IRIS
VOTTERO, Alessandra
 Distribuzione geografica
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Continente #
NA - Nord America 2.386
EU - Europa 1.955
AS - Asia 931
Continente sconosciuto - Info sul continente non disponibili 8
AF - Africa 4
OC - Oceania 4
Totale 5.288
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Nazione #
US - Stati Uniti d'America 2.315
CN - Cina 764
UA - Ucraina 428
IE - Irlanda 410
SE - Svezia 361
FI - Finlandia 318
DE - Germania 303
SG - Singapore 77
CA - Canada 70
IT - Italia 58
TR - Turchia 43
IN - India 38
GB - Regno Unito 34
BE - Belgio 14
EU - Europa 8
FR - Francia 8
AT - Austria 6
BG - Bulgaria 4
CI - Costa d'Avorio 4
CZ - Repubblica Ceca 4
IR - Iran 4
JP - Giappone 3
NL - Olanda 3
NZ - Nuova Zelanda 3
AU - Australia 1
BY - Bielorussia 1
ES - Italia 1
HU - Ungheria 1
IL - Israele 1
PA - Panama 1
PK - Pakistan 1
PL - Polonia 1
Totale 5.288
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Città #
Jacksonville 454
Chandler 426
Dublin 410
Dearborn 225
Beijing 201
Nanjing 125
Ashburn 108
San Mateo 99
Bremen 95
Princeton 95
Ann Arbor 72
Toronto 64
New York 63
Shanghai 55
Boardman 45
Kunming 45
Helsinki 40
Izmir 40
Wilmington 39
Hefei 36
Nanchang 36
Shenyang 36
Singapore 35
Hebei 28
Jiaxing 24
Jinan 24
Woodbridge 24
Des Moines 19
Norwalk 18
Leawood 16
Augusta 14
Brussels 14
Guangzhou 13
Parma 13
Tianjin 11
Seattle 10
Changsha 9
Los Angeles 9
Borås 6
Chengdu 6
Ningbo 6
Vienna 6
Hangzhou 5
Monmouth Junction 5
Munich 5
Pune 5
Abidjan 4
Ardabil 4
Auburn Hills 4
Brno 4
Haikou 4
Shaoxing 4
Sofia 4
Torino 4
Auckland 3
Cutrofiano 3
Eastbourne 3
Elmendorf 3
Fremont 3
Kocaeli 3
Milan 3
Zhengzhou 3
Angri 2
Chicago 2
Chongqing 2
Düsseldorf 2
Lanzhou 2
Mestre 2
Mumbai 2
Quzhou 2
Rockville 2
Santa Clara 2
Tokyo 2
Verona 2
Wenzhou 2
Abano Terme 1
Altavilla Silentina 1
Baotou 1
Brampton 1
Brunico 1
Budapest 1
Changchun 1
Dallas 1
Dolianova 1
Edinburgh 1
Enid 1
Forest City 1
Formigine 1
Frankfurt am Main 1
Fuzhou 1
Gandhi Nagar 1
Geislingen an der Steige 1
Grafing 1
Huzhou 1
Laval 1
Madrid 1
Moncton 1
Monteroni D'arbia 1
Panama City 1
Paris 1
Totale 3.241
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Nome #
Altezza finale di bambine affette da pubertà precoce centrale idiopatica trattate con l’analogo del GnRH ed oxandrolone 120
Evidence fo Epigenetic Abnormalities of the Androgen Receptor Gene in Foreskin from Children with Hypospadias 115
Irsutismo e poi.... 81
Adrenal androgens 80
Androgen receptor-mediated hypersensitivity to androgens in women with nonhyperandrogenic hirsutism: skewing of X-chromosome inactivation 79
17 HYDROXYLASE DEFICIENCY IN A 46XY FEMALE WITH HYPERTENSION 78
Androgen receptor gene methylation pattern in normal children and adults, and in premature pubarche patients 75
Spontaneous GH secretion is not directly affected by ghrelin either in short-normal prepubertal children or in children with GH neurosecretory dysfunction 74
A novel mutation in the nr0b1 gene in a family with monozygotic twin sisters and congenital adrenal hypoplasia affected children. 74
A novel dominant negative mutation of the glucocorticoid receptor causing familial glucocorticoid resistance: defective interaction P160 coactivators 72
Absence of functional interaction between p23 and DNA methyltransferase 1 in steroid-stimulated fibroblasts 71
Leptin inhibits steroid biosynthesis by human granulosa-lutein cells 70
Androgen receptor CAG repeats and gene methylation in children with premature pubarche 69
Aromatase is differentially expressed in peripheral blood leukocytes from children, and adult female and male subjects. 69
A novel mutation of the NR0B1 (DAX-1)gene in a family with two monozygotic twin sisters and a congenital adrenal ipoplasia affected child 69
Final height in girls with idiopathic central precocious puberty treated with GnRH analogue and olaxandrolone 66
A clinical assay of the human growth hormone receptor (GHR) isoforms in peripheral blood lymphocytes (PBL) 65
Clinical significance of parental origin of the X chromosome in Turner syndrome (TS) 64
