CRIS Current Research Information System

BALSAMO, ANTONIO
 Distribuzione geografica
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Continente #
EU - Europa 6.405
NA - Nord America 4.485
AS - Asia 1.872
AF - Africa 290
OC - Oceania 17
SA - Sud America 14
Continente sconosciuto - Info sul continente non disponibili 1
Totale 13.084
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Nazione #
US - Stati Uniti d'America 4.451
IT - Italia 2.592
GB - Regno Unito 1.225
DE - Germania 624
CN - Cina 619
UA - Ucraina 547
SG - Singapore 500
SE - Svezia 444
VN - Vietnam 392
RU - Federazione Russa 258
FR - Francia 224
IN - India 224
IE - Irlanda 155
ZA - Sudafrica 90
EE - Estonia 68
TG - Togo 60
CH - Svizzera 56
CI - Costa d'Avorio 56
NG - Nigeria 42
FI - Finlandia 38
NL - Olanda 38
SC - Seychelles 36
JO - Giordania 32
JP - Giappone 31
CA - Canada 29
BG - Bulgaria 25
BE - Belgio 23
PL - Polonia 19
GR - Grecia 18
IL - Israele 17
AU - Australia 16
HK - Hong Kong 12
RO - Romania 11
AT - Austria 10
IR - Iran 9
ES - Italia 8
EG - Egitto 6
CL - Cile 5
LT - Lituania 5
TR - Turchia 5
TW - Taiwan 5
AE - Emirati Arabi Uniti 4
BR - Brasile 4
LB - Libano 4
PK - Pakistan 4
TH - Thailandia 4
AL - Albania 3
MD - Moldavia 3
PH - Filippine 3
AR - Argentina 2
CO - Colombia 2
DK - Danimarca 2
ID - Indonesia 2
LU - Lussemburgo 2
MX - Messico 2
RS - Serbia 2
A2 - ???statistics.table.value.countryCode.A2??? 1
BA - Bosnia-Erzegovina 1
BD - Bangladesh 1
BZ - Belize 1
CR - Costa Rica 1
CZ - Repubblica Ceca 1
HN - Honduras 1
IQ - Iraq 1
KZ - Kazakistan 1
ME - Montenegro 1
NO - Norvegia 1
NZ - Nuova Zelanda 1
PE - Perù 1
PT - Portogallo 1
SA - Arabia Saudita 1
UZ - Uzbekistan 1
Totale 13.084
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Città #
Southend 1.080
Singapore 433
Chandler 383
Fairfield 371
Jacksonville 336
Ashburn 290
Princeton 238
Santa Clara 226
Wilmington 216
Dong Ket 209
Milan 200
Houston 197
Woodbridge 183
Ann Arbor 169
Rome 158
Dublin 147
Seattle 145
Cambridge 134
Boardman 118
Padova 112
Westminster 109
Nanjing 102
Berlin 90
Bologna 82
Turin 81
Naples 79
Saint Petersburg 71
Medford 69
Lomé 60
Abidjan 56
Mülheim 53
Shenyang 44
Abeokuta 41
Redwood City 39
Beijing 38
Nanchang 36
Mahé 35
Palermo 34
Tianjin 34
Verona 34
Falls Church 33
Jinan 33
Amman 32
Florence 31
Helsinki 31
Changsha 29
Bari 28
Dallas 28
Tokyo 28
Bern 26
Hebei 26
San Diego 24
Sofia 24
Bremen 23
Catania 22
Dearborn 21
Brussels 19
Redmond 19
Genoa 18
Salerno 18
Norwalk 17
Parma 17
Jiaxing 16
Perugia 16
Falkenstein 15
Guangzhou 15
Modena 15
Zhengzhou 15
Salt Lake City 14
Frankfurt am Main 13
Los Angeles 13
Olalla 13
Shanghai 13
Taizhou 12
Andover 11
Athens 11
Bergamo 11
Chicago 11
Mountain View 11
Napoli 11
Ningbo 11
Phoenix 11
Pisa 11
Tacoma 11
Hong Kong 10
New York 10
Cagliari 9
Des Moines 9
Haikou 9
Imola 9
Ravenna 9
Brookhaven 8
Caserta 8
Chennai 8
Dortmund 8
Fuzhou 8
Kansas City 8
Rishon LeTsiyyon 8
Toronto 8
Trento 8
Totale 7.496
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Nome #
Terapia e follow-up dell’iperplasia surrenale congenita 1.166
I deficit congeniti della steroidogenesi 918
CYP21A2 AND CYP11B1: FIRST REPORT OF A DIGENIC INHERITANCE IN CAH. 420
Nuove acquisizioni sulla genetica dell’ipogonadismo ipogonadotropo. 304
Screening e diagnosi dell’iperplasia surrenale congenita: dalle vecchie alle nuove tecnologie. 212
Severe obesity and cardiometabolic risk in children: comparison from two international classification systems. 207
A new DAX1 gene mutation associated with congenital adrenal hypoplasia and hypogonadotropic hypogonadism 192
Tra obesità e percentili 156
A new case of familial mutation in the SRY gene implicated in the pure gonadal dysgenesis in two sisters and in their unaffected father 154
A sequence variation in 3’UTR of CYP21A2 gene correlates with a mild form of Congenital Adrenal Hyperplasia 152
Characterization of deletions at 9p affecting the candidate regions for sex reversal and deletion 9p syndrome by MLPA. 140
Effect on adult height of pubertal growth hormone retesting and withdrawal of therapy in patients with previously diagnosed growth hormone deficiency. 138
Italian cross-sectional growth charts for height, weight and BMI (2 to 20 yr). 137
