statistiche ricercatore

SALVATONI, ALESSANDRO

Distribuzione geografica

Continente	#
NA - Nord America	14.425
EU - Europa	13.574
AS - Asia	2.945
OC - Oceania	21
Continente sconosciuto - Info sul continente non disponibili	20
AF - Africa	11
SA - Sud America	10
Totale	31.006

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Nazione	#
US - Stati Uniti d'America	14.404
IT - Italia	7.441
UA - Ucraina	2.505
TR - Turchia	1.208
SE - Svezia	968
CN - Cina	776
VN - Vietnam	702
DE - Germania	684
FI - Finlandia	604
IE - Irlanda	583
FR - Francia	376
GB - Regno Unito	272
SG - Singapore	176
JP - Giappone	37
RU - Federazione Russa	37
CZ - Repubblica Ceca	26
NL - Olanda	26
IN - India	22
EU - Europa	19
CA - Canada	17
AU - Australia	16
BE - Belgio	14
CH - Svizzera	9
EG - Egitto	8
ES - Italia	8
BR - Brasile	5
NZ - Nuova Zelanda	5
ID - Indonesia	4
IR - Iran	4
MX - Messico	4
PL - Polonia	4
AT - Austria	3
RO - Romania	3
AR - Argentina	2
DK - Danimarca	2
GR - Grecia	2
HK - Hong Kong	2
LK - Sri Lanka	2
MA - Marocco	2
OM - Oman	2
SA - Arabia Saudita	2
A2 - ???statistics.table.value.countryCode.A2???	1
BG - Bulgaria	1
CL - Cile	1
CO - Colombia	1
GE - Georgia	1
HU - Ungheria	1
LB - Libano	1
ME - Montenegro	1
MK - Macedonia	1
MN - Mongolia	1
MT - Malta	1
MY - Malesia	1
NO - Norvegia	1
PE - Perù	1
PK - Pakistan	1
PS - Palestinian Territory	1
PT - Portogallo	1
SN - Senegal	1
TW - Taiwan	1
UZ - Uzbekistan	1
Totale	31.006

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Città	#
Milan	5.246
Jacksonville	1.906
Fairfield	1.492
Chandler	1.342
Woodbridge	1.197
Ashburn	911
Houston	904
Wilmington	662
Princeton	646
Izmir	624
Dearborn	620
Ann Arbor	597
Dublin	578
Cambridge	480
Seattle	476
Nyköping	457
Rome	410
Boardman	352
Dong Ket	345
San Mateo	258
Beijing	210
New York	175
Singapore	175
San Diego	143
Ogden	126
Hefei	81
Como	70
Düsseldorf	68
Santa Clara	68
Kunming	62
Washington	62
Nanjing	59
Chicago	58
Verona	53
Nanchang	42
Norwalk	39
London	36
Tokyo	36
Guangzhou	35
Jinan	31
Munich	29
Fuzhou	25
Helsinki	25
Brno	24
Los Angeles	16
Berlin	14
Dallas	13
Kilburn	13
Brussels	12
Chengdu	12
Naples	12
Sydney	12
Torino	12
Wuhan	12
Zhengzhou	12
Bologna	11
Frankfurt am Main	11
Redmond	11
Redwood City	11
Shenyang	11
Hebei	10
Kocaeli	10
Mcallen	10
Brescia	9
Baotou	8
Chongqing	8
Ningbo	8
Padova	8
Toronto	8
Changsha	7
Falls Church	7
Florence	7
Napoli	7
Phoenix	7
Xian	7
Amsterdam	6
Ferrara	6
Hangzhou	6
Jiaxing	6
Nanning	6
San Francisco	6
Shanghai	6
Shaoxing	6
Acton	5
Caserta	5
Catanzaro	5
Detroit	5
Edinburgh	5
Genova	5
Spinea	5
Venice	5
Busto Arsizio	4
Cairo	4
Catania	4
Chaoyang	4
Colli del Tronto	4
Latina	4
Monza	4
Pune	4
Quzhou	4
Totale	21.675

