Andrea Rossi researcher (ORCID 0000-0001-8575-700X)
Rossi, Andrea, médecin
Rossi, Andrea, MD
Rossi, Andrea 19..-.... neuroradiologue
Rossi, Andrea, 1967 January 8-
VIAF ID: 66745183 (Personal)
Permalink: http://viaf.org/viaf/66745183
Preferred Forms
- 100 0 _ ‡a Andrea Rossi ‡c researcher (ORCID 0000-0001-8575-700X)
- 200 _ | ‡a Rossi ‡b Andrea ‡f 19..-.... ‡c neuroradiologue
- 100 1 _ ‡a Rossi, Andrea ‡c médecin
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- 100 1 _ ‡a Rossi, Andrea, ‡c médecin
- 100 1 _ ‡a Rossi, Andrea, ‡d 1967 January 8-
Works
Title | Sources |
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Brain imaging with MRI and CT, 2014 : | |
Imaging of acute disseminated encephalomyelitis. | |
Immunomodulatory therapy in recurrent acute necrotizing encephalopathy ANE1: is it useful? | |
Improvement in White Matter Tract Reconstruction with Constrained Spherical Deconvolution and Track Density Mapping in Low Angular Resolution Data: A Pediatric Study and Literature Review | |
Incidental findings on routine brain MRI scans in preterm infants | |
Inferior olivary nucleus involvement in pediatric neurodegenerative disorders: does it play a role in neuroimaging pattern-recognition approach? | |
Intermittent-relapsing pyruvate dehydrogenase complex deficiency: a case with clinical, biochemical, and neuroradiological reversibility. | |
Internal jugular vein phlebectasia and duplication: case report with magnetic resonance angiography features | |
Intracerebral schwannoma in a child. | |
Intracranial contrast-enhancing masses in infants with capillary haemangioma of the head and neck: intracranial capillary haemangioma? | |
An Italian severe Salla disease variant associated with a SLC17A5 mutation earlier described in infantile sialic acid storage disease | |
Langerhans cell histiocytosis presenting as a lumbosacral intradural-extramedullary mass | |
Laryngeal schwannoma in an 8-year-old boy with inspiratory dyspnea. | |
Late Persistent Increased Putaminal 18F-DOPA Uptake Following Ipsilateral Frontal Resection: Evidence for Corticostriatal Synaptic Plasticity? | |
Low-grade intraventricular hemorrhage: is ultrasound good enough? | |
Magnetic resonance imaging in childhood leukemia survivors treated with cranial radiotherapy: A cross sectional, single center study | |
Magnetic resonance imaging spectrum of medulloblastoma. | |
Magnetic resonance imaging "tigroid pattern" in Alexander disease. | |
Management of diabetes insipidus and adipsia in the child | |
Medulloblastoma in children: CT and MRI findings. | |
Medulloblastoma variants: age-dependent occurrence and relation to Gorlin syndrome--a new clinical perspective | |
Microcephaly, sensorineural deafness and Currarino triad with duplication-deletion of distal 7q. | |
Midbrain-hindbrain involvement in septo-optic dysplasia. | |
Middle interhemispheric variant of holoprosencephaly: a very mild clinical case | |
Molecular genetic analysis of the PLP1 gene in 38 families with PLP1-related disorders: identification and functional characterization of 11 novel PLP1 mutations | |
Moyamoya Vasculopathy in PHACE Syndrome: Six New Cases and Review of the Literature. | |
MR Imaging Diagnosis of Diencephalic-Mesencephalic Junction Dysplasia in Fetuses with Developmental Ventriculomegaly | |
MR imaging of neonatal brain infections | |
MRI in an unusual case of congenital spinal mesenchymal proliferation | |
Multimodal magnetic resonance imaging and 18F-L-dihydroxyphenylalanine positron emission tomography in early characterization of pseudoresponse and nonenhancing tumor progression in a pediatric patient with malignant transformation of ganglioglioma | |
Multimodality imaging of Hodgkin disease and non-Hodgkin lymphomas in children. | |
Muscle and the cerebellum | |
NANS-mediated synthesis of sialic acid is required for brain and skeletal development | |
Natural history of cavernous malformations in children with brain tumors treated with radiotherapy and chemotherapy | |
Natural history of familial cerebral cavernous malformation syndrome in children: a multicenter cohort study | |
Neonatal Developmental Venous Anomalies: Clinicoradiologic Characterization and Follow-Up | |
New insights into central nervous system involvement in FOP: Case report and review of the literature. | |
New MR sequences (diffusion, perfusion, spectroscopy) in brain tumours | |
No major role for theEMX2gene in schizencephaly | |
Noninvasive Assessment of Hemodynamic Stress Distribution after Indirect Revascularization for Pediatric Moyamoya Vasculopathy | |
Novel asymptomatic CNS findings in patients with ACVR1/ALK2 mutations causing fibrodysplasia ossificans progressiva. | |
Novel dynein DYNC1H1 neck and motor domain mutations link distal spinal muscular atrophy and abnormal cortical development | |
A novel mutation in the SURF1 gene in a child with Leigh disease, peripheral neuropathy, and cytochrome-c oxidase deficiency. | |
