IRIS
POLIZZI, Agata Rita Maria
 Distribuzione geografica
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Continente #
NA - Nord America 8.171
EU - Europa 4.246
AS - Asia 3.974
SA - Sud America 845
AF - Africa 475
OC - Oceania 16
Continente sconosciuto - Info sul continente non disponibili 1
Totale 17.728
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Nazione #
US - Stati Uniti d'America 7.890
SG - Singapore 2.043
RU - Federazione Russa 1.488
CN - Cina 1.200
IT - Italia 1.013
BR - Brasile 731
IE - Irlanda 603
UA - Ucraina 511
CI - Costa d'Avorio 341
CA - Canada 224
VN - Vietnam 209
IN - India 160
DE - Germania 141
SE - Svezia 108
GB - Regno Unito 103
KR - Corea 103
SN - Senegal 57
AR - Argentina 52
FI - Finlandia 42
MX - Messico 41
JP - Giappone 38
BD - Bangladesh 36
NL - Olanda 35
PL - Polonia 34
FR - Francia 31
TR - Turchia 31
CH - Svizzera 27
HK - Hong Kong 25
ZA - Sudafrica 23
UZ - Uzbekistan 22
ES - Italia 21
CZ - Repubblica Ceca 20
ID - Indonesia 18
EC - Ecuador 17
IQ - Iraq 16
CO - Colombia 15
GR - Grecia 14
AT - Austria 13
AU - Australia 13
BJ - Benin 13
IR - Iran 12
MA - Marocco 12
PK - Pakistan 11
BE - Belgio 10
NG - Nigeria 10
PY - Paraguay 8
LB - Libano 7
UY - Uruguay 6
PE - Perù 5
SA - Arabia Saudita 5
AE - Emirati Arabi Uniti 4
AZ - Azerbaigian 4
BG - Bulgaria 4
CL - Cile 4
IL - Israele 4
JM - Giamaica 4
KE - Kenya 4
LT - Lituania 4
NP - Nepal 4
TN - Tunisia 4
VE - Venezuela 4
AL - Albania 3
BO - Bolivia 3
DO - Repubblica Dominicana 3
DZ - Algeria 3
EE - Estonia 3
EG - Egitto 3
HN - Honduras 3
JO - Giordania 3
MY - Malesia 3
NZ - Nuova Zelanda 3
QA - Qatar 3
AM - Armenia 2
BT - Bhutan 2
BY - Bielorussia 2
CR - Costa Rica 2
GA - Gabon 2
HU - Ungheria 2
LU - Lussemburgo 2
MK - Macedonia 2
OM - Oman 2
PH - Filippine 2
SI - Slovenia 2
SK - Slovacchia (Repubblica Slovacca) 2
AO - Angola 1
BA - Bosnia-Erzegovina 1
BN - Brunei Darussalam 1
DK - Danimarca 1
ET - Etiopia 1
EU - Europa 1
GD - Grenada 1
GT - Guatemala 1
HR - Croazia 1
IS - Islanda 1
KH - Cambogia 1
KZ - Kazakistan 1
LA - Repubblica Popolare Democratica del Laos 1
MD - Moldavia 1
NE - Niger 1
NI - Nicaragua 1
Totale 17.725
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Città #
Dallas 1.405
Singapore 1.188
Santa Clara 895
Chandler 791
Moscow 645
Jacksonville 601
Dublin 600
Houston 587
Abidjan 341
Ashburn 315
Chicago 304
Boardman 289
Hefei 255
Los Angeles 238
Catania 215
Lawrence 176
Cambridge 174
Andover 173
Nanjing 173
Beijing 165
Toronto 154
Des Moines 108
Seoul 100
Kochi 91
Wilmington 86
Civitanova Marche 82
San Mateo 78
Ho Chi Minh City 69
Nanchang 62
New York 59
São Paulo 58
Dakar 57
Hebei 54
Buffalo 51
Shenyang 51
Bremen 50
Rome 41
Ottawa 40
Hanoi 38
Palermo 38
The Dalles 37
Tokyo 37
Columbus 32
Council Bluffs 32
Grafing 32
Saint Petersburg 32
Tianjin 32
Milan 31
Jiaxing 30
Oakland 30
Changsha 29
Warsaw 24
Belo Horizonte 23
Denver 23
Hong Kong 23
Rio de Janeiro 23
Brooklyn 22
Falls Church 22
Orem 22
Bussero 21
Montreal 19
Redondo Beach 19
Washington 19
Dong Ket 18
Boston 17
Curitiba 17
Lappeenranta 17
San Francisco 17
Turku 17
London 16
Mumbai 16
Poplar 16
Seattle 16
Amsterdam 15
Johannesburg 15
Mexico City 15
Munich 15
Phoenix 15
Bari 14
Chennai 14
Redmond 14
San Jose 14
Stockholm 14
Atlanta 13
Cotonou 13
Kunming 13
Manchester 13
Biên Hòa 12
Brasília 12
Den Haag 12
Gela 11
Ningbo 11
Abuja 10
Ann Arbor 10
Bologna 10
Haiphong 10
Hangzhou 10
Milazzo 10
Pune 10
Redwood City 10
Totale 12.013
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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] 268
A pilot study on neurological manifestations and antibodies against neuronal antigens in children with haematological and other cancers 229
Natural history of neurofibromatosis type 2 with onset before the age of 1 year. 212
A mosaic pattern of INI1/SMARCB1 protein expression distinguishes Schwannomatosis and NF2-associated peripheral schwannomas from solitary peripheral schwannomas and NF2-associated vestibular schwannomas 188
Speckled Lentiginous Nevus Syndrome 183
