CRIS Current Research Information System

CICOGNANI, ALESSANDRO
 Distribuzione geografica
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Continente #
NA - Nord America 5.962
EU - Europa 5.521
AS - Asia 5.462
AF - Africa 417
SA - Sud America 295
OC - Oceania 9
Continente sconosciuto - Info sul continente non disponibili 3
Totale 17.669
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Nazione #
US - Stati Uniti d'America 5.900
SG - Singapore 1.551
GB - Regno Unito 1.521
CN - Cina 1.460
VN - Vietnam 1.390
DE - Germania 808
IT - Italia 692
SE - Svezia 640
UA - Ucraina 569
HK - Hong Kong 417
RU - Federazione Russa 293
IN - India 284
FR - Francia 250
IE - Irlanda 209
BR - Brasile 201
JP - Giappone 140
NL - Olanda 116
ZA - Sudafrica 115
TG - Togo 98
EE - Estonia 90
CI - Costa d'Avorio 89
KR - Corea 78
FI - Finlandia 69
BG - Bulgaria 68
CH - Svizzera 56
NG - Nigeria 51
JO - Giordania 48
SC - Seychelles 47
AR - Argentina 45
BE - Belgio 43
CA - Canada 30
MX - Messico 22
PL - Polonia 21
BD - Bangladesh 16
LT - Lituania 16
AT - Austria 13
EC - Ecuador 13
IR - Iran 13
GR - Grecia 12
ID - Indonesia 12
CL - Cile 11
TR - Turchia 11
CO - Colombia 9
LB - Libano 8
AU - Australia 7
EG - Egitto 7
ES - Italia 7
PY - Paraguay 7
RO - Romania 7
IQ - Iraq 5
PE - Perù 5
TW - Taiwan 5
HN - Honduras 4
MA - Marocco 4
MY - Malesia 4
PK - Pakistan 4
CZ - Repubblica Ceca 3
DK - Danimarca 3
RS - Serbia 3
AE - Emirati Arabi Uniti 2
DO - Repubblica Dominicana 2
DZ - Algeria 2
ET - Etiopia 2
EU - Europa 2
HU - Ungheria 2
KG - Kirghizistan 2
KZ - Kazakistan 2
LU - Lussemburgo 2
SA - Arabia Saudita 2
SK - Slovacchia (Repubblica Slovacca) 2
UY - Uruguay 2
UZ - Uzbekistan 2
A2 - ???statistics.table.value.countryCode.A2??? 1
AL - Albania 1
BO - Bolivia 1
BZ - Belize 1
CR - Costa Rica 1
HR - Croazia 1
IL - Israele 1
JM - Giamaica 1
KE - Kenya 1
KH - Cambogia 1
KI - Kiribati 1
LK - Sri Lanka 1
MD - Moldavia 1
ME - Montenegro 1
NO - Norvegia 1
NP - Nepal 1
NZ - Nuova Zelanda 1
PH - Filippine 1
PT - Portogallo 1
SY - Repubblica araba siriana 1
TN - Tunisia 1
TT - Trinidad e Tobago 1
VE - Venezuela 1
Totale 17.669
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Città #
Southend 1.332
Singapore 1.064
Ashburn 646
Chandler 633
Jacksonville 437
Hong Kong 414
Fairfield 365
Dong Ket 334
Hefei 312
Santa Clara 288
Princeton 276
Ho Chi Minh City 270
Wilmington 263
Ann Arbor 238
Houston 235
Hanoi 215
Dublin 206
Beijing 201
Woodbridge 200
Seattle 154
Cambridge 144
Boardman 139
Tokyo 134
Nanjing 128
Westminster 126
Padova 125
Berlin 101
Lomé 98
Los Angeles 94
Abidjan 89
Medford 81
Seoul 78
Turin 77
Saint Petersburg 74
Mülheim 71
Munich 70
Bologna 68
Sofia 68
Shenyang 64
Buffalo 63
Milan 59
Jinan 57
Abeokuta 48
Amman 48
Helsinki 47
Mahé 46
Bern 43
Frankfurt am Main 43
Brussels 41
Nanchang 39
Tianjin 33
Dallas 31
Haiphong 31
Bengaluru 30
Hebei 30
Bremen 29
San Diego 29
São Paulo 27
Da Nang 26
Mountain View 25
Olalla 25
Dearborn 24
Falls Church 24
Changsha 23
Falkenstein 23
Guangzhou 23
Jiaxing 23
Verona 23
Redwood City 22
Norwalk 21
Turku 20
Zhengzhou 20
Phoenix 19
New York 18
Redondo Beach 18
Rome 18
Quận Bình Thạnh 17
Ningbo 16
Shanghai 16
Yubileyny 15
Düsseldorf 14
London 14
Biên Hòa 13
Ha Long 13
Hải Dương 13
Des Moines 12
Haikou 12
Hangzhou 12
Kunming 12
Parma 12
Toronto 12
Ninh Bình 11
Taizhou 11
The Dalles 11
Can Tho 10
Redmond 10
Thái Nguyên 10
Vũng Tàu 10
Fuzhou 9
Hòa Bình 9
Totale 11.375
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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 374
Turner syndrome, insulin sensitivity and growth hormone treatment 253
Lung function in children with diabetes mellitus. 245
A new DAX1 gene mutation associated with congenital adrenal hypoplasia and hypogonadotropic hypogonadism 238
Role of intratesticular ultrasonographic and Doppler flow analyses in evaluating gonadal status in male survivors of childhood malignancy. 228
High glucose levels induce membrane antioxidants, in terms of vitamin E and Coenzyme Q10, in children and adolescents with type 1 diabetes 219
A sequence variation in 3’UTR of CYP21A2 gene correlates with a mild form of Congenital Adrenal Hyperplasia 217
UN CASO COMPLICATO DI TBC 215
Active and total ghrelin concentrations in the newborn 213
Acanthosis Nigricans (AN), Glucose Tolerance and Turner Syndrome: Influence of GH-Therapy 212
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. 203
Reproductive outcome in girls with congenital and acquired autoimmune thyroid pathology 190
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 190
