SALPIETRO DAMIANO, Carmelo
 Distribuzione geografica
Continente #
NA - Nord America 17.689
EU - Europa 15.111
AS - Asia 8.639
SA - Sud America 4.216
AF - Africa 250
OC - Oceania 19
Continente sconosciuto - Info sul continente non disponibili 11
Totale 45.935
Nazione #
US - Stati Uniti d'America 17.431
IT - Italia 4.621
SG - Singapore 3.886
BR - Brasile 3.683
IE - Irlanda 2.957
SE - Svezia 2.571
CN - Cina 2.329
DE - Germania 1.143
UA - Ucraina 1.082
HK - Hong Kong 1.068
FI - Finlandia 633
VN - Vietnam 503
RU - Federazione Russa 484
GB - Regno Unito 445
PL - Polonia 397
FR - Francia 267
AR - Argentina 211
IN - India 152
TR - Turchia 108
MX - Messico 103
CA - Canada 95
NL - Olanda 90
EC - Ecuador 88
AT - Austria 86
BE - Belgio 86
BD - Bangladesh 82
IQ - Iraq 73
ZA - Sudafrica 73
VE - Venezuela 62
MA - Marocco 58
JP - Giappone 50
CO - Colombia 48
ID - Indonesia 48
UZ - Uzbekistan 48
ES - Italia 46
PY - Paraguay 42
PK - Pakistan 38
CZ - Repubblica Ceca 32
KE - Kenya 30
AZ - Azerbaigian 29
IR - Iran 29
CL - Cile 26
EG - Egitto 26
PE - Perù 25
JO - Giordania 23
CH - Svizzera 21
TN - Tunisia 20
IL - Israele 19
UY - Uruguay 19
KZ - Kazakistan 18
LT - Lituania 18
PT - Portogallo 17
AE - Emirati Arabi Uniti 16
AU - Australia 15
DO - Repubblica Dominicana 13
HN - Honduras 13
NP - Nepal 13
OM - Oman 13
DK - Danimarca 12
KG - Kirghizistan 12
RO - Romania 12
RS - Serbia 12
GR - Grecia 11
BO - Bolivia 10
JM - Giamaica 10
LB - Libano 10
SA - Arabia Saudita 10
BG - Bulgaria 9
BY - Bielorussia 9
DZ - Algeria 9
PA - Panama 9
SN - Senegal 8
AL - Albania 7
EU - Europa 7
KW - Kuwait 7
LV - Lettonia 7
MY - Malesia 7
AO - Angola 6
CI - Costa d'Avorio 6
GE - Georgia 6
NO - Norvegia 6
QA - Qatar 6
BN - Brunei Darussalam 5
LK - Sri Lanka 5
LU - Lussemburgo 5
MD - Moldavia 5
NG - Nigeria 5
CY - Cipro 4
EE - Estonia 4
GT - Guatemala 4
MK - Macedonia 4
NI - Nicaragua 4
NZ - Nuova Zelanda 4
PH - Filippine 4
AM - Armenia 3
GA - Gabon 3
PS - Palestinian Territory 3
SK - Slovacchia (Repubblica Slovacca) 3
SM - San Marino 3
XK - ???statistics.table.value.countryCode.XK??? 3
Totale 45.901
Città #
Dublin 2.953
Chandler 2.290
Jacksonville 2.249
Dallas 2.006
Singapore 1.833
Ashburn 1.567
Hong Kong 1.065
Nyköping 1.048
Beijing 1.010
Dearborn 668
Princeton 544
Cambridge 509
Medford 465
Des Moines 427
The Dalles 365
Ann Arbor 358
Warsaw 357
Messina 354
Boardman 351
Los Angeles 349
Rome 325
Milan 284
São Paulo 266
Buffalo 263
Munich 245
New York 216
Ho Chi Minh City 182
Moscow 181
Woodbridge 156
Wilmington 152
Redondo Beach 137
Jinan 124
San Mateo 118
Lancaster 111
Belo Horizonte 105
Rio de Janeiro 105
Tianjin 104
Hanoi 101
Naples 100
Catania 83
Shenyang 83
Turku 79
Brussels 78
Houston 76
Nanjing 70
Brasília 67
Seattle 63
Vienna 63
Porto Alegre 60
Curitiba 59
Helsinki 58
Bologna 55
Florence 51
Pune 51
Nuremberg 50
Turin 48
Zhengzhou 48
Bremen 47
Hebei 46
Campinas 44
Ningbo 44
Palermo 42
Tashkent 42
Genoa 41
Haikou 41
Tokyo 41
Frankfurt am Main 40
Johannesburg 40
Guarulhos 39
Taizhou 37
Bari 36
Guayaquil 36
Stockholm 36
Baghdad 35
Nanchang 35
Salvador 35
Washington 35
Düsseldorf 34
Hangzhou 34
Norwalk 33
Dong Ket 31
London 31
Montreal 31
Padova 31
Chicago 30
Ribeirão Preto 30
Brooklyn 29
Santa Clara 28
Baku 27
Chennai 27
Fuzhou 27
Guangzhou 26
Tehran 26
Boston 25
Dhaka 25
Fortaleza 25
Jakarta 25
Manchester 25
Nairobi 25
San Francisco 25
Totale 26.627
