IRIS
RUGGIERI, MARTINO
 Distribuzione geografica
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Continente #
NA - Nord America 25.270
EU - Europa 16.405
AS - Asia 13.974
SA - Sud America 2.664
AF - Africa 1.499
Continente sconosciuto - Info sul continente non disponibili 889
OC - Oceania 34
Totale 60.735
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Nazione #
US - Stati Uniti d'America 24.192
SG - Singapore 6.789
IT - Italia 5.943
RU - Federazione Russa 4.107
CN - Cina 3.763
BR - Brasile 2.172
IE - Irlanda 1.770
UA - Ucraina 1.682
VN - Vietnam 1.073
CA - Canada 795
CI - Costa d'Avorio 731
FR - Francia 705
IN - India 556
KR - Corea 538
SE - Svezia 483
DE - Germania 438
NG - Nigeria 322
BD - Bangladesh 316
GB - Regno Unito 291
NL - Olanda 212
FI - Finlandia 186
AR - Argentina 180
MX - Messico 141
HK - Hong Kong 139
SN - Senegal 125
ZA - Sudafrica 113
PL - Polonia 109
TR - Turchia 91
IQ - Iraq 90
JP - Giappone 88
EC - Ecuador 85
ID - Indonesia 82
CH - Svizzera 78
ES - Italia 75
PK - Pakistan 72
CO - Colombia 71
UZ - Uzbekistan 69
AT - Austria 55
GR - Grecia 48
BJ - Benin 46
MA - Marocco 42
VE - Venezuela 42
JM - Giamaica 39
IR - Iran 38
CZ - Repubblica Ceca 36
CL - Cile 33
LT - Lituania 31
JO - Giordania 29
AU - Australia 28
PY - Paraguay 27
EG - Egitto 26
KE - Kenya 26
PH - Filippine 26
SA - Arabia Saudita 26
LB - Libano 25
RO - Romania 25
AE - Emirati Arabi Uniti 21
MY - Malesia 21
BE - Belgio 20
CR - Costa Rica 19
DZ - Algeria 19
TN - Tunisia 18
UY - Uruguay 17
BO - Bolivia 16
PE - Perù 16
IL - Israele 14
AL - Albania 13
BG - Bulgaria 13
ET - Etiopia 13
KZ - Kazakistan 13
HN - Honduras 12
TT - Trinidad e Tobago 11
AZ - Azerbaigian 10
BY - Bielorussia 10
EU - Europa 10
HU - Ungheria 9
NP - Nepal 9
PT - Portogallo 9
SV - El Salvador 9
DO - Repubblica Dominicana 8
GT - Guatemala 8
OM - Oman 8
AO - Angola 7
HR - Croazia 7
KH - Cambogia 7
PR - Porto Rico 7
RS - Serbia 7
BB - Barbados 6
DK - Danimarca 6
KW - Kuwait 6
SK - Slovacchia (Repubblica Slovacca) 6
TH - Thailandia 6
BN - Brunei Darussalam 5
EE - Estonia 5
PA - Panama 5
PS - Palestinian Territory 5
SI - Slovenia 5
SY - Repubblica araba siriana 5
BA - Bosnia-Erzegovina 4
CY - Cipro 4
Totale 59.769
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Città #
Dallas 4.074
Singapore 3.949
Santa Clara 2.312
Chandler 1.871
Jacksonville 1.818
Dublin 1.752
Moscow 1.735
San Jose 1.683
Ashburn 1.239
Boardman 834
Hefei 797
Chicago 773
Abidjan 730
Council Bluffs 680
Houston 644
Catania 632
Los Angeles 577
Nanjing 553
Seoul 530
Lauterbourg 524
Lawrence 493
Andover 487
Cambridge 487
Toronto 473
Beijing 446
Milan 416
Ho Chi Minh City 382
Rome 375
Des Moines 290
Kochi 288
San Mateo 256
New York 241
Wilmington 236
Hanoi 232
Civitanova Marche 221
São Paulo 206
Nanchang 178
Abuja 176
Palermo 162
Shenyang 158
Buffalo 151
Munich 140
Dakar 125
Hebei 125
Hong Kong 125
Lagos 119
Jiaxing 117
Ottawa 113
Saint Petersburg 111
Naples 103
Florence 102
Changsha 101
Montreal 98
Bremen 97
Orem 93
Bologna 87
Tianjin 85
Tokyo 82
Amsterdam 79
Warsaw 79
Helsinki 76
Bari 75
Johannesburg 75
Rio de Janeiro 75
Seattle 73
Brooklyn 70
Phoenix 69
Turin 68
Lappeenranta 67
The Dalles 66
Padova 59
Chennai 54
Atlanta 53
Denver 53
Belo Horizonte 52
Columbus 52
Grafing 51
London 51
Stockholm 51
Cotonou 46
Dong Ket 46
Da Nang 45
Frankfurt am Main 45
Boston 44
Poplar 44
Mexico City 43
Mumbai 42
Curitiba 41
San Francisco 40
Hangzhou 39
Haiphong 38
Redondo Beach 38
Augusta 37
Pune 37
Turku 37
Baghdad 36
Tashkent 35
Jinan 34
Liberty Lake 34
Genoa 33
Totale 38.066
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Nome #
Dislocazione atlanto-occipitale e atlanto-assiale con grave compressione del midollo spinale nella Sindrome di Down 1.017
Encefalite da Anticorpi anti-GluR3 in sei pazienti in età pediatrica 929
Sindromi Neurocutanee 738
ESAME NEUROLOGICO 521
Expanding genotype-phenotype correlation of Kenny-Caffey syndrome type 1 451
CUTIS TRICOLOR (RUGGIERI-HAPPLE SYNDROME) 423
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] 286
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders 273
A pilot study on neurological manifestations and antibodies against neuronal antigens in children with haematological and other cancers 250
