IRIS
RUGGIERI, MARTINO
 Distribuzione geografica
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Continente #
NA - Nord America 20.640
EU - Europa 11.299
AS - Asia 10.662
SA - Sud America 2.325
AF - Africa 1.076
OC - Oceania 24
Continente sconosciuto - Info sul continente non disponibili 15
Totale 46.041
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Nazione #
US - Stati Uniti d'America 19.858
SG - Singapore 5.358
IT - Italia 5.208
CN - Cina 3.366
BR - Brasile 2.000
IE - Irlanda 1.780
UA - Ucraina 1.664
RU - Federazione Russa 904
CI - Costa d'Avorio 731
CA - Canada 650
VN - Vietnam 520
IN - India 468
DE - Germania 382
KR - Corea 328
SE - Svezia 275
GB - Regno Unito 223
FI - Finlandia 152
NL - Olanda 149
AR - Argentina 136
FR - Francia 128
SN - Senegal 123
MX - Messico 93
PL - Polonia 83
BD - Bangladesh 81
CH - Svizzera 70
ZA - Sudafrica 68
JP - Giappone 66
EC - Ecuador 63
UZ - Uzbekistan 61
ID - Indonesia 59
TR - Turchia 59
ES - Italia 50
AT - Austria 49
BJ - Benin 46
GR - Grecia 40
IQ - Iraq 39
HK - Hong Kong 38
IR - Iran 38
PK - Pakistan 35
CO - Colombia 32
CZ - Repubblica Ceca 28
MA - Marocco 27
LB - Libano 22
VE - Venezuela 21
NG - Nigeria 20
PY - Paraguay 19
RO - Romania 19
AU - Australia 18
AE - Emirati Arabi Uniti 17
BE - Belgio 17
LT - Lituania 16
SA - Arabia Saudita 16
CL - Cile 15
PE - Perù 14
EG - Egitto 13
KE - Kenya 13
UY - Uruguay 13
TN - Tunisia 12
BG - Bulgaria 11
EU - Europa 11
IL - Israele 11
JO - Giordania 10
AZ - Azerbaigian 8
BO - Bolivia 8
DZ - Algeria 8
KZ - Kazakistan 8
AL - Albania 6
BY - Bielorussia 6
DO - Repubblica Dominicana 6
JM - Giamaica 6
MY - Malesia 6
NP - Nepal 6
BN - Brunei Darussalam 5
CR - Costa Rica 5
EE - Estonia 5
AO - Angola 4
DK - Danimarca 4
GD - Grenada 4
HR - Croazia 4
HU - Ungheria 4
KW - Kuwait 4
OM - Oman 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
PS - Palestinian Territory 3
RS - Serbia 3
SK - Slovacchia (Repubblica Slovacca) 3
AM - Armenia 2
BA - Bosnia-Erzegovina 2
BW - Botswana 2
Totale 46.003
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Città #
Dallas 4.056
Singapore 2.778
Santa Clara 2.221
Chandler 1.877
Jacksonville 1.827
Dublin 1.762
Boardman 836
Hefei 796
Chicago 756
Abidjan 731
Ashburn 707
Houston 624
Catania 590
Nanjing 557
Lawrence 497
Andover 491
Cambridge 491
Los Angeles 482
Toronto 453
Beijing 378
Milan 358
Seoul 322
Rome 321
Moscow 311
Des Moines 290
Kochi 288
San Mateo 257
Wilmington 233
Civitanova Marche 222
Ho Chi Minh City 196
Nanchang 180
São Paulo 175
Shenyang 158
Munich 140
Palermo 131
Hebei 126
New York 124
Dakar 123
Jiaxing 118
Buffalo 116
Saint Petersburg 111
Ottawa 109
Changsha 101
Bremen 98
Hanoi 97
Florence 91
Naples 89
Tianjin 84
Bologna 71
Helsinki 70
Rio de Janeiro 68
Seattle 67
Council Bluffs 66
The Dalles 62
Tokyo 62
Turin 62
Padova 59
Bari 58
Warsaw 57
Belo Horizonte 52
Grafing 51
Brooklyn 50
Columbus 50
Cotonou 46
Dong Ket 46
Johannesburg 44
Montreal 44
Phoenix 42
Amsterdam 40
Lappeenranta 39
Redondo Beach 38
Denver 37
Turku 37
Boston 36
Hong Kong 36
Stockholm 36
Chennai 35
Augusta 34
Curitiba 34
Hangzhou 34
Jinan 34
Liberty Lake 34
Pune 34
Norwalk 33
Den Haag 32
Falls Church 32
Poplar 32
San Francisco 31
Washington 31
Atlanta 30
Oakland 30
Genoa 28
London 28
Tashkent 28
Ann Arbor 27
Brescia 27
Kunming 27
Mexico City 27
Mumbai 27
Taormina 27
Totale 30.041
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Nome #
Dislocazione atlanto-occipitale e atlanto-assiale con grave compressione del midollo spinale nella Sindrome di Down 966
Encefalite da Anticorpi anti-GluR3 in sei pazienti in età pediatrica 813
Sindromi Neurocutanee 616
ESAME NEUROLOGICO 429
Expanding genotype-phenotype correlation of Kenny-Caffey syndrome type 1 400
CUTIS TRICOLOR (RUGGIERI-HAPPLE SYNDROME) 381
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] 248
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders 229
