Cesar Alves, MD, PhD
Associate Program Director, Neuroradiology Fellowship Program; Neuroradiologist, Department of Radiology
Assistant Professor of Radiology, Harvard Medical School
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Cesar Alves, MD, PhD
Associate Program Director, Neuroradiology Fellowship Program; Neuroradiologist, Department of Radiology
Assistant Professor of Radiology, Harvard Medical School
Medical Services
Languages
English
Publications
Pediatric-Type Diffuse Low-Grade Gliomas with MYB Alterations: Neuroimaging of the Diffuse Astrocytomas, MYB- or MYBL1-Altered. View Abstract
MAPK signaling and angiopoietin-2 contribute to endothelial permeability in capillary malformations. View Abstract
Spinal Cord Leptomeningeal Enhancement as a Marker of Extensive Spinal Cord Involvement in Children With MOGAD. View Abstract
Imaging patterns of paediatric CNS mitochondrial disorders. View Abstract
Extensive Cerebellitis as a Key Neuroimaging Feature in a Child With MT-ATP6 Pathogenic Variant. View Abstract
Mutations in the Key Autophagy Tethering Factor EPG5 Link Neurodevelopmental and Neurodegenerative Disorders Including Early-Onset Parkinsonism. View Abstract
Neuroimaging Findings in Carbonic Anhydrase VA Deficiency: A Case Series Highlighting Diagnostic and Prognostic Patterns in a Potentially Reversible Mitochondrial Dysfunction. View Abstract
Comprehensive genotypic, phenotypic, and biochemical characterization of GOT2 deficiency: A progressive neurodevelopmental disorder with epilepsy and abnormal movements. View Abstract
An Emerging Pediatric CNS Tumor: Imaging Evaluation of H3K27M and BRAF V600E Comutated Midline Tumors. View Abstract
A programmed decline in ribosome levels governs human early neurodevelopment. View Abstract
Frontal Paraventricular Cysts: Refined Definitions and Outcomes. View Abstract
Central Dysmyelination in SSADH-Deficient Humans and Mice. View Abstract
Neuroimaging patterns in patients with mitochondrial leukoencephalopathies. View Abstract
Variable Flip Angle Optimization for Fetal Brain Imaging With Reduced Specific Absorption Rate. View Abstract
Contributions of clinical simulation in the care of women in situations of violence for training. View Abstract
ELFN1 deficiency: The mechanistic basis and phenotypic spectrum of a neurodevelopmental disorder with epilepsy. View Abstract
High-resolution modelling of particulate matter chemical composition over Europe: brake wear pollution. View Abstract
Single Large-Scale Mitochondrial Deletion Syndromes: Neuroimaging Phenotypes and Longitudinal Progression in Pediatric Patients. View Abstract
MAPK Signaling and Angiopoietin-2 Contribute to Endothelial Permeability in Capillary Malformations. View Abstract
PM10 exposure in beauty salons: impact on A549 cell viability, cell cycle, oxidative stress, and mutagenicity. View Abstract
PM10-bound elements in Luanda's urban atmosphere: Concentrations, sources, and their environmental and health impacts. View Abstract
Magnetic resonance imaging findings in SCN1A-related epilepsies and Dravet syndrome: A systematic review. View Abstract
Clinical simulation on intimate partner violence in adolescent girls: contributions to health teaching. View Abstract
Overview of neuroimaging in primary mitochondrial disorders. View Abstract
Biallelic variants in GTF3C3 encoding a subunit of the TFIIIC2 complex are associated with neurodevelopmental phenotypes in humans and zebrafish. View Abstract
Cortically Based Brain Tumors in Children: A Decision-Tree Approach in the Radiology Reading Room. View Abstract
Cancer Predisposition Syndromes With Involvement of the Head and Neck Regions in Children: An Imaging Guide. View Abstract
Icodextrin versus Glucose 2.5% on markers of hypervolemia and survival of patients undergoing automated peritoneal dialysis with an unplanned start: a randomized controlled trial. View Abstract
Frequency and Distribution of Perinatal Arterial Ischemic Stroke in a Cohort of Patients With Cerebral Palsy Using Delayed MRI. View Abstract
Clinical and neuroradiological spectrum of biallelic variants in NOTCH3. View Abstract
Loss of symmetric cell division of apical neural progenitors drives DENND5A-related developmental and epileptic encephalopathy. View Abstract
Fetal Brain MRI Abnormalities in Pyruvate Dehydrogenase Complex Deficiency. View Abstract
Approaches to supratentorial brain tumours in children. View Abstract
Incomplete partition type II in its various manifestations: isolated, in association with EVA, syndromic, and beyond; a multicentre international study. View Abstract
Characteristic Fetal Brain MRI Abnormalities in Pyruvate Dehydrogenase Complex Deficiency. View Abstract
Clinical and Molecular Spectrum of Autosomal Recessive CA8-Related Cerebellar Ataxia. View Abstract
Biallelic variants in GTF3C5, a regulator of RNA polymerase III-mediated transcription, cause a multisystem developmental disorder. View Abstract
Advancing the neuroimaging diagnosis and understanding of mitochondrial disorders. View Abstract
Loss of symmetric cell division of apical neural progenitors drives DENND5A-related developmental and epileptic encephalopathy. View Abstract
Distinguishing multicystic from focal encephalomalacia on delayed MRI in children with term hypoxic ischemic injury. View Abstract
An inappropriate decline in ribosome levels drives a diverse set of neurodevelopmental disorders. View Abstract
Frequency of Cerebellar Abnormalities Associated With the Differing Magnetic Resonance Imaging Patterns of Term Hypoxic-Ischemic Injury in Children. View Abstract
