CRIS Current Research Information System

BALSAMO, ANTONIO
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
EU - Europa 6.931
NA - Nord America 5.027
AS - Asia 4.546
AF - Africa 332
SA - Sud America 320
OC - Oceania 17
Continente sconosciuto - Info sul continente non disponibili 1
Totale 17.174
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 4.956
IT - Italia 2.848
SG - Singapore 1.267
GB - Regno Unito 1.254
CN - Cina 1.199
VN - Vietnam 1.141
DE - Germania 686
UA - Ucraina 550
SE - Svezia 448
HK - Hong Kong 343
RU - Federazione Russa 273
FR - Francia 259
IN - India 252
BR - Brasile 237
IE - Irlanda 159
NL - Olanda 116
JP - Giappone 106
ZA - Sudafrica 101
KR - Corea 84
CI - Costa d'Avorio 68
EE - Estonia 68
TG - Togo 60
CH - Svizzera 57
FI - Finlandia 50
NG - Nigeria 42
CA - Canada 38
SC - Seychelles 37
AR - Argentina 34
JO - Giordania 33
BG - Bulgaria 26
PL - Polonia 25
BE - Belgio 23
AT - Austria 20
GR - Grecia 20
MX - Messico 18
IL - Israele 17
AU - Australia 16
TR - Turchia 13
BD - Bangladesh 12
ID - Indonesia 12
CL - Cile 11
CO - Colombia 11
EC - Ecuador 11
ES - Italia 11
RO - Romania 11
IR - Iran 10
EG - Egitto 9
LT - Lituania 9
PE - Perù 8
TH - Thailandia 8
PH - Filippine 7
TW - Taiwan 7
MA - Marocco 6
PK - Pakistan 6
AE - Emirati Arabi Uniti 5
HN - Honduras 5
IQ - Iraq 5
DO - Repubblica Dominicana 4
LB - Libano 4
MY - Malesia 4
PY - Paraguay 4
AL - Albania 3
CR - Costa Rica 3
KE - Kenya 3
MD - Moldavia 3
UY - Uruguay 3
UZ - Uzbekistan 3
DK - Danimarca 2
KW - Kuwait 2
KZ - Kazakistan 2
LU - Lussemburgo 2
RS - Serbia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
BA - Bosnia-Erzegovina 1
BB - Barbados 1
BH - Bahrain 1
BZ - Belize 1
CZ - Repubblica Ceca 1
DJ - Gibuti 1
DZ - Algeria 1
ET - Etiopia 1
GH - Ghana 1
JM - Giamaica 1
KG - Kirghizistan 1
ME - Montenegro 1
MR - Mauritania 1
NO - Norvegia 1
NZ - Nuova Zelanda 1
PS - Palestinian Territory 1
PT - Portogallo 1
SA - Arabia Saudita 1
SK - Slovacchia (Repubblica Slovacca) 1
TN - Tunisia 1
VE - Venezuela 1
Totale 17.174
Salva come PNG Salva come JPEG
Città #
Southend 1.080
Singapore 826
Ashburn 499
Chandler 383
Fairfield 371
Hong Kong 336
Jacksonville 336
Hefei 266
Ho Chi Minh City 250
Princeton 236
Santa Clara 229
Milan 223
Wilmington 218
Dong Ket 209
Hanoi 203
Houston 200
Woodbridge 183
Rome 175
Ann Arbor 169
Dublin 151
Seattle 146
Cambridge 134
Beijing 133
Boardman 120
Padova 112
Westminster 109
Tokyo 103
Nanjing 102
Bologna 101
Berlin 90
Naples 87
Seoul 84
Turin 83
Los Angeles 72
Saint Petersburg 71
Medford 69
Abidjan 68
Lomé 60
Buffalo 56
Mülheim 53
Dallas 48
Shenyang 46
Abeokuta 40
Bari 39
Redwood City 39
Munich 38
Palermo 37
Nanchang 36
Tianjin 36
Mahé 35
Verona 35
Changsha 34
Florence 34
Jinan 34
Amman 33
Falls Church 33
São Paulo 33
Helsinki 31
Bern 26
Hebei 26
Da Nang 25
Frankfurt am Main 25
Haiphong 25
Redondo Beach 25
Sofia 25
San Diego 24
Bremen 23
Catania 23
New York 22
Dearborn 21
Bengaluru 20
Genoa 20
Salerno 20
Brussels 19
Guangzhou 19
Redmond 19
Modena 18
Parma 18
Norwalk 17
Phoenix 17
Chicago 16
Jiaxing 16
Perugia 16
Salt Lake City 16
Shanghai 16
Zhengzhou 16
Biên Hòa 15
Can Tho 15
Falkenstein 15
Bergamo 14
Quận Bình Thạnh 14
Düsseldorf 13
Olalla 13
Vienna 13
London 12
Taizhou 12
Toronto 12
Vũng Tàu 12
Andover 11
Athens 11
Totale 9.812
Salva come PNG Salva come JPEG
Nome #
Terapia e follow-up dell’iperplasia surrenale congenita 1.227
I deficit congeniti della steroidogenesi 1.057
CYP21A2 AND CYP11B1: FIRST REPORT OF A DIGENIC INHERITANCE IN CAH. 470
