IRIS
ROSSI, ANDREA
 Distribuzione geografica
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Continente #
EU - Europa 11.088
Totale 11.088
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Nazione #
IT - Italia 11.088
Totale 11.088
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Città #
Genova 8.028
Genoa 1.627
Rapallo 1.387
Bordighera 37
Vado Ligure 9
Totale 11.088
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Nome #
A 3-year-old boy with drug-resistant complex partial seizures 140
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 137
Congenital segmental lymphedema in tuberous sclerosis complex with associated subependymal giant cell astrocytomas treated with Mammalian target of rapamycin inhibitors. 135
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? 130
Phenotypic characterization of hypomyelination and congenital cataract 129
PITUITARY HYPOPLASIA AND GROWTH HORMONE DEFICIENCY IN COFFIN-SIRIS SYNDROME 129
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. 126
Management of diabetes insipidus and adipsia in the child. 125
Early-onset cobalamin C/D deficiency: epilepsy and electroencephalographic features. 125
White matter lesions in spastic paraplegia with mutations in SPG5/CYP7B1. 124
Structural connectivity analysis in children with segmental callosal agenesis 123
Epilepsy associated with supratentorial brain tumors under 3 years of life. 122
Licorice-associated reversible cerebral vasoconstriction with PRES. 122
POMT2 gene mutation in limb-girdle muscular dystrophy with inflammatory changes. 122
Aicardi-Goutières syndrome presenting atypically as a sub-acute leukoencephalopathy 121
Cerebellar atrophy without cerebellar cortex hyperintensity in infantile neuroaxonal dystrophy (INAD) due to PLA2G6 mutation. 120
Deficiency of hyccin, a newly identified membrane protein, causes hypomyelination and congenital cataract 120
Rhombencephalosynapsis in a patient with mental retardation, epilepsy, and dysmorphisms. 119
A novel mutation in the SURF1 gene in a child with Leigh disease, peripheral neuropathy, and cytochrome-c oxidase deficiency. 118
Erratum to: Treatment and outcome of children with cerebral cavernomas: a survey on 32 patients. 118
Posterior pituitary (PP) evaluation in patients with anterior pituitary defect associated with ectopic PP and septo-optic dysplasia. 116
Dissecting the neurological phenotype in children with callosal agenesis, interhemispheric cysts and malformations of cortical development 115
Prevalence and Prognostic Impact of Chronic Obstructive Pulmonary Disease in Patients with Chronic Heart Failure: Data from the GISSI-HF Trial 113
Widening the Heterogeneity of Leigh Syndrome: Clinical, Biochemical, and Neuroradiologic Features in a Patient Harboring a NDUFA10 Mutation 113
Anti-N-methyl-D-aspartate-receptor encephalitis in a four-year-old girl. 112
Apparently isolated borderline ventriculomegaly and lissencephaly. 110
CEREBELLAR WHITE MATTER INVOLVEMENT IN SALLA DISEASE 110
Sirenomelia. Pathological features, antenatal ultrasonographic clues, and a review of current embryogenic theories. 109
Central diabetes insipidus in children and young adults: etiological diagnosis and long-term outcome of idiopathic cases. 109
Pituitary Tumors: Advances in Neuroimaging. 108
Enhancement of Tumor Homing by Chemotherapy-Loaded Nanoparticles 108
Neuroimaging in Growth hormone deficiency 107
The use of neuroimaging for assessing disorders of pituitary development. 107
Temporal lobe epilepsy and hippocampal malrotation: is there a causal association? 107
EXOSC3 mutations in isolated cerebellar hypoplasia and spinal anterior horn involvement. 107
Hypomyelination and Congenital Cataract: Neuroimaging Features of a Novel Inherited White Matter Disorder 106
Novel FAM126A mutations in hypomyelination and congenital cataract disease. 106
MR imaging findings in 2 cases of late infantile GM1 gangliosidosis. 105
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
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
Magnetic Resonance Imaging "Tigroid Pattern" in Alexander Disease. 101
New insights into central nervous system involvement in FOP: Case report and review of the literature 101
GFAP mutations and polymorphisms in 13 unrelated Italian patients affected by Alexander disease 101
ABCC6 mutations and early onset stroke: Two cases of a typical Pseudoxanthoma Elasticum 101
Early classification of childhood focal idiopathic epilepsies: Is it possible at the first seizure? 100
Expanding the spectrum of congenital anomalies of the diencephalic–mesencephalic junction 100
Medulloblastoma variants: age-dependent occurrence and relation to Gorlin syndrome--a new clinical perspective. 97
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