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) 227
Natural history of neurofibromatosis type 2 with onset before the age of 1 year. 223
A mosaic pattern of INI1/SMARCB1 protein expression distinguishes Schwannomatosis and NF2-associated peripheral schwannomas from solitary peripheral schwannomas and NF2-associated vestibular schwannomas 210
Speckled Lentiginous Nevus Syndrome 210
A boy born with multiple lesions of atrophoderma 205
PARALISI CEREBRALI INFANTILI E PARAPLEGIE SPASTICHE EREDITARIE 205
Anti-MOG Antibody Syndrome and Cerebral Sinovenous Thrombosis: A Cause-Effect Hypothesis 203
Becker's Nevus Syndrome 201
Manuale di Pediatria, quinta edizione. Capitolo 2 "Anamnesi ed esame obiettivo". Capitolo 29 "Malattie Neurologiche". 198
Anti-mog associated encephalitis: when steroid therapy is not enough 197
Encephalocraniocutaneous Lipomatosis (Haberland Syndrome or Fishman Syndrome) 196
Phacomatosis Pigmentovascularis 187
A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment 186
A New Patient with Potocki-Lupski Syndrome: A Literature Review 181
Blue Rubber Bleb Nevus Syndrome 180
A girl with a 14.7 Mb 3q26.32-q28 duplication: a new report of 3q duplication syndrome and a literature review 178
A highly sensitive colorimetric approach based on tris (bipyridine) Ruthenium (II/III) mediator for the enzymatic detection of phenylalanine 177
Nevus Sebaceous Syndrome 175
Astenia: una maschera per tante identità. Ruolo della patologia della placca neuromuscolare 174
Phacomatosis Pigmentokeratotica 172
A Phenylalanine sensor exploiting a capacitive readout strategy embedding a selective enzymatic mechanism 170
Complex malformation (Ruggieri-Happle) phenotype with “cutis tricolor” in a 10-year-old girl 169
Autoimmune encephalitis and CSF anti-AMPA GluR3 antibodies in childhood: a case report and literature review 168
A case of extreme brain lesions: Which pathogenetic mechanism? 167
Aneurysmal bone cyst of the acromion: a case report 167
Cutis Tricolor 166
Aicardi-Goutières Syndrome Type 2: A Report on Two Cases with Different Phenotypes Caused by RNASEH2B Gene Mutations 165
Cerebellotrigeminal Dermal Dysplasia (Gómez-López-Hernández Syndrome) 163
A critical appraisal of neurological evidence on paediatric COVID-19 patients. A systematic literature review 161
Megalencephaly Capillary Malformation Syndrome 161
PURA-Related Neurodevelopmental Disorders with Epilepsy Treated with Ketogenic Diet: A Case-Based Review 160
Craniofacial anomalies, severe cerebellar hypoplasia, psychomotor and growth delay in a child with congenital hypothyroidism 159
Paracelso: vita e contributo all'evoluzione delle scienze mediche, umane e neuropsichiatriche 159
Electrocardiographic Evaluation in Patients With Spinal Muscular Atrophy: A Case-Control Study 158
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. 158
Wyburn-Mason Syndrome 158
Correlazione genotipo/fenotipo nella Sclerosi Tuberosa (TSC1 vs. TSC2) in 81 pazienti siciliani 155
Familial osteoma of the cranial vault 155
Acute disseminated encephalomyelitis: a long-term prospective study and meta-analysis 154
A child with rhombencephalosynapsis, agenesis of the trigeminal ganglion and optic coloboma (without alopecia): A variant of the cerebellotrigeminal dermal dysplasia? 154
Need for palliative care from birth to infancy in pediatric patients with neurological diseases 153
Archetypical Patterns of Skin Manifestations in Neurocutaneous Disorders 152
A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease 151
Microcephaly-Capillary Malformation Syndrome 151
Malformazioni vascolari nella neurofibromatosi di tipo 1 (NF1) 151
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 149
An 11-year follow-up of neonatal onset bath-induced alternating hemiplegia of childhood in monozygotic twins 148
Anomalies of Midbrain/Hindbrain Development and Related Disabilities: Pontocerebellar Hypoplasia, Congenital Disorders of Glycosylation, and Cerebellar Hemisphere Hypoplasia 147
Short Efficacy Evaluation of External Ventricular Drains Versus Ventriculosubgaleal Shunt in the Management of Neonatal Posthemorrhagic Hydrocephalus: A Retrospective Single-Center Cohort Study 147
