CRIS Current Research Information System

CICOGNANI, ALESSANDRO
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
AS - Asia 7.528
NA - Nord America 6.690
EU - Europa 5.787
AF - Africa 434
SA - Sud America 338
OC - Oceania 10
Continente sconosciuto - Info sul continente non disponibili 4
Totale 20.791
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 6.608
VN - Vietnam 2.746
SG - Singapore 1.716
CN - Cina 1.702
GB - Regno Unito 1.533
DE - Germania 816
IT - Italia 729
SE - Svezia 645
UA - Ucraina 576
HK - Hong Kong 481
FR - Francia 386
IN - India 318
RU - Federazione Russa 294
BR - Brasile 225
IE - Irlanda 211
JP - Giappone 163
NL - Olanda 119
ZA - Sudafrica 118
FI - Finlandia 107
TG - Togo 98
KR - Corea 95
CI - Costa d'Avorio 90
EE - Estonia 90
BG - Bulgaria 68
CH - Svizzera 56
JO - Giordania 53
NG - Nigeria 52
AR - Argentina 51
SC - Seychelles 47
BE - Belgio 46
CA - Canada 45
BD - Bangladesh 30
PH - Filippine 28
TW - Taiwan 26
PL - Polonia 25
TH - Thailandia 25
TR - Turchia 25
IQ - Iraq 24
MX - Messico 23
LT - Lituania 16
EC - Ecuador 15
ID - Indonesia 15
AT - Austria 13
CL - Cile 13
GR - Grecia 13
IR - Iran 13
PK - Pakistan 12
CO - Colombia 10
EG - Egitto 10
PY - Paraguay 10
ES - Italia 9
SA - Arabia Saudita 9
AU - Australia 8
LB - Libano 8
UZ - Uzbekistan 8
RO - Romania 7
MA - Marocco 6
PE - Perù 6
MY - Malesia 5
HN - Honduras 4
OM - Oman 4
AE - Emirati Arabi Uniti 3
CZ - Repubblica Ceca 3
DK - Danimarca 3
DZ - Algeria 3
KH - Cambogia 3
KZ - Kazakistan 3
MK - Macedonia 3
PS - Palestinian Territory 3
RS - Serbia 3
SY - Repubblica araba siriana 3
UY - Uruguay 3
VE - Venezuela 3
BO - Bolivia 2
DO - Repubblica Dominicana 2
ET - Etiopia 2
EU - Europa 2
HR - Croazia 2
HU - Ungheria 2
KE - Kenya 2
KG - Kirghizistan 2
LU - Lussemburgo 2
LV - Lettonia 2
NI - Nicaragua 2
NP - Nepal 2
PT - Portogallo 2
SK - Slovacchia (Repubblica Slovacca) 2
TT - Trinidad e Tobago 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AL - Albania 1
BZ - Belize 1
CG - Congo 1
CR - Costa Rica 1
GH - Ghana 1
IL - Israele 1
JM - Giamaica 1
KI - Kiribati 1
KM - Comore 1
LK - Sri Lanka 1
LY - Libia 1
Totale 20.782
Salva come PNG Salva come JPEG
Città #
Southend 1.332
Singapore 1.210
Ashburn 692
Ho Chi Minh City 647
Chandler 633
Hanoi 555
San Jose 512
Hong Kong 445
Jacksonville 437
Fairfield 365
Dong Ket 334
Hefei 314
Santa Clara 293
Princeton 276
Wilmington 263
Ann Arbor 238
Houston 236
Beijing 210
Dublin 208
Woodbridge 200
Seattle 154
Cambridge 144
Tokyo 144
Boardman 139
Lauterbourg 135
Nanjing 130
Westminster 126
Padova 125
Da Nang 116
Los Angeles 106
Berlin 101
Lomé 98
Abidjan 90
Haiphong 85
Helsinki 85
Medford 81
Seoul 79
Turin 77
Saint Petersburg 74
Bologna 73
Mülheim 71
Munich 70
Milan 68
Sofia 68
Shenyang 67
Buffalo 64
Jinan 63
Amman 51
Frankfurt am Main 49
Abeokuta 48
Mahé 46
Guangzhou 44
Bern 43
Brussels 43
Nanchang 39
Dallas 37
Tianjin 37
New York 33
Hải Dương 32
Bengaluru 31
Changsha 31
São Paulo 31
Hebei 30
Bremen 29
San Diego 29
Mountain View 25
Olalla 25
Biên Hòa 24
Dearborn 24
Falls Church 24
Shanghai 24
Falkenstein 23
Jiaxing 23
Verona 23
Redwood City 22
Zhengzhou 22
Can Tho 21
Norwalk 21
Thái Nguyên 21
Phoenix 20
Quận Bình Thạnh 20
Turku 20
Ninh Bình 19
Rome 19
The Dalles 19
Hangzhou 18
Redondo Beach 18
Thái Bình 18
Bến Tre 17
London 17
Ningbo 17
Toronto 17
Bắc Ninh 16
Ha Long 15
Yubileyny 15
Düsseldorf 14
Shenzhen 14
Vũng Tàu 14
Des Moines 13
Orem 13
Totale 13.391
Salva come PNG Salva come JPEG
Nome #
A new case of familial mutation in the SRY gene implicated in the pure gonadal dysgenesis in two sisters and in their unaffected father 398
