IRIS
ROSSI, ANDREA
 Distribuzione geografica
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Continente #
EU - Europa 17.546
AS - Asia 2.804
NA - Nord America 2.288
Continente sconosciuto - Info sul continente non disponibili 350
SA - Sud America 254
AF - Africa 61
OC - Oceania 4
Totale 23.307
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Nazione #
IT - Italia 17.151
US - Stati Uniti d'America 2.119
SG - Singapore 1.042
CN - Cina 747
VN - Vietnam 521
BD - Bangladesh 221
FR - Francia 173
BR - Brasile 149
HK - Hong Kong 93
CA - Canada 65
DE - Germania 53
AR - Argentina 45
MX - Messico 35
GB - Regno Unito 33
FI - Finlandia 32
TR - Turchia 26
EC - Ecuador 21
IN - India 19
JM - Giamaica 19
JP - Giappone 19
ZA - Sudafrica 19
ID - Indonesia 17
PK - Pakistan 17
IQ - Iraq 14
NL - Olanda 14
CO - Colombia 12
CH - Svizzera 10
CR - Costa Rica 10
CL - Cile 9
RU - Federazione Russa 9
TH - Thailandia 9
VE - Venezuela 9
ES - Italia 8
GT - Guatemala 8
MA - Marocco 8
PH - Filippine 8
SA - Arabia Saudita 8
IE - Irlanda 7
TT - Trinidad e Tobago 7
UA - Ucraina 7
EG - Egitto 6
HN - Honduras 6
JO - Giordania 6
UZ - Uzbekistan 6
KR - Corea 5
AL - Albania 4
AU - Australia 4
BG - Bulgaria 4
DK - Danimarca 4
DZ - Algeria 4
GR - Grecia 4
KE - Kenya 4
KZ - Kazakistan 4
RO - Romania 4
RS - Serbia 4
SC - Seychelles 4
TN - Tunisia 4
BB - Barbados 3
BS - Bahamas 3
DO - Repubblica Dominicana 3
HR - Croazia 3
KH - Cambogia 3
MY - Malesia 3
NI - Nicaragua 3
PE - Perù 3
PL - Polonia 3
TW - Taiwan 3
UY - Uruguay 3
AT - Austria 2
AZ - Azerbaigian 2
BA - Bosnia-Erzegovina 2
CY - Cipro 2
ET - Etiopia 2
LC - Santa Lucia 2
MT - Malta 2
NP - Nepal 2
PT - Portogallo 2
PY - Paraguay 2
SE - Svezia 2
SK - Slovacchia (Repubblica Slovacca) 2
AE - Emirati Arabi Uniti 1
AG - Antigua e Barbuda 1
AM - Armenia 1
BE - Belgio 1
BH - Bahrain 1
BO - Bolivia 1
BY - Bielorussia 1
BZ - Belize 1
CI - Costa d'Avorio 1
CV - Capo Verde 1
GA - Gabon 1
GD - Grenada 1
GH - Ghana 1
GP - Guadalupe 1
HU - Ungheria 1
IL - Israele 1
LT - Lituania 1
LY - Libia 1
MD - Moldavia 1
MK - Macedonia 1
Totale 22.947
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Città #
Genova 8.028
Genoa 5.899
Vado Ligure 1.512
Rapallo 1.387
San Jose 539
Singapore 515
Ashburn 286
Ho Chi Minh City 180
Beijing 160
Lauterbourg 158
Hanoi 126
Hong Kong 85
New York 85
Los Angeles 71
Santa Clara 46
Milan 42
Bordighera 37
Frankfurt am Main 34
Chicago 30
Da Nang 30
Buffalo 28
Council Bluffs 27
Orem 26
Dallas 22
Mexico City 21
Rome 20
Boardman 19
Helsinki 18
Atlanta 17
Tianjin 17
Brooklyn 16
Montreal 16
Haiphong 15
Phoenix 15
Guangzhou 14
Tokyo 14
Izmir 13
Johannesburg 13
São Paulo 13
Turin 13
Lappeenranta 12
Biên Hòa 11
Can Tho 11
Kingston 11
Las Vegas 10
Naples 10
Philadelphia 10
Washington 10
Houston 9
Memphis 9
San José 9
Toronto 9
Amsterdam 8
Curitiba 8
Guayaquil 8
Istanbul 8
Jacksonville 8
London 8
Palermo 8
Poplar 8
San Antonio 8
Bologna 7
Cagliari 7
Cleveland 7
Des Moines 7
Dublin 7
Florence 7
Guatemala City 7
Newark 7
Shanghai 7
Shenzhen 7
The Bronx 7
Baghdad 6
Chennai 6
Collingswood 6
Columbus 6
Dhaka 6
Elgin 6
Madrid 6
Manchester 6
Nuremberg 6
San Francisco 6
Albuquerque 5
Cairo 5
Caracas 5
Cardiff 5
Charlotte 5
City of London 5
Denver 5
Hải Dương 5
Indpls 5
Lahore 5
Ninh Bình 5
Oklahoma City 5
Orlando 5
Paris 5
Piscataway 5
Rio de Janeiro 5
Seattle 5
Tashkent 5
Totale 20.027
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Nome #
