IRIS
POLIZZI, Agata Rita Maria
 Distribuzione geografica
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Continente #
NA - Nord America 9.688
AS - Asia 4.986
EU - Europa 4.826
SA - Sud America 977
AF - Africa 631
OC - Oceania 20
Continente sconosciuto - Info sul continente non disponibili 1
Totale 21.129
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Nazione #
US - Stati Uniti d'America 9.323
SG - Singapore 2.367
RU - Federazione Russa 1.529
CN - Cina 1.343
IT - Italia 1.186
BR - Brasile 805
IE - Irlanda 605
UA - Ucraina 525
VN - Vietnam 411
CI - Costa d'Avorio 346
CA - Canada 259
FR - Francia 237
IN - India 189
KR - Corea 175
DE - Germania 161
BD - Bangladesh 133
NG - Nigeria 121
GB - Regno Unito 120
SE - Svezia 116
AR - Argentina 71
NL - Olanda 68
MX - Messico 60
SN - Senegal 59
FI - Finlandia 56
HK - Hong Kong 54
JP - Giappone 46
TR - Turchia 39
IQ - Iraq 37
PL - Polonia 37
ZA - Sudafrica 36
CH - Svizzera 31
PK - Pakistan 29
CO - Colombia 28
ES - Italia 27
ID - Indonesia 27
CZ - Repubblica Ceca 25
UZ - Uzbekistan 25
EC - Ecuador 22
AT - Austria 20
AU - Australia 17
GR - Grecia 17
MA - Marocco 17
BJ - Benin 14
JM - Giamaica 14
PY - Paraguay 14
IR - Iran 12
BE - Belgio 11
JO - Giordania 11
VE - Venezuela 11
PH - Filippine 9
SA - Arabia Saudita 9
CL - Cile 8
DZ - Algeria 8
HN - Honduras 8
KE - Kenya 8
LB - Libano 8
AE - Emirati Arabi Uniti 7
PE - Perù 7
EG - Egitto 6
LT - Lituania 6
MY - Malesia 6
NP - Nepal 6
UY - Uruguay 6
AL - Albania 5
BG - Bulgaria 5
BO - Bolivia 5
GT - Guatemala 5
RO - Romania 5
TN - Tunisia 5
AZ - Azerbaigian 4
CR - Costa Rica 4
DO - Repubblica Dominicana 4
ET - Etiopia 4
HU - Ungheria 4
IL - Israele 4
KZ - Kazakistan 4
OM - Oman 4
SK - Slovacchia (Repubblica Slovacca) 4
BY - Bielorussia 3
EE - Estonia 3
HR - Croazia 3
LU - Lussemburgo 3
NZ - Nuova Zelanda 3
PS - Palestinian Territory 3
QA - Qatar 3
SI - Slovenia 3
TT - Trinidad e Tobago 3
AM - Armenia 2
AO - Angola 2
BA - Bosnia-Erzegovina 2
BT - Bhutan 2
CY - Cipro 2
GA - Gabon 2
GE - Georgia 2
KG - Kirghizistan 2
KH - Cambogia 2
MK - Macedonia 2
NI - Nicaragua 2
PT - Portogallo 2
SV - El Salvador 2
Totale 21.107
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Città #
Dallas 1.591
Singapore 1.406
Santa Clara 925
Chandler 791
Moscow 664
San Jose 625
Dublin 602
Jacksonville 601
Houston 588
Ashburn 457
Abidjan 346
Chicago 310
Boardman 290
Los Angeles 272
Hefei 262
Catania 233
Lauterbourg 187
Beijing 182
Lawrence 176
Cambridge 174
Andover 173
Nanjing 173
Seoul 171
Toronto 162
Ho Chi Minh City 134
Des Moines 108
New York 102
Kochi 91
Hanoi 89
Wilmington 88
Civitanova Marche 82
San Mateo 78
Council Bluffs 77
São Paulo 73
Abuja 64
Nanchang 62
Palermo 61
Buffalo 60
Dakar 59
Rome 55
Hebei 54
Shenyang 51
Bremen 50
Hong Kong 50
Lagos 47
Amsterdam 44
Tokyo 42
Ottawa 41
Orem 37
The Dalles 37
Milan 36
Montreal 34
Columbus 33
Grafing 32
Saint Petersburg 32
Tianjin 32
Changsha 31
Jiaxing 30
Oakland 30
Denver 28
Brooklyn 27
Warsaw 27
Lappeenranta 26
Rio de Janeiro 26
Belo Horizonte 25
Atlanta 23
Johannesburg 23
Mexico City 23
Falls Church 22
San Francisco 22
Bussero 21
London 21
Phoenix 21
Washington 21
Bari 20
Seattle 20
Chennai 19
Da Nang 19
Mumbai 19
Redondo Beach 19
Curitiba 18
Dong Ket 18
Frankfurt am Main 18
Poplar 18
Bologna 17
Boston 17
Turku 17
Biên Hòa 16
Haiphong 16
Stockholm 16
Munich 15
Baghdad 14
Cotonou 14
Redmond 14
Brasília 13
Helsinki 13
Kunming 13
Manchester 13
Den Haag 12
Hangzhou 12
Totale 14.163
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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] 285
A pilot study on neurological manifestations and antibodies against neuronal antigens in children with haematological and other cancers 249
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 209
Speckled Lentiginous Nevus Syndrome 207
Becker's Nevus Syndrome 196
Manuale di Pediatria, quinta edizione. Capitolo 2 "Anamnesi ed esame obiettivo". Capitolo 29 "Malattie Neurologiche". 196
Encephalocraniocutaneous Lipomatosis (Haberland Syndrome or Fishman Syndrome) 194
Familial osteoma of the cranial vault 185
Phacomatosis Pigmentovascularis 183
