SALPIETRO DAMIANO, VINCENZO
 Distribuzione geografica
Continente #
EU - Europa 1.360
NA - Nord America 735
AS - Asia 292
SA - Sud America 16
AF - Africa 4
OC - Oceania 3
Continente sconosciuto - Info sul continente non disponibili 2
Totale 2.412
Nazione #
US - Stati Uniti d'America 731
IT - Italia 722
IE - Irlanda 228
SE - Svezia 157
SG - Singapore 131
CN - Cina 129
DE - Germania 90
FI - Finlandia 66
GB - Regno Unito 24
PL - Polonia 19
IN - India 14
UA - Ucraina 14
BR - Brasile 12
FR - Francia 8
BE - Belgio 7
CH - Svizzera 7
TR - Turchia 7
AT - Austria 3
AU - Australia 3
CA - Canada 3
ES - Italia 3
ID - Indonesia 3
RU - Federazione Russa 3
CZ - Repubblica Ceca 2
EU - Europa 2
GR - Grecia 2
MA - Marocco 2
NL - Olanda 2
PE - Perù 2
VN - Vietnam 2
AZ - Azerbaigian 1
EC - Ecuador 1
EG - Egitto 1
HK - Hong Kong 1
IR - Iran 1
KE - Kenya 1
KG - Kirghizistan 1
LT - Lituania 1
MX - Messico 1
RO - Romania 1
SA - Arabia Saudita 1
SK - Slovacchia (Repubblica Slovacca) 1
UZ - Uzbekistan 1
VE - Venezuela 1
Totale 2.412
Città #
Dublin 228
Chandler 168
Nyköping 98
Singapore 90
Messina 82
Munich 68
Ashburn 63
Beijing 52
Milan 45
Jacksonville 43
Helsinki 40
Naples 37
New York 32
Medford 28
Princeton 28
Padova 27
Ann Arbor 26
Rome 26
Cambridge 23
Des Moines 23
Bari 22
Dearborn 21
Warsaw 18
Boardman 17
Bologna 16
Lancaster 15
Mascali 13
Catania 12
Palermo 12
Jinan 10
Lodi 10
Rovereto 10
Florence 9
Hyderabad 9
Wilmington 9
San Mateo 8
Vicenza 8
Brescia 7
Brussels 7
Houston 7
Turin 7
Hangzhou 6
Los Angeles 6
Nanjing 6
Shenyang 6
Woodbridge 6
Alessandria 5
Haikou 5
Rende 5
Romano d'Ezzelino 5
Sant'Antonio Abate 5
Venice 5
Busto Arsizio 4
Casalnuovo di Napoli 4
Hebei 4
Manduria 4
Nanchang 4
Nuremberg 4
Pune 4
Seattle 4
Verona 4
Cassano Magnago 3
Cassina de' Pecchi 3
Fisciano 3
Frankfurt am Main 3
Gela 3
Istanbul 3
Jakarta 3
Lappeenranta 3
Lucca 3
Madrid 3
Melbourne 3
Parma 3
Peio 3
Rimini 3
Sant'Ambrogio di Valpolicella 3
Sarno 3
Stefania 3
Tianjin 3
Washington 3
Zhengzhou 3
Angri 2
Athens 2
Bagheria 2
Basilicanova 2
Bellante 2
Bellinzona 2
Bovolone 2
Brno 2
Cagliari 2
Caltagirone 2
Campi Bisenzio 2
Campobasso 2
Carmiano 2
Catanzaro 2
Changsha 2
Chieti 2
Coccaglio 2
Como 2
Corsico 2
Totale 1.668
Nome #
IDROCEFALO BENIGNO ESTERNO: CONSIDERAZIONI FISIOPATOLOGICHE E POSSIBILI COMPLICANZE DI COMPETENZA NEURORADIOLOGICA. 615
De novo mutation in SLC25A22 gene: expansion of the clinical and electroencephalographic phenotype 138
Adrenal Disorders and the Paediatric Brain: Pathophysiological Considerations and Clinical Implications. 110
A de novo 0.63 Mb 6q25.1 deletion associated with growth failure, congenital heart defect, underdeveloped cerebellar vermis, abnormal cutaneous elasticity and joint laxity. 84
A novel SLC1A4 homozygous mutation causing congenital microcephaly, epileptic encephalopathy and spastic tetraparesis: a video-EEG and tractography – case study 83
Central precocious puberty: from physiopathological mechanisms to treatment. 81
Idiopathic Bilateral Relapsing-Remitting Painful Ophthalmoplegia co-occurring with Hashimoto thyroiditis and hyperhomocysteinemia 77
Sudden cardiac arrest in a child with nemaline myopathy 76
Primary nocturnal enuresis in children with allergic rhinitis and severe adenotonsillar hypertrophy: a single center pilot study 74
