UNICA IRIS Institutional Research Information System

SAVASTA, SALVATORE
 Distribuzione geografica
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Continente #
EU - Europa 5.011
AS - Asia 2.615
NA - Nord America 2.470
SA - Sud America 407
AF - Africa 84
OC - Oceania 5
Totale 10.592
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Nazione #
IT - Italia 4.071
US - Stati Uniti d'America 2.400
SG - Singapore 1.153
CN - Cina 683
BR - Brasile 302
SE - Svezia 231
VN - Vietnam 192
DE - Germania 178
HK - Hong Kong 168
FI - Finlandia 161
FR - Francia 109
IN - India 92
KR - Corea 65
GB - Regno Unito 62
BD - Bangladesh 47
AT - Austria 39
AR - Argentina 35
NL - Olanda 31
CA - Canada 30
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 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
KE - Kenya 9
SA - Arabia Saudita 9
UA - Ucraina 9
UZ - Uzbekistan 9
IE - Irlanda 8
EG - Egitto 7
DK - Danimarca 6
PY - Paraguay 6
CR - Costa Rica 5
CZ - Repubblica Ceca 5
DZ - Algeria 5
GR - Grecia 5
LB - Libano 5
NP - Nepal 5
AU - Australia 4
AZ - Azerbaigian 4
CI - Costa d'Avorio 4
ET - Etiopia 4
IR - Iran 4
JM - Giamaica 4
KZ - Kazakistan 4
LT - Lituania 4
RO - Romania 4
AO - Angola 3
BY - Bielorussia 3
IL - Israele 3
KG - Kirghizistan 3
MD - Moldavia 3
OM - Oman 3
PE - Perù 3
PT - Portogallo 3
SN - Senegal 3
TH - Thailandia 3
BA - Bosnia-Erzegovina 2
BH - Bahrain 2
BO - Bolivia 2
CH - Svizzera 2
DO - Repubblica Dominicana 2
GT - Guatemala 2
ML - Mali 2
MN - Mongolia 2
NG - Nigeria 2
NO - Norvegia 2
PA - Panama 2
RS - Serbia 2
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
PR - Porto Rico 1
PS - Palestinian Territory 1
QA - Qatar 1
SC - Seychelles 1
Totale 10.586
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Città #
Cagliari 3.479
Singapore 622
Boardman 536
Ashburn 370
Uta 284
San Jose 262
Hong Kong 157
Dallas 152
Nyköping 152
Hefei 146
Los Angeles 127
Helsinki 124
Santa Clara 115
Beijing 97
Council Bluffs 82
Ho Chi Minh City 67
Seoul 64
Lauterbourg 61
Hanoi 47
Redondo Beach 47
Buffalo 37
Nuremberg 37
Pune 36
Milan 35
Rome 33
Shanghai 33
New York 31
The Dalles 27
São Paulo 26
Chicago 25
Lappeenranta 24
Warsaw 23
Kerken 21
Baghdad 17
Guangzhou 17
Vienna 17
London 16
Orem 16
Tokyo 15
Fairfield 14
Frankfurt am Main 14
Munich 13
Seattle 13
Dottingen 12
Houston 12
Johannesburg 12
Turku 12
Belo Horizonte 11
Amsterdam 10
Denver 10
Kuala Lumpur 10
Montreal 10
Naples 10
Turin 10
Amman 9
Brooklyn 9
Caracas 9
Stockholm 9
Tashkent 9
Toronto 9
Atlanta 8
New Delhi 8
Newark 8
Shenzhen 8
Washington 8
Wilmington 8
Xi'an 8
Boston 7
Da Nang 7
Dhaka 7
Dublin 7
Haiphong 7
Mexico City 7
Rio de Janeiro 7
San Francisco 7
Brasília 6
Brescia 6
Cairo 6
Chennai 6
Kazan' 6
Montevideo 6
Palermo 6
Phoenix 6
Salt Lake City 6
Tunis 6
Wuhan 6
Boca Raton 5
Cape Town 5
Casablanca 5
Cavenago di Brianza 5
Chandler 5
Changsha 5
Des Moines 5
Düsseldorf 5
Indianapolis 5
Karachi 5
Lahore 5
Mumbai 5
Nairobi 5
Paris 5
Totale 7.952
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Nome #
Targeting Inflammatory Mediators in Epilepsy: A Systematic Review of Its Molecular Basis and Clinical Applications 830
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders 679
Pulmonary Tuberculosis in Children: A Forgotten Disease? 481
Improving molecular diagnosis in epilepsy by a dedicated high-throughput sequencing platform 459
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 414
Epilepsy in “Sunflower syndrome”: electroclinical features, therapeutic response, and long-term follow-up 365
Human Herpesvirus 6 Encephalitis in Immunocompetent and Immunocompromised Hosts 320
Children with special health care needs attending emergency department in Italy: analysis of 3479 cases 231
Rasmussen's encephalitis: From immune pathogenesis towards targeted-therapy 192
Clinical and Genetic Heterogeneity of HCM: The Possible Role of a Deletion Involving MYH6 and MYH7 141
Bi-allelic JAM2 Variants Lead to Early-Onset Recessive Primary Familial Brain Calcification 139
CDKL5 deficiency-related neurodevelopmental disorders: a multi-center cohort study in Italy 135
The role of inflammatory mediators in epilepsy: Focus on developmental and epileptic encephalopathies and therapeutic implications 134
Abdominal pain as first manifestation of lyme neuroborreliosis in children, case report and review of literature 132
