UNICA IRIS Institutional Research Information System

SAVASTA, SALVATORE
 Distribuzione geografica
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Continente #
EU - Europa 5.152
NA - Nord America 3.168
AS - Asia 2.689
SA - Sud America 408
AF - Africa 86
OC - Oceania 5
Totale 11.508
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Nazione #
IT - Italia 4.199
US - Stati Uniti d'America 3.057
SG - Singapore 1.156
CN - Cina 687
BR - Brasile 303
SE - Svezia 233
VN - Vietnam 192
DE - Germania 178
HK - Hong Kong 171
FI - Finlandia 161
BD - Bangladesh 111
FR - Francia 110
IN - India 92
GB - Regno Unito 65
KR - Corea 65
CA - Canada 55
AT - Austria 39
AR - Argentina 35
NL - Olanda 34
IQ - Iraq 28
RU - Federazione Russa 28
PL - Polonia 27
JP - Giappone 22
MX - Messico 21
PK - Pakistan 21
ZA - Sudafrica 19
ID - Indonesia 18
VE - Venezuela 18
TR - Turchia 17
MY - Malesia 14
ES - Italia 13
JM - Giamaica 12
MA - Marocco 12
UY - Uruguay 12
JO - Giordania 11
PH - Filippine 11
CO - Colombia 10
EC - Ecuador 10
TN - Tunisia 10
AE - Emirati Arabi Uniti 9
CL - Cile 9
EG - Egitto 9
KE - Kenya 9
SA - Arabia Saudita 9
UA - Ucraina 9
UZ - Uzbekistan 9
IE - Irlanda 8
CR - Costa Rica 6
CZ - Repubblica Ceca 6
DK - Danimarca 6
PY - Paraguay 6
DZ - Algeria 5
GR - Grecia 5
LB - Libano 5
NP - Nepal 5
RO - Romania 5
AU - Australia 4
AZ - Azerbaigian 4
CI - Costa d'Avorio 4
ET - Etiopia 4
IR - Iran 4
KZ - Kazakistan 4
LT - Lituania 4
AO - Angola 3
BA - Bosnia-Erzegovina 3
BY - Bielorussia 3
GT - Guatemala 3
IL - Israele 3
KG - Kirghizistan 3
MD - Moldavia 3
OM - Oman 3
PE - Perù 3
PR - Porto Rico 3
PT - Portogallo 3
SN - Senegal 3
TH - Thailandia 3
BH - Bahrain 2
BO - Bolivia 2
CH - Svizzera 2
DO - Repubblica Dominicana 2
ML - Mali 2
MN - Mongolia 2
NG - Nigeria 2
NO - Norvegia 2
PA - Panama 2
RS - Serbia 2
SV - El Salvador 2
TT - Trinidad e Tobago 2
AW - Aruba 1
BE - Belgio 1
BG - Bulgaria 1
BJ - Benin 1
BS - Bahamas 1
CY - Cipro 1
HN - Honduras 1
KW - Kuwait 1
LA - Repubblica Popolare Democratica del Laos 1
ME - Montenegro 1
MG - Madagascar 1
NZ - Nuova Zelanda 1
Totale 11.500
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Città #
Cagliari 3.541
Singapore 625
Boardman 542
San Jose 408
Ashburn 390
Uta 284
Hong Kong 160
Dallas 156
Nyköping 152
Hefei 146
Council Bluffs 143
Los Angeles 136
Helsinki 124
Santa Clara 118
Beijing 98
Ho Chi Minh City 67
Seoul 64
New York 62
Lauterbourg 61
Buffalo 47
Hanoi 47
Redondo Beach 47
Rome 42
Milan 41
Nuremberg 37
Pune 36
Shanghai 34
Chicago 29
The Dalles 27
São Paulo 26
Lappeenranta 24
Warsaw 23
Kerken 21
Houston 19
Orem 18
Vienna 18
Atlanta 17
Baghdad 17
Guangzhou 17
London 17
Brooklyn 15
Tokyo 15
Fairfield 14
Frankfurt am Main 14
Montreal 13
Munich 13
Seattle 13
Toronto 13
Dottingen 12
Johannesburg 12
Naples 12
San Francisco 12
Turku 12
Washington 12
Belo Horizonte 11
Boston 11
Philadelphia 11
Turin 11
Amsterdam 10
Denver 10
Kuala Lumpur 10
Amman 9
Caracas 9
Newark 9
Palermo 9
Stockholm 9
Tashkent 9
Cairo 8
New Delhi 8
Phoenix 8
Rio de Janeiro 8
Shenzhen 8
The Bronx 8
Wilmington 8
Xi'an 8
Brescia 7
Charlotte 7
Da Nang 7
Dhaka 7
Dublin 7
Haiphong 7
Mexico City 7
Secaucus 7
Boca Raton 6
Brasília 6
Chennai 6
Indianapolis 6
Kazan' 6
Kingston 6
Montevideo 6
Salt Lake City 6
Tunis 6
Wuhan 6
Bari 5
Cape Town 5
Casablanca 5
Cavenago di Brianza 5
Chandler 5
Changsha 5
Des Moines 5
Totale 8.406
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Nome #
Targeting Inflammatory Mediators in Epilepsy: A Systematic Review of Its Molecular Basis and Clinical Applications 859
