IRIS
RUGGIERI, MARTINO
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
NA - Nord America 20.330
EU - Europa 10.813
AS - Asia 9.356
SA - Sud America 2.278
AF - Africa 1.061
OC - Oceania 24
Continente sconosciuto - Info sul continente non disponibili 15
Totale 43.877
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 19.569
IT - Italia 5.185
SG - Singapore 4.209
CN - Cina 3.355
BR - Brasile 1.974
IE - Irlanda 1.780
UA - Ucraina 1.661
CI - Costa d'Avorio 731
CA - Canada 641
RU - Federazione Russa 480
IN - India 462
VN - Vietnam 418
DE - Germania 381
KR - Corea 327
SE - Svezia 270
GB - Regno Unito 208
FI - Finlandia 151
NL - Olanda 146
FR - Francia 128
AR - Argentina 124
SN - Senegal 123
MX - Messico 83
PL - Polonia 78
BD - Bangladesh 75
CH - Svizzera 70
ZA - Sudafrica 62
EC - Ecuador 59
UZ - Uzbekistan 59
TR - Turchia 58
JP - Giappone 57
ID - Indonesia 55
AT - Austria 49
ES - Italia 49
BJ - Benin 46
GR - Grecia 40
IR - Iran 37
HK - Hong Kong 36
IQ - Iraq 36
PK - Pakistan 33
CO - Colombia 32
CZ - Repubblica Ceca 28
MA - Marocco 26
LB - Libano 22
NG - Nigeria 20
VE - Venezuela 20
PY - Paraguay 19
AU - Australia 18
BE - Belgio 17
RO - Romania 16
SA - Arabia Saudita 16
AE - Emirati Arabi Uniti 15
CL - Cile 14
LT - Lituania 14
EG - Egitto 13
PE - Perù 13
UY - Uruguay 12
BG - Bulgaria 11
EU - Europa 11
IL - Israele 11
TN - Tunisia 10
JO - Giordania 9
KE - Kenya 9
AZ - Azerbaigian 8
BO - Bolivia 7
DZ - Algeria 7
KZ - Kazakistan 7
AL - Albania 6
BY - Bielorussia 6
DO - Repubblica Dominicana 6
NP - Nepal 6
BN - Brunei Darussalam 5
EE - Estonia 5
JM - Giamaica 5
AO - Angola 4
CR - Costa Rica 4
DK - Danimarca 4
GD - Grenada 4
HR - Croazia 4
HU - Ungheria 4
KW - Kuwait 4
MY - Malesia 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 43.841
Salva come PNG Salva come JPEG
Città #
Dallas 4.049
Santa Clara 2.220
Singapore 2.202
Chandler 1.877
Jacksonville 1.827
Dublin 1.762
Boardman 836
Hefei 796
Chicago 755
Abidjan 731
Ashburn 631
Houston 619
Catania 587
Nanjing 557
Lawrence 497
Andover 491
Cambridge 491
Toronto 452
Los Angeles 432
Beijing 377
Milan 358
Seoul 322
Rome 321
Des Moines 290
Kochi 288
San Mateo 257
Wilmington 233
Civitanova Marche 222
Nanchang 180
São Paulo 172
Shenyang 157
Ho Chi Minh City 155
Munich 140
Palermo 131
Hebei 126
Dakar 123
Jiaxing 118
New York 118
Saint Petersburg 111
Ottawa 109
Changsha 101
Bremen 98
Florence 91
Naples 89
Tianjin 84
Hanoi 79
Helsinki 70
Bologna 69
Buffalo 67
Rio de Janeiro 67
Council Bluffs 65
Seattle 65
The Dalles 62
Turin 62
Padova 59
Bari 57
Tokyo 53
Moscow 52
Warsaw 52
Belo Horizonte 51
Grafing 51
Columbus 50
Brooklyn 48
Cotonou 46
Dong Ket 46
Phoenix 40
Amsterdam 39
Johannesburg 39
Lappeenranta 38
Montreal 38
Redondo Beach 38
Turku 37
Curitiba 34
Hangzhou 34
Hong Kong 34
Jinan 34
Liberty Lake 34
Pune 34
Chennai 33
Norwalk 33
Boston 32
Den Haag 32
Falls Church 32
Augusta 31
Denver 31
San Francisco 31
Stockholm 31
Washington 31
Oakland 30
Atlanta 28
Genoa 28
Ann Arbor 27
Kunming 27
Taormina 27
Tashkent 27
Brasília 26
Brescia 26
Mumbai 26
Poplar 26
Mexico City 25
Totale 28.867
Salva come PNG Salva come JPEG
Nome #
Dislocazione atlanto-occipitale e atlanto-assiale con grave compressione del midollo spinale nella Sindrome di Down 964
Encefalite da Anticorpi anti-GluR3 in sei pazienti in età pediatrica 803
Sindromi Neurocutanee 612
ESAME NEUROLOGICO 425
Expanding genotype-phenotype correlation of Kenny-Caffey syndrome type 1 396
CUTIS TRICOLOR (RUGGIERI-HAPPLE SYNDROME) 377
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] 244
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders 227
Natural history of neurofibromatosis type 2 with onset before the age of 1 year. 207
A pilot study on neurological manifestations and antibodies against neuronal antigens in children with haematological and other cancers 203
