IRIS
SALPIETRO DAMIANO, Carmelo
 Distribuzione geografica
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Continente #
EU - Europa 26.446
NA - Nord America 19.565
AS - Asia 10.638
SA - Sud America 4.410
AF - Africa 327
OC - Oceania 23
Continente sconosciuto - Info sul continente non disponibili 11
Totale 61.420
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Nazione #
US - Stati Uniti d'America 19.275
RU - Federazione Russa 11.024
IT - Italia 4.753
SG - Singapore 4.721
BR - Brasile 3.773
CN - Cina 2.964
IE - Irlanda 2.953
SE - Svezia 2.571
DE - Germania 1.195
HK - Hong Kong 1.099
UA - Ucraina 1.086
FR - Francia 753
FI - Finlandia 629
VN - Vietnam 623
GB - Regno Unito 507
PL - Polonia 407
IN - India 250
AR - Argentina 239
TR - Turchia 133
BD - Bangladesh 128
IQ - Iraq 117
MX - Messico 115
CA - Canada 105
NL - Olanda 104
EC - Ecuador 103
ZA - Sudafrica 92
AT - Austria 89
BE - Belgio 87
VE - Venezuela 80
JP - Giappone 77
CO - Colombia 69
MA - Marocco 66
PK - Pakistan 64
ES - Italia 62
ID - Indonesia 59
UZ - Uzbekistan 58
PY - Paraguay 43
KE - Kenya 38
CL - Cile 37
AZ - Azerbaigian 35
CZ - Repubblica Ceca 33
EG - Egitto 32
TN - Tunisia 30
IR - Iran 29
JO - Giordania 28
PE - Perù 27
SA - Arabia Saudita 27
UY - Uruguay 23
CH - Svizzera 21
IL - Israele 21
AU - Australia 19
KZ - Kazakistan 19
LT - Lituania 19
NP - Nepal 19
OM - Oman 19
AE - Emirati Arabi Uniti 18
PT - Portogallo 18
MY - Malesia 16
PH - Filippine 16
RS - Serbia 16
KG - Kirghizistan 15
DK - Danimarca 14
DO - Repubblica Dominicana 14
HN - Honduras 14
BO - Bolivia 13
JM - Giamaica 13
LB - Libano 12
RO - Romania 12
AL - Albania 11
DZ - Algeria 11
GR - Grecia 11
BG - Bulgaria 10
BY - Bielorussia 10
TH - Thailandia 10
PA - Panama 9
SN - Senegal 9
CI - Costa d'Avorio 8
LV - Lettonia 8
AO - Angola 7
EU - Europa 7
GE - Georgia 7
KW - Kuwait 7
CR - Costa Rica 6
MD - Moldavia 6
NG - Nigeria 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
LY - Libia 5
NI - Nicaragua 5
AM - Armenia 4
BA - Bosnia-Erzegovina 4
CY - Cipro 4
EE - Estonia 4
GA - Gabon 4
GT - Guatemala 4
Totale 61.355
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Città #
Moscow 3.438
Dublin 2.947
Singapore 2.488
Ashburn 2.297
Chandler 2.279
Jacksonville 2.247
Dallas 2.015
Hong Kong 1.096
Nyköping 1.046
Beijing 1.014
The Dalles 675
Dearborn 665
Princeton 541
Cambridge 506
San Jose 491
Lauterbourg 466
Medford 462
Des Moines 427
Warsaw 366
Messina 363
Los Angeles 361
Ann Arbor 357
Boardman 350
Rome 338
Milan 300
São Paulo 272
Buffalo 262
Munich 245
New York 233
Ho Chi Minh City 213
Woodbridge 154
Wilmington 150
Tianjin 148
Redondo Beach 135
Hanoi 123
Jinan 123
San Mateo 117
Lancaster 111
Rio de Janeiro 109
Belo Horizonte 106
Naples 104
Guangzhou 96
Catania 83
Shenyang 82
Houston 80
Turku 79
Brussels 78
Frankfurt am Main 78
Orem 72
Nanjing 70
Brasília 67
Tokyo 67
Vienna 65
Seattle 64
Curitiba 63
Porto Alegre 61
Helsinki 57
Nuremberg 56
Bologna 55
Baghdad 54
Santa Clara 54
Chennai 53
Florence 52
Pune 51
Tashkent 51
Manchester 49
Shenzhen 48
Turin 48
Zhengzhou 48
Bremen 47
Johannesburg 47
Hebei 46
Campinas 44
Genoa 44
Ningbo 44
Shanghai 43
Palermo 42
Guarulhos 41
Guayaquil 41
Haikou 41
London 40
Chicago 39
Salvador 39
Bari 38
Montreal 37
Stockholm 37
Taizhou 37
Council Bluffs 36
Hangzhou 36
Nanchang 36
Brooklyn 35
Mumbai 35
Washington 35
Baku 33
Düsseldorf 33
Norwalk 33
Dong Ket 31
Nairobi 31
Padova 31
Istanbul 30
Totale 33.103
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Nome #
Lipodistrofia parziale tipo Dunnigan: aspetti clinici e genetici 1.089
Sindrome del vomito ciclico: identificazione della mutazione 3243 del DNA mitocondriale 794
Descrizione del primo caso italiano di sindrome di Ohdo 701
Su un caso di sindrome da Iper-IGD con eredità triallelica 406
TRISOMIA 14 A MOSAICO:DESCRIZIONE DI UN CASO 346
Acute pulmonary exacerbation and lung function decline in patients with cystic fibrosis: high-mobility group box 1 (HMGB1) between inflammation and infection. 260
"Cumulative Stress": The Effects of Maternal and Neonatal Oxidative Stress and Oxidative Stress-Inducible Genes on Programming of Atopy 249
Individuazione del locus genico della sindrome di Nablus 239
Identificazione di una nuova famiglia italiana con geniospasmo ereditario 239
Anemia emolitica autoimmune da CMV: descrizione di un caso in bambino immunocompetente 237
