Search research articles
Contact Us
Filters
Showing results (91-100 of 149) with videos related to
Page
of 15
Sort By:
American Journal of Medical Genetics. Part A
|
September 3, 2020
Severe intellectual disability, absence of language, epilepsy, microcephaly and progressive cerebellar atrophy related to the recurrent de novo variant p.(P139L) of the CAMK2B gene: A case report and brief review
Susanna Rizzi, Carlotta Spagnoli, Grazia Gabriella Salerno, et al.
Frontiers in Neurology
|
October 11, 2021
Infantile-Onset Charcot-Marie-Tooth Disease With Pyramidal Features and White Matter Abnormalities Due to a <i>De novo MORC2</i> Gene Variant: A Case Report and Brief Review of the Literature
Ivana Frongia, Susanna Rizzi, Margherita Baga, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
October 29, 2024
Transition and management of patients with Duchenne Muscular Dystrophy: a narrative review based on Italian experts' opinion and real-world experience
Carlotta Spagnoli, Rachele Adorisio, Luca Bello, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
February 26, 2024
Continuitiy of care with ataluren in Duchenne Muscular Dystrophy patients with nonsense mutations after loss of ambulation. Personal experience
Carlotta Spagnoli, Rachele Adorisio, Luca Bello, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape
|
July 21, 2010
Partial epilepsy complicated by convulsive and nonconvulsive episodes of status epilepticus in a patient with ring chromosome 14 syndrome
Simona Giovannini, Daniele Frattini, Angela Scarano, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
March 3, 2026
A Systematic Review about Neuropathies in Spinal Muscular Atrophy (SMA): Current Insights and Future Directions
Carlo Alberto Cesaroni, Martina Gnazzo, Giulia Pisanò, et al.
Parkinsonism & Related Disorders
|
August 19, 2020
Paroxysmal movement disorder with response to carbamazepine in a patient with RHOBTB2 developmental and epileptic encephalopathy
Carlotta Spagnoli, Luca Soliani, Stefano Giuseppe Caraffi, et al.
Journal of Clinical Medicine
|
May 13, 2026
Phenotypic Heterogeneity in Titinopathies with Peripheral Nerve Involvement in Pediatric Age: Two Case Reports
Carlo Alberto Cesaroni, Giulia Pisanò, Massimiliano Marton, et al.
Ebiomedicine
|
March 6, 2018
Reciprocal modulation of mesenchymal stem cells and tumor cells promotes lung cancer metastasis
Giulia Fregni, Mathieu Quinodoz, Emely Möller, et al.
The Neurohospitalist
|
January 18, 2024
Tick-Borne Encephalitis in a 6-Year-Old Patient: A Case Report
Carlo Alberto Cesaroni, Daniele Frattini, Marco Lecis, et al.
Page
of 15
Search research articles
Search
Showing results (91-100 of 149) with videos related to
Sort By:
Page
of 15
American Journal of Medical Genetics. Part A
|
September 3, 2020
Severe intellectual disability, absence of language, epilepsy, microcephaly and progressive cerebellar atrophy related to the recurrent de novo variant p.(P139L) of the CAMK2B gene: A case report and brief review
Susanna Rizzi, Carlotta Spagnoli, Grazia Gabriella Salerno, et al.
Frontiers in Neurology
|
October 11, 2021
Infantile-Onset Charcot-Marie-Tooth Disease With Pyramidal Features and White Matter Abnormalities Due to a <i>De novo MORC2</i> Gene Variant: A Case Report and Brief Review of the Literature
Ivana Frongia, Susanna Rizzi, Margherita Baga, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
October 29, 2024
Transition and management of patients with Duchenne Muscular Dystrophy: a narrative review based on Italian experts' opinion and real-world experience
Carlotta Spagnoli, Rachele Adorisio, Luca Bello, et al.
Acta Myologica : Myopathies and Cardiomyopathies : Official Journal of the Mediterranean Society of Myology
|
February 26, 2024
Continuitiy of care with ataluren in Duchenne Muscular Dystrophy patients with nonsense mutations after loss of ambulation. Personal experience
Carlotta Spagnoli, Rachele Adorisio, Luca Bello, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape
|
July 21, 2010
Partial epilepsy complicated by convulsive and nonconvulsive episodes of status epilepticus in a patient with ring chromosome 14 syndrome
Simona Giovannini, Daniele Frattini, Angela Scarano, et al.
The Canadian Journal of Neurological Sciences. Le Journal Canadien Des Sciences Neurologiques
|
March 3, 2026
A Systematic Review about Neuropathies in Spinal Muscular Atrophy (SMA): Current Insights and Future Directions
Carlo Alberto Cesaroni, Martina Gnazzo, Giulia Pisanò, et al.
Parkinsonism & Related Disorders
|
August 19, 2020
Paroxysmal movement disorder with response to carbamazepine in a patient with RHOBTB2 developmental and epileptic encephalopathy
Carlotta Spagnoli, Luca Soliani, Stefano Giuseppe Caraffi, et al.
Journal of Clinical Medicine
|
May 13, 2026
Phenotypic Heterogeneity in Titinopathies with Peripheral Nerve Involvement in Pediatric Age: Two Case Reports
Carlo Alberto Cesaroni, Giulia Pisanò, Massimiliano Marton, et al.
Ebiomedicine
|
March 6, 2018
Reciprocal modulation of mesenchymal stem cells and tumor cells promotes lung cancer metastasis
Giulia Fregni, Mathieu Quinodoz, Emely Möller, et al.
The Neurohospitalist
|
January 18, 2024
Tick-Borne Encephalitis in a 6-Year-Old Patient: A Case Report
Carlo Alberto Cesaroni, Daniele Frattini, Marco Lecis, et al.
Page
of 15