A 3-year-old boy with drug-resistant complex partial seizures 236
Quantitative susceptibility map analysis in preterm neonates with germinal matrix-intraventricular hemorrhage 204
Brainstem anomalies in two patients affected by congenital central hypoventilation syndrome 203
A novel mutation in the SURF1 gene in a child with Leigh disease, peripheral neuropathy, and cytochrome-c oxidase deficiency. 199
Dissecting the neurological phenotype in children with callosal agenesis, interhemispheric cysts and malformations of cortical development 197
A New Tool for Extracting Static and Dynamic Parameters from [18F]F-DOPA PET/CT in Pediatric Gliomas 196
Congenital segmental lymphedema in tuberous sclerosis complex with associated subependymal giant cell astrocytomas treated with Mammalian target of rapamycin inhibitors. 194
Anti-N-methyl-D-aspartate-receptor encephalitis in a four-year-old girl. 193
ABCC6 mutations and early onset stroke: Two cases of a typical Pseudoxanthoma Elasticum 191
Inferior olivary nucleus involvement in pediatric neurodegenerative disorders: does it play a role in neuroimaging pattern-recognition approach? 190
Structural connectivity analysis in children with segmental callosal agenesis 190
Management of diabetes insipidus and adipsia in the child. 189
Epilepsy associated with supratentorial brain tumors under 3 years of life. 186
PITUITARY HYPOPLASIA AND GROWTH HORMONE DEFICIENCY IN COFFIN-SIRIS SYNDROME 186
Deficiency of hyccin, a newly identified membrane protein, causes hypomyelination and congenital cataract 185
Early-onset cobalamin C/D deficiency: epilepsy and electroencephalographic features. 183
Hypomyelination and congenital cataract: Identification of novel mutations in two unrelated families. 182
Aicardi-Goutières syndrome presenting atypically as a sub-acute leukoencephalopathy 177
Apparently isolated borderline ventriculomegaly and lissencephaly. 177
Clinical and electrophysiological features of epilepsy in Italian patients with CLN8 mutations. 174
Treatment and outcome of children with cerebral cavernomas: a survey on 32 patients. 173
Phenotypic characterization of hypomyelination and congenital cataract 169
Erratum to: Treatment and outcome of children with cerebral cavernomas: a survey on 32 patients. 169
Posterior pituitary (PP) evaluation in patients with anterior pituitary defect associated with ectopic PP and septo-optic dysplasia. 168
Rhombencephalosynapsis in a patient with mental retardation, epilepsy, and dysmorphisms. 166
Novel FAM126A mutations in hypomyelination and congenital cataract disease. 166
Widening the Heterogeneity of Leigh Syndrome: Clinical, Biochemical, and Neuroradiologic Features in a Patient Harboring a NDUFA10 Mutation 165
Genetic abnormalities and CNS tumors: Report of two cases of ependymoma associated with Klinefelter's Syndrome (KS). 165
White matter lesions in spastic paraplegia with mutations in SPG5/CYP7B1. 163
Role of MRI T2-DRIVE in the assessment of pituitary stalk abnormalities without gadolinium in pituitary diseases 161
EXOSC3 mutations in isolated cerebellar hypoplasia and spinal anterior horn involvement. 161
POMT2 gene mutation in limb-girdle muscular dystrophy with inflammatory changes. 159
Beyond spinal muscular atrophy with lower extremity dominance: Cerebellar hypoplasia associated with a novel mutation in BICD2 158
Cognitive and White Matter Microstructure Development in Congenital Hypothyroidism and Familial Thyroid Disorders 158