Opposing Effects of CREBBP Mutations Govern the Phenotype of Rubinstein-Taybi Syndrome and Adult SHH Medulloblastoma. | |
Orbital and Periorbital Extension of Congenital Dacryocystoceles: Suggested Mechanism and Management. | |
The pathogenesis of hydrocephalus in inborn errors of the single carbon transfer pathway. | |
Pediatric Inflammatory Diseases. Part IV: Miscellaneous, Reye, PRES, Sarcoidosis. | |
Pediatric neuroradiology | |
Pediatric Orbital Osteoradionecrosis | |
Pediatric spinal infection and inflammation. | |
Perinatal Arterial Ischemic Stroke in Fetal Vascular Malperfusion: A Case Series and Literature Review | |
Pharyngeal enterogenous cyst associated with canalis basilaris medianus in a newborn | |
Pituitary deficiency and congenital infiltrating lipomatosis of the face in a girl with deletion of chromosome 1q24.3q31.1. | |
Pituitary hypoplasia and growth hormone deficiency in Coffin-Siris syndrome | |
POMGnT1 mutations in congenital muscular dystrophy: genotype-phenotype correlation and expanded clinical spectrum. | |
POMT2 gene mutation in limb-girdle muscular dystrophy with inflammatory changes. | |
Pontine Tegmental Cap Dysplasia: developmental and cognitive outcome in three adolescent patients | |
Pontocerebellar hypoplasia: clinical, pathologic, and genetic studies | |
Post-chemotherapy maturation of a pineoblastoma. | |
Posterior fossa and arterial abnormalities in patients with facial capillary haemangioma: presumed incomplete phenotypic expression of PHACES syndrome | |
Posterior pituitary (PP) evaluation in patients with anterior pituitary defect associated with ectopic PP and septo-optic dysplasia. | |
Prematurity and brain perfusion: Arterial spin labeling MRI. | |
Prenatal diagnosis of a nasal glioma in the mid trimester. | |
Prenatal MR imaging features of isolated cerebellar haemorrhagic lesions | |
Prenatal MR imaging of dural sinus malformation: a case report | |
Presence of delayed myelination and macrocephaly in the sister of a patient with vacuolating leukoencephalopathy with subcortical cysts | |
Primary diffuse leptomeningeal gliomatosis in children: a clinical pathologic correlation. | |
Primary Hydatid Cyst of the Brain in a Child: A Case Report | |
Reversible cerebral vasoconstriction mimicking posterior reversible encephalopathy syndrome in an infant with end-stage renal disease. | |
Rhabdoid meningioma of the tentorium with expression of desmin in a 12-year-old Turner syndrome patient | |
Rhombencephalosynapsis in a patient with mental retardation, epilepsy, and dysmorphisms. | |
The shrunken, bright cerebellum: a characteristic MRI finding in congenital disorders of glycosylation type 1a. | |
Sinus pericranii: diagnosis and management in 21 pediatric patients | |
Sirenomelia. Pathological features, antenatal ultrasonographic clues, and a review of current embryogenic theories. | |
Skull base osteomyelitis and potential cerebrovascular complications in children. | |
Spatial coefficient of variation applied to arterial spin labeling MRI may contribute to predict surgical revascularization outcomes in pediatric moyamoya vasculopathy | |
Spectrum of nonterminal myelocystoceles. | |
Spinal dysraphism: MR imaging rationale. | |
Spinal lipoma as a dysembryogenetic anomaly: Four unusual cases of ectopic iliac rib within the spinal lipoma. | |
Spontaneously regressing leukoencephalopathy with bilateral temporal cysts in congenital rubella infection. | |
Structural Connectivity Analysis in Children with Segmental Callosal Agenesis | |
T2*-based MR imaging (gradient echo or susceptibility-weighted imaging) in midline and off-midline intracranial germ cell tumors: a pilot study. | |
Teaching NeuroImages: Figure of 8: The clue to the diagnosis of AMPD2 pontocerebellar hypoplasia (PCH9) | |
Temporal lobe epilepsy and hippocampal malrotation: is there a causal association? | |
Torcular pseudomass: a potential diagnostic pitfall in infants and young children. | |
TUBB4A-related hypomyelinating leukodystrophy: New insights from a series of 12 patients. | |
Tubulin-related cerebellar dysplasia: definition of a distinct pattern of cerebellar malformation. | |
Tumors of the spine in children. | |
Unusual white matter involvement in EAST syndrome associated with novel KCNJ10 mutations. | |
The use of neuroimaging for assessing disorders of pituitary development. | |
Value of 18F-3,4-dihydroxyphenylalanine PET/MR image fusion in pediatric supratentorial infiltrative astrocytomas: a prospective pilot study. | |
Variability of Cerebral Deep Venous System in Preterm and Term Neonates Evaluated on MR SWI Venography. | |
Vein of Galen aneurysmal malformation (VGAM) in the fetus: retrospective analysis of perinatal prognostic indicators in a two-center series of 49 cases. | |
White matter and cerebellar involvement in alternating hemiplegia of childhood | |
White matter lesions in spastic paraplegia with mutations in SPG5/CYP7B1. |