Functional studies of two novel and two rare mutations in the 21-hydroxylase gene. 135
Comparison between Liquid and Tablet Formulations of Levothyroxine in the Initial Treatment of Congenital Hypothyroidism 135
A molecular analysis of candidate genes for hypospadias in Italian subjects 134
Disorders of sexual development 133
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. 132
Birth length and weight in congenital adrenal hyperplasia according to the different phenotypes. 132
A molecular analysis of candidate genes for hypospadias in Italian subjects 132
Obesità essenziale: diagnosi 132
Alterazioni endocrino metaboliche nell’obesità dell’età evolutiva. 131
Comment on "complete androgen insensitivity syndrome: optimizing diagnosis and management" 131
46, XX DSD due to androgen excess in monogenic disorders of steroidogenesis: Genetic, biochemical, and clinical features 131
A genetic epidemiology study of congenital adrenal hyperplasia in Italy 126
Metabolic Aspects of Patients Followed for Severe Obesity 123
Bone Mineral Density in Women Living with Complete Androgen Insensitivity Syndrome and Intact Testes or Removed Gonads. 122
Congenital adrenal hyperplasia due to 11-beta-hydroxylase deficiency: functional consequences of four CYP11B1 mutations 120
Changes over time in sex assignment for disorders of sex development 119
A new case of familial mutation in the SRY gene implicated in the pure gonadal dysgenesis in two sisters and their unaffected father 117
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 117
Reproductive outcome in patients treated and not treated for idiopathic early puberty: long-term results of a randomized trial in adults. 117
Studio della funzionalità polmonare nel bambino obeso. 116
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. 116
Le complicanze metaboliche dell'obesità in età evolutiva 115
High prevalence of precocious puberty and obesity in childhood narcolepsy with cataplexy. 115
Final height and Pubertal development in congenital hypothyroidism before and after neonatal screening programs. 112
Two Moroccan Sisters Presenting with a Severe Salt-Wasting Form of Congenital Adrenal Hyperplasia but Normal Female Genitalia 112
17beta-Hydroxysteroid dehydrogenase-3 deficiency: from pregnancy to adolescence 110
Relationships between ghrelin, hypothalamic-pituitary-adrenal- and GH/IGF1 axes in patients treated for congenital adrenal hyperplasia 109
Impact of molecular genetics on congenital adrenal hyperplasia management. 108
Identification of rare alleles in an Italian population of 284 patients with 21- hydroxylase deficiency by complete sequencing of the CYP21 gene 107
High Variability of Sexual Ambiguity and Clinical Expression in two Patients with a 46,XY del(9p) Kariotype 106
Due casi falsi negativi con forma classica allo screening neonatale per la sindrome adreno-genitale congenita della Regione Emilia-Romagna (1980-83, 1991-2003). 106
Behavioural and emotional aspects in obese children. 105
Birth length and weight in congenital adrenal hyperplasia according to the different phenotype. 105
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 103
Rare diseases research and practice 103
SRD5A2 gene analysis in an Italian population of under-masculinized 46,XY subjects. 103
Functional characterization of naturally occurring NR3C2 gene mutations in Italian patients suffering from pseudohypoaldosteronism type 1 102
Functional analysis of two recurrent amino acid substitutions in the CYP21 gene from Italian patients with congenital adrenal hyperplasia. 102
Insulin resistance is a risk factor for high blood pressure regardless of body size and fat distribution in obese children. 102
Altri agenti farmacologici 100
Prevalence of pathogenetic MC4R mutations in Italian children with early onset obesity, tall stature and familial history of obesity. 100
CYP11B1 gene analysis in 3 Italian patients: identification of a new mutation. 99
Hirsutism and virilization 98
Molecular and phenotypical characterization of 10 families with 11ß-hydroxylase deficiency 98
CYP21 genotype, adult height, and pubertal development in 55 patients treated for 21-hydroxylase deficiency. 98
Futuro endocrino a lungo termine nella pubertà precoce centrale trattata e non trattata (PPC). 97