Analisi dei geni dell’asse melanocortinico in bambini con obesità ad esordio precoce: risultati preliminari di uno studio multicentrico 64
Glucocorticoid resistance and hypersensitivity syndromes 64
A novel mutation of the glucocorticoid receptor in familial glucocorticoid resistance 64
Clinical significance of the parental origin of the X chromosome in Turner Syndrome. 64
Relationship of CYP21A2 genotype and serum 17-hydroxyprogesterone and cortisol levels in a large cohort of Italian children with premature pubarche. 64
Glucocorticoid receptor beta: view I 63
Aromatase overexpression 63
Epigenetic abnormalities of the androgen receptor gene in hypospadia 63
In vitro modulation of androgen receptor gene methylation by steroids. 63
Clinical significance of the parental origin of the X chromosome in Turner Syndrome. 62
Cross talk between leptin, cortisol, GH, and TSH 62
Spontaneous growth hormone (GH) secretion is not directly affected by Ghrelin in either short normal prepubertal children or in children with neurosecretory dysfunction 61
Catecholamines in Asymptomatic and symptomatic pseudohypoaldosteronism 61
Una nuova mutazione dominante negativa del recettore per i glucocorticoidi causa la sindrome da resistenza familiare ai glucocorticoidi: difetto nell’interazione con I coattivatori p160 61
A novel, C-terminal dominant negative mutation of the GR causing familial glucocorticoid resistance through abnormal interactions with p160 steroid receptor coactivators 61
Interactions of leptin and thyrotropin 24-hour secretory profiles in short-normal children 61
Inhibitory effect of ghrelin on human ovarian steroidogenesis. 60
Adrenal hyperandrogenism in children 60
The human glucocorticoid receptor (hGR) beta isoform suppresses the transcriptional activity of hGRalpha by interfering with formation of active coactivator complexes 60
Physical activity and hypothalamic-pituitary-gonadal axis (HPG) function 59
P-043 RUOLO E POSSIBILI MECCANISMI DEGLI ENDOCRINE DISRUPTERS NELL'EZIOPATOGENESI DELL'IPOSPADIA 59
The Role of SHOX Gene in Idiopathic Short Stature: an Italian Multicenter Study 58
Glucocorticoid resistance syndromes and states 57
Aromatase overexpression 57
Imbalanced expression of the glucocorticoid receptor isoforms in cultured lymphocytes from a patient with systemic glucocorticoid resistance and chronic lymphocytic leukemia 57
Absence of functional interaction between p23 and DNA methyltransferase 1 in steroid-stimulated fibroblasts. 57
Ginecomastia 56
Studio del numero delle triplette CAG e della metilazione del gene per il recettore degli androgeni in bambine prepuberi, donne e pazienti con pubarca prematuro 56
DNA methyl transferase 3A -448A >G variant in foreskin tissue from children with hypospadia 56
Premature pubarche as epiphenomenon of non-random androgen receptor gene methylation 55
Glucocorticoid resistance and hypersensitivity states 55
The human glucocorticoid receptor (hGR) beta isoform suppresses the transcriptional activity of hGR alpha by interfering with binding of hGR alpha to coactivators molecules through its preserved activation function (AF)-1 54
Corticotropin-releasing hormone is directly affecting human adipose tissue functions 54
Glucocorticoid resistance in inflammatory diseases: no evidence for IL-4 and IL-2 regulation of glucocorticoid receptor RNA splicing to its two major isoforms 53
The human glucocorticoid receptor (GR) beta isoform interacts with coactivators only through its transcriptional activation function (AF) 1 region and suppresses both AF1 and AF2 activities of GR beta 51
Transcriptional and translational regulation of the splicing isoforms of the growth hormone receptor by glucocorticoids 48
Familial autosomal dominant pseudohypoaldosteronism (PHA): alteration in the expression of the glucocorticoid receptor 48
Ghrelin-dependent regulation of estradiol secretion by human granulosa lutein cells. 48
Crescita ed espressione del gene dell’aromatasi 48
Long-term results with growth hormone (GH) therapy in idiopathic hypopituitarism 48
Postreceptor insulin resistance contributes to human dyslipidemia and hepatic steatosis. 48
