IRIS
RUGGIERI, MARTINO
 Distribuzione geografica
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Continente #
NA - Nord America 24.221
EU - Europa 16.066
AS - Asia 13.867
SA - Sud America 2.632
AF - Africa 1.498
OC - Oceania 33
Continente sconosciuto - Info sul continente non disponibili 14
Totale 58.331
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Nazione #
US - Stati Uniti d'America 23.217
SG - Singapore 6.768
IT - Italia 5.770
RU - Federazione Russa 4.107
CN - Cina 3.726
BR - Brasile 2.171
IE - Irlanda 1.770
UA - Ucraina 1.679
VN - Vietnam 1.066
CA - Canada 763
CI - Costa d'Avorio 731
FR - Francia 699
IN - India 555
KR - Corea 538
DE - Germania 431
SE - Svezia 345
NG - Nigeria 322
BD - Bangladesh 296
GB - Regno Unito 288
NL - Olanda 209
FI - Finlandia 186
AR - Argentina 180
MX - Messico 138
HK - Hong Kong 128
SN - Senegal 125
ZA - Sudafrica 113
PL - Polonia 108
TR - Turchia 91
IQ - Iraq 90
JP - Giappone 88
ID - Indonesia 80
EC - Ecuador 78
CH - Svizzera 77
ES - Italia 73
PK - Pakistan 71
UZ - Uzbekistan 69
AT - Austria 55
CO - Colombia 54
GR - Grecia 48
BJ - Benin 46
MA - Marocco 42
IR - Iran 38
VE - Venezuela 37
CZ - Repubblica Ceca 36
CL - Cile 33
JM - Giamaica 31
LT - Lituania 31
JO - Giordania 29
AU - Australia 27
PY - Paraguay 27
EG - Egitto 26
KE - Kenya 26
SA - Arabia Saudita 26
RO - Romania 25
LB - Libano 24
PH - Filippine 24
AE - Emirati Arabi Uniti 21
BE - Belgio 20
DZ - Algeria 18
MY - Malesia 18
TN - Tunisia 18
UY - Uruguay 17
PE - Perù 16
BO - Bolivia 14
IL - Israele 14
BG - Bulgaria 13
ET - Etiopia 13
KZ - Kazakistan 13
AL - Albania 11
AZ - Azerbaigian 10
BY - Bielorussia 10
EU - Europa 10
HN - Honduras 10
TT - Trinidad e Tobago 10
HU - Ungheria 9
NP - Nepal 9
PT - Portogallo 9
CR - Costa Rica 8
DO - Repubblica Dominicana 8
GT - Guatemala 8
OM - Oman 8
AO - Angola 7
HR - Croazia 7
KH - Cambogia 7
RS - Serbia 7
DK - Danimarca 6
KW - Kuwait 6
SK - Slovacchia (Repubblica Slovacca) 6
TH - Thailandia 6
BN - Brunei Darussalam 5
EE - Estonia 5
PS - Palestinian Territory 5
SI - Slovenia 5
SV - El Salvador 5
SY - Repubblica araba siriana 5
BA - Bosnia-Erzegovina 4
BB - Barbados 4
CY - Cipro 4
GD - Grenada 4
GE - Georgia 4
Totale 58.248
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Città #
Dallas 4.067
Singapore 3.932
Santa Clara 2.280
Chandler 1.871
Jacksonville 1.817
Dublin 1.752
Moscow 1.735
San Jose 1.645
Ashburn 1.180
Boardman 833
Hefei 797
Chicago 768
Abidjan 730
Houston 644
Catania 624
Los Angeles 567
Nanjing 553
Seoul 530
Lauterbourg 524
Lawrence 493
Andover 487
Cambridge 487
Toronto 469
Beijing 416
Milan 394
Ho Chi Minh City 380
Rome 357
Des Moines 290
Kochi 288
San Mateo 256
Wilmington 234
Hanoi 230
New York 228
Civitanova Marche 220
São Paulo 206
Council Bluffs 194
Nanchang 178
Abuja 176
Palermo 158
Shenyang 158
Buffalo 149
Munich 140
Dakar 125
Hebei 125
Lagos 119
Jiaxing 117
Hong Kong 114
Saint Petersburg 111
Ottawa 110
Changsha 101
Florence 101
Naples 98
Bremen 97
Montreal 93
Orem 93
Tianjin 85
Tokyo 82
Amsterdam 79
Warsaw 79
Bologna 77
Helsinki 76
Johannesburg 75
Rio de Janeiro 75
Seattle 73
Bari 67
Lappeenranta 67
Turin 67
Brooklyn 66
The Dalles 66
Padova 59
Phoenix 59
Chennai 54
Atlanta 52
Belo Horizonte 52
Denver 52
Columbus 51
Grafing 51
Stockholm 51
London 49
Cotonou 46
Dong Ket 46
Da Nang 45
Frankfurt am Main 45
Poplar 44
Mexico City 42
Mumbai 42
Curitiba 41
Boston 39
Hangzhou 39
Redondo Beach 38
Augusta 37
Haiphong 37
Pune 37
San Francisco 37
Turku 37
Baghdad 36
Tashkent 35
Jinan 34
Liberty Lake 34
Norwalk 33
Totale 37.229
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Nome #
Dislocazione atlanto-occipitale e atlanto-assiale con grave compressione del midollo spinale nella Sindrome di Down 1.008
Encefalite da Anticorpi anti-GluR3 in sei pazienti in età pediatrica 923
Sindromi Neurocutanee 712
ESAME NEUROLOGICO 500
Expanding genotype-phenotype correlation of Kenny-Caffey syndrome type 1 445
CUTIS TRICOLOR (RUGGIERI-HAPPLE SYNDROME) 408
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] 285
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders 269
A pilot study on neurological manifestations and antibodies against neuronal antigens in children with haematological and other cancers 248