Allergic rhinitis and adenoid hypertrophy in chilrden: is adeinoidectomy always really useful? 233
Ipernatriemia e Febbre di ndd 231
Age and sex prevalence estimate of Joubert syndrome in Italy 224
Ace and angiotensin type 2 receptor genes genotype distributions in italian childhood with congenital uropathies 222
A gene for familial isolated chronic nail candidiasis maps to chromosome 11p12-q12.1 215
Effects of strontium ranelate on bone mass and bone turnover in women with thalassemia major-related osteoporosis 215
A New Hypothesis: correlation between Phlogosis Allergic Minimum Persistent (P.A.M.P.) and Recurrent Respiratory Infections (R.R.I.) 214
Atopy and autoimmune thyroid diseases: melatonin can be useful? 214
5. Sindrome di Borjeson-Forssman-Lehmann: descrizione di un caso 211
Co-inheritance of Hb Hershey [beta70(E14) Ala-->Gly] and Hb La Pommeraie [beta133(H11)Val-->Met] in a Sicilian subject 209
An unusual and malignant intussusception in a child 209
Allelic association of gene markers on chromosome 11q in Italian families with atopy 203
Analisi molecolare di polimorfismi dei geni ACE e AT2R in bambini affetti da patologie congenite del rene e delle vie urinarie 201
Affective Control and Life Satisfaction in Thalassemics 201
A case of Mondor's disease in a patient with Beta Thalassemia Syndrome 199
Caudal Regression and Encephalocele: Rare Manifestations of Expanded Goldenhar Complex 199
Different concentration of human cord blood HMGB1 according to delivery and labour: A pilot study 197
Almond milk: A potential therapeutic weapon against cow's milk protein allergy 195
CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders 194
Bacteraemia caused by Clostridium baratii and Kawasaki syndrome. First case report 193
Atopic dermatitis: expression of immunological imbalance 193
Serum interleukin 17, interleukin 23, and interleukin 10 values in children with atopic eczema/dermatitis syndrome (AEDS): Association with clinical severity and phenotype. 191
Febbre Mediterranea Familiare e mutazioni in eterozigosi: forma di ereditarietà pseudodominante? 191
Central precocious puberty: from physiopathological mechanisms to treatment. 190
Correlation of s-IgA and IL-6 Salivary with Caries Disease and Oral Hygiene Parameters in Children 189
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
BONE MASS AND BONE TURNOVER IN WOMEN WITH THALASSEMIA MAJOR RELATED OSTEOPOROSIS: EFFECTS OF STRONTIUM RANELATE 187
Covid-19 and cardiac involvement in childhood: state of the art 186
Association of the T14709C mutation of mitochondrial DNA with maternally inherited diabetes mellitus and deafness in an Italian family 185
Allergen immunotherapy, routes of administration and cytokine networks: an update 185
Valutazione citofluorimetrica della fagocitosi e del burst ossidativo di neutrofili e monociti in talassemici politrasfusi 184
ACE I/D gene polymorphism in congenital uropathies 184
Clostridium baratii bacteremia associated with Kawasaki syndrome. First case report 184
Geniospasmo ereditario: identificata una nuova fratria 183
Angiotensin-converting enzyme and angiotensin type 2 receptor gene genotype distributions in Italian children with congenital uropathies 183
Access in pediatric emergency department for respiratory infectious disease 183
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
Molecular analysis of the CART gene in overweight and obese Italian children using family-based association methods. 180
HIF1α and Glut1 receptor in transfused and untransfused thalassemic patients 180
Local Allergic Rhinitis in Pediatric Patients: Is IgE Dosage in Nasal Lavage Fluid a Useful Diagnostic Method in Children? 179
Local therapy with ozone in the management of the exit site in a patient undergoing peritoneal dialysis 178
3243 BP Mitochondrial DNA mutation in an Italian family with cyclic vomiting syndrome 177
High-mobility group protein B1 (HMGB1): a new biomarker of metabolic syndrome in obese children 177
Allelic association of gene markers on chromosome 11q in Italian families with atopy 176
Criteri trasfusionali restrittivi vs terapia con rHuEPO in neonati pretermine esperienza dell’ultimo quinquennio 176
High-mobility group protein B1: a new biomarker of metabolic syndrome in obese children 175
Cardiac dysfunction in children with essential obesity: preliminary data 174
Gastroesophageal reflux and congenital gastrointestinal malformations 173
