SALPIETRO DAMIANO, VINCENZO
 Distribuzione geografica
Continente #
EU - Europa 1.562
NA - Nord America 862
AS - Asia 447
SA - Sud America 266
AF - Africa 20
OC - Oceania 3
Continente sconosciuto - Info sul continente non disponibili 2
Totale 3.162
Nazione #
US - Stati Uniti d'America 846
IT - Italia 792
BR - Brasile 245
IE - Irlanda 229
SE - Svezia 158
SG - Singapore 155
DE - Germania 144
CN - Cina 141
FI - Finlandia 92
HK - Hong Kong 90
GB - Regno Unito 28
PL - Polonia 22
FR - Francia 21
UA - Ucraina 20
IN - India 16
RU - Federazione Russa 9
TR - Turchia 9
BE - Belgio 7
CH - Svizzera 7
NL - Olanda 7
CA - Canada 6
CZ - Repubblica Ceca 6
IQ - Iraq 6
KE - Kenya 6
MA - Marocco 6
AR - Argentina 5
MX - Messico 5
AT - Austria 4
AZ - Azerbaigian 4
BD - Bangladesh 4
EC - Ecuador 4
UZ - Uzbekistan 4
ZA - Sudafrica 4
AU - Australia 3
ES - Italia 3
ID - Indonesia 3
PK - Pakistan 3
RO - Romania 3
VE - Venezuela 3
VN - Vietnam 3
BO - Bolivia 2
CO - Colombia 2
EG - Egitto 2
EU - Europa 2
GR - Grecia 2
HN - Honduras 2
KZ - Kazakistan 2
LV - Lettonia 2
PA - Panama 2
PE - Perù 2
PY - Paraguay 2
SK - Slovacchia (Repubblica Slovacca) 2
TN - Tunisia 2
BG - Bulgaria 1
CR - Costa Rica 1
IR - Iran 1
JP - Giappone 1
KG - Kirghizistan 1
KH - Cambogia 1
LB - Libano 1
LT - Lituania 1
NP - Nepal 1
PT - Portogallo 1
RS - Serbia 1
SA - Arabia Saudita 1
UY - Uruguay 1
Totale 3.162
Città #
Dublin 229
Chandler 168
Munich 113
Nyköping 98
Singapore 96
Hong Kong 89
Messina 82
Milan 79
Ashburn 64
Beijing 62
The Dalles 62
Helsinki 53
Jacksonville 43
Naples 37
New York 35
Padova 30
Rome 30
Medford 28
Princeton 28
Ann Arbor 26
São Paulo 25
Bari 24
Cambridge 23
Des Moines 23
Dearborn 21
Warsaw 20
Bologna 19
Boardman 17
Lancaster 15
Catania 14
Mascali 13
Palermo 13
Rio de Janeiro 12
Turku 12
Los Angeles 11
Jinan 10
Lodi 10
Rovereto 10
Brescia 9
Florence 9
Hyderabad 9
Wilmington 9
Frankfurt am Main 8
San Mateo 8
Vicenza 8
Belo Horizonte 7
Brussels 7
Houston 7
Turin 7
Woodbridge 7
Hangzhou 6
Lauterbourg 6
Livorno 6
Nanjing 6
Shenyang 6
Alessandria 5
Campinas 5
Haikou 5
Moscow 5
Nairobi 5
Nuremberg 5
Rende 5
Romano d'Ezzelino 5
Sant'Antonio Abate 5
Santo André 5
Venice 5
Baku 4
Brasília 4
Busto Arsizio 4
Casalnuovo di Napoli 4
Hebei 4
London 4
Manduria 4
Nanchang 4
Pune 4
Seattle 4
Tashkent 4
Verona 4
Araruama 3
Casablanca 3
Cassano Magnago 3
Cassina de' Pecchi 3
Curitiba 3
Düsseldorf 3
Fisciano 3
Gela 3
Istanbul 3
Jakarta 3
Lappeenranta 3
Lucca 3
Madrid 3
Melbourne 3
Olomouc 3
Osasco 3
Parma 3
Peio 3
Pescara 3
Ribeirão Preto 3
Rimini 3
Sant'Ambrogio di Valpolicella 3
Totale 2.038
Nome #
IDROCEFALO BENIGNO ESTERNO: CONSIDERAZIONI FISIOPATOLOGICHE E POSSIBILI COMPLICANZE DI COMPETENZA NEURORADIOLOGICA. 701
De novo mutation in SLC25A22 gene: expansion of the clinical and electroencephalographic phenotype 202
Adrenal Disorders and the Paediatric Brain: Pathophysiological Considerations and Clinical Implications. 132
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. 109
A novel SLC1A4 homozygous mutation causing congenital microcephaly, epileptic encephalopathy and spastic tetraparesis: a video-EEG and tractography – case study 104
Central precocious puberty: from physiopathological mechanisms to treatment. 97
Idiopathic Bilateral Relapsing-Remitting Painful Ophthalmoplegia co-occurring with Hashimoto thyroiditis and hyperhomocysteinemia 96
