IRIS
POLIZZI, Agata Rita Maria
 Distribuzione geografica
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Continente #
NA - Nord America 5.938
EU - Europa 2.727
AS - Asia 2.267
SA - Sud America 535
AF - Africa 321
OC - Oceania 16
Continente sconosciuto - Info sul continente non disponibili 1
Totale 11.805
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Nazione #
US - Stati Uniti d'America 5.715
SG - Singapore 1.149
IT - Italia 933
CN - Cina 755
IE - Irlanda 611
UA - Ucraina 512
BR - Brasile 486
CI - Costa d'Avorio 227
CA - Canada 199
RU - Federazione Russa 166
DE - Germania 140
IN - India 140
SE - Svezia 96
GB - Regno Unito 58
SN - Senegal 57
KR - Corea 35
FI - Finlandia 33
FR - Francia 29
VN - Vietnam 28
CH - Svizzera 26
TR - Turchia 24
NL - Olanda 23
BD - Bangladesh 20
UZ - Uzbekistan 20
JP - Giappone 19
PL - Polonia 19
AR - Argentina 18
CZ - Repubblica Ceca 18
MX - Messico 15
GR - Grecia 14
AU - Australia 13
IQ - Iraq 13
AT - Austria 12
HK - Hong Kong 10
NG - Nigeria 10
ZA - Sudafrica 10
BE - Belgio 9
PK - Pakistan 8
LB - Libano 7
MA - Marocco 7
EC - Ecuador 6
ES - Italia 6
IR - Iran 6
PY - Paraguay 6
CO - Colombia 5
SA - Arabia Saudita 5
BG - Bulgaria 4
CL - Cile 4
IL - Israele 4
JM - Giamaica 4
NP - Nepal 4
UY - Uruguay 4
AZ - Azerbaigian 3
BO - Bolivia 3
EE - Estonia 3
KE - Kenya 3
NZ - Nuova Zelanda 3
QA - Qatar 3
VE - Venezuela 3
AE - Emirati Arabi Uniti 2
AL - Albania 2
BT - Bhutan 2
EG - Egitto 2
HU - Ungheria 2
JO - Giordania 2
LU - Lussemburgo 2
PH - Filippine 2
SI - Slovenia 2
SK - Slovacchia (Repubblica Slovacca) 2
TN - Tunisia 2
AM - Armenia 1
AO - Angola 1
BA - Bosnia-Erzegovina 1
BY - Bielorussia 1
CR - Costa Rica 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
EU - Europa 1
GA - Gabon 1
HN - Honduras 1
HR - Croazia 1
ID - Indonesia 1
IS - Islanda 1
KH - Cambogia 1
LA - Repubblica Popolare Democratica del Laos 1
LT - Lituania 1
MY - Malesia 1
NI - Nicaragua 1
OM - Oman 1
TT - Trinidad e Tobago 1
Totale 11.805
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Città #
Santa Clara 885
Chandler 791
Singapore 722
Dublin 608
Jacksonville 607
Houston 575
Chicago 301
Boardman 291
Abidjan 227
Catania 203
Lawrence 178
Cambridge 176
Andover 175
Nanjing 174
Ashburn 155
Toronto 150
Des Moines 108
Kochi 92
Wilmington 87
Civitanova Marche 82
Hefei 79
San Mateo 78
Nanchang 64
Beijing 57
Dakar 57
Hebei 54
Shenyang 51
Bremen 50
Ottawa 40
The Dalles 37
Palermo 36
Rome 34
Seoul 33
Columbus 32
Grafing 32
Saint Petersburg 32
Tianjin 32
Jiaxing 31
Changsha 30
Oakland 30
São Paulo 29
Los Angeles 28
Council Bluffs 27
Milan 26
Falls Church 22
Bussero 21
Dong Ket 18
Tokyo 18
Washington 18
Turku 17
Rio de Janeiro 16
Belo Horizonte 15
Munich 15
New York 15
Redmond 15
Moscow 14
San Francisco 14
Kunming 13
Den Haag 12
Seattle 12
Gela 11
Mumbai 11
Ningbo 11
Abuja 10
Ann Arbor 10
Bologna 10
Hangzhou 10
Milazzo 10
Pune 10
Redwood City 10
Brussels 9
Curitiba 9
Guangzhou 9
Jinan 9
Warsaw 9
Brasília 8
Helsinki 8
Hong Kong 8
Istanbul 8
Lago 8
Lappeenranta 8
Torino 8
Augusta 7
Baghdad 7
Bari 7
Dallas 7
Genova 7
Liberty Lake 7
Melbourne 7
Norwalk 7
Reggio Emilia 7
Tappahannock 7
Betim 6
Brooklyn 6
Dhaka 6
Florence 6
Leawood 6
Lipari 6
Messina 6
Milo 6
Totale 8.163
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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] 219
Natural history of neurofibromatosis type 2 with onset before the age of 1 year. 188
A pilot study on neurological manifestations and antibodies against neuronal antigens in children with haematological and other cancers 176
Familial osteoma of the cranial vault 149
Speckled Lentiginous Nevus Syndrome 138
Encephalocraniocutaneous Lipomatosis (Haberland Syndrome or Fishman Syndrome) 127
Familial osteoma of the cranial vault 112
Blue Rubber Bleb Nevus Syndrome 110
Phacomatosis Pigmentokeratotica 109
Becker's Nevus Syndrome 107
Phacomatosis Pigmentovascularis 105
