IRIS
ROSSI, ANDREA
 Distribuzione geografica
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Continente #
EU - Europa 12.626
Totale 12.626
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Nazione #
IT - Italia 12.626
Totale 12.626
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Città #
Genova 8.028
Genoa 1.655
Vado Ligure 1.519
Rapallo 1.387
Bordighera 37
Totale 12.626
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Nome #
A 3-year-old boy with drug-resistant complex partial seizures 156
Quantitative susceptibility map analysis in preterm neonates with germinal matrix-intraventricular hemorrhage 145
Treatment and outcome of children with cerebral cavernomas: a survey on 32 patients. 144
Clinical and electrophysiological features of epilepsy in Italian patients with CLN8 mutations. 143
Congenital segmental lymphedema in tuberous sclerosis complex with associated subependymal giant cell astrocytomas treated with Mammalian target of rapamycin inhibitors. 143
Brainstem anomalies in two patients affected by congenital central hypoventilation syndrome 140
Inferior olivary nucleus involvement in pediatric neurodegenerative disorders: does it play a role in neuroimaging pattern-recognition approach? 137
Genetic abnormalities and CNS tumors: Report of two cases of ependymoma associated with Klinefelter's Syndrome (KS). 135
PITUITARY HYPOPLASIA AND GROWTH HORMONE DEFICIENCY IN COFFIN-SIRIS SYNDROME 134
Management of diabetes insipidus and adipsia in the child. 134
Phenotypic characterization of hypomyelination and congenital cataract 133
Early-onset cobalamin C/D deficiency: epilepsy and electroencephalographic features. 133
White matter lesions in spastic paraplegia with mutations in SPG5/CYP7B1. 132
Hypomyelination and congenital cataract: Identification of novel mutations in two unrelated families. 132
A novel mutation in the SURF1 gene in a child with Leigh disease, peripheral neuropathy, and cytochrome-c oxidase deficiency. 132
Structural connectivity analysis in children with segmental callosal agenesis 131
Epilepsy associated with supratentorial brain tumors under 3 years of life. 129
Aicardi-Goutières syndrome presenting atypically as a sub-acute leukoencephalopathy 128
Licorice-associated reversible cerebral vasoconstriction with PRES. 128
Cerebellar atrophy without cerebellar cortex hyperintensity in infantile neuroaxonal dystrophy (INAD) due to PLA2G6 mutation. 127
Rhombencephalosynapsis in a patient with mental retardation, epilepsy, and dysmorphisms. 127
POMT2 gene mutation in limb-girdle muscular dystrophy with inflammatory changes. 127
Deficiency of hyccin, a newly identified membrane protein, causes hypomyelination and congenital cataract 125
Dissecting the neurological phenotype in children with callosal agenesis, interhemispheric cysts and malformations of cortical development 125
Posterior pituitary (PP) evaluation in patients with anterior pituitary defect associated with ectopic PP and septo-optic dysplasia. 123
Erratum to: Treatment and outcome of children with cerebral cavernomas: a survey on 32 patients. 123
EXOSC3 mutations in isolated cerebellar hypoplasia and spinal anterior horn involvement. 121
Prevalence and Prognostic Impact of Chronic Obstructive Pulmonary Disease in Patients with Chronic Heart Failure: Data from the GISSI-HF Trial 120
Widening the Heterogeneity of Leigh Syndrome: Clinical, Biochemical, and Neuroradiologic Features in a Patient Harboring a NDUFA10 Mutation 120
Anti-N-methyl-D-aspartate-receptor encephalitis in a four-year-old girl. 119
CEREBELLAR WHITE MATTER INVOLVEMENT IN SALLA DISEASE 118
Apparently isolated borderline ventriculomegaly and lissencephaly. 116
Central diabetes insipidus in children and young adults: etiological diagnosis and long-term outcome of idiopathic cases. 116
Neuroimaging in Growth hormone deficiency 114
Sirenomelia. Pathological features, antenatal ultrasonographic clues, and a review of current embryogenic theories. 114
The use of neuroimaging for assessing disorders of pituitary development. 113
Pituitary Tumors: Advances in Neuroimaging. 113
Enhancement of Tumor Homing by Chemotherapy-Loaded Nanoparticles 113
Novel FAM126A mutations in hypomyelination and congenital cataract disease. 112
MR imaging findings in 2 cases of late infantile GM1 gangliosidosis. 111
Epilepsia partialis continua in type 1 diabetes: evolution into epileptic encephalopathy with continuous spike-waves during slow sleep 111
Hypomyelination and Congenital Cataract: Neuroimaging Features of a Novel Inherited White Matter Disorder 111
Temporal lobe epilepsy and hippocampal malrotation: is there a causal association? 111
ABCC6 mutations and early onset stroke: Two cases of a typical Pseudoxanthoma Elasticum 111
Chronic inflammatory demyelinating polyneuropathy of childhood: clinical and neuroradiological findings. 111
Prenatal diagnosis of a nasal glioma in the mid trimester 110
Focal leptomeningeal enhancement and corticopial calcifications underlying a parietal convexity lipoma: a rare association of findings in 2 pediatric epileptic patients. 109
New insights into central nervous system involvement in FOP: Case report and review of the literature 109
