RUGGIERI, MARTINO
 Distribuzione geografica
Continente #
NA - Nord America 14.180
EU - Europa 9.645
AS - Asia 3.729
AF - Africa 593
SA - Sud America 337
OC - Oceania 20
Continente sconosciuto - Info sul continente non disponibili 11
Totale 28.515
Nazione #
US - Stati Uniti d'America 13.596
IT - Italia 4.560
CN - Cina 1.862
IE - Irlanda 1.787
UA - Ucraina 1.653
SG - Singapore 1.551
CA - Canada 567
RU - Federazione Russa 453
CI - Costa d'Avorio 431
DE - Germania 321
BR - Brasile 302
SE - Svezia 238
SN - Senegal 121
FR - Francia 115
GB - Regno Unito 92
NL - Olanda 86
IN - India 69
CH - Svizzera 66
FI - Finlandia 66
VN - Vietnam 52
AT - Austria 39
GR - Grecia 39
UZ - Uzbekistan 35
TR - Turchia 31
PL - Polonia 28
NG - Nigeria 19
AU - Australia 18
HK - Hong Kong 18
LB - Libano 18
CZ - Repubblica Ceca 17
JP - Giappone 17
BE - Belgio 16
ES - Italia 14
MX - Messico 14
IR - Iran 13
RO - Romania 12
AR - Argentina 11
EU - Europa 11
PK - Pakistan 10
BD - Bangladesh 9
BG - Bulgaria 8
ZA - Sudafrica 7
CO - Colombia 6
CL - Cile 5
EE - Estonia 5
IQ - Iraq 5
MA - Marocco 5
AE - Emirati Arabi Uniti 4
AZ - Azerbaigian 4
EC - Ecuador 4
EG - Egitto 4
HR - Croazia 4
HU - Ungheria 4
IL - Israele 4
TN - Tunisia 4
BY - Bielorussia 3
ID - Indonesia 3
KH - Cambogia 3
KZ - Kazakistan 3
RS - Serbia 3
VE - Venezuela 3
BA - Bosnia-Erzegovina 2
BN - Brunei Darussalam 2
BO - Bolivia 2
DK - Danimarca 2
KR - Corea 2
NO - Norvegia 2
NZ - Nuova Zelanda 2
PE - Perù 2
PT - Portogallo 2
QA - Qatar 2
SK - Slovacchia (Repubblica Slovacca) 2
UY - Uruguay 2
AF - Afghanistan, Repubblica islamica di 1
AL - Albania 1
AO - Angola 1
BT - Bhutan 1
GE - Georgia 1
GL - Groenlandia 1
IS - Islanda 1
JO - Giordania 1
KE - Kenya 1
KW - Kuwait 1
LA - Repubblica Popolare Democratica del Laos 1
LT - Lituania 1
LU - Lussemburgo 1
MM - Myanmar 1
MT - Malta 1
NI - Nicaragua 1
NP - Nepal 1
OM - Oman 1
PA - Panama 1
PH - Filippine 1
PS - Palestinian Territory 1
SA - Arabia Saudita 1
SI - Slovenia 1
Totale 28.515
Città #
Santa Clara 2.186
Chandler 1.877
Jacksonville 1.838
Dublin 1.771
Singapore 1.035
Boardman 839
Chicago 729
Houston 589
Nanjing 561
Catania 513
Lawrence 500
Andover 494
Cambridge 494
Toronto 442
Abidjan 431
Ashburn 323
Milan 298
Des Moines 289
Rome 263
San Mateo 259
Wilmington 236
Civitanova Marche 222
Nanchang 182
Shenyang 158
Hebei 126
Dakar 121
Jiaxing 119
Saint Petersburg 113
Ottawa 106
Changsha 101
Bremen 98
Munich 92
Palermo 88
Tianjin 86
Florence 76
Naples 65
Council Bluffs 60
Turin 60
Padova 58
Helsinki 55
Seattle 55
Beijing 54
Bologna 51
Grafing 51
Los Angeles 51
Moscow 47
Dong Ket 46
Bari 39
Hangzhou 34
Jinan 34
Liberty Lake 34
Norwalk 33
Den Haag 32
Falls Church 32
Pune 31
Oakland 30
Ann Arbor 28
Kunming 27
Taormina 27
Brescia 26
Genoa 26
Ningbo 25
Washington 25
Redwood City 23
Riposto 23
Augusta 22
Leawood 22
São Paulo 22
Ferrara 19
Abuja 18
Gravina di Catania 17
Reggio Emilia 17
Zhengzhou 17
Adrano 16
Hong Kong 16
Tokyo 16
Ragusa 15
Campobasso 14
Catanzaro 14
Gela 14
Napoli 14
Rio de Janeiro 14
Vicenza 14
Amsterdam 13
Cagliari 13
Lago 13
Lipari 13
Pozzallo 13
Redmond 13
Brussels 12
Frankfurt Am Main 12
Guangzhou 12
Verona 12
Ancona 11
Belo Horizonte 11
Castelnovo 11
Dallas 11
Dearborn 11
Frattamaggiore 11
Lappeenranta 11
Totale 19.341
Nome #
Dislocazione atlanto-occipitale e atlanto-assiale con grave compressione del midollo spinale nella Sindrome di Down 903
Encefalite da Anticorpi anti-GluR3 in sei pazienti in età pediatrica 678
Sindromi Neurocutanee 477
ESAME NEUROLOGICO 360
CUTIS TRICOLOR (RUGGIERI-HAPPLE SYNDROME) 320
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] 212
Natural history of neurofibromatosis type 2 with onset before the age of 1 year. 179
