IRIS
RUGGIERI, MARTINO
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 23.238
EU - Europa 15.740
AS - Asia 13.520
SA - Sud America 2.611
AF - Africa 1.497
OC - Oceania 33
Continente sconosciuto - Info sul continente non disponibili 14
Totale 56.653
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 22.318
SG - Singapore 6.675
IT - Italia 5.530
RU - Federazione Russa 4.107
CN - Cina 3.641
BR - Brasile 2.159
IE - Irlanda 1.770
UA - Ucraina 1.676
VN - Vietnam 1.065
CI - Costa d'Avorio 731
CA - Canada 724
FR - Francia 696
IN - India 553
KR - Corea 537
DE - Germania 428
NG - Nigeria 322
SE - Svezia 290
GB - Regno Unito 287
NL - Olanda 206
FI - Finlandia 186
AR - Argentina 176
BD - Bangladesh 152
MX - Messico 130
SN - Senegal 125
HK - Hong Kong 114
ZA - Sudafrica 113
PL - Polonia 107
TR - Turchia 91
IQ - Iraq 90
JP - Giappone 88
EC - Ecuador 78
ID - Indonesia 78
CH - Svizzera 77
PK - Pakistan 70
UZ - Uzbekistan 69
ES - Italia 67
AT - Austria 55
CO - Colombia 51
BJ - Benin 46
GR - Grecia 46
MA - Marocco 42
IR - Iran 38
CZ - Repubblica Ceca 36
VE - Venezuela 36
CL - Cile 33
JO - Giordania 29
LT - Lituania 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
JM - Giamaica 20
BE - Belgio 19
DZ - Algeria 18
MY - Malesia 18
TN - Tunisia 18
PE - Perù 16
UY - Uruguay 16
BO - Bolivia 14
IL - Israele 14
BG - Bulgaria 13
ET - Etiopia 13
KZ - Kazakistan 13
AL - Albania 10
AZ - Azerbaigian 10
BY - Bielorussia 10
EU - Europa 10
CR - Costa Rica 8
DO - Repubblica Dominicana 8
HU - Ungheria 8
NP - Nepal 8
OM - Oman 8
PT - Portogallo 8
AO - Angola 7
HR - Croazia 7
KH - Cambogia 7
DK - Danimarca 6
KW - Kuwait 6
RS - Serbia 6
SK - Slovacchia (Repubblica Slovacca) 6
TH - Thailandia 6
TT - Trinidad e Tobago 6
BN - Brunei Darussalam 5
EE - Estonia 5
PS - Palestinian Territory 5
SI - Slovenia 5
SY - Repubblica araba siriana 5
GD - Grenada 4
GE - Georgia 4
KG - Kirghizistan 4
MT - Malta 4
PA - Panama 4
QA - Qatar 4
XK - ???statistics.table.value.countryCode.XK??? 4
AM - Armenia 3
Totale 56.586
Salva come PNG Salva come JPEG
Città #
Dallas 4.054
Singapore 3.922
Santa Clara 2.241
Chandler 1.870
Jacksonville 1.815
Dublin 1.752
Moscow 1.735
San Jose 1.263
Ashburn 1.131
Boardman 832
Hefei 796
Chicago 759
Abidjan 730
Houston 639
Catania 602
Nanjing 553
Los Angeles 547
Seoul 530
Lauterbourg 524
Lawrence 493
Andover 487
Cambridge 487
Toronto 465
Beijing 403
Milan 383
Ho Chi Minh City 380
Rome 335
Des Moines 290
Kochi 288
San Mateo 256
Wilmington 232
Hanoi 229
Civitanova Marche 220
São Paulo 205
Council Bluffs 192
New York 192
Nanchang 178
Abuja 176
Shenyang 158
Palermo 144
Munich 140
Buffalo 128
Dakar 125
Hebei 125
Lagos 119
Jiaxing 117
Saint Petersburg 111
Ottawa 110
Changsha 101
Hong Kong 100
Bremen 97
Florence 96
Naples 92
Orem 89
Tianjin 85
Montreal 82
Tokyo 82
Amsterdam 79
Warsaw 78
Helsinki 76
Bologna 75
Johannesburg 75
Rio de Janeiro 75
Seattle 71
Lappeenranta 67
The Dalles 66
Bari 65
Turin 63
Brooklyn 59
Padova 59
Chennai 54
Phoenix 54
Belo Horizonte 52
Denver 52
Grafing 51
Stockholm 51
Atlanta 50
Columbus 50
London 48
Cotonou 46
Dong Ket 46
Da Nang 45
Frankfurt am Main 45
Poplar 44
Curitiba 41
Mumbai 40
Boston 39
Redondo Beach 38
Augusta 37
Haiphong 37
Hangzhou 37
Pune 37
Turku 37
Baghdad 36
San Francisco 35
Tashkent 35
Jinan 34
Liberty Lake 34
Mexico City 34
Norwalk 33
Totale 36.467
Salva come PNG Salva come JPEG
Nome #
Dislocazione atlanto-occipitale e atlanto-assiale con grave compressione del midollo spinale nella Sindrome di Down 992
Encefalite da Anticorpi anti-GluR3 in sei pazienti in età pediatrica 910
Sindromi Neurocutanee 698
ESAME NEUROLOGICO 486
Expanding genotype-phenotype correlation of Kenny-Caffey syndrome type 1 443
CUTIS TRICOLOR (RUGGIERI-HAPPLE SYNDROME) 404
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] 281
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders 268
A pilot study on neurological manifestations and antibodies against neuronal antigens in children with haematological and other cancers 242
Natural history of neurofibromatosis type 2 with onset before the age of 1 year. 218