Adoptive immunotherapies in neuro-oncology: classification, recent advances, and translational challenges 127
Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome 127
Advanced pharmacological therapies for neurofibromatosis type 1-related tumors 118
Mowat-Wilson syndrome: growth charts 117
Early-infantile onset epilepsy and developmental delay caused by bi-allelic GAD1 variants 116
Pai syndrome: a review 113
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) 112
Psychopathological Impact in Patients with History of Rheumatic Fever with or without Sydenham’s Chorea: A Multicenter Prospective Study 107
Pediatric Moyamoya Disease and Syndrome in Italy: A Multicenter Cohort 106
Epilepsy after acute central nervous system complications of pediatric hematopoietic cell transplantation: A retrospective, multicenter study 102
Children under 6 years with acute headache in Pediatric Emergency Departments. A 2-year retrospective exploratory multicenter Italian study 101
Cell-based assays for the detection of MOG antibodies: a comparative study 101
Seizures and myelin oligodendrocyte glycoprotein (MOG) antibodies: Two paradigmatic cases and a review of the literature 99
Gonosomal mosaicism for a novel col5a1 pathogenic variant in classic ehlers-danlos syndrome 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) 96
Challenges and management of neurological and psychiatric manifestations in SARS-CoV-2 (COVID-19) patients 96
Neuroinflammation and status epilepticus: a narrative review unraveling a complex interplay 93
Vascular Abnormalities and Neurofibromatosis Type 1: A Paediatric Case Series 93
Potential roads for reaching the summit: an overview on target therapies for high-grade gliomas 92
Management, treatment, and clinical approach of Sydenham's chorea in children: Italian survey on expert-based experience 89
The impact of stem cells in neuro-oncology: applications, evidence, limitations and challenges 89
Post-traumatic stress, anxiety, and depressive symptoms in caregivers of children tested for COVID-19 in the acute phase of the Italian outbreak 88
Expanding the Spectrum of Autosomal Dominant ATP6V1A-Related Disease: Case Report and Literature Review 86
Biallelic mutations in neurofascin cause neurodevelopmental impairment and peripheral demyelination 86
Innovative therapies for malignant brain tumors: the road to a tailored cure 86
A novel missense variant of FBN1 gene in a Sardinian family with Marfan syndrome: a case report 84
Impact of novel coronavirus Disease-19 (COVID-19) pandemic in Italian pediatric emergency departments: a national survey 84
Gene therapies for high-grade gliomas: From the bench to the bedside 83
Targeting the medulloblastoma: A molecular-based approach 83
Novel "T-Dimension" Therapies for Pediatric Optic Pathway Glioma: A Timely, Targeted, and Tailored Treatment Trend 80
Clinical and Genetic Characteristics of Pediatric Patients with Inflammatory Bowel Disease Transitioning to Adult Medicine: A Single-Center Ten-Year Experience 79
Human Herpes Virus 7-related encephalopathy in children 78
Understanding Childhood Neuroimmune Diseases of the Central Nervous System 76
Acneiform rash as a side effect of selumetinib in a child with neurofibromatosis type 1 treated for inoperable plexiform neurofibromas: Good results with doxycycline 74
Mutations in the Neuronal Vesicular SNARE VAMP2 Affect Synaptic Membrane Fusion and Impair Human Neurodevelopment 73
Postural analysis in a pediatric cohort of patients with Ehlers-Danlos Syndrome: a pilot study 72
Melkersson–rosenthal syndrome in childhood: Report of three paediatric cases and a review of the literature 71
Headache in progressive facial hemiatrophy (Parry-Romberg syndrome): A paradigmatic case and systematic review of the literature 67
Lower airway microbiota 66
KIRREL3-related disorders: a case report confirming the radiological features and expanding the clinical spectrum to a less severe phenotype 66
Impact of Fundoplication Surgery and Multidisciplinary Approach on Quality of Life in Children with Neurological Impairment and Gastroesophageal Reflux Disease 65
Pediatric optic neuritis and anti MOG antibodies: a cohort of Italian patients 65
An Overview of The Role of Tumor Necrosis Factor-Alpha in Epileptogenesis and Its Terapeutic Implications 64
