IRIS
RUGGIERI, MARTINO
 Distribuzione geografica
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Continente #
NA - Nord America 20.499
EU - Europa 10.853
AS - Asia 10.067
SA - Sud America 2.316
AF - Africa 1.069
OC - Oceania 24
Continente sconosciuto - Info sul continente non disponibili 15
Totale 44.843
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Nazione #
US - Stati Uniti d'America 19.727
IT - Italia 5.199
SG - Singapore 4.786
CN - Cina 3.361
BR - Brasile 1.993
IE - Irlanda 1.780
UA - Ucraina 1.664
CI - Costa d'Avorio 731
CA - Canada 645
VN - Vietnam 518
RU - Federazione Russa 485
IN - India 466
DE - Germania 381
KR - Corea 327
SE - Svezia 273
GB - Regno Unito 217
FI - Finlandia 152
NL - Olanda 147
AR - Argentina 134
FR - Francia 128
SN - Senegal 123
MX - Messico 89
BD - Bangladesh 80
PL - Polonia 80
CH - Svizzera 70
ZA - Sudafrica 65
EC - Ecuador 63
JP - Giappone 62
UZ - Uzbekistan 60
ID - Indonesia 59
TR - Turchia 58
AT - Austria 49
ES - Italia 49
BJ - Benin 46
GR - Grecia 40
HK - Hong Kong 38
IR - Iran 38
IQ - Iraq 37
PK - Pakistan 34
CO - Colombia 32
CZ - Repubblica Ceca 28
MA - Marocco 27
LB - Libano 22
VE - Venezuela 21
NG - Nigeria 20
PY - Paraguay 19
AU - Australia 18
BE - Belgio 17
RO - Romania 17
AE - Emirati Arabi Uniti 16
SA - Arabia Saudita 16
CL - Cile 15
LT - Lituania 15
PE - Perù 14
EG - Egitto 13
UY - Uruguay 13
BG - Bulgaria 11
EU - Europa 11
IL - Israele 11
TN - Tunisia 11
JO - Giordania 10
KE - Kenya 10
AZ - Azerbaigian 8
BO - Bolivia 8
DZ - Algeria 8
KZ - Kazakistan 7
AL - Albania 6
BY - Bielorussia 6
DO - Repubblica Dominicana 6
JM - Giamaica 6
NP - Nepal 6
BN - Brunei Darussalam 5
EE - Estonia 5
MY - Malesia 5
AO - Angola 4
CR - Costa Rica 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 44.805
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Città #
Dallas 4.054
Santa Clara 2.220
Singapore 2.214
Chandler 1.877
Jacksonville 1.827
Dublin 1.762
Boardman 836
Hefei 796
Chicago 756
Abidjan 731
Ashburn 669
Houston 623
Catania 590
Nanjing 557
Lawrence 497
Andover 491
Cambridge 491
Los Angeles 460
Toronto 452
Beijing 377
Milan 358
Seoul 322
Rome 321
Des Moines 290
Kochi 288
San Mateo 257
Wilmington 233
Civitanova Marche 222
Ho Chi Minh City 195
Nanchang 180
São Paulo 173
Shenyang 157
Munich 140
Palermo 131
Hebei 126
Dakar 123
New York 120
Jiaxing 118
Saint Petersburg 111
Ottawa 109
Buffalo 104
Changsha 101
Bremen 98
Hanoi 96
Florence 91
Naples 89
Tianjin 84
Bologna 71
Helsinki 70
Rio de Janeiro 67
Council Bluffs 65
Seattle 65
The Dalles 62
Turin 62
Padova 59
Bari 58
Tokyo 58
Warsaw 54
Moscow 52
Belo Horizonte 51
Grafing 51
Brooklyn 50
Columbus 50
Cotonou 46
Dong Ket 46
Johannesburg 41
Montreal 41
Amsterdam 40
Phoenix 40
Lappeenranta 39
Redondo Beach 38
Turku 37
Hong Kong 36
Chennai 34
Curitiba 34
Hangzhou 34
Jinan 34
Liberty Lake 34
Pune 34
Stockholm 34
Boston 33
Norwalk 33
Den Haag 32
Denver 32
Falls Church 32
Augusta 31
San Francisco 31
Washington 31
Oakland 30
Atlanta 29
Poplar 29
Genoa 28
Tashkent 28
Ann Arbor 27
Brescia 27
Kunming 27
London 27
Taormina 27
Brasília 26
Mexico City 26
Totale 29.090
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Nome #
Dislocazione atlanto-occipitale e atlanto-assiale con grave compressione del midollo spinale nella Sindrome di Down 965
Encefalite da Anticorpi anti-GluR3 in sei pazienti in età pediatrica 806
Sindromi Neurocutanee 614
ESAME NEUROLOGICO 427
Expanding genotype-phenotype correlation of Kenny-Caffey syndrome type 1 398
CUTIS TRICOLOR (RUGGIERI-HAPPLE SYNDROME) 379
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] 247
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders 228
Natural history of neurofibromatosis type 2 with onset before the age of 1 year. 208
A pilot study on neurological manifestations and antibodies against neuronal antigens in children with haematological and other cancers 205