Blue Rubber Bleb Nevus Syndrome 176
At the Origin of Brain Malformations: Embryology of the Central and Peripheral Nervous System 175
Nevus Sebaceous Syndrome 173
Periventricular Heterotopias: Neuroependymal Abnormalities 171
Phacomatosis Pigmentokeratotica 170
Cutis Tricolor 162
Aicardi-Goutières Syndrome Type 2: A Report on Two Cases with Different Phenotypes Caused by RNASEH2B Gene Mutations 162
Cerebellotrigeminal Dermal Dysplasia (Gómez-López-Hernández Syndrome) 161
Megalencephaly Capillary Malformation Syndrome 158
Wyburn-Mason Syndrome 156
GRIN2A and GRIN2B and Their Related Phenotypes 156
Prefazione a: La complessità della cultura. Flussi, identità, valori. 155
Another "new" form, the palagonia type of acrofacial dysostosis in a sicilian family 154
Archetypical Patterns of Skin Manifestations in Neurocutaneous Disorders 150
Familial osteoma of the cranial vault 149
A child with rhombencephalosynapsis, agenesis of the trigeminal ganglion and optic coloboma (without alopecia): A variant of the cerebellotrigeminal dermal dysplasia? 149
Acute disseminated encephalomyelitis: a long-term prospective study and meta-analysis 148
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 148
Microcephaly-Capillary Malformation Syndrome 146
An 11-year follow-up of neonatal onset bath-induced alternating hemiplegia of childhood in monozygotic twins 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 145
Klippel-Trenaunay Syndrome, Segmental/Focal Overgrowth Malformations: A Review 143
SCN1B gene: A close relative to SCN1A 143
Anomalies of Midbrain/Hindbrain Development and Related Disabilities: Pontocerebellar Hypoplasia, Congenital Disorders of Glycosylation, and Cerebellar Hemisphere Hypoplasia 141
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 141
Hypomelanosis of Ito 140
Microcephaly and Its Related Syndromes: Classification, Genetic, Clinical, and Rehabilitative Considerations 139
Maternal Phenylketonuria and Offspring Outcome: A Retrospective Study with a Systematic Review of the Literature 134
Mixed Vascular Nevus Syndrome 133
Autoimmune thyroiditis and acquired demyelinating poliradiculoneuropathy 133
Motor imagery for paediatric neurorehabilitation: how much do we know? Perspectives from a systematic review 132
Did Cro-Magnon 1 have neurofibromatosis type 2? 132
Neurocutaneous melanocytosis (melanosis) 132
Genotype–Phenotype Correlation in a Large Cohort of Eastern Sicilian Patients Affected by Phenylketonuria: Newborn Screening Program, Clinical Features, and Follow-Up 131
ANOMALIE MALFORMATIVE CEREBRALI ED ENDOCRINOPATIE 131
Anomalies of Midbrain/Hindbrain Development: Malformations of Cerebellum: Diagnosis, Classification, and Rehabilitative Hypothesis 130
Adrenal Disorders and the Paediatric Brain: Pathophysiological Considerations and Clinical Implications 127
Analgetic thalamic syndrome in association with thalamic symmetrical abnormalities during measles encephalitis 126
Antibodies to voltage-gated (VG) ion channels and glutamic acid decarboxylase (GAD) in childhood forms of epilepsies 126
Cognitive disabilities and bioethical implications in down syndrome 126
Cutis tricolor: a literature review and report of five new cases 125
The natural history of Spinal Neurofibromatosis: A critical review of clinical and genetic features 124
TSC1 and TSC2: Tuberous Sclerosis Complex and Its Related Epilepsy Phenotype 120
Near-infrared spectroscopy (NIRS) as a tool to prevent cerebral desaturation in newborns with bradycardia events: A systematic review 119
Earliest clinical manifestations and natural history of neurofibromatosis type 2 in childhood: a study of 24 patients 117
Introduction to phacomatoses (neurocutaneous disorders) in childhood 117
Mixed vascular nevus syndrome: a report of four new cases and a literature review 115
Polydactyly and syndactyly linked to GLI3 and TBX5 mutations: A pediatric case report 114
Hypotonia, congenital nystagmus, ataxia and abnormal auditory brainstem responses. Report on the first white Caucasian patient 113
Multiple Sclerosis in Childhood and other Immune-Mediated Disorders of the Central Nervous System in the Pediatric Age 113
