IRIS
ROSSI, ANDREA
 Distribuzione geografica
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Continente #
EU - Europa 17.323
AS - Asia 2.499
NA - Nord America 939
SA - Sud America 227
AF - Africa 58
OC - Oceania 2
Totale 21.048
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Nazione #
IT - Italia 16.956
SG - Singapore 1.025
US - Stati Uniti d'America 874
CN - Cina 686
VN - Vietnam 508
FR - Francia 168
BR - Brasile 137
HK - Hong Kong 89
DE - Germania 49
AR - Argentina 41
MX - Messico 35
FI - Finlandia 32
GB - Regno Unito 30
TR - Turchia 25
BD - Bangladesh 21
CA - Canada 21
IN - India 19
ZA - Sudafrica 19
EC - Ecuador 17
JP - Giappone 17
PK - Pakistan 17
ID - Indonesia 15
IQ - Iraq 14
NL - Olanda 12
RU - Federazione Russa 9
VE - Venezuela 9
CO - Colombia 8
MA - Marocco 8
PH - Filippine 8
SA - Arabia Saudita 8
TH - Thailandia 8
CL - Cile 7
ES - Italia 7
CH - Svizzera 6
EG - Egitto 6
IE - Irlanda 6
UA - Ucraina 6
UZ - Uzbekistan 6
KR - Corea 5
AL - Albania 4
DK - Danimarca 4
DZ - Algeria 4
GR - Grecia 4
JO - Giordania 4
KE - Kenya 4
KZ - Kazakistan 4
RO - Romania 4
TN - Tunisia 4
BG - Bulgaria 3
DO - Repubblica Dominicana 3
HR - Croazia 3
KH - Cambogia 3
PE - Perù 3
RS - Serbia 3
TW - Taiwan 3
UY - Uruguay 3
AT - Austria 2
AU - Australia 2
AZ - Azerbaigian 2
BA - Bosnia-Erzegovina 2
CY - Cipro 2
ET - Etiopia 2
GT - Guatemala 2
MT - Malta 2
NP - Nepal 2
PL - Polonia 2
SE - Svezia 2
TT - Trinidad e Tobago 2
AE - Emirati Arabi Uniti 1
AM - Armenia 1
BE - Belgio 1
BH - Bahrain 1
BO - Bolivia 1
BY - Bielorussia 1
CI - Costa d'Avorio 1
CR - Costa Rica 1
CV - Capo Verde 1
GA - Gabon 1
GH - Ghana 1
HN - Honduras 1
HU - Ungheria 1
IL - Israele 1
LT - Lituania 1
LY - Libia 1
MD - Moldavia 1
MK - Macedonia 1
MN - Mongolia 1
MU - Mauritius 1
MY - Malesia 1
NA - Namibia 1
OM - Oman 1
PY - Paraguay 1
QA - Qatar 1
SC - Seychelles 1
SI - Slovenia 1
SN - Senegal 1
TG - Togo 1
ZM - Zambia 1
Totale 21.048
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Città #
Genova 8.028
Genoa 5.883
Vado Ligure 1.512
Rapallo 1.387
Singapore 501
San Jose 329
Ho Chi Minh City 175
Lauterbourg 158
Ashburn 153
Hanoi 118
Beijing 116
Hong Kong 83
Los Angeles 39
New York 38
Bordighera 37
Frankfurt am Main 31
Santa Clara 31
Da Nang 30
Council Bluffs 26
Orem 24
Mexico City 21
Helsinki 18
Tianjin 17
Haiphong 15
Guangzhou 14
Milan 14
Tokyo 14
Izmir 13
Johannesburg 13
Chicago 12
Lappeenranta 12
São Paulo 12
Biên Hòa 11
Can Tho 11
Montreal 10
Amsterdam 8
Poplar 8
Buffalo 7
Guayaquil 7
Istanbul 7
Shanghai 7
Shenzhen 7
Baghdad 6
Chennai 6
Curitiba 6
Dallas 6
Dublin 6
Madrid 6
Nuremberg 6
Rome 6
Turin 6
Atlanta 5
Caracas 5
Cardiff 5
City of London 5
Hải Dương 5
Lahore 5
Manchester 5
Ninh Bình 5
Rio de Janeiro 5
Tashkent 5
Thái Bình 5
Amman 4
Bangkok 4
Brasília 4
Cairo 4
Chongqing 4
Dhaka 4
Jeddah 4
London 4
Marrakesh 4
Marseille 4
Nairobi 4
Nha Trang 4
Paris 4
Piscataway 4
Ahmedabad 3
Bogotá 3
Denver 3
Des Moines 3
Durban 3
Goiânia 3
Hamburg 3
Hưng Yên 3
Iztapalapa 3
Mumbai 3
Nanjing 3
Naples 3
Phnom Penh 3
Phoenix 3
Quito 3
Quận Bình Thạnh 3
Resistencia 3
Riyadh 3
Thái Nguyên 3
Toronto 3
Wuppertal 3
Zurich 3
Addis Ababa 2
Alessandria 2
Totale 19.192
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Nome #
A 3-year-old boy with drug-resistant complex partial seizures 228
Quantitative susceptibility map analysis in preterm neonates with germinal matrix-intraventricular hemorrhage 193
Brainstem anomalies in two patients affected by congenital central hypoventilation syndrome 191
A novel mutation in the SURF1 gene in a child with Leigh disease, peripheral neuropathy, and cytochrome-c oxidase deficiency. 190
A New Tool for Extracting Static and Dynamic Parameters from [18F]F-DOPA PET/CT in Pediatric Gliomas 188
Dissecting the neurological phenotype in children with callosal agenesis, interhemispheric cysts and malformations of cortical development 188
Congenital segmental lymphedema in tuberous sclerosis complex with associated subependymal giant cell astrocytomas treated with Mammalian target of rapamycin inhibitors. 186
Inferior olivary nucleus involvement in pediatric neurodegenerative disorders: does it play a role in neuroimaging pattern-recognition approach? 185
ABCC6 mutations and early onset stroke: Two cases of a typical Pseudoxanthoma Elasticum 185
Management of diabetes insipidus and adipsia in the child. 184
Structural connectivity analysis in children with segmental callosal agenesis 183
Anti-N-methyl-D-aspartate-receptor encephalitis in a four-year-old girl. 182