DEVELOPMENTAL SYNDROMES: GROWTH HORMONE DEFICIENCY AND TREATMENT. 184
Age at onset do not influence long-term glycemic control in children with type 1 diabetes mellitus 183
Disorders of sexual development 182
Analysis of the TSHR gene in patients with isolated hyperthyrotropinemia 182
Glucose tolerance and insulin sensitivity in Turner patients treated with GH: Follow-up until the young adult age 180
Airway inflammation and lung function decline in childhood post-infectious bronchiolitis obliterans. 180
A novel frame-shift mutation in the SHOX gene in a subject with Léri-Weill dyschondrosteosis 180
Functional studies of two novel and two rare mutations in the 21-hydroxylase gene. 179
Long-term clinical significance of thyroid autoimmunity in children with celiac disease. 176
Effect on adult height of pubertal growth hormone retesting and withdrawal of therapy in patients with previously diagnosed growth hormone deficiency. 172
Italian cross-sectional growth charts for height, weight and BMI (2 to 20 yr). 169
Metabolic Aspects of Patients Followed for Severe Obesity 166
Thyroid status in children and adolescents after bone marrow transplantation(BMT) with and without total body irradiation (TBI)conditioning 164
Le complicanze metaboliche dell'obesità in età evolutiva 164
Cardiofaciocutaneous Syndrome (CFC): A New Case with GH-Deficit and without Mental Retardation (MR) 163
Final Height Related to Growth Hormone Levels (Stimulated and Physiological) Evaluated in Short Children Before and After Growth Hormone Therapy 162
A molecular analysis of candidate genes for hypospadias in Italian subjects 162
Prevalence of Aortic Dilation in Turner Patients without Congenital Heart Disease (CHD) Studied at Echocardiography and Transthoracic MRI 160
Diagnosis and Successful Intrauterine Treatment of Fetal Goiter: A Case Report 159
Correlations of phenotype and genotype in relation to mor phologic remodelling of the aortic root in patients with Turner's syndrome 159
psychological and behavioural aspects in children and adolescents with congenital hypothyroidism diagnosed by neonatal screening:comparison between parents' and children's perceptions 159
SCREENING NEONATALE DELLA FIBROSI CISTICA IN EMILIA ROMAGNA: BENEFICI E RISCHI 158
Gonadoblastoma in Turner syndrome and Y-chromosome-derived material. 156
Il bambino oncologico "guarito": quali alterazioni endocrinologiche temere? 155
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 155
A novel PRKAR1A mutation associated with hepatocellular carcinoma in a young patient and a variable Carney complex phenotype in affected subjects in older generations. 155
Final height and Pubertal development in congenital hypothyroidism before and after neonatal screening programs. 153
Identification of rare alleles in an Italian population of 284 patients with 21- hydroxylase deficiency by complete sequencing of the CYP21 gene 152
Two Novel Missense mutations in the GnRHR Gene in Two Siblings with Isolated Hypogonadotropic Hypogonadism 152
Body Mass Index (BMI) evaluation in survivors from childhood cancer 152
Thyrotropin-stimulating hormone receptor gene analysis in pediatric patients with non-autoimmune subclinical hypothyroidism 152
Relationships between ghrelin, hypothalamic-pituitary-adrenal- and GH/IGF1 axes in patients treated for congenital adrenal hyperplasia 151
INTRAVENOUS HIGH-DOSE IMMUNOGLOBULIN TREATMENT IN RECENT ONSET CHILDHOOD NARCOLEPSY WITH CATAPLEXY 150
High Variability of Sexual Ambiguity and Clinical Expression in two Patients with a 46,XY del(9p) Kariotype 149
A molecular analysis of candidate genes for hypospadias in Italian subjects 149
Growth patterns in children treated for Acute Lymphoblastic Leukemia (ALL): Relationship with cranial irradiation 147
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 144
Thyroid neoplasms after head and neck irradiation (RT) in childhood cancer survivors 143
Influence of gender and pubertal stage at diagnosis on growth outcome in childhood thyrotoxicosis: results of a collaborative study. 142
A new case of familial mutation in the SRY gene implicated in the pure gonadal dysgenesis in two sisters and their unaffected father 141
Quality of life, psychological adjustment and metabolic control in youths with type 1 diabetes: a study with self- and parent-report questionnaires. 141
Tre nuove variazioni di sequenza nel gene dell’AMH in un paziente con sindrome da persistenza dei dotti di Muller. 140
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. 140
17beta-Hydroxysteroid dehydrogenase-3 deficiency: from pregnancy to adolescence 140