Lung function in children with diabetes mellitus. 270
Turner syndrome, insulin sensitivity and growth hormone treatment 269
Disorders of sexual development 265
A sequence variation in 3’UTR of CYP21A2 gene correlates with a mild form of Congenital Adrenal Hyperplasia 256
A new DAX1 gene mutation associated with congenital adrenal hypoplasia and hypogonadotropic hypogonadism 254
High glucose levels induce membrane antioxidants, in terms of vitamin E and Coenzyme Q10, in children and adolescents with type 1 diabetes 242
psychological and behavioural aspects in children and adolescents with congenital hypothyroidism diagnosed by neonatal screening:comparison between parents' and children's perceptions 242
Acanthosis Nigricans (AN), Glucose Tolerance and Turner Syndrome: Influence of GH-Therapy 240
Correlations of phenotype and genotype in relation to mor phologic remodelling of the aortic root in patients with Turner's syndrome 236
UN CASO COMPLICATO DI TBC 236
Active and total ghrelin concentrations in the newborn 236
Role of intratesticular ultrasonographic and Doppler flow analyses in evaluating gonadal status in male survivors of childhood malignancy. 235
Impact of molecular genetics on congenital adrenal hyperplasia management. 232
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. 226
A rare association of inlet patch with laryngospasm: a report of two children and literature review. 223
Age at onset do not influence long-term glycemic control in children with type 1 diabetes mellitus 219
High Rate of Regression From Micro-Macroalbuminuria to Normoalbuminuria in Children and Adolescents With Type 1 Diabetes Treated or Not With Enalapril: The influence of HDL cholesterol 218
Hearing Growth Defects in Turner Syndrome 215
Reproductive outcome in girls with congenital and acquired autoimmune thyroid pathology 213
DEVELOPMENTAL SYNDROMES: GROWTH HORMONE DEFICIENCY AND TREATMENT. 211
Glucose tolerance and insulin sensitivity in Turner patients treated with GH: Follow-up until the young adult age 209
Functional studies of two novel and two rare mutations in the 21-hydroxylase gene. 205
Airway inflammation and lung function decline in childhood post-infectious bronchiolitis obliterans. 205
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 205
Effect on adult height of pubertal growth hormone retesting and withdrawal of therapy in patients with previously diagnosed growth hormone deficiency. 202
Long-term clinical significance of thyroid autoimmunity in children with celiac disease. 202
Gonadoblastoma in Turner syndrome and Y-chromosome-derived material. 200
Analysis of the TSHR gene in patients with isolated hyperthyrotropinemia 199
Cardiofaciocutaneous Syndrome (CFC): A New Case with GH-Deficit and without Mental Retardation (MR) 199
A novel frame-shift mutation in the SHOX gene in a subject with Léri-Weill dyschondrosteosis 199
Italian cross-sectional growth charts for height, weight and BMI (2 to 20 yr). 198
Le complicanze metaboliche dell'obesità in età evolutiva 189
Diagnosis and Successful Intrauterine Treatment of Fetal Goiter: A Case Report 188
A molecular analysis of candidate genes for hypospadias in Italian subjects 188
Final Height Related to Growth Hormone Levels (Stimulated and Physiological) Evaluated in Short Children Before and After Growth Hormone Therapy 187
Relationships between ghrelin, hypothalamic-pituitary-adrenal- and GH/IGF1 axes in patients treated for congenital adrenal hyperplasia 184