Epilepsy associated with supratentorial brain tumors under 3 years of life. 179
PITUITARY HYPOPLASIA AND GROWTH HORMONE DEFICIENCY IN COFFIN-SIRIS SYNDROME 178
Deficiency of hyccin, a newly identified membrane protein, causes hypomyelination and congenital cataract 176
Hypomyelination and congenital cataract: Identification of novel mutations in two unrelated families. 175
Early-onset cobalamin C/D deficiency: epilepsy and electroencephalographic features. 173
Aicardi-Goutières syndrome presenting atypically as a sub-acute leukoencephalopathy 172
Apparently isolated borderline ventriculomegaly and lissencephaly. 171
Treatment and outcome of children with cerebral cavernomas: a survey on 32 patients. 168
Phenotypic characterization of hypomyelination and congenital cataract 165
Clinical and electrophysiological features of epilepsy in Italian patients with CLN8 mutations. 164
Erratum to: Treatment and outcome of children with cerebral cavernomas: a survey on 32 patients. 164
Rhombencephalosynapsis in a patient with mental retardation, epilepsy, and dysmorphisms. 161
Widening the Heterogeneity of Leigh Syndrome: Clinical, Biochemical, and Neuroradiologic Features in a Patient Harboring a NDUFA10 Mutation 159
Genetic abnormalities and CNS tumors: Report of two cases of ependymoma associated with Klinefelter's Syndrome (KS). 159
Posterior pituitary (PP) evaluation in patients with anterior pituitary defect associated with ectopic PP and septo-optic dysplasia. 158
Novel FAM126A mutations in hypomyelination and congenital cataract disease. 158
White matter lesions in spastic paraplegia with mutations in SPG5/CYP7B1. 157
EXOSC3 mutations in isolated cerebellar hypoplasia and spinal anterior horn involvement. 157
Central diabetes insipidus in children and young adults: etiological diagnosis and long-term outcome of idiopathic cases. 155
Cerebellar atrophy without cerebellar cortex hyperintensity in infantile neuroaxonal dystrophy (INAD) due to PLA2G6 mutation. 152
Beyond spinal muscular atrophy with lower extremity dominance: Cerebellar hypoplasia associated with a novel mutation in BICD2 152
Cognitive and White Matter Microstructure Development in Congenital Hypothyroidism and Familial Thyroid Disorders 152
Role of MRI T2-DRIVE in the assessment of pituitary stalk abnormalities without gadolinium in pituitary diseases 151
POMT2 gene mutation in limb-girdle muscular dystrophy with inflammatory changes. 150
Novel asymptomatic CNS findings in patients with ACVR1/ALK2 mutations causing fibrodysplasia ossificans progressiva 147
Acute superior vena cava syndrome after insertion of implantable cardioverter defibrillator 146
CEREBELLAR WHITE MATTER INVOLVEMENT IN SALLA DISEASE 146
Neuroimaging in Growth hormone deficiency 145
Cobalamin (Cbl)C/D deficiency: clinical, neurophysiological and neuroradiologic finding in 14 cases 145
Licorice-associated reversible cerebral vasoconstriction with PRES. 143
New insights into central nervous system involvement in FOP: Case report and review of the literature 143
Midbrain-hindbrain involvement in septo-optic dysplasia. 142
Early Pain Exposure Influences Functional Brain Connectivity in Very Preterm Neonates 142
Early classification of childhood focal idiopathic epilepsies: Is it possible at the first seizure? 141
Enhancement of Tumor Homing by Chemotherapy-Loaded Nanoparticles 141
Crossed pontine hemiatrophy associated with unilateral cerebellar hemorrhage in premature infants 141
EARLY-ONSET COMBINED METHYLMALONIC ACIDURIA AND HOMOCYSTINURIA: NEURORADIOLOGICAL FINDINGS 140
Sirenomelia. Pathological features, antenatal ultrasonographic clues, and a review of current embryogenic theories. 140
Prevalence and Prognostic Impact of Chronic Obstructive Pulmonary Disease in Patients with Chronic Heart Failure: Data from the GISSI-HF Trial 140
Severe epilepsy in X-linked creatine transporter defect (CRTR-D) 139
Focal leptomeningeal enhancement and corticopial calcifications underlying a parietal convexity lipoma: a rare association of findings in 2 pediatric epileptic patients. 139
Accuracy of ultrasound in assessing cerebellar haemorrhages in very low birthweight babies 139
Chronic inflammatory demyelinating polyneuropathy of childhood: clinical and neuroradiological findings. 139
The use of neuroimaging for assessing disorders of pituitary development. 138
Adenosine Blood Level: A Biomarker of White Matter Damage in Very Low Birth Weight Infants 138