Nome #
Lipodistrofia parziale tipo Dunnigan: aspetti clinici e genetici 1.034
Sindrome del vomito ciclico: identificazione della mutazione 3243 del DNA mitocondriale 749
Descrizione del primo caso italiano di sindrome di Ohdo 653
Su un caso di sindrome da Iper-IGD con eredità triallelica 389
TRISOMIA 14 A MOSAICO:DESCRIZIONE DI UN CASO 329
Anemia emolitica autoimmune da CMV: descrizione di un caso in bambino immunocompetente 220
Individuazione del locus genico della sindrome di Nablus 213
Identificazione di una nuova famiglia italiana con geniospasmo ereditario 208
"Cumulative Stress": The Effects of Maternal and Neonatal Oxidative Stress and Oxidative Stress-Inducible Genes on Programming of Atopy 189
Acute pulmonary exacerbation and lung function decline in patients with cystic fibrosis: high-mobility group box 1 (HMGB1) between inflammation and infection. 186
Ipernatriemia e Febbre di ndd 183
Ace and angiotensin type 2 receptor genes genotype distributions in italian childhood with congenital uropathies 169
Stimolazione atriale trans-esofagea (SATE): la nostra esperienza 169
Febbre Mediterranea Familiare e mutazioni in eterozigosi: forma di ereditarietà pseudodominante? 167
Allergic rhinitis and adenoid hypertrophy in chilrden: is adeinoidectomy always really useful? 167
Valutazione citofluorimetrica della fagocitosi e del burst ossidativo di neutrofili e monociti in talassemici politrasfusi 165
Geniospasmo ereditario: identificata una nuova fratria 157
5. Sindrome di Borjeson-Forssman-Lehmann: descrizione di un caso 157
A gene for familial isolated chronic nail candidiasis maps to chromosome 11p12-q12.1 155
Analisi molecolare di polimorfismi dei geni ACE e AT2R in bambini affetti da patologie congenite del rene e delle vie urinarie 153
A New Hypothesis: correlation between Phlogosis Allergic Minimum Persistent (P.A.M.P.) and Recurrent Respiratory Infections (R.R.I.) 153
Co-inheritance of Hb Hershey [beta70(E14) Ala-->Gly] and Hb La Pommeraie [beta133(H11)Val-->Met] in a Sicilian subject 152
Miosite da Mycoplasma 149
Effects of strontium ranelate on bone mass and bone turnover in women with thalassemia major-related osteoporosis 148
Atopy and autoimmune thyroid diseases: melatonin can be useful? 147
Caudal Regression and Encephalocele: Rare Manifestations of Expanded Goldenhar Complex 147
An unusual and malignant intussusception in a child 145
Age and sex prevalence estimate of Joubert syndrome in Italy 145
Serum interleukin 17, interleukin 23, and interleukin 10 values in children with atopic eczema/dermatitis syndrome (AEDS): Association with clinical severity and phenotype. 144
Bacteraemia caused by Clostridium baratii and Kawasaki syndrome. First case report 144
A case of Mondor's disease in a patient with Beta Thalassemia Syndrome 142
Allelic association of gene markers on chromosome 11q in Italian families with atopy 141
Different concentration of human cord blood HMGB1 according to delivery and labour: A pilot study 138
Allelic association of gene markers in the FC epsilon receptor I beta gene and IL-4 gene promoter in Italian atopic children 136
Local Allergic Rhinitis in Pediatric Patients: Is IgE Dosage in Nasal Lavage Fluid a Useful Diagnostic Method in Children? 136
Role of the diet as a link between oxidative stress and liver diseases 135
Allelic association of gene markers on chromosome 11q in Italian families with atopy 135