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Nome	#
Iperinsulinismo congenito nell'infanzia: registro nazionale degli iperinsulinismi congeniti; ruolo dell'ipoglicemia iperinsulinemica negli eventi ad apparente rischio di vita (ALTE)e sindrome della morte improvvisa (SIDS); valutazione clinica e metabolica; caratterizzazione genetica; individuazione di nuovi geni candidati.	350
Studio di linkage in famiglie di pazienti affetti da Iperinsulinismo Congenito dell'Infanzia (CHI) mediante tecnologie di genotipizzazione ad alta risoluzione di SNP	274
Deficit di 3beta-idrossisteroido deidrogenasi di tipo 2: una diagnosi mondiale.	224
Obesità, microalbuminemia ed ipertensione in soggetti con T1DM in età pediatrica	194
Vitamin D status, enterovirus infection, and type 1 diabetes in Italian children/adolescents	169
Subcutaneous Immunoglobulin in Infantile Chronic Inflammatory Demyelinating Polyneuropathy: A Case Report.	167
Intrafamilial spread of enterovirus infections at the clinical onset of type 1 diabetes	164
Disorders of glucose metabolism in Prader–Willi syndrome: Results of a multicenter Italian cohort study	162
Health-related quality of life and treatment preferences in adolescents with type 1 diabetes. The VIPKIDS study.	161
Behind the (impedance) baseline in children	159
The Effect of Alginate in Gastroesophageal Reflux in Infants	158
Anthropometric characteristics of newborns with Prader-Willi syndrome	158
Increasing burden, younger age at onset and worst metabolic control in migrant than in Italian children with type 1 diabetes: An emerging problem in pediatric clinics	157
A Multicenter Retrospective Survey regarding Diabetic Ketoacidosis Management in Italian Children with Type 1 Diabetes	154
Emerging effects of early environmental factors over genetic background for type 1 diabetes susceptibility: Evidence from a nationwide Italian twin study	154
Metabolic syndrome in adult patients with Prader-Willi syndrome	153
A "hot spot" in the Pit-1 gene responsible for combined pituitary hormone deficiency: clinical and molecular correlates.	148
Ketoacidosis at diagnosis in childhood-onset diabetes and the risk of retinopathy 20 years later	148
Severe hypoglycemia and ketoacidosis over one year in Italian pediatric population with type 1 diabetes mellitus: A multi center retrospective observational study	147
Molecular cytogenetics, RFLP analysis and clinical characterization of a de novo trisomy 10p case	145
Whole genome SNP genotyping and exome sequencing reveal novel genetic variants and putative causative genes in congenital hyperinsulinism	145
Long-term side effects of growth hormone treatment in children with Prader-Willi syndrome	145
Insulin pump failures in Italian children with Type 1 diabetes: retrospective 1-year cohort study.	145
Diabetic ketoacidosis at the onset of disease during a national awareness campaign: A 2-year observational study in children aged 0-18 years	145
Leptin in children and adolescents with Type 1 Diabetes. A 2-year longitunidal study	145
Pediatric Dehydration Assessment at Triage: Prospective Study on Refilling Time.	144
Trattamento della pubertà precoce con Ciproterone Acetato	143
How Accurate Is a Single Cutpoint to Identify High Blood Pressure in Adolescents?	143
Thyroid function in patients with Prader-Willi syndrome: an Italian multicenter study of 339 patients	142
POI: a score to modulate GH treatment in children with Prader-Willi Syndrome.	141
The role of socio-economic and clinical factors on HbA1c in children and adolescents with type 1 diabetes: an Italian multicentre survey	141
Uniparental disomy and pretreatment IGF-1 may predict elevated IGF-1 levels in Prader-Willi patients on GH treatment	140
Assessment of central adrenal insufficiency in children and adolescents with Prader-Willi syndrome	139
Evaluation Of Retinal Thickness In Young Patients With Type 1 Diabetes Mellitus	139
Retinal thinning in young patients with type 1 diabetes mellitus: is it the first sign of diabetic retinopathy?	139
Prevalence of pathogenetic MC4R mutations in Italian Children with early onset obesity, tall stature and familial history of obesity	138
Recommendations for self-monitoring in pediatric diabetes: a consensus statement by the ISPED	137
High frequency of diabetic ketoacidosis at diagnosis of type 1 diabetes in Italian children: A nationwide longitudinal study, 2004-2013	137
Younger age at diagnosis of type 1 diabetes mellitus in children of immigrated families born in Italy	135
A survey on Prader-Willi syndrome in the Italian population: prevalence of historical and clinical signs.	135
Bone mineral density in diabetic children and adolescents: a follow-up study	134
Potential celiac disease in type 1 diabetes:A multicenter study	133
Urinary hydroxylysine and hydroxylysyl glycosides excretion in patients with Turner's syndrome.	133
Bone metabolism and glucose control in children and adolescents with T1DM	130
Growth hormone therapy and respiratory disorders: Long-term follow-up in PWS children	130
The Italian National Survey for Prader-Willi syndrome: An epidemiologic study	129
Body Composition and Growth in Asthmatic Children Treated with Inhaled Steroids	129
Esophageal impedance and esophagitis in children: any correlation?	128
Enteroviruses and causality of type 1 diabetes: how close we are?	128
Homozygousity mapping of congenital hyperinsulinism of infancy (CHI) in Italian patients	127
Variability of the 13C-acetate breath test for gastric emptying of liquids in healthy children.	127