Hypomyelination and Congenital Cataract: Neuroimaging Features of a Novel Inherited White Matter Disorder 137
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 137
Magnetic Resonance Imaging "Tigroid Pattern" in Alexander Disease. 135
T2*-based MR imaging (gradient echo or susceptibility-weighted imaging) in midline and off-midline intracranial germ cell tumors: a pilot study 135
Prenatal diagnosis of a nasal glioma in the mid trimester 133
Novel dynein DYNC1H1 neck and motor domain mutations link distal spinal muscular atrophy and abnormal cortical development. 133
Cognitive Profiles and Brain Volume Are Affected in Patients with Silver-Russell Syndrome 133
Temporal lobe epilepsy and hippocampal malrotation: is there a causal association? 132
Pediatric Brain Tissue Segmentation from MRI using Clustering: A Preliminary Study 132
Epilepsia partialis continua in type 1 diabetes: evolution into epileptic encephalopathy with continuous spike-waves during slow sleep 131
Prenatal MR imaging of dural sinus malformation: a case report 131
MR imaging findings in 2 cases of late infantile GM1 gangliosidosis. 130
Pituitary Tumors: Advances in Neuroimaging. 130
An Italian severe Salla disease variant associated with a SLC17A5 mutation 130
Medulloblastoma variants: age-dependent occurrence and relation to Gorlin syndrome--a new clinical perspective. 127
Pediatric optic neuritis and anti MOG antibodies: a cohort of Italian patients 127
GFAP mutations and polymorphisms in 13 unrelated Italian patients affected by Alexander disease 126
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 125
THE DIAGNOSIS OF CHILDREN WITH CENTRAL DIABETES INSIPIDUS. 125
Expanding the spectrum of congenital anomalies of the diencephalic–mesencephalic junction 122
Middle interhemispheric variant of holoprosencepaly: a very mild clinical case 121
White matter and cerebellar involvement in alternating hemiplegia of childhood 121
Placental Pathology Findings and the Risk of Intraventricular and Cerebellar Hemorrhage in Preterm Neonates 121
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 120
Focal status and acute encephalopathy in a 13-year-old boy with de novo DNM1L mutation: Video-polygraphic pattern and clues for differential diagnosis 120
Incidental findings on routine brain MRI scans in preterm infants 117
Differences in subependymal vein anatomy may predispose preterm infants to GMH–IVH 116
Diabetes insipidus--diagnosis and management. 116
Brown-Vialetto-Van Laere syndrome: Cinical and neuroradiological findings of a genetically proven patient. 114
Arterial spin labeling perfusion in neonates 114
Expanding the clinical and neuroimaging features of post-varicella arteriopathy of childhood 114
Unusual white matter involvement in EAST syndrome associated with novel KCNJ10 mutations 113
The effects of mild germinal matrix-intraventricular haemorrhage on the developmental white matter microstructure of preterm neonates: a DTI study 112
Different gestational ages and changing vulnerability of the premature brain 112
[Acute urinary retention in a child with acute disseminatedencephalomyelitis] 110
Leucoencefalopatie su base genetica in età pediatrica 110
Tonsillar herniation spectrum: more than just Chiari I. Update and controversies on classification and management 110
Low-grade intraventricular hemorrhage: Is ultrasound good enough? 109
Endocrine Outcomes In Central Diabetes Insipidus: the Predictive Value of Neuroimaging "Mismatch Pattern" 108
Correction to: Spatial coefficient of variation applied to arterial spin labeling MRI may contribute to predict surgical revascularization outcomes in pediatric moyamoya vasculopathy 107
Comparison between NODDI metrics acquired at 3T and 7T in the human brain 107
Agenesis of the putamen and globus pallidus caused by recessive mutations in the homeobox gene GSX2 105
Comparison of Diffusion Tensor and Diffusion Kurtosis Metrics acquired at 3T and 7T in Human Brain 104
Totale 14.375
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Categoria #
all - tutte 75.537
article - articoli 71.180
book - libri 0
conference - conferenze 2.568
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 1.789
Totale 151.074
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021418 0 0 0 0 0 0 0 0 0 174 130 114
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
2023/20241.313 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
2025/20266.146 912 197 411 599 1.025 494 1.096 305 489 618 0 0
Totale 21.378