Central diabetes insipidus in children and young adults: etiological diagnosis and long-term outcome of idiopathic cases. 157
Cerebellar atrophy without cerebellar cortex hyperintensity in infantile neuroaxonal dystrophy (INAD) due to PLA2G6 mutation. 156
Cobalamin (Cbl)C/D deficiency: clinical, neurophysiological and neuroradiologic finding in 14 cases 155
CEREBELLAR WHITE MATTER INVOLVEMENT IN SALLA DISEASE 155
The use of neuroimaging for assessing disorders of pituitary development. 153
Novel asymptomatic CNS findings in patients with ACVR1/ALK2 mutations causing fibrodysplasia ossificans progressiva 153
Accuracy of ultrasound in assessing cerebellar haemorrhages in very low birthweight babies 153
Licorice-associated reversible cerebral vasoconstriction with PRES. 152
Acute superior vena cava syndrome after insertion of implantable cardioverter defibrillator 152
Cognitive Profiles and Brain Volume Are Affected in Patients with Silver-Russell Syndrome 151
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 151
Neuroimaging in Growth hormone deficiency 150
Early classification of childhood focal idiopathic epilepsies: Is it possible at the first seizure? 150
Early Pain Exposure Influences Functional Brain Connectivity in Very Preterm Neonates 150
Midbrain-hindbrain involvement in septo-optic dysplasia. 149
New insights into central nervous system involvement in FOP: Case report and review of the literature 149
Crossed pontine hemiatrophy associated with unilateral cerebellar hemorrhage in premature infants 149
Adenosine Blood Level: A Biomarker of White Matter Damage in Very Low Birth Weight Infants 149
EARLY-ONSET COMBINED METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA: NEURORADIOLOGICAL FINDINGS 148
Sirenomelia. Pathological features, antenatal ultrasonographic clues, and a review of current embryogenic theories. 148
Prevalence and Prognostic Impact of Chronic Obstructive Pulmonary Disease in Patients with Chronic Heart Failure: Data from the GISSI-HF Trial 147
Enhancement of Tumor Homing by Chemotherapy-Loaded Nanoparticles 147
T2*-based MR imaging (gradient echo or susceptibility-weighted imaging) in midline and off-midline intracranial germ cell tumors: a pilot study 147
Severe epilepsy in X-linked creatine transporter defect (CRTR-D) 146
Focal leptomeningeal enhancement and corticopial calcifications underlying a parietal convexity lipoma: a rare association of findings in 2 pediatric epileptic patients. 146
Chronic inflammatory demyelinating polyneuropathy of childhood: clinical and neuroradiological findings. 146
Hypomyelination and Congenital Cataract: Neuroimaging Features of a Novel Inherited White Matter Disorder 143
Magnetic Resonance Imaging "Tigroid Pattern" in Alexander Disease. 143
MR imaging findings in 2 cases of late infantile GM1 gangliosidosis. 142
Temporal lobe epilepsy and hippocampal malrotation: is there a causal association? 141
Prenatal diagnosis of a nasal glioma in the mid trimester 140
An Italian severe Salla disease variant associated with a SLC17A5 mutation 139
GFAP mutations and polymorphisms in 13 unrelated Italian patients affected by Alexander disease 138
Pediatric Brain Tissue Segmentation from MRI using Clustering: A Preliminary Study 138
Epilepsia partialis continua in type 1 diabetes: evolution into epileptic encephalopathy with continuous spike-waves during slow sleep 137