SCN8A and Its Related Epileptic Phenotypes 112
Life-threatening neurological syndrome in Down's syndrome 111
Bilateral periventricular nodular heterotopia and amniotic band syndrome 110
Two siblings with a homozygous MTHFR C677T (G80A-RFC1) mutation and stroke 110
Spinal neurofibromatosis with central nervous system involvement in a set of twin girls and a boy: further expansion of the phenotype 110
Bilateral (perisylvian and opercular) polymicrogyria and Neurofibromatosis type 1 110
Progressive Depletion of B and T Lymphocytes in Patients with Ataxia Telangiectasia: Results of the Italian Primary Immunodeficiency Network 110
Malattie neuromuscolari 109
Reconstructive Surgery in Children with Down's Syndrome: Bioethical Implications 109
SCN1A and its related epileptic phenotypes 109
Investigating the Role of the Zinc Finger Protein ZC2HC1C on Autism Spectrum Disorder Susceptibility 107
Case report: A gain-of-function of hamartin may lead to a distinct "inverse TSC1-hamartin" phenotype characterized by reduced cell growth 107
Ossifying fibroma of the skull in a patient with neurofibromatosis type 1 - Case report 107
Nevus vascularis mixtus (cutaneous vascular twin nevi) associated with intracranial vascular malformation of the Dyke-Davidoff-Masson type in two patients 107
CNS findings in three cases of septo-optic dysplasia, including one with semilobar holoprosencephaly 106
NEUROEMBRIOLOGIA 105
A mouse model for fetal abnormalities caused by maternal autoantibodies to neuronal or muscle antigens 105
Multiple sclerosis with onset at 35 months of age 103
Competing to raise awareness of rare diseases 103
Highlights on Genomics Applications for Lysosomal Storage Diseases 103
Malformations of the Spinal Cord: From Genetics to Diagnosis and Rehabilitation 102
Clinical spectrum of woolly hair: Indications for cerebral involvement 102
ATAXIA-TELANGIECTASIA 101
The natural history of L-aminoacid decarboxylase (AADC) deficiency: report of two never treated ault patients. 101
Design and validation of a custom ngs panel targeting a set of lysosomal storage diseases candidate for nbs applications 100
Influence of the cerebellum in paediatric epilepsy: A comprehensive systematic literature review focusing on neurodevelopmental/neuropsychological implications 99
Tuberculosis of the ankle in childhood: Clinical, roentgenographic and computed tomography findings 99
Neonatal Hyperekplexia: Is It Still a Diagnostic Challenge? Evidence From a Systematic Review 98
Neurofibromatosis type 1 and infantile spasms 97
Dominant myopia? Report on a large Italian family 97
MALATTIE NEURODEGENERATIVE E MALATTIE DA ALTERAZIONE DEI NEUROTRASMETTITORI 97
Congenital myasthenic syndromes: Clinical and molecular report on 7 Sicilian patients 97
At the Basis of Brain Malformations: Brain Plasticity, Developmental Neurobiology, and Considerations for Rehabilitation 96
Rediagnosing one of Smith's patients (John McCann) with "neuromas tumours" (1849). 95
Displasia setto-ottica ad esordio precoce. Descrizione di un caso con follow-up. Min Pediatr, 54(1): 57-62, 2002 95
Biological Approaches to the Treatment of Saline Oily Waste(waters) Originated from Marine Transportation 95
Unusual form of recurrent multinucleated giant cell granuloma of the mandible and lower extremities in a patient with neurofirbomatosis type 1 94
Confronto tra differenti metodi di recupero microbiologico (bioremediation) per il trattamento di “Bilge water 94
Spectrum of skeletal abnormalities in a complex malformation syndrome with cutis tricolor (Ruggieri-Happle syndrome) 94
Ohtahara syndrome with emphasis on recent genetic discovery. 93
Totale 13.247
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Categoria #
all - tutte 68.174
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 68.174
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
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
2024/20254.007 41 585 241 220 715 459 131 162 297 398 411 347
2025/20269.542 535 736 1.665 624 1.324 1.739 1.024 253 579 467 318 278
2026/2027147 147 0 0 0 0 0 0 0 0 0 0 0
Totale 21.473