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders 689
Pulmonary Tuberculosis in Children: A Forgotten Disease? 493
Improving molecular diagnosis in epilepsy by a dedicated high-throughput sequencing platform 464
The Impact of the COVID-19 Epidemic During the Lockdown on Children With the Pediatric Acute-Onset Neuropsychiatric Syndrome (PANDAS/PANS): The Importance of Environmental Factors on Clinical Conditions 446
Epilepsy in “Sunflower syndrome”: electroclinical features, therapeutic response, and long-term follow-up 370
Human Herpesvirus 6 Encephalitis in Immunocompetent and Immunocompromised Hosts 330
Children with special health care needs attending emergency department in Italy: analysis of 3479 cases 238
Rasmussen's encephalitis: From immune pathogenesis towards targeted-therapy 204
CDKL5 deficiency-related neurodevelopmental disorders: a multi-center cohort study in Italy 158
Clinical and Genetic Heterogeneity of HCM: The Possible Role of a Deletion Involving MYH6 and MYH7 155
Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome 154
Bi-allelic JAM2 Variants Lead to Early-Onset Recessive Primary Familial Brain Calcification 146
The role of inflammatory mediators in epilepsy: Focus on developmental and epileptic encephalopathies and therapeutic implications 142
Abdominal pain as first manifestation of lyme neuroborreliosis in children, case report and review of literature 138
Adoptive immunotherapies in neuro-oncology: classification, recent advances, and translational challenges 135
Mowat-Wilson syndrome: growth charts 125
Advanced pharmacological therapies for neurofibromatosis type 1-related tumors 125
Early-infantile onset epilepsy and developmental delay caused by bi-allelic GAD1 variants 120
Psychopathological Impact in Patients with History of Rheumatic Fever with or without Sydenham’s Chorea: A Multicenter Prospective Study 120
Pai syndrome: a review 116
Cyclic vomiting syndrome in children: a nationwide survey of current practice on behalf of the Italian Society of Pediatric Gastroenterology, Hepatology and Nutrition (SIGENP) and Italian Society of Pediatric Neurology (SINP) 114
Pediatric Moyamoya Disease and Syndrome in Italy: A Multicenter Cohort 112
Cell-based assays for the detection of MOG antibodies: a comparative study 112
Neuroinflammation and status epilepticus: a narrative review unraveling a complex interplay 110
Epilepsy after acute central nervous system complications of pediatric hematopoietic cell transplantation: A retrospective, multicenter study 109
Children under 6 years with acute headache in Pediatric Emergency Departments. A 2-year retrospective exploratory multicenter Italian study 108
Gonosomal mosaicism for a novel col5a1 pathogenic variant in classic ehlers-danlos syndrome 108
Seizures and myelin oligodendrocyte glycoprotein (MOG) antibodies: Two paradigmatic cases and a review of the literature 105
Vascular Abnormalities and Neurofibromatosis Type 1: A Paediatric Case Series 102
Post-traumatic stress, anxiety, and depressive symptoms in caregivers of children tested for COVID-19 in the acute phase of the Italian outbreak 99
Correction to: CDKL5 deficiency-related neurodevelopmental disorders: a multi-center cohort study in Italy (Journal of Neurology, (2024), 271, 8, (5368-5377), 10.1007/s00415-024-12421-1) 99
Challenges and management of neurological and psychiatric manifestations in SARS-CoV-2 (COVID-19) patients 99
A novel missense variant of FBN1 gene in a Sardinian family with Marfan syndrome: a case report 96