Novel dynein DYNC1H1 neck and motor domain mutations link distal spinal muscular atrophy and abnormal cortical development. 137
Early Extra-Uterine Growth Restriction in Very-Low-Birth-Weight Neonates with Normal or Mildly Abnormal Brain MRI: Effects on a 2-3-Year Neurodevelopmental Outcome 135
Prenatal MR imaging of dural sinus malformation: a case report 135
Pituitary Tumors: Advances in Neuroimaging. 134
Pediatric optic neuritis and anti MOG antibodies: a cohort of Italian patients 132
Medulloblastoma variants: age-dependent occurrence and relation to Gorlin syndrome--a new clinical perspective. 131
Placental Pathology Findings and the Risk of Intraventricular and Cerebellar Hemorrhage in Preterm Neonates 130
Differences in subependymal vein anatomy may predispose preterm infants to GMH–IVH 129
Focal status and acute encephalopathy in a 13-year-old boy with de novo DNM1L mutation: Video-polygraphic pattern and clues for differential diagnosis 129
Middle interhemispheric variant of holoprosencepaly: a very mild clinical case 128
THE DIAGNOSIS OF CHILDREN WITH CENTRAL DIABETES INSIPIDUS. 128
Punctate white matter lesions of preterm infants: Risk factor analysis 128
Expanding the spectrum of congenital anomalies of the diencephalic–mesencephalic junction 127
White matter and cerebellar involvement in alternating hemiplegia of childhood 127
Incidental findings on routine brain MRI scans in preterm infants 125
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 123
Diabetes insipidus--diagnosis and management. 123
Expanding the clinical and neuroimaging features of post-varicella arteriopathy of childhood 123
Arterial spin labeling perfusion in neonates 122
Different gestational ages and changing vulnerability of the premature brain 122
The Importance of Neuroimaging Follow-Up in Bilirubin-Induced Encephalopathy: A Clinical Case Review 121
Agenesis of the putamen and globus pallidus caused by recessive mutations in the homeobox gene GSX2 121
[Acute urinary retention in a child with acute disseminatedencephalomyelitis] 120
Leucoencefalopatie su base genetica in età pediatrica 119
Comparison between NODDI metrics acquired at 3T and 7T in the human brain 119
The effects of mild germinal matrix-intraventricular haemorrhage on the developmental white matter microstructure of preterm neonates: a DTI study 119
Correction to: Spatial coefficient of variation applied to arterial spin labeling MRI may contribute to predict surgical revascularization outcomes in pediatric moyamoya vasculopathy 117
Low-grade intraventricular hemorrhage: Is ultrasound good enough? 117
Unusual white matter involvement in EAST syndrome associated with novel KCNJ10 mutations 117
Brown-Vialetto-Van Laere syndrome: Cinical and neuroradiological findings of a genetically proven patient. 116
Endocrine Outcomes In Central Diabetes Insipidus: the Predictive Value of Neuroimaging "Mismatch Pattern" 116
Totale 15.173
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Categoria #
all - tutte 84.255
article - articoli 79.416
book - libri 0
conference - conferenze 2.848
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.991
Totale 168.510
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
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
2023/20241.313 63 160 34 170 98 211 75 74 86 55 72 215
2024/20253.985 185 272 74 290 461 418 310 645 192 239 443 456
2025/20267.309 912 197 411 599 1.025 494 1.096 305 489 705 451 625
2026/2027766 766 0 0 0 0 0 0 0 0 0 0 0
Totale 23.307