Improving the diagnosis of 11β-hydroxylase deficiency using home-made MLPA probes: identification of a novel chimeric CYP11B2/CYP11B1 gene in a Sicilian patient 97
Obesità infantile: organizzazione dell'assistenza ospedaliera. 96
Quality of Life and Psychological Adjustment of Women Living with 46,XY Differences of Sex Development 96
Transient 21-OHase deficiency in newborns suspected for CAH: May hydrocortisone treatment be beneficial or is simply inappropriate? 95
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 94
Tre nuove variazioni di sequenza nel gene dell’AMH in un paziente con sindrome da persistenza dei dotti di Muller. 92
Obesity in children and adolescents: an increasing metabolic problem. 91
Valutazione clinica del soggetto sovrappeso e dell'obeso 90
Journal of Endocrinological Investigation 89
Analisi dei geni dell’asse melanocortinico in bambini con obesità ad esordio precoce: risultati preliminari di uno studio multicentrico. 89
Clinical Management of CAH 86
A sequence variation in 3’UTR of CYP21A2 gene correlates with a mild form of congenital adrenal hyperplasia. 86
Triglycerides-to-HDL cholesterol ratio as screening tool for impaired glucose tolerance in obese children and adolescents 86
Height outcome and pubertal development in CYP21 genotyped CAH male patients 86
SRD5A2 gene analysis in Italian patients with male pseudohermaphroditism. 85
Two novel GnRHR gene mutations in two siblings with hypogonadotropic hypogonadism. Eur J Endocrinol 85
Novel associations in disorders of sex development: findings from the I-DSD Registry 83
PREDEX - Prenatal assessment and treatment of Congenital Adrenal Hyperplasia with Dexamethasone - A longitudinal Study of outcome measures for mother and child 81
Three new sequence variations of the AMH gene in an Italian patient with persistent Mullerian duct syndrome. 79
Emotion recognition and expression in young obese partecipants: preliminary study 79
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) 79
Insufficienza cortico-surrenalica in età pediatrica 76
Sindrome adreno-genitale congenita da deficit di 21-idrossilasi 74
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 74
Newborn screening importance in detection of asymptomatic forms of epimerase deficiency galactosemia (EDG) 74
Trattamento dell’ipogonadismo in età evolutiva: indagine conoscitiva SIEDP. 73
Three Novel AMHGene Mutations in a Patient with Persistent Mullerian Duct Syndrome and Normal AMH Serum Dosage. 73
Evaluation of GH-IGF-1 axis in PHP1a children and adolescents. 72
Gonadal dysgenesis and XY sex reversal in one patient with a deletion of the distal short arm of chromosome 9 (9p). 72
X-linked hypophosphatemic rickets: An Italian experts' opinion survey 71
Valutazione dell'adiposità 70
Preliminary data on the Italian experience of the prenatal diagnosis and treatment of 21-hydroxylase deficiency. 68
Definizione di "sovrappeso" ed "obesità" in età evolutiva 67
Non classical CAH: molecular evaluation of 287 subjects from northern and southern Italy with comparison between genetical and hormonal results. 66
Endocrinopatie 65
Misurazioni come indicatori del follow up 65
I deficit enzimatici surrenalici ad insorgenza tardiva 65
GH secretion in a cohort of children with pseudohypoparathyroidism type Ia. 65
Increased large artery intima media thickness in adolescents with either classical or non-classical congenital adrenal hyperplasia 65
Dati preliminari sull’esperienza Italiana di diagnosi e terapia prenatale nel deficit di 21-idrossilasi. 63
Disorders of sexual development: new definitions and specific recommendations regarding gender assignment in 17 beta-hydroxysteroid dehydrogenase type 3 deficiency 62
Totale 12.786
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Categoria #
all - tutte 29.326
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 29.326
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020439 0 0 0 0 0 0 0 0 0 184 74 181
2020/20212.051 339 144 172 154 99 146 77 130 124 125 105 436
2021/20222.143 235 109 128 201 181 160 61 133 90 71 386 388
2022/20232.283 215 335 127 270 149 169 68 133 384 55 232 146
2023/20241.110 53 113 110 128 94 96 85 111 54 83 90 93
2024/20251.964 160 451 195 251 383 160 175 114 68 7 0 0
Totale 13.291