IRIS
POLIZZI, Agata Rita Maria
 Distribuzione geografica
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Continente #
NA - Nord America 5.677
EU - Europa 2.590
AS - Asia 1.828
SA - Sud America 367
AF - Africa 305
OC - Oceania 16
Continente sconosciuto - Info sul continente non disponibili 1
Totale 10.784
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Nazione #
US - Stati Uniti d'America 5.474
SG - Singapore 1.006
IT - Italia 868
CN - Cina 658
IE - Irlanda 611
UA - Ucraina 507
BR - Brasile 339
CI - Costa d'Avorio 227
CA - Canada 188
RU - Federazione Russa 164
DE - Germania 127
SE - Svezia 93
SN - Senegal 56
GB - Regno Unito 46
IN - India 28
FR - Francia 27
CH - Svizzera 26
NL - Olanda 23
TR - Turchia 19
JP - Giappone 18
UZ - Uzbekistan 18
VN - Vietnam 18
CZ - Repubblica Ceca 15
FI - Finlandia 14
GR - Grecia 14
AU - Australia 13
PL - Polonia 13
AT - Austria 11
HK - Hong Kong 10
MX - Messico 10
NG - Nigeria 10
AR - Argentina 9
BE - Belgio 9
BD - Bangladesh 7
LB - Libano 7
IR - Iran 6
PK - Pakistan 5
BG - Bulgaria 4
CL - Cile 4
CO - Colombia 4
IL - Israele 4
MA - Marocco 4
ZA - Sudafrica 4
EC - Ecuador 3
EE - Estonia 3
IQ - Iraq 3
NZ - Nuova Zelanda 3
PY - Paraguay 3
QA - Qatar 3
BT - Bhutan 2
ES - Italia 2
HU - Ungheria 2
JO - Giordania 2
LU - Lussemburgo 2
NP - Nepal 2
PH - Filippine 2
SI - Slovenia 2
SK - Slovacchia (Repubblica Slovacca) 2
UY - Uruguay 2
VE - Venezuela 2
AE - Emirati Arabi Uniti 1
AM - Armenia 1
AZ - Azerbaigian 1
BA - Bosnia-Erzegovina 1
BO - Bolivia 1
BY - Bielorussia 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
EG - Egitto 1
EU - Europa 1
HN - Honduras 1
HR - Croazia 1
ID - Indonesia 1
IS - Islanda 1
JM - Giamaica 1
KE - Kenya 1
KH - Cambogia 1
KR - Corea 1
LA - Repubblica Popolare Democratica del Laos 1
LT - Lituania 1
MY - Malesia 1
NI - Nicaragua 1
OM - Oman 1
SA - Arabia Saudita 1
TN - Tunisia 1
TT - Trinidad e Tobago 1
Totale 10.784
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Città #
Santa Clara 877
Chandler 791
Dublin 608
Jacksonville 607
Singapore 578
Houston 571
Chicago 298
Boardman 291
Abidjan 227
Catania 183
Lawrence 178
Cambridge 176
Andover 175
Nanjing 174
Toronto 146
Ashburn 130
Des Moines 108
Wilmington 87
Civitanova Marche 82
San Mateo 78
Nanchang 64
Dakar 56
Hebei 54
Shenyang 51
Bremen 50
Beijing 41
Ottawa 40
Rome 33
Grafing 32
Saint Petersburg 32
Tianjin 32
Jiaxing 31
Changsha 30
Oakland 30
Council Bluffs 27
Milan 25
Palermo 23
Falls Church 22
Bussero 21
Los Angeles 21
Dong Ket 18
Tokyo 17
Redmond 15
São Paulo 15
Washington 15
Belo Horizonte 13
Kunming 13
Moscow 13
Den Haag 12
Rio de Janeiro 12
Seattle 12
Gela 11
Ningbo 11
Abuja 10
Ann Arbor 10
Bologna 10
Hangzhou 10
Milazzo 10
Redwood City 10
San Francisco 10
Brussels 9
Guangzhou 9
Jinan 9
Pune 9
Curitiba 8
Helsinki 8
Hong Kong 8
Lago 8
Mumbai 8
The Dalles 8
Torino 8
Augusta 7
Bari 7
Genova 7
Istanbul 7
Liberty Lake 7
Melbourne 7
Norwalk 7
Reggio Emilia 7
Tappahannock 7
Brasília 6
Florence 6
Lappeenranta 6
Leawood 6
Lipari 6
Milo 6
Riposto 6
Alvignano 5
Belford Roxo 5
Betim 5
Campinas 5
Casalnuovo Di Napoli 5
Dearborn 5
Edinburgh 5
Hanover 5
Messina 5
Mestre 5
Munich 5
Providence 5
Vicenza 5
Totale 7.589
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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] 215
Natural history of neurofibromatosis type 2 with onset before the age of 1 year. 182
A pilot study on neurological manifestations and antibodies against neuronal antigens in children with haematological and other cancers 168
Familial osteoma of the cranial vault 141
Speckled Lentiginous Nevus Syndrome 133
Encephalocraniocutaneous Lipomatosis (Haberland Syndrome or Fishman Syndrome) 117
Familial osteoma of the cranial vault 105
Phacomatosis Pigmentokeratotica 104
Blue Rubber Bleb Nevus Syndrome 103
