IRIS
SALPIETRO DAMIANO, Carmelo
 Distribuzione geografica
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Continente #
EU - Europa 20.092
NA - Nord America 17.805
AS - Asia 8.899
SA - Sud America 4.230
AF - Africa 253
OC - Oceania 19
Continente sconosciuto - Info sul continente non disponibili 11
Totale 51.309
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Nazione #
US - Stati Uniti d'America 17.542
RU - Federazione Russa 5.440
IT - Italia 4.633
SG - Singapore 4.065
BR - Brasile 3.694
IE - Irlanda 2.957
SE - Svezia 2.571
CN - Cina 2.392
DE - Germania 1.145
UA - Ucraina 1.082
HK - Hong Kong 1.070
FI - Finlandia 633
VN - Vietnam 504
GB - Regno Unito 448
PL - Polonia 402
FR - Francia 267
AR - Argentina 212
IN - India 156
TR - Turchia 108
MX - Messico 105
CA - Canada 98
NL - Olanda 90
EC - Ecuador 88
AT - Austria 86
BE - Belgio 86
BD - Bangladesh 83
IQ - Iraq 74
ZA - Sudafrica 74
VE - Venezuela 62
MA - Marocco 58
JP - Giappone 53
ID - Indonesia 49
UZ - Uzbekistan 49
CO - Colombia 48
ES - Italia 47
PY - Paraguay 42
PK - Pakistan 38
CZ - Repubblica Ceca 32
KE - Kenya 31
AZ - Azerbaigian 29
IR - Iran 29
CL - Cile 27
EG - Egitto 27
PE - Perù 25
JO - Giordania 24
CH - Svizzera 21
TN - Tunisia 20
UY - Uruguay 20
IL - Israele 19
KZ - Kazakistan 18
LT - Lituania 18
PT - Portogallo 17
AE - Emirati Arabi Uniti 16
AU - Australia 15
DK - Danimarca 13
DO - Repubblica Dominicana 13
HN - Honduras 13
NP - Nepal 13
OM - Oman 13
RS - Serbia 13
KG - Kirghizistan 12
RO - Romania 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
GE - Georgia 7
KW - Kuwait 7
LV - Lettonia 7
MY - Malesia 7
AO - Angola 6
CI - Costa d'Avorio 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
TH - Thailandia 4
AM - Armenia 3
GA - Gabon 3
PS - Palestinian Territory 3
SK - Slovacchia (Repubblica Slovacca) 3
SM - San Marino 3
Totale 51.274
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Città #
Dublin 2.953
Moscow 2.842
Chandler 2.290
Jacksonville 2.249
Singapore 2.012
Dallas 2.006
Ashburn 1.617
Hong Kong 1.067
Nyköping 1.048
Beijing 1.010
Dearborn 668
Princeton 544
Cambridge 509
Medford 465
Des Moines 427
The Dalles 365
Warsaw 362
Ann Arbor 358
Messina 354
Los Angeles 353
Boardman 351
Rome 325
Milan 284
São Paulo 269
Buffalo 263
Munich 245
New York 222
Ho Chi Minh City 183
Woodbridge 156
Wilmington 152
Redondo Beach 137
Jinan 124
San Mateo 118
Tianjin 117
Lancaster 111
Belo Horizonte 105
Rio de Janeiro 105
Hanoi 101
Naples 100
Catania 83
Shenyang 83
Turku 79
Brussels 78
Houston 77
Nanjing 70
Brasília 67
Seattle 64
Vienna 63
Porto Alegre 60
Curitiba 59
Helsinki 58
Bologna 55
Florence 52
Nuremberg 51
Pune 51
Turin 48
Zhengzhou 48
Bremen 47
Hebei 46
Campinas 44
Ningbo 44
Tokyo 44
Tashkent 43
Palermo 42
Genoa 41
Haikou 41
Johannesburg 41
Frankfurt am Main 40
Guarulhos 40
Taizhou 37
Baghdad 36
Bari 36
Guayaquil 36
Stockholm 36
Nanchang 35
Salvador 35
Washington 35
Düsseldorf 34
Hangzhou 34
Brooklyn 33
London 33
Norwalk 33
Chicago 32
Montreal 32
Dong Ket 31
Padova 31
Ribeirão Preto 30
Santa Clara 30
Guangzhou 29
Chennai 28
Baku 27
Fuzhou 27
Boston 26
Denver 26
Jakarta 26
Nairobi 26
Tehran 26
Buenos Aires 25
Dhaka 25
Fortaleza 25
Totale 29.581
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Nome #
Lipodistrofia parziale tipo Dunnigan: aspetti clinici e genetici 1.051
Sindrome del vomito ciclico: identificazione della mutazione 3243 del DNA mitocondriale 760
Descrizione del primo caso italiano di sindrome di Ohdo 667
Su un caso di sindrome da Iper-IGD con eredità triallelica 396
TRISOMIA 14 A MOSAICO:DESCRIZIONE DI UN CASO 337
Anemia emolitica autoimmune da CMV: descrizione di un caso in bambino immunocompetente 227
Individuazione del locus genico della sindrome di Nablus 222
Identificazione di una nuova famiglia italiana con geniospasmo ereditario 214
Acute pulmonary exacerbation and lung function decline in patients with cystic fibrosis: high-mobility group box 1 (HMGB1) between inflammation and infection. 206
"Cumulative Stress": The Effects of Maternal and Neonatal Oxidative Stress and Oxidative Stress-Inducible Genes on Programming of Atopy 206
Ipernatriemia e Febbre di ndd 199
Ace and angiotensin type 2 receptor genes genotype distributions in italian childhood with congenital uropathies 188
Allergic rhinitis and adenoid hypertrophy in chilrden: is adeinoidectomy always really useful? 184
