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Movement Disorders Clinical Practice
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February 13, 2019
Substantia Nigra Swelling and Dentate Nucleus T2 Hyperintensity May Be Early Magnetic Resonance Imaging Signs of β-Propeller Protein-Associated Neurodegeneration
Camilla Russo, Anna Ardissone, Elena Freri, et al.
Human Mutation
|
November 3, 2016
Clinical and Molecular Characteristics of SLC16A2 (MCT8) Mutations in Three Families with the Allan-Herndon-Dudley Syndrome
Francesca Novara, Stefan Groeneweg, Elena Freri, et al.
Brain & Development
|
October 27, 2009
Dravet syndrome: early clinical manifestations and cognitive outcome in 37 Italian patients
Francesca Ragona, Daniela Brazzo, Ilaria De Giorgi, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape
|
July 14, 2021
Paroxysmal tonic upgaze in a child with SCN8A-related encephalopathy
Roberta Solazzi, Barbara Castellotti, Laura Canafoglia, et al.
Neurosci
|
November 24, 2025
Compound Heterozygous <i>PNKP</i> Variants Causing Developmental and Epileptic Encephalopathy with Severe Microcephaly: Natural History of Two New Cases and Literature Review
Francesca Ragona, Giuliana Messina, Stefania Magri, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
September 19, 2015
Clinical and genetic features of paroxysmal kinesigenic dyskinesia in Italian patients
Costanza Lamperti, Federica Invernizzi, Roberta Solazzi, et al.
Seizure
|
April 25, 2021
Severe epilepsy in CNTNAP2-related Pitt-Hopkins-like syndrome successfully treated with stiripentol
Elena Freri, Barbara Castellotti, Laura Canafoglia, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 21, 2024
Cortical Myoclonus and Complex Paroxysmal Dyskinesias in a Patient with NAA15 Variant
Elena Freri, Laura Canafoglia, Claudia Ciaccio, et al.
Orphanet Journal of Rare Diseases
|
June 23, 2019
Treatment with metformin in twelve patients with Lafora disease
Francesca Bisulli, Lorenzo Muccioli, Giuseppe d'Orsi, et al.
Neuroimage. Clinical
|
March 15, 2026
Pediatric anti-NMDAR encephalitis: Neuroradiological presentation, cognitive outcome and volumetric MRI analysis
Fabio M Doniselli, Anna Paola Savoldi, João Ramos, et al.
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of 11
Search research articles
Search
Showing results (31-40 of 109) with videos related to
Sort By:
Page
of 11
Movement Disorders Clinical Practice
|
February 13, 2019
Substantia Nigra Swelling and Dentate Nucleus T2 Hyperintensity May Be Early Magnetic Resonance Imaging Signs of β-Propeller Protein-Associated Neurodegeneration
Camilla Russo, Anna Ardissone, Elena Freri, et al.
Human Mutation
|
November 3, 2016
Clinical and Molecular Characteristics of SLC16A2 (MCT8) Mutations in Three Families with the Allan-Herndon-Dudley Syndrome
Francesca Novara, Stefan Groeneweg, Elena Freri, et al.
Brain & Development
|
October 27, 2009
Dravet syndrome: early clinical manifestations and cognitive outcome in 37 Italian patients
Francesca Ragona, Daniela Brazzo, Ilaria De Giorgi, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape
|
July 14, 2021
Paroxysmal tonic upgaze in a child with SCN8A-related encephalopathy
Roberta Solazzi, Barbara Castellotti, Laura Canafoglia, et al.
Neurosci
|
November 24, 2025
Compound Heterozygous <i>PNKP</i> Variants Causing Developmental and Epileptic Encephalopathy with Severe Microcephaly: Natural History of Two New Cases and Literature Review
Francesca Ragona, Giuliana Messina, Stefania Magri, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
September 19, 2015
Clinical and genetic features of paroxysmal kinesigenic dyskinesia in Italian patients
Costanza Lamperti, Federica Invernizzi, Roberta Solazzi, et al.
Seizure
|
April 25, 2021
Severe epilepsy in CNTNAP2-related Pitt-Hopkins-like syndrome successfully treated with stiripentol
Elena Freri, Barbara Castellotti, Laura Canafoglia, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
April 21, 2024
Cortical Myoclonus and Complex Paroxysmal Dyskinesias in a Patient with NAA15 Variant
Elena Freri, Laura Canafoglia, Claudia Ciaccio, et al.
Orphanet Journal of Rare Diseases
|
June 23, 2019
Treatment with metformin in twelve patients with Lafora disease
Francesca Bisulli, Lorenzo Muccioli, Giuseppe d'Orsi, et al.
Neuroimage. Clinical
|
March 15, 2026
Pediatric anti-NMDAR encephalitis: Neuroradiological presentation, cognitive outcome and volumetric MRI analysis
Fabio M Doniselli, Anna Paola Savoldi, João Ramos, et al.
Page
of 11