IRIS
RUGGIERI, MARTINO
 Distribuzione geografica
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Continente #
NA - Nord America 19.497
EU - Europa 10.587
AS - Asia 8.412
SA - Sud America 2.037
AF - Africa 992
OC - Oceania 24
Continente sconosciuto - Info sul continente non disponibili 13
Totale 41.562
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Nazione #
US - Stati Uniti d'America 18.784
IT - Italia 5.083
SG - Singapore 3.597
CN - Cina 3.268
BR - Brasile 1.782
IE - Irlanda 1.779
UA - Ucraina 1.658
CI - Costa d'Avorio 731
CA - Canada 612
RU - Federazione Russa 478
IN - India 432
DE - Germania 381
KR - Corea 327
VN - Vietnam 278
SE - Svezia 256
GB - Regno Unito 171
FI - Finlandia 150
FR - Francia 127
NL - Olanda 123
SN - Senegal 123
AR - Argentina 97
CH - Svizzera 70
BD - Bangladesh 66
MX - Messico 66
PL - Polonia 57
UZ - Uzbekistan 57
TR - Turchia 53
EC - Ecuador 52
AT - Austria 49
ID - Indonesia 44
ZA - Sudafrica 44
JP - Giappone 43
GR - Grecia 40
IQ - Iraq 36
ES - Italia 35
HK - Hong Kong 34
PK - Pakistan 32
CZ - Repubblica Ceca 27
CO - Colombia 25
MA - Marocco 24
LB - Libano 22
NG - Nigeria 20
AU - Australia 18
PY - Paraguay 18
BE - Belgio 17
RO - Romania 16
SA - Arabia Saudita 16
VE - Venezuela 16
CL - Cile 13
IR - Iran 13
LT - Lituania 13
AE - Emirati Arabi Uniti 12
EG - Egitto 12
PE - Perù 12
BG - Bulgaria 11
EU - Europa 11
UY - Uruguay 11
IL - Israele 10
JO - Giordania 9
KE - Kenya 9
TN - Tunisia 9
AZ - Azerbaigian 8
BO - Bolivia 7
BY - Bielorussia 6
DO - Repubblica Dominicana 6
DZ - Algeria 6
KZ - Kazakistan 6
NP - Nepal 6
EE - Estonia 5
JM - Giamaica 5
AL - Albania 4
AO - Angola 4
BN - Brunei Darussalam 4
GD - Grenada 4
HR - Croazia 4
HU - Ungheria 4
KW - Kuwait 4
MY - Malesia 4
PH - Filippine 4
PT - Portogallo 4
QA - Qatar 4
TT - Trinidad e Tobago 4
BB - Barbados 3
BH - Bahrain 3
CR - Costa Rica 3
DK - Danimarca 3
ET - Etiopia 3
GY - Guiana 3
KH - Cambogia 3
NO - Norvegia 3
OM - Oman 3
PS - Palestinian Territory 3
RS - Serbia 3
SK - Slovacchia (Repubblica Slovacca) 3
AM - Armenia 2
BA - Bosnia-Erzegovina 2
BW - Botswana 2
HN - Honduras 2
LA - Repubblica Popolare Democratica del Laos 2
NI - Nicaragua 2
Totale 41.530
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Città #
Dallas 4.042
Santa Clara 2.215
Singapore 2.178
Chandler 1.877
Jacksonville 1.827
Dublin 1.761
Boardman 836
Hefei 796
Chicago 751
Abidjan 731
Houston 597
Catania 564
Nanjing 557
Lawrence 497
Andover 491
Cambridge 491
Ashburn 476
Toronto 447
Milan 356
Beijing 339
Seoul 322
Los Angeles 318
Rome 316
Des Moines 289
Kochi 288
San Mateo 257
Wilmington 233
Civitanova Marche 222
Nanchang 180
Shenyang 157
São Paulo 147
Munich 140
Palermo 127
Hebei 126
Dakar 123
Jiaxing 118
Saint Petersburg 111
Ottawa 109
Changsha 101
Bremen 98
Ho Chi Minh City 97
Naples 86
Tianjin 84
Florence 81
Helsinki 70
New York 68
Bologna 67
Council Bluffs 65
Rio de Janeiro 63
Seattle 62
The Dalles 62
Turin 62
Padova 59
Hanoi 54
Moscow 52
Grafing 51
Columbus 50
Bari 49
Dong Ket 46
Belo Horizonte 45
Brooklyn 41
Tokyo 39
Lappeenranta 37
Turku 37
Hangzhou 34
Jinan 34
Liberty Lake 34
Pune 34
Norwalk 33
Den Haag 32
Falls Church 32
Hong Kong 32
San Francisco 31
Warsaw 31
Oakland 30
Washington 30
Curitiba 29
Augusta 28
Boston 28
Genoa 28
Ann Arbor 27
Kunming 27
Taormina 27
Brescia 26
Ningbo 25
Phoenix 25
Tashkent 25
Redwood City 23
Riposto 23
Brasília 22
Johannesburg 22
Leawood 22
Dhaka 21
Montreal 21
Salvador 21
Campinas 19
Ferrara 19
Mexico City 19
Mumbai 19
Abuja 18
Totale 27.989
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Nome #
Dislocazione atlanto-occipitale e atlanto-assiale con grave compressione del midollo spinale nella Sindrome di Down 960
Encefalite da Anticorpi anti-GluR3 in sei pazienti in età pediatrica 794
Sindromi Neurocutanee 594
ESAME NEUROLOGICO 416
Expanding genotype-phenotype correlation of Kenny-Caffey syndrome type 1 386
CUTIS TRICOLOR (RUGGIERI-HAPPLE SYNDROME) 365