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) 209
A mosaic pattern of INI1/SMARCB1 protein expression distinguishes Schwannomatosis and NF2-associated peripheral schwannomas from solitary peripheral schwannomas and NF2-associated vestibular schwannomas 204
A boy born with multiple lesions of atrophoderma 201
Speckled Lentiginous Nevus Syndrome 200
Anti-MOG Antibody Syndrome and Cerebral Sinovenous Thrombosis: A Cause-Effect Hypothesis 197
PARALISI CEREBRALI INFANTILI E PARAPLEGIE SPASTICHE EREDITARIE 196
Manuale di Pediatria, quinta edizione. Capitolo 2 "Anamnesi ed esame obiettivo". Capitolo 29 "Malattie Neurologiche". 196
Encephalocraniocutaneous Lipomatosis (Haberland Syndrome or Fishman Syndrome) 193
Becker's Nevus Syndrome 193
Anti-mog associated encephalitis: when steroid therapy is not enough 190
A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment 182
A New Patient with Potocki-Lupski Syndrome: A Literature Review 176
Blue Rubber Bleb Nevus Syndrome 174
A girl with a 14.7 Mb 3q26.32-q28 duplication: a new report of 3q duplication syndrome and a literature review 172
Nevus Sebaceous Syndrome 172
Astenia: una maschera per tante identità. Ruolo della patologia della placca neuromuscolare 171
A highly sensitive colorimetric approach based on tris (bipyridine) Ruthenium (II/III) mediator for the enzymatic detection of phenylalanine 169
Phacomatosis Pigmentovascularis 169
Phacomatosis Pigmentokeratotica 169
Complex malformation (Ruggieri-Happle) phenotype with “cutis tricolor” in a 10-year-old girl 165
A case of extreme brain lesions: Which pathogenetic mechanism? 163
Aneurysmal bone cyst of the acromion: a case report 159
Aicardi-Goutières Syndrome Type 2: A Report on Two Cases with Different Phenotypes Caused by RNASEH2B Gene Mutations 159
A Phenylalanine sensor exploiting a capacitive readout strategy embedding a selective enzymatic mechanism 158
Cerebellotrigeminal Dermal Dysplasia (Gómez-López-Hernández Syndrome) 158
A critical appraisal of neurological evidence on paediatric COVID-19 patients. A systematic literature review 156
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. 153
Wyburn-Mason Syndrome 152
Electrocardiographic Evaluation in Patients With Spinal Muscular Atrophy: A Case-Control Study 151
Autoimmune encephalitis and CSF anti-AMPA GluR3 antibodies in childhood: a case report and literature review 149
Megalencephaly Capillary Malformation Syndrome 149
Correlazione genotipo/fenotipo nella Sclerosi Tuberosa (TSC1 vs. TSC2) in 81 pazienti siciliani 148
Paracelso: vita e contributo all'evoluzione delle scienze mediche, umane e neuropsichiatriche 148
Malformazioni vascolari nella neurofibromatosi di tipo 1 (NF1) 148
Need for palliative care from birth to infancy in pediatric patients with neurological diseases 147
Archetypical Patterns of Skin Manifestations in Neurocutaneous Disorders 147
Craniofacial anomalies, severe cerebellar hypoplasia, psychomotor and growth delay in a child with congenital hypothyroidism 146
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 146
Acute disseminated encephalomyelitis: a long-term prospective study and meta-analysis 145
A child with rhombencephalosynapsis, agenesis of the trigeminal ganglion and optic coloboma (without alopecia): A variant of the cerebellotrigeminal dermal dysplasia? 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 143
Microcephaly-Capillary Malformation Syndrome 143
An 11-year follow-up of neonatal onset bath-induced alternating hemiplegia of childhood in monozygotic twins 142
Mutazione PRRT2 in un bambino con caratteristiche dismorfiche, microcefalia congenita e convulsioni epilettiche gravi 142
Familial osteoma of the cranial vault 142
Anomalies of Midbrain/Hindbrain Development and Related Disabilities: Pontocerebellar Hypoplasia, Congenital Disorders of Glycosylation, and Cerebellar Hemisphere Hypoplasia 140
A child with congenital heart disease and situs viscerum inversus 139
A Probable Topiramate-induced Limbs Paraesthesia and Rigid Fingers Flexion 139
E se non fossero solo incubi notturni? 139