5. Sindrome di Borjeson-Forssman-Lehmann: descrizione di un caso 176
Febbre Mediterranea Familiare e mutazioni in eterozigosi: forma di ereditarietà pseudodominante? 175
A gene for familial isolated chronic nail candidiasis maps to chromosome 11p12-q12.1 174
Stimolazione atriale trans-esofagea (SATE): la nostra esperienza 174
Valutazione citofluorimetrica della fagocitosi e del burst ossidativo di neutrofili e monociti in talassemici politrasfusi 171
Age and sex prevalence estimate of Joubert syndrome in Italy 169
Analisi molecolare di polimorfismi dei geni ACE e AT2R in bambini affetti da patologie congenite del rene e delle vie urinarie 168
A New Hypothesis: correlation between Phlogosis Allergic Minimum Persistent (P.A.M.P.) and Recurrent Respiratory Infections (R.R.I.) 168
Effects of strontium ranelate on bone mass and bone turnover in women with thalassemia major-related osteoporosis 166
Geniospasmo ereditario: identificata una nuova fratria 164
Allelic association of gene markers on chromosome 11q in Italian families with atopy 164
Caudal Regression and Encephalocele: Rare Manifestations of Expanded Goldenhar Complex 164
Co-inheritance of Hb Hershey [beta70(E14) Ala-->Gly] and Hb La Pommeraie [beta133(H11)Val-->Met] in a Sicilian subject 163
Atopy and autoimmune thyroid diseases: melatonin can be useful? 163
Bacteraemia caused by Clostridium baratii and Kawasaki syndrome. First case report 160
An unusual and malignant intussusception in a child 160
A case of Mondor's disease in a patient with Beta Thalassemia Syndrome 159
Serum interleukin 17, interleukin 23, and interleukin 10 values in children with atopic eczema/dermatitis syndrome (AEDS): Association with clinical severity and phenotype. 158
Miosite da Mycoplasma 158
Allelic association of gene markers in the FC epsilon receptor I beta gene and IL-4 gene promoter in Italian atopic children 154
Allelic association of gene markers on chromosome 11q in Italian families with atopy 154
Different concentration of human cord blood HMGB1 according to delivery and labour: A pilot study 154
ACE I/D gene polymorphism in congenital uropathies 153
Angiotensin-converting enzyme and angiotensin type 2 receptor gene genotype distributions in Italian children with congenital uropathies 152
Clostridium baratii bacteremia associated with Kawasaki syndrome. First case report 152
Atopic dermatitis: expression of immunological imbalance 149
Association of the T14709C mutation of mitochondrial DNA with maternally inherited diabetes mellitus and deafness in an Italian family 148
CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders 148
Local Allergic Rhinitis in Pediatric Patients: Is IgE Dosage in Nasal Lavage Fluid a Useful Diagnostic Method in Children? 148
Almond milk: A potential therapeutic weapon against cow's milk protein allergy 147
Correlation of s-IgA and IL-6 Salivary with Caries Disease and Oral Hygiene Parameters in Children 147
Affective Control and Life Satisfaction in Thalassemics 147
Central precocious puberty: from physiopathological mechanisms to treatment. 145
3243 BP Mitochondrial DNA mutation in an Italian family with cyclic vomiting syndrome 145
Covid-19 and cardiac involvement in childhood: state of the art 145
BONE MASS AND BONE TURNOVER IN WOMEN WITH THALASSEMIA MAJOR RELATED OSTEOPOROSIS: EFFECTS OF STRONTIUM RANELATE 144
Allergen immunotherapy, routes of administration and cytokine networks: an update 144
Role of the diet as a link between oxidative stress and liver diseases 143
A mitochondrial DNA mutation (A3243G mtDNA) in a family with cyclic vomiting 143
Access in pediatric emergency department for respiratory infectious disease 143
Analisi molecolare dei polimorfismi del gene ACE e ATR in bambini italiani affetti da malformazioni congenite renali 142
HIF1α and Glut1 receptor in transfused and untransfused thalassemic patients 142
Paraplegia agli arti inferiori dopo intervento di coartazione aortica 141
Local therapy with ozone in the management of the exit site in a patient undergoing peritoneal dialysis 141
Molecular analysis of the CART gene in overweight and obese Italian children using family-based association methods. 140
Porpora di Schonlein Henoch e Febbre Mediterranea Familiare: descrizione di un caso clinico con mutazione del gene MEFV 140
