IRIS
RUGGIERI, MARTINO
 Distribuzione geografica
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Continente #
NA - Nord America 20.155
EU - Europa 10.743
AS - Asia 9.292
SA - Sud America 2.251
AF - Africa 1.014
OC - Oceania 24
Continente sconosciuto - Info sul continente non disponibili 15
Totale 43.494
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Nazione #
US - Stati Uniti d'America 19.399
IT - Italia 5.152
SG - Singapore 4.197
CN - Cina 3.345
BR - Brasile 1.963
IE - Irlanda 1.779
UA - Ucraina 1.660
CI - Costa d'Avorio 731
CA - Canada 637
RU - Federazione Russa 479
IN - India 459
VN - Vietnam 386
DE - Germania 381
KR - Corea 327
SE - Svezia 269
GB - Regno Unito 205
FI - Finlandia 150
FR - Francia 127
NL - Olanda 126
SN - Senegal 123
AR - Argentina 112
MX - Messico 82
BD - Bangladesh 75
PL - Polonia 75
CH - Svizzera 70
ZA - Sudafrica 61
UZ - Uzbekistan 59
EC - Ecuador 58
TR - Turchia 57
JP - Giappone 54
ID - Indonesia 53
AT - Austria 49
ES - Italia 46
GR - Grecia 40
IR - Iran 37
HK - Hong Kong 36
IQ - Iraq 36
PK - Pakistan 33
CO - Colombia 30
CZ - Repubblica Ceca 28
MA - Marocco 26
LB - Libano 22
NG - Nigeria 20
VE - Venezuela 20
PY - Paraguay 19
AU - Australia 18
BE - Belgio 17
RO - Romania 16
SA - Arabia Saudita 16
AE - Emirati Arabi Uniti 15
CL - Cile 14
LT - Lituania 14
EG - Egitto 13
PE - Perù 13
BG - Bulgaria 11
EU - Europa 11
IL - Israele 11
UY - Uruguay 11
TN - Tunisia 10
JO - Giordania 9
KE - Kenya 9
AZ - Azerbaigian 8
BO - Bolivia 7
DZ - Algeria 7
KZ - Kazakistan 7
BY - Bielorussia 6
DO - Repubblica Dominicana 6
NP - Nepal 6
BN - Brunei Darussalam 5
EE - Estonia 5
JM - Giamaica 5
AL - Albania 4
AO - Angola 4
CR - Costa Rica 4
DK - Danimarca 4
GD - Grenada 4
HR - Croazia 4
HU - Ungheria 4
KW - Kuwait 4
MY - Malesia 4
PH - Filippine 4
PT - Portogallo 4
QA - Qatar 4
TT - Trinidad e Tobago 4
XK - ???statistics.table.value.countryCode.XK??? 4
BB - Barbados 3
BH - Bahrain 3
ET - Etiopia 3
GY - Guiana 3
HN - Honduras 3
KH - Cambogia 3
NO - Norvegia 3
OM - Oman 3
PS - Palestinian Territory 3
RS - Serbia 3
SK - Slovacchia (Repubblica Slovacca) 3
AM - Armenia 2
BA - Bosnia-Erzegovina 2
BW - Botswana 2
LA - Repubblica Popolare Democratica del Laos 2
Totale 43.460
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Città #
Dallas 4.047
Santa Clara 2.219
Singapore 2.199
Chandler 1.877
Jacksonville 1.827
Dublin 1.761
Boardman 836
Hefei 796
Chicago 755
Abidjan 731
Houston 617
Ashburn 578
Catania 567
Nanjing 557
Lawrence 497
Andover 491
Cambridge 491
Toronto 452
Los Angeles 394
Beijing 373
Milan 358
Seoul 322
Rome 321
Des Moines 290
Kochi 288
San Mateo 257
Wilmington 233
Civitanova Marche 222
Nanchang 180
São Paulo 168
Shenyang 157
Ho Chi Minh City 145
Munich 140
Palermo 129
Hebei 126
Dakar 123
Jiaxing 118
New York 115
Saint Petersburg 111
Ottawa 109
Changsha 101
Bremen 98
Florence 91
Naples 89
Tianjin 84
Hanoi 71
Helsinki 70
Bologna 67
Rio de Janeiro 67
Council Bluffs 65
Seattle 65
The Dalles 62
Turin 62
Padova 59
Bari 57
Moscow 52
Belo Horizonte 51
Grafing 51
Columbus 50
Tokyo 50
Warsaw 49
Brooklyn 48
Dong Ket 46
Phoenix 40
Johannesburg 38
Redondo Beach 38
Lappeenranta 37
Turku 37
Montreal 35
Curitiba 34
Hangzhou 34
Hong Kong 34
Jinan 34
Liberty Lake 34
Pune 34
Buffalo 33
Chennai 33
Norwalk 33
Boston 32
Den Haag 32
Falls Church 32
Augusta 31
San Francisco 31
Washington 31
Denver 30
Oakland 30
Stockholm 30
Genoa 28
Ann Arbor 27
Kunming 27
Taormina 27
Tashkent 27
Atlanta 26
Brasília 26
Brescia 26
Mexico City 25
Mumbai 25
Ningbo 25
London 24
Tehran 24
Totale 28.626
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Nome #
Dislocazione atlanto-occipitale e atlanto-assiale con grave compressione del midollo spinale nella Sindrome di Down 963
Encefalite da Anticorpi anti-GluR3 in sei pazienti in età pediatrica 800
Sindromi Neurocutanee 609
ESAME NEUROLOGICO 423
Expanding genotype-phenotype correlation of Kenny-Caffey syndrome type 1 394
CUTIS TRICOLOR (RUGGIERI-HAPPLE SYNDROME) 377
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] 240