Prevalence of Aortic Dilation in Turner Patients without Congenital Heart Disease (CHD) Studied at Echocardiography and Transthoracic MRI 183
Metabolic Aspects of Patients Followed for Severe Obesity 182
Thyroid status in children and adolescents after bone marrow transplantation(BMT) with and without total body irradiation (TBI)conditioning 179
Thyrotropin-stimulating hormone receptor gene analysis in pediatric patients with non-autoimmune subclinical hypothyroidism 179
High Variability of Sexual Ambiguity and Clinical Expression in two Patients with a 46,XY del(9p) Kariotype 178
Identification of rare alleles in an Italian population of 284 patients with 21- hydroxylase deficiency by complete sequencing of the CYP21 gene 175
Final height and Pubertal development in congenital hypothyroidism before and after neonatal screening programs. 175
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 175
Two Novel Missense mutations in the GnRHR Gene in Two Siblings with Isolated Hypogonadotropic Hypogonadism 174
A new case of familial mutation in the SRY gene implicated in the pure gonadal dysgenesis in two sisters and their unaffected father 173
SCREENING NEONATALE DELLA FIBROSI CISTICA IN EMILIA ROMAGNA: BENEFICI E RISCHI 173
Body Mass Index (BMI) evaluation in survivors from childhood cancer 171
Il bambino oncologico "guarito": quali alterazioni endocrinologiche temere? 170
Hashimoto encepahlopathy in an adolescent boy. 170
A novel PRKAR1A mutation associated with hepatocellular carcinoma in a young patient and a variable Carney complex phenotype in affected subjects in older generations. 170
INTRAVENOUS HIGH-DOSE IMMUNOGLOBULIN TREATMENT IN RECENT ONSET CHILDHOOD NARCOLEPSY WITH CATAPLEXY 169
Follow-Up of Homocysteine, Folate and Vitamin B12 in Children and Young Adults with Type 1 Diabetes Mellitus 168
Functional analysis of two recurrent amino acid substitutions in the CYP21 gene from Italian patients with congenital adrenal hyperplasia. 167
Growth patterns in children treated for Acute Lymphoblastic Leukemia (ALL): Relationship with cranial irradiation 166
Interruption of GH Therapy on the Basis of GH Retesting at Puberty in Previously Diagnosed GHD Patients: Final Height Results 164
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 163
Quality of life, psychological adjustment and metabolic control in youths with type 1 diabetes: a study with self- and parent-report questionnaires. 162
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. 160
17beta-Hydroxysteroid dehydrogenase-3 deficiency: from pregnancy to adolescence 160
Thyroid neoplasms after head and neck irradiation (RT) in childhood cancer survivors 159
Tre nuove variazioni di sequenza nel gene dell’AMH in un paziente con sindrome da persistenza dei dotti di Muller. 158
Futuro endocrino a lungo termine nella pubertà precoce centrale trattata e non trattata (PPC). 156
CYP11B1 gene analysis in 3 Italian patients: identification of a new mutation. 156
A molecular analysis of candidate genes for hypospadias in Italian subjects 156
SRD5A2 gene analysis in an Italian population of under-masculinized 46,XY subjects. 155
Hearing loss in Turner syndrome: results of a multicentric study. 154
A sequence variation in 3’UTR of CYP21A2 gene correlates with a mild form of congenital adrenal hyperplasia. 154
Influence of gender and pubertal stage at diagnosis on growth outcome in childhood thyrotoxicosis: results of a collaborative study. 154
Studio della funzionalità polmonare nel bambino obeso. 153
Growth and adult height in atypical coeliac patients, with or without growth hormone deficiency. 153