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] 232
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders 220
Natural history of neurofibromatosis type 2 with onset before the age of 1 year. 205
A pilot study on neurological manifestations and antibodies against neuronal antigens in children with haematological and other cancers 200
PARALISI CEREBRALI INFANTILI E PARAPLEGIE SPASTICHE EREDITARIE 177
A boy born with multiple lesions of atrophoderma 157
Speckled Lentiginous Nevus Syndrome 155
Manuale di Pediatria, quinta edizione. Capitolo 2 "Anamnesi ed esame obiettivo". Capitolo 29 "Malattie Neurologiche". 151
Complex malformation (Ruggieri-Happle) phenotype with “cutis tricolor” in a 10-year-old girl 150
A mosaic pattern of INI1/SMARCB1 protein expression distinguishes Schwannomatosis and NF2-associated peripheral schwannomas from solitary peripheral schwannomas and NF2-associated vestibular schwannomas 147
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) 145
Encephalocraniocutaneous Lipomatosis (Haberland Syndrome or Fishman Syndrome) 144
Becker's Nevus Syndrome 142
Anti-mog associated encephalitis: when steroid therapy is not enough 133
Anti-MOG Antibody Syndrome and Cerebral Sinovenous Thrombosis: A Cause-Effect Hypothesis 131
A girl with a 14.7 Mb 3q26.32-q28 duplication: a new report of 3q duplication syndrome and a literature review 130
Blue Rubber Bleb Nevus Syndrome 128
Craniofacial anomalies, severe cerebellar hypoplasia, psychomotor and growth delay in a child with congenital hypothyroidism 127
Phacomatosis Pigmentokeratotica 127
Autoimmune encephalitis and CSF anti-AMPA GluR3 antibodies in childhood: a case report and literature review 123
Phacomatosis Pigmentovascularis 123
Familial osteoma of the cranial vault 122
Astenia: una maschera per tante identità. Ruolo della patologia della placca neuromuscolare 121
A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment 120
A case of extreme brain lesions: Which pathogenetic mechanism? 118
Nevus Sebaceous Syndrome 116
Malattie neurocutanee 116
Aneurysmal bone cyst of the acromion: a case report 113
An 11-year follow-up of neonatal onset bath-induced alternating hemiplegia of childhood in monozygotic twins 110
Correlazione genotipo/fenotipo nella Sclerosi Tuberosa (TSC1 vs. TSC2) in 81 pazienti siciliani 110
A New Patient with Potocki-Lupski Syndrome: A Literature Review 110
Paracelso: vita e contributo all'evoluzione delle scienze mediche, umane e neuropsichiatriche 110
Aicardi-Goutières Syndrome Type 2: A Report on Two Cases with Different Phenotypes Caused by RNASEH2B Gene Mutations 109
A highly sensitive colorimetric approach based on tris (bipyridine) Ruthenium (II/III) mediator for the enzymatic detection of phenylalanine 108
Displasia ossea della volta cranica in un paziente con neurofibromatosi tipo 1 108
The natural history of Spinal Neurofibromatosis: A critical review of clinical and genetic features 108
Cerebellotrigeminal Dermal Dysplasia (Gómez-López-Hernández Syndrome) 108
E se non fossero solo incubi notturni? 107
Congenital bone malformations in patients with neurofibromatosis type 1 (Nf1) 105
Congenital muscular dystrophy: from muscle to brain 105
Wyburn-Mason Syndrome 104
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 103
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 102
Melorheostosis: case report with 20-year follow-up 101
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. 101
Chromosome 2p15-p16.1 microduplication in a boy with congenital anomalies: Is it a distinctive syndrome? 101
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] 100
Did Cro-Magnon 1 have neurofibromatosis type 2? 100
Microcephaly-Capillary Malformation Syndrome 99
Malformazioni vascolari nella neurofibromatosi di tipo 1 (NF1) 99
Cognitive disabilities and bioethical implications in down syndrome 98
Clinical course of N-methyl-D-aspartate receptor encephalitis and the effectiveness of cyclophosphamide treatment 97
