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Plos One
|
May 26, 2011
Identification of prognostic molecular features in the reactive stroma of human breast and prostate cancer
Anne Planche, Marina Bacac, Paolo Provero, et al.
Brain & Development
|
July 24, 2010
Cerebellar atrophy in a child with hereditary methemoglobinemia type II
Carlo Fusco, Giuliana Soncini, Daniele Frattini, et al.
Italian Journal of Pediatrics
|
November 28, 2023
Tolosa-Hunt syndrome and recurrent painful ophthalmoplegic neuropathy, case reports: what to do and when?
Daniele Frattini, Alessandro Iodice, Carlotta Spagnoli, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
December 2, 2015
CMV-associated axonal sensory-motor Guillain-Barré syndrome in a child: Case report and review of the literature
Carlotta Spagnoli, Alessandro Iodice, Grazia Gabriella Salerno, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
February 16, 2016
Expanding phenotype of PRRT2 gene mutations: A new case with epilepsy and benign myoclonus of early infancy
Ilenia Maini, Alessandro Iodice, Carlotta Spagnoli, et al.
Movement Disorders Clinical Practice
|
January 9, 2026
The Criss-Cross Gait Is Not Child's Play
Susanna Rizzi, Carlo Alberto Cesaroni, Daniele Frattini, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape
|
October 5, 2021
Beneficial effects of the ketogenic diet on drug-resistant epileptic encephalopathy associated with a de novo NBEA pathogenic variant
Silvia Schiavoni, Carlotta Spagnoli, Susanna Rizzi, et al.
Cerebellum (London, England)
|
November 14, 2020
Infantile-Onset Spinocerebellar Ataxia Type 5 (SCA5) with Optic Atrophy and Peripheral Neuropathy
Carlotta Spagnoli, Daniele Frattini, Fabrizio Gozzi, et al.
Developmental Medicine and Child Neurology
|
April 12, 2020
Paediatric-onset hereditary spastic paraplegias: a retrospective cohort study
Silvia Schiavoni, Carlotta Spagnoli, Susanna Rizzi, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
October 28, 2021
Growth hormone deficiency in a child with benign hereditary chorea caused by a <i>de novo</i> mutation of the TITF1/NKX2-1 gene
Viola Trevisani, Barbara Predieri, Simona Filomena Madeo, et al.
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Search research articles
Search
Showing results (51-60 of 148) with videos related to
Sort By:
Page
of 15
Plos One
|
May 26, 2011
Identification of prognostic molecular features in the reactive stroma of human breast and prostate cancer
Anne Planche, Marina Bacac, Paolo Provero, et al.
Brain & Development
|
July 24, 2010
Cerebellar atrophy in a child with hereditary methemoglobinemia type II
Carlo Fusco, Giuliana Soncini, Daniele Frattini, et al.
Italian Journal of Pediatrics
|
November 28, 2023
Tolosa-Hunt syndrome and recurrent painful ophthalmoplegic neuropathy, case reports: what to do and when?
Daniele Frattini, Alessandro Iodice, Carlotta Spagnoli, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
December 2, 2015
CMV-associated axonal sensory-motor Guillain-Barré syndrome in a child: Case report and review of the literature
Carlotta Spagnoli, Alessandro Iodice, Grazia Gabriella Salerno, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
February 16, 2016
Expanding phenotype of PRRT2 gene mutations: A new case with epilepsy and benign myoclonus of early infancy
Ilenia Maini, Alessandro Iodice, Carlotta Spagnoli, et al.
Movement Disorders Clinical Practice
|
January 9, 2026
The Criss-Cross Gait Is Not Child's Play
Susanna Rizzi, Carlo Alberto Cesaroni, Daniele Frattini, et al.
Epileptic Disorders : International Epilepsy Journal with Videotape
|
October 5, 2021
Beneficial effects of the ketogenic diet on drug-resistant epileptic encephalopathy associated with a de novo NBEA pathogenic variant
Silvia Schiavoni, Carlotta Spagnoli, Susanna Rizzi, et al.
Cerebellum (London, England)
|
November 14, 2020
Infantile-Onset Spinocerebellar Ataxia Type 5 (SCA5) with Optic Atrophy and Peripheral Neuropathy
Carlotta Spagnoli, Daniele Frattini, Fabrizio Gozzi, et al.
Developmental Medicine and Child Neurology
|
April 12, 2020
Paediatric-onset hereditary spastic paraplegias: a retrospective cohort study
Silvia Schiavoni, Carlotta Spagnoli, Susanna Rizzi, et al.
Journal of Pediatric Endocrinology & Metabolism : JPEM
|
October 28, 2021
Growth hormone deficiency in a child with benign hereditary chorea caused by a <i>de novo</i> mutation of the TITF1/NKX2-1 gene
Viola Trevisani, Barbara Predieri, Simona Filomena Madeo, et al.
Page
of 15