IRIS
ROSSI, ANDREA
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
EU - Europa 10.592
Totale 10.592
Salva come PNG Salva come JPEG
Nazione #
IT - Italia 10.592
Totale 10.592
Salva come PNG Salva come JPEG
Città #
Genova 7.924
Rapallo 1.387
Genoa 1.244
Bordighera 37
Totale 10.592
Salva come PNG Salva come JPEG
Nome #
Treatment and outcome of children with cerebral cavernomas: a survey on 32 patients. 139
Clinical and electrophysiological features of epilepsy in Italian patients with CLN8 mutations. 137
Quantitative susceptibility map analysis in preterm neonates with germinal matrix-intraventricular hemorrhage 136
A 3-year-old boy with drug-resistant complex partial seizures 135
Congenital segmental lymphedema in tuberous sclerosis complex with associated subependymal giant cell astrocytomas treated with Mammalian target of rapamycin inhibitors. 133
Brainstem anomalies in two patients affected by congenital central hypoventilation syndrome 132
Inferior olivary nucleus involvement in pediatric neurodegenerative disorders: does it play a role in neuroimaging pattern-recognition approach? 129
Phenotypic characterization of hypomyelination and congenital cataract 128
PITUITARY HYPOPLASIA AND GROWTH HORMONE DEFICIENCY IN COFFIN-SIRIS SYNDROME 128
Genetic abnormalities and CNS tumors: Report of two cases of ependymoma associated with Klinefelter's Syndrome (KS). 127
Hypomyelination and congenital cataract: Identification of novel mutations in two unrelated families. 125
Management of diabetes insipidus and adipsia in the child. 124
White matter lesions in spastic paraplegia with mutations in SPG5/CYP7B1. 123
Early-onset cobalamin C/D deficiency: epilepsy and electroencephalographic features. 123
Licorice-associated reversible cerebral vasoconstriction with PRES. 122
Structural connectivity analysis in children with segmental callosal agenesis 122
POMT2 gene mutation in limb-girdle muscular dystrophy with inflammatory changes. 122
Epilepsy associated with supratentorial brain tumors under 3 years of life. 119
Cerebellar atrophy without cerebellar cortex hyperintensity in infantile neuroaxonal dystrophy (INAD) due to PLA2G6 mutation. 119
Rhombencephalosynapsis in a patient with mental retardation, epilepsy, and dysmorphisms. 119
Deficiency of hyccin, a newly identified membrane protein, causes hypomyelination and congenital cataract 119
Aicardi-Goutières syndrome presenting atypically as a sub-acute leukoencephalopathy 116
Dissecting the neurological phenotype in children with callosal agenesis, interhemispheric cysts and malformations of cortical development 115
Posterior pituitary (PP) evaluation in patients with anterior pituitary defect associated with ectopic PP and septo-optic dysplasia. 114
A novel mutation in the SURF1 gene in a child with Leigh disease, peripheral neuropathy, and cytochrome-c oxidase deficiency. 114
Erratum to: Treatment and outcome of children with cerebral cavernomas: a survey on 32 patients. 114
Prevalence and Prognostic Impact of Chronic Obstructive Pulmonary Disease in Patients with Chronic Heart Failure: Data from the GISSI-HF Trial 113
Anti-N-methyl-D-aspartate-receptor encephalitis in a four-year-old girl. 110
CEREBELLAR WHITE MATTER INVOLVEMENT IN SALLA DISEASE 110
Sirenomelia. Pathological features, antenatal ultrasonographic clues, and a review of current embryogenic theories. 109
Widening the Heterogeneity of Leigh Syndrome: Clinical, Biochemical, and Neuroradiologic Features in a Patient Harboring a NDUFA10 Mutation 109
Temporal lobe epilepsy and hippocampal malrotation: is there a causal association? 107
Apparently isolated borderline ventriculomegaly and lissencephaly. 106
The use of neuroimaging for assessing disorders of pituitary development. 106
Hypomyelination and Congenital Cataract: Neuroimaging Features of a Novel Inherited White Matter Disorder 106
EXOSC3 mutations in isolated cerebellar hypoplasia and spinal anterior horn involvement. 106
Enhancement of Tumor Homing by Chemotherapy-Loaded Nanoparticles 106
Central diabetes insipidus in children and young adults: etiological diagnosis and long-term outcome of idiopathic cases. 106
Epilepsia partialis continua in type 1 diabetes: evolution into epileptic encephalopathy with continuous spike-waves during slow sleep 105
Chronic inflammatory demyelinating polyneuropathy of childhood: clinical and neuroradiological findings. 105
MR imaging findings in 2 cases of late infantile GM1 gangliosidosis. 104
Novel FAM126A mutations in hypomyelination and congenital cataract disease. 104
Neuroimaging in Growth hormone deficiency 103
Prenatal diagnosis of a nasal glioma in the mid trimester 102
Focal leptomeningeal enhancement and corticopial calcifications underlying a parietal convexity lipoma: a rare association of findings in 2 pediatric epileptic patients. 102
GFAP mutations and polymorphisms in 13 unrelated Italian patients affected by Alexander disease 101
New insights into central nervous system involvement in FOP: Case report and review of the literature 100
Expanding the spectrum of congenital anomalies of the diencephalic–mesencephalic junction 100
Early classification of childhood focal idiopathic epilepsies: Is it possible at the first seizure? 99
Magnetic Resonance Imaging "Tigroid Pattern" in Alexander Disease. 99