A child with congenital heart disease and situs viscerum inversus 146
A Probable Topiramate-induced Limbs Paraesthesia and Rigid Fingers Flexion 146
Mutazione PRRT2 in un bambino con caratteristiche dismorfiche, microcefalia congenita e convulsioni epilettiche gravi 146
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 146
Off-label use of drugs and adverse drug reactions in pediatric units: A prospective, multicenter study 146
A novel GABRB3 variant in Dravet syndrome: Case report and literature review 146
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 145
Klippel-Trenaunay Syndrome, Segmental/Focal Overgrowth Malformations: A Review 144
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] 144
Neurologia e psichiatria dello sviluppo 144
Hypomelanosis of Ito 144
E se non fossero solo incubi notturni? 143
Aneurismal bone cyst of the acromion: a case report 142
Encefalite GluR3: fenotipo clinico e strumentale di quattro pazienti 141
Neurocutaneous melanocytosis (melanosis) 140
Malformations of cortical development, cognitive involvement and epilepsy: A single institution experience in 19 young patients 140
Sindrome del vomito ciclico: analisi di una popolazione di 20 bambini e revisione della letteratura 139
Esame obiettivo neurologico nel bambino 138
A Young Boy with 21q21.1 Microdeletion Showing Speech Delay, Spastic Diplegia, and MRI Abnormalities: Original Case Report 137
Disturbi del sonno: uno studio prospettico pilota basato sulla somministrazione di questionario online. 137
Long-term follow-up and novel genotype-phenotype analysis of monozygotic twins with ATP1A3 mutation in Alternating Hemiplegia of Childhood-2 137
Maternal Phenylketonuria and Offspring Outcome: A Retrospective Study with a Systematic Review of the Literature 136
Mixed Vascular Nevus Syndrome 136
7q31.32 partial duplication: First report of a child with dysmorphism, autistic spectrum disorder, moderate intellectual disability and, epilepsy. Literature review 136
A neurocutaneous phenotype with paired hypo- and hyperpigmented macules, microcephaly and stunted growth as prominent features 135
Short-term neurodevelopmental outcome in term neonates treated with phenobarbital versus levetiracetam: A single-center experience 135
Motor imagery for paediatric neurorehabilitation: how much do we know? Perspectives from a systematic review 134
PPP5C pathogenic variant identified: a potential key to gaining insight into developmental and epileptic encephalopathy? 134
A Complex Brain Malformation Syndrome with Rhombencephalosynapsis, Preaxial Hexadactyly plus Facial and Skull Anomalies 134
Autoimmune thyroiditis and acquired demyelinating poliradiculoneuropathy 134
Malattie neurocutanee 134
Urea/Creatinine Ratio’s Correlation with Creatine Kinase Normalization in Pediatric COVID-19 Patients with Myositis: Evaluating Prognostic and Predictive Value 133
Did Cro-Magnon 1 have neurofibromatosis type 2? 133
Genotype–Phenotype Correlation in a Large Cohort of Eastern Sicilian Patients Affected by Phenylketonuria: Newborn Screening Program, Clinical Features, and Follow-Up 132
Anomalies of Midbrain/Hindbrain Development: Malformations of Cerebellum: Diagnosis, Classification, and Rehabilitative Hypothesis 132
The use of selegiline in the treatment of cognitive deficits in elderly patients 132
Citalopram in the treatment of depression in the elderly 132
Chronic atrial fibrillation and asymptomatic cerebral infarction in elderly patients 132
Displasia ossea della volta cranica in un paziente con neurofibromatosi tipo 1 131
Ataxia in children: early recognition and clinical evaluation 131
Point-of-care ultrasound (POCUS) pediatric resident training course: a cross-sectional survey 131
Recurrent obstructive hydrocephalus in a 4-month-old infant 130
Totale 19.137
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Categoria #
all - tutte 201.379
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 201.379
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20223.118 0 0 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
2026/20271.656 500 1.124 32 0 0 0 0 0 0 0 0 0
Totale 60.735