IRIS
RUGGIERI, MARTINO
 Distribuzione geografica
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Continente #
NA - Nord America 20.731
EU - Europa 11.441
AS - Asia 11.067
SA - Sud America 2.334
AF - Africa 1.079
OC - Oceania 24
Continente sconosciuto - Info sul continente non disponibili 15
Totale 46.691
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Nazione #
US - Stati Uniti d'America 19.942
SG - Singapore 5.734
IT - Italia 5.236
CN - Cina 3.374
BR - Brasile 2.006
IE - Irlanda 1.780
UA - Ucraina 1.664
RU - Federazione Russa 994
CI - Costa d'Avorio 731
CA - Canada 653
VN - Vietnam 521
IN - India 474
DE - Germania 382
KR - Corea 328
SE - Svezia 277
GB - Regno Unito 226
NL - Olanda 153
FI - Finlandia 152
AR - Argentina 137
FR - Francia 128
SN - Senegal 123
MX - Messico 97
PL - Polonia 89
BD - Bangladesh 82
ZA - Sudafrica 71
CH - Svizzera 70
JP - Giappone 67
EC - Ecuador 64
UZ - Uzbekistan 61
TR - Turchia 60
ID - Indonesia 59
ES - Italia 53
AT - Austria 49
BJ - Benin 46
IQ - Iraq 42
HK - Hong Kong 41
GR - Grecia 40
IR - Iran 38
PK - Pakistan 36
CO - Colombia 32
CZ - Repubblica Ceca 28
MA - Marocco 27
LB - Libano 22
VE - Venezuela 21
NG - Nigeria 20
PY - Paraguay 19
RO - Romania 19
AE - Emirati Arabi Uniti 18
AU - Australia 18
BE - Belgio 18
LT - Lituania 18
SA - Arabia Saudita 16
CL - Cile 15
PE - Perù 14
EG - Egitto 13
KE - Kenya 13
UY - Uruguay 13
IL - Israele 12
TN - Tunisia 12
BG - Bulgaria 11
EU - Europa 11
JO - Giordania 11
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 46.653
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Città #
Dallas 4.057
Singapore 3.137
Santa Clara 2.223
Chandler 1.877
Jacksonville 1.827
Dublin 1.762
Boardman 836
Hefei 796
Chicago 756
Ashburn 747
Abidjan 731
Houston 627
Catania 590
Nanjing 557
Lawrence 497
Andover 491
Cambridge 491
Los Angeles 483
Toronto 453
Beijing 378
Milan 358
Seoul 322
Rome 321
Moscow 311
Des Moines 290
Kochi 288
San Mateo 257
Wilmington 233
Civitanova Marche 222
Ho Chi Minh City 196
Nanchang 180
São Paulo 178
Shenyang 158
Munich 140
Palermo 131
Hebei 126
New York 126
Dakar 123
Jiaxing 118
Buffalo 116
Saint Petersburg 111
Ottawa 109
Changsha 102
Bremen 98
Hanoi 97
Florence 92
Naples 90
Tianjin 84
Bologna 71
Helsinki 70
Rio de Janeiro 68
Council Bluffs 67
Seattle 67
The Dalles 64
Tokyo 63
Warsaw 63
Turin 62
Bari 59
Padova 59
Belo Horizonte 52
Brooklyn 52
Grafing 51
Columbus 50
Cotonou 46
Dong Ket 46
Johannesburg 46
Montreal 45
Phoenix 42
Amsterdam 41
Chennai 40
Hong Kong 39
Lappeenranta 39
Redondo Beach 38
Stockholm 38
Boston 37
Denver 37
Turku 37
Augusta 35
Curitiba 35
Hangzhou 34
Jinan 34
Liberty Lake 34
Poplar 34
Pune 34
Norwalk 33
Den Haag 32
Falls Church 32
Orem 32
San Francisco 31
Washington 31
Atlanta 30
Genoa 30
Oakland 30
London 28
Mumbai 28
Tashkent 28
Ann Arbor 27
Brescia 27
Kunming 27
Mexico City 27
Totale 30.495
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Nome #
Dislocazione atlanto-occipitale e atlanto-assiale con grave compressione del midollo spinale nella Sindrome di Down 971
Encefalite da Anticorpi anti-GluR3 in sei pazienti in età pediatrica 823
Sindromi Neurocutanee 623
ESAME NEUROLOGICO 431
Expanding genotype-phenotype correlation of Kenny-Caffey syndrome type 1 401
CUTIS TRICOLOR (RUGGIERI-HAPPLE SYNDROME) 383
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] 251
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders 233
A pilot study on neurological manifestations and antibodies against neuronal antigens in children with haematological and other cancers 211
Natural history of neurofibromatosis type 2 with onset before the age of 1 year. 210
PARALISI CEREBRALI INFANTILI E PARAPLEGIE SPASTICHE EREDITARIE 181