ABCC6 mutations and early onset stroke: Two cases of a typical Pseudoxanthoma Elasticum 99
Deterioration of growth hormone (GH) response and anterior pituitary function in young adults with childhood-onset GH deficiency and ectopic posterior pituitary: a two-year prospective follow-up study 97
Medulloblastoma variants: age-dependent occurrence and relation to Gorlin syndrome--a new clinical perspective. 96
Midbrain-hindbrain involvement in septo-optic dysplasia. 95
Severe epilepsy in X-linked creatine transporter defect (CRTR-D) 92
Novel asymptomatic CNS findings in patients with ACVR1/ALK2 mutations causing fibrodysplasia ossificans progressiva 92
Improvement of white matter tract reconstruction with constrained spherical deconvolution and track-density mapping in low angular resolution data: a pediatric study and literature review 92
Role of MRI T2-DRIVE in the assessment of pituitary stalk abnormalities without gadolinium in pituitary diseases 91
Cobalamin (Cbl)C/D deficiency: clinical, neurophysiological and neuroradiologic finding in 14 cases 90
Prenatal MR imaging of dural sinus malformation: a case report 90
EARLY-ONSET COMBINED METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA: NEURORADIOLOGICAL FINDINGS 86
Novel dynein DYNC1H1 neck and motor domain mutations link distal spinal muscular atrophy and abnormal cortical development. 86
Beyond spinal muscular atrophy with lower extremity dominance: Cerebellar hypoplasia associated with a novel mutation in BICD2 86
Acute superior vena cava syndrome after insertion of implantable cardioverter defibrillator 85
Diabetes insipidus--diagnosis and management. 84
THE DIAGNOSIS OF CHILDREN WITH CENTRAL DIABETES INSIPIDUS. 83
Tonsillar herniation spectrum: more than just Chiari I. Update and controversies on classification and management 82
T2*-based MR imaging (gradient echo or susceptibility-weighted imaging) in midline and off-midline intracranial germ cell tumors: a pilot study 79
Pediatric Brain Tissue Segmentation from MRI using Clustering: A Preliminary Study 78
Middle interhemispheric variant of holoprosencepaly: a very mild clinical case 75
Unusual white matter involvement in EAST syndrome associated with novel KCNJ10 mutations 74
Brown-Vialetto-Van Laere syndrome: Cinical and neuroradiological findings of a genetically proven patient. 73
An Italian severe Salla disease variant associated with a SLC17A5 mutation 72
NO MAJOR ROLE FOR THE EMX2 GENE IN SCHIZENCEPHALY. 70
Hybrid imaging in pediatric central nervous system disorders 69
Pediatric optic neuritis and anti MOG antibodies: a cohort of Italian patients 68
Accuracy of ultrasound in assessing cerebellar haemorrhages in very low birthweight babies 68
Incidental findings on routine brain MRI scans in preterm infants 65
Epileptic encephalopathy and type 1 diabetes mellitus 64
Early Pain Exposure Influences Functional Brain Connectivity in Very Preterm Neonates 63
Leucoencefalopatie su base genetica in età pediatrica 62
Low-grade intraventricular hemorrhage: Is ultrasound good enough? 62
Management: opinions from different centers—the Istituto Giannina Gaslini experience 60
Cognitive Profiles and Brain Volume Are Affected in Patients with Silver-Russell Syndrome 60
Crossed pontine hemiatrophy associated with unilateral cerebellar hemorrhage in premature infants 60
Different gestational ages and changing vulnerability of the premature brain 60
Hypomyelination and congenital cataract: broadening the clinical phenotype. 59
Developmental abnormalities of the posterior pituitary gland. 59
Clinical and neuroradiological features in two patients with Leigh syndrome and cytochrome c oxidase deficiency 58
Targeted re-sequencing in pediatric and perinatal stroke 57
Differences in subependymal vein anatomy may predispose preterm infants to GMH–IVH 57
White matter and cerebellar involvement in alternating hemiplegia of childhood 56
The effects of mild germinal matrix-intraventricular haemorrhage on the developmental white matter microstructure of preterm neonates: a DTI study 53
Presence of delayed myelination and macrocephaly in the sister of a patient with vacuolating leukoencephalopathy with subcortical cystis. 52
POMGnT1 mutations in congenital muscular dystrophy: genotype-phenotype correlation and expanded clinical spectrum 52
Leucodistrofia con macrocefalia e decorso clinico sorprendentemente lieve. 49
Feasibility of constrained spherical deconvolution in diffusion imaging of children 49
Placental Pathology Findings and the Risk of Intraventricular and Cerebellar Hemorrhage in Preterm Neonates 47
Prenatal MR imaging features of isolated cerebellar haemorrhagic lesions 46
Punctate white matter lesions of preterm infants: Risk factor analysis 45
Totale 9.299
Salva come PNG Salva come JPEG
Categoria #
all - tutte 36.689
article - articoli 34.923
book - libri 0
conference - conferenze 997
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 769
Totale 73.378
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019468 0 0 0 0 0 0 0 0 0 0 251 217
2019/20202.650 118 69 98 166 230 271 456 200 256 433 265 88
2020/20211.327 60 60 86 215 146 76 43 141 83 173 130 114
2021/20221.484 70 32 139 130 58 100 75 374 69 176 55 206
2022/20231.717 144 133 24 148 239 294 5 139 291 8 254 38
2023/20241.035 63 160 35 171 98 213 76 74 86 55 4 0
Totale 10.864