High constitutive glucocorticoid receptor beta in human neutriphils enables them to reduce their spontaneous rate of cell death in response to glucocorticoids 47
Interactions of leptin and thyrotropin 24-hour secretory profiles in short-normal children. 47
In vitro modulation of androgen receptor gene methylation by steroids. 47
Mitochondrial dysfunction in patients with primary congenital insulin resistance. 47
Patologia della corteccia e della midollare del surrene 47
Leptin, Cortisol and GH Secretion Interactions in Short Normal Prepubertal Children 46
Hormonal regulation of interleukin-6 production in human adipocytes 46
Individual expression and tissue distribution of the splice isoforms of the human growth hormone receptor (GHR) 46
Quantificazione del trascritto del gene dell’aromatasi nei leucociti di donne, uomini e bambini 46
Interazioni tra leptina e cortisolo, GH e TSH 46
Magnetic Beads-Based Extraction and Liquid Chromatography-Electrospray-Linear lon Trap Mass Specrometry for a Sensitive Analysis of Estrogens in Children Serum 46
Endocrine modulators of interlukin-6 secretion by human adypocites 46
Interleukin-6 promotes insulin resistance and lypolysis in human adipocytes 45
Dyslipidaemia, hepatic steatosis and selective post-receptor insulin resistance: insights from humans with insulin receptor and post-receptor signaling defects. 45
Heterozygous mutation of HESX1 causing hypopituitarism and multiple anatomical malformations without feature of septo-ptic dysplasia 45
Prevalence of pathogenetic MC4R mutations in Italian children with early onset obesity, tall stature and familial history of obesity. 45
Increased glucocorticoid receptor beta expression converts mouse hybridoma cells to a corticoid resistant phenotype 44
Peripheral IL-6 is not involved in the activation of the hypothalamic-pituitary-adrenal (HPA) axis by insulin-induced hypoglicemia 44
Secrezione spontanea delle 24 ore di Ghrelina in bambini prepuberi con bassa statura 44
Transcriptional and translational regulation of the splicing isoforms of the GH receptor by glucocorticoids 44
Natural glucocorticoid receptor mutants causing generalized glucocorticoid resistance: molecular genotype, genetic transmission, and clinical phenotype 44
Genotype and 17-hydroxyprogesterone blood levels in italian children with premature pubarche due to nonclassic 21-hydroxylase. 44
Differential interaction and activation function 2 of natural glucocorticoid receptor mutants causing familial glucocorticoid resistance 43
Low glucocorticoid receptor GRalpha/GRbeta ratio in T-cell lymphoblastic leukemia 41
Relative abundance of growth hormone receptor isoforms in Rhesus monkey tissues and human transformed lymphocytes 41
Quantification of human aromatase gene expression in peripheral blood leukocytes (PBLS) 41
Novità in endocrinologia pediatrica 41
Mineralocorticoid and glucocorticoid receptors 40
Familial/sporadic glucocorticoid resistance syndrome and hypertension 40
Glucocorticoid receptor isoforms alpha and beta: potential physiologic and pathologic importance 39
Relazione tra genotipo e livelli sierici di 17-idrossiprogesterone in bambini italiani con pubarca prematuro secondario a deficit non classico di 21-idrossilasi. 39
Nuovi geni coinvolti nella funzione dell'asse ipofisi-surrene. 38
Gender difference in lymphocytes aromatase gene expression 38
Interlukin-6 and tumor necrosis factor alpha in asymptomatic and symptomatic pseudohypoaldosteronism 34
Glucocorticoid resistance syndromes and states 34
Spontaneous 24-hour Ghrelin secretion in short-normal prepubertal children 31
Totale 5.295
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Categoria #
all - tutte 16.581
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 16.581
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20201.372 199 267 98 33 125 147 159 26 104 93 26 95
2020/2021689 3 96 84 1 87 5 92 4 130 11 172 4
2021/2022420 4 1 2 13 13 2 65 78 21 30 58 133
2022/20231.655 193 143 108 118 214 176 14 92 513 7 62 15
2023/2024467 25 60 14 12 42 146 23 22 10 14 32 67
2024/202553 53 0 0 0 0 0 0 0 0 0 0 0
Totale 5.295