IRIS
RUGGIERI, MARTINO
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 20.581
EU - Europa 10.989
AS - Asia 10.437
SA - Sud America 2.319
AF - Africa 1.073
OC - Oceania 24
Continente sconosciuto - Info sul continente non disponibili 15
Totale 45.438
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 19.808
IT - Italia 5.201
SG - Singapore 5.147
CN - Cina 3.361
BR - Brasile 1.994
IE - Irlanda 1.780
UA - Ucraina 1.664
CI - Costa d'Avorio 731
CA - Canada 646
RU - Federazione Russa 613
VN - Vietnam 519
IN - India 468
DE - Germania 381
KR - Corea 327
SE - Svezia 273
GB - Regno Unito 219
FI - Finlandia 152
NL - Olanda 147
AR - Argentina 136
FR - Francia 128
SN - Senegal 123
MX - Messico 89
PL - Polonia 81
BD - Bangladesh 80
CH - Svizzera 70
ZA - Sudafrica 66
JP - Giappone 65
EC - Ecuador 63
UZ - Uzbekistan 61
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 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 17
AE - Emirati Arabi Uniti 16
LT - Lituania 16
SA - Arabia Saudita 16
CL - Cile 15
PE - Perù 14
EG - Egitto 13
UY - Uruguay 13
KE - Kenya 12
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 7
AL - Albania 6
BY - Bielorussia 6
DO - Repubblica Dominicana 6
JM - Giamaica 6
MY - Malesia 6
NP - Nepal 6
BN - Brunei Darussalam 5
EE - Estonia 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 45.400
Salva come PNG Salva come JPEG
Città #
Dallas 4.055
Singapore 2.567
Santa Clara 2.220
Chandler 1.877
Jacksonville 1.827
Dublin 1.762
Boardman 836
Hefei 796
Chicago 756
Abidjan 731
Ashburn 700
Houston 623
Catania 590
Nanjing 557
Lawrence 497
Andover 491
Cambridge 491
Los Angeles 475
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 174
Moscow 161
Shenyang 157
Munich 140
Palermo 131
Hebei 126
New York 124
Dakar 123
Jiaxing 118
Buffalo 112
Saint Petersburg 111
Ottawa 109
Changsha 101
Bremen 98
Hanoi 97
Florence 91
Naples 89
Tianjin 84
Bologna 71
Helsinki 70
Rio de Janeiro 67
Council Bluffs 66
Seattle 65
The Dalles 62
Turin 62
Tokyo 61
Padova 59
Bari 58
Warsaw 55
Belo Horizonte 51
Grafing 51
Brooklyn 50
Columbus 50
Cotonou 46
Dong Ket 46
Johannesburg 42
Montreal 42
Phoenix 41
Amsterdam 40
Lappeenranta 39
Redondo Beach 38
Turku 37
Hong Kong 36
Chennai 35
Curitiba 34
Denver 34
Hangzhou 34
Jinan 34
Liberty Lake 34
Pune 34
Stockholm 34
Boston 33
Norwalk 33
Den Haag 32
Falls Church 32
Augusta 31
Poplar 31
San Francisco 31
Washington 31
Atlanta 30
Oakland 30
Genoa 28
Tashkent 28
Ann Arbor 27
Brescia 27
Kunming 27
London 27
Mumbai 27
Taormina 27
Brasília 26
Totale 29.628
Salva come PNG Salva come JPEG
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 808
Sindromi Neurocutanee 616
ESAME NEUROLOGICO 428
Expanding genotype-phenotype correlation of Kenny-Caffey syndrome type 1 399
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] 248
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders 229
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 207
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 165
Speckled Lentiginous Nevus Syndrome 165
A boy born with multiple lesions of atrophoderma 163
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) 161
Manuale di Pediatria, quinta edizione. Capitolo 2 "Anamnesi ed esame obiettivo". Capitolo 29 "Malattie Neurologiche". 159
Encephalocraniocutaneous Lipomatosis (Haberland Syndrome or Fishman Syndrome) 158
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 152
Becker's Nevus Syndrome 148
Anti-mog associated encephalitis: when steroid therapy is not enough 146
A girl with a 14.7 Mb 3q26.32-q28 duplication: a new report of 3q duplication syndrome and a literature review 137
Astenia: una maschera per tante identità. Ruolo della patologia della placca neuromuscolare 137
A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment 137
Phacomatosis Pigmentovascularis 136
Blue Rubber Bleb Nevus Syndrome 135
Phacomatosis Pigmentokeratotica 135
Nevus Sebaceous Syndrome 132
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
Autoimmune encephalitis and CSF anti-AMPA GluR3 antibodies in childhood: a case report and literature review 129
A case of extreme brain lesions: Which pathogenetic mechanism? 128
Familial osteoma of the cranial vault 126
A highly sensitive colorimetric approach based on tris (bipyridine) Ruthenium (II/III) mediator for the enzymatic detection of phenylalanine 124
Aicardi-Goutières Syndrome Type 2: A Report on Two Cases with Different Phenotypes Caused by RNASEH2B Gene Mutations 123
Paracelso: vita e contributo all'evoluzione delle scienze mediche, umane e neuropsichiatriche 120
Cerebellotrigeminal Dermal Dysplasia (Gómez-López-Hernández Syndrome) 120
Malattie neurocutanee 119
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. 118
An 11-year follow-up of neonatal onset bath-induced alternating hemiplegia of childhood in monozygotic twins 117
Aneurysmal bone cyst of the acromion: a case report 117