A mosaic pattern of INI1/SMARCB1 protein expression distinguishes Schwannomatosis and NF2-associated peripheral schwannomas from solitary peripheral schwannomas and NF2-associated vestibular schwannomas 168
Speckled Lentiginous Nevus Syndrome 168
A boy born with multiple lesions of atrophoderma 167
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) 165
Encephalocraniocutaneous Lipomatosis (Haberland Syndrome or Fishman Syndrome) 164
Manuale di Pediatria, quinta edizione. Capitolo 2 "Anamnesi ed esame obiettivo". Capitolo 29 "Malattie Neurologiche". 162
Complex malformation (Ruggieri-Happle) phenotype with “cutis tricolor” in a 10-year-old girl 157
Anti-MOG Antibody Syndrome and Cerebral Sinovenous Thrombosis: A Cause-Effect Hypothesis 155
Becker's Nevus Syndrome 150
Anti-mog associated encephalitis: when steroid therapy is not enough 149
A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment 144
Phacomatosis Pigmentovascularis 140
Blue Rubber Bleb Nevus Syndrome 139
Phacomatosis Pigmentokeratotica 139
A girl with a 14.7 Mb 3q26.32-q28 duplication: a new report of 3q duplication syndrome and a literature review 138
Astenia: una maschera per tante identità. Ruolo della patologia della placca neuromuscolare 138
Nevus Sebaceous Syndrome 136
A New Patient with Potocki-Lupski Syndrome: A Literature Review 134
Autoimmune encephalitis and CSF anti-AMPA GluR3 antibodies in childhood: a case report and literature review 132
Craniofacial anomalies, severe cerebellar hypoplasia, psychomotor and growth delay in a child with congenital hypothyroidism 132
Familial osteoma of the cranial vault 129
A highly sensitive colorimetric approach based on tris (bipyridine) Ruthenium (II/III) mediator for the enzymatic detection of phenylalanine 128
A case of extreme brain lesions: Which pathogenetic mechanism? 128
Aicardi-Goutières Syndrome Type 2: A Report on Two Cases with Different Phenotypes Caused by RNASEH2B Gene Mutations 128
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. 126
Cerebellotrigeminal Dermal Dysplasia (Gómez-López-Hernández Syndrome) 124
Paracelso: vita e contributo all'evoluzione delle scienze mediche, umane e neuropsichiatriche 123
Malattie neurocutanee 122
Correlazione genotipo/fenotipo nella Sclerosi Tuberosa (TSC1 vs. TSC2) in 81 pazienti siciliani 120
E se non fossero solo incubi notturni? 120
Megalencephaly Capillary Malformation Syndrome 120
Aneurysmal bone cyst of the acromion: a case report 119
An 11-year follow-up of neonatal onset bath-induced alternating hemiplegia of childhood in monozygotic twins 118
Wyburn-Mason Syndrome 118
Electrocardiographic Evaluation in Patients With Spinal Muscular Atrophy: A Case-Control Study 117
A critical appraisal of neurological evidence on paediatric COVID-19 patients. A systematic literature review 115
A Phenylalanine sensor exploiting a capacitive readout strategy embedding a selective enzymatic mechanism 115
Congenital muscular dystrophy: from muscle to brain 115
A child with rhombencephalosynapsis, agenesis of the trigeminal ganglion and optic coloboma (without alopecia): A variant of the cerebellotrigeminal dermal dysplasia? 115
The natural history of Spinal Neurofibromatosis: A critical review of clinical and genetic features 114
Displasia ossea della volta cranica in un paziente con neurofibromatosi tipo 1 113
Acute disseminated encephalomyelitis: a long-term prospective study and meta-analysis 113
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 113
Congenital bone malformations in patients with neurofibromatosis type 1 (Nf1) 112
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 112
Off-label use of drugs and adverse drug reactions in pediatric units: A prospective, multicenter study 112
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] 111
Malformazioni vascolari nella neurofibromatosi di tipo 1 (NF1) 111
