IRIS
RUGGIERI, MARTINO
 Distribuzione geografica
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Continente #
NA - Nord America 14.834
EU - Europa 10.265
AS - Asia 6.447
SA - Sud America 1.428
AF - Africa 642
OC - Oceania 20
Continente sconosciuto - Info sul continente non disponibili 12
Totale 33.648
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Nazione #
US - Stati Uniti d'America 14.178
IT - Italia 4.901
SG - Singapore 3.318
CN - Cina 2.167
IE - Irlanda 1.789
UA - Ucraina 1.663
BR - Brasile 1.321
CA - Canada 592
RU - Federazione Russa 471
CI - Costa d'Avorio 431
IN - India 407
DE - Germania 373
SE - Svezia 246
FI - Finlandia 132
GB - Regno Unito 129
SN - Senegal 123
FR - Francia 121
KR - Corea 115
NL - Olanda 112
VN - Vietnam 70
CH - Svizzera 69
UZ - Uzbekistan 53
TR - Turchia 48
AT - Austria 44
BD - Bangladesh 44
PL - Polonia 42
GR - Grecia 40
MX - Messico 37
AR - Argentina 32
PK - Pakistan 29
IQ - Iraq 27
CZ - Repubblica Ceca 25
ES - Italia 24
HK - Hong Kong 24
ZA - Sudafrica 24
JP - Giappone 22
LB - Libano 22
NG - Nigeria 20
AU - Australia 18
EC - Ecuador 17
BE - Belgio 16
MA - Marocco 14
IR - Iran 13
RO - Romania 12
SA - Arabia Saudita 12
CL - Cile 11
CO - Colombia 11
EU - Europa 11
BG - Bulgaria 10
JO - Giordania 10
IL - Israele 9
PY - Paraguay 9
VE - Venezuela 9
AE - Emirati Arabi Uniti 8
EG - Egitto 8
TN - Tunisia 8
UY - Uruguay 8
AZ - Azerbaigian 7
KE - Kenya 7
KZ - Kazakistan 6
LT - Lituania 6
NP - Nepal 6
BO - Bolivia 5
EE - Estonia 5
JM - Giamaica 5
BY - Bielorussia 4
HR - Croazia 4
HU - Ungheria 4
PE - Perù 4
PT - Portogallo 4
TT - Trinidad e Tobago 4
BN - Brunei Darussalam 3
DO - Repubblica Dominicana 3
DZ - Algeria 3
GD - Grenada 3
ID - Indonesia 3
KH - Cambogia 3
KW - Kuwait 3
NO - Norvegia 3
PH - Filippine 3
PS - Palestinian Territory 3
QA - Qatar 3
RS - Serbia 3
SK - Slovacchia (Repubblica Slovacca) 3
AL - Albania 2
AO - Angola 2
BA - Bosnia-Erzegovina 2
BB - Barbados 2
CR - Costa Rica 2
DK - Danimarca 2
HN - Honduras 2
NZ - Nuova Zelanda 2
PA - Panama 2
AF - Afghanistan, Repubblica islamica di 1
AM - Armenia 1
BH - Bahrain 1
BS - Bahamas 1
BT - Bhutan 1
BW - Botswana 1
GA - Gabon 1
Totale 33.634
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Città #
Santa Clara 2.201
Singapore 2.022
Chandler 1.877
Jacksonville 1.840
Dublin 1.772
Boardman 839
Chicago 742
Houston 596
Nanjing 561
Catania 552
Lawrence 500
Andover 494
Cambridge 494
Toronto 445
Abidjan 431
Ashburn 378
Milan 339
Rome 306
Kochi 290
Des Moines 289
San Mateo 259
Hefei 257
Wilmington 236
Civitanova Marche 222
Nanchang 182
Shenyang 158
Munich 140
Hebei 126
Dakar 123
Jiaxing 119
Palermo 114
Saint Petersburg 113
Seoul 112
Ottawa 109
Beijing 101
Changsha 101
Bremen 98
São Paulo 89
Tianjin 86
Florence 81
Naples 72
Helsinki 70
Los Angeles 68
Bologna 63
Council Bluffs 62
The Dalles 62
Turin 62
Padova 59
Seattle 59
Grafing 51
Moscow 51
Columbus 50
Dong Ket 46
Rio de Janeiro 42
Bari 41
New York 39
Turku 37
Belo Horizonte 34
Hangzhou 34
Jinan 34
Liberty Lake 34
Norwalk 33
Pune 33
Den Haag 32
Falls Church 32
Oakland 30
Ann Arbor 28
Augusta 28
Genoa 28
Washington 28
Kunming 27
Taormina 27
Brescia 26
Ningbo 25
Brooklyn 23
Redwood City 23
Riposto 23
San Francisco 23
Curitiba 22
Hong Kong 22
Leawood 22
Tokyo 21
Tashkent 20
Ferrara 19
Lappeenranta 19
Abuja 18
Reggio Emilia 18
Gravina di Catania 17
Mumbai 17
Phoenix 17
Warsaw 17
Zhengzhou 17
Adrano 16
Brasília 16
Dhaka 16
Pozzallo 16
Cagliari 15
Campinas 15
Dallas 15
Ragusa 15
Totale 21.723
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Nome #
Dislocazione atlanto-occipitale e atlanto-assiale con grave compressione del midollo spinale nella Sindrome di Down 928
Encefalite da Anticorpi anti-GluR3 in sei pazienti in età pediatrica 750
Sindromi Neurocutanee 559
ESAME NEUROLOGICO 386
