IRIS
POLIZZI, Agata Rita Maria
 Distribuzione geografica
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Continente #
NA - Nord America 9.002
AS - Asia 4.734
EU - Europa 4.633
SA - Sud America 958
AF - Africa 615
OC - Oceania 20
Continente sconosciuto - Info sul continente non disponibili 1
Totale 19.963
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Nazione #
US - Stati Uniti d'America 8.680
SG - Singapore 2.277
RU - Federazione Russa 1.489
CN - Cina 1.288
IT - Italia 1.070
BR - Brasile 792
IE - Irlanda 604
UA - Ucraina 522
VN - Vietnam 404
CI - Costa d'Avorio 342
CA - Canada 243
FR - Francia 230
IN - India 188
KR - Corea 167
DE - Germania 158
GB - Regno Unito 117
NG - Nigeria 115
SE - Svezia 110
AR - Argentina 68
NL - Olanda 64
BD - Bangladesh 61
SN - Senegal 59
FI - Finlandia 54
MX - Messico 52
HK - Hong Kong 47
JP - Giappone 41
TR - Turchia 39
PL - Polonia 36
IQ - Iraq 35
ZA - Sudafrica 33
CH - Svizzera 31
PK - Pakistan 28
ID - Indonesia 26
CO - Colombia 25
CZ - Repubblica Ceca 25
UZ - Uzbekistan 25
ES - Italia 24
EC - Ecuador 22
AT - Austria 20
AU - Australia 17
GR - Grecia 17
MA - Marocco 17
PY - Paraguay 14
BJ - Benin 13
IR - Iran 12
BE - Belgio 11
JO - Giordania 11
VE - Venezuela 11
JM - Giamaica 9
PH - Filippine 9
SA - Arabia Saudita 9
CL - Cile 8
DZ - Algeria 8
LB - Libano 8
PE - Perù 7
AE - Emirati Arabi Uniti 6
EG - Egitto 6
KE - Kenya 6
LT - Lituania 6
MY - Malesia 6
NP - Nepal 6
UY - Uruguay 6
BG - Bulgaria 5
BO - Bolivia 5
TN - Tunisia 5
AL - Albania 4
AZ - Azerbaigian 4
CR - Costa Rica 4
DO - Repubblica Dominicana 4
ET - Etiopia 4
IL - Israele 4
KZ - Kazakistan 4
OM - Oman 4
RO - Romania 4
SK - Slovacchia (Repubblica Slovacca) 4
BY - Bielorussia 3
EE - Estonia 3
HN - Honduras 3
HR - Croazia 3
HU - Ungheria 3
LU - Lussemburgo 3
NZ - Nuova Zelanda 3
PS - Palestinian Territory 3
QA - Qatar 3
SI - Slovenia 3
AM - Armenia 2
AO - Angola 2
BT - Bhutan 2
GA - Gabon 2
GE - Georgia 2
KG - Kirghizistan 2
KH - Cambogia 2
MK - Macedonia 2
NI - Nicaragua 2
PT - Portogallo 2
TH - Thailandia 2
TT - Trinidad e Tobago 2
BA - Bosnia-Erzegovina 1
BN - Brunei Darussalam 1
CY - Cipro 1
Totale 19.946
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Città #
Dallas 1.408
Singapore 1.368
Santa Clara 907
Chandler 791
Moscow 645
Dublin 601
Jacksonville 601
Houston 587
San Jose 466
Ashburn 418
Abidjan 342
Chicago 305
Boardman 289
Los Angeles 258
Hefei 255
Catania 217
Lauterbourg 182
Lawrence 176
Beijing 174
Cambridge 174
Andover 173
Nanjing 173
Seoul 164
Toronto 158
Ho Chi Minh City 132
Des Moines 108
Kochi 91
Wilmington 86
Hanoi 85
Civitanova Marche 82
San Mateo 78
Council Bluffs 76
New York 73
São Paulo 67
Abuja 63
Nanchang 62
Dakar 59
Hebei 54
Palermo 54
Buffalo 53
Shenyang 51
Bremen 50
Hong Kong 43
Rome 43
Lagos 42
Amsterdam 41
Ottawa 40
Tokyo 40
The Dalles 37
Milan 35
Columbus 32
Grafing 32
Orem 32
Saint Petersburg 32
Tianjin 32
Changsha 31
Jiaxing 30
Oakland 30
Montreal 28
Rio de Janeiro 26
Warsaw 26
Belo Horizonte 24
Lappeenranta 24
Denver 23
Brooklyn 22
Falls Church 22
Bussero 21
Johannesburg 20
London 20
Atlanta 19
Bari 19
Mexico City 19
Mumbai 19
Redondo Beach 19
Washington 19
Chennai 18
Curitiba 18
Da Nang 18
Dong Ket 18
Frankfurt am Main 18
San Francisco 18
Boston 17
Phoenix 17
Seattle 17
Turku 17
Biên Hòa 16
Haiphong 16
Poplar 16