Need for palliative care from birth to infancy in pediatric patients with neurological diseases 110
A Complex Brain Malformation Syndrome with Rhombencephalosynapsis, Preaxial Hexadactyly plus Facial and Skull Anomalies 109
Aneurismal bone cyst of the acromion: a case report 109
Chromosome 2p15-p16.1 microduplication in a boy with congenital anomalies: Is it a distinctive syndrome? 109
Esame obiettivo neurologico nel bambino 108
Autoimmune thyroiditis and acquired demyelinating poliradiculoneuropathy 108
Microcephaly-Capillary Malformation Syndrome 108
Melorheostosis: case report with 20-year follow-up 107
Mixed Vascular Nevus Syndrome 107
Archetypical Patterns of Skin Manifestations in Neurocutaneous Disorders 107
The use of selegiline in the treatment of cognitive deficits in elderly patients 106
A child with congenital heart disease and situs viscerum inversus 106
Did Cro-Magnon 1 have neurofibromatosis type 2? 106
Hormesis, cellular stress response, and redox homeostasis in autism spectrum disorders 105
A Probable Topiramate-induced Limbs Paraesthesia and Rigid Fingers Flexion 105
Mutazione PRRT2 in un bambino con caratteristiche dismorfiche, microcefalia congenita e convulsioni epilettiche gravi 105
Hypomelanosis of Ito 105
Cutis Tricolor 105
Neurocutaneous melanocytosis (melanosis) 105
Recurrent obstructive hydrocephalus in a 4-month-old infant 104
Citalopram in the treatment of depression in the elderly 104
Zellweger Syndrome coupled to secondary mitochondrial cytopathy in skeletal muscle cells in an infant: a pattern of biochemical overlapping in metabolic myopathies 104
Cognitive disabilities and bioethical implications in down syndrome 104
Short-term neurodevelopmental outcome in term neonates treated with phenobarbital versus levetiracetam: A single-center experience 104
A novel GABRB3 variant in Dravet syndrome: Case report and literature review 104
Sindrome del vomito ciclico: analisi di una popolazione di 20 bambini e revisione della letteratura 103
Ataxia in children: early recognition and clinical evaluation 103
Klippel-Trenaunay Syndrome, Segmental/Focal Overgrowth Malformations: A Review 102
Clinical course of N-methyl-D-aspartate receptor encephalitis and the effectiveness of cyclophosphamide treatment 102
A clinical and molecular study in a child under 1 year of age affected by Neurofibromatosis type 2 102
Disturbi del sonno: uno studio prospettico pilota basato sulla somministrazione di questionario online. 102
A homozygous MED11 C-terminal variant causes a lethal neurodegenerative disease 101
Two siblings with a homozygous MTHFR C677T (G80A-RFC1) mutation and stroke 101
Bilateral (perisylvian and opercular) polymicrogyria and Neurofibromatosis type 1 101
A neurocutaneous phenotype with paired hypo- and hyperpigmented macules, microcephaly and stunted growth as prominent features 101
Neurologia e psichiatria dello sviluppo 101
A Young Boy with 21q21.1 Microdeletion Showing Speech Delay, Spastic Diplegia, and MRI Abnormalities: Original Case Report 100
Hypotonia, congenital nystagmus, ataxia and abnormal auditory brainstem responses. Report on the first white Caucasian patient 100
Encefalite GluR3: fenotipo clinico e strumentale di quattro pazienti 100
La morte di Iulia Florentina: ipotesi mediche e diagnostiche 100
Bilateral periventricular nodular heterotopia and amniotic band syndrome 99
Totale 15.278
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Categoria #
all - tutte 157.837
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 157.837
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211.768 0 0 0 0 0 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
2025/202613.766 1.397 1.624 4.754 1.788 3.707 496 0 0 0 0 0 0
Totale 47.546