Medulloblastoma variants: age-dependent occurrence and relation to Gorlin syndrome--a new clinical perspective. 108
Magnetic Resonance Imaging "Tigroid Pattern" in Alexander Disease. 108
Early classification of childhood focal idiopathic epilepsies: Is it possible at the first seizure? 107
GFAP mutations and polymorphisms in 13 unrelated Italian patients affected by Alexander disease 106
Expanding the spectrum of congenital anomalies of the diencephalic–mesencephalic junction 106
Cobalamin (Cbl)C/D deficiency: clinical, neurophysiological and neuroradiologic finding in 14 cases 105
Role of MRI T2-DRIVE in the assessment of pituitary stalk abnormalities without gadolinium in pituitary diseases 105
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 104
Midbrain-hindbrain involvement in septo-optic dysplasia. 100
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 100
Severe epilepsy in X-linked creatine transporter defect (CRTR-D) 99
Novel asymptomatic CNS findings in patients with ACVR1/ALK2 mutations causing fibrodysplasia ossificans progressiva 99
EARLY-ONSET COMBINED METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA: NEURORADIOLOGICAL FINDINGS 97
Beyond spinal muscular atrophy with lower extremity dominance: Cerebellar hypoplasia associated with a novel mutation in BICD2 96
Prenatal MR imaging of dural sinus malformation: a case report 95
Acute superior vena cava syndrome after insertion of implantable cardioverter defibrillator 95
Novel dynein DYNC1H1 neck and motor domain mutations link distal spinal muscular atrophy and abnormal cortical development. 93
T2*-based MR imaging (gradient echo or susceptibility-weighted imaging) in midline and off-midline intracranial germ cell tumors: a pilot study 93
Diabetes insipidus--diagnosis and management. 92
THE DIAGNOSIS OF CHILDREN WITH CENTRAL DIABETES INSIPIDUS. 88
Tonsillar herniation spectrum: more than just Chiari I. Update and controversies on classification and management 88
Pediatric Brain Tissue Segmentation from MRI using Clustering: A Preliminary Study 88
An Italian severe Salla disease variant associated with a SLC17A5 mutation 84
Accuracy of ultrasound in assessing cerebellar haemorrhages in very low birthweight babies 84
Brown-Vialetto-Van Laere syndrome: Cinical and neuroradiological findings of a genetically proven patient. 82
Middle interhemispheric variant of holoprosencepaly: a very mild clinical case 80
Unusual white matter involvement in EAST syndrome associated with novel KCNJ10 mutations 80
NO MAJOR ROLE FOR THE EMX2 GENE IN SCHIZENCEPHALY. 78
Pediatric optic neuritis and anti MOG antibodies: a cohort of Italian patients 78
Incidental findings on routine brain MRI scans in preterm infants 78
Hybrid imaging in pediatric central nervous system disorders 77
Early Pain Exposure Influences Functional Brain Connectivity in Very Preterm Neonates 77
Low-grade intraventricular hemorrhage: Is ultrasound good enough? 73
Leucoencefalopatie su base genetica in età pediatrica 72
Cognitive Profiles and Brain Volume Are Affected in Patients with Silver-Russell Syndrome 72
Crossed pontine hemiatrophy associated with unilateral cerebellar hemorrhage in premature infants 72
Different gestational ages and changing vulnerability of the premature brain 72
Differences in subependymal vein anatomy may predispose preterm infants to GMH–IVH 71
Epileptic encephalopathy and type 1 diabetes mellitus 70
Targeted re-sequencing in pediatric and perinatal stroke 69
Developmental abnormalities of the posterior pituitary gland. 68
Hypomyelination and congenital cataract: broadening the clinical phenotype. 65
Management: opinions from different centers—the Istituto Giannina Gaslini experience 65
The effects of mild germinal matrix-intraventricular haemorrhage on the developmental white matter microstructure of preterm neonates: a DTI study 65
White matter and cerebellar involvement in alternating hemiplegia of childhood 64
Clinical and neuroradiological features in two patients with Leigh syndrome and cytochrome c oxidase deficiency 63
Presence of delayed myelination and macrocephaly in the sister of a patient with vacuolating leukoencephalopathy with subcortical cystis. 58
Placental Pathology Findings and the Risk of Intraventricular and Cerebellar Hemorrhage in Preterm Neonates 58
[Acute urinary retention in a child with acute disseminatedencephalomyelitis] 57
POMGnT1 mutations in congenital muscular dystrophy: genotype-phenotype correlation and expanded clinical spectrum 57
Arterial spin labeling perfusion in neonates 57
Focal status and acute encephalopathy in a 13-year-old boy with de novo DNM1L mutation: Video-polygraphic pattern and clues for differential diagnosis 57
Totale 10.244
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Categoria #
all - tutte 49.673
article - articoli 46.952
book - libri 0
conference - conferenze 1.474
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.247
Totale 99.346
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.991 0 0 0 0 0 274 460 204 259 438 268 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
2024/20251.667 188 273 75 292 462 377 0 0 0 0 0 0
Totale 12.921