variant in a Patient With Congenital Fibrosis of the Extraocular Muscles With a Syndromic CFEOM PhenotypeLuca Soliani, Carlotta Spagnoli, Grazia G Salerno, et al.
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Showing results (1-10 of 5) with videos related to

Sort By:
Pageof 1
American Journal of Medical Genetics. Part A|November 16, 2019
IRF2BPL gene variants: One new caseCarlotta Spagnoli, Susanna Rizzi, Grazia G Salerno, et al.
American Journal of Medical Genetics. Part A|July 26, 2022
Novel CTNNB1 variant leading to neurodevelopmental disorder with spastic diplegia and visual defects plus peripheral neuropathy: A case reportCarlotta Spagnoli, Grazia G Salerno, Susanna Rizzi, et al.
Journal of Pediatric Neurosciences|September 25, 2014
Neuropsychological implications of adjunctive levetiracetam in childhood epilepsyAnnio Posar, Grazia G Salerno, Morena Monti, et al.
Developmental Medicine and Child Neurology|April 12, 2020
Paediatric-onset hereditary spastic paraplegias: a retrospective cohort studySilvia Schiavoni, Carlotta Spagnoli, Susanna Rizzi, et al.
Journal of Neuro-Ophthalmology : the Official Journal of the North American Neuro-Ophthalmology Society|March 7, 2020
A Novel De Novo KIF21A Variant in a Patient With Congenital Fibrosis of the Extraocular Muscles With a Syndromic CFEOM PhenotypeLuca Soliani, Carlotta Spagnoli, Grazia G Salerno, et al.
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