Potential roads for reaching the summit: an overview on target therapies for high-grade gliomas 96
Management, treatment, and clinical approach of Sydenham's chorea in children: Italian survey on expert-based experience 95
The impact of stem cells in neuro-oncology: applications, evidence, limitations and challenges 95
Gene therapies for high-grade gliomas: From the bench to the bedside 93
Innovative therapies for malignant brain tumors: the road to a tailored cure 92
Impact of novel coronavirus Disease-19 (COVID-19) pandemic in Italian pediatric emergency departments: a national survey 92
Expanding the Spectrum of Autosomal Dominant ATP6V1A-Related Disease: Case Report and Literature Review 90
Biallelic mutations in neurofascin cause neurodevelopmental impairment and peripheral demyelination 89
Clinical and Genetic Characteristics of Pediatric Patients with Inflammatory Bowel Disease Transitioning to Adult Medicine: A Single-Center Ten-Year Experience 89
Targeting the medulloblastoma: A molecular-based approach 88
Novel "T-Dimension" Therapies for Pediatric Optic Pathway Glioma: A Timely, Targeted, and Tailored Treatment Trend 86
Melkersson–rosenthal syndrome in childhood: Report of three paediatric cases and a review of the literature 84
Human Herpes Virus 7-related encephalopathy in children 84
Understanding Childhood Neuroimmune Diseases of the Central Nervous System 81
Acneiform rash as a side effect of selumetinib in a child with neurofibromatosis type 1 treated for inoperable plexiform neurofibromas: Good results with doxycycline 80
Cyclic Vomiting Syndrome in Children 79
Postural analysis in a pediatric cohort of patients with Ehlers-Danlos Syndrome: a pilot study 79
Mutations in the Neuronal Vesicular SNARE VAMP2 Affect Synaptic Membrane Fusion and Impair Human Neurodevelopment 77
Pyridostigmine as a therapeutic option for pediatric gastrointestinal dysmotilities in ATR-X syndrome. Case report and literature review 73
Lower airway microbiota 72
An Overview of The Role of Tumor Necrosis Factor-Alpha in Epileptogenesis and Its Terapeutic Implications 71
Headache in progressive facial hemiatrophy (Parry-Romberg syndrome): A paradigmatic case and systematic review of the literature 70
Pediatric optic neuritis and anti MOG antibodies: a cohort of Italian patients 70
Impact of Fundoplication Surgery and Multidisciplinary Approach on Quality of Life in Children with Neurological Impairment and Gastroesophageal Reflux Disease 69
KIRREL3-related disorders: a case report confirming the radiological features and expanding the clinical spectrum to a less severe phenotype 69
A Novel Intronic Variant in the KH3 Domain of HNRNPK Leads to a Mild Form of Au-Kline Syndrome 69
PPP2R5D-Related Neurodevelopmental Disorder and Multiple Haemangiomas: A Novel Phenotypic Trait? 67
MCM5: A new actor in the link between DNA replication and Meier-Gorlin syndrome 63
SLK is mutated in individuals with a neurodevelopmental disorder 63
Case Report: Hereditary neuropathy with liability to pressure palsy (HNPP): the role of genetic investigation in diagnostic assessment 61
Gelastic seizures not associated with hypothalamic hamartoma: A long-term follow-up study 61
Infantile spasms followed by childhood absence epilepsy: A case series 58
PDXK mutations cause polyneuropathy responsive to pyridoxal 5′-phosphate supplementation 58
Clinical variability in children with dolichoarteriopathies of the internal carotid artery 57