A new case of familial mutation in the SRY gene implicated in the pure gonadal dysgenesis in two sisters and in their unaffected father 375
Nuove acquisizioni sulla genetica dell’ipogonadismo ipogonadotropo. 351
Screening e diagnosi dell’iperplasia surrenale congenita: dalle vecchie alle nuove tecnologie. 289
The role of 21-hydroxylase in the pathogenesis of adrenal masses: Review of the literature and focus on our own experience. 259
A new DAX1 gene mutation associated with congenital adrenal hypoplasia and hypogonadotropic hypogonadism 240
Severe obesity and cardiometabolic risk in children: comparison from two international classification systems. 224
A sequence variation in 3’UTR of CYP21A2 gene correlates with a mild form of Congenital Adrenal Hyperplasia 219
Study of the NR5A1 gene in a cohort of Italian patients with 46,XY Disorders of Sex Development (DSD) without adrenal insufficiency: identification of 7 novel mutations. 203
Studio del gene CYP21A2 in una casistica del centro-nord Italia con deficit di 21-idrossialasi nella fascia di sovrapposizione tra eterozigote e forma non classica (17-OH-progesterone dopo stimolo: 24-76 nmol/L) al fine di individuare nuove mutazioni del gene associate a tale condizione; studio funzionale, confronto con i risultati ottenuti in una casisitica Siciliana e ricerca di indicatori per la necessità di terapia 191
Disorders of sexual development 185
Functional studies of two novel and two rare mutations in the 21-hydroxylase gene. 180
Tra obesità e percentili 177
Obesità essenziale: diagnosi 177
Effect on adult height of pubertal growth hormone retesting and withdrawal of therapy in patients with previously diagnosed growth hormone deficiency. 176
Characterization of deletions at 9p affecting the candidate regions for sex reversal and deletion 9p syndrome by MLPA. 176
Italian cross-sectional growth charts for height, weight and BMI (2 to 20 yr). 169
Metabolic Aspects of Patients Followed for Severe Obesity 168
Le complicanze metaboliche dell'obesità in età evolutiva 167
46, XX DSD due to androgen excess in monogenic disorders of steroidogenesis: Genetic, biochemical, and clinical features 167
Comparison between Liquid and Tablet Formulations of Levothyroxine in the Initial Treatment of Congenital Hypothyroidism 166
A molecular analysis of candidate genes for hypospadias in Italian subjects 163
Birth length and weight in congenital adrenal hyperplasia according to the different phenotypes. 160
Comment on "complete androgen insensitivity syndrome: optimizing diagnosis and management" 157
Autosomal dominant pseudohypoaldosteronism type 1 (PHA1) in the Italian population: functional characterization of two novel hMR (NR3C2) gene mutations and frequency and function of three gene SNPs 156
Relationships between ghrelin, hypothalamic-pituitary-adrenal- and GH/IGF1 axes in patients treated for congenital adrenal hyperplasia 155
Final height and Pubertal development in congenital hypothyroidism before and after neonatal screening programs. 155
A genetic epidemiology study of congenital adrenal hyperplasia in Italy 155
High Variability of Sexual Ambiguity and Clinical Expression in two Patients with a 46,XY del(9p) Kariotype 153
Identification of rare alleles in an Italian population of 284 patients with 21- hydroxylase deficiency by complete sequencing of the CYP21 gene 153
Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations 153
Alterazioni endocrino metaboliche nell’obesità dell’età evolutiva. 150
X-linked hypophosphatemic rickets: An Italian experts' opinion survey 150
A molecular analysis of candidate genes for hypospadias in Italian subjects 149