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) 223
Natural history of neurofibromatosis type 2 with onset before the age of 1 year. 218
A mosaic pattern of INI1/SMARCB1 protein expression distinguishes Schwannomatosis and NF2-associated peripheral schwannomas from solitary peripheral schwannomas and NF2-associated vestibular schwannomas 209
Speckled Lentiginous Nevus Syndrome 205
A boy born with multiple lesions of atrophoderma 204
PARALISI CEREBRALI INFANTILI E PARAPLEGIE SPASTICHE EREDITARIE 202
Anti-MOG Antibody Syndrome and Cerebral Sinovenous Thrombosis: A Cause-Effect Hypothesis 201
Becker's Nevus Syndrome 196
Manuale di Pediatria, quinta edizione. Capitolo 2 "Anamnesi ed esame obiettivo". Capitolo 29 "Malattie Neurologiche". 196
Encephalocraniocutaneous Lipomatosis (Haberland Syndrome or Fishman Syndrome) 194
Anti-mog associated encephalitis: when steroid therapy is not enough 194
A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment 186
Phacomatosis Pigmentovascularis 182
A New Patient with Potocki-Lupski Syndrome: A Literature Review 180
A girl with a 14.7 Mb 3q26.32-q28 duplication: a new report of 3q duplication syndrome and a literature review 176
Blue Rubber Bleb Nevus Syndrome 176
A highly sensitive colorimetric approach based on tris (bipyridine) Ruthenium (II/III) mediator for the enzymatic detection of phenylalanine 175
Astenia: una maschera per tante identità. Ruolo della patologia della placca neuromuscolare 173
Nevus Sebaceous Syndrome 173
Phacomatosis Pigmentokeratotica 170
Autoimmune encephalitis and CSF anti-AMPA GluR3 antibodies in childhood: a case report and literature review 166
A Phenylalanine sensor exploiting a capacitive readout strategy embedding a selective enzymatic mechanism 166
A case of extreme brain lesions: Which pathogenetic mechanism? 166
Complex malformation (Ruggieri-Happle) phenotype with “cutis tricolor” in a 10-year-old girl 166
Aneurysmal bone cyst of the acromion: a case report 163
Aicardi-Goutières Syndrome Type 2: A Report on Two Cases with Different Phenotypes Caused by RNASEH2B Gene Mutations 162
Cerebellotrigeminal Dermal Dysplasia (Gómez-López-Hernández Syndrome) 161
Cutis Tricolor 161
A critical appraisal of neurological evidence on paediatric COVID-19 patients. A systematic literature review 159
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. 156
Paracelso: vita e contributo all'evoluzione delle scienze mediche, umane e neuropsichiatriche 156
Wyburn-Mason Syndrome 155
Electrocardiographic Evaluation in Patients With Spinal Muscular Atrophy: A Case-Control Study 153
Megalencephaly Capillary Malformation Syndrome 153
Correlazione genotipo/fenotipo nella Sclerosi Tuberosa (TSC1 vs. TSC2) in 81 pazienti siciliani 151
Need for palliative care from birth to infancy in pediatric patients with neurological diseases 150
Craniofacial anomalies, severe cerebellar hypoplasia, psychomotor and growth delay in a child with congenital hypothyroidism 150
Archetypical Patterns of Skin Manifestations in Neurocutaneous Disorders 150
Malformazioni vascolari nella neurofibromatosi di tipo 1 (NF1) 149
A child with rhombencephalosynapsis, agenesis of the trigeminal ganglion and optic coloboma (without alopecia): A variant of the cerebellotrigeminal dermal dysplasia? 149
A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease 148
Acute disseminated encephalomyelitis: a long-term prospective study and meta-analysis 148
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 148
Familial osteoma of the cranial vault 147
An 11-year follow-up of neonatal onset bath-induced alternating hemiplegia of childhood in monozygotic twins 145
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 145
Microcephaly-Capillary Malformation Syndrome 145
A Probable Topiramate-induced Limbs Paraesthesia and Rigid Fingers Flexion 144
Mutazione PRRT2 in un bambino con caratteristiche dismorfiche, microcefalia congenita e convulsioni epilettiche gravi 144
A novel GABRB3 variant in Dravet syndrome: Case report and literature review 144
Short Efficacy Evaluation of External Ventricular Drains Versus Ventriculosubgaleal Shunt in the Management of Neonatal Posthemorrhagic Hydrocephalus: A Retrospective Single-Center Cohort Study 143