PARALISI CEREBRALI INFANTILI E PARAPLEGIE SPASTICHE EREDITARIE 178
A mosaic pattern of INI1/SMARCB1 protein expression distinguishes Schwannomatosis and NF2-associated peripheral schwannomas from solitary peripheral schwannomas and NF2-associated vestibular schwannomas 163
A boy born with multiple lesions of atrophoderma 160
Speckled Lentiginous Nevus Syndrome 160
Manuale di Pediatria, quinta edizione. Capitolo 2 "Anamnesi ed esame obiettivo". Capitolo 29 "Malattie Neurologiche". 157
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) 156
Encephalocraniocutaneous Lipomatosis (Haberland Syndrome or Fishman Syndrome) 156
Complex malformation (Ruggieri-Happle) phenotype with “cutis tricolor” in a 10-year-old girl 152
Anti-MOG Antibody Syndrome and Cerebral Sinovenous Thrombosis: A Cause-Effect Hypothesis 146
Becker's Nevus Syndrome 144
Anti-mog associated encephalitis: when steroid therapy is not enough 143
Astenia: una maschera per tante identità. Ruolo della patologia della placca neuromuscolare 133
Phacomatosis Pigmentovascularis 133
A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment 133
Blue Rubber Bleb Nevus Syndrome 132
A girl with a 14.7 Mb 3q26.32-q28 duplication: a new report of 3q duplication syndrome and a literature review 131
Phacomatosis Pigmentokeratotica 130
Craniofacial anomalies, severe cerebellar hypoplasia, psychomotor and growth delay in a child with congenital hypothyroidism 128
Nevus Sebaceous Syndrome 127
Autoimmune encephalitis and CSF anti-AMPA GluR3 antibodies in childhood: a case report and literature review 125
Familial osteoma of the cranial vault 125
A New Patient with Potocki-Lupski Syndrome: A Literature Review 124
A case of extreme brain lesions: Which pathogenetic mechanism? 122
A highly sensitive colorimetric approach based on tris (bipyridine) Ruthenium (II/III) mediator for the enzymatic detection of phenylalanine 121
Aicardi-Goutières Syndrome Type 2: A Report on Two Cases with Different Phenotypes Caused by RNASEH2B Gene Mutations 121
Malattie neurocutanee 118
Paracelso: vita e contributo all'evoluzione delle scienze mediche, umane e neuropsichiatriche 117
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. 116
Cerebellotrigeminal Dermal Dysplasia (Gómez-López-Hernández Syndrome) 116
Aneurysmal bone cyst of the acromion: a case report 114
An 11-year follow-up of neonatal onset bath-induced alternating hemiplegia of childhood in monozygotic twins 113
E se non fossero solo incubi notturni? 113
Correlazione genotipo/fenotipo nella Sclerosi Tuberosa (TSC1 vs. TSC2) in 81 pazienti siciliani 112
Electrocardiographic Evaluation in Patients With Spinal Muscular Atrophy: A Case-Control Study 111
Wyburn-Mason Syndrome 111
Displasia ossea della volta cranica in un paziente con neurofibromatosi tipo 1 110
Congenital muscular dystrophy: from muscle to brain 110
Megalencephaly Capillary Malformation Syndrome 110
The natural history of Spinal Neurofibromatosis: A critical review of clinical and genetic features 109
A critical appraisal of neurological evidence on paediatric COVID-19 patients. A systematic literature review 107
Congenital bone malformations in patients with neurofibromatosis type 1 (Nf1) 107
A child with rhombencephalosynapsis, agenesis of the trigeminal ganglion and optic coloboma (without alopecia): A variant of the cerebellotrigeminal dermal dysplasia? 107
A Phenylalanine sensor exploiting a capacitive readout strategy embedding a selective enzymatic mechanism 106
Acute disseminated encephalomyelitis: a long-term prospective study and meta-analysis 106
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 106
Malformazioni vascolari nella neurofibromatosi di tipo 1 (NF1) 106