A pilot study on neurological manifestations and antibodies against neuronal antigens in children with haematological and other cancers 211
Natural history of neurofibromatosis type 2 with onset before the age of 1 year. 210
PARALISI CEREBRALI INFANTILI E PARAPLEGIE SPASTICHE EREDITARIE 180
A mosaic pattern of INI1/SMARCB1 protein expression distinguishes Schwannomatosis and NF2-associated peripheral schwannomas from solitary peripheral schwannomas and NF2-associated vestibular schwannomas 167
Speckled Lentiginous Nevus Syndrome 166
A boy born with multiple lesions of atrophoderma 165
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) 163
Encephalocraniocutaneous Lipomatosis (Haberland Syndrome or Fishman Syndrome) 159
Manuale di Pediatria, quinta edizione. Capitolo 2 "Anamnesi ed esame obiettivo". Capitolo 29 "Malattie Neurologiche". 159
Complex malformation (Ruggieri-Happle) phenotype with “cutis tricolor” in a 10-year-old girl 156
Anti-MOG Antibody Syndrome and Cerebral Sinovenous Thrombosis: A Cause-Effect Hypothesis 152
Becker's Nevus Syndrome 149
Anti-mog associated encephalitis: when steroid therapy is not enough 148
A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment 139
A girl with a 14.7 Mb 3q26.32-q28 duplication: a new report of 3q duplication syndrome and a literature review 138
Astenia: una maschera per tante identità. Ruolo della patologia della placca neuromuscolare 137
Phacomatosis Pigmentovascularis 137
Blue Rubber Bleb Nevus Syndrome 136
Phacomatosis Pigmentokeratotica 135
Nevus Sebaceous Syndrome 134
Autoimmune encephalitis and CSF anti-AMPA GluR3 antibodies in childhood: a case report and literature review 131
Craniofacial anomalies, severe cerebellar hypoplasia, psychomotor and growth delay in a child with congenital hypothyroidism 131
A New Patient with Potocki-Lupski Syndrome: A Literature Review 130
Familial osteoma of the cranial vault 129
A case of extreme brain lesions: Which pathogenetic mechanism? 128
A highly sensitive colorimetric approach based on tris (bipyridine) Ruthenium (II/III) mediator for the enzymatic detection of phenylalanine 127
Aicardi-Goutières Syndrome Type 2: A Report on Two Cases with Different Phenotypes Caused by RNASEH2B Gene Mutations 127
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. 121
Paracelso: vita e contributo all'evoluzione delle scienze mediche, umane e neuropsichiatriche 121
Cerebellotrigeminal Dermal Dysplasia (Gómez-López-Hernández Syndrome) 121
Malattie neurocutanee 120
Aneurysmal bone cyst of the acromion: a case report 119
Correlazione genotipo/fenotipo nella Sclerosi Tuberosa (TSC1 vs. TSC2) in 81 pazienti siciliani 119
An 11-year follow-up of neonatal onset bath-induced alternating hemiplegia of childhood in monozygotic twins 118
Wyburn-Mason Syndrome 117
Megalencephaly Capillary Malformation Syndrome 117
Electrocardiographic Evaluation in Patients With Spinal Muscular Atrophy: A Case-Control Study 116
E se non fossero solo incubi notturni? 116
Congenital muscular dystrophy: from muscle to brain 114
A critical appraisal of neurological evidence on paediatric COVID-19 patients. A systematic literature review 113
Displasia ossea della volta cranica in un paziente con neurofibromatosi tipo 1 113
A Phenylalanine sensor exploiting a capacitive readout strategy embedding a selective enzymatic mechanism 112
The natural history of Spinal Neurofibromatosis: A critical review of clinical and genetic features 112
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 112
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 112
Acute disseminated encephalomyelitis: a long-term prospective study and meta-analysis 111
Malformazioni vascolari nella neurofibromatosi di tipo 1 (NF1) 111
A child with rhombencephalosynapsis, agenesis of the trigeminal ganglion and optic coloboma (without alopecia): A variant of the cerebellotrigeminal dermal dysplasia? 111
Off-label use of drugs and adverse drug reactions in pediatric units: A prospective, multicenter study 111