Prefazione a: La complessità della cultura. Flussi, identità, valori. 100
The natural history of Spinal Neurofibromatosis: A critical review of clinical and genetic features 99
Nevus Sebaceous Syndrome 98
Another "new" form, the palagonia type of acrofacial dysostosis in a sicilian family 92
Cerebellotrigeminal Dermal Dysplasia (Gómez-López-Hernández Syndrome) 92
SCN1B gene: A close relative to SCN1A 92
An 11-year follow-up of neonatal onset bath-induced alternating hemiplegia of childhood in monozygotic twins 91
Cognitive disabilities and bioethical implications in down syndrome 89
Autoimmune thyroiditis and acquired demyelinating poliradiculoneuropathy 88
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 88
Did Cro-Magnon 1 have neurofibromatosis type 2? 87
GRIN2A and GRIN2B and Their Related Phenotypes 87
Two siblings with a homozygous MTHFR C677T (G80A-RFC1) mutation and stroke 85
NEUROEMBRIOLOGIA 84
Mixed Vascular Nevus Syndrome 84
Wyburn-Mason Syndrome 84
Bilateral (perisylvian and opercular) polymicrogyria and Neurofibromatosis type 1 82
Microcephaly-Capillary Malformation Syndrome 82
Hypotonia, congenital nystagmus, ataxia and abnormal auditory brainstem responses. Report on the first white Caucasian patient 81
Bilateral periventricular nodular heterotopia and amniotic band syndrome 80
Multiple Sclerosis in Childhood and other Immune-Mediated Disorders of the Central Nervous System in the Pediatric Age 80
Life-threatening neurological syndrome in Down's syndrome 79
ANOMALIE MALFORMATIVE CEREBRALI ED ENDOCRINOPATIE 79
Archetypical Patterns of Skin Manifestations in Neurocutaneous Disorders 79
Cutis Tricolor 79
Aicardi-Goutières Syndrome Type 2: A Report on Two Cases with Different Phenotypes Caused by RNASEH2B Gene Mutations 79
Analgetic thalamic syndrome in association with thalamic symmetrical abnormalities during measles encephalitis 78
Acute disseminated encephalomyelitis: a long-term prospective study and meta-analysis 78
Multiple sclerosis with onset at 35 months of age 76
Mixed vascular nevus syndrome: a report of four new cases and a literature review 76
ATAXIA-TELANGIECTASIA 76
Hypomelanosis of Ito 76
Manuale di Pediatria, quinta edizione. Capitolo 2 "Anamnesi ed esame obiettivo". Capitolo 29 "Malattie Neurologiche". 75
Earliest clinical manifestations and natural history of neurofibromatosis type 2 in childhood: a study of 24 patients 74
The natural history of L-aminoacid decarboxylase (AADC) deficiency: report of two never treated ault patients. 73
Clinical spectrum of woolly hair: Indications for cerebral involvement 73
Reconstructive Surgery in Children with Down's Syndrome: Bioethical Implications 73
TSC1 and TSC2: Tuberous Sclerosis Complex and Its Related Epilepsy Phenotype 73
Adrenal Disorders and the Paediatric Brain: Pathophysiological Considerations and Clinical Implications 72
Megalencephaly Capillary Malformation Syndrome 72
Antibodies to voltage-gated (VG) ion channels and glutamic acid decarboxylase (GAD) in childhood forms of epilepsies 72
Ossifying fibroma of the skull in a patient with neurofibromatosis type 1 - Case report 71
Dall’ infanzia all’ eta’ adulta: storia naturale del deficit di decarbossilasi degli aminoacidi aromatici. 71
CNS findings in three cases of septo-optic dysplasia, including one with semilobar holoprosencephaly 70
Spinal neurofibromatosis with central nervous system involvement in a set of twin girls and a boy: further expansion of the phenotype 70
Malattie neuromuscolari 70
A mosaic pattern of INI1/SMARCB1 protein expression distinguishes Schwannomatosis and NF2-associated peripheral schwannomas from solitary peripheral schwannomas and NF2-associated vestibular schwannomas 70
Neurofibromatosis type 1 and infantile spasms 69
Dominant myopia? Report on a large Italian family 69
Competing to raise awareness of rare diseases 69