Need for palliative care from birth to infancy in pediatric patients with neurological diseases 105
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] 105
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 105
A Complex Brain Malformation Syndrome with Rhombencephalosynapsis, Preaxial Hexadactyly plus Facial and Skull Anomalies 104
Chromosome 2p15-p16.1 microduplication in a boy with congenital anomalies: Is it a distinctive syndrome? 104
Melorheostosis: case report with 20-year follow-up 103
Autoimmune thyroiditis and acquired demyelinating poliradiculoneuropathy 103
Off-label use of drugs and adverse drug reactions in pediatric units: A prospective, multicenter study 103
A child with congenital heart disease and situs viscerum inversus 101
Did Cro-Magnon 1 have neurofibromatosis type 2? 101
Microcephaly-Capillary Malformation Syndrome 101
Archetypical Patterns of Skin Manifestations in Neurocutaneous Disorders 101
Aneurismal bone cyst of the acromion: a case report 100
Esame obiettivo neurologico nel bambino 100
Mixed Vascular Nevus Syndrome 100
Cognitive disabilities and bioethical implications in down syndrome 100
Neurocutaneous melanocytosis (melanosis) 100
A novel GABRB3 variant in Dravet syndrome: Case report and literature review 100
Clinical course of N-methyl-D-aspartate receptor encephalitis and the effectiveness of cyclophosphamide treatment 99
Mutazione PRRT2 in un bambino con caratteristiche dismorfiche, microcefalia congenita e convulsioni epilettiche gravi 99
Zellweger Syndrome coupled to secondary mitochondrial cytopathy in skeletal muscle cells in an infant: a pattern of biochemical overlapping in metabolic myopathies 99
Ataxia in children: early recognition and clinical evaluation 99
Cutis Tricolor 99
The use of selegiline in the treatment of cognitive deficits in elderly patients 98
Two siblings with a homozygous MTHFR C677T (G80A-RFC1) mutation and stroke 97
Recurrent obstructive hydrocephalus in a 4-month-old infant 97
Neurologia e psichiatria dello sviluppo 97
La morte di Iulia Florentina: ipotesi mediche e diagnostiche 97
Bilateral (perisylvian and opercular) polymicrogyria and Neurofibromatosis type 1 96
Hormesis, cellular stress response, and redox homeostasis in autism spectrum disorders 96
A Probable Topiramate-induced Limbs Paraesthesia and Rigid Fingers Flexion 96
A clinical and molecular study in a child under 1 year of age affected by Neurofibromatosis type 2 96
Hypomelanosis of Ito 96
Disturbi del sonno: uno studio prospettico pilota basato sulla somministrazione di questionario online. 96
Short-term neurodevelopmental outcome in term neonates treated with phenobarbital versus levetiracetam: A single-center experience 96
Klippel-Trenaunay Syndrome, Segmental/Focal Overgrowth Malformations: A Review 95
Hypotonia, congenital nystagmus, ataxia and abnormal auditory brainstem responses. Report on the first white Caucasian patient 95
Sindrome del vomito ciclico: analisi di una popolazione di 20 bambini e revisione della letteratura 95
Bilateral periventricular nodular heterotopia and amniotic band syndrome 94
Citalopram in the treatment of depression in the elderly 94
NEUROEMBRIOLOGIA 94
Analgetic thalamic syndrome in association with thalamic symmetrical abnormalities during measles encephalitis 94
Encefalite GluR3: fenotipo clinico e strumentale di quattro pazienti 94
A Young Boy with 21q21.1 Microdeletion Showing Speech Delay, Spastic Diplegia, and MRI Abnormalities: Original Case Report 93
Totale 14.620
Salva come PNG Salva come JPEG
Categoria #
all - tutte 153.079
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 153.079
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
2025/202610.951 1.397 1.624 4.754 1.788 1.388 0 0 0 0 0 0 0
Totale 44.731