PARALISI CEREBRALI INFANTILI E PARAPLEGIE SPASTICHE EREDITARIE 179
A mosaic pattern of INI1/SMARCB1 protein expression distinguishes Schwannomatosis and NF2-associated peripheral schwannomas from solitary peripheral schwannomas and NF2-associated vestibular schwannomas 164
Speckled Lentiginous Nevus Syndrome 163
A boy born with multiple lesions of atrophoderma 162
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) 160
Manuale di Pediatria, quinta edizione. Capitolo 2 "Anamnesi ed esame obiettivo". Capitolo 29 "Malattie Neurologiche". 158
Encephalocraniocutaneous Lipomatosis (Haberland Syndrome or Fishman Syndrome) 157
Complex malformation (Ruggieri-Happle) phenotype with “cutis tricolor” in a 10-year-old girl 153
Anti-MOG Antibody Syndrome and Cerebral Sinovenous Thrombosis: A Cause-Effect Hypothesis 149
Becker's Nevus Syndrome 145
Anti-mog associated encephalitis: when steroid therapy is not enough 144
A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment 136
A girl with a 14.7 Mb 3q26.32-q28 duplication: a new report of 3q duplication syndrome and a literature review 135
Astenia: una maschera per tante identità. Ruolo della patologia della placca neuromuscolare 135
Phacomatosis Pigmentovascularis 135
Blue Rubber Bleb Nevus Syndrome 134
Phacomatosis Pigmentokeratotica 134
Nevus Sebaceous Syndrome 130
Craniofacial anomalies, severe cerebellar hypoplasia, psychomotor and growth delay in a child with congenital hypothyroidism 129
A New Patient with Potocki-Lupski Syndrome: A Literature Review 128
Autoimmune encephalitis and CSF anti-AMPA GluR3 antibodies in childhood: a case report and literature review 127
Familial osteoma of the cranial vault 126
A case of extreme brain lesions: Which pathogenetic mechanism? 124
A highly sensitive colorimetric approach based on tris (bipyridine) Ruthenium (II/III) mediator for the enzymatic detection of phenylalanine 122
Aicardi-Goutières Syndrome Type 2: A Report on Two Cases with Different Phenotypes Caused by RNASEH2B Gene Mutations 122
Malattie neurocutanee 119
Paracelso: vita e contributo all'evoluzione delle scienze mediche, umane e neuropsichiatriche 118
Cerebellotrigeminal Dermal Dysplasia (Gómez-López-Hernández Syndrome) 118
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. 117
Aneurysmal bone cyst of the acromion: a case report 116
Correlazione genotipo/fenotipo nella Sclerosi Tuberosa (TSC1 vs. TSC2) in 81 pazienti siciliani 115
An 11-year follow-up of neonatal onset bath-induced alternating hemiplegia of childhood in monozygotic twins 114
Electrocardiographic Evaluation in Patients With Spinal Muscular Atrophy: A Case-Control Study 114
E se non fossero solo incubi notturni? 114
Megalencephaly Capillary Malformation Syndrome 114
Wyburn-Mason Syndrome 113
Displasia ossea della volta cranica in un paziente con neurofibromatosi tipo 1 111
Congenital muscular dystrophy: from muscle to brain 111
A critical appraisal of neurological evidence on paediatric COVID-19 patients. A systematic literature review 110
Congenital bone malformations in patients with neurofibromatosis type 1 (Nf1) 110
The natural history of Spinal Neurofibromatosis: A critical review of clinical and genetic features 110
A Phenylalanine sensor exploiting a capacitive readout strategy embedding a selective enzymatic mechanism 109
Acute disseminated encephalomyelitis: a long-term prospective study and meta-analysis 109
A child with rhombencephalosynapsis, agenesis of the trigeminal ganglion and optic coloboma (without alopecia): A variant of the cerebellotrigeminal dermal dysplasia? 109
Off-label use of drugs and adverse drug reactions in pediatric units: A prospective, multicenter study 109
Need for palliative care from birth to infancy in pediatric patients with neurological diseases 108
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] 108
