CRIS Current Research Information System

BALSAMO, ANTONIO
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
EU - Europa 7.453
NA - Nord America 7.368
AS - Asia 6.001
SA - Sud America 368
AF - Africa 353
Continente sconosciuto - Info sul continente non disponibili 237
OC - Oceania 21
Totale 21.801
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 7.235
IT - Italia 3.135
VN - Vietnam 1.967
SG - Singapore 1.397
CN - Cina 1.366
GB - Regno Unito 1.268
DE - Germania 702
UA - Ucraina 555
SE - Svezia 449
FR - Francia 384
HK - Hong Kong 376
IN - India 276
RU - Federazione Russa 275
BR - Brasile 269
IE - Irlanda 163
JP - Giappone 140
NL - Olanda 131
ZA - Sudafrica 106
BD - Bangladesh 100
KR - Corea 100
FI - Finlandia 74
CA - Canada 70
CI - Costa d'Avorio 70
EE - Estonia 68
CH - Svizzera 60
TG - Togo 60
NG - Nigeria 42
AR - Argentina 38
SC - Seychelles 37
PH - Filippine 36
TH - Thailandia 35
JO - Giordania 33
MX - Messico 28
PL - Polonia 28
BE - Belgio 27
BG - Bulgaria 26
TR - Turchia 24
TW - Taiwan 24
GR - Grecia 22
AT - Austria 20
AU - Australia 20
IL - Israele 19
IQ - Iraq 19
ID - Indonesia 18
CO - Colombia 15
PK - Pakistan 15
ES - Italia 14
RO - Romania 13
EC - Ecuador 12
CL - Cile 11
EG - Egitto 11
IR - Iran 10
LT - Lituania 9
MA - Marocco 9
MY - Malesia 9
JM - Giamaica 8
PE - Perù 8
AE - Emirati Arabi Uniti 7
AL - Albania 7
PY - Paraguay 6
DO - Repubblica Dominicana 5
HN - Honduras 5
KE - Kenya 5
UZ - Uzbekistan 5
CR - Costa Rica 4
LB - Libano 4
MD - Moldavia 4
SA - Arabia Saudita 4
UY - Uruguay 4
VE - Venezuela 4
GH - Ghana 3
KZ - Kazakistan 3
NI - Nicaragua 3
OM - Oman 3
SK - Slovacchia (Repubblica Slovacca) 3
BB - Barbados 2
BS - Bahamas 2
BZ - Belize 2
DK - Danimarca 2
DZ - Algeria 2
ET - Etiopia 2
KW - Kuwait 2
LU - Lussemburgo 2
LV - Lettonia 2
NP - Nepal 2
PS - Palestinian Territory 2
PT - Portogallo 2
RS - Serbia 2
SY - Repubblica araba siriana 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AG - Antigua e Barbuda 1
AO - Angola 1
BA - Bosnia-Erzegovina 1
BH - Bahrain 1
BO - Bolivia 1
CZ - Repubblica Ceca 1
DJ - Gibuti 1
GT - Guatemala 1
HR - Croazia 1
KG - Kirghizistan 1
Totale 21.554
Salva come PNG Salva come JPEG
Città #
Southend 1.080
Singapore 935
Ashburn 603
San Jose 556
Ho Chi Minh City 495
Chandler 383
Hanoi 383
Fairfield 372
Hong Kong 354
Jacksonville 337
Hefei 268
Milan 244
Santa Clara 244
Princeton 237
Wilmington 220
Council Bluffs 214
Dong Ket 209
Houston 206
Rome 189
Woodbridge 184
Ann Arbor 169
Dublin 154
Seattle 152
Beijing 140
Cambridge 134
Tokyo 130
Lauterbourg 123
Boardman 121
Padova 112
Westminster 109
Bologna 106
Los Angeles 106
Nanjing 104
Naples 96
Dallas 92
Berlin 91
Turin 88
Seoul 85
New York 73
Da Nang 72
Saint Petersburg 71
Abidjan 70
Medford 69
Buffalo 61
Haiphong 61
Lomé 60
Helsinki 55
Mülheim 53
São Paulo 48
Shenyang 47
Bari 46
Atlanta 44
Palermo 44
Florence 42
Abeokuta 40
Redwood City 39
Munich 38
Tianjin 38
Nanchang 37
Verona 37
Changsha 36
Jinan 36
Mahé 35
Amman 33
Falls Church 33
Frankfurt am Main 33
Guangzhou 32
Catania 28
Bern 26
Hebei 26
Can Tho 25
Redondo Beach 25
Shanghai 25
Sofia 25
Phoenix 24
San Diego 24
San Francisco 24
Bremen 23
Brussels 23
Chicago 23
Bengaluru 21
Biên Hòa 21
Dearborn 21
London 21
Salerno 21
Genoa 20
Hải Dương 20
Toronto 20
Redmond 19
Modena 18
Parma 18
Norwalk 17
Orem 17
Perugia 17
Zhengzhou 17
Brooklyn 16
Denver 16
Jiaxing 16
Quận Bình Thạnh 16
Salt Lake City 16
Totale 11.897
Salva come PNG Salva come JPEG
Nome #
Terapia e follow-up dell’iperplasia surrenale congenita 1.369
Italian cross-sectional growth charts for height, weight and BMI (2 to 20 yr). 1.283
I deficit congeniti della steroidogenesi 1.225
CYP21A2 AND CYP11B1: FIRST REPORT OF A DIGENIC INHERITANCE IN CAH. 529
A new case of familial mutation in the SRY gene implicated in the pure gonadal dysgenesis in two sisters and in their unaffected father 405
Nuove acquisizioni sulla genetica dell’ipogonadismo ipogonadotropo. 395
Screening e diagnosi dell’iperplasia surrenale congenita: dalle vecchie alle nuove tecnologie. 321
The role of 21-hydroxylase in the pathogenesis of adrenal masses: Review of the literature and focus on our own experience. 275
Disorders of sexual development 269
A sequence variation in 3’UTR of CYP21A2 gene correlates with a mild form of Congenital Adrenal Hyperplasia 264
A new DAX1 gene mutation associated with congenital adrenal hypoplasia and hypogonadotropic hypogonadism 262