Changes over time in sex assignment for disorders of sex development 148
Bone Mineral Density in Women Living with Complete Androgen Insensitivity Syndrome and Intact Testes or Removed Gonads. 146
Autosomal dominant pseudohypoaldosteronism type 1 (PHA1) in the Italian population: functional characterization of two novel hMR (NR3C2) gene mutations and frequency and function of three NR3C2 gene SNPs 145
Functional analysis of two recurrent amino acid substitutions in the CYP21 gene from Italian patients with congenital adrenal hyperplasia. 143
A new case of familial mutation in the SRY gene implicated in the pure gonadal dysgenesis in two sisters and their unaffected father 142
Gene dosage imbalances in patients with 46,XY gonadal DSD detected by an in-house-designed synthetic probe set for multiplex ligation-dependent probe amplification analysis. 141
Impact of molecular genetics on congenital adrenal hyperplasia management. 141
17beta-Hydroxysteroid dehydrogenase-3 deficiency: from pregnancy to adolescence 141
Tre nuove variazioni di sequenza nel gene dell’AMH in un paziente con sindrome da persistenza dei dotti di Muller. 140
CYP11B1 gene analysis in 3 Italian patients: identification of a new mutation. 140
Studio della funzionalità polmonare nel bambino obeso. 140
High prevalence of precocious puberty and obesity in childhood narcolepsy with cataplexy. 140
Two Moroccan Sisters Presenting with a Severe Salt-Wasting Form of Congenital Adrenal Hyperplasia but Normal Female Genitalia 139
Futuro endocrino a lungo termine nella pubertà precoce centrale trattata e non trattata (PPC). 138
Improving the diagnosis of 11β-hydroxylase deficiency using home-made MLPA probes: identification of a novel chimeric CYP11B2/CYP11B1 gene in a Sicilian patient 136
Journal of Endocrinological Investigation 135
Hirsutism and virilization 135
Birth length and weight in congenital adrenal hyperplasia according to the different phenotype. 133
SRD5A2 gene analysis in an Italian population of under-masculinized 46,XY subjects. 133
Insulin resistance is a risk factor for high blood pressure regardless of body size and fat distribution in obese children. 131
Reproductive outcome in patients treated and not treated for idiopathic early puberty: long-term results of a randomized trial in adults. 131
Obesity in children and adolescents: an increasing metabolic problem. 130
Behavioural and emotional aspects in obese children. 129
Molecular and phenotypical characterization of 10 families with 11ß-hydroxylase deficiency 129
Quality of Life and Psychological Adjustment of Women Living with 46,XY Differences of Sex Development 128
A sequence variation in 3’UTR of CYP21A2 gene correlates with a mild form of congenital adrenal hyperplasia. 128
Rare diseases research and practice 127
Altri agenti farmacologici 126
Functional characterization of naturally occurring NR3C2 gene mutations in Italian patients suffering from pseudohypoaldosteronism type 1 126
Due casi falsi negativi con forma classica allo screening neonatale per la sindrome adreno-genitale congenita della Regione Emilia-Romagna (1980-83, 1991-2003). 126
Transient 21-OHase deficiency in newborns suspected for CAH: May hydrocortisone treatment be beneficial or is simply inappropriate? 125
CYP21 genotype, adult height, and pubertal development in 55 patients treated for 21-hydroxylase deficiency. 125
Triglycerides-to-HDL cholesterol ratio as screening tool for impaired glucose tolerance in obese children and adolescents 124