Phacomatosis Pigmentovascularis 100
Becker's Nevus Syndrome 96
Prefazione a: La complessità della cultura. Flussi, identità, valori. 94
The natural history of Spinal Neurofibromatosis: A critical review of clinical and genetic features 93
Nevus Sebaceous Syndrome 93
SCN1B gene: A close relative to SCN1A 91
Another "new" form, the palagonia type of acrofacial dysostosis in a sicilian family 87
An 11-year follow-up of neonatal onset bath-induced alternating hemiplegia of childhood in monozygotic twins 86
Autoimmune thyroiditis and acquired demyelinating poliradiculoneuropathy 84
Cerebellotrigeminal Dermal Dysplasia (Gómez-López-Hernández Syndrome) 83
Did Cro-Magnon 1 have neurofibromatosis type 2? 82
NEUROEMBRIOLOGIA 81
Cognitive disabilities and bioethical implications in down syndrome 81
GRIN2A and GRIN2B and Their Related Phenotypes 81
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 79
Two siblings with a homozygous MTHFR C677T (G80A-RFC1) mutation and stroke 78
Wyburn-Mason Syndrome 78
Hypotonia, congenital nystagmus, ataxia and abnormal auditory brainstem responses. Report on the first white Caucasian patient 77
Bilateral periventricular nodular heterotopia and amniotic band syndrome 77
Bilateral (perisylvian and opercular) polymicrogyria and Neurofibromatosis type 1 77
Analgetic thalamic syndrome in association with thalamic symmetrical abnormalities during measles encephalitis 75
Multiple Sclerosis in Childhood and other Immune-Mediated Disorders of the Central Nervous System in the Pediatric Age 75
Mixed Vascular Nevus Syndrome 75
ANOMALIE MALFORMATIVE CEREBRALI ED ENDOCRINOPATIE 74
Archetypical Patterns of Skin Manifestations in Neurocutaneous Disorders 74
Cutis Tricolor 74
Microcephaly-Capillary Malformation Syndrome 73
Acute disseminated encephalomyelitis: a long-term prospective study and meta-analysis 72
Multiple sclerosis with onset at 35 months of age 71
Life-threatening neurological syndrome in Down's syndrome 71
Earliest clinical manifestations and natural history of neurofibromatosis type 2 in childhood: a study of 24 patients 71
Hypomelanosis of Ito 71
ATAXIA-TELANGIECTASIA 70
Clinical spectrum of woolly hair: Indications for cerebral involvement 70
The natural history of L-aminoacid decarboxylase (AADC) deficiency: report of two never treated ault patients. 69
Mixed vascular nevus syndrome: a report of four new cases and a literature review 68
Dominant myopia? Report on a large Italian family 68
Dall’ infanzia all’ eta’ adulta: storia naturale del deficit di decarbossilasi degli aminoacidi aromatici. 68
Adrenal Disorders and the Paediatric Brain: Pathophysiological Considerations and Clinical Implications 68
Aicardi-Goutières Syndrome Type 2: A Report on Two Cases with Different Phenotypes Caused by RNASEH2B Gene Mutations 68
TSC1 and TSC2: Tuberous Sclerosis Complex and Its Related Epilepsy Phenotype 68
Malattie neuromuscolari 67
Biological Approaches to the Treatment of Saline Oily Waste(waters) Originated from Marine Transportation 67
Antibodies to voltage-gated (VG) ion channels and glutamic acid decarboxylase (GAD) in childhood forms of epilepsies 67
CNS findings in three cases of septo-optic dysplasia, including one with semilobar holoprosencephaly 66
Reconstructive Surgery in Children with Down's Syndrome: Bioethical Implications 66
Unusual form of recurrent multinucleated giant cell granuloma of the mandible and lower extremities in a patient with neurofirbomatosis type 1 65
Megalencephaly Capillary Malformation Syndrome 65
Manuale di Pediatria, quinta edizione. Capitolo 2 "Anamnesi ed esame obiettivo". Capitolo 29 "Malattie Neurologiche". 65
Rediagnosing one of Smith's patients (John McCann) with "neuromas tumours" (1849). 64
Neurofibromatosis type 1 and infantile spasms 64
