IRIS
SALPIETRO DAMIANO, Carmelo
 Distribuzione geografica
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Continente #
EU - Europa 26.379
NA - Nord America 20.210
AS - Asia 10.633
SA - Sud America 4.352
AF - Africa 322
OC - Oceania 23
Continente sconosciuto - Info sul continente non disponibili 11
Totale 61.930
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Nazione #
US - Stati Uniti d'America 19.885
RU - Federazione Russa 10.948
IT - Italia 4.819
SG - Singapore 4.701
BR - Brasile 3.719
CN - Cina 2.980
IE - Irlanda 2.927
SE - Svezia 2.558
DE - Germania 1.190
HK - Hong Kong 1.086
UA - Ucraina 1.079
FR - Francia 749
FI - Finlandia 624
VN - Vietnam 618
GB - Regno Unito 507
PL - Polonia 407
IN - India 248
AR - Argentina 234
BD - Bangladesh 149
TR - Turchia 130
CA - Canada 128
IQ - Iraq 116
MX - Messico 116
NL - Olanda 106
EC - Ecuador 102
ZA - Sudafrica 91
AT - Austria 89
BE - Belgio 87
VE - Venezuela 80
JP - Giappone 79
CO - Colombia 69
MA - Marocco 65
ES - Italia 63
PK - Pakistan 63
ID - Indonesia 60
UZ - Uzbekistan 58
PY - Paraguay 43
CL - Cile 39
KE - Kenya 37
AZ - Azerbaigian 35
CZ - Repubblica Ceca 33
EG - Egitto 33
IR - Iran 29
JO - Giordania 28
PE - Perù 27
SA - Arabia Saudita 27
TN - Tunisia 27
UY - Uruguay 23
CH - Svizzera 22
IL - Israele 21
AE - Emirati Arabi Uniti 19
AU - Australia 19
KZ - Kazakistan 19
LT - Lituania 19
NP - Nepal 19
MY - Malesia 18
OM - Oman 18
PT - Portogallo 18
JM - Giamaica 17
PH - Filippine 16
RS - Serbia 16
HN - Honduras 15
KG - Kirghizistan 15
DK - Danimarca 14
DO - Repubblica Dominicana 14
BO - Bolivia 13
DZ - Algeria 12
LB - Libano 12
RO - Romania 12
AL - Albania 11
GR - Grecia 11
BG - Bulgaria 10
BY - Bielorussia 10
PA - Panama 9
SN - Senegal 9
CI - Costa d'Avorio 8
CR - Costa Rica 8
AO - Angola 7
EU - Europa 7
GE - Georgia 7
KW - Kuwait 7
LV - Lettonia 7
TH - Thailandia 7
MD - Moldavia 6
NG - Nigeria 6
NI - Nicaragua 6
NO - Norvegia 6
PS - Palestinian Territory 6
QA - Qatar 6
BN - Brunei Darussalam 5
ET - Etiopia 5
LK - Sri Lanka 5
LU - Lussemburgo 5
AM - Armenia 4
BA - Bosnia-Erzegovina 4
CY - Cipro 4
EE - Estonia 4
GA - Gabon 4
GT - Guatemala 4
LY - Libia 4
Totale 61.861
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Città #
Moscow 3.412
Dublin 2.921
Ashburn 2.484
Singapore 2.476
Chandler 2.271
Jacksonville 2.235
Dallas 2.013
Hong Kong 1.083
Nyköping 1.040
Beijing 1.007
The Dalles 678
Dearborn 660
San Jose 648
Princeton 536
Cambridge 501
Lauterbourg 462
Medford 457
Des Moines 422
Messina 372
Los Angeles 366
Warsaw 365
Ann Arbor 356
Boardman 350
Rome 340
Milan 306
São Paulo 266
Buffalo 261
Munich 245
New York 241
Ho Chi Minh City 204
Council Bluffs 155
Woodbridge 152
Wilmington 150
Tianjin 147
Redondo Beach 133
Hanoi 127
Jinan 123
San Mateo 116
Lancaster 111
Rio de Janeiro 109
Naples 107
Belo Horizonte 103
Guangzhou 95
Catania 84
Houston 83
Shenyang 82
Turku 79
Brussels 78
Orem 78
Frankfurt am Main 77
Santa Clara 71
Nanjing 70
Tokyo 67
Brasília 65
Vienna 65
Seattle 64
Curitiba 63
Porto Alegre 60
Helsinki 57
Bologna 56
Nuremberg 56
Florence 54
Baghdad 53
Chennai 52
Tashkent 51
Manchester 50
Pune 50
Turin 49
Shenzhen 48
Zhengzhou 48
Bremen 47
Johannesburg 47
Hebei 46
Campinas 44
Genoa 44
London 44
Montreal 44
Ningbo 44
Palermo 44
Shanghai 43
Chicago 41
Guayaquil 40
Haikou 40
Salvador 39
Bari 38
Guarulhos 38
Stockholm 37
Taizhou 37
Washington 37
Brooklyn 36
Hangzhou 36