CUTIS TRICOLOR (RUGGIERI-HAPPLE SYNDROME) 343
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
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders 205
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
PARALISI CEREBRALI INFANTILI E PARAPLEGIE SPASTICHE EREDITARIE 163
Complex malformation (Ruggieri-Happle) phenotype with “cutis tricolor” in a 10-year-old girl 144
Speckled Lentiginous Nevus Syndrome 137
Encephalocraniocutaneous Lipomatosis (Haberland Syndrome or Fishman Syndrome) 127
Craniofacial anomalies, severe cerebellar hypoplasia, psychomotor and growth delay in a child with congenital hypothyroidism 112
Familial osteoma of the cranial vault 112
Blue Rubber Bleb Nevus Syndrome 110
Anti-MOG Antibody Syndrome and Cerebral Sinovenous Thrombosis: A Cause-Effect Hypothesis 110
Phacomatosis Pigmentokeratotica 109
Malattie neurocutanee 109
Anti-mog associated encephalitis: when steroid therapy is not enough 108
Becker's Nevus Syndrome 106
Phacomatosis Pigmentovascularis 104
Astenia: una maschera per tante identità. Ruolo della patologia della placca neuromuscolare 102
Correction to: Analysis of common methodological flaws in the highest cited e-cigarette epidemiology research (Internal and Emergency Medicine, (2022), 17, 3, (887-909), 10.1007/s11739-022-02967-1) 101
Correlazione genotipo/fenotipo nella Sclerosi Tuberosa (TSC1 vs. TSC2) in 81 pazienti siciliani 101
Congenital muscular dystrophy: from muscle to brain 101
Displasia ossea della volta cranica in un paziente con neurofibromatosi tipo 1 100
The natural history of Spinal Neurofibromatosis: A critical review of clinical and genetic features 99
Paracelso: vita e contributo all'evoluzione delle scienze mediche, umane e neuropsichiatriche 99
Nevus Sebaceous Syndrome 98
A boy born with multiple lesions of atrophoderma 96
Chromosome 2p15-p16.1 microduplication in a boy with congenital anomalies: Is it a distinctive syndrome? 94
A girl with a 14.7 Mb 3q26.32-q28 duplication: a new report of 3q duplication syndrome and a literature review 92
An 11-year follow-up of neonatal onset bath-induced alternating hemiplegia of childhood in monozygotic twins 91
Cerebellotrigeminal Dermal Dysplasia (Gómez-López-Hernández Syndrome) 91
Congenital bone malformations in patients with neurofibromatosis type 1 (Nf1) 90
Melorheostosis: case report with 20-year follow-up 89
Cognitive disabilities and bioethical implications in down syndrome 89
Esame obiettivo neurologico nel bambino 88
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
A case of extreme brain lesions: Which pathogenetic mechanism? 87
Did Cro-Magnon 1 have neurofibromatosis type 2? 87
Malformazioni vascolari nella neurofibromatosi di tipo 1 (NF1) 87
A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment 86
Two siblings with a homozygous MTHFR C677T (G80A-RFC1) mutation and stroke 85
Electrocardiographic Evaluation in Patients With Spinal Muscular Atrophy: A Case-Control Study 85
E se non fossero solo incubi notturni? 85
NEUROEMBRIOLOGIA 84
Hormesis, cellular stress response and neuroinflammation in schizophrenia: early onset versus late onset state 84
Mixed Vascular Nevus Syndrome 84
Recurrent obstructive hydrocephalus in a 4-month-old infant 83
Wyburn-Mason Syndrome 83
Bilateral (perisylvian and opercular) polymicrogyria and Neurofibromatosis type 1 82
Hormesis, cellular stress response, and redox homeostasis in autism spectrum disorders 82
Microcephaly-Capillary Malformation Syndrome 82
Encefalite GluR3: fenotipo clinico e strumentale di quattro pazienti 82
Hypotonia, congenital nystagmus, ataxia and abnormal auditory brainstem responses. Report on the first white Caucasian patient 81
Mutazione PRRT2 in un bambino con caratteristiche dismorfiche, microcefalia congenita e convulsioni epilettiche gravi 81