Stockholm 16
Munich 15
Baghdad 14
Redmond 14
Cotonou 13
Helsinki 13
Kunming 13
Manchester 13
Brasília 12
Den Haag 12
Pune 12
Gela 11
Totale 13.480
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Nome #
Childhood neurofibromatosis type 2 (NF2) and related disorders: From bench to bedside and biologically targeted therapies [Neurofibromatosi tipo 2 (NF2) e sindromi correlate in età infantile: dalla biologia molecolare alla pratica clinica e nuove terapie con farmaci biologici] 281
A pilot study on neurological manifestations and antibodies against neuronal antigens in children with haematological and other cancers 242
Natural history of neurofibromatosis type 2 with onset before the age of 1 year. 218
A mosaic pattern of INI1/SMARCB1 protein expression distinguishes Schwannomatosis and NF2-associated peripheral schwannomas from solitary peripheral schwannomas and NF2-associated vestibular schwannomas 204
Speckled Lentiginous Nevus Syndrome 200
Manuale di Pediatria, quinta edizione. Capitolo 2 "Anamnesi ed esame obiettivo". Capitolo 29 "Malattie Neurologiche". 196
Encephalocraniocutaneous Lipomatosis (Haberland Syndrome or Fishman Syndrome) 193
Becker's Nevus Syndrome 193
Familial osteoma of the cranial vault 181
Blue Rubber Bleb Nevus Syndrome 174
Nevus Sebaceous Syndrome 172
At the Origin of Brain Malformations: Embryology of the Central and Peripheral Nervous System 169
Phacomatosis Pigmentovascularis 169
Phacomatosis Pigmentokeratotica 169
Aicardi-Goutières Syndrome Type 2: A Report on Two Cases with Different Phenotypes Caused by RNASEH2B Gene Mutations 159
Cerebellotrigeminal Dermal Dysplasia (Gómez-López-Hernández Syndrome) 158
Prefazione a: La complessità della cultura. Flussi, identità, valori. 155
GRIN2A and GRIN2B and Their Related Phenotypes 155
Another "new" form, the palagonia type of acrofacial dysostosis in a sicilian family 152
Wyburn-Mason Syndrome 152
Megalencephaly Capillary Malformation Syndrome 149
Archetypical Patterns of Skin Manifestations in Neurocutaneous Disorders 147
Chromosome 15q BP3 to BP5 deletion is a likely locus for speech delay and language impairment: Report on a four-member family and an unrelated boy 146
Acute disseminated encephalomyelitis: a long-term prospective study and meta-analysis 145
A child with rhombencephalosynapsis, agenesis of the trigeminal ganglion and optic coloboma (without alopecia): A variant of the cerebellotrigeminal dermal dysplasia? 145
A de novo 0.63 Mb 6q25.1 deletion associated to growth failure, congenital heart defect, underdeveloped cerebellar vermis and abnormal cutaneous elasticity and joint laxity 143
Microcephaly-Capillary Malformation Syndrome 143
An 11-year follow-up of neonatal onset bath-induced alternating hemiplegia of childhood in monozygotic twins 142
Familial osteoma of the cranial vault 142
SCN1B gene: A close relative to SCN1A 141
Anomalies of Midbrain/Hindbrain Development and Related Disabilities: Pontocerebellar Hypoplasia, Congenital Disorders of Glycosylation, and Cerebellar Hemisphere Hypoplasia 140
Klippel-Trenaunay Syndrome, Segmental/Focal Overgrowth Malformations: A Review 138
Anomalies of Midbrain Hindbrain Development: Midbrain Clefts, Cerebellar Nodular Heterotopia with Overlying Dysgenesis, Cerebellar Foliation Disorder, Pontine Tegmental Cap Dysplasia; Joubert Syndrome; Lhermitte Duclos Syndrome. Diagnosis, Classification and Rehabilitation Hypothesis 137
