UNICA IRIS Institutional Research Information System

SAVASTA, SALVATORE
 Distribuzione geografica
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Continente #
EU - Europa 4.637
AS - Asia 1.831
NA - Nord America 1.822
SA - Sud America 300
AF - Africa 43
OC - Oceania 4
Totale 8.637
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Nazione #
IT - Italia 3.945
US - Stati Uniti d'America 1.784
SG - Singapore 832
CN - Cina 549
BR - Brasile 240
SE - Svezia 228
DE - Germania 169
VN - Vietnam 95
HK - Hong Kong 94
KR - Corea 65
IN - India 63
GB - Regno Unito 57
FR - Francia 47
AT - Austria 36
FI - Finlandia 35
NL - Olanda 26
BD - Bangladesh 25
PL - Polonia 25
RU - Federazione Russa 24
AR - Argentina 21
CA - Canada 19
ZA - Sudafrica 16
JP - Giappone 14
ID - Indonesia 13
MX - Messico 10
MY - Malesia 10
PK - Pakistan 9
TR - Turchia 9
UY - Uruguay 9
ES - Italia 8
IQ - Iraq 8
AE - Emirati Arabi Uniti 7
MA - Marocco 7
VE - Venezuela 7
DK - Danimarca 6
EC - Ecuador 6
CL - Cile 5
PY - Paraguay 5
CZ - Repubblica Ceca 4
IE - Irlanda 4
IR - Iran 4
PH - Filippine 4
RO - Romania 4
TN - Tunisia 4
UA - Ucraina 4
UZ - Uzbekistan 4
AU - Australia 3
CI - Costa d'Avorio 3
CO - Colombia 3
EG - Egitto 3
JO - Giordania 3
KE - Kenya 3
LB - Libano 3
LT - Lituania 3
PE - Perù 3
SA - Arabia Saudita 3
AZ - Azerbaigian 2
BY - Bielorussia 2
CH - Svizzera 2
CR - Costa Rica 2
DZ - Algeria 2
GT - Guatemala 2
KZ - Kazakistan 2
NO - Norvegia 2
NP - Nepal 2
PT - Portogallo 2
SN - Senegal 2
AO - Angola 1
BA - Bosnia-Erzegovina 1
BG - Bulgaria 1
BH - Bahrain 1
BO - Bolivia 1
BS - Bahamas 1
CY - Cipro 1
ET - Etiopia 1
GR - Grecia 1
HN - Honduras 1
IL - Israele 1
JM - Giamaica 1
KW - Kuwait 1
LA - Repubblica Popolare Democratica del Laos 1
ML - Mali 1
MN - Mongolia 1
NZ - Nuova Zelanda 1
OM - Oman 1
PR - Porto Rico 1
PS - Palestinian Territory 1
QA - Qatar 1
SK - Slovacchia (Repubblica Slovacca) 1
TH - Thailandia 1
TJ - Tagikistan 1
TT - Trinidad e Tobago 1
Totale 8.637
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Città #
Cagliari 3.405
Boardman 535
Singapore 362
Uta 284
Ashburn 262
Nyköping 152
Dallas 150
Hefei 146
Santa Clara 112
Beijing 94
Los Angeles 94
Hong Kong 90
Seoul 64
Redondo Beach 47
Nuremberg 37
Ho Chi Minh City 36
Pune 36
Buffalo 35
Shanghai 33
Rome 27
Milan 25
New York 22
Warsaw 22
Kerken 21
São Paulo 20
Chicago 18
Hanoi 18
London 16
Helsinki 15
Vienna 15
Fairfield 14
Guangzhou 13
Seattle 13
Dottingen 12
Munich 12
The Dalles 12
Turku 12
Houston 11
Johannesburg 11
Belo Horizonte 10
Denver 10
Tokyo 10
Turin 10
Council Bluffs 9
Kuala Lumpur 9
Stockholm 9
Atlanta 8
Brooklyn 8
Frankfurt am Main 8
Montreal 8
Washington 8
Wilmington 8
Amsterdam 7
Boston 7
Lappeenranta 7
Lauterbourg 7
Mexico City 7
Naples 7
Rio de Janeiro 7
San Francisco 7
Xi'an 7
Kazan' 6
Newark 6
Palermo 6
Wuhan 6
Boca Raton 5
Brasília 5
Cavenago di Brianza 5
Chandler 5
Chennai 5
Da Nang 5
Düsseldorf 5
Mumbai 5
Orem 5
Paris 5
Phoenix 5
Roubaix 5
Salt Lake City 5
Secaucus 5
Toronto 5
Woodbridge 5
Ankara 4
Arezzo 4
Bexley 4
Cape Town 4
Caracas 4
Casablanca 4
Curitiba 4
Fortaleza 4
Messina 4
Montevideo 4
Moscow 4
Osaka 4
Shatki 4
Shenzhen 4
São José 4
Tashkent 4
Amman 3
Baghdad 3
Bengaluru 3
Totale 6.658
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Nome #
Targeting Inflammatory Mediators in Epilepsy: A Systematic Review of Its Molecular Basis and Clinical Applications 786
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders 648
Improving molecular diagnosis in epilepsy by a dedicated high-throughput sequencing platform 438
Pulmonary Tuberculosis in Children: A Forgotten Disease? 432
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 399
Epilepsy in “Sunflower syndrome”: electroclinical features, therapeutic response, and long-term follow-up 333
Human Herpesvirus 6 Encephalitis in Immunocompetent and Immunocompromised Hosts 288
Children with special health care needs attending emergency department in Italy: analysis of 3479 cases 195
Rasmussen's encephalitis: From immune pathogenesis towards targeted-therapy 177
The role of inflammatory mediators in epilepsy: Focus on developmental and epileptic encephalopathies and therapeutic implications 120
Bi-allelic JAM2 Variants Lead to Early-Onset Recessive Primary Familial Brain Calcification 118
Adoptive immunotherapies in neuro-oncology: classification, recent advances, and translational challenges 113