Electrocardiographic Evaluation in Patients With Spinal Muscular Atrophy: A Case-Control Study 97
Mixed Vascular Nevus Syndrome 97
Ataxia in children: early recognition and clinical evaluation 97
Archetypical Patterns of Skin Manifestations in Neurocutaneous Disorders 97
Recurrent obstructive hydrocephalus in a 4-month-old infant 95
Esame obiettivo neurologico nel bambino 95
Hormesis, cellular stress response, and redox homeostasis in autism spectrum disorders 95
Zellweger Syndrome coupled to secondary mitochondrial cytopathy in skeletal muscle cells in an infant: a pattern of biochemical overlapping in metabolic myopathies 95
Megalencephaly Capillary Malformation Syndrome 95
Disturbi del sonno: uno studio prospettico pilota basato sulla somministrazione di questionario online. 95
Two siblings with a homozygous MTHFR C677T (G80A-RFC1) mutation and stroke 94
Bilateral (perisylvian and opercular) polymicrogyria and Neurofibromatosis type 1 94
A Probable Topiramate-induced Limbs Paraesthesia and Rigid Fingers Flexion 94
A critical appraisal of neurological evidence on paediatric COVID-19 patients. A systematic literature review 93
Hypotonia, congenital nystagmus, ataxia and abnormal auditory brainstem responses. Report on the first white Caucasian patient 93
Mutazione PRRT2 in un bambino con caratteristiche dismorfiche, microcefalia congenita e convulsioni epilettiche gravi 93
Autoimmune thyroiditis and acquired demyelinating poliradiculoneuropathy 93
Hypomelanosis of Ito 93
Cutis Tricolor 93
A Phenylalanine sensor exploiting a capacitive readout strategy embedding a selective enzymatic mechanism 92
Citalopram in the treatment of depression in the elderly 92
A novel missense mutation of the NF2 gene in a severely affected boy and his healthy father 92
Acute disseminated encephalomyelitis: a long-term prospective study and meta-analysis 92
A child with rhombencephalosynapsis, agenesis of the trigeminal ganglion and optic coloboma (without alopecia): A variant of the cerebellotrigeminal dermal dysplasia? 92
A novel GABRB3 variant in Dravet syndrome: Case report and literature review 92
La morte di Iulia Florentina: ipotesi mediche e diagnostiche 92
Need for palliative care from birth to infancy in pediatric patients with neurological diseases 91
Bilateral periventricular nodular heterotopia and amniotic band syndrome 91
A Complex Brain Malformation Syndrome with Rhombencephalosynapsis, Preaxial Hexadactyly plus Facial and Skull Anomalies 91
Aneurismal bone cyst of the acromion: a case report 91
NEUROEMBRIOLOGIA 91
Analgetic thalamic syndrome in association with thalamic symmetrical abnormalities during measles encephalitis 91
Life-threatening neurological syndrome in Down's syndrome 90
Neurologia Pediatrica 90
Hormesis, cellular stress response and neuroinflammation in schizophrenia: early onset versus late onset state 90
A clinical and molecular study in a child under 1 year of age affected by Neurofibromatosis type 2 90
Encefalite GluR3: fenotipo clinico e strumentale di quattro pazienti 90
Neurological manifestations in individuals with isolated or syndromic (Ruggieri-Happle syndrome) phenotypes with “cutis tricolor”: a study of 14 cases 89
A neurocutaneous phenotype with paired hypo- and hyperpigmented macules, microcephaly and stunted growth as prominent features 89
Neurologia e psichiatria dello sviluppo 89
Off-label use of drugs and adverse drug reactions in pediatric units: A prospective, multicenter study 89
The use of selegiline in the treatment of cognitive deficits in elderly patients 88
Totale 13.973
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Categoria #
all - tutte 147.977
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 147.977
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20212.603 0 0 0 43 792 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
2025/20268.633 1.397 1.624 4.754 858 0 0 0 0 0 0 0 0
Totale 42.413