IRIS
RUGGIERI, MARTINO
 Distribuzione geografica
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Continente #
NA - Nord America 20.672
EU - Europa 11.394
AS - Asia 10.798
SA - Sud America 2.326
AF - Africa 1.076
OC - Oceania 24
Continente sconosciuto - Info sul continente non disponibili 15
Totale 46.305
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Nazione #
US - Stati Uniti d'America 19.890
SG - Singapore 5.488
IT - Italia 5.212
CN - Cina 3.368
BR - Brasile 2.000
IE - Irlanda 1.780
UA - Ucraina 1.664
RU - Federazione Russa 993
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 137
FR - Francia 128
SN - Senegal 123
MX - Messico 93
PL - Polonia 83
BD - Bangladesh 82
CH - Svizzera 70
ZA - Sudafrica 68
JP - Giappone 67
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 40
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
BE - Belgio 18
AE - Emirati Arabi Uniti 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 9
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
HU - Ungheria 5
AO - Angola 4
DK - Danimarca 4
GD - Grenada 4
HR - Croazia 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 46.267
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Città #
Dallas 4.056
Singapore 2.908
Santa Clara 2.221
Chandler 1.877
Jacksonville 1.827
Dublin 1.762
Boardman 836
Hefei 796
Chicago 756
Ashburn 732
Abidjan 731
Houston 625
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 125
Dakar 123
Jiaxing 118
Buffalo 116
Saint Petersburg 111
Ottawa 109
Changsha 101
Bremen 98
Hanoi 97
Florence 92
Naples 89
Tianjin 84
Bologna 71
Helsinki 70
Rio de Janeiro 68
Council Bluffs 67
Seattle 67
The Dalles 64
Tokyo 63
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 30.203
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Nome #
Dislocazione atlanto-occipitale e atlanto-assiale con grave compressione del midollo spinale nella Sindrome di Down 967
Encefalite da Anticorpi anti-GluR3 in sei pazienti in età pediatrica 814
Sindromi Neurocutanee 616
ESAME NEUROLOGICO 431
Expanding genotype-phenotype correlation of Kenny-Caffey syndrome type 1 400
CUTIS TRICOLOR (RUGGIERI-HAPPLE SYNDROME) 382
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] 249
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders 230
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
Speckled Lentiginous Nevus Syndrome 168
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
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) 162
Manuale di Pediatria, quinta edizione. Capitolo 2 "Anamnesi ed esame obiettivo". Capitolo 29 "Malattie Neurologiche". 160
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 153
Becker's Nevus Syndrome 150
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 141
A girl with a 14.7 Mb 3q26.32-q28 duplication: a new report of 3q duplication syndrome and a literature review 138
Phacomatosis Pigmentovascularis 138
Phacomatosis Pigmentokeratotica 138
Astenia: una maschera per tante identità. Ruolo della patologia della placca neuromuscolare 137
Blue Rubber Bleb Nevus Syndrome 136
Nevus Sebaceous Syndrome 135
Autoimmune encephalitis and CSF anti-AMPA GluR3 antibodies in childhood: a case report and literature review 132
Craniofacial anomalies, severe cerebellar hypoplasia, psychomotor and growth delay in a child with congenital hypothyroidism 132
A New Patient with Potocki-Lupski Syndrome: A Literature Review 132
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
Cerebellotrigeminal Dermal Dysplasia (Gómez-López-Hernández Syndrome) 123
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. 122
Malattie neurocutanee 122
Paracelso: vita e contributo all'evoluzione delle scienze mediche, umane e neuropsichiatriche 121
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
E se non fossero solo incubi notturni? 117
Wyburn-Mason Syndrome 117
Megalencephaly Capillary Malformation Syndrome 117
Electrocardiographic Evaluation in Patients With Spinal Muscular Atrophy: A Case-Control Study 116
Congenital muscular dystrophy: from muscle to brain 115
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
The natural history of Spinal Neurofibromatosis: A critical review of clinical and genetic features 113
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 113
A Phenylalanine sensor exploiting a capacitive readout strategy embedding a selective enzymatic mechanism 112
Congenital bone malformations in patients with neurofibromatosis type 1 (Nf1) 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
A child with rhombencephalosynapsis, agenesis of the trigeminal ganglion and optic coloboma (without alopecia): A variant of the cerebellotrigeminal dermal dysplasia? 112
Acute disseminated encephalomyelitis: a long-term prospective study and meta-analysis 111
Malformazioni vascolari nella neurofibromatosi di tipo 1 (NF1) 111
Off-label use of drugs and adverse drug reactions in pediatric units: A prospective, multicenter study 111
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
Chromosome 2p15-p16.1 microduplication in a boy with congenital anomalies: Is it a distinctive syndrome? 109
Aneurismal bone cyst of the acromion: a case report 108
Esame obiettivo neurologico nel bambino 108
Microcephaly-Capillary Malformation Syndrome 108
Autoimmune thyroiditis and acquired demyelinating poliradiculoneuropathy 107
Melorheostosis: case report with 20-year follow-up 106
A Complex Brain Malformation Syndrome with Rhombencephalosynapsis, Preaxial Hexadactyly plus Facial and Skull Anomalies 106
Did Cro-Magnon 1 have neurofibromatosis type 2? 106
Mixed Vascular Nevus Syndrome 106
A child with congenital heart disease and situs viscerum inversus 105
A Probable Topiramate-induced Limbs Paraesthesia and Rigid Fingers Flexion 105
Mutazione PRRT2 in un bambino con caratteristiche dismorfiche, microcefalia congenita e convulsioni epilettiche gravi 105
Hypomelanosis of Ito 105
Archetypical Patterns of Skin Manifestations in Neurocutaneous Disorders 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
Cutis Tricolor 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
Klippel-Trenaunay Syndrome, Segmental/Focal Overgrowth Malformations: A Review 101
Two siblings with a homozygous MTHFR C677T (G80A-RFC1) mutation and stroke 101
Neurologia e psichiatria dello sviluppo 101
Disturbi del sonno: uno studio prospettico pilota basato sulla somministrazione di questionario online. 101
Short-term neurodevelopmental outcome in term neonates treated with phenobarbital versus levetiracetam: A single-center experience 101
Hypotonia, congenital nystagmus, ataxia and abnormal auditory brainstem responses. Report on the first white Caucasian patient 100
Bilateral (perisylvian and opercular) polymicrogyria and Neurofibromatosis type 1 100
A clinical and molecular study in a child under 1 year of age affected by Neurofibromatosis type 2 100
La morte di Iulia Florentina: ipotesi mediche e diagnostiche 100
A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease 99
A Young Boy with 21q21.1 Microdeletion Showing Speech Delay, Spastic Diplegia, and MRI Abnormalities: Original Case Report 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
Encefalite GluR3: fenotipo clinico e strumentale di quattro pazienti 99
Totale 15.157
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Categoria #
all - tutte 157.065
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 157.065
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211.768 0 0 0 0 0 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
2025/202613.380 1.397 1.624 4.754 1.788 3.707 110 0 0 0 0 0 0
Totale 47.160