The prevalence of celiac disease in children with type 1 diabetes mellitus increased in the mid nineties: an 18-yr longitudinal study based on anti-endomysial antibodies 151
OSSIDO NITRICO ESALATO E FLOGOSI DELLE VIE AEREE IN SOGGETTI ALLERGICI 150
Statural growth and final height after transsphenoidal surgery for Cushing's disease in 7 children 148
Psychological problems in diabetic children and adolescents are related to disease duration and metabolic control: a study with children and parent questionnaires 147
Three new mutations in androgen receptor gene identified in patients with 46,XY SDS: Complications for genetic counselling 147
Obesity in children and adolescents: an increasing metabolic problem. 144
Early corticosteroid treatment in 4 Duchenne muscular dystrophy patients: 14-years follow-up 144
Behavioural and emotional aspects in obese children. 143
Transient 21-OHase deficiency in newborns suspected for CAH: May hydrocortisone treatment be beneficial or is simply inappropriate? 143
Functional characterization of naturally occurring NR3C2 gene mutations in Italian patients suffering from pseudohypoaldosteronism type 1 143
Due casi falsi negativi con forma classica allo screening neonatale per la sindrome adreno-genitale congenita della Regione Emilia-Romagna (1980-83, 1991-2003). 143
The impact of maternal thyroid disorders on neonatal screening for congenital hypothyroidism (CH): a regional experience 142
Genotypic and phenotypic variability in 54 subjects with congenital hypopituitarism 142
Reproductive outcome in patients treated and not treated for idiopathic early puberty: long-term results of a randomized trial in adults. 142
Height as a risk factor for osteosarcoma. 141
Height outcome and pubertal development in CYP21 genotyped CAH male patients 141
CYP21 genotype, adult height, and pubertal development in 55 patients treated for 21-hydroxylase deficiency. 141
High risk of congenital hypothyroidism in multiple pregnancies. 140
Behavioural and emotional aspects in children with early-treated congenital hypothyroidism 140
Valutazione della funzionalità tiroidea nei pazienti irradiati per neoplasie insorte in età pediatrica. 139
PREDEX - Prenatal assessment and treatment of Congenital Adrenal Hyperplasia with Dexamethasone - A longitudinal Study of outcome measures for mother and child 137
Altri agenti farmacologici 136
Noonan syndrome and PTPN11 mutations: clinical findings and growth follow-up with long-term GH therapy 136
Interstitial 6q deletion: a new patient with empty sella and GH deficiency 135
Update on age at menarche in Italy: toward the leveling off of the secular trend. 134
Three new sequence variations of the AMH gene in an Italian patient with persistent Mullerian duct syndrome. 130
SRD5A2 gene analysis in Italian patients with male pseudohermaphroditism. 130
HESX1 gene analysis in a population of 45 patients with posterior pituitari ectopia (PPE) and GH deficiency (GHD): two novel mutations associated with a mild phenotype. 130
Totale 18.048
Salva come PNG Salva come JPEG
Categoria #
all - tutte 48.153
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 48.153
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021752 0 0 0 0 0 0 0 0 0 100 101 551
2021/20222.458 297 102 118 231 179 176 42 121 73 105 563 451
2022/20232.718 266 439 159 322 169 206 57 135 503 60 265 137
2023/2024575 25 100 31 65 63 126 34 42 17 40 9 23
2024/20252.698 112 445 194 233 454 148 110 90 22 155 72 663
2025/20266.758 898 687 564 495 778 377 1.005 423 1.161 370 0 0
Totale 21.037