Encephalocraniocutaneous Lipomatosis (Haberland Syndrome or Fishman Syndrome) 182
Manuale di Pediatria, quinta edizione. Capitolo 2 "Anamnesi ed esame obiettivo". Capitolo 29 "Malattie Neurologiche". 179
Familial osteoma of the cranial vault 170
Becker's Nevus Syndrome 170
Nevus Sebaceous Syndrome 156
Blue Rubber Bleb Nevus Syndrome 153
Phacomatosis Pigmentovascularis 153
Phacomatosis Pigmentokeratotica 151
Cerebellotrigeminal Dermal Dysplasia (Gómez-López-Hernández Syndrome) 145
At the Origin of Brain Malformations: Embryology of the Central and Peripheral Nervous System 144
Aicardi-Goutières Syndrome Type 2: A Report on Two Cases with Different Phenotypes Caused by RNASEH2B Gene Mutations 142
Prefazione a: La complessità della cultura. Flussi, identità, valori. 140
Another "new" form, the palagonia type of acrofacial dysostosis in a sicilian family 139
GRIN2A and GRIN2B and Their Related Phenotypes 138
Megalencephaly Capillary Malformation Syndrome 137
Wyburn-Mason Syndrome 135
A child with rhombencephalosynapsis, agenesis of the trigeminal ganglion and optic coloboma (without alopecia): A variant of the cerebellotrigeminal dermal dysplasia? 134
Familial osteoma of the cranial vault 133
An 11-year follow-up of neonatal onset bath-induced alternating hemiplegia of childhood in monozygotic twins 132
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 131
Acute disseminated encephalomyelitis: a long-term prospective study and meta-analysis 130
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 129
Archetypical Patterns of Skin Manifestations in Neurocutaneous Disorders 128
SCN1B gene: A close relative to SCN1A 126
Autoimmune thyroiditis and acquired demyelinating poliradiculoneuropathy 124
Microcephaly-Capillary Malformation Syndrome 124
Hypomelanosis of Ito 122
Klippel-Trenaunay Syndrome, Segmental/Focal Overgrowth Malformations: A Review 118
Did Cro-Magnon 1 have neurofibromatosis type 2? 118
Cutis Tricolor 118
The natural history of Spinal Neurofibromatosis: A critical review of clinical and genetic features 117
ANOMALIE MALFORMATIVE CEREBRALI ED ENDOCRINOPATIE 116
Mixed Vascular Nevus Syndrome 115
Neurocutaneous melanocytosis (melanosis) 115
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 113
Antibodies to voltage-gated (VG) ion channels and glutamic acid decarboxylase (GAD) in childhood forms of epilepsies 113
Adrenal Disorders and the Paediatric Brain: Pathophysiological Considerations and Clinical Implications 112
Analgetic thalamic syndrome in association with thalamic symmetrical abnormalities during measles encephalitis 110
Cognitive disabilities and bioethical implications in down syndrome 108
Maternal Phenylketonuria and Offspring Outcome: A Retrospective Study with a Systematic Review of the Literature 105
Anomalies of Midbrain/Hindbrain Development and Related Disabilities: Pontocerebellar Hypoplasia, Congenital Disorders of Glycosylation, and Cerebellar Hemisphere Hypoplasia 105
Anomalies of Midbrain/Hindbrain Development: Malformations of Cerebellum: Diagnosis, Classification, and Rehabilitative Hypothesis 105
Introduction to phacomatoses (neurocutaneous disorders) in childhood 105
Hypotonia, congenital nystagmus, ataxia and abnormal auditory brainstem responses. Report on the first white Caucasian patient 104
Two siblings with a homozygous MTHFR C677T (G80A-RFC1) mutation and stroke 104
Earliest clinical manifestations and natural history of neurofibromatosis type 2 in childhood: a study of 24 patients 104
Cutis tricolor: a literature review and report of five new cases 104
TSC1 and TSC2: Tuberous Sclerosis Complex and Its Related Epilepsy Phenotype 104
Bilateral (perisylvian and opercular) polymicrogyria and Neurofibromatosis type 1 103
Mixed vascular nevus syndrome: a report of four new cases and a literature review 102
Bilateral periventricular nodular heterotopia and amniotic band syndrome 101
Multiple Sclerosis in Childhood and other Immune-Mediated Disorders of the Central Nervous System in the Pediatric Age 101