Hereditary Multiple Osteochondromas and Acute Lymphoblastic Leukemia: A Possible Role for EXT1 and EXT2 in Hematopoietic Malignancies 49
Rethinking Otorhinolaryngologic Care Pathways in Children with Down Syndrome: A Multidisciplinary Framework for Early Diagnosis and Management 46
Erratum: Wolf-Hirschhorn syndrome-associated chromosome changes are not mediated by olfactory receptor gene clusters nor by inversion polymorphism on 4p16 (Human Genetics (2007) vol. 122 (423-430) 10.1007/ s00439-007-0412-5) 44
Specifications and validation of the ACMG/AMP criteria for clinical interpretation of sequence variants in collagen genes associated with joint hypermobility 43
Whole-Exome Sequencing Identifies Novel Genetic Variants Associated with Unexplained Neurodevelopmental Disorders in Children 36
West-Nile virus encephalitis in an immunocompetent pediatric patient: successful recovery 30
Neuroimaging findings in Mowat-Wilson syndrome: a study of 54 patients 29
La sincope vasovagale 29
Intermittent acute porphyria in an 11 year-old girl suffering from oneiric crises: treatment with folic acid 29
Acute ataxia in paediatric emergency departments: a multicentre Italian study 28
Adenoidal immune response in the context of inflammation and allergy 27
Biotin-Thiamine Responsive Encephalopathy: Report of an Egyptian Family with a Novel SLC19A3 Mutation and Review of the Literature 27
Microcephaly associated with Legg-Calvè-Perthes disease in two siblings 26
Severe hyponatremia followed by extrapontine myelinolysis (vol 69, pg 423, 2006) 26
ANGIOMATOSI CAVERNOSA CEREBRALE FAMILIARE: DESCRIZIONE DI UN NUOVO CASO 25
Broncopolmoniti recidivanti da anomalie dell’epitelio ciliare in una bambina di otto anni. 25
Aplasia of the radial artery. 25
Bickerstaff Brainstem Encephalitis and overlapping Guillain-Barre syndrome in children: Report of two cases and review of the literature 24
Problemi della nutrizione in pazienti con patologia cronica 24
Phenotype and genotype of 87 patients with Mowat-Wilson syndrome and recommendations for care 23
Benign convulsions associated with mild gastroenteritis: A multicenter clinical study 23
Beneficial effects of pharmacological treatment in patients with infantil mitochondrial encephalomyopathies 23
Lacosamide in pediatric and adult patients: Comparison of efficacy and safety 22
Disabilità intellettiva e fenotipi correlati 22
2 pathologies with supernumerary microtubules - evidence of a peculiar HLA haplotpe association 22
Autosomal recessive congenital total lipodystophy of Berardinelli-Seip Type: clinical features in 15 new patients. 22
Topiramate in frontal lobe epilepsy 21
Electroclinical findings and long-term outcomes in epileptic patients with inv dup (15) 21
Aspetti EEG precoci nella sindrome di Angelman 21
Specificità del quadro clinico della duplicazione del braccio corto del cromosoma 8. Due nuove osservazioni. 21
Agenesis of internal carotid artery and hypopituitarism: case report and review of literature. 21
A Rare Cause of Recurrent Spontaneous Pneumothorax 20
Totale 10.594
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Categoria #
all - tutte 43.489
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 43.489
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202117 0 0 0 0 0 0 0 0 0 0 0 17
2021/2022229 18 14 17 4 12 27 11 17 8 32 42 27
2022/2023810 21 18 75 34 90 303 23 52 96 30 44 24
2023/20241.657 94 69 96 164 114 223 276 114 81 84 129 213
2024/20253.737 451 562 614 389 271 263 254 85 271 142 188 247
2025/20265.222 316 206 505 482 463 448 711 305 459 641 481 205
Totale 11.846