Criteri trasfusionali restrittivi vs terapia con rHuEPO in neonati pretermine esperienza dell’ultimo quinquennio 139
High-mobility group protein B1 (HMGB1): a new biomarker of metabolic syndrome in obese children 138
GSTP1 gene methylation and AHR rs2066853 variant predict resistance to first generation somatostatin analogs in patients with acromegaly 138
Allelic association of gene markers on chromosome 11q in Italian families with atopy 137
Gastroesophageal reflux and congenital gastrointestinal malformations 136
Due anni di studi epidemiologici sulla diffusione di anticorpi anti-Borrelia burgdorferi in ruminanti domestici dei monti Nebrodi 135
Sindrome di Joubert e altre sindromi con segno del dente molare: prevalenza e spettro fenotipico dei geni noti 135
Valutazione della genotossicità in talassemici politrasfusi trattati con terapia ferrochelante:risultati preliminari 134
Pontine Tegmental Cap Dysplasia: developmental and cognitive outcome in three adolescent patients 133
Clinical significance of NOD2/CARD15 and Toll-like receptor 4 gene single nucleotide polymorphisms in inflammatory bowel disease. 133
High-mobility group protein B1: a new biomarker of metabolic syndrome in obese children 133
Identification of a new Beta globin variant (beta133 GTG>ATG) in a family from Messina (Sicily-Italy). 132
Cardiac dysfunction in children with essential obesity: preliminary data 132
Apparent third patient with cutaneous mastocytosis, microcephaly, conductive hearing loss, and microtia 132
Molecular analysis of beta-thalassaemia patients in a high incidence area of southern Italy. 131
The role of anaemia in oxidative and genotoxic damage in transfused β-thalassaemic patients 130
Allelic association of gene markers on chromosome 11q in Italian families with atopy 129
Febbri ricorrenti ed eredità oligogenica 129
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 129
PREVENZIONE DEL DANNO OSSIDATIVO E GENOTOSSICO NELLA TALASSEMIA MAJOR: RUOLO DELLE COMPLICANZE CLINICHE, DELL'ANEMIA E DELLA SIDEROSI 128
BACTERIAL EMERGING INFECTIONS IN CHILDHOOD 126
Emopoiesi Extramidollare e trattamento con idrossiurea nella talassemia intermedia: case report 126
A forced expiratory flow at 25-75% value <65% of predicted should be considered abnormal: a real-world, cross-sectional study 126
HMGB1 levels in children with atopic eczema/dermatitis syndrome (AEDS) 126
Serum levels of interleukin-18 in splenectomized and nonsplenectomized thalassemic patients: preliminary considerations. 125
Mixed Botryoid and Spindle Cell Bladder Rhabdomyosarcoma: an outstanding pediatric case 125
CO(2) pneumoperitoneum induces in vitro hypoxic response culminating in apoptosis of human neuroblastoma cells 125
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. 125
Adipokines and their role in allergies 125
Sindrome di Fahr senza ipoparatiroidismo? 124
Correlazione tra stress ossidativo e concentrazione di O2 utilizzata per rianimare neonati pretermine alla nascita 124
Uteroglobin-related protein 1 gene -112G/a polymorphism and atopic asthma in Sicilian children. 123
EFFECT OF WEIGHT REDUCTION ON LEPTIN, TOTAL GHRELIN AND OBESTATIN CONCENTRATIONS IN PREPUBERTAL CHILDREN 123
Genetic analysis of the human insulin-like 3 gene in pediatric patients with testicular torsion 123
Antihistamines: Recommended Dosage-Divergence between Clinical Practice and Guideline Recommendations 123
Pontine Tegmental Cap Dysplasia: neurosviluppo e profilo cognitivo di un paziente adolescente 122
Genotoxicity biomarkers in thalassaemic patients 122
Increased frequency of the rs2066853 variant of aryl hydrocarbon receptor gene in patients with acromegaly 122
Detection of respiratory syncytial virus (RSV) at birth in a newborn with respiratory distress 122
Failure to thrive: the importance of measuring the electrolytes 122
Analisi molecolare di polimorfismi genetici del recettore FcεIβ della regione promotrice dell' IL-4 in famiglie del Sud.Italia con atopia 121
Totale 17.225
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Categoria #
all - tutte 178.045
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 178.045
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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
2025/202614.535 1.111 1.900 1.946 1.994 1.978 5.606 0 0 0 0 0 0
Totale 51.909