Nanchang 36
Mumbai 35
Norwalk 34
San Francisco 34
Baku 33
Düsseldorf 33
Dong Ket 31
Padova 31
Nairobi 30
Totale 33.479
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Nome #
Lipodistrofia parziale tipo Dunnigan: aspetti clinici e genetici 1.120
Sindrome del vomito ciclico: identificazione della mutazione 3243 del DNA mitocondriale 800
Descrizione del primo caso italiano di sindrome di Ohdo 708
Su un caso di sindrome da Iper-IGD con eredità triallelica 406
TRISOMIA 14 A MOSAICO:DESCRIZIONE DI UN CASO 349
Acute pulmonary exacerbation and lung function decline in patients with cystic fibrosis: high-mobility group box 1 (HMGB1) between inflammation and infection. 263
"Cumulative Stress": The Effects of Maternal and Neonatal Oxidative Stress and Oxidative Stress-Inducible Genes on Programming of Atopy 252
Identificazione di una nuova famiglia italiana con geniospasmo ereditario 243
Allergic rhinitis and adenoid hypertrophy in chilrden: is adeinoidectomy always really useful? 240
Individuazione del locus genico della sindrome di Nablus 239
Anemia emolitica autoimmune da CMV: descrizione di un caso in bambino immunocompetente 238
Ipernatriemia e Febbre di ndd 232
Age and sex prevalence estimate of Joubert syndrome in Italy 226
Ace and angiotensin type 2 receptor genes genotype distributions in italian childhood with congenital uropathies 224
A gene for familial isolated chronic nail candidiasis maps to chromosome 11p12-q12.1 217
A New Hypothesis: correlation between Phlogosis Allergic Minimum Persistent (P.A.M.P.) and Recurrent Respiratory Infections (R.R.I.) 217
Atopy and autoimmune thyroid diseases: melatonin can be useful? 217
Effects of strontium ranelate on bone mass and bone turnover in women with thalassemia major-related osteoporosis 216
Co-inheritance of Hb Hershey [beta70(E14) Ala-->Gly] and Hb La Pommeraie [beta133(H11)Val-->Met] in a Sicilian subject 213
5. Sindrome di Borjeson-Forssman-Lehmann: descrizione di un caso 212
An unusual and malignant intussusception in a child 210
Affective Control and Life Satisfaction in Thalassemics 208
Allelic association of gene markers on chromosome 11q in Italian families with atopy 205
Analisi molecolare di polimorfismi dei geni ACE e AT2R in bambini affetti da patologie congenite del rene e delle vie urinarie 204
Febbre Mediterranea Familiare e mutazioni in eterozigosi: forma di ereditarietà pseudodominante? 204
Bacteraemia caused by Clostridium baratii and Kawasaki syndrome. First case report 202
Different concentration of human cord blood HMGB1 according to delivery and labour: A pilot study 202
A case of Mondor's disease in a patient with Beta Thalassemia Syndrome 201
Caudal Regression and Encephalocele: Rare Manifestations of Expanded Goldenhar Complex 201
Almond milk: A potential therapeutic weapon against cow's milk protein allergy 198
CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders 197
Serum interleukin 17, interleukin 23, and interleukin 10 values in children with atopic eczema/dermatitis syndrome (AEDS): Association with clinical severity and phenotype. 194
Central precocious puberty: from physiopathological mechanisms to treatment. 194
Atopic dermatitis: expression of immunological imbalance 193
BONE MASS AND BONE TURNOVER IN WOMEN WITH THALASSEMIA MAJOR RELATED OSTEOPOROSIS: EFFECTS OF STRONTIUM RANELATE 192
