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Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology
|
December 25, 2023
The long-term impact of irradiation on functional connectivity in brain circuits involved in memory processes after pediatric posterior fossa tumor
Eloïse Baudou, Patrice Peran, Fatima Tensaouti, et al.
Journal of Child Neurology
|
January 28, 2021
Reading Comprehension Impairment in Children With Neurofibromatosis Type 1 (NF1): The Need of Multimodal Assessment of Attention
Maëlle Biotteau, Elodie Tournay, Eloise Baudou, et al.
Orphanet Journal of Rare Diseases
|
April 18, 2015
Natural disease history and characterisation of SUMF1 molecular defects in ten unrelated patients with multiple sulfatase deficiency
Frédérique Sabourdy, Lionel Mourey, Emmanuelle Le Trionnaire, et al.
International Journal of Molecular Sciences
|
April 3, 2021
Refining Genotypes and Phenotypes in <i>KCNA2</i>-Related Neurological Disorders
Jan H Döring, Julian Schröter, Jerome Jüngling, et al.
Annals of Clinical and Translational Neurology
|
February 23, 2018
Effect of desipramine on patients with breathing disorders in RETT syndrome
Josette Mancini, Jean-Christophe Dubus, Elisabeth Jouve, et al.
Clinical and Translational Radiation Oncology
|
January 6, 2022
A prospective behavioral and imaging study exploring the impact on long-term memory of radiotherapy delivered for a brain tumor in childhood and adolescence
Eloïse Baudou, Jérémie Pariente, Patrice Péran, et al.
Immunity
|
September 14, 2010
Human TRAF3 adaptor molecule deficiency leads to impaired Toll-like receptor 3 response and susceptibility to herpes simplex encephalitis
Rebeca Pérez de Diego, Vanessa Sancho-Shimizu, Lazaro Lorenzo, et al.
Orphanet Journal of Rare Diseases
|
October 30, 2013
Phenotypic variability in ARCA2 and identification of a core ataxic phenotype with slow progression
Cyril Mignot, Emmanuelle Apartis, Alexandra Durr, et al.
Annals of Neurology
|
August 23, 2024
Electro-Clinical Features and Functional Connectivity Analysis in SYN1-Related Epilepsy
Vincent Moya Quiros, Ahmed Adham, Philippe Convers, et al.
Journal of Child Psychology and Psychiatry, and Allied Disciplines
|
December 12, 2012
Predictors of developmental dyslexia in European orthographies with varying complexity
Karin Landerl, Franck Ramus, Kristina Moll, et al.
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of 8
Search research articles
Search
Showing results (61-70 of 72) with videos related to
Sort By:
Page
of 8
Radiotherapy and Oncology : Journal of the European Society for Therapeutic Radiology and Oncology
|
December 25, 2023
The long-term impact of irradiation on functional connectivity in brain circuits involved in memory processes after pediatric posterior fossa tumor
Eloïse Baudou, Patrice Peran, Fatima Tensaouti, et al.
Journal of Child Neurology
|
January 28, 2021
Reading Comprehension Impairment in Children With Neurofibromatosis Type 1 (NF1): The Need of Multimodal Assessment of Attention
Maëlle Biotteau, Elodie Tournay, Eloise Baudou, et al.
Orphanet Journal of Rare Diseases
|
April 18, 2015
Natural disease history and characterisation of SUMF1 molecular defects in ten unrelated patients with multiple sulfatase deficiency
Frédérique Sabourdy, Lionel Mourey, Emmanuelle Le Trionnaire, et al.
International Journal of Molecular Sciences
|
April 3, 2021
Refining Genotypes and Phenotypes in <i>KCNA2</i>-Related Neurological Disorders
Jan H Döring, Julian Schröter, Jerome Jüngling, et al.
Annals of Clinical and Translational Neurology
|
February 23, 2018
Effect of desipramine on patients with breathing disorders in RETT syndrome
Josette Mancini, Jean-Christophe Dubus, Elisabeth Jouve, et al.
Clinical and Translational Radiation Oncology
|
January 6, 2022
A prospective behavioral and imaging study exploring the impact on long-term memory of radiotherapy delivered for a brain tumor in childhood and adolescence
Eloïse Baudou, Jérémie Pariente, Patrice Péran, et al.
Immunity
|
September 14, 2010
Human TRAF3 adaptor molecule deficiency leads to impaired Toll-like receptor 3 response and susceptibility to herpes simplex encephalitis
Rebeca Pérez de Diego, Vanessa Sancho-Shimizu, Lazaro Lorenzo, et al.
Orphanet Journal of Rare Diseases
|
October 30, 2013
Phenotypic variability in ARCA2 and identification of a core ataxic phenotype with slow progression
Cyril Mignot, Emmanuelle Apartis, Alexandra Durr, et al.
Annals of Neurology
|
August 23, 2024
Electro-Clinical Features and Functional Connectivity Analysis in SYN1-Related Epilepsy
Vincent Moya Quiros, Ahmed Adham, Philippe Convers, et al.
Journal of Child Psychology and Psychiatry, and Allied Disciplines
|
December 12, 2012
Predictors of developmental dyslexia in European orthographies with varying complexity
Karin Landerl, Franck Ramus, Kristina Moll, et al.
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of 8