Congenital myasthenic syndromes: Clinical and molecular report on 7 Sicilian patients 69
The multiple faces of artwork diagnoses. 69
At the Origin of Brain Malformations: Embryology of the Central and Peripheral Nervous System 68
Rediagnosing one of Smith's patients (John McCann) with "neuromas tumours" (1849). 68
Unusual form of recurrent multinucleated giant cell granuloma of the mandible and lower extremities in a patient with neurofirbomatosis type 1 68
Biological Approaches to the Treatment of Saline Oily Waste(waters) Originated from Marine Transportation 68
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 68
Confronto tra differenti metodi di recupero microbiologico (bioremediation) per il trattamento di “Bilge water 67
MALATTIE NEURODEGENERATIVE E MALATTIE DA ALTERAZIONE DEI NEUROTRASMETTITORI 67
Displasia setto-ottica ad esordio precoce. Descrizione di un caso con follow-up. Min Pediatr, 54(1): 57-62, 2002 67
SCN1A and its related epileptic phenotypes 67
Septo-optic dysplasia complex: a complex malformation syndrome 65
La condrodisplasia di Schmid: Reperti clinici e radiologici su due pazienti 65
The "pubertal switch" in pediatric multiple sclerosis 65
Progressive encephalopathy, with oedema, hypsarrhythmia, and optic atrophy (PEHO syndrome): report of the first italian cases 65
Cutis tricolor: a literature review and report of five new cases 65
Tuberculosis of the ankle in childhood: Clinical, roentgenographic and computed tomography findings 65
Familial broad terminal phalanges with one individual showing additional anomalies 64
NEUROEMBRIOLOGIA 64
Two novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus 64
Spectrum of skeletal abnormalities in a complex malformation syndrome with cutis tricolor (Ruggieri-Happle syndrome) 64
Rett syndrome phenotype following infantile acute encephalopathy. J Child Neurol 2002, 17(9):700-702 IF 1.333 63
Nevus vascularis mixtus (cutaneous vascular twin nevi) associated with intracranial vascular malformation of the Dyke-Davidoff-Masson type in two patients 63
Early history of neurofibromatosis type 2 and related forms: earliest descriptions of acoustic neuromas, medical curiosities, misconceptions, landmarks and the pioneers behind the eponyms 63
Neurocutaneous melanocytosis (melanosis) 63
Multiple sclerosis in children under 10 years of age 62
THE NEUROFIBROMATOSES: CLINICAL MANIFESTATIONS, NATURAL HISTORY, AND MANAGEMENT 62
SHORT syndrome: a new case with probable AD inheritance 61
Lack of progression of brain atrophy in Aicardi-Goutièeres syndrome 61
Childhood multiple sclerosis (MS) with onset at pre-school age 61
Neuroimaging findings in hypomelanosis of Ito 60
Dystonia as acute adverse reaction to cough suppressant in a 3 year old girl 60
Hyperphenylalaninemia: from diagnosis to therapy. 60
MALATTIE DA DIFETTO DI RIPARAZIONE DEL DNA 60
A mouse model for fetal abnormalities caused by maternal autoantibodies to neuronal or muscle antigens 60
A child with rhombencephalosynapsis, agenesis of the trigeminal ganglion and optic coloboma (without alopecia): A variant of the cerebellotrigeminal dermal dysplasia? 60
The Neurofibromatoses: clinical manifestations, natural history and management 59
Trattamento di Biorigenerazione di Carboni Attivi Saturi per il Recupero di Reflui di Navigazione 59
Neurological Findings in Anderson-Fabry Disease 59
Totale 8.014
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Categoria #
all - tutte 44.513
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 44.513
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211.083 20 86 122 15 270 28 142 23 117 12 194 54
2021/20221.471 135 181 51 36 220 27 205 70 108 18 25 395
2022/20232.293 213 118 44 230 237 390 18 375 515 25 78 50
2023/2024981 59 221 37 49 37 150 33 61 21 22 209 82
2024/20254.027 41 590 243 220 721 462 131 163 297 400 413 346
2025/2026277 277 0 0 0 0 0 0 0 0 0 0 0
Totale 12.131