CRIS Current Research Information System

CICOGNANI, ALESSANDRO
 Distribuzione geografica
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Continente #
NA - Nord America 8.426
AS - Asia 7.647
EU - Europa 5.881
AF - Africa 434
SA - Sud America 363
Continente sconosciuto - Info sul continente non disponibili 250
OC - Oceania 10
Totale 23.011
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Nazione #
US - Stati Uniti d'America 8.302
VN - Vietnam 2.746
SG - Singapore 1.738
CN - Cina 1.719
GB - Regno Unito 1.539
DE - Germania 818
IT - Italia 807
SE - Svezia 645
UA - Ucraina 576
HK - Hong Kong 493
FR - Francia 387
IN - India 318
RU - Federazione Russa 294
BR - Brasile 247
IE - Irlanda 211
JP - Giappone 163
NL - Olanda 120
ZA - Sudafrica 118
FI - Finlandia 107
TG - Togo 98
BD - Bangladesh 95
KR - Corea 95
CI - Costa d'Avorio 90
EE - Estonia 90
BG - Bulgaria 68
CA - Canada 64
CH - Svizzera 57
JO - Giordania 53
NG - Nigeria 52
AR - Argentina 51
BE - Belgio 47
SC - Seychelles 47
MX - Messico 30
PH - Filippine 28
TW - Taiwan 26
PL - Polonia 25
TH - Thailandia 25
TR - Turchia 25
IQ - Iraq 24
LT - Lituania 18
EC - Ecuador 16
ID - Indonesia 15
AT - Austria 13
CL - Cile 13
GR - Grecia 13
IR - Iran 13
PK - Pakistan 13
CO - Colombia 12
EG - Egitto 10
ES - Italia 10
PY - Paraguay 10
SA - Arabia Saudita 9
AU - Australia 8
JM - Giamaica 8
LB - Libano 8
UZ - Uzbekistan 8
RO - Romania 7
HN - Honduras 6
MA - Marocco 6
MY - Malesia 6
PE - Perù 6
OM - Oman 4
AE - Emirati Arabi Uniti 3
CZ - Repubblica Ceca 3
DK - Danimarca 3
DZ - Algeria 3
GT - Guatemala 3
KH - Cambogia 3
KZ - Kazakistan 3
MK - Macedonia 3
NI - Nicaragua 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
IL - Israele 2
KE - Kenya 2
KG - Kirghizistan 2
LU - Lussemburgo 2
LV - Lettonia 2
MD - Moldavia 2
NP - Nepal 2
PT - Portogallo 2
SK - Slovacchia (Repubblica Slovacca) 2
TT - Trinidad e Tobago 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AG - Antigua e Barbuda 1
AL - Albania 1
BS - Bahamas 1
BZ - Belize 1
CG - Congo 1
CR - Costa Rica 1
GH - Ghana 1
Totale 22.752
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Città #
Southend 1.332
Singapore 1.226
Ashburn 762
Ho Chi Minh City 647
Chandler 634
San Jose 619
Hanoi 555
Hong Kong 457
Jacksonville 439
Fairfield 366
Dong Ket 334
Hefei 314
Santa Clara 310
Princeton 277
Wilmington 264
Houston 241
Ann Arbor 238
Council Bluffs 234
Beijing 218
Dublin 208
Woodbridge 200
Seattle 159
Cambridge 144
Tokyo 144
Boardman 139
Lauterbourg 135
Los Angeles 134
Nanjing 130
Westminster 126
Padova 125
Da Nang 116
Berlin 101
Lomé 98
Abidjan 90
Haiphong 85
Helsinki 85
Medford 81
Turin 80
Seoul 79
Milan 78
Bologna 74
Saint Petersburg 74
Mülheim 71
Munich 70
Buffalo 69
Dallas 68
Sofia 68
New York 67
Shenyang 67
Jinan 63
Amman 51
Frankfurt am Main 51
Abeokuta 48
Mahé 46
São Paulo 45
Guangzhou 44
Bern 43
Brussels 43
Atlanta 42
Nanchang 39
Tianjin 37
Hải Dương 32
Bengaluru 31
Changsha 31
Hebei 30
San Diego 30
Bremen 29
Rome 28
Phoenix 27
Shanghai 27
Mountain View 25
Olalla 25
Verona 25
Biên Hòa 24
Dearborn 24
Falls Church 24
Falkenstein 23
Jiaxing 23
London 22
Redwood City 22
Zhengzhou 22
Can Tho 21
Norwalk 21
Thái Nguyên 21
Orem 20
Quận Bình Thạnh 20
Turku 20
Ninh Bình 19
San Francisco 19
The Dalles 19
Toronto 19
Chicago 18
Hangzhou 18
Redondo Beach 18
Thái Bình 18
Bến Tre 17
Ningbo 17
Bắc Ninh 16
Montreal 16
Ha Long 15
Totale 14.060
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Nome #
Italian cross-sectional growth charts for height, weight and BMI (2 to 20 yr). 1.283
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
Lung function in children with diabetes mellitus. 278
Turner syndrome, insulin sensitivity and growth hormone treatment 277
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
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 260
High glucose levels induce membrane antioxidants, in terms of vitamin E and Coenzyme Q10, in children and adolescents with type 1 diabetes 253
psychological and behavioural aspects in children and adolescents with congenital hypothyroidism diagnosed by neonatal screening:comparison between parents' and children's perceptions 251