Clinical significance of NOD2/CARD15 and Toll-like receptor 4 gene single nucleotide polymorphisms in inflammatory bowel disease. 172
A forced expiratory flow at 25-75% value <65% of predicted should be considered abnormal: a real-world, cross-sectional study 171
Analisi molecolare dei polimorfismi del gene ACE e ATR in bambini italiani affetti da malformazioni congenite renali 170
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 170
Due anni di studi epidemiologici sulla diffusione di anticorpi anti-Borrelia burgdorferi in ruminanti domestici dei monti Nebrodi 169
Molecular analysis of beta-thalassaemia patients in a high incidence area of southern Italy. 169
Miosite da Mycoplasma 168
CO(2) pneumoperitoneum induces in vitro hypoxic response culminating in apoptosis of human neuroblastoma cells 168
Mixed Botryoid and Spindle Cell Bladder Rhabdomyosarcoma: an outstanding pediatric case 166
Pontine Tegmental Cap Dysplasia: developmental and cognitive outcome in three adolescent patients 165
Apparent third patient with cutaneous mastocytosis, microcephaly, conductive hearing loss, and microtia 165
GSTP1 gene methylation and AHR rs2066853 variant predict resistance to first generation somatostatin analogs in patients with acromegaly 164
Identification of a new Beta globin variant (beta133 GTG>ATG) in a family from Messina (Sicily-Italy). 163
Pneumomediastinum, subcutaneous emphysema and pneumorrhachis in asthmatic children 163
Role of the diet as a link between oxidative stress and liver diseases 162
Association between Allergies and Hypercholesterolemia: A Systematic Review 162
Febbri ricorrenti ed eredità oligogenica 161
Allelic association of gene markers on chromosome 11q in Italian families with atopy 160
A systematic review of food protein–induced enterocolitis syndrome from the last 40 years 160
Genetic analysis of the human insulin-like 3 gene in pediatric patients with testicular torsion 160
Oxidative damage and genotoxicity biomarkers in transfused and untransfused thalassemic subjects. 159
Increased frequency of the rs2066853 variant of aryl hydrocarbon receptor gene in patients with acromegaly 159
High-mobility group box 1 in allergic and non allergic upper airway inflammation 159
Breastfeeding and IL-10 levels in children affected by cow's milk protein allergy: A restrospective study 159
BACTERIAL EMERGING INFECTIONS IN CHILDHOOD 158
Correlazione tra stress ossidativo e concentrazione di O2 utilizzata per rianimare neonati pretermine alla nascita 158
Valutazione della genotossicità in talassemici politrasfusi trattati con terapia ferrochelante:risultati preliminari 158
Genotoxicity biomarkers in thalassaemic patients 158
Strontium ranelate improves bone mineral density in thalassemia major related osteoporosis and reduces sclerostin levels 158
EFFECT OF WEIGHT REDUCTION ON LEPTIN, TOTAL GHRELIN AND OBESTATIN CONCENTRATIONS IN PREPUBERTAL CHILDREN 157
aCGH nella diagnostica delle sindromi dismorfiche: nostra casistica 156
Uteroglobin-related protein 1 gene -112G/a polymorphism and atopic asthma in Sicilian children. 155
PREVENZIONE DEL DANNO OSSIDATIVO E GENOTOSSICO NELLA TALASSEMIA MAJOR: RUOLO DELLE COMPLICANZE CLINICHE, DELL'ANEMIA E DELLA SIDEROSI 155
Congenital heart disease in down syndrome 155
Paraplegia agli arti inferiori dopo intervento di coartazione aortica 154
The role of anaemia in oxidative and genotoxic damage in transfused β-thalassaemic patients 154
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. 154
Adipokines and their role in allergies 154
Analisi molecolare del gene della filaggrina in bambini affetti da dermatite atopica 153
Sindrome di Joubert e altre sindromi con segno del dente molare: prevalenza e spettro fenotipico dei geni noti 153
Totale 20.650
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Categoria #
all - tutte 193.813
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 193.813
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021781 0 0 0 0 0 0 0 0 0 376 201 204
2021/20223.680 29 385 63 167 97 36 217 171 63 767 504 1.181
2022/20238.783 759 629 356 719 782 825 80 502 3.652 76 293 110
2023/20242.935 211 356 188 318 583 432 106 208 52 78 116 287
2024/20259.780 148 140 221 586 474 318 180 2.264 2.642 565 742 1.500
2025/202624.761 1.105 1.894 1.936 1.984 1.967 5.922 2.968 3.019 3.149 817 0 0
Totale 62.019