Association of the T14709C mutation of mitochondrial DNA with maternally inherited diabetes mellitus and deafness in an Italian family 134
ACE I/D gene polymorphism in congenital uropathies 134
Angiotensin-converting enzyme and angiotensin type 2 receptor gene genotype distributions in Italian children with congenital uropathies 134
Porpora di Schonlein Henoch e Febbre Mediterranea Familiare: descrizione di un caso clinico con mutazione del gene MEFV 134
Paraplegia agli arti inferiori dopo intervento di coartazione aortica 133
Clostridium baratii bacteremia associated with Kawasaki syndrome. First case report 131
3243 BP Mitochondrial DNA mutation in an Italian family with cyclic vomiting syndrome 130
Correlation of s-IgA and IL-6 Salivary with Caries Disease and Oral Hygiene Parameters in Children 130
Atopic dermatitis: expression of immunological imbalance 130
CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders 129
Affective Control and Life Satisfaction in Thalassemics 129
Sindrome di Joubert e altre sindromi con segno del dente molare: prevalenza e spettro fenotipico dei geni noti 128
Central precocious puberty: from physiopathological mechanisms to treatment. 127
Almond milk: A potential therapeutic weapon against cow's milk protein allergy 127
BONE MASS AND BONE TURNOVER IN WOMEN WITH THALASSEMIA MAJOR RELATED OSTEOPOROSIS: EFFECTS OF STRONTIUM RANELATE 127
Allergen immunotherapy, routes of administration and cytokine networks: an update 127
Molecular analysis of the CART gene in overweight and obese Italian children using family-based association methods. 126
Local therapy with ozone in the management of the exit site in a patient undergoing peritoneal dialysis 126
Access in pediatric emergency department for respiratory infectious disease 125
A mitochondrial DNA mutation (A3243G mtDNA) in a family with cyclic vomiting 124
Valutazione della genotossicità in talassemici politrasfusi trattati con terapia ferrochelante:risultati preliminari 124
GSTP1 gene methylation and AHR rs2066853 variant predict resistance to first generation somatostatin analogs in patients with acromegaly 124
HIF1α and Glut1 receptor in transfused and untransfused thalassemic patients 124
Covid-19 and cardiac involvement in childhood: state of the art 124
Analisi molecolare dei polimorfismi del gene ACE e ATR in bambini italiani affetti da malformazioni congenite renali 123
Pontine Tegmental Cap Dysplasia: developmental and cognitive outcome in three adolescent patients 122
Criteri trasfusionali restrittivi vs terapia con rHuEPO in neonati pretermine esperienza dell’ultimo quinquennio 121
Due anni di studi epidemiologici sulla diffusione di anticorpi anti-Borrelia burgdorferi in ruminanti domestici dei monti Nebrodi 120
Allelic association of gene markers on chromosome 11q in Italian families with atopy 120
High-mobility group protein B1 (HMGB1): a new biomarker of metabolic syndrome in obese children 120
Clinical significance of NOD2/CARD15 and Toll-like receptor 4 gene single nucleotide polymorphisms in inflammatory bowel disease. 119
Cardiac dysfunction in children with essential obesity: preliminary data 119
Gastroesophageal reflux and congenital gastrointestinal malformations 119
Apparent third patient with cutaneous mastocytosis, microcephaly, conductive hearing loss, and microtia 119