A pilot study on neurological manifestations and antibodies against neuronal antigens in children with haematological and other cancers 164
PARALISI CEREBRALI INFANTILI E PARAPLEGIE SPASTICHE EREDITARIE 151
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders 141
Complex malformation (Ruggieri-Happle) phenotype with “cutis tricolor” in a 10-year-old girl 139
Speckled Lentiginous Nevus Syndrome 127
Encephalocraniocutaneous Lipomatosis (Haberland Syndrome or Fishman Syndrome) 114
Craniofacial anomalies, severe cerebellar hypoplasia, psychomotor and growth delay in a child with congenital hypothyroidism 104
Familial osteoma of the cranial vault 103
Malattie neurocutanee 103
Blue Rubber Bleb Nevus Syndrome 100
Astenia: una maschera per tante identità. Ruolo della patologia della placca neuromuscolare 99
Phacomatosis Pigmentokeratotica 97
Anti-MOG Antibody Syndrome and Cerebral Sinovenous Thrombosis: A Cause-Effect Hypothesis 97
Anti-mog associated encephalitis: when steroid therapy is not enough 96
Phacomatosis Pigmentovascularis 95
Displasia ossea della volta cranica in un paziente con neurofibromatosi tipo 1 93
Correlazione genotipo/fenotipo nella Sclerosi Tuberosa (TSC1 vs. TSC2) in 81 pazienti siciliani 92
Becker's Nevus Syndrome 92
Paracelso: vita e contributo all'evoluzione delle scienze mediche, umane e neuropsichiatriche 91
Nevus Sebaceous Syndrome 91
The natural history of Spinal Neurofibromatosis: A critical review of clinical and genetic features 90
Congenital muscular dystrophy: from muscle to brain 88
Chromosome 2p15-p16.1 microduplication in a boy with congenital anomalies: Is it a distinctive syndrome? 85
A boy born with multiple lesions of atrophoderma 84
Congenital bone malformations in patients with neurofibromatosis type 1 (Nf1) 80
A case of extreme brain lesions: Which pathogenetic mechanism? 80
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) 79
Melorheostosis: case report with 20-year follow-up 79
NEUROEMBRIOLOGIA 79
Autoimmune thyroiditis and acquired demyelinating poliradiculoneuropathy 79
A girl with a 14.7 Mb 3q26.32-q28 duplication: a new report of 3q duplication syndrome and a literature review 78
An 11-year follow-up of neonatal onset bath-induced alternating hemiplegia of childhood in monozygotic twins 78
Did Cro-Magnon 1 have neurofibromatosis type 2? 78
Malformazioni vascolari nella neurofibromatosi di tipo 1 (NF1) 78
Wyburn-Mason Syndrome 76
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 76
Hormesis, cellular stress response and neuroinflammation in schizophrenia: early onset versus late onset state 75
Cerebellotrigeminal Dermal Dysplasia (Gómez-López-Hernández Syndrome) 75
Cognitive disabilities and bioethical implications in down syndrome 75
Two siblings with a homozygous MTHFR C677T (G80A-RFC1) mutation and stroke 74
Hypotonia, congenital nystagmus, ataxia and abnormal auditory brainstem responses. Report on the first white Caucasian patient 73
Bilateral periventricular nodular heterotopia and amniotic band syndrome 73
Mutazione PRRT2 in un bambino con caratteristiche dismorfiche, microcefalia congenita e convulsioni epilettiche gravi 73
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] 72
Bilateral (perisylvian and opercular) polymicrogyria and Neurofibromatosis type 1 72
Hormesis, cellular stress response, and redox homeostasis in autism spectrum disorders 72
Citalopram in the treatment of depression in the elderly 71
Multiple Sclerosis in Childhood and other Immune-Mediated Disorders of the Central Nervous System in the Pediatric Age 71
MALATTIE NEUROCUTANEE 71
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. 71