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 108
Malformazioni vascolari nella neurofibromatosi di tipo 1 (NF1) 108
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 108
A Complex Brain Malformation Syndrome with Rhombencephalosynapsis, Preaxial Hexadactyly plus Facial and Skull Anomalies 105
Aneurismal bone cyst of the acromion: a case report 105
Chromosome 2p15-p16.1 microduplication in a boy with congenital anomalies: Is it a distinctive syndrome? 105
Melorheostosis: case report with 20-year follow-up 104
Autoimmune thyroiditis and acquired demyelinating poliradiculoneuropathy 104
Microcephaly-Capillary Malformation Syndrome 104
Esame obiettivo neurologico nel bambino 103
A child with congenital heart disease and situs viscerum inversus 103
Did Cro-Magnon 1 have neurofibromatosis type 2? 103
Archetypical Patterns of Skin Manifestations in Neurocutaneous Disorders 103
The use of selegiline in the treatment of cognitive deficits in elderly patients 102
Mixed Vascular Nevus Syndrome 102
Neurocutaneous melanocytosis (melanosis) 102
Mutazione PRRT2 in un bambino con caratteristiche dismorfiche, microcefalia congenita e convulsioni epilettiche gravi 101
Zellweger Syndrome coupled to secondary mitochondrial cytopathy in skeletal muscle cells in an infant: a pattern of biochemical overlapping in metabolic myopathies 101
Ataxia in children: early recognition and clinical evaluation 101
Cutis Tricolor 101
Cognitive disabilities and bioethical implications in down syndrome 101
A novel GABRB3 variant in Dravet syndrome: Case report and literature review 101
Clinical course of N-methyl-D-aspartate receptor encephalitis and the effectiveness of cyclophosphamide treatment 100
Citalopram in the treatment of depression in the elderly 100
Neurologia e psichiatria dello sviluppo 100
Sindrome del vomito ciclico: analisi di una popolazione di 20 bambini e revisione della letteratura 100
Hypomelanosis of Ito 100
Disturbi del sonno: uno studio prospettico pilota basato sulla somministrazione di questionario online. 100
Short-term neurodevelopmental outcome in term neonates treated with phenobarbital versus levetiracetam: A single-center experience 100
Recurrent obstructive hydrocephalus in a 4-month-old infant 99
Hormesis, cellular stress response, and redox homeostasis in autism spectrum disorders 99
A Probable Topiramate-induced Limbs Paraesthesia and Rigid Fingers Flexion 99
Klippel-Trenaunay Syndrome, Segmental/Focal Overgrowth Malformations: A Review 98
Hypotonia, congenital nystagmus, ataxia and abnormal auditory brainstem responses. Report on the first white Caucasian patient 98
Two siblings with a homozygous MTHFR C677T (G80A-RFC1) mutation and stroke 98
La morte di Iulia Florentina: ipotesi mediche e diagnostiche 98
Bilateral (perisylvian and opercular) polymicrogyria and Neurofibromatosis type 1 97
A clinical and molecular study in a child under 1 year of age affected by Neurofibromatosis type 2 97
A Young Boy with 21q21.1 Microdeletion Showing Speech Delay, Spastic Diplegia, and MRI Abnormalities: Original Case Report 96
Encefalite GluR3: fenotipo clinico e strumentale di quattro pazienti 96
Bilateral periventricular nodular heterotopia and amniotic band syndrome 95
A neurocutaneous phenotype with paired hypo- and hyperpigmented macules, microcephaly and stunted growth as prominent features 95
Analgetic thalamic syndrome in association with thalamic symmetrical abnormalities during measles encephalitis 95
Totale 14.839
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Categoria #
all - tutte 155.009
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 155.009
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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
2025/202611.916 1.397 1.624 4.754 1.788 2.353 0 0 0 0 0 0 0
Totale 45.696