Ossifying fibroma of the skull in a patient with neurofibromatosis type 1 - Case report 64
Confronto tra differenti metodi di recupero microbiologico (bioremediation) per il trattamento di “Bilge water 64
Displasia setto-ottica ad esordio precoce. Descrizione di un caso con follow-up. Min Pediatr, 54(1): 57-62, 2002 64
The multiple faces of artwork diagnoses. 64
SCN1A and its related epileptic phenotypes 64
Septo-optic dysplasia complex: a complex malformation syndrome 63
NEUROEMBRIOLOGIA 63
MALATTIE NEURODEGENERATIVE E MALATTIE DA ALTERAZIONE DEI NEUROTRASMETTITORI 63
A mosaic pattern of INI1/SMARCB1 protein expression distinguishes Schwannomatosis and NF2-associated peripheral schwannomas from solitary peripheral schwannomas and NF2-associated vestibular schwannomas 63
Competing to raise awareness of rare diseases 63
Congenital myasthenic syndromes: Clinical and molecular report on 7 Sicilian patients 63
La condrodisplasia di Schmid: Reperti clinici e radiologici su due pazienti 62
Spinal neurofibromatosis with central nervous system involvement in a set of twin girls and a boy: further expansion of the phenotype 62
Progressive encephalopathy, with oedema, hypsarrhythmia, and optic atrophy (PEHO syndrome): report of the first italian cases 61
Early history of neurofibromatosis type 2 and related forms: earliest descriptions of acoustic neuromas, medical curiosities, misconceptions, landmarks and the pioneers behind the eponyms 61
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 61
The "pubertal switch" in pediatric multiple sclerosis 60
Multiple sclerosis in children under 10 years of age 60
Cutis tricolor: a literature review and report of five new cases 60
Spectrum of skeletal abnormalities in a complex malformation syndrome with cutis tricolor (Ruggieri-Happle syndrome) 60
Neuroimaging findings in hypomelanosis of Ito 59
THE NEUROFIBROMATOSES: CLINICAL MANIFESTATIONS, NATURAL HISTORY, AND MANAGEMENT 59
Two novel SCN1A missense mutations in generalized epilepsy with febrile seizures plus 59
Tuberculosis of the ankle in childhood: Clinical, roentgenographic and computed tomography findings 59
SHORT syndrome: a new case with probable AD inheritance 58
Rett syndrome phenotype following infantile acute encephalopathy. J Child Neurol 2002, 17(9):700-702 IF 1.333 58
Fatal biphasic brainstem and spinal leptomeningitis with Cryptococcus neoformans in a non-immunocompromised child. Acta Paediatr 58
Familial broad terminal phalanges with one individual showing additional anomalies 58
Nevus vascularis mixtus (cutaneous vascular twin nevi) associated with intracranial vascular malformation of the Dyke-Davidoff-Masson type in two patients 58
Recurrent facial paralysis in a child with renovascular hypertension 57
Dystonia as acute adverse reaction to cough suppressant in a 3 year old girl 57
Childhood multiple sclerosis (MS) with onset at pre-school age 57
The Neurofibromatoses: clinical manifestations, natural history and management 57
MALATTIE DA DIFETTO DI RIPARAZIONE DEL DNA 57
Trattamento di Biorigenerazione di Carboni Attivi Saturi per il Recupero di Reflui di Navigazione 56
Neurological Findings in Anderson-Fabry Disease 56
Lack of progression of brain atrophy in Aicardi-Goutièeres syndrome 55
Neuronopathic Gaucher disease 55
Hyperphenylalaninemia: from diagnosis to therapy. 55
Pediatric idiopathic intracranial hypertension and the underlying endocrine-metabolic dysfunction: a pilot study. 55
Totale 7.503
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Categoria #
all - tutte 40.000
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 40.000
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020165 0 0 0 0 0 0 0 0 0 0 109 56
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
2024/20253.280 41 590 243 220 721 463 133 163 297 402 7 0
Totale 11.107