IRIS
RUGGIERI, MARTINO
 Distribuzione geografica
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Continente #
NA - Nord America 20.729
EU - Europa 14.560
AS - Asia 11.332
SA - Sud America 2.336
AF - Africa 1.082
OC - Oceania 24
Continente sconosciuto - Info sul continente non disponibili 14
Totale 50.077
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Nazione #
US - Stati Uniti d'America 19.937
SG - Singapore 5.926
IT - Italia 5.256
RU - Federazione Russa 4.103
CN - Cina 3.407
BR - Brasile 2.002
IE - Irlanda 1.764
UA - Ucraina 1.655
CI - Costa d'Avorio 728
CA - Canada 654
VN - Vietnam 548
IN - India 477
DE - Germania 382
KR - Corea 328
SE - Svezia 278
GB - Regno Unito 231
NL - Olanda 154
FI - Finlandia 152
AR - Argentina 138
FR - Francia 129
SN - Senegal 121
MX - Messico 99
PL - Polonia 92
BD - Bangladesh 83
ZA - Sudafrica 75
CH - Svizzera 70
JP - Giappone 68
EC - Ecuador 65
TR - Turchia 61
ID - Indonesia 59
UZ - Uzbekistan 59
ES - Italia 55
HK - Hong Kong 49
AT - Austria 48
BJ - Benin 46
IQ - Iraq 42
GR - Grecia 40
IR - Iran 38
PK - Pakistan 37
CO - Colombia 33
CZ - Repubblica Ceca 28
MA - Marocco 27
LB - Libano 22
LT - Lituania 21
NG - Nigeria 20
VE - Venezuela 20
PY - Paraguay 19
RO - Romania 19
AE - Emirati Arabi Uniti 18
AU - Australia 18
BE - Belgio 18
CL - Cile 18
KE - Kenya 17
SA - Arabia Saudita 16
PE - Perù 14
EG - Egitto 13
UY - Uruguay 13
TN - Tunisia 12
BG - Bulgaria 11
IL - Israele 11
JO - Giordania 11
EU - Europa 10
AZ - Azerbaigian 9
BO - Bolivia 9
DZ - Algeria 8
KZ - Kazakistan 8
BY - Bielorussia 7
AL - Albania 6
DO - Repubblica Dominicana 6
JM - Giamaica 6
MY - Malesia 6
NP - Nepal 6
BN - Brunei Darussalam 5
CR - Costa Rica 5
DK - Danimarca 5
EE - Estonia 5
HU - Ungheria 5
AO - Angola 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 50.037
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Città #
Dallas 4.038
Singapore 3.341
Santa Clara 2.211
Chandler 1.870
Jacksonville 1.815
Dublin 1.746
Moscow 1.734
Boardman 832
Hefei 796
Ashburn 770
Chicago 752
Abidjan 728
Houston 629
Catania 591
Nanjing 553
Lawrence 493
Andover 487
Cambridge 487
Los Angeles 483
Toronto 449
Beijing 377
Milan 361
Rome 323
Seoul 322
Des Moines 289
Kochi 287
San Mateo 256
Wilmington 231
Civitanova Marche 220
Ho Chi Minh City 209
São Paulo 181
Nanchang 178
Shenyang 158
Munich 140
New York 132
Palermo 131
Hebei 125
Dakar 121
Jiaxing 117
Buffalo 116
Saint Petersburg 111
Ottawa 109
Hanoi 103
Changsha 100
Bremen 97
Florence 90
Naples 90
Tianjin 84
Bologna 71
Helsinki 70
Council Bluffs 69
Seattle 68
Rio de Janeiro 65
Warsaw 65
The Dalles 64
Tokyo 64
Turin 62
Bari 59
Padova 59
Brooklyn 53
Belo Horizonte 51
Grafing 51
Columbus 50
Johannesburg 50
Montreal 49
Cotonou 46
Dong Ket 46
Hong Kong 46
Phoenix 45
Denver 43
Amsterdam 41
Chennai 41
Lappeenranta 39
Stockholm 39
Redondo Beach 38
Boston 37
Poplar 37
Turku 37
Augusta 35
Curitiba 35
Orem 35
Hangzhou 34
Jinan 34
Liberty Lake 34
Pune 34
Atlanta 33
Norwalk 33
Den Haag 32
Falls Church 32
San Francisco 31
Genoa 30
Oakland 30
Washington 30
London 29
Mumbai 29
San Jose 28
Ann Arbor 27
Brescia 27
Kunming 27
Mexico City 27
Totale 32.104
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Nome #
Dislocazione atlanto-occipitale e atlanto-assiale con grave compressione del midollo spinale nella Sindrome di Down 974
Encefalite da Anticorpi anti-GluR3 in sei pazienti in età pediatrica 848
Sindromi Neurocutanee 637
ESAME NEUROLOGICO 433
Expanding genotype-phenotype correlation of Kenny-Caffey syndrome type 1 421
CUTIS TRICOLOR (RUGGIERI-HAPPLE SYNDROME) 385
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] 266
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders 248
A pilot study on neurological manifestations and antibodies against neuronal antigens in children with haematological and other cancers 228
Natural history of neurofibromatosis type 2 with onset before the age of 1 year. 211
PARALISI CEREBRALI INFANTILI E PARAPLEGIE SPASTICHE EREDITARIE 187
A mosaic pattern of INI1/SMARCB1 protein expression distinguishes Schwannomatosis and NF2-associated peripheral schwannomas from solitary peripheral schwannomas and NF2-associated vestibular schwannomas 187
