CRIS Current Research Information System

BALSAMO, ANTONIO
 Distribuzione geografica
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Continente #
EU - Europa 7.357
NA - Nord America 6.601
AS - Asia 5.963
SA - Sud America 364
AF - Africa 353
OC - Oceania 17
Continente sconosciuto - Info sul continente non disponibili 2
Totale 20.657
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Nazione #
US - Stati Uniti d'America 6.490
IT - Italia 3.045
VN - Vietnam 1.967
SG - Singapore 1.387
CN - Cina 1.362
GB - Regno Unito 1.266
DE - Germania 701
UA - Ucraina 555
SE - Svezia 449
FR - Francia 384
HK - Hong Kong 372
IN - India 275
RU - Federazione Russa 275
BR - Brasile 267
IE - Irlanda 162
JP - Giappone 140
NL - Olanda 130
ZA - Sudafrica 106
KR - Corea 100
BD - Bangladesh 83
FI - Finlandia 74
CI - Costa d'Avorio 70
EE - Estonia 68
CA - Canada 60
CH - Svizzera 60
TG - Togo 60
NG - Nigeria 42
AR - Argentina 37
SC - Seychelles 37
PH - Filippine 36
TH - Thailandia 35
JO - Giordania 33
PL - Polonia 28
BE - Belgio 27
BG - Bulgaria 26
MX - Messico 25
TR - Turchia 24
TW - Taiwan 24
GR - Grecia 21
AT - Austria 20
IQ - Iraq 19
IL - Israele 18
ID - Indonesia 17
AU - Australia 16
PK - Pakistan 15
CO - Colombia 14
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
PE - Perù 8
AE - Emirati Arabi Uniti 7
AL - Albania 7
JM - Giamaica 6
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
OM - Oman 3
SK - Slovacchia (Repubblica Slovacca) 3
BB - Barbados 2
DK - Danimarca 2
DZ - Algeria 2
ET - Etiopia 2
KW - Kuwait 2
LU - Lussemburgo 2
LV - Lettonia 2
NI - Nicaragua 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
AO - Angola 1
BA - Bosnia-Erzegovina 1
BH - Bahrain 1
BO - Bolivia 1
BZ - Belize 1
CZ - Repubblica Ceca 1
DJ - Gibuti 1
GT - Guatemala 1
HR - Croazia 1
KG - Kirghizistan 1
KH - Cambogia 1
KM - Comore 1
Totale 20.649
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Città #
Southend 1.080
Singapore 926
Ashburn 586
San Jose 528
Ho Chi Minh City 495
Chandler 383
Hanoi 383
Fairfield 371
Hong Kong 351
Jacksonville 337
Hefei 268
Milan 239
Santa Clara 237
Princeton 236
Wilmington 218
Dong Ket 209
Houston 204
Rome 184
Woodbridge 184
Ann Arbor 169
Dublin 153
Seattle 150
Beijing 139
Cambridge 134
Tokyo 130
Lauterbourg 123
Boardman 121
Council Bluffs 113
Padova 112
Westminster 109
Nanjing 104
Bologna 103
Los Angeles 100
Naples 93
Berlin 91
Seoul 85
Turin 85
Dallas 73
Da Nang 72
Saint Petersburg 71
Abidjan 70
Medford 69
New York 62
Haiphong 61
Buffalo 60
Lomé 60
Helsinki 55
Mülheim 53
São Paulo 48
Shenyang 47
Bari 45
Palermo 42
Abeokuta 40
Redwood City 39
Munich 38
Tianjin 38
Florence 37
Nanchang 37
Changsha 36
Jinan 36
Mahé 35
Verona 35
Amman 33
Falls Church 33
Frankfurt am Main 32
Guangzhou 32
Bern 26
Catania 26
Hebei 26
Atlanta 25
Can Tho 25
Redondo Beach 25
Sofia 25
San Diego 24
Shanghai 24
Bremen 23
Brussels 23
San Francisco 23
Bengaluru 21
Biên Hòa 21
Dearborn 21
London 21
Genoa 20
Hải Dương 20
Salerno 20
Redmond 19
Toronto 19
Chicago 18
Modena 18
Parma 18
Phoenix 18
Norwalk 17
Perugia 17
Zhengzhou 17
Jiaxing 16
Quận Bình Thạnh 16
Salt Lake City 16
Bangkok 15
Brooklyn 15
Falkenstein 15
Totale 11.615
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Nome #
Terapia e follow-up dell’iperplasia surrenale congenita 1.318
I deficit congeniti della steroidogenesi 1.174
Italian cross-sectional growth charts for height, weight and BMI (2 to 20 yr). 770
CYP21A2 AND CYP11B1: FIRST REPORT OF A DIGENIC INHERITANCE IN CAH. 515
A new case of familial mutation in the SRY gene implicated in the pure gonadal dysgenesis in two sisters and in their unaffected father 403
Nuove acquisizioni sulla genetica dell’ipogonadismo ipogonadotropo. 388
Screening e diagnosi dell’iperplasia surrenale congenita: dalle vecchie alle nuove tecnologie. 317
The role of 21-hydroxylase in the pathogenesis of adrenal masses: Review of the literature and focus on our own experience. 273
Disorders of sexual development 267
A sequence variation in 3’UTR of CYP21A2 gene correlates with a mild form of Congenital Adrenal Hyperplasia 261
A new DAX1 gene mutation associated with congenital adrenal hypoplasia and hypogonadotropic hypogonadism 260
Severe obesity and cardiometabolic risk in children: comparison from two international classification systems. 248
