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Epilepsia
|
May 8, 2016
Epileptic networks are strongly connected with and without the effects of interictal discharges
Giannina R Iannotti, Frédéric Grouiller, Maria Centeno, et al.
Frontiers in Immunology
|
February 14, 2022
Childhood-Onset Movement Disorders Can Mask a Primary Immunodeficiency: 6 Cases of Classical Ataxia-Telangiectasia and Variant Forms
Geraldine Blanchard-Rohner, Anna Peirolo, Ludivine Coulon, et al.
Frontiers in Neurology
|
February 14, 2025
Evaluating NfL and NTproBNP as predictive biomarkers of intracranial injuries after mild traumatic brain injury in children presenting to emergency departments
Anne-Cécile Chiollaz, Virginie Pouillard, Michelle Seiler, et al.
Frontiers in Neurology
|
July 26, 2024
Diagnostic potential of IL6 and other blood-based inflammatory biomarkers in mild traumatic brain injury among children
Anne-Cécile Chiollaz, Virginie Pouillard, Céline Habre, et al.
Journal of Neurotrauma
|
October 7, 2025
IL6 in Combination with Either NfL, NTproBNP, or GFAP to Safely Discharge Children with Mild Traumatic Brain Injury
Anne-Cécile Chiollaz, Virginie Pouillard, Michelle Seiler, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 18, 2015
Severe phenotypic spectrum of biallelic mutations in PRRT2 gene
Marion Delcourt, Florence Riant, Josette Mancini, et al.
Neurotrauma Reports
|
July 29, 2024
Management of Pediatric Mild Traumatic Brain Injury Patients: S100b, Glial Fibrillary Acidic Protein, and Heart Fatty-Acid-Binding Protein Promising Biomarkers
Anne-Cécile Chiollaz, Virginie Pouillard, Fabian Spigariol, et al.
Epilepsia
|
February 16, 2013
Reduction of seizure frequency after epilepsy surgery in a patient with STXBP1 encephalopathy and clinical description of six novel mutation carriers
Sarah Weckhuysen, Philip Holmgren, Rik Hendrickx, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
October 16, 2024
Developmental and epileptic encephalopathy 56 due to YWHAG variants: 12 new cases and review of the literature
Maria Eugenia Amato, Sol Balsells, Loreto Martorell, et al.
Clinical Genetics
|
July 3, 2021
ZMYND11 variants are a novel cause of centrotemporal and generalised epilepsies with neurodevelopmental disorder
Stephanie Oates, Michael Absoud, Sushma Goyal, et al.
Page
of 4
Search research articles
Search
Showing results (21-30 of 38) with videos related to
Sort By:
Page
of 4
Epilepsia
|
May 8, 2016
Epileptic networks are strongly connected with and without the effects of interictal discharges
Giannina R Iannotti, Frédéric Grouiller, Maria Centeno, et al.
Frontiers in Immunology
|
February 14, 2022
Childhood-Onset Movement Disorders Can Mask a Primary Immunodeficiency: 6 Cases of Classical Ataxia-Telangiectasia and Variant Forms
Geraldine Blanchard-Rohner, Anna Peirolo, Ludivine Coulon, et al.
Frontiers in Neurology
|
February 14, 2025
Evaluating NfL and NTproBNP as predictive biomarkers of intracranial injuries after mild traumatic brain injury in children presenting to emergency departments
Anne-Cécile Chiollaz, Virginie Pouillard, Michelle Seiler, et al.
Frontiers in Neurology
|
July 26, 2024
Diagnostic potential of IL6 and other blood-based inflammatory biomarkers in mild traumatic brain injury among children
Anne-Cécile Chiollaz, Virginie Pouillard, Céline Habre, et al.
Journal of Neurotrauma
|
October 7, 2025
IL6 in Combination with Either NfL, NTproBNP, or GFAP to Safely Discharge Children with Mild Traumatic Brain Injury
Anne-Cécile Chiollaz, Virginie Pouillard, Michelle Seiler, et al.
Journal of Neurology, Neurosurgery, and Psychiatry
|
January 18, 2015
Severe phenotypic spectrum of biallelic mutations in PRRT2 gene
Marion Delcourt, Florence Riant, Josette Mancini, et al.
Neurotrauma Reports
|
July 29, 2024
Management of Pediatric Mild Traumatic Brain Injury Patients: S100b, Glial Fibrillary Acidic Protein, and Heart Fatty-Acid-Binding Protein Promising Biomarkers
Anne-Cécile Chiollaz, Virginie Pouillard, Fabian Spigariol, et al.
Epilepsia
|
February 16, 2013
Reduction of seizure frequency after epilepsy surgery in a patient with STXBP1 encephalopathy and clinical description of six novel mutation carriers
Sarah Weckhuysen, Philip Holmgren, Rik Hendrickx, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
October 16, 2024
Developmental and epileptic encephalopathy 56 due to YWHAG variants: 12 new cases and review of the literature
Maria Eugenia Amato, Sol Balsells, Loreto Martorell, et al.
Clinical Genetics
|
July 3, 2021
ZMYND11 variants are a novel cause of centrotemporal and generalised epilepsies with neurodevelopmental disorder
Stephanie Oates, Michael Absoud, Sushma Goyal, et al.
Page
of 4