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) 186
A boy born with multiple lesions of atrophoderma 185
Speckled Lentiginous Nevus Syndrome 182
Encephalocraniocutaneous Lipomatosis (Haberland Syndrome or Fishman Syndrome) 181
Manuale di Pediatria, quinta edizione. Capitolo 2 "Anamnesi ed esame obiettivo". Capitolo 29 "Malattie Neurologiche". 178
Anti-MOG Antibody Syndrome and Cerebral Sinovenous Thrombosis: A Cause-Effect Hypothesis 173
Becker's Nevus Syndrome 169
Anti-mog associated encephalitis: when steroid therapy is not enough 168
A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment 164
Complex malformation (Ruggieri-Happle) phenotype with “cutis tricolor” in a 10-year-old girl 158
Nevus Sebaceous Syndrome 155
A girl with a 14.7 Mb 3q26.32-q28 duplication: a new report of 3q duplication syndrome and a literature review 154
Astenia: una maschera per tante identità. Ruolo della patologia della placca neuromuscolare 154
A New Patient with Potocki-Lupski Syndrome: A Literature Review 153
Blue Rubber Bleb Nevus Syndrome 152
Phacomatosis Pigmentovascularis 152
Phacomatosis Pigmentokeratotica 150
A highly sensitive colorimetric approach based on tris (bipyridine) Ruthenium (II/III) mediator for the enzymatic detection of phenylalanine 148
A case of extreme brain lesions: Which pathogenetic mechanism? 145
Autoimmune encephalitis and CSF anti-AMPA GluR3 antibodies in childhood: a case report and literature review 144
Cerebellotrigeminal Dermal Dysplasia (Gómez-López-Hernández Syndrome) 144
Aneurysmal bone cyst of the acromion: a case report 142
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. 142
Aicardi-Goutières Syndrome Type 2: A Report on Two Cases with Different Phenotypes Caused by RNASEH2B Gene Mutations 141
A Phenylalanine sensor exploiting a capacitive readout strategy embedding a selective enzymatic mechanism 138
A critical appraisal of neurological evidence on paediatric COVID-19 patients. A systematic literature review 136
Megalencephaly Capillary Malformation Syndrome 136
Paracelso: vita e contributo all'evoluzione delle scienze mediche, umane e neuropsichiatriche 135
Craniofacial anomalies, severe cerebellar hypoplasia, psychomotor and growth delay in a child with congenital hypothyroidism 134
Wyburn-Mason Syndrome 134
A child with rhombencephalosynapsis, agenesis of the trigeminal ganglion and optic coloboma (without alopecia): A variant of the cerebellotrigeminal dermal dysplasia? 134
Correlazione genotipo/fenotipo nella Sclerosi Tuberosa (TSC1 vs. TSC2) in 81 pazienti siciliani 133
Electrocardiographic Evaluation in Patients With Spinal Muscular Atrophy: A Case-Control Study 132
Familial osteoma of the cranial vault 132
An 11-year follow-up of neonatal onset bath-induced alternating hemiplegia of childhood in monozygotic twins 131
Malformazioni vascolari nella neurofibromatosi di tipo 1 (NF1) 131
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 130
Need for palliative care from birth to infancy in pediatric patients with neurological diseases 129
Acute disseminated encephalomyelitis: a long-term prospective study and meta-analysis 129
E se non fossero solo incubi notturni? 128
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 128
Archetypical Patterns of Skin Manifestations in Neurocutaneous Disorders 127
Malattie neurocutanee 126
A child with congenital heart disease and situs viscerum inversus 124
A Probable Topiramate-induced Limbs Paraesthesia and Rigid Fingers Flexion 124
A novel GABRB3 variant in Dravet syndrome: Case report and literature review 124
A Complex Brain Malformation Syndrome with Rhombencephalosynapsis, Preaxial Hexadactyly plus Facial and Skull Anomalies 123
Autoimmune thyroiditis and acquired demyelinating poliradiculoneuropathy 123
Microcephaly-Capillary Malformation Syndrome 123
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] 122
Aneurismal bone cyst of the acromion: a case report 122
Mutazione PRRT2 in un bambino con caratteristiche dismorfiche, microcefalia congenita e convulsioni epilettiche gravi 122