Midbrain-hindbrain involvement in septo-optic dysplasia. 96
Severe epilepsy in X-linked creatine transporter defect (CRTR-D) 93
Role of MRI T2-DRIVE in the assessment of pituitary stalk abnormalities without gadolinium in pituitary diseases 93
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 93
Cobalamin (Cbl)C/D deficiency: clinical, neurophysiological and neuroradiologic finding in 14 cases 92
Novel asymptomatic CNS findings in patients with ACVR1/ALK2 mutations causing fibrodysplasia ossificans progressiva 92
Prenatal MR imaging of dural sinus malformation: a case report 91
EARLY-ONSET COMBINED METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA: NEURORADIOLOGICAL FINDINGS 89
Novel dynein DYNC1H1 neck and motor domain mutations link distal spinal muscular atrophy and abnormal cortical development. 88
Beyond spinal muscular atrophy with lower extremity dominance: Cerebellar hypoplasia associated with a novel mutation in BICD2 88
Acute superior vena cava syndrome after insertion of implantable cardioverter defibrillator 88
THE DIAGNOSIS OF CHILDREN WITH CENTRAL DIABETES INSIPIDUS. 84
Tonsillar herniation spectrum: more than just Chiari I. Update and controversies on classification and management 84
Diabetes insipidus--diagnosis and management. 84
T2*-based MR imaging (gradient echo or susceptibility-weighted imaging) in midline and off-midline intracranial germ cell tumors: a pilot study 83
Pediatric Brain Tissue Segmentation from MRI using Clustering: A Preliminary Study 80
Middle interhemispheric variant of holoprosencepaly: a very mild clinical case 77
Brown-Vialetto-Van Laere syndrome: Cinical and neuroradiological findings of a genetically proven patient. 75
An Italian severe Salla disease variant associated with a SLC17A5 mutation 75
Unusual white matter involvement in EAST syndrome associated with novel KCNJ10 mutations 75
Hybrid imaging in pediatric central nervous system disorders 72
Accuracy of ultrasound in assessing cerebellar haemorrhages in very low birthweight babies 72
NO MAJOR ROLE FOR THE EMX2 GENE IN SCHIZENCEPHALY. 71
Pediatric optic neuritis and anti MOG antibodies: a cohort of Italian patients 69
Incidental findings on routine brain MRI scans in preterm infants 69
Early Pain Exposure Influences Functional Brain Connectivity in Very Preterm Neonates 68
Epileptic encephalopathy and type 1 diabetes mellitus 64
Leucoencefalopatie su base genetica in età pediatrica 63
Cognitive Profiles and Brain Volume Are Affected in Patients with Silver-Russell Syndrome 63
Crossed pontine hemiatrophy associated with unilateral cerebellar hemorrhage in premature infants 63
Low-grade intraventricular hemorrhage: Is ultrasound good enough? 63
Different gestational ages and changing vulnerability of the premature brain 62
Management: opinions from different centers—the Istituto Giannina Gaslini experience 61
Hypomyelination and congenital cataract: broadening the clinical phenotype. 60
Targeted re-sequencing in pediatric and perinatal stroke 60
Developmental abnormalities of the posterior pituitary gland. 60
Differences in subependymal vein anatomy may predispose preterm infants to GMH–IVH 59
Clinical and neuroradiological features in two patients with Leigh syndrome and cytochrome c oxidase deficiency 58
White matter and cerebellar involvement in alternating hemiplegia of childhood 57
The effects of mild germinal matrix-intraventricular haemorrhage on the developmental white matter microstructure of preterm neonates: a DTI study 54
Presence of delayed myelination and macrocephaly in the sister of a patient with vacuolating leukoencephalopathy with subcortical cystis. 53
POMGnT1 mutations in congenital muscular dystrophy: genotype-phenotype correlation and expanded clinical spectrum 53
Leucodistrofia con macrocefalia e decorso clinico sorprendentemente lieve. 50
Feasibility of constrained spherical deconvolution in diffusion imaging of children 50
Arterial spin labeling perfusion in neonates 48
Placental Pathology Findings and the Risk of Intraventricular and Cerebellar Hemorrhage in Preterm Neonates 48
Totale 9.510
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Categoria #
all - tutte 40.297
article - articoli 38.130
book - libri 0
conference - conferenze 1.107
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.060
Totale 80.594
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20202.677 118 69 99 168 232 274 460 204 259 438 268 88
2020/20211.332 61 61 86 215 147 76 43 142 83 174 130 114
2021/20221.499 70 33 140 131 58 100 77 381 69 178 55 207
2022/20231.718 145 133 24 148 239 294 5 139 291 8 254 38
2023/20241.320 63 160 35 171 98 213 76 74 86 55 73 216
2024/2025115 115 0 0 0 0 0 0 0 0 0 0 0
Totale 11.369