"A Man Has to Show That He Is a Man From a Young Age": Intimate Partner Violence for Young Male University Students in Brazil. View Abstract
Clinical, radiological, biochemical and molecular characterization of a new case with multiple mitochondrial dysfunction syndrome due to IBA57: Lysine and tryptophan metabolites as potential biomarkers. View Abstract
Heterozygous nonsense variants in the ferritin heavy-chain gene FTH1 cause a neuroferritinopathy. View Abstract
Dandy-Walker Phenotype with Brainstem Involvement: 2 Distinct Subgroups with Different Prognosis. View Abstract
Expansion of clinical and variant spectrum of EEF2-related neurodevelopmental disorder: Report of two additional cases. View Abstract
MELAS: Phenotype Classification into Classic-versus-Atypical Presentations. View Abstract
Subdural Hemorrhage as an Early Presentation in a Case of Sotos Syndrome. View Abstract
Acquired hump of the corpus callosum: a rare morphologic complication after CSF shunting. View Abstract
Heterozygous Nonsense Variants in the Ferritin Heavy Chain Gene FTH1 Cause a Novel Pediatric Neuroferritinopathy. View Abstract
Magnetic resonance imaging protocols in pediatric stroke. View Abstract
Malate dehydrogenase 2 deficiency is an emerging cause of pediatric epileptic encephalopathy with a recognizable biochemical signature. View Abstract
Teaching NeuroImage: Selectively Bright Inferior Cerebellum in Christianson Syndrome. View Abstract
Natural history of familial cerebral cavernous malformation syndrome in children: a multicenter cohort study. View Abstract
Refining the Neuroimaging Definition of the Dandy-Walker Phenotype. View Abstract
Imaging of Suspected Stroke in Children, From the AJR Special Series on Emergency Radiology. View Abstract
Brain Abnormalities in Patients with Germline Variants in H3F3: Novel Imaging Findings and Neurologic Symptoms Beyond Somatic Variants and Brain Tumors. View Abstract
Spinal involvement in pediatric familial cavernous malformation syndrome. View Abstract
Current understanding and future potential applications of cerebral microvascular imaging in infants. View Abstract
Correction to: Genetic and Clinical Predictors of Ataxia in Pediatric Primary Mitochondrial Disorders. View Abstract
ACTA2-Related Dysgyria: An Under-Recognized Malformation of Cortical Development. View Abstract
Comparison of Spinal Cord Magnetic Resonance Imaging Features Among Children With Acquired Demyelinating Syndromes. View Abstract
Neuroimaging of paediatric pineal, sellar and suprasellar tumours: a guide to differential diagnosis. View Abstract
Acquisition of Developmental Milestones in Hypomyelination With Atrophy of the Basal Ganglia and Cerebellum and Other TUBB4A-Related Leukoencephalopathy. View Abstract
Widening the MRI Findings of PLA2G6-Associated Neurodegeneration. View Abstract
Genetic and Clinical Predictors of Ataxia in Pediatric Primary Mitochondrial Disorders. View Abstract
Bi-allelic KARS1 pathogenic variants affecting functions of cytosolic and mitochondrial isoforms are associated with a progressive and multisystem disease. View Abstract
Imaging of brain tumors in children: the basics-a narrative review. View Abstract
Arteriopathy in pediatric stroke: an underestimated clinical entity. View Abstract
Imaging Patterns Characterizing Mitochondrial Leukodystrophies. View Abstract
A Diagnostic Algorithm for Posterior Fossa Tumors in Children: A Validation Study. View Abstract
Reply to "Pediatric Leigh Syndrome: Neuroimaging Features and Genetic Correlations". View Abstract
Involvement of the Spinal Cord in Primary Mitochondrial Disorders: A Neuroimaging Mimicker of Inflammation and Ischemia in Children. View Abstract
Primary Mitochondrial Disorders of the Pediatric Central Nervous System: Neuroimaging Findings. View Abstract
Characteristic Cochlear Hypoplasia in Patients with Walker-Warburg Syndrome: A Radiologic Study of the Inner Ear in a-Dystroglycan-Related Muscular Disorders. View Abstract
Understanding brain resilience in superagers: a systematic review. View Abstract
Intracranial calcifications in childhood: Part 1. View Abstract
Intracranial calcifications in childhood: Part 2. View Abstract
Pediatric Leigh Syndrome: Neuroimaging Features and Genetic Correlations. View Abstract
The Perirolandic Sign: A Unique Imaging Finding Observed in Association with Polymerase ?-Related Disorders. View Abstract
Updates in Pediatric Malignant Gliomas. View Abstract
Brain abnormalities in myelomeningocele patients. View Abstract
Teaching NeuroImages: Lacunar stroke and polyarteritis nodosa: Consider ADA2 deficiency (DADA2). View Abstract
Childhood Medulloblastoma Revisited. View Abstract
Expanding the Distinctive Neuroimaging Phenotype of ACTA2 Mutations. View Abstract
Neuroimaging of Mitochondrial Cytopathies. View Abstract
Cerebellar Ataxia in Children: A Clinical and MRI Approach to the Differential Diagnosis. View Abstract
Atypical subependymal giant cell astrocytoma and neonatal tuberous sclerosis. View Abstract
T2*-based MR imaging (gradient echo or susceptibility-weighted imaging) in midline and off-midline intracranial germ cell tumors: a pilot study. View Abstract
Decaying molar tooth sign in Joubert syndrome and related disorders is correlated to a displacement of the corticospinal tract. View Abstract
Added value of diffusion weighted imaging in pediatric central nervous system embryonal tumors surveillance. View Abstract
Congenital Myoepithelial Carcinoma of Soft Tissue Associated With Cystic Myoepithelioma. View Abstract
Thrombus Features in Hyperacute Ischemic Stroke: A Perspective on Using Length and Density Evaluation. View Abstract