Hypomelanosis of Ito 134
Motor imagery for paediatric neurorehabilitation: how much do we know? Perspectives from a systematic review 131
Did Cro-Magnon 1 have neurofibromatosis type 2? 131
Autoimmune thyroiditis and acquired demyelinating poliradiculoneuropathy 131
ANOMALIE MALFORMATIVE CEREBRALI ED ENDOCRINOPATIE 130
Cutis Tricolor 130
Maternal Phenylketonuria and Offspring Outcome: A Retrospective Study with a Systematic Review of the Literature 126
Genotype–Phenotype Correlation in a Large Cohort of Eastern Sicilian Patients Affected by Phenylketonuria: Newborn Screening Program, Clinical Features, and Follow-Up 126
Mixed Vascular Nevus Syndrome 126
Neurocutaneous melanocytosis (melanosis) 126
Adrenal Disorders and the Paediatric Brain: Pathophysiological Considerations and Clinical Implications 125
The natural history of Spinal Neurofibromatosis: A critical review of clinical and genetic features 124
Cognitive disabilities and bioethical implications in down syndrome 124
Anomalies of Midbrain/Hindbrain Development: Malformations of Cerebellum: Diagnosis, Classification, and Rehabilitative Hypothesis 123
Cutis tricolor: a literature review and report of five new cases 123
Antibodies to voltage-gated (VG) ion channels and glutamic acid decarboxylase (GAD) in childhood forms of epilepsies 120
Analgetic thalamic syndrome in association with thalamic symmetrical abnormalities during measles encephalitis 119
Introduction to phacomatoses (neurocutaneous disorders) in childhood 116
TSC1 and TSC2: Tuberous Sclerosis Complex and Its Related Epilepsy Phenotype 116
Earliest clinical manifestations and natural history of neurofibromatosis type 2 in childhood: a study of 24 patients 115
Hypotonia, congenital nystagmus, ataxia and abnormal auditory brainstem responses. Report on the first white Caucasian patient 112
Multiple Sclerosis in Childhood and other Immune-Mediated Disorders of the Central Nervous System in the Pediatric Age 111
Two siblings with a homozygous MTHFR C677T (G80A-RFC1) mutation and stroke 109
Bilateral (perisylvian and opercular) polymicrogyria and Neurofibromatosis type 1 109
Mixed vascular nevus syndrome: a report of four new cases and a literature review 109
Bilateral periventricular nodular heterotopia and amniotic band syndrome 108
Life-threatening neurological syndrome in Down's syndrome 108
SCN1A and its related epileptic phenotypes 107
Case report: A gain-of-function of hamartin may lead to a distinct "inverse TSC1-hamartin" phenotype characterized by reduced cell growth 105
Polydactyly and syndactyly linked to GLI3 and TBX5 mutations: A pediatric case report 105
Ossifying fibroma of the skull in a patient with neurofibromatosis type 1 - Case report 105
NEUROEMBRIOLOGIA 104
A mouse model for fetal abnormalities caused by maternal autoantibodies to neuronal or muscle antigens 104
Reconstructive Surgery in Children with Down's Syndrome: Bioethical Implications 104
Multiple sclerosis with onset at 35 months of age 103
Competing to raise awareness of rare diseases 103
CNS findings in three cases of septo-optic dysplasia, including one with semilobar holoprosencephaly 102