Correlazione genotipo/fenotipo nella Sclerosi Tuberosa (TSC1 vs. TSC2) in 81 pazienti siciliani 117
Megalencephaly Capillary Malformation Syndrome 117
Electrocardiographic Evaluation in Patients With Spinal Muscular Atrophy: A Case-Control Study 114
E se non fossero solo incubi notturni? 114
Wyburn-Mason Syndrome 114
A critical appraisal of neurological evidence on paediatric COVID-19 patients. A systematic literature review 112
Displasia ossea della volta cranica in un paziente con neurofibromatosi tipo 1 112
Congenital muscular dystrophy: from muscle to brain 112
A Phenylalanine sensor exploiting a capacitive readout strategy embedding a selective enzymatic mechanism 111
The natural history of Spinal Neurofibromatosis: A critical review of clinical and genetic features 111
Acute disseminated encephalomyelitis: a long-term prospective study and meta-analysis 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
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 110
Malformazioni vascolari nella neurofibromatosi di tipo 1 (NF1) 110
A child with rhombencephalosynapsis, agenesis of the trigeminal ganglion and optic coloboma (without alopecia): A variant of the cerebellotrigeminal dermal dysplasia? 110
Need for palliative care from birth to infancy in pediatric patients with neurological diseases 109
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 109
Off-label use of drugs and adverse drug reactions in pediatric units: A prospective, multicenter study 109
Aneurismal bone cyst of the acromion: a case report 107
Chromosome 2p15-p16.1 microduplication in a boy with congenital anomalies: Is it a distinctive syndrome? 107
A Complex Brain Malformation Syndrome with Rhombencephalosynapsis, Preaxial Hexadactyly plus Facial and Skull Anomalies 106
Microcephaly-Capillary Malformation Syndrome 106
Autoimmune thyroiditis and acquired demyelinating poliradiculoneuropathy 105
Melorheostosis: case report with 20-year follow-up 104
A child with congenital heart disease and situs viscerum inversus 104
Did Cro-Magnon 1 have neurofibromatosis type 2? 104
Mixed Vascular Nevus Syndrome 104
The use of selegiline in the treatment of cognitive deficits in elderly patients 103
Esame obiettivo neurologico nel bambino 103
A Probable Topiramate-induced Limbs Paraesthesia and Rigid Fingers Flexion 103
Mutazione PRRT2 in un bambino con caratteristiche dismorfiche, microcefalia congenita e convulsioni epilettiche gravi 103
Ataxia in children: early recognition and clinical evaluation 103
Archetypical Patterns of Skin Manifestations in Neurocutaneous Disorders 103
Cognitive disabilities and bioethical implications in down syndrome 103
Hormesis, cellular stress response, and redox homeostasis in autism spectrum disorders 102
Hypomelanosis of Ito 102
Cutis Tricolor 102
Neurocutaneous melanocytosis (melanosis) 102
A novel GABRB3 variant in Dravet syndrome: Case report and literature review 102
Recurrent obstructive hydrocephalus in a 4-month-old infant 101
Citalopram in the treatment of depression in the elderly 101
Sindrome del vomito ciclico: analisi di una popolazione di 20 bambini e revisione della letteratura 101
Zellweger Syndrome coupled to secondary mitochondrial cytopathy in skeletal muscle cells in an infant: a pattern of biochemical overlapping in metabolic myopathies 101
Disturbi del sonno: uno studio prospettico pilota basato sulla somministrazione di questionario online. 101
Klippel-Trenaunay Syndrome, Segmental/Focal Overgrowth Malformations: A Review 100
Clinical course of N-methyl-D-aspartate receptor encephalitis and the effectiveness of cyclophosphamide treatment 100
Neurologia e psichiatria dello sviluppo 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
Two siblings with a homozygous MTHFR C677T (G80A-RFC1) mutation and stroke 99
Encefalite GluR3: fenotipo clinico e strumentale di quattro pazienti 99
A Young Boy with 21q21.1 Microdeletion Showing Speech Delay, Spastic Diplegia, and MRI Abnormalities: Original Case Report 98
Hypotonia, congenital nystagmus, ataxia and abnormal auditory brainstem responses. Report on the first white Caucasian patient 98
Bilateral (perisylvian and opercular) polymicrogyria and Neurofibromatosis type 1 98
A clinical and molecular study in a child under 1 year of age affected by Neurofibromatosis type 2 98
A neurocutaneous phenotype with paired hypo- and hyperpigmented macules, microcephaly and stunted growth as prominent features 97
A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease 96
Bilateral periventricular nodular heterotopia and amniotic band syndrome 96
Totale 14.973
Salva come PNG Salva come JPEG
Categoria #
all - tutte 155.790
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 155.790
Salva come PNG Salva come JPEG


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
2025/202612.513 1.397 1.624 4.754 1.788 2.950 0 0 0 0 0 0 0
Totale 46.293