Abdominal pain as first manifestation of lyme neuroborreliosis in children, case report and review of literature 111
Clinical and Genetic Heterogeneity of HCM: The Possible Role of a Deletion Involving MYH6 and MYH7 105
Pai syndrome: a review 102
Advanced pharmacological therapies for neurofibromatosis type 1-related tumors 99
Mowat-Wilson syndrome: growth charts 98
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) 92
Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome 91
CDKL5 deficiency-related neurodevelopmental disorders: a multi-center cohort study in Italy 90
Cell-based assays for the detection of MOG antibodies: a comparative study 89
Early-infantile onset epilepsy and developmental delay caused by bi-allelic GAD1 variants 85
Pediatric Moyamoya Disease and Syndrome in Italy: A Multicenter Cohort 84
Seizures and myelin oligodendrocyte glycoprotein (MOG) antibodies: Two paradigmatic cases and a review of the literature 84
Psychopathological Impact in Patients with History of Rheumatic Fever with or without Sydenham’s Chorea: A Multicenter Prospective Study 82
Challenges and management of neurological and psychiatric manifestations in SARS-CoV-2 (COVID-19) patients 76
Epilepsy after acute central nervous system complications of pediatric hematopoietic cell transplantation: A retrospective, multicenter study 74
Potential roads for reaching the summit: an overview on target therapies for high-grade gliomas 73
Gonosomal mosaicism for a novel col5a1 pathogenic variant in classic ehlers-danlos syndrome 71
Novel "T-Dimension" Therapies for Pediatric Optic Pathway Glioma: A Timely, Targeted, and Tailored Treatment Trend 70
Children under 6 years with acute headache in Pediatric Emergency Departments. A 2-year retrospective exploratory multicenter Italian study 69
The impact of stem cells in neuro-oncology: applications, evidence, limitations and challenges 69
Post-traumatic stress, anxiety, and depressive symptoms in caregivers of children tested for COVID-19 in the acute phase of the Italian outbreak 68
Vascular Abnormalities and Neurofibromatosis Type 1: A Paediatric Case Series 68
Innovative therapies for malignant brain tumors: the road to a tailored cure 65
Human Herpes Virus 7-related encephalopathy in children 65
Expanding the Spectrum of Autosomal Dominant ATP6V1A-Related Disease: Case Report and Literature Review 63
Targeting the medulloblastoma: A molecular-based approach 63
Acneiform rash as a side effect of selumetinib in a child with neurofibromatosis type 1 treated for inoperable plexiform neurofibromas: Good results with doxycycline 63
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) 62
Impact of novel coronavirus Disease-19 (COVID-19) pandemic in Italian pediatric emergency departments: a national survey 61
Gene therapies for high-grade gliomas: From the bench to the bedside 61
Postural analysis in a pediatric cohort of patients with Ehlers-Danlos Syndrome: a pilot study 59
Biallelic mutations in neurofascin cause neurodevelopmental impairment and peripheral demyelination 57
Headache in progressive facial hemiatrophy (Parry-Romberg syndrome): A paradigmatic case and systematic review of the literature 57
Management, treatment, and clinical approach of Sydenham's chorea in children: Italian survey on expert-based experience 57
Mutations in the Neuronal Vesicular SNARE VAMP2 Affect Synaptic Membrane Fusion and Impair Human Neurodevelopment 55
A novel missense variant of FBN1 gene in a Sardinian family with Marfan syndrome: a case report 54
Pediatric optic neuritis and anti MOG antibodies: a cohort of Italian patients 54
Melkersson–rosenthal syndrome in childhood: Report of three paediatric cases and a review of the literature 53
Cyclic Vomiting Syndrome in Children 52
Understanding Childhood Neuroimmune Diseases of the Central Nervous System 52
An Overview of The Role of Tumor Necrosis Factor-Alpha in Epileptogenesis and Its Terapeutic Implications 51
Lower airway microbiota 49
MCM5: A new actor in the link between DNA replication and Meier-Gorlin syndrome 48
KIRREL3-related disorders: a case report confirming the radiological features and expanding the clinical spectrum to a less severe phenotype 46
Neuroinflammation and status epilepticus: a narrative review unraveling a complex interplay 44
Gelastic seizures not associated with hypothalamic hamartoma: A long-term follow-up study 44