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders 226
Natural history of neurofibromatosis type 2 with onset before the age of 1 year. 207
A pilot study on neurological manifestations and antibodies against neuronal antigens in children with haematological and other cancers 202
PARALISI CEREBRALI INFANTILI E PARAPLEGIE SPASTICHE EREDITARIE 178
A boy born with multiple lesions of atrophoderma 159
A mosaic pattern of INI1/SMARCB1 protein expression distinguishes Schwannomatosis and NF2-associated peripheral schwannomas from solitary peripheral schwannomas and NF2-associated vestibular schwannomas 159
Speckled Lentiginous Nevus Syndrome 158
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) 156
Manuale di Pediatria, quinta edizione. Capitolo 2 "Anamnesi ed esame obiettivo". Capitolo 29 "Malattie Neurologiche". 155
Encephalocraniocutaneous Lipomatosis (Haberland Syndrome or Fishman Syndrome) 154
Complex malformation (Ruggieri-Happle) phenotype with “cutis tricolor” in a 10-year-old girl 152
Becker's Nevus Syndrome 143
Anti-MOG Antibody Syndrome and Cerebral Sinovenous Thrombosis: A Cause-Effect Hypothesis 143
Anti-mog associated encephalitis: when steroid therapy is not enough 140
Astenia: una maschera per tante identità. Ruolo della patologia della placca neuromuscolare 133
Blue Rubber Bleb Nevus Syndrome 132
Phacomatosis Pigmentovascularis 132
A girl with a 14.7 Mb 3q26.32-q28 duplication: a new report of 3q duplication syndrome and a literature review 131
Phacomatosis Pigmentokeratotica 130
A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment 129
Craniofacial anomalies, severe cerebellar hypoplasia, psychomotor and growth delay in a child with congenital hypothyroidism 128
Autoimmune encephalitis and CSF anti-AMPA GluR3 antibodies in childhood: a case report and literature review 125
Familial osteoma of the cranial vault 125
Nevus Sebaceous Syndrome 124
A case of extreme brain lesions: Which pathogenetic mechanism? 120
A New Patient with Potocki-Lupski Syndrome: A Literature Review 120
Aicardi-Goutières Syndrome Type 2: A Report on Two Cases with Different Phenotypes Caused by RNASEH2B Gene Mutations 120
A highly sensitive colorimetric approach based on tris (bipyridine) Ruthenium (II/III) mediator for the enzymatic detection of phenylalanine 118
Malattie neurocutanee 118
Paracelso: vita e contributo all'evoluzione delle scienze mediche, umane e neuropsichiatriche 117
Cerebellotrigeminal Dermal Dysplasia (Gómez-López-Hernández Syndrome) 116
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. 115
Aneurysmal bone cyst of the acromion: a case report 114
An 11-year follow-up of neonatal onset bath-induced alternating hemiplegia of childhood in monozygotic twins 113
Correlazione genotipo/fenotipo nella Sclerosi Tuberosa (TSC1 vs. TSC2) in 81 pazienti siciliani 112
E se non fossero solo incubi notturni? 112
Displasia ossea della volta cranica in un paziente con neurofibromatosi tipo 1 110
Congenital muscular dystrophy: from muscle to brain 110
Wyburn-Mason Syndrome 110
The natural history of Spinal Neurofibromatosis: A critical review of clinical and genetic features 109
Electrocardiographic Evaluation in Patients With Spinal Muscular Atrophy: A Case-Control Study 109
Congenital bone malformations in patients with neurofibromatosis type 1 (Nf1) 107
Megalencephaly Capillary Malformation Syndrome 107
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] 105
Malformazioni vascolari nella neurofibromatosi di tipo 1 (NF1) 105
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 104
Chromosome 2p15-p16.1 microduplication in a boy with congenital anomalies: Is it a distinctive syndrome? 104
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 104
A critical appraisal of neurological evidence on paediatric COVID-19 patients. A systematic literature review 103
Autoimmune thyroiditis and acquired demyelinating poliradiculoneuropathy 103
A child with rhombencephalosynapsis, agenesis of the trigeminal ganglion and optic coloboma (without alopecia): A variant of the cerebellotrigeminal dermal dysplasia? 103
