140 results on '"Arrigoni, Filippo"'
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102. Diaphragm excursion in Duchenne muscolar distrophy (DMD) by magnetic resonance imaging (MRI)
103. A diffusion tensor magnetic resonance imaging study of paediatric patients with severe non-traumatic brain injury
104. SU66 - THE DCDC2/INTRON 2 DELETION AND MAGNOCELLULAR VISUAL STREAM: A PRELIMINARY FMRI STUDY IN DEVELOPMENTAL DYSLEXIA TESTING MAIN EFFECTS AND INTERACTIONS
105. Clinical Characterization, Genetics, and Long-Term Follow-up of a Large Cohort of Patients With Agenesis of the Corpus Callosum
106. Sleep/Wake Modulation of Polysomnographic Patterns has Prognostic Value in Pediatric Unresponsive Wakefulness Syndrome
107. A Study of Lobar Atrophy and White Matter Tract Damage in Pediatric Patients with Traumatic Brain Injury (P3.261)
108. Cortico-Cerebellar Connectivity in Autism Spectrum Disorder: What Do We Know So Far?
109. Aberrant supracallosal longitudinal bundle: MR features, pathogenesis and associated clinical phenotype
110. Learning to live without the cerebellum
111. A de-novo STXBP1 gene mutation in a patient showing the Rett syndrome phenotype
112. Altered Recruitment of the Attention Network Is Associated with Disability and Cognitive Impairment in Pediatric Patients with Acquired Brain Injury
113. Constructing fMRI connectivity networks: A whole brain functional parcellation method for node definition
114. Brain malformations and mutations inα- andβ-tubulin genes: a review of the literature and description of two new cases
115. Mutations in CYP2U1, DDHD2 and GBA2 genes are rare causes of complicated forms of hereditary spastic paraparesis
116. Delineation and diagnostic criteria of Oral-Facial-Digital Syndrome type VI
117. A Novel Mutation in STXBP1 Gene in a Child With Epileptic Encephalopathy and an Atypical Electroclinical Pattern
118. Bedside assessment of residual functional activation in minimally conscious state using NIRS and general linear models
119. Cerebroretinal Microangiopathy With Calcifications and Cysts Associated With CTC1 and NDP Mutations
120. Early Formative Stage of Human Focal Cortical Gyration Anomalies: Fetal MRI
121. Early Cerebral Lesions in Cytomegalovirus Infection: Prenatal MR Imaging
122. Early Prenatal Magnetic Resonance Imaging of Glutaric Aciduria Type 1
123. A Novel Mutation in STXBP1 Gene in a Child With Epileptic Encephalopathy and an Atypical Electroclinical Pattern.
124. Cerebroretinal Microangiopathy With Calcifications and Cysts Associated With CTC1 and NDP Mutations.
125. A de-novo STXBP1gene mutation in a patient showing the Rett syndrome phenotype
126. A Study of Lobar Atrophy and White Matter Tract Dam age in Pediatric Patients with Traumatic Brain Injury
127. The spectrum of brainstem malformations associated to mutations of the tubulin genes family: MRI and DTI analysis
128. Reply letter: Neurocognitive and behavioral outcomes in a nearly drowned child with cardiac arrest and hypothermia resuscitated after 43 min of no flow-time: A case study
129. Neurocognitive and behavioral outcomes in a nearly drowned child with cardiac arrest and hypothermia resuscitated after 43 min of no flow-time: A case study
130. When one is Enough: Impaired Multisensory Integration in Cerebellar Agenesis
131. Neurocognitive and behavioral outcomes in a nearly drowned child with cardiac arrest and hypothermia resuscitated after 43min of no flow-time: A case study.
132. Clinical Characterization, Genetics, and Long-Term Follow-up of a Large Cohort of Patients With Agenesis of the Corpus Callosum.
133. A framework for the automatic detection and characterization of brain malformations: Validation on the corpus callosum.
134. Aberrant supracallosal longitudinal bundle: MR features, pathogenesis and associated clinical phenotype.
135. Cognitive rehabilitation in a child with Joubert Syndrome: Developmental trends and adaptive changes in a single case report.
136. Mutations in α- and β-tubulin encoding genes: implications in brain malformations.
137. Novel SETX variants in a patient with ataxia, neuropathy, and oculomotor apraxia are associated with normal sensitivity to oxidative DNA damaging agents.
138. Detection of corpus callosum malformations in pediatric population using the discriminative direction in multiple kernel learning.
139. Bedside assessment of residual functional activation in minimally conscious state using NIRS and general linear models.
140. Early formative stage of human focal cortical gyration anomalies: fetal MRI.
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