IRIS
RUGGIERI, MARTINO
 Distribuzione geografica
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Continente #
NA - Nord America 20.415
EU - Europa 10.839
AS - Asia 9.643
SA - Sud America 2.300
AF - Africa 1.066
OC - Oceania 24
Continente sconosciuto - Info sul continente non disponibili 15
Totale 44.302
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Nazione #
US - Stati Uniti d'America 19.649
IT - Italia 5.199
SG - Singapore 4.384
CN - Cina 3.356
BR - Brasile 1.982
IE - Irlanda 1.780
UA - Ucraina 1.662
CI - Costa d'Avorio 731
CA - Canada 642
VN - Vietnam 512
RU - Federazione Russa 483
IN - India 464
DE - Germania 381
KR - Corea 327
SE - Svezia 272
GB - Regno Unito 211
FI - Finlandia 152
NL - Olanda 147
AR - Argentina 131
FR - Francia 128
SN - Senegal 123
MX - Messico 86
PL - Polonia 78
BD - Bangladesh 77
CH - Svizzera 70
ZA - Sudafrica 64
EC - Ecuador 63
JP - Giappone 60
UZ - Uzbekistan 59
ID - Indonesia 58
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 26
LB - Libano 22
VE - Venezuela 21
NG - Nigeria 20
PY - Paraguay 19
AU - Australia 18
BE - Belgio 17
RO - Romania 17
SA - Arabia Saudita 16
AE - Emirati Arabi Uniti 15
CL - Cile 14
LT - Lituania 14
PE - Perù 14
EG - Egitto 13
UY - Uruguay 12
BG - Bulgaria 11
EU - Europa 11
IL - Israele 11
TN - Tunisia 11
JO - Giordania 9
KE - Kenya 9
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 44.264
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Città #
Dallas 4.053
Santa Clara 2.220
Singapore 2.204
Chandler 1.877
Jacksonville 1.827
Dublin 1.762
Boardman 836
Hefei 796
Chicago 755
Abidjan 731
Ashburn 655
Houston 621
Catania 590
Nanjing 557
Lawrence 497
Andover 491
Cambridge 491
Toronto 452
Los Angeles 447
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 193
Nanchang 180
São Paulo 173
Shenyang 157
Munich 140
Palermo 131
Hebei 126
Dakar 123
Jiaxing 118
New York 118
Saint Petersburg 111
Ottawa 109
Changsha 101
Bremen 98
Hanoi 96
Florence 91
Naples 89
Tianjin 84
Buffalo 83
Bologna 71
Helsinki 70
Rio de Janeiro 67
Council Bluffs 65
Seattle 65
The Dalles 62
Turin 62
Padova 59
Bari 58
Tokyo 56
Moscow 52
Warsaw 52
Belo Horizonte 51
Grafing 51
Columbus 50
Brooklyn 49
Cotonou 46
Dong Ket 46
Amsterdam 40
Johannesburg 40
Phoenix 40
Lappeenranta 39
Montreal 39
Redondo Beach 38
Turku 37
Hong Kong 36
Curitiba 34
Hangzhou 34
Jinan 34
Liberty Lake 34
Pune 34
Chennai 33
Norwalk 33
Stockholm 33
Boston 32
Den Haag 32
Denver 32
Falls Church 32
Augusta 31
San Francisco 31
Washington 31
Oakland 30
Atlanta 28
Genoa 28
Ann Arbor 27
Brescia 27
Kunming 27
Taormina 27
Tashkent 27
Brasília 26
London 26
Mexico City 26
Mumbai 26
Totale 29.007
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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 805
Sindromi Neurocutanee 613
ESAME NEUROLOGICO 427
Expanding genotype-phenotype correlation of Kenny-Caffey syndrome type 1 397
CUTIS TRICOLOR (RUGGIERI-HAPPLE SYNDROME) 378
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] 246
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders 227
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 204
PARALISI CEREBRALI INFANTILI E PARAPLEGIE SPASTICHE EREDITARIE 178
A mosaic pattern of INI1/SMARCB1 protein expression distinguishes Schwannomatosis and NF2-associated peripheral schwannomas from solitary peripheral schwannomas and NF2-associated vestibular schwannomas 163
A boy born with multiple lesions of atrophoderma 161
Speckled Lentiginous Nevus Syndrome 161
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) 158
Manuale di Pediatria, quinta edizione. Capitolo 2 "Anamnesi ed esame obiettivo". Capitolo 29 "Malattie Neurologiche". 157
Encephalocraniocutaneous Lipomatosis (Haberland Syndrome or Fishman Syndrome) 156
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 148
Becker's Nevus Syndrome 144
Anti-mog associated encephalitis: when steroid therapy is not enough 143
A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment 135
Astenia: una maschera per tante identità. Ruolo della patologia della placca neuromuscolare 134
Phacomatosis Pigmentovascularis 134
Blue Rubber Bleb Nevus Syndrome 133
A girl with a 14.7 Mb 3q26.32-q28 duplication: a new report of 3q duplication syndrome and a literature review 132
Phacomatosis Pigmentokeratotica 132
Craniofacial anomalies, severe cerebellar hypoplasia, psychomotor and growth delay in a child with congenital hypothyroidism 129
Nevus Sebaceous Syndrome 129
Autoimmune encephalitis and CSF anti-AMPA GluR3 antibodies in childhood: a case report and literature review 126
A New Patient with Potocki-Lupski Syndrome: A Literature Review 126
Familial osteoma of the cranial vault 126
A case of extreme brain lesions: Which pathogenetic mechanism? 122
A highly sensitive colorimetric approach based on tris (bipyridine) Ruthenium (II/III) mediator for the enzymatic detection of phenylalanine 121
Aicardi-Goutières Syndrome Type 2: A Report on Two Cases with Different Phenotypes Caused by RNASEH2B Gene Mutations 121
Malattie neurocutanee 119
Paracelso: vita e contributo all'evoluzione delle scienze mediche, umane e neuropsichiatriche 118
Cerebellotrigeminal Dermal Dysplasia (Gómez-López-Hernández Syndrome) 117