Mixed Vascular Nevus Syndrome 71
La genetica delle maggiori sindromi neurocutanee 71
Cutis Tricolor 71
Electrocardiographic Evaluation in Patients With Spinal Muscular Atrophy: A Case-Control Study 70
Microcephaly-Capillary Malformation Syndrome 70
Archetypical Patterns of Skin Manifestations in Neurocutaneous Disorders 70
Recurrent obstructive hydrocephalus in a 4-month-old infant 69
Clinical course of N-methyl-D-aspartate receptor encephalitis and the effectiveness of cyclophosphamide treatment 69
Acute disseminated encephalomyelitis: a long-term prospective study and meta-analysis 69
Aneurysmal bone cyst of the acromion: a case report 69
Ataxia in children: early recognition and clinical evaluation. 69
Encefalite GluR3: fenotipo clinico e strumentale di quattro pazienti 69
Neurological manifestations in individuals with isolated or syndromic (Ruggieri-Happle syndrome) phenotypes with “cutis tricolor”: a study of 14 cases 68
Analgetic thalamic syndrome in association with thalamic symmetrical abnormalities during measles encephalitis 68
Sindrome del vomito ciclico: analisi di una popolazione di 20 bambini e revisione della letteratura 68
Hypomelanosis of Ito 68
Life-threatening neurological syndrome in Down's syndrome 67
E se non fossero solo incubi notturni? 67
La morte di Iulia Florentina: ipotesi mediche e diagnostiche 67
Multiple sclerosis with onset at 35 months of age 66
ATAXIA-TELANGIECTASIA 66
Disturbi del sonno: uno studio prospettico pilota basato sulla somministrazione di questionario online. 66
Aneurismal bone cyst of the acromion: a case report 65
Neurologia Pediatrica 65
Chronic atrial fibrillation and asymptomatic cerebral infarction in elderly patients 65
The natural history of L-aminoacid decarboxylase (AADC) deficiency: report of two never treated ault patients. 65
Therapy of panic attacks in the elderly 65
A clinical review on megalencephaly: A large brain as a possible sign of cerebral impairment 65
Reconstructive Surgery in Children with Down's Syndrome: Bioethical Implications 65
Aicardi-Goutières Syndrome Type 2: A Report on Two Cases with Different Phenotypes Caused by RNASEH2B Gene Mutations 65
CNS findings in three cases of septo-optic dysplasia, including one with semilobar holoprosencephaly 64
A novel missense mutation of the NF2 gene in a severely affected boy and his healthy father 64
Neurologia e psichiatria dello sviluppo 64
Cervical neurenteric cyst and Klippel-Feil syndrome: An abrupt onset of myelopathic signs in a young patient 64
Clinical spectrum of woolly hair: Indications for cerebral involvement 64
The use of selegiline in the treatment of cognitive deficits in elderly patients 63
Dominant myopia? Report on a large Italian family 63
MALFORMAZIONI CEREBRALI ED IDROCEFALO 63
Malattie neuromuscolari 63
Earliest clinical manifestations and natural history of neurofibromatosis type 2 in childhood: a study of 24 patients 63
A clinical and molecular study in a child under 1 year of age affected by Neurofibromatosis type 2 63
Megalencephaly Capillary Malformation Syndrome 63
SCN1A and its related epileptic phenotypes 63
Totale 10.475
Categoria #
all - tutte 103.998
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 103.998


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020783 0 0 0 0 0 0 0 20 275 52 291 145
2020/20213.301 33 264 385 43 798 98 429 65 340 135 543 168
2021/20224.137 454 532 57 112 596 79 581 189 405 41 124 967
2022/20236.471 562 258 104 561 644 1.099 75 1.026 1.487 138 303 214
2023/20243.593 233 446 282 308 182 483 152 247 65 142 609 444
2024/20257.097 205 1.702 736 589 2.085 1.108 463 209 0 0 0 0
Totale 29.364