UNICA IRIS Institutional Research Information System

SAVASTA, SALVATORE
 Distribuzione geografica
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Continente #
EU - Europa 5.448
NA - Nord America 5.123
AS - Asia 2.740
SA - Sud America 424
Continente sconosciuto - Info sul continente non disponibili 345
AF - Africa 94
OC - Oceania 5
Totale 14.179
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Nazione #
US - Stati Uniti d'America 4.911
IT - Italia 4.402
SG - Singapore 1.163
CN - Cina 699
BR - Brasile 317
SE - Svezia 241
VN - Vietnam 192
DE - Germania 185
HK - Hong Kong 171
FI - Finlandia 161
BD - Bangladesh 132
FR - Francia 113
CA - Canada 109
IN - India 92
GB - Regno Unito 88
KR - Corea 65
NL - Olanda 40
RU - Federazione Russa 40
AT - Austria 39
AR - Argentina 36
PL - Polonia 29
IQ - Iraq 28
JP - Giappone 26
LT - Lituania 26
MX - Messico 22
PK - Pakistan 21
ZA - Sudafrica 20
ID - Indonesia 19
ES - Italia 18
JM - Giamaica 18
VE - Venezuela 18
TR - Turchia 17
CR - Costa Rica 15
MY - Malesia 14
MA - Marocco 12
UY - Uruguay 12
EC - Ecuador 11
GT - Guatemala 11
JO - Giordania 11
PH - Filippine 11
AE - Emirati Arabi Uniti 10
CO - Colombia 10
TN - Tunisia 10
UA - Ucraina 10
CL - Cile 9
EG - Egitto 9
KE - Kenya 9
SA - Arabia Saudita 9
UZ - Uzbekistan 9
IE - Irlanda 8
IL - Israele 8
DK - Danimarca 7
SC - Seychelles 7
SV - El Salvador 7
CZ - Repubblica Ceca 6
PY - Paraguay 6
DZ - Algeria 5
GR - Grecia 5
HN - Honduras 5
LB - Libano 5
NP - Nepal 5
PR - Porto Rico 5
RO - Romania 5
TT - Trinidad e Tobago 5
AU - Australia 4
AZ - Azerbaigian 4
CI - Costa d'Avorio 4
ET - Etiopia 4
IR - Iran 4
KZ - Kazakistan 4
AO - Angola 3
BA - Bosnia-Erzegovina 3
BY - Bielorussia 3
KG - Kirghizistan 3
MD - Moldavia 3
OM - Oman 3
PE - Perù 3
PT - Portogallo 3
RS - Serbia 3
SN - Senegal 3
TH - Thailandia 3
BH - Bahrain 2
BO - Bolivia 2
CH - Svizzera 2
DO - Repubblica Dominicana 2
EE - Estonia 2
HT - Haiti 2
ML - Mali 2
MN - Mongolia 2
NG - Nigeria 2
NI - Nicaragua 2
NO - Norvegia 2
PA - Panama 2
AW - Aruba 1
BB - Barbados 1
BE - Belgio 1
BG - Bulgaria 1
BJ - Benin 1
BS - Bahamas 1
BZ - Belize 1
Totale 13.817
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Città #
Cagliari 3.595
Ashburn 829
Singapore 629
San Jose 584
Boardman 542
Uta 284
Council Bluffs 263
Los Angeles 192
Dallas 185
Hong Kong 160
Santa Clara 154
Nyköping 152
Hefei 146
Helsinki 124
Beijing 107
New York 81
Ho Chi Minh City 67
Columbus 66
Seoul 64
Lauterbourg 61
Milan 61
Rome 55
Buffalo 53
Hanoi 47
Redondo Beach 47
Chicago 43
Nuremberg 40
Phoenix 38
Pune 36
Shanghai 35
Brooklyn 29
São Paulo 29
The Dalles 27
Atlanta 26
San Francisco 25
Lappeenranta 24
Warsaw 24
Houston 23
Montreal 23
Orem 23
Vilnius 23
London 22
Kerken 21
Naples 20
North Bergen 19
Tokyo 19
Turin 19
Vienna 18
Baghdad 17
Guangzhou 17
Toronto 17
Richmond 16
Washington 16
Newark 15
Philadelphia 15
The Bronx 15
Fairfield 14
Frankfurt am Main 14
Princeton 14
Seattle 14
Boston 13
Munich 13
Belo Horizonte 12
Charlotte 12
Dottingen 12
Johannesburg 12
Turku 12
Amsterdam 11
Denver 11
Kingston 11
Miami 11
Indianapolis 10
Kuala Lumpur 10
Palermo 10
Amman 9
Caracas 9
San Diego 9
San José 9
Stockholm 9
Tashkent 9
Wilmington 9
Agrolândia 8
Brasília 8
Brescia 8
Cairo 8
Las Vegas 8
Mexico City 8
Modena 8
New Delhi 8
Rio de Janeiro 8
Shenzhen 8
Xi'an 8
Austin 7
Bologna 7
Da Nang 7
Detroit 7
Dhaka 7
Dublin 7
Guatemala City 7
Haiphong 7
Totale 9.705
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Nome #
Targeting Inflammatory Mediators in Epilepsy: A Systematic Review of Its Molecular Basis and Clinical Applications 868
AMPA receptor GluA2 subunit defects are a cause of neurodevelopmental disorders 698
Pulmonary Tuberculosis in Children: A Forgotten Disease? 508
Improving molecular diagnosis in epilepsy by a dedicated high-throughput sequencing platform 471
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 468
Epilepsy in “Sunflower syndrome”: electroclinical features, therapeutic response, and long-term follow-up 394
Human Herpesvirus 6 Encephalitis in Immunocompetent and Immunocompromised Hosts 344
Children with special health care needs attending emergency department in Italy: analysis of 3479 cases 280
Neuroinflammation and status epilepticus: a narrative review unraveling a complex interplay 229
Cyclic Vomiting Syndrome in Children 221
Rasmussen's encephalitis: From immune pathogenesis towards targeted-therapy 212
Clinical and Genetic Heterogeneity of HCM: The Possible Role of a Deletion Involving MYH6 and MYH7 197