A rare association of inlet patch with laryngospasm: a report of two children and literature review. 140
CYP11B1 gene analysis in 3 Italian patients: identification of a new mutation. 139
Hearing loss in Turner syndrome: results of a multicentric study. 139
Functional analysis of two recurrent amino acid substitutions in the CYP21 gene from Italian patients with congenital adrenal hyperplasia. 139
Studio della funzionalità polmonare nel bambino obeso. 138
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 137
Follow-Up of Homocysteine, Folate and Vitamin B12 in Children and Young Adults with Type 1 Diabetes Mellitus 137
Interruption of GH Therapy on the Basis of GH Retesting at Puberty in Previously Diagnosed GHD Patients: Final Height Results 137
Futuro endocrino a lungo termine nella pubertà precoce centrale trattata e non trattata (PPC). 136
Impact of molecular genetics on congenital adrenal hyperplasia management. 135
Hearing Growth Defects in Turner Syndrome 133
SRD5A2 gene analysis in an Italian population of under-masculinized 46,XY subjects. 131
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 131
Reproductive outcome in patients treated and not treated for idiopathic early puberty: long-term results of a randomized trial in adults. 131
Growth and adult height in atypical coeliac patients, with or without growth hormone deficiency. 130
Behavioural and emotional aspects in obese children. 129
Psychological problems in diabetic children and adolescents are related to disease duration and metabolic control: a study with children and parent questionnaires 129
Statural growth and final height after transsphenoidal surgery for Cushing's disease in 7 children 128
Obesity in children and adolescents: an increasing metabolic problem. 128
A sequence variation in 3’UTR of CYP21A2 gene correlates with a mild form of congenital adrenal hyperplasia. 127
Altri agenti farmacologici 126
Height as a risk factor for osteosarcoma. 126
OSSIDO NITRICO ESALATO E FLOGOSI DELLE VIE AEREE IN SOGGETTI ALLERGICI 126
Valutazione della funzionalità tiroidea nei pazienti irradiati per neoplasie insorte in età pediatrica. 126
Behavioural and emotional aspects in children with early-treated congenital hypothyroidism 126
Transient 21-OHase deficiency in newborns suspected for CAH: May hydrocortisone treatment be beneficial or is simply inappropriate? 125
High risk of congenital hypothyroidism in multiple pregnancies. 125
Due casi falsi negativi con forma classica allo screening neonatale per la sindrome adreno-genitale congenita della Regione Emilia-Romagna (1980-83, 1991-2003). 124
The impact of maternal thyroid disorders on neonatal screening for congenital hypothyroidism (CH): a regional experience 123
Functional characterization of naturally occurring NR3C2 gene mutations in Italian patients suffering from pseudohypoaldosteronism type 1 123
CYP21 genotype, adult height, and pubertal development in 55 patients treated for 21-hydroxylase deficiency. 123
Early corticosteroid treatment in 4 Duchenne muscular dystrophy patients: 14-years follow-up 122
Three new mutations in androgen receptor gene identified in patients with 46,XY SDS: Complications for genetic counselling 121
SRD5A2 gene analysis in Italian patients with male pseudohermaphroditism. 119
Genotypic and phenotypic variability in 54 subjects with congenital hypopituitarism 119
Interstitial 6q deletion: a new patient with empty sella and GH deficiency 119
Update on age at menarche in Italy: toward the leveling off of the secular trend. 119
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 116
Height outcome and pubertal development in CYP21 genotyped CAH male patients 115
Two novel GnRHR gene mutations in two siblings with hypogonadotropic hypogonadism. Eur J Endocrinol 113
Comparative data on reproductive axis suppression by quarterly or monthly triptorelin depot in girls with central precocious puberty (CPP) 112
Noonan syndrome and PTPN11 mutations: clinical findings and growth follow-up with long-term GH therapy 112
AutoimmunePolyendocrinopathyCandidiasisEctodermalDystrophy Syndrome(APECED) clinical and molecular features in three patients from southernItaly. 112
Totale 15.445
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Categoria #
all - tutte 43.309
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 43.309
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211.036 0 0 0 0 0 97 25 110 52 100 101 551
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
2025/20263.605 898 687 564 495 778 183 0 0 0 0 0 0
Totale 17.884