Idiopathic intracranial hypertension: a unifying neuroendocrine hypothesis through the adrenal-brain axis 64
Pseudotumor cerebri e Papilledema Idiopatico: un'analisi retrospettiva di tre centri pediatrici italiani. 61
High-mobility group protein B1: a new biomarker of metabolic syndrome in obese children 59
Bassa statura e sindromi genetiche 56
  Hypoprolactinemia in obese children: a bridge between inflammation and metabolic-endocrine dysfunction 47
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME (PRES) IN ETA’ PEDIATRICA: PECULIARITA’ CLINICHE E NEURORADIOLOGICHE. 47
null 46
High-Mobility Group Box 1 (HMGB1) in the childhood: latest findings and future prospects 46
Is there a risk of pubertal worsening in primary intestinal lymphangiectasia? 46
Prominent and regressive brain developmental disorders associated with nance-horan syndrome 46
aCGH nella diagnostica delle sindromi dismorfiche: nostra casistica 42
Pediatric idiopathic intracranial hypertension and extreme childhood obesity: a role for weight gain 40
A de novo truncating mutation in ASXL1 associated with segmental overgrowth 40
Natural history of neurofibromatosis type 2 with onset before the age of 1 year 39
Pediatric idiopathic intracranial hypertension and the underlying endocrine-metabolic dysfunction: a pilot study 39
null 35
A rare PANK2 deletion in the first north African patient affected with pantothenate kinase associated neurodegeneration 34
Spinal neurofibromatosis with central nervous system involvement in a set of twin girls and a boy: further expansion of the phenotype. 32
LMNA gene mutation as a model of cardiometabolic dysfunction: From genetic analysis to treatment response. 32
null 29
KCNQ2-Related Neonatal Epilepsy Treated With Vitamin B6: A Report of Two Cases and Literature Review 28
Thyroid dysfunction in thalassaemic patients: ferritin as a prognostic marker and combined iron chelators as an ideal therapy 28
null 23
Synaptopathies in Developmental and Epileptic Encephalopathies: A Focus on Pre-synaptic Dysfunction 22
Gain and loss of function variants in EZH1 disrupt neurogenesis and cause dominant and recessive neurodevelopmental disorders 21
Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome 21
New insights on the relationship between pseudotumor cerebri and secondary hyperaldosteronism in children 21
null 19
Upper respiratory tract infection and torticollis in children: differential diagnosis of Grisel's syndrome 16
ATP6V1B2-related disorders featuring Lennox-Gastaut-syndrome: A case-based overview 12
Sputum high mobility group box-1 in asthmatic children: A noninvasive sensitive biomarker reflecting disease status 11
Bardet-Biedl Syndrome: A Brief Overview on Clinics and Genetics 11
Age-Related Neurodevelopmental Features in Children with Joubert Syndrome 11
Early-infantile onset epilepsy and developmental delay caused by bi-allelic GAD1 variants 9
Totale 2.471
Categoria #
all - tutte 10.060
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 10.060


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202091 0 0 0 0 0 0 0 12 3 48 21 7
2020/2021181 15 2 42 11 29 7 18 5 18 22 5 7
2021/2022221 1 17 7 9 9 2 19 10 6 47 24 70
2022/2023752 43 65 35 48 43 75 17 42 307 28 21 28
2023/2024440 22 32 39 33 25 61 60 24 7 27 24 86
2024/2025496 42 28 42 78 63 89 117 37 0 0 0 0
Totale 2.471