Impact of molecular genetics on congenital adrenal hyperplasia management. 237
Tra obesità e percentili 234
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. 231
Functional studies of two novel and two rare mutations in the 21-hydroxylase gene. 212
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 210
Effect on adult height of pubertal growth hormone retesting and withdrawal of therapy in patients with previously diagnosed growth hormone deficiency. 209
46, XX DSD due to androgen excess in monogenic disorders of steroidogenesis: Genetic, biochemical, and clinical features 209
Characterization of deletions at 9p affecting the candidate regions for sex reversal and deletion 9p syndrome by MLPA. 207
Comparison between Liquid and Tablet Formulations of Levothyroxine in the Initial Treatment of Congenital Hypothyroidism 203
Obesità essenziale: diagnosi 199
Relationships between ghrelin, hypothalamic-pituitary-adrenal- and GH/IGF1 axes in patients treated for congenital adrenal hyperplasia 196
A molecular analysis of candidate genes for hypospadias in Italian subjects 193
Le complicanze metaboliche dell'obesità in età evolutiva 192
Metabolic Aspects of Patients Followed for Severe Obesity 190
Identification of rare alleles in an Italian population of 284 patients with 21- hydroxylase deficiency by complete sequencing of the CYP21 gene 188
A genetic epidemiology study of congenital adrenal hyperplasia in Italy 185
High Variability of Sexual Ambiguity and Clinical Expression in two Patients with a 46,XY del(9p) Kariotype 183
X-linked hypophosphatemic rickets: An Italian experts' opinion survey 182
A new case of familial mutation in the SRY gene implicated in the pure gonadal dysgenesis in two sisters and their unaffected father 181
Comment on "complete androgen insensitivity syndrome: optimizing diagnosis and management" 181
Changes over time in sex assignment for disorders of sex development 181
Final height and Pubertal development in congenital hypothyroidism before and after neonatal screening programs. 180
Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations 179
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 179
Alterazioni endocrino metaboliche nell’obesità dell’età evolutiva. 178
Two Moroccan Sisters Presenting with a Severe Salt-Wasting Form of Congenital Adrenal Hyperplasia but Normal Female Genitalia 176
Birth length and weight in congenital adrenal hyperplasia according to the different phenotypes. 173
Bone Mineral Density in Women Living with Complete Androgen Insensitivity Syndrome and Intact Testes or Removed Gonads. 173
Functional analysis of two recurrent amino acid substitutions in the CYP21 gene from Italian patients with congenital adrenal hyperplasia. 171
High prevalence of precocious puberty and obesity in childhood narcolepsy with cataplexy. 168
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. 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 165
17beta-Hydroxysteroid dehydrogenase-3 deficiency: from pregnancy to adolescence 165
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 164
SRD5A2 gene analysis in an Italian population of under-masculinized 46,XY subjects. 164
CYP11B1 gene analysis in 3 Italian patients: identification of a new mutation. 162
Auxological and endocrine findings in narcolepsy type 1: seventeen-year follow-up from a pediatric endocrinology center 161
Rare diseases research and practice 160
Tre nuove variazioni di sequenza nel gene dell’AMH in un paziente con sindrome da persistenza dei dotti di Muller. 159
Futuro endocrino a lungo termine nella pubertà precoce centrale trattata e non trattata (PPC). 159
Studio della funzionalità polmonare nel bambino obeso. 159
A molecular analysis of candidate genes for hypospadias in Italian subjects 158
A sequence variation in 3’UTR of CYP21A2 gene correlates with a mild form of congenital adrenal hyperplasia. 158
Quality of Life and Psychological Adjustment of Women Living with 46,XY Differences of Sex Development 157
Hirsutism and virilization 155
Insulin resistance is a risk factor for high blood pressure regardless of body size and fat distribution in obese children. 153
Obesity in children and adolescents: an increasing metabolic problem. 152