Primary nocturnal enuresis in children with allergic rhinitis and severe adenotonsillar hypertrophy: a single center pilot study 94
Idiopathic intracranial hypertension: a unifying neuroendocrine hypothesis through the adrenal-brain axis 89
Sudden cardiac arrest in a child with nemaline myopathy 86
Bassa statura e sindromi genetiche 79
Pseudotumor cerebri e Papilledema Idiopatico: un'analisi retrospettiva di tre centri pediatrici italiani. 77
High-mobility group protein B1: a new biomarker of metabolic syndrome in obese children 76
Is there a risk of pubertal worsening in primary intestinal lymphangiectasia? 66
A de novo truncating mutation in ASXL1 associated with segmental overgrowth 65
Pediatric idiopathic intracranial hypertension and extreme childhood obesity: a role for weight gain 63
High-Mobility Group Box 1 (HMGB1) in the childhood: latest findings and future prospects 63
  Hypoprolactinemia in obese children: a bridge between inflammation and metabolic-endocrine dysfunction 61
Prominent and regressive brain developmental disorders associated with nance-horan syndrome 60
aCGH nella diagnostica delle sindromi dismorfiche: nostra casistica 57
POSTERIOR REVERSIBLE ENCEPHALOPATHY SYNDROME (PRES) IN ETA’ PEDIATRICA: PECULIARITA’ CLINICHE E NEURORADIOLOGICHE. 56
LMNA gene mutation as a model of cardiometabolic dysfunction: From genetic analysis to treatment response. 55
Pediatric idiopathic intracranial hypertension and the underlying endocrine-metabolic dysfunction: a pilot study 53
A rare PANK2 deletion in the first north African patient affected with pantothenate kinase associated neurodegeneration 53
Gain and loss of function variants in EZH1 disrupt neurogenesis and cause dominant and recessive neurodevelopmental disorders 50
Natural history of neurofibromatosis type 2 with onset before the age of 1 year 48
Spinal neurofibromatosis with central nervous system involvement in a set of twin girls and a boy: further expansion of the phenotype. 47
null 46
Thyroid dysfunction in thalassaemic patients: ferritin as a prognostic marker and combined iron chelators as an ideal therapy 46
KCNQ2-Related Neonatal Epilepsy Treated With Vitamin B6: A Report of Two Cases and Literature Review 41
Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome 40
null 35
Synaptopathies in Developmental and Epileptic Encephalopathies: A Focus on Pre-synaptic Dysfunction 34
Age-Related Neurodevelopmental Features in Children with Joubert Syndrome 32
New insights on the relationship between pseudotumor cerebri and secondary hyperaldosteronism in children 29
null 29
Upper respiratory tract infection and torticollis in children: differential diagnosis of Grisel's syndrome 26
Bardet-Biedl Syndrome: A Brief Overview on Clinics and Genetics 25
null 23
ATP6V1B2-related disorders featuring Lennox-Gastaut-syndrome: A case-based overview 21
Early-infantile onset epilepsy and developmental delay caused by bi-allelic GAD1 variants 20
null 19
Sputum high mobility group box-1 in asthmatic children: A noninvasive sensitive biomarker reflecting disease status 16
Totale 3.221
Categoria #
all - tutte 12.130
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 12.130


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20207 0 0 0 0 0 0 0 0 0 0 0 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
2024/20251.246 42 28 42 78 63 89 117 227 249 101 102 108
Totale 3.221