A novel GABRB3 variant in Dravet syndrome: Case report and literature review 139
Klippel-Trenaunay Syndrome, Segmental/Focal Overgrowth Malformations: A Review 138
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 137
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] 137
Encefalite GluR3: fenotipo clinico e strumentale di quattro pazienti 136
A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease 135
Aneurismal bone cyst of the acromion: a case report 135
Off-label use of drugs and adverse drug reactions in pediatric units: A prospective, multicenter study 135
Hypomelanosis of Ito 134
Sindrome del vomito ciclico: analisi di una popolazione di 20 bambini e revisione della letteratura 133
A Complex Brain Malformation Syndrome with Rhombencephalosynapsis, Preaxial Hexadactyly plus Facial and Skull Anomalies 132
Motor imagery for paediatric neurorehabilitation: how much do we know? Perspectives from a systematic review 131
Neurologia e psichiatria dello sviluppo 131
Did Cro-Magnon 1 have neurofibromatosis type 2? 131
Autoimmune thyroiditis and acquired demyelinating poliradiculoneuropathy 131
Malattie neurocutanee 131
Short-term neurodevelopmental outcome in term neonates treated with phenobarbital versus levetiracetam: A single-center experience 131
Displasia ossea della volta cranica in un paziente con neurofibromatosi tipo 1 130
Cutis Tricolor 130
Disturbi del sonno: uno studio prospettico pilota basato sulla somministrazione di questionario online. 130
Short Efficacy Evaluation of External Ventricular Drains Versus Ventriculosubgaleal Shunt in the Management of Neonatal Posthemorrhagic Hydrocephalus: A Retrospective Single-Center Cohort Study 129
A neurocutaneous phenotype with paired hypo- and hyperpigmented macules, microcephaly and stunted growth as prominent features 129
A Young Boy with 21q21.1 Microdeletion Showing Speech Delay, Spastic Diplegia, and MRI Abnormalities: Original Case Report 128
Esame obiettivo neurologico nel bambino 128
Maternal Phenylketonuria and Offspring Outcome: A Retrospective Study with a Systematic Review of the Literature 127
Congenital muscular dystrophy: from muscle to brain 127
A clinical and molecular study in a child under 1 year of age affected by Neurofibromatosis type 2 127
Long-term follow-up and novel genotype-phenotype analysis of monozygotic twins with ATP1A3 mutation in Alternating Hemiplegia of Childhood-2 127
Genotype–Phenotype Correlation in a Large Cohort of Eastern Sicilian Patients Affected by Phenylketonuria: Newborn Screening Program, Clinical Features, and Follow-Up 126
Recurrent obstructive hydrocephalus in a 4-month-old infant 126
The use of selegiline in the treatment of cognitive deficits in elderly patients 126
Mixed Vascular Nevus Syndrome 126
Neurocutaneous melanocytosis (melanosis) 126
7q31.32 partial duplication: First report of a child with dysmorphism, autistic spectrum disorder, moderate intellectual disability and, epilepsy. Literature review 126
Malformations of cortical development, cognitive involvement and epilepsy: A single institution experience in 19 young patients 126
Citalopram in the treatment of depression in the elderly 125
Adrenal Disorders and the Paediatric Brain: Pathophysiological Considerations and Clinical Implications 125
Ataxia in children: early recognition and clinical evaluation 125
Chromosome 2p15-p16.1 microduplication in a boy with congenital anomalies: Is it a distinctive syndrome? 125
PPP5C pathogenic variant identified: a potential key to gaining insight into developmental and epileptic encephalopathy? 124
The natural history of Spinal Neurofibromatosis: A critical review of clinical and genetic features 124
Totale 18.255
Salva come PNG Salva come JPEG
Categoria #
all - tutte 175.861
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 175.861
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021842 0 0 0 0 0 0 0 0 0 135 539 168
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
2025/202623.897 1.391 1.619 4.732 1.772 3.689 4.639 2.848 640 1.414 1.153 0 0
Totale 57.503