1,601 results on '"Boddaert, Nathalie"'
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152. Reduced‐order Models of Blood Flow: Application to Arterial Stenoses
153. Suleiman-El-Hattab syndrome: a histone modification disorder caused by TASP1 deficiency
154. Recessive PRDM13 mutations cause fatal perinatal brainstem dysfunction with cerebellar hypoplasia and disrupt Purkinje cell differentiation
155. Interrelations humaines, cognition sociale et sillon temporal supérieur
156. Impact of aortic arch curvature in flow haemodynamics in patients with transposition of the great arteries after arterial switch operation
157. WDR81 mutations cause extreme microcephaly and impair mitotic progression in human fibroblasts and Drosophila neural stem cells
158. Mutations in DNM1L, as in OPA1, result indominant optic atrophy despite opposite effectson mitochondrial fusion and fission
159. Prenatal and Postnatal Presentations of Corpus Callosum Agenesis with Polymicrogyria Caused By EGP5 Mutation
160. A novel recurrent LIS1 splice site mutation in classic lissencephaly
161. Preoperative Detection of Subtle Focal Cortical Dysplasia in Children by Combined Arterial Spin Labeling, Voxel-Based Morphometry, Electroencephalography-Synchronized Functional MRI, Resting-State Regional Homogeneity, and 18F-fluorodeoxyglucose...
162. Focal polymicrogyria are associated with submicroscopic chromosomal rearrangements detected by CGH microarray analysis
163. Mutation in a primate-conserved retrotransposon reveals a noncoding RNA as a mediator of infantile encephalopathy
164. Neurodegeneration With Brain Iron Accumulation: A Diagnostic Algorithm
165. Author Correction: Targeted therapy in patients with PIK3CA-related overgrowth syndrome
166. Biallelic variants in SLC35B2 cause a novel chondrodysplasia with hypomyelinating leukodystrophy
167. A partial form of inherited human USP18 deficiency underlies infection and inflammation
168. Systemic inflammatory syndrome in children with FARSA deficiency
169. Central Nervous System Complications in Cystinosis: The Role of Neuroimaging
170. Additional file 1 of Posterior fossa ependymoma H3 K27-mutant: an integrated radiological and histomolecular tumor analysis
171. Additional file 2 of Posterior fossa ependymoma H3 K27-mutant: an integrated radiological and histomolecular tumor analysis
172. Additional file 1 of A novel LARGE1-AFF2 fusion expanding the molecular alterations associated with the methylation class of neuroepithelial tumors with PATZ1 fusions
173. FGFR3 overactivation in the brain is responsible for memory impairments in Crouzon syndrome mouse model
174. Chapitre 4 - Crises convulsives
175. Chapitre 5 - Augmentation du périmètre crânien
176. Chapitre 3 - Syndrome cérébelleux
177. Chapitre 1 - Céphalées
178. A novel LARGE1-AFF2 fusion expanding the molecular alterations associated with the methylation class of neuroepithelial tumors with PATZ1 fusions
179. Polyradiculoneuritis on MRI: An Overlooked Feature of Biallelic POLG Gene Mutations in Infancy.
180. Feature selection and classification of imbalanced datasets: Application to PET images of children with autistic spectrum disorders
181. New Approach to Accelerated Image Annotation by Leveraging Virtual Reality and Cloud Computing
182. Treatment of two infants with PIK3CA-related overgrowth spectrum by alpelisib
183. Arterial Spin Labeling for the Etiological Workup of Intracerebral Hemorrhage in Children
184. Pulmonary Perfusion Asymmetry in Patients after Repair of Tetralogy of Fallot: A 4D Flow MRI-Based Study
185. Object Detection Improves Tumour Segmentation in MR Images of Rare Brain Tumours
186. Prevalence of Venovenous Shunting and High-Output State Quantified with 4D Flow MRI in Patients with Fontan Circulation
187. Deciphering the genetic and epigenetic landscape of pediatric bithalamic tumors
188. The Role of Irinotecan-Bevacizumab as Rescue Regimen in Children With Low-Grade Gliomas: A Retrospective Nationwide Study in 72 Patients
189. Impact of ComBat and a Multi-Model approach to deal with multi-scanner and missing MRI data in a small cohort study. Application to H3K27M mutation prediction in patients with DIPG
190. Variants in the MIPEP gene presenting with complex neurological phenotype without cardiomyopathy, impair OXPHOS protein maturation and lead to a reduced OXPHOS abundance in patient cells
191. Expanding the clinical and mutational spectrum of Kaufman oculocerebrofacial syndrome with biallelic UBE3B mutations
192. Tuning Eye-Gaze Perception by Transitory STS Inhibition
193. Sulfonylurea Therapy Benefits Neurological and Psychomotor Functions in Patients With Neonatal Diabetes Owing to Potassium Channel Mutations
194. Arterial abnormalities identified in kidneys transplanted into children during the COVID-19 pandemic
195. Optimisation d'une métrique de forme basée sur la théorie de l'information pour la fusion et l'évaluation de méthodes de segmentation de tumeurs GITC en IRM multimodale 3D
196. Pediatric brain arteriovenous malformation recurrence: a cohort study, systematic review and meta-analysis
197. Prenatal‐onset of congenital neuronal ceroid lipofuscinosis with a novel CTSD mutation
198. Cardiac MRI prediction of recovery in children with acute myocarditis
199. A malignant choroid plexus tumour with prevailing immature blastematous elements
200. IFT81, encoding an IFT-B core protein, as a very rare cause of a ciliopathy phenotype
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