Bilateral periventricular nodular heterotopia and amniotic band syndrome 80
Neurological manifestations in individuals with isolated or syndromic (Ruggieri-Happle syndrome) phenotypes with “cutis tricolor”: a study of 14 cases 80
Multiple Sclerosis in Childhood and other Immune-Mediated Disorders of the Central Nervous System in the Pediatric Age 80
Neurologia Pediatrica 80
Acute deep vein thrombosis (DVT) of the lower limbs in a 32-year-old man with chronic hypoplasia of the inferior vena cava (HIVC) without risk factors. 80
Ataxia in children: early recognition and clinical evaluation 80
Life-threatening neurological syndrome in Down's syndrome 79
Clinical course of N-methyl-D-aspartate receptor encephalitis and the effectiveness of cyclophosphamide treatment 79
Astenia: Una maschera per tante identità. ruolo della patologia della placca neuromuscolare [Asthenia: A mask for many identities. the role of dysfunction of the neuromuscular junction] 79
Aneurysmal bone cyst of the acromion: a case report 79
Archetypical Patterns of Skin Manifestations in Neurocutaneous Disorders 79
Cutis Tricolor 79
Analgetic thalamic syndrome in association with thalamic symmetrical abnormalities during measles encephalitis 78
Disturbi del sonno: uno studio prospettico pilota basato sulla somministrazione di questionario online. 78
Aicardi-Goutières Syndrome Type 2: A Report on Two Cases with Different Phenotypes Caused by RNASEH2B Gene Mutations 78
MALATTIE NEUROCUTANEE 77
Neurologia e psichiatria dello sviluppo 77
Sindrome del vomito ciclico: analisi di una popolazione di 20 bambini e revisione della letteratura 77
La genetica delle maggiori sindromi neurocutanee 77
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
Acute disseminated encephalomyelitis: a long-term prospective study and meta-analysis 76
Hypomelanosis of Ito 76
Citalopram in the treatment of depression in the elderly 75
Zellweger Syndrome coupled to secondary mitochondrial cytopathy in skeletal muscle cells in an infant: a pattern of biochemical overlapping in metabolic myopathies 75
Earliest clinical manifestations and natural history of neurofibromatosis type 2 in childhood: a study of 24 patients 74
The use of selegiline in the treatment of cognitive deficits in elderly patients 73
Congenital generalized hypertrichosis: the skin as a clue to complex malformation Syndromes. 73
A New Patient with Potocki-Lupski Syndrome: A Literature Review 73
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
Manuale di Pediatria, quinta edizione. Capitolo 2 "Anamnesi ed esame obiettivo". Capitolo 29 "Malattie Neurologiche". 73
Reconstructive Surgery in Children with Down's Syndrome: Bioethical Implications 73
TSC1 and TSC2: Tuberous Sclerosis Complex and Its Related Epilepsy Phenotype 73
Megalencephaly Capillary Malformation Syndrome 72
Off-label use of drugs and adverse drug reactions in pediatric units: A prospective, multicenter study 72
La morte di Iulia Florentina: ipotesi mediche e diagnostiche 72
Aneurismal bone cyst of the acromion: a case report 71
Ossifying fibroma of the skull in a patient with neurofibromatosis type 1 - Case report 71
MALFORMAZIONI CEREBRALI ED IDROCEFALO 71
Totale 11.725
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Categoria #
all - tutte 126.025
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 126.025
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20213.301 33 264 385 43 798 98 429 65 340 135 543 168
2021/20224.137 454 532 57 112 596 79 581 189 405 41 124 967
2022/20236.471 562 258 104 561 644 1.099 75 1.026 1.487 138 303 214
2023/20243.593 233 446 282 308 182 483 152 247 65 142 609 444
2024/202511.657 205 1.702 736 589 2.085 1.107 461 516 904 1.177 1.174 1.001
2025/2026580 580 0 0 0 0 0 0 0 0 0 0 0
Totale 34.504