Acanthosis Nigricans (AN), Glucose Tolerance and Turner Syndrome: Influence of GH-Therapy 248
UN CASO COMPLICATO DI TBC 243
Age at onset do not influence long-term glycemic control in children with type 1 diabetes mellitus 241
Active and total ghrelin concentrations in the newborn 241
Role of intratesticular ultrasonographic and Doppler flow analyses in evaluating gonadal status in male survivors of childhood malignancy. 240
Correlations of phenotype and genotype in relation to mor phologic remodelling of the aortic root in patients with Turner's syndrome 239
Impact of molecular genetics on congenital adrenal hyperplasia management. 239
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
A rare association of inlet patch with laryngospasm: a report of two children and literature review. 227
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
DEVELOPMENTAL SYNDROMES: GROWTH HORMONE DEFICIENCY AND TREATMENT. 219
Reproductive outcome in girls with congenital and acquired autoimmune thyroid pathology 218
Hearing Growth Defects in Turner Syndrome 218
Airway inflammation and lung function decline in childhood post-infectious bronchiolitis obliterans. 215
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
Glucose tolerance and insulin sensitivity in Turner patients treated with GH: Follow-up until the young adult age 212
Gonadoblastoma in Turner syndrome and Y-chromosome-derived material. 210
Effect on adult height of pubertal growth hormone retesting and withdrawal of therapy in patients with previously diagnosed growth hormone deficiency. 209
Long-term clinical significance of thyroid autoimmunity in children with celiac disease. 208
Cardiofaciocutaneous Syndrome (CFC): A New Case with GH-Deficit and without Mental Retardation (MR) 206
Analysis of the TSHR gene in patients with isolated hyperthyrotropinemia 205
A novel frame-shift mutation in the SHOX gene in a subject with Léri-Weill dyschondrosteosis 203
Final Height Related to Growth Hormone Levels (Stimulated and Physiological) Evaluated in Short Children Before and After Growth Hormone Therapy 198
Le complicanze metaboliche dell'obesità in età evolutiva 197
Diagnosis and Successful Intrauterine Treatment of Fetal Goiter: A Case Report 196
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
Prevalence of Aortic Dilation in Turner Patients without Congenital Heart Disease (CHD) Studied at Echocardiography and Transthoracic MRI 192
High Variability of Sexual Ambiguity and Clinical Expression in two Patients with a 46,XY del(9p) Kariotype 186
Thyroid status in children and adolescents after bone marrow transplantation(BMT) with and without total body irradiation (TBI)conditioning 184
A new case of familial mutation in the SRY gene implicated in the pure gonadal dysgenesis in two sisters and their unaffected father 184
Thyrotropin-stimulating hormone receptor gene analysis in pediatric patients with non-autoimmune subclinical hypothyroidism 184
Final height and Pubertal development in congenital hypothyroidism before and after neonatal screening programs. 182
High risk of congenital hypothyroidism in multiple pregnancies. 182
Two Novel Missense mutations in the GnRHR Gene in Two Siblings with Isolated Hypogonadotropic Hypogonadism 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
A novel PRKAR1A mutation associated with hepatocellular carcinoma in a young patient and a variable Carney complex phenotype in affected subjects in older generations. 179
Il bambino oncologico "guarito": quali alterazioni endocrinologiche temere? 178
Body Mass Index (BMI) evaluation in survivors from childhood cancer 177
SCREENING NEONATALE DELLA FIBROSI CISTICA IN EMILIA ROMAGNA: BENEFICI E RISCHI 176
Follow-Up of Homocysteine, Folate and Vitamin B12 in Children and Young Adults with Type 1 Diabetes Mellitus 175
Hashimoto encepahlopathy in an adolescent boy. 174
Growth patterns in children treated for Acute Lymphoblastic Leukemia (ALL): Relationship with cranial irradiation 173