Motor imagery for paediatric neurorehabilitation: how much do we know? Perspectives from a systematic review 100
Life-threatening neurological syndrome in Down's syndrome 100
Genotype–Phenotype Correlation in a Large Cohort of Eastern Sicilian Patients Affected by Phenylketonuria: Newborn Screening Program, Clinical Features, and Follow-Up 99
Multiple sclerosis with onset at 35 months of age 96
NEUROEMBRIOLOGIA 96
Ossifying fibroma of the skull in a patient with neurofibromatosis type 1 - Case report 94
Competing to raise awareness of rare diseases 94
SCN1A and its related epileptic phenotypes 94
Case report: A gain-of-function of hamartin may lead to a distinct "inverse TSC1-hamartin" phenotype characterized by reduced cell growth 93
A mouse model for fetal abnormalities caused by maternal autoantibodies to neuronal or muscle antigens 93
CNS findings in three cases of septo-optic dysplasia, including one with semilobar holoprosencephaly 92
ATAXIA-TELANGIECTASIA 92
Clinical spectrum of woolly hair: Indications for cerebral involvement 92
Spinal neurofibromatosis with central nervous system involvement in a set of twin girls and a boy: further expansion of the phenotype 91
Neurofibromatosis type 1 and infantile spasms 89
The natural history of L-aminoacid decarboxylase (AADC) deficiency: report of two never treated ault patients. 89
Highlights on Genomics Applications for Lysosomal Storage Diseases 89
Design and validation of a custom ngs panel targeting a set of lysosomal storage diseases candidate for nbs applications 88
Unusual form of recurrent multinucleated giant cell granuloma of the mandible and lower extremities in a patient with neurofirbomatosis type 1 87
Biological Approaches to the Treatment of Saline Oily Waste(waters) Originated from Marine Transportation 87
Rett syndrome phenotype following infantile acute encephalopathy. J Child Neurol 2002, 17(9):700-702 IF 1.333 86
Malattie neuromuscolari 86
Congenital myasthenic syndromes: Clinical and molecular report on 7 Sicilian patients 86
SHORT syndrome: a new case with probable AD inheritance 85
The "pubertal switch" in pediatric multiple sclerosis 85
MALATTIE NEURODEGENERATIVE E MALATTIE DA ALTERAZIONE DEI NEUROTRASMETTITORI 85
Two novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus 85
Polydactyly and syndactyly linked to GLI3 and TBX5 mutations: A pediatric case report 84
Dominant myopia? Report on a large Italian family 84
Confronto tra differenti metodi di recupero microbiologico (bioremediation) per il trattamento di “Bilge water 84
Dall’ infanzia all’ eta’ adulta: storia naturale del deficit di decarbossilasi degli aminoacidi aromatici. 84
Displasia setto-ottica ad esordio precoce. Descrizione di un caso con follow-up. Min Pediatr, 54(1): 57-62, 2002 84
Tuberculosis of the ankle in childhood: Clinical, roentgenographic and computed tomography findings 84
Reconstructive Surgery in Children with Down's Syndrome: Bioethical Implications 84
Spectrum of skeletal abnormalities in a complex malformation syndrome with cutis tricolor (Ruggieri-Happle syndrome) 83
Lack of progression of brain atrophy in Aicardi-Goutièeres syndrome 82
Rediagnosing one of Smith's patients (John McCann) with "neuromas tumours" (1849). 82
Septo-optic dysplasia complex: a complex malformation syndrome 82
La condrodisplasia di Schmid: Reperti clinici e radiologici su due pazienti 82
Nevus vascularis mixtus (cutaneous vascular twin nevi) associated with intracranial vascular malformation of the Dyke-Davidoff-Masson type in two patients 82
NEUROEMBRIOLOGIA 81
The multiple faces of artwork diagnoses. 81
Progressive encephalopathy, with oedema, hypsarrhythmia, and optic atrophy (PEHO syndrome): report of the first italian cases 80
Totale 11.423
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Categoria #
all - tutte 57.591
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 57.591
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021567 0 0 0 0 0 27 141 23 117 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
2025/20266.273 533 580 1.635 610 1.266 1.649 0 0 0 0 0 0
Totale 18.052