High-mobility group protein B1: a new biomarker of metabolic syndrome in obese children 118
Emopoiesi Extramidollare e trattamento con idrossiurea nella talassemia intermedia: case report 117
Sindrome di Fahr senza ipoparatiroidismo? 117
Febbri ricorrenti ed eredità oligogenica 117
Identification of a new Beta globin variant (beta133 GTG>ATG) in a family from Messina (Sicily-Italy). 116
Molecular analysis of beta-thalassaemia patients in a high incidence area of southern Italy. 116
PREVENZIONE DEL DANNO OSSIDATIVO E GENOTOSSICO NELLA TALASSEMIA MAJOR: RUOLO DELLE COMPLICANZE CLINICHE, DELL'ANEMIA E DELLA SIDEROSI 115
The role of anaemia in oxidative and genotoxic damage in transfused β-thalassaemic patients 115
Uteroglobin-related protein 1 gene -112G/a polymorphism and atopic asthma in Sicilian children. 113
Endocrinopathies, metabolic disorders, and iron overload in major and intermedia thalassemia: Serum ferritin as diagnostic and predictive marker associated with liver and cardiac T2* MRI assessment 113
On the use of conventional and tissue Doppler echocardiography in patients with β-Thalassemia major and myocardial iron-overload: Preliminary data by a single centre study. 113
BACTERIAL EMERGING INFECTIONS IN CHILDHOOD 111
Allelic association of gene markers on chromosome 11q in Italian families with atopy 111
Serum levels of interleukin-18 in splenectomized and nonsplenectomized thalassemic patients: preliminary considerations. 111
Pontine Tegmental Cap Dysplasia: neurosviluppo e profilo cognitivo di un paziente adolescente 111
A forced expiratory flow at 25-75% value <65% of predicted should be considered abnormal: a real-world, cross-sectional study 111
HMGB1 levels in children with atopic eczema/dermatitis syndrome (AEDS) 110
Correlazione tra stress ossidativo e concentrazione di O2 utilizzata per rianimare neonati pretermine alla nascita 109
Mixed Botryoid and Spindle Cell Bladder Rhabdomyosarcoma: an outstanding pediatric case 109
Renal anomalies in newborns with vacterel association: case series and literature review 109
Adipokines and their role in allergies 109
EFFECT OF WEIGHT REDUCTION ON LEPTIN, TOTAL GHRELIN AND OBESTATIN CONCENTRATIONS IN PREPUBERTAL CHILDREN 108
Detection of respiratory syncytial virus (RSV) at birth in a newborn with respiratory distress 108
Genotoxicity biomarkers in thalassaemic patients 107
Genetic analysis of the human insulin-like 3 gene in pediatric patients with testicular torsion 107
Allergic reactions to foods by inhalation in children. 106
Candidiasi mucocutanea cronica tra storia e novità 106
Analisi molecolare di polimorfismi genetici del recettore FcεIβ della regione promotrice dell' IL-4 in famiglie del Sud.Italia con atopia 106
Analisi molecolare del gene della filaggrina in bambini affetti da dermatite atopica 106
Totale 15.757
Categoria #
all - tutte 169.856
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 169.856


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211.753 0 0 0 0 0 427 92 313 140 376 201 204
2021/20223.691 29 386 63 168 97 36 217 173 63 767 505 1.187
2022/20238.817 762 631 356 722 785 827 80 506 3.667 76 295 110
2023/20242.947 212 358 189 319 585 434 107 208 52 78 116 289
2024/20259.811 148 140 223 588 475 318 180 2.268 2.653 567 744 1.507
2025/20269.161 1.111 1.900 1.946 1.994 1.978 232 0 0 0 0 0 0
Totale 46.535