Off-label use of drugs and adverse drug reactions in pediatric units: A prospective, multicenter study 122
Hypomelanosis of Ito 121
A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease 120
Short-term neurodevelopmental outcome in term neonates treated with phenobarbital versus levetiracetam: A single-center experience 119
The use of selegiline in the treatment of cognitive deficits in elderly patients 118
A neurocutaneous phenotype with paired hypo- and hyperpigmented macules, microcephaly and stunted growth as prominent features 118
Klippel-Trenaunay Syndrome, Segmental/Focal Overgrowth Malformations: A Review 117
Sindrome del vomito ciclico: analisi di una popolazione di 20 bambini e revisione della letteratura 117
Did Cro-Magnon 1 have neurofibromatosis type 2? 117
Congenital muscular dystrophy: from muscle to brain 117
Cutis Tricolor 117
Disturbi del sonno: uno studio prospettico pilota basato sulla somministrazione di questionario online. 117
Displasia ossea della volta cranica in un paziente con neurofibromatosi tipo 1 116
The natural history of Spinal Neurofibromatosis: A critical review of clinical and genetic features 116
Ataxia in children: early recognition and clinical evaluation 116
A Young Boy with 21q21.1 Microdeletion Showing Speech Delay, Spastic Diplegia, and MRI Abnormalities: Original Case Report 115
Congenital bone malformations in patients with neurofibromatosis type 1 (Nf1) 115
Citalopram in the treatment of depression in the elderly 115
Recurrent obstructive hydrocephalus in a 4-month-old infant 114
Mixed Vascular Nevus Syndrome 114
Neurocutaneous melanocytosis (melanosis) 114
A clinical and molecular study in a child under 1 year of age affected by Neurofibromatosis type 2 113
Encefalite GluR3: fenotipo clinico e strumentale di quattro pazienti 113
Long-term follow-up and novel genotype-phenotype analysis of monozygotic twins with ATP1A3 mutation in Alternating Hemiplegia of Childhood-2 113
Anomalies of Midbrain Hindbrain Development: Midbrain Clefts, Cerebellar Nodular Heterotopia with Overlying Dysgenesis, Cerebellar Foliation Disorder, Pontine Tegmental Cap Dysplasia; Joubert Syndrome; Lhermitte Duclos Syndrome. Diagnosis, Classification and Rehabilitation Hypothesis 112
Esame obiettivo neurologico nel bambino 111
Adrenal Disorders and the Paediatric Brain: Pathophysiological Considerations and Clinical Implications 111
Chromosome 2p15-p16.1 microduplication in a boy with congenital anomalies: Is it a distinctive syndrome? 111
7q31.32 partial duplication: First report of a child with dysmorphism, autistic spectrum disorder, moderate intellectual disability and, epilepsy. Literature review 110
aEEG vs cEEG's sensivity for seizure detection in the setting of neonatal intensive care units: A systematic review and meta-analysis 109
Short Efficacy Evaluation of External Ventricular Drains Versus Ventriculosubgaleal Shunt in the Management of Neonatal Posthemorrhagic Hydrocephalus: A Retrospective Single-Center Cohort Study 109
Analgetic thalamic syndrome in association with thalamic symmetrical abnormalities during measles encephalitis 109
Hormesis, cellular stress response, and redox homeostasis in autism spectrum disorders 109
Chronic atrial fibrillation and asymptomatic cerebral infarction in elderly patients 109
121 novel mutations revealed by DHPLC analysis of the neurofibromatosis type 1 (NF1) gene in southern Italian NF1 patients 109
Melorheostosis: case report with 20-year follow-up 108
Totale 16.566
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Categoria #
all - tutte 163.204
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 163.204
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211.762 0 0 0 0 0 95 424 64 337 135 539 168
2021/20224.090 447 525 57 112 588 79 574 188 400 41 122 957
2022/20236.425 555 257 103 560 642 1.090 75 1.018 1.471 138 302 214
2023/20243.578 233 444 280 307 182 482 152 247 65 142 603 441
2024/202511.542 204 1.689 730 586 2.065 1.092 454 509 900 1.161 1.161 991
2025/202617.321 1.391 1.619 4.732 1.772 3.689 4.118 0 0 0 0 0 0
Totale 50.927