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] 143
Off-label use of drugs and adverse drug reactions in pediatric units: A prospective, multicenter study 143
Klippel-Trenaunay Syndrome, Segmental/Focal Overgrowth Malformations: A Review 142
Anomalies of Midbrain/Hindbrain Development and Related Disabilities: Pontocerebellar Hypoplasia, Congenital Disorders of Glycosylation, and Cerebellar Hemisphere Hypoplasia 141
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 141
Neurologia e psichiatria dello sviluppo 141
E se non fossero solo incubi notturni? 141
A child with congenital heart disease and situs viscerum inversus 140
Hypomelanosis of Ito 140
Aneurismal bone cyst of the acromion: a case report 139
Encefalite GluR3: fenotipo clinico e strumentale di quattro pazienti 139
Esame obiettivo neurologico nel bambino 136
Sindrome del vomito ciclico: analisi di una popolazione di 20 bambini e revisione della letteratura 135
Short-term neurodevelopmental outcome in term neonates treated with phenobarbital versus levetiracetam: A single-center experience 135
Long-term follow-up and novel genotype-phenotype analysis of monozygotic twins with ATP1A3 mutation in Alternating Hemiplegia of Childhood-2 135
Malformations of cortical development, cognitive involvement and epilepsy: A single institution experience in 19 young patients 135
Maternal Phenylketonuria and Offspring Outcome: A Retrospective Study with a Systematic Review of the Literature 134
A Young Boy with 21q21.1 Microdeletion Showing Speech Delay, Spastic Diplegia, and MRI Abnormalities: Original Case Report 133
A Complex Brain Malformation Syndrome with Rhombencephalosynapsis, Preaxial Hexadactyly plus Facial and Skull Anomalies 133
Autoimmune thyroiditis and acquired demyelinating poliradiculoneuropathy 133
Disturbi del sonno: uno studio prospettico pilota basato sulla somministrazione di questionario online. 133
Malattie neurocutanee 133
Urea/Creatinine Ratio’s Correlation with Creatine Kinase Normalization in Pediatric COVID-19 Patients with Myositis: Evaluating Prognostic and Predictive Value 132
Motor imagery for paediatric neurorehabilitation: how much do we know? Perspectives from a systematic review 132
PPP5C pathogenic variant identified: a potential key to gaining insight into developmental and epileptic encephalopathy? 132
Did Cro-Magnon 1 have neurofibromatosis type 2? 132
Mixed Vascular Nevus Syndrome 132
Neurocutaneous melanocytosis (melanosis) 132
Genotype–Phenotype Correlation in a Large Cohort of Eastern Sicilian Patients Affected by Phenylketonuria: Newborn Screening Program, Clinical Features, and Follow-Up 131
The use of selegiline in the treatment of cognitive deficits in elderly patients 131
A neurocutaneous phenotype with paired hypo- and hyperpigmented macules, microcephaly and stunted growth as prominent features 131
7q31.32 partial duplication: First report of a child with dysmorphism, autistic spectrum disorder, moderate intellectual disability and, epilepsy. Literature review 131
Displasia ossea della volta cranica in un paziente con neurofibromatosi tipo 1 130
Anomalies of Midbrain/Hindbrain Development: Malformations of Cerebellum: Diagnosis, Classification, and Rehabilitative Hypothesis 129
Chronic atrial fibrillation and asymptomatic cerebral infarction in elderly patients 129
Point-of-care ultrasound (POCUS) pediatric resident training course: a cross-sectional survey 129
aEEG vs cEEG's sensivity for seizure detection in the setting of neonatal intensive care units: A systematic review and meta-analysis 128
Recurrent obstructive hydrocephalus in a 4-month-old infant 128
Citalopram in the treatment of depression in the elderly 128
A clinical and molecular study in a child under 1 year of age affected by Neurofibromatosis type 2 128
Totale 18.744
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Categoria #
all - tutte 189.138
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 189.138
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
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
2025/202625.473 1.391 1.619 4.732 1.772 3.689 4.639 2.848 640 1.414 1.235 875 619
2026/2027127 127 0 0 0 0 0 0 0 0 0 0 0
Totale 59.206