Auxological and endocrine findings in narcolepsy type 1: seventeen-year follow-up from a pediatric endocrinology center 122
SRD5A2 gene analysis in Italian patients with male pseudohermaphroditism. 119
Height outcome and pubertal development in CYP21 genotyped CAH male patients 119
Obesità infantile: organizzazione dell'assistenza ospedaliera. 117
Two novel GnRHR gene mutations in two siblings with hypogonadotropic hypogonadism. Eur J Endocrinol 114
Prevalence of pathogenetic MC4R mutations in Italian children with early onset obesity, tall stature and familial history of obesity. 113
PREDEX - Prenatal assessment and treatment of Congenital Adrenal Hyperplasia with Dexamethasone - A longitudinal Study of outcome measures for mother and child 113
Three new sequence variations of the AMH gene in an Italian patient with persistent Mullerian duct syndrome. 111
Sindrome adreno-genitale congenita da deficit di 21-idrossilasi 110
Valutazione clinica del soggetto sovrappeso e dell'obeso 110
Insufficienza cortico-surrenalica in età pediatrica 109
Clinical Management of CAH 108
Novel associations in disorders of sex development: findings from the I-DSD Registry 108
Three Novel AMHGene Mutations in a Patient with Persistent Mullerian Duct Syndrome and Normal AMH Serum Dosage. 108
Genotyping Patients with Differences of Sex Development: 25 Years of Investigation of an Italian Population of 308 Cases (194 46,XY and 114 46,XX) 108
Newborn screening importance in detection of asymptomatic forms of epimerase deficiency galactosemia (EDG) 102
Analisi dei geni dell’asse melanocortinico in bambini con obesità ad esordio precoce: risultati preliminari di uno studio multicentrico. 101
Preliminary data on the Italian experience of the prenatal diagnosis and treatment of 21-hydroxylase deficiency. 100
Evaluation of GH-IGF-1 axis in PHP1a children and adolescents. 100
Melanocortin-4-receptor molecular screening in a group of phenotypically selected obese children: report of two new mutations and lack of association to the early onset of the disease 100
Increased large artery intima media thickness in adolescents with either classical or non-classical congenital adrenal hyperplasia 99
Endocrinopatie 95
Emotion recognition and expression in young obese partecipants: preliminary study 95
Definizione di "sovrappeso" ed "obesità" in età evolutiva 94
Valutazione dell'adiposità 94
Non classical CAH: molecular evaluation of 287 subjects from northern and southern Italy with comparison between genetical and hormonal results. 94
Misurazioni come indicatori del follow up 91
Dati preliminari sull’esperienza Italiana di diagnosi e terapia prenatale nel deficit di 21-idrossilasi. 91
Trattamento dell’ipogonadismo in età evolutiva: indagine conoscitiva SIEDP. 88
Gonadal dysgenesis and XY sex reversal in one patient with a deletion of the distal short arm of chromosome 9 (9p). 88
Disorders of sexual development: new definitions and specific recommendations regarding gender assignment in 17 beta-hydroxysteroid dehydrogenase type 3 deficiency 84
Totale 16.668
Salva come PNG Salva come JPEG
Categoria #
all - tutte 39.530
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 39.530
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211.143 0 0 0 0 0 146 77 130 124 125 105 436
2021/20222.143 235 109 128 201 181 160 61 133 90 71 386 388
2022/20232.273 213 335 127 268 148 169 68 133 382 54 231 145
2023/20241.106 53 112 109 127 94 96 84 111 54 83 90 93
2024/20252.713 160 449 193 251 380 159 174 114 68 148 111 506
2025/20263.355 864 615 543 492 552 289 0 0 0 0 0 0
Totale 17.381