Severe obesity and cardiometabolic risk in children: comparison from two international classification systems. 249
Impact of molecular genetics on congenital adrenal hyperplasia management. 239
Tra obesità e percentili 236
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. 233
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 224
Relationships between ghrelin, hypothalamic-pituitary-adrenal- and GH/IGF1 axes in patients treated for congenital adrenal hyperplasia 213
Functional studies of two novel and two rare mutations in the 21-hydroxylase gene. 213
46, XX DSD due to androgen excess in monogenic disorders of steroidogenesis: Genetic, biochemical, and clinical features 210
Effect on adult height of pubertal growth hormone retesting and withdrawal of therapy in patients with previously diagnosed growth hormone deficiency. 209
Characterization of deletions at 9p affecting the candidate regions for sex reversal and deletion 9p syndrome by MLPA. 209
Comparison between Liquid and Tablet Formulations of Levothyroxine in the Initial Treatment of Congenital Hypothyroidism 205
Obesità essenziale: diagnosi 203
Le complicanze metaboliche dell'obesità in età evolutiva 197
A molecular analysis of candidate genes for hypospadias in Italian subjects 195
Metabolic Aspects of Patients Followed for Severe Obesity 193
Identification of rare alleles in an Italian population of 284 patients with 21- hydroxylase deficiency by complete sequencing of the CYP21 gene 193
A genetic epidemiology study of congenital adrenal hyperplasia in Italy 187
High Variability of Sexual Ambiguity and Clinical Expression in two Patients with a 46,XY del(9p) Kariotype 186
X-linked hypophosphatemic rickets: An Italian experts' opinion survey 186
A new case of familial mutation in the SRY gene implicated in the pure gonadal dysgenesis in two sisters and their unaffected father 184
Comment on "complete androgen insensitivity syndrome: optimizing diagnosis and management" 184
Changes over time in sex assignment for disorders of sex development 184
Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations 183
Final height and Pubertal development in congenital hypothyroidism before and after neonatal screening programs. 182
Alterazioni endocrino metaboliche nell’obesità dell’età evolutiva. 182
Two Moroccan Sisters Presenting with a Severe Salt-Wasting Form of Congenital Adrenal Hyperplasia but Normal Female Genitalia 181
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 180
Bone Mineral Density in Women Living with Complete Androgen Insensitivity Syndrome and Intact Testes or Removed Gonads. 177
Birth length and weight in congenital adrenal hyperplasia according to the different phenotypes. 176
Functional analysis of two recurrent amino acid substitutions in the CYP21 gene from Italian patients with congenital adrenal hyperplasia. 172
High prevalence of precocious puberty and obesity in childhood narcolepsy with cataplexy. 172
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. 170
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 167
Improving the diagnosis of 11β-hydroxylase deficiency using home-made MLPA probes: identification of a novel chimeric CYP11B2/CYP11B1 gene in a Sicilian patient 167
SRD5A2 gene analysis in an Italian population of under-masculinized 46,XY subjects. 167
17beta-Hydroxysteroid dehydrogenase-3 deficiency: from pregnancy to adolescence 167
Auxological and endocrine findings in narcolepsy type 1: seventeen-year follow-up from a pediatric endocrinology center 165
CYP11B1 gene analysis in 3 Italian patients: identification of a new mutation. 165
Quality of Life and Psychological Adjustment of Women Living with 46,XY Differences of Sex Development 163
Tre nuove variazioni di sequenza nel gene dell’AMH in un paziente con sindrome da persistenza dei dotti di Muller. 162
Rare diseases research and practice 162
Futuro endocrino a lungo termine nella pubertà precoce centrale trattata e non trattata (PPC). 161
Studio della funzionalità polmonare nel bambino obeso. 161
A sequence variation in 3’UTR of CYP21A2 gene correlates with a mild form of congenital adrenal hyperplasia. 160
A molecular analysis of candidate genes for hypospadias in Italian subjects 159
Hirsutism and virilization 157
Triglycerides-to-HDL cholesterol ratio as screening tool for impaired glucose tolerance in obese children and adolescents 154