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. 116
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 113
Electrocardiographic Evaluation in Patients With Spinal Muscular Atrophy: A Case-Control Study 113
E se non fossero solo incubi notturni? 113
Megalencephaly Capillary Malformation Syndrome 113
Wyburn-Mason Syndrome 112
Displasia ossea della volta cranica in un paziente con neurofibromatosi tipo 1 111
Congenital muscular dystrophy: from muscle to brain 110
Congenital bone malformations in patients with neurofibromatosis type 1 (Nf1) 109
The natural history of Spinal Neurofibromatosis: A critical review of clinical and genetic features 109
A critical appraisal of neurological evidence on paediatric COVID-19 patients. A systematic literature review 108
A child with rhombencephalosynapsis, agenesis of the trigeminal ganglion and optic coloboma (without alopecia): A variant of the cerebellotrigeminal dermal dysplasia? 108
A Phenylalanine sensor exploiting a capacitive readout strategy embedding a selective enzymatic mechanism 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] 107
Acute disseminated encephalomyelitis: a long-term prospective study and meta-analysis 107
Malformazioni vascolari nella neurofibromatosi di tipo 1 (NF1) 107
Need for palliative care from birth to infancy in pediatric patients with neurological diseases 106
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 106
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 106
Off-label use of drugs and adverse drug reactions in pediatric units: A prospective, multicenter study 106
A Complex Brain Malformation Syndrome with Rhombencephalosynapsis, Preaxial Hexadactyly plus Facial and Skull Anomalies 105
Aneurismal bone cyst of the acromion: a case report 104
Autoimmune thyroiditis and acquired demyelinating poliradiculoneuropathy 104
Chromosome 2p15-p16.1 microduplication in a boy with congenital anomalies: Is it a distinctive syndrome? 104
Melorheostosis: case report with 20-year follow-up 103
Microcephaly-Capillary Malformation Syndrome 103
Esame obiettivo neurologico nel bambino 102
A child with congenital heart disease and situs viscerum inversus 102
Did Cro-Magnon 1 have neurofibromatosis type 2? 102
Mixed Vascular Nevus Syndrome 101
Ataxia in children: early recognition and clinical evaluation 101
Archetypical Patterns of Skin Manifestations in Neurocutaneous Disorders 101
Neurocutaneous melanocytosis (melanosis) 101
Clinical course of N-methyl-D-aspartate receptor encephalitis and the effectiveness of cyclophosphamide treatment 100
Mutazione PRRT2 in un bambino con caratteristiche dismorfiche, microcefalia congenita e convulsioni epilettiche gravi 100
Zellweger Syndrome coupled to secondary mitochondrial cytopathy in skeletal muscle cells in an infant: a pattern of biochemical overlapping in metabolic myopathies 100
Cognitive disabilities and bioethical implications in down syndrome 100
A novel GABRB3 variant in Dravet syndrome: Case report and literature review 100
Recurrent obstructive hydrocephalus in a 4-month-old infant 99
The use of selegiline in the treatment of cognitive deficits in elderly patients 99
Neurologia e psichiatria dello sviluppo 99
Hypomelanosis of Ito 99
Cutis Tricolor 99
Two siblings with a homozygous MTHFR C677T (G80A-RFC1) mutation and stroke 98
Citalopram in the treatment of depression in the elderly 98
Bilateral (perisylvian and opercular) polymicrogyria and Neurofibromatosis type 1 97
Sindrome del vomito ciclico: analisi di una popolazione di 20 bambini e revisione della letteratura 97
Hormesis, cellular stress response, and redox homeostasis in autism spectrum disorders 97
A Probable Topiramate-induced Limbs Paraesthesia and Rigid Fingers Flexion 97
A clinical and molecular study in a child under 1 year of age affected by Neurofibromatosis type 2 97
Disturbi del sonno: uno studio prospettico pilota basato sulla somministrazione di questionario online. 97
Short-term neurodevelopmental outcome in term neonates treated with phenobarbital versus levetiracetam: A single-center experience 97
La morte di Iulia Florentina: ipotesi mediche e diagnostiche 97
Klippel-Trenaunay Syndrome, Segmental/Focal Overgrowth Malformations: A Review 96
Hypotonia, congenital nystagmus, ataxia and abnormal auditory brainstem responses. Report on the first white Caucasian patient 96
Bilateral periventricular nodular heterotopia and amniotic band syndrome 95
Analgetic thalamic syndrome in association with thalamic symmetrical abnormalities during measles encephalitis 95
Encefalite GluR3: fenotipo clinico e strumentale di quattro pazienti 95
A Young Boy with 21q21.1 Microdeletion Showing Speech Delay, Spastic Diplegia, and MRI Abnormalities: Original Case Report 94
A neurocutaneous phenotype with paired hypo- and hyperpigmented macules, microcephaly and stunted growth as prominent features 94
Totale 14.725
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Categoria #
all - tutte 154.038
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 154.038
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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
2025/202611.375 1.397 1.624 4.754 1.788 1.812 0 0 0 0 0 0 0
Totale 45.155