Variability of the 13C-octanoic acid breath test for gastricemptying of solids in healthy children	127
Oral ranitidine and gastric acid buffering in infants with persisting reflux-symptoms.	125
Metabolic syndrome in children with Prader-Willi syndrome: the effect of obesity	125
Peripheral nerve conduction study in children and adolescents at the clinical onset of type 1 diabetes and at five of more years postdiagnosis	125
Thyroid Function Anomalies in Children with Down Syndrome: Early TSH Alteration can Predict Future Hypothyroidism Development?	125
Hypothyroidism and sodium valproate	124
Assessment of the efficacy of a psychological aiming at improving the quality of life in patients with diabetes mellitus type 1 and their families	124
Cyproterone acetate treatment in precocious puberty.	123
Symptomatic threshold of hypoglycemia and predictors of severe hypoglycemia in children and adolescent with T1DM	123
Low mean impedance in 24-hour tracings and esophagitis in children: a strong connection	123
Children with Prader-Willi syndrome exhibit more evident meal-induced responses in plasma ghrelin and peptide YY levels than obese and lean children	122
Oral ranitidine and duration of gastric pH >4.0 in infants with persisting reflux symptoms	121
The influence of dietary education in diabetic children.	121
Macular Thickness Evaluation in Young Patients With Type 1 Diabetes Mellitus and Healthy Controls	121
Erratum: Organization and regional distribution of centers for the management of children and adolescents with diabetes in Italy	121
Novel mutation in HADHSC gene in a Italian infant with congenital hyperinsulinism.	120
Enterovirus infection and low Treg function: two possible biomarkers of progression to autoimmune T1D.	120
Enteroviruses in Blood Diabetes and Viruses	119
Nationwide cross-sectional survey of 3560 children and adolescents with diabetes in Italy.	119
Hyponatremia and seizures during desmopressin acetate treatment in hypothyroidism.	119
Is dopamine responsible for a reduction in nocturnal blood pressure fall in children with type 1 diabetes?	118
Adrenal function and type III procollagen propeptide in obese children with striae	118
Effect of purified somatomedins on thymidine incorporation into lectin activated human lymphocytes	117
N323K mutation of HSD3B2 gene in two siblings: sexual ambiguity limited to male gender	117
Italian Study Group on Idiopathic Central Hypogonadism (ICH). Germline prokineticin receptor 2 (PROKR2) variants associated with central hypogonadism cause differental modulation of distinct intracellular pathways.	117
Whole genome SNP genotyping and exome sequencing reveal novel genetic variants and putative causative genes in congenital hyperinsulinism.	117
Ambulatory 24 hrs blood pressure minitoring in diabetic children and adolescent: a pilot study	116
Sleep disordered breathing in Prader-Willi patients treated with rhGH	116
IDDM in a Boy with 10pTrisomy: Is GAD2 Gene Involved?	115
Short-term effects of growth hormone treatment on the upper airways of non severely obese children with Prader-Willi syndrome.	115
A rare genetic disorder causing persistent severe neonatalhypoglycaemia the diagnostic workup.	115
Frequent detection of enteroviruses in children with newly-diagnosed type 1 diabetes	114
LH-RH test in Bartter's Syndrome before and during treatment with prostaglandin synthesis inhibitors	113
Esophageal impedance baseline is age dependent	113
Physical activity and diabetes.	112
Organization and regional distribution of centers for the management of children and adolescents with diabetes in Italy	112
Alla base della ridotta caduta pressoria notturna in giovani diabetici vi è un eccesso di dopamina?	111
Infant and Toddler Type 1 Diabetes: Complications after 20 years' duration	111
Growth hormone dependency of the effect of human serum on thymidine uptake by lectin-activated human lymphocytes.	111
PEDIATRIC GIST PRESENTING AS ANEMIA	110
Metabolic syndrome in children and adolescents with Prader-Willi syndrome: Preliminary results-	109
A rare complication of T1DM in a female teenager: Mauriac syndrome?	109
GH/IGF-I axis in Prader-Willi syndrome: Evaluation of IGF-I levels and the somatotroph responsiveness to various provocative stimuli	108
Enterovirus genomes in the blood of children with T1DM at disease onset and one year later	108
Revealing enterovirus infection in chronic human disorders: An integrated diagnostic approach	108
Multiple pituitary hormone deficiency: management of puberty for optimal auxological results	106
The natural history of euthyroid hashimoto's thyroiditis in children	106
Treg function as a marker to define the susceptibility to T1DM clinical onset in a healthy subject with antibodies positivity?	105
The effect of prolonged GH treatment on upper airways and sleep-disordered breathing of 50 non-severely obese children with Prader-Willi syndrome	105
Totale	13.491

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Categoria	#
all - tutte	104.345
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	104.345

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	Totale	Lug	Ago	Sett	Ott	Nov	Dic	Gen	Feb	Mar	Apr	Mag	Giu
2019/2020	4.509	0	0	0	792	190	580	995	715	284	480	82	391
2020/2021	4.229	49	431	88	406	147	498	262	393	732	148	387	688
2021/2022	2.910	273	362	293	192	166	56	94	211	193	385	230	455
2022/2023	3.617	447	167	189	385	259	859	12	461	525	110	102	101
2023/2024	8.103	1.330	1.303	1.364	1.432	1.549	571	62	84	228	30	66	84
2024/2025	852	63	37	750	2	0	0	0	0	0	0	0	0
Totale													31.119