Congenital bone malformations in patients with neurofibromatosis type 1 (Nf1) 110
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] 110
Need for palliative care from birth to infancy in pediatric patients with neurological diseases 109
Aneurismal bone cyst of the acromion: a case report 108
Chromosome 2p15-p16.1 microduplication in a boy with congenital anomalies: Is it a distinctive syndrome? 108
Microcephaly-Capillary Malformation Syndrome 107
A Complex Brain Malformation Syndrome with Rhombencephalosynapsis, Preaxial Hexadactyly plus Facial and Skull Anomalies 106
Esame obiettivo neurologico nel bambino 106
Did Cro-Magnon 1 have neurofibromatosis type 2? 106
Mixed Vascular Nevus Syndrome 106
Autoimmune thyroiditis and acquired demyelinating poliradiculoneuropathy 106
Melorheostosis: case report with 20-year follow-up 105
A child with congenital heart disease and situs viscerum inversus 105
A Probable Topiramate-induced Limbs Paraesthesia and Rigid Fingers Flexion 105
The use of selegiline in the treatment of cognitive deficits in elderly patients 104
Hormesis, cellular stress response, and redox homeostasis in autism spectrum disorders 104
Mutazione PRRT2 in un bambino con caratteristiche dismorfiche, microcefalia congenita e convulsioni epilettiche gravi 104
Hypomelanosis of Ito 104
Archetypical Patterns of Skin Manifestations in Neurocutaneous Disorders 104
Cognitive disabilities and bioethical implications in down syndrome 104
Neurocutaneous melanocytosis (melanosis) 104
Citalopram in the treatment of depression in the elderly 103
Sindrome del vomito ciclico: analisi di una popolazione di 20 bambini e revisione della letteratura 103
Ataxia in children: early recognition and clinical evaluation 103
A novel GABRB3 variant in Dravet syndrome: Case report and literature review 103
Recurrent obstructive hydrocephalus in a 4-month-old infant 102
Clinical course of N-methyl-D-aspartate receptor encephalitis and the effectiveness of cyclophosphamide treatment 102
Zellweger Syndrome coupled to secondary mitochondrial cytopathy in skeletal muscle cells in an infant: a pattern of biochemical overlapping in metabolic myopathies 102
Cutis Tricolor 102
Klippel-Trenaunay Syndrome, Segmental/Focal Overgrowth Malformations: A Review 101
Neurologia e psichiatria dello sviluppo 101
Disturbi del sonno: uno studio prospettico pilota basato sulla somministrazione di questionario online. 101
Two siblings with a homozygous MTHFR C677T (G80A-RFC1) mutation and stroke 100
Bilateral (perisylvian and opercular) polymicrogyria and Neurofibromatosis type 1 100
Short-term neurodevelopmental outcome in term neonates treated with phenobarbital versus levetiracetam: A single-center experience 100
La morte di Iulia Florentina: ipotesi mediche e diagnostiche 100
A Young Boy with 21q21.1 Microdeletion Showing Speech Delay, Spastic Diplegia, and MRI Abnormalities: Original Case Report 99
Hypotonia, congenital nystagmus, ataxia and abnormal auditory brainstem responses. Report on the first white Caucasian patient 99
Bilateral periventricular nodular heterotopia and amniotic band syndrome 99
A neurocutaneous phenotype with paired hypo- and hyperpigmented macules, microcephaly and stunted growth as prominent features 99
A clinical and molecular study in a child under 1 year of age affected by Neurofibromatosis type 2 99
Encefalite GluR3: fenotipo clinico e strumentale di quattro pazienti 99
Hormesis, cellular stress response and neuroinflammation in schizophrenia: early onset versus late onset state 98
Totale 15.103
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Categoria #
all - tutte 156.661
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 156.661
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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
2025/202613.116 1.397 1.624 4.754 1.788 3.553 0 0 0 0 0 0 0
Totale 46.896