CDKL5 deficiency-related neurodevelopmental disorders: a multi-center cohort study in Italy 184
Impact of Fundoplication Surgery and Multidisciplinary Approach on Quality of Life in Children with Neurological Impairment and Gastroesophageal Reflux Disease 176
Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome 173
Bi-allelic JAM2 Variants Lead to Early-Onset Recessive Primary Familial Brain Calcification 154
Abdominal pain as first manifestation of lyme neuroborreliosis in children, case report and review of literature 151
The role of inflammatory mediators in epilepsy: Focus on developmental and epileptic encephalopathies and therapeutic implications 148
Adoptive immunotherapies in neuro-oncology: classification, recent advances, and translational challenges 145
A novel missense variant of FBN1 gene in a Sardinian family with Marfan syndrome: a case report 138
Mowat-Wilson syndrome: growth charts 135
Advanced pharmacological therapies for neurofibromatosis type 1-related tumors 132
Early-infantile onset epilepsy and developmental delay caused by bi-allelic GAD1 variants 130
Psychopathological Impact in Patients with History of Rheumatic Fever with or without Sydenham’s Chorea: A Multicenter Prospective Study 130
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) 127
Children under 6 years with acute headache in Pediatric Emergency Departments. A 2-year retrospective exploratory multicenter Italian study 126
Pediatric Moyamoya Disease and Syndrome in Italy: A Multicenter Cohort 125
Pai syndrome: a review 125
Cell-based assays for the detection of MOG antibodies: a comparative study 124
Expanding the Spectrum of Autosomal Dominant ATP6V1A-Related Disease: Case Report and Literature Review 122
Epilepsy after acute central nervous system complications of pediatric hematopoietic cell transplantation: A retrospective, multicenter study 122
Human Herpes Virus 7-related encephalopathy in children 122
Vascular Abnormalities and Neurofibromatosis Type 1: A Paediatric Case Series 122
Gonosomal mosaicism for a novel col5a1 pathogenic variant in classic ehlers-danlos syndrome 119
Post-traumatic stress, anxiety, and depressive symptoms in caregivers of children tested for COVID-19 in the acute phase of the Italian outbreak 115
Seizures and myelin oligodendrocyte glycoprotein (MOG) antibodies: Two paradigmatic cases and a review of the literature 114
Challenges and management of neurological and psychiatric manifestations in SARS-CoV-2 (COVID-19) patients 111
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) 110
Management, treatment, and clinical approach of Sydenham's chorea in children: Italian survey on expert-based experience 109
Clinical and Genetic Characteristics of Pediatric Patients with Inflammatory Bowel Disease Transitioning to Adult Medicine: A Single-Center Ten-Year Experience 108
The impact of stem cells in neuro-oncology: applications, evidence, limitations and challenges 107
Gene therapies for high-grade gliomas: From the bench to the bedside 106
Potential roads for reaching the summit: an overview on target therapies for high-grade gliomas 106
PPP2R5D-Related Neurodevelopmental Disorder and Multiple Haemangiomas: A Novel Phenotypic Trait? 104
Impact of novel coronavirus Disease-19 (COVID-19) pandemic in Italian pediatric emergency departments: a national survey 104
Biallelic mutations in neurofascin cause neurodevelopmental impairment and peripheral demyelination 101
Innovative therapies for malignant brain tumors: the road to a tailored cure 101
Targeting the medulloblastoma: A molecular-based approach 99
Novel "T-Dimension" Therapies for Pediatric Optic Pathway Glioma: A Timely, Targeted, and Tailored Treatment Trend 95
An Overview of The Role of Tumor Necrosis Factor-Alpha in Epileptogenesis and Its Terapeutic Implications 93
Postural analysis in a pediatric cohort of patients with Ehlers-Danlos Syndrome: a pilot study 93
Melkersson–rosenthal syndrome in childhood: Report of three paediatric cases and a review of the literature 90
Acneiform rash as a side effect of selumetinib in a child with neurofibromatosis type 1 treated for inoperable plexiform neurofibromas: Good results with doxycycline 89
Understanding Childhood Neuroimmune Diseases of the Central Nervous System 88
KIRREL3-related disorders: a case report confirming the radiological features and expanding the clinical spectrum to a less severe phenotype 88
A Novel Intronic Variant in the KH3 Domain of HNRNPK Leads to a Mild Form of Au-Kline Syndrome 88