Association of the T14709C mutation of mitochondrial DNA with maternally inherited diabetes mellitus and deafness in an Italian family 191
Correlation of s-IgA and IL-6 Salivary with Caries Disease and Oral Hygiene Parameters in Children 191
Angiotensin-converting enzyme and angiotensin type 2 receptor gene genotype distributions in Italian children with congenital uropathies 189
Covid-19 and cardiac involvement in childhood: state of the art 189
Geniospasmo ereditario: identificata una nuova fratria 188
Allergen immunotherapy, routes of administration and cytokine networks: an update 188
Allelic association of gene markers in the FC epsilon receptor I beta gene and IL-4 gene promoter in Italian atopic children 187
Stimolazione atriale trans-esofagea (SATE): la nostra esperienza 187
Access in pediatric emergency department for respiratory infectious disease 186
ACE I/D gene polymorphism in congenital uropathies 185
Clostridium baratii bacteremia associated with Kawasaki syndrome. First case report 185
Valutazione citofluorimetrica della fagocitosi e del burst ossidativo di neutrofili e monociti in talassemici politrasfusi 184
Molecular analysis of the CART gene in overweight and obese Italian children using family-based association methods. 184
Local Allergic Rhinitis in Pediatric Patients: Is IgE Dosage in Nasal Lavage Fluid a Useful Diagnostic Method in Children? 184
HIF1α and Glut1 receptor in transfused and untransfused thalassemic patients 182
Local therapy with ozone in the management of the exit site in a patient undergoing peritoneal dialysis 181
Allelic association of gene markers on chromosome 11q in Italian families with atopy 180
A mitochondrial DNA mutation (A3243G mtDNA) in a family with cyclic vomiting 180
Allelic association of gene markers on chromosome 11q in Italian families with atopy 180
High-mobility group protein B1 (HMGB1): a new biomarker of metabolic syndrome in obese children 179
3243 BP Mitochondrial DNA mutation in an Italian family with cyclic vomiting syndrome 178
Criteri trasfusionali restrittivi vs terapia con rHuEPO in neonati pretermine esperienza dell’ultimo quinquennio 178
High-mobility group protein B1: a new biomarker of metabolic syndrome in obese children 177
Cardiac dysfunction in children with essential obesity: preliminary data 177
Clinical significance of NOD2/CARD15 and Toll-like receptor 4 gene single nucleotide polymorphisms in inflammatory bowel disease. 176
Molecular analysis of beta-thalassaemia patients in a high incidence area of southern Italy. 175
Gastroesophageal reflux and congenital gastrointestinal malformations 174
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 174
A forced expiratory flow at 25-75% value <65% of predicted should be considered abnormal: a real-world, cross-sectional study 173
Analisi molecolare dei polimorfismi del gene ACE e ATR in bambini italiani affetti da malformazioni congenite renali 172
Mixed Botryoid and Spindle Cell Bladder Rhabdomyosarcoma: an outstanding pediatric case 172
CO(2) pneumoperitoneum induces in vitro hypoxic response culminating in apoptosis of human neuroblastoma cells 171
Miosite da Mycoplasma 170
Due anni di studi epidemiologici sulla diffusione di anticorpi anti-Borrelia burgdorferi in ruminanti domestici dei monti Nebrodi 169
Pontine Tegmental Cap Dysplasia: developmental and cognitive outcome in three adolescent patients 168