Pyridostigmine as a therapeutic option for pediatric gastrointestinal dysmotilities in ATR-X syndrome. Case report and literature review 64
Cyclic Vomiting Syndrome in Children 63
MCM5: A new actor in the link between DNA replication and Meier-Gorlin syndrome 59
PPP2R5D-Related Neurodevelopmental Disorder and Multiple Haemangiomas: A Novel Phenotypic Trait? 58
A Novel Intronic Variant in the KH3 Domain of HNRNPK Leads to a Mild Form of Au-Kline Syndrome 58
Case Report: Hereditary neuropathy with liability to pressure palsy (HNPP): the role of genetic investigation in diagnostic assessment 57
Gelastic seizures not associated with hypothalamic hamartoma: A long-term follow-up study 56
SLK is mutated in individuals with a neurodevelopmental disorder 54
PDXK mutations cause polyneuropathy responsive to pyridoxal 5′-phosphate supplementation 52
Infantile spasms followed by childhood absence epilepsy: A case series 49
Hereditary Multiple Osteochondromas and Acute Lymphoblastic Leukemia: A Possible Role for EXT1 and EXT2 in Hematopoietic Malignancies 46
Rethinking Otorhinolaryngologic Care Pathways in Children with Down Syndrome: A Multidisciplinary Framework for Early Diagnosis and Management 41
Clinical variability in children with dolichoarteriopathies of the internal carotid artery 37
Specifications and validation of the ACMG/AMP criteria for clinical interpretation of sequence variants in collagen genes associated with joint hypermobility 36
Intermittent acute porphyria in an 11 year-old girl suffering from oneiric crises: treatment with folic acid 28
West-Nile virus encephalitis in an immunocompetent pediatric patient: successful recovery 28
Acute ataxia in paediatric emergency departments: a multicentre Italian study 25
Neuroimaging findings in Mowat-Wilson syndrome: a study of 54 patients 25
Biotin-Thiamine Responsive Encephalopathy: Report of an Egyptian Family with a Novel SLC19A3 Mutation and Review of the Literature 24
Whole-Exome Sequencing Identifies Novel Genetic Variants Associated with Unexplained Neurodevelopmental Disorders in Children 24
La sincope vasovagale 24
Severe hyponatremia followed by extrapontine myelinolysis (vol 69, pg 423, 2006) 23
ANGIOMATOSI CAVERNOSA CEREBRALE FAMILIARE: DESCRIZIONE DI UN NUOVO CASO 23
Microcephaly associated with Legg-Calvè-Perthes disease in two siblings 22
Problemi della nutrizione in pazienti con patologia cronica 22
Aplasia of the radial artery. 22
Bickerstaff Brainstem Encephalitis and overlapping Guillain-Barre syndrome in children: Report of two cases and review of the literature 21
Benign convulsions associated with mild gastroenteritis: A multicenter clinical study 21
2 pathologies with supernumerary microtubules - evidence of a peculiar HLA haplotpe association 21
Autosomal recessive congenital total lipodystophy of Berardinelli-Seip Type: clinical features in 15 new patients. 21
Aspetti EEG precoci nella sindrome di Angelman 20
Beneficial effects of pharmacological treatment in patients with infantil mitochondrial encephalomyopathies 20
Agenesis of internal carotid artery and hypopituitarism: case report and review of literature. 20
Adenoidal immune response in the context of inflammation and allergy 19
Phenotype and genotype of 87 patients with Mowat-Wilson syndrome and recommendations for care 19
A Rare Cause of Recurrent Spontaneous Pneumothorax 19
Specificità del quadro clinico della duplicazione del braccio corto del cromosoma 8. Due nuove osservazioni. 19
Lacosamide in pediatric and adult patients: Comparison of efficacy and safety 18
Electroclinical findings and long-term outcomes in epileptic patients with inv dup (15) 18
Topiramate in frontal lobe epilepsy 17
Novel FAM126A mutations in hypomyelination and congenital cataract disease 17
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) 16
CHARGE-like presentation, craniosynostosis and mild Mowat-Wilson Syndrome diagnosed by recognition of the distinctive facial gestalt in a cohort of 28 new cases 16
Totale 9.863
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Categoria #
all - tutte 39.307
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 39.307
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202134 0 0 0 0 0 0 0 0 0 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
2025/20264.306 316 206 505 482 463 448 711 305 459 411 0 0
Totale 10.930