Need for palliative care from birth to infancy in pediatric patients with neurological diseases 102
A Phenylalanine sensor exploiting a capacitive readout strategy embedding a selective enzymatic mechanism 102
Melorheostosis: case report with 20-year follow-up 102
Acute disseminated encephalomyelitis: a long-term prospective study and meta-analysis 102
A Complex Brain Malformation Syndrome with Rhombencephalosynapsis, Preaxial Hexadactyly plus Facial and Skull Anomalies 101
Did Cro-Magnon 1 have neurofibromatosis type 2? 101
Microcephaly-Capillary Malformation Syndrome 101
Mixed Vascular Nevus Syndrome 100
Archetypical Patterns of Skin Manifestations in Neurocutaneous Disorders 100
Cognitive disabilities and bioethical implications in down syndrome 100
Off-label use of drugs and adverse drug reactions in pediatric units: A prospective, multicenter study 100
Clinical course of N-methyl-D-aspartate receptor encephalitis and the effectiveness of cyclophosphamide treatment 99
Esame obiettivo neurologico nel bambino 99
Mutazione PRRT2 in un bambino con caratteristiche dismorfiche, microcefalia congenita e convulsioni epilettiche gravi 99
Ataxia in children: early recognition and clinical evaluation 99
Neurocutaneous melanocytosis (melanosis) 99
The use of selegiline in the treatment of cognitive deficits in elderly patients 98
Aneurismal bone cyst of the acromion: a case report 98
Cutis Tricolor 98
A novel GABRB3 variant in Dravet syndrome: Case report and literature review 98
Recurrent obstructive hydrocephalus in a 4-month-old infant 97
Zellweger Syndrome coupled to secondary mitochondrial cytopathy in skeletal muscle cells in an infant: a pattern of biochemical overlapping in metabolic myopathies 97
Two siblings with a homozygous MTHFR C677T (G80A-RFC1) mutation and stroke 96
A child with congenital heart disease and situs viscerum inversus 96
Hormesis, cellular stress response, and redox homeostasis in autism spectrum disorders 96
A clinical and molecular study in a child under 1 year of age affected by Neurofibromatosis type 2 96
Hypomelanosis of Ito 96
Disturbi del sonno: uno studio prospettico pilota basato sulla somministrazione di questionario online. 96
La morte di Iulia Florentina: ipotesi mediche e diagnostiche 96
Hypotonia, congenital nystagmus, ataxia and abnormal auditory brainstem responses. Report on the first white Caucasian patient 95
Bilateral (perisylvian and opercular) polymicrogyria and Neurofibromatosis type 1 95
Neurologia e psichiatria dello sviluppo 95
Sindrome del vomito ciclico: analisi di una popolazione di 20 bambini e revisione della letteratura 95
A Probable Topiramate-induced Limbs Paraesthesia and Rigid Fingers Flexion 95
Citalopram in the treatment of depression in the elderly 94
Short-term neurodevelopmental outcome in term neonates treated with phenobarbital versus levetiracetam: A single-center experience 94
Klippel-Trenaunay Syndrome, Segmental/Focal Overgrowth Malformations: A Review 93
Bilateral periventricular nodular heterotopia and amniotic band syndrome 93
Life-threatening neurological syndrome in Down's syndrome 93
NEUROEMBRIOLOGIA 93
A novel missense mutation of the NF2 gene in a severely affected boy and his healthy father 93
Analgetic thalamic syndrome in association with thalamic symmetrical abnormalities during measles encephalitis 92
Totale 14.499
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Categoria #
all - tutte 152.230
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 152.230
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20212.560 0 0 0 0 792 96 427 64 337 135 541 168
2021/20224.116 451 529 57 112 592 79 578 188 401 41 124 964
2022/20236.458 559 258 104 561 644 1.097 75 1.024 1.481 138 303 214
2023/20243.589 233 446 282 307 182 483 152 247 65 142 606 444
2024/202511.600 205 1.699 734 589 2.079 1.098 454 512 904 1.168 1.165 993
2025/202610.565 1.397 1.624 4.754 1.788 1.002 0 0 0 0 0 0 0
Totale 44.345