Spinal neurofibromatosis with central nervous system involvement in a set of twin girls and a boy: further expansion of the phenotype 102
Malattie neuromuscolari 102
The natural history of L-aminoacid decarboxylase (AADC) deficiency: report of two never treated ault patients. 100
Clinical spectrum of woolly hair: Indications for cerebral involvement 100
Design and validation of a custom ngs panel targeting a set of lysosomal storage diseases candidate for nbs applications 99
ATAXIA-TELANGIECTASIA 98
Highlights on Genomics Applications for Lysosomal Storage Diseases 98
Neurofibromatosis type 1 and infantile spasms 97
Near-infrared spectroscopy (NIRS) as a tool to prevent cerebral desaturation in newborns with bradycardia events: A systematic review 97
Progressive Depletion of B and T Lymphocytes in Patients with Ataxia Telangiectasia: Results of the Italian Primary Immunodeficiency Network 96
Dominant myopia? Report on a large Italian family 95
MALATTIE NEURODEGENERATIVE E MALATTIE DA ALTERAZIONE DEI NEUROTRASMETTITORI 95
At the Basis of Brain Malformations: Brain Plasticity, Developmental Neurobiology, and Considerations for Rehabilitation 94
Biological Approaches to the Treatment of Saline Oily Waste(waters) Originated from Marine Transportation 94
Tuberculosis of the ankle in childhood: Clinical, roentgenographic and computed tomography findings 94
Congenital myasthenic syndromes: Clinical and molecular report on 7 Sicilian patients 94
Ohtahara syndrome with emphasis on recent genetic discovery. 93
Unusual form of recurrent multinucleated giant cell granuloma of the mandible and lower extremities in a patient with neurofirbomatosis type 1 93
SCN8A and Its Related Epileptic Phenotypes 93
Influence of the cerebellum in paediatric epilepsy: A comprehensive systematic literature review focusing on neurodevelopmental/neuropsychological implications 92
Malformations of the Spinal Cord: From Genetics to Diagnosis and Rehabilitation 92
SHORT syndrome: a new case with probable AD inheritance 92
Rett syndrome phenotype following infantile acute encephalopathy. J Child Neurol 2002, 17(9):700-702 IF 1.333 92
Confronto tra differenti metodi di recupero microbiologico (bioremediation) per il trattamento di “Bilge water 92
Displasia setto-ottica ad esordio precoce. Descrizione di un caso con follow-up. Min Pediatr, 54(1): 57-62, 2002 92
La condrodisplasia di Schmid: Reperti clinici e radiologici su due pazienti 91
Nevus vascularis mixtus (cutaneous vascular twin nevi) associated with intracranial vascular malformation of the Dyke-Davidoff-Masson type in two patients 91
Two novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus 91
Rediagnosing one of Smith's patients (John McCann) with "neuromas tumours" (1849). 90
Septo-optic dysplasia complex: a complex malformation syndrome 90
Totale 12.693
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Categoria #
all - tutte 61.789
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 61.789
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021259 0 0 0 0 0 0 0 0 0 12 193 54
2021/20221.458 133 179 51 36 218 27 203 70 108 18 24 391
2022/20232.283 211 118 44 230 237 388 18 373 511 25 78 50
2023/2024978 59 221 37 49 37 149 33 61 21 22 208 81
2024/20254.002 41 585 241 220 715 459 131 162 296 397 410 345
2025/20268.508 533 580 1.635 610 1.266 1.688 992 236 556 412 0 0
Totale 20.287