Pneumomediastinum, subcutaneous emphysema and pneumorrhachis in asthmatic children 167
Genotoxicity biomarkers in thalassaemic patients 166
A systematic review of food protein–induced enterocolitis syndrome from the last 40 years 166
Apparent third patient with cutaneous mastocytosis, microcephaly, conductive hearing loss, and microtia 166
Role of the diet as a link between oxidative stress and liver diseases 165
Breastfeeding and IL-10 levels in children affected by cow's milk protein allergy: A restrospective study 164
GSTP1 gene methylation and AHR rs2066853 variant predict resistance to first generation somatostatin analogs in patients with acromegaly 164
Febbri ricorrenti ed eredità oligogenica 163
Identification of a new Beta globin variant (beta133 GTG>ATG) in a family from Messina (Sicily-Italy). 163
Increased frequency of the rs2066853 variant of aryl hydrocarbon receptor gene in patients with acromegaly 162
Genetic analysis of the human insulin-like 3 gene in pediatric patients with testicular torsion 162
Association between Allergies and Hypercholesterolemia: A Systematic Review 162
Oxidative damage and genotoxicity biomarkers in transfused and untransfused thalassemic subjects. 161
Allelic association of gene markers on chromosome 11q in Italian families with atopy 160
EFFECT OF WEIGHT REDUCTION ON LEPTIN, TOTAL GHRELIN AND OBESTATIN CONCENTRATIONS IN PREPUBERTAL CHILDREN 160
High-mobility group box 1 in allergic and non allergic upper airway inflammation 160
Strontium ranelate improves bone mineral density in thalassemia major related osteoporosis and reduces sclerostin levels 160
BACTERIAL EMERGING INFECTIONS IN CHILDHOOD 159
Correlazione tra stress ossidativo e concentrazione di O2 utilizzata per rianimare neonati pretermine alla nascita 159
Valutazione della genotossicità in talassemici politrasfusi trattati con terapia ferrochelante:risultati preliminari 159
PREVENZIONE DEL DANNO OSSIDATIVO E GENOTOSSICO NELLA TALASSEMIA MAJOR: RUOLO DELLE COMPLICANZE CLINICHE, DELL'ANEMIA E DELLA SIDEROSI 159
aCGH nella diagnostica delle sindromi dismorfiche: nostra casistica 159
Congenital heart disease in down syndrome 157
Cardiovascular risk factors in childhood obesity 156
Analisi molecolare del gene della filaggrina in bambini affetti da dermatite atopica 156
Uteroglobin-related protein 1 gene -112G/a polymorphism and atopic asthma in Sicilian children. 156
High-Mobility Group Box 1 (HMGB1) in the childhood: latest findings and future prospects 156
The role of anaemia in oxidative and genotoxic damage in transfused β-thalassaemic patients 156
Serum levels of interleukin-18 in splenectomized and nonsplenectomized thalassemic patients: preliminary considerations. 155
Paraplegia agli arti inferiori dopo intervento di coartazione aortica 155
Totale 20.954
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Categoria #
all - tutte 202.172
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 202.172
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021204 0 0 0 0 0 0 0 0 0 0 0 204
2021/20223.655 29 385 63 166 97 36 216 171 63 760 499 1.170
2022/20238.736 753 626 354 718 782 821 80 502 3.624 76 292 108
2023/20242.924 210 356 186 318 582 431 105 208 52 78 114 284
2024/20259.698 147 140 221 585 470 316 177 2.229 2.626 561 738 1.488
2025/202625.511 1.089 1.875 1.915 1.956 1.953 5.876 2.942 2.992 3.127 891 505 390
Totale 62.525