Impact of Fundoplication Surgery and Multidisciplinary Approach on Quality of Life in Children with Neurological Impairment and Gastroesophageal Reflux Disease 41
Infantile spasms followed by childhood absence epilepsy: A case series 41
Clinical and Genetic Characteristics of Pediatric Patients with Inflammatory Bowel Disease Transitioning to Adult Medicine: A Single-Center Ten-Year Experience 39
Pyridostigmine as a therapeutic option for pediatric gastrointestinal dysmotilities in ATR-X syndrome. Case report and literature review 35
Case Report: Hereditary neuropathy with liability to pressure palsy (HNPP): the role of genetic investigation in diagnostic assessment 33
A Novel Intronic Variant in the KH3 Domain of HNRNPK Leads to a Mild Form of Au-Kline Syndrome 31
PDXK mutations cause polyneuropathy responsive to pyridoxal 5′-phosphate supplementation 29
Clinical variability in children with dolichoarteriopathies of the internal carotid artery 27
Intermittent acute porphyria in an 11 year-old girl suffering from oneiric crises: treatment with folic acid 26
West-Nile virus encephalitis in an immunocompetent pediatric patient: successful recovery 26
PPP2R5D-Related Neurodevelopmental Disorder and Multiple Haemangiomas: A Novel Phenotypic Trait? 24
Acute ataxia in paediatric emergency departments: a multicentre Italian study 21
ANGIOMATOSI CAVERNOSA CEREBRALE FAMILIARE: DESCRIZIONE DI UN NUOVO CASO 21
Hereditary Multiple Osteochondromas and Acute Lymphoblastic Leukemia: A Possible Role for EXT1 and EXT2 in Hematopoietic Malignancies 20
Microcephaly associated with Legg-Calvè-Perthes disease in two siblings 19
Severe hyponatremia followed by extrapontine myelinolysis (vol 69, pg 423, 2006) 19
Biotin-Thiamine Responsive Encephalopathy: Report of an Egyptian Family with a Novel SLC19A3 Mutation and Review of the Literature 19
Specifications and validation of the ACMG/AMP criteria for clinical interpretation of sequence variants in collagen genes associated with joint hypermobility 19
Benign convulsions associated with mild gastroenteritis: A multicenter clinical study 19
Bickerstaff Brainstem Encephalitis and overlapping Guillain-Barre syndrome in children: Report of two cases and review of the literature 18
A Rare Cause of Recurrent Spontaneous Pneumothorax 18
Aspetti EEG precoci nella sindrome di Angelman 18
2 pathologies with supernumerary microtubules - evidence of a peculiar HLA haplotpe association 18
Autosomal recessive congenital total lipodystophy of Berardinelli-Seip Type: clinical features in 15 new patients. 18
La sincope vasovagale 18
Agenesis of internal carotid artery and hypopituitarism: case report and review of literature. 18
Neuroimaging findings in Mowat-Wilson syndrome: a study of 54 patients 17
Beneficial effects of pharmacological treatment in patients with infantil mitochondrial encephalomyopathies 17
Aplasia of the radial artery. 17
Adenoidal immune response in the context of inflammation and allergy 16
Lacosamide in pediatric and adult patients: Comparison of efficacy and safety 16
Specificità del quadro clinico della duplicazione del braccio corto del cromosoma 8. Due nuove osservazioni. 16
Rethinking Otorhinolaryngologic Care Pathways in Children with Down Syndrome: A Multidisciplinary Framework for Early Diagnosis and Management 15
Novel FAM126A mutations in hypomyelination and congenital cataract disease 15
Electroclinical findings and long-term outcomes in epileptic patients with inv dup (15) 15
SLK is mutated in individuals with a neurodevelopmental disorder 15
Topiramate in frontal lobe epilepsy 14
Porfiria acuta intermittente con stato onirico in una bambina di 11 anni 14
Broncopolmoniti recidivanti da anomalie dell’epitelio ciliare in una bambina di otto anni. 14
Phenotype and genotype of 87 patients with Mowat-Wilson syndrome and recommendations for care 13
Transient symptomatic zinc deficiency in a breast-fed African infant: case report and literature review 13
CHARGE-like presentation, craniosynostosis and mild Mowat-Wilson Syndrome diagnosed by recognition of the distinctive facial gestalt in a cohort of 28 new cases 13
Totale 8.107
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Categoria #
all - tutte 36.130
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 36.130
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202162 0 0 0 0 0 11 3 8 6 13 4 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
2025/20262.348 316 206 505 482 463 376 0 0 0 0 0 0
Totale 8.972