Triglycerides-to-HDL cholesterol ratio as screening tool for impaired glucose tolerance in obese children and adolescents 152
Birth length and weight in congenital adrenal hyperplasia according to the different phenotype. 150
Transient 21-OHase deficiency in newborns suspected for CAH: May hydrocortisone treatment be beneficial or is simply inappropriate? 148
Behavioural and emotional aspects in obese children. 147
Journal of Endocrinological Investigation 147
Molecular and phenotypical characterization of 10 families with 11ß-hydroxylase deficiency 147
Functional characterization of naturally occurring NR3C2 gene mutations in Italian patients suffering from pseudohypoaldosteronism type 1 146
Due casi falsi negativi con forma classica allo screening neonatale per la sindrome adreno-genitale congenita della Regione Emilia-Romagna (1980-83, 1991-2003). 146
Novel associations in disorders of sex development: findings from the I-DSD Registry 145
CYP21 genotype, adult height, and pubertal development in 55 patients treated for 21-hydroxylase deficiency. 145
Height outcome and pubertal development in CYP21 genotyped CAH male patients 144
Reproductive outcome in patients treated and not treated for idiopathic early puberty: long-term results of a randomized trial in adults. 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) 142
Valutazione clinica del soggetto sovrappeso e dell'obeso 141
Altri agenti farmacologici 140
Obesità infantile: organizzazione dell'assistenza ospedaliera. 140
PREDEX - Prenatal assessment and treatment of Congenital Adrenal Hyperplasia with Dexamethasone - A longitudinal Study of outcome measures for mother and child 140
SRD5A2 gene analysis in Italian patients with male pseudohermaphroditism. 137
Prevalence of pathogenetic MC4R mutations in Italian children with early onset obesity, tall stature and familial history of obesity. 136
Increased large artery intima media thickness in adolescents with either classical or non-classical congenital adrenal hyperplasia 134
Three new sequence variations of the AMH gene in an Italian patient with persistent Mullerian duct syndrome. 133
Two novel GnRHR gene mutations in two siblings with hypogonadotropic hypogonadism. Eur J Endocrinol 130
Three Novel AMHGene Mutations in a Patient with Persistent Mullerian Duct Syndrome and Normal AMH Serum Dosage. 128
Newborn screening importance in detection of asymptomatic forms of epimerase deficiency galactosemia (EDG) 127
Insufficienza cortico-surrenalica in età pediatrica 125
Clinical Management of CAH 124
Sindrome adreno-genitale congenita da deficit di 21-idrossilasi 123
Evaluation of GH-IGF-1 axis in PHP1a children and adolescents. 120
Analisi dei geni dell’asse melanocortinico in bambini con obesità ad esordio precoce: risultati preliminari di uno studio multicentrico. 118
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 117
Preliminary data on the Italian experience of the prenatal diagnosis and treatment of 21-hydroxylase deficiency. 114
Emotion recognition and expression in young obese partecipants: preliminary study 113
Non classical CAH: molecular evaluation of 287 subjects from northern and southern Italy with comparison between genetical and hormonal results. 112
Endocrinopatie 110
Valutazione dell'adiposità 109
Dati preliminari sull’esperienza Italiana di diagnosi e terapia prenatale nel deficit di 21-idrossilasi. 108
Definizione di "sovrappeso" ed "obesità" in età evolutiva 106
Misurazioni come indicatori del follow up 104
Disorders of sexual development: new definitions and specific recommendations regarding gender assignment in 17 beta-hydroxysteroid dehydrogenase type 3 deficiency 104
Gonadal dysgenesis and XY sex reversal in one patient with a deletion of the distal short arm of chromosome 9 (9p). 103
Trattamento dell’ipogonadismo in età evolutiva: indagine conoscitiva SIEDP. 100
Totale 19.991
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Categoria #
all - tutte 46.058
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 46.058
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021436 0 0 0 0 0 0 0 0 0 0 0 436
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
2025/20266.866 864 615 543 492 552 299 574 438 1.033 408 248 800
Totale 20.892