Pyridostigmine as a therapeutic option for pediatric gastrointestinal dysmotilities in ATR-X syndrome. Case report and literature review 86
Mutations in the Neuronal Vesicular SNARE VAMP2 Affect Synaptic Membrane Fusion and Impair Human Neurodevelopment 85
Case Report: Hereditary neuropathy with liability to pressure palsy (HNPP): the role of genetic investigation in diagnostic assessment 84
SLK is mutated in individuals with a neurodevelopmental disorder 83
Lower airway microbiota 81
Headache in progressive facial hemiatrophy (Parry-Romberg syndrome): A paradigmatic case and systematic review of the literature 81
Pediatric optic neuritis and anti MOG antibodies: a cohort of Italian patients 81
Hereditary Multiple Osteochondromas and Acute Lymphoblastic Leukemia: A Possible Role for EXT1 and EXT2 in Hematopoietic Malignancies 73
PDXK mutations cause polyneuropathy responsive to pyridoxal 5′-phosphate supplementation 72
Gelastic seizures not associated with hypothalamic hamartoma: A long-term follow-up study 69
MCM5: A new actor in the link between DNA replication and Meier-Gorlin syndrome 68
Adenoidal immune response in the context of inflammation and allergy 67
Clinical variability in children with dolichoarteriopathies of the internal carotid artery 67
Infantile spasms followed by childhood absence epilepsy: A case series 66
Whole-Exome Sequencing Identifies Novel Genetic Variants Associated with Unexplained Neurodevelopmental Disorders in Children 66
Rethinking Otorhinolaryngologic Care Pathways in Children with Down Syndrome: A Multidisciplinary Framework for Early Diagnosis and Management 65
Specifications and validation of the ACMG/AMP criteria for clinical interpretation of sequence variants in collagen genes associated with joint hypermobility 56
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) 50
West-Nile virus encephalitis in an immunocompetent pediatric patient: successful recovery 41
Biotin-Thiamine Responsive Encephalopathy: Report of an Egyptian Family with a Novel SLC19A3 Mutation and Review of the Literature 38
Neuroimaging findings in Mowat-Wilson syndrome: a study of 54 patients 37
Argo Delphi consensus statement on red flags and clinical gateways towards rare disease diagnosis 36
Acute ataxia in paediatric emergency departments: a multicentre Italian study 35
La sincope vasovagale 35
Aplasia of the radial artery. 33
Microcephaly associated with Legg-Calvè-Perthes disease in two siblings 32
Bickerstaff Brainstem Encephalitis and overlapping Guillain-Barre syndrome in children: Report of two cases and review of the literature 32
Intermittent acute porphyria in an 11 year-old girl suffering from oneiric crises: treatment with folic acid 32
Severe hyponatremia followed by extrapontine myelinolysis (vol 69, pg 423, 2006) 31
ANGIOMATOSI CAVERNOSA CEREBRALE FAMILIARE: DESCRIZIONE DI UN NUOVO CASO 31
Identification of the gene altered in Berardinelli-Seip congenital lipodystrophy on chromosome 11q13. 31
Electroclinical findings and long-term outcomes in epileptic patients with inv dup (15) 29
Topiramate in frontal lobe epilepsy 28
Diagnosi precoce e trattamento di un caso di disrafismo spinale occulto con “diastematomielia” e doppio seno dermico. 28
Problemi della nutrizione in pazienti con patologia cronica 27
Specificità del quadro clinico della duplicazione del braccio corto del cromosoma 8. Due nuove osservazioni. 27
2 pathologies with supernumerary microtubules - evidence of a peculiar HLA haplotpe association 27
Phenotype and genotype of 87 patients with Mowat-Wilson syndrome and recommendations for care 26
Benign convulsions associated with mild gastroenteritis: A multicenter clinical study 26
Beneficial effects of pharmacological treatment in patients with infantil mitochondrial encephalomyopathies 26
Broncopolmoniti recidivanti da anomalie dell’epitelio ciliare in una bambina di otto anni. 26
Autosomal recessive congenital total lipodystophy of Berardinelli-Seip Type: clinical features in 15 new patients. 26
Lacosamide in pediatric and adult patients: Comparison of efficacy and safety 25
A Rare Cause of Recurrent Spontaneous Pneumothorax 25
Totale 12.229
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Categoria #
all - tutte 51.471
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 51.471
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022176 0 0 0 0 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
2025/20265.239 316 206 505 482 463 448 711 305 459 641 481 222
2026/20272.316 343 332 703 797 141 0 0 0 0 0 0 0
Totale 14.179