INTRAVENOUS HIGH-DOSE IMMUNOGLOBULIN TREATMENT IN RECENT ONSET CHILDHOOD NARCOLEPSY WITH CATAPLEXY 173
Functional analysis of two recurrent amino acid substitutions in the CYP21 gene from Italian patients with congenital adrenal hyperplasia. 172
Interruption of GH Therapy on the Basis of GH Retesting at Puberty in Previously Diagnosed GHD Patients: Final Height Results 171
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
Quality of life, psychological adjustment and metabolic control in youths with type 1 diabetes: a study with self- and parent-report questionnaires. 169
Thyroid neoplasms after head and neck irradiation (RT) in childhood cancer survivors 168
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
SRD5A2 gene analysis in an Italian population of under-masculinized 46,XY subjects. 167
17beta-Hydroxysteroid dehydrogenase-3 deficiency: from pregnancy to adolescence 167
CYP11B1 gene analysis in 3 Italian patients: identification of a new mutation. 165
Tre nuove variazioni di sequenza nel gene dell’AMH in un paziente con sindrome da persistenza dei dotti di Muller. 162
Futuro endocrino a lungo termine nella pubertà precoce centrale trattata e non trattata (PPC). 161
Studio della funzionalità polmonare nel bambino obeso. 161
Hearing loss in Turner syndrome: results of a multicentric study. 160
Growth and adult height in atypical coeliac patients, with or without growth hormone deficiency. 160
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
Influence of gender and pubertal stage at diagnosis on growth outcome in childhood thyrotoxicosis: results of a collaborative study. 158
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 157
OSSIDO NITRICO ESALATO E FLOGOSI DELLE VIE AEREE IN SOGGETTI ALLERGICI 155
Genotypic and phenotypic variability in 54 subjects with congenital hypopituitarism 155
Psychological problems in diabetic children and adolescents are related to disease duration and metabolic control: a study with children and parent questionnaires 154
Obesity in children and adolescents: an increasing metabolic problem. 153
Statural growth and final height after transsphenoidal surgery for Cushing's disease in 7 children 152
Three new mutations in androgen receptor gene identified in patients with 46,XY SDS: Complications for genetic counselling 151
Height as a risk factor for osteosarcoma. 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
The impact of maternal thyroid disorders on neonatal screening for congenital hypothyroidism (CH): a regional experience 147
Early corticosteroid treatment in 4 Duchenne muscular dystrophy patients: 14-years follow-up 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
Reproductive outcome in patients treated and not treated for idiopathic early puberty: long-term results of a randomized trial in adults. 145
Noonan syndrome and PTPN11 mutations: clinical findings and growth follow-up with long-term GH therapy 143
Valutazione della funzionalità tiroidea nei pazienti irradiati per neoplasie insorte in età pediatrica. 143
PREDEX - Prenatal assessment and treatment of Congenital Adrenal Hyperplasia with Dexamethasone - A longitudinal Study of outcome measures for mother and child 142
Behavioural and emotional aspects in children with early-treated congenital hypothyroidism 142
Altri agenti farmacologici 141
Interstitial 6q deletion: a new patient with empty sella and GH deficiency 141
SRD5A2 gene analysis in Italian patients with male pseudohermaphroditism. 139
Impact of insulin glargine on metabolic control and on occurrence of severe hypoglycemia in type 1 diabetic children and adolescents in the last three years 137
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
Totale 19.906
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Categoria #
all - tutte 54.186
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 54.186
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20222.161 0 102 118 231 179 176 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
2025/20267.972 898 687 564 495 778 377 1.005 423 1.161 462 281 841
2026/2027760 558 202 0 0 0 0 0 0 0 0 0 0
Totale 23.011