Insulin resistance is a risk factor for high blood pressure regardless of body size and fat distribution in obese children. 154
Obesity in children and adolescents: an increasing metabolic problem. 153
Molecular and phenotypical characterization of 10 families with 11ß-hydroxylase deficiency 152
Birth length and weight in congenital adrenal hyperplasia according to the different phenotype. 151
Journal of Endocrinological Investigation 150
Transient 21-OHase deficiency in newborns suspected for CAH: May hydrocortisone treatment be beneficial or is simply inappropriate? 149
Due casi falsi negativi con forma classica allo screening neonatale per la sindrome adreno-genitale congenita della Regione Emilia-Romagna (1980-83, 1991-2003). 149
Behavioural and emotional aspects in obese children. 148
Novel associations in disorders of sex development: findings from the I-DSD Registry 147
Functional characterization of naturally occurring NR3C2 gene mutations in Italian patients suffering from pseudohypoaldosteronism type 1 146
Height outcome and pubertal development in CYP21 genotyped CAH male patients 146
CYP21 genotype, adult height, and pubertal development in 55 patients treated for 21-hydroxylase deficiency. 146
Valutazione clinica del soggetto sovrappeso e dell'obeso 145
Reproductive outcome in patients treated and not treated for idiopathic early puberty: long-term results of a randomized trial in adults. 145
Obesità infantile: organizzazione dell'assistenza ospedaliera. 144
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) 143
PREDEX - Prenatal assessment and treatment of Congenital Adrenal Hyperplasia with Dexamethasone - A longitudinal Study of outcome measures for mother and child 142
Altri agenti farmacologici 141
SRD5A2 gene analysis in Italian patients with male pseudohermaphroditism. 139
Increased large artery intima media thickness in adolescents with either classical or non-classical congenital adrenal hyperplasia 137
Three new sequence variations of the AMH gene in an Italian patient with persistent Mullerian duct syndrome. 136
Prevalence of pathogenetic MC4R mutations in Italian children with early onset obesity, tall stature and familial history of obesity. 136
Two novel GnRHR gene mutations in two siblings with hypogonadotropic hypogonadism. Eur J Endocrinol 132
Insufficienza cortico-surrenalica in età pediatrica 129
Three Novel AMHGene Mutations in a Patient with Persistent Mullerian Duct Syndrome and Normal AMH Serum Dosage. 129
Newborn screening importance in detection of asymptomatic forms of epimerase deficiency galactosemia (EDG) 129
Sindrome adreno-genitale congenita da deficit di 21-idrossilasi 125
Evaluation of GH-IGF-1 axis in PHP1a children and adolescents. 125
Clinical Management of CAH 125
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 122
Analisi dei geni dell’asse melanocortinico in bambini con obesità ad esordio precoce: risultati preliminari di uno studio multicentrico. 120
Preliminary data on the Italian experience of the prenatal diagnosis and treatment of 21-hydroxylase deficiency. 116
Emotion recognition and expression in young obese partecipants: preliminary study 115
Non classical CAH: molecular evaluation of 287 subjects from northern and southern Italy with comparison between genetical and hormonal results. 114
Endocrinopatie 112
Valutazione dell'adiposità 111
Dati preliminari sull’esperienza Italiana di diagnosi e terapia prenatale nel deficit di 21-idrossilasi. 110
Definizione di "sovrappeso" ed "obesità" in età evolutiva 108
Misurazioni come indicatori del follow up 106
Disorders of sexual development: new definitions and specific recommendations regarding gender assignment in 17 beta-hydroxysteroid dehydrogenase type 3 deficiency 106
Gonadal dysgenesis and XY sex reversal in one patient with a deletion of the distal short arm of chromosome 9 (9p). 104
Trattamento dell’ipogonadismo in età evolutiva: indagine conoscitiva SIEDP. 101
Totale 20.879
Salva come PNG Salva come JPEG
Categoria #
all - tutte 48.303
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 48.303
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.908 0 109 128 201 181 160 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
2025/20266.919 864 615 543 492 552 299 574 438 1.033 408 248 853
2026/2027856 617 239 0 0 0 0 0 0 0 0 0 0
Totale 21.801