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Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
December 20, 2019
Neurosurgical treatment of subependymal giant cell astrocytomas in tuberous sclerosis complex: a series of 44 surgical procedures in 31 patients
Flavio Giordano, Carla Moscheo, Matteo Lenge, et al.
American Journal of Medical Genetics. Part A
|
June 12, 2008
A 7 Mb duplication at 22q13 in a girl with bipolar disorder and hippocampal malformation
Tiziano Pramparo, Manuela de Gregori, Stefania Gimelli, et al.
Fetal and Pediatric Pathology
|
September 1, 2022
Fetal Presentation of Walker-Warburg Syndrome with Compound Heterozygous <i>POMT2</i> Missense Mutations
Silvia Zago, Evelina Silvestri, Tiziana Arcangeli, et al.
Neuroradiology
|
July 6, 2026
Enhanced detection of subtle cortical abnormalities in focal epilepsy using 7 T MRI surface-based models and graph neural networks
Matteo Lenge, Simona Fiori, Pietro Cappelletto, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
August 26, 2023
GNAO1 Haploinsufficiency: The Milder End of the GNAO1 Phenotypic Spectrum
Serena Galosi, Maria Novelli, Martina Di Rocco, et al.
Plos One
|
July 16, 2015
Early Diagnosis and Monitoring of Neurodegenerative Langerhans Cell Histiocytosis
Elena Sieni, Carmen Barba, Marzia Mortilla, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
April 27, 2017
Leigh-like neuroimaging features associated with new biallelic mutations in OPA1
Anna Rubegni, Tiziana Pisano, Giacomo Bacci, et al.
Journal of Medical Genetics
|
March 11, 2015
Familial periventricular nodular heterotopia, epilepsy and Melnick-Needles Syndrome caused by a single FLNA mutation with combined gain-of-function and loss-of-function effects
Elena Parrini, Davide Mei, Maria Antonietta Pisanti, et al.
Neurobiology of Disease
|
April 5, 2011
Autism with seizures and intellectual disability: possible causative role of gain-of-function of the inwardly-rectifying K+ channel Kir4.1
Federico Sicca, Paola Imbrici, Maria Cristina D'Adamo, et al.
Orphanet Journal of Rare Diseases
|
August 7, 2013
Galactosialidosis: review and analysis of CTSA gene mutations
Anna Caciotti, Serena Catarzi, Rodolfo Tonin, et al.
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of 62
Search research articles
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Showing results (261-270 of 611) with videos related to
Sort By:
Page
of 62
Child'S Nervous System : Chns : Official Journal of the International Society for Pediatric Neurosurgery
|
December 20, 2019
Neurosurgical treatment of subependymal giant cell astrocytomas in tuberous sclerosis complex: a series of 44 surgical procedures in 31 patients
Flavio Giordano, Carla Moscheo, Matteo Lenge, et al.
American Journal of Medical Genetics. Part A
|
June 12, 2008
A 7 Mb duplication at 22q13 in a girl with bipolar disorder and hippocampal malformation
Tiziano Pramparo, Manuela de Gregori, Stefania Gimelli, et al.
Fetal and Pediatric Pathology
|
September 1, 2022
Fetal Presentation of Walker-Warburg Syndrome with Compound Heterozygous <i>POMT2</i> Missense Mutations
Silvia Zago, Evelina Silvestri, Tiziana Arcangeli, et al.
Neuroradiology
|
July 6, 2026
Enhanced detection of subtle cortical abnormalities in focal epilepsy using 7 T MRI surface-based models and graph neural networks
Matteo Lenge, Simona Fiori, Pietro Cappelletto, et al.
Movement Disorders : Official Journal of the Movement Disorder Society
|
August 26, 2023
GNAO1 Haploinsufficiency: The Milder End of the GNAO1 Phenotypic Spectrum
Serena Galosi, Maria Novelli, Martina Di Rocco, et al.
Plos One
|
July 16, 2015
Early Diagnosis and Monitoring of Neurodegenerative Langerhans Cell Histiocytosis
Elena Sieni, Carmen Barba, Marzia Mortilla, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
April 27, 2017
Leigh-like neuroimaging features associated with new biallelic mutations in OPA1
Anna Rubegni, Tiziana Pisano, Giacomo Bacci, et al.
Journal of Medical Genetics
|
March 11, 2015
Familial periventricular nodular heterotopia, epilepsy and Melnick-Needles Syndrome caused by a single FLNA mutation with combined gain-of-function and loss-of-function effects
Elena Parrini, Davide Mei, Maria Antonietta Pisanti, et al.
Neurobiology of Disease
|
April 5, 2011
Autism with seizures and intellectual disability: possible causative role of gain-of-function of the inwardly-rectifying K+ channel Kir4.1
Federico Sicca, Paola Imbrici, Maria Cristina D'Adamo, et al.
Orphanet Journal of Rare Diseases
|
August 7, 2013
Galactosialidosis: review and analysis of CTSA gene mutations
Anna Caciotti, Serena Catarzi, Rodolfo Tonin, et al.
Page
of 62