CRIS Current Research Information System

CASSIO, ALESSANDRA
 Distribuzione geografica
Salva come PNG Salva come JPEG
Continente #
AS - Asia 6.038
NA - Nord America 5.787
EU - Europa 4.110
AF - Africa 418
SA - Sud America 364
OC - Oceania 16
Continente sconosciuto - Info sul continente non disponibili 5
Totale 16.738
Salva come PNG Salva come JPEG
Nazione #
US - Stati Uniti d'America 5.684
VN - Vietnam 1.614
CN - Cina 1.541
SG - Singapore 1.531
GB - Regno Unito 1.012
IT - Italia 625
DE - Germania 548
HK - Hong Kong 421
SE - Svezia 411
FR - Francia 316
IN - India 287
UA - Ucraina 265
RU - Federazione Russa 250
BR - Brasile 248
IE - Irlanda 172
KR - Corea 162
JP - Giappone 140
FI - Finlandia 104
ZA - Sudafrica 103
CI - Costa d'Avorio 100
NL - Olanda 81
NG - Nigeria 58
EE - Estonia 55
AR - Argentina 54
CA - Canada 54
TG - Togo 53
TR - Turchia 53
CH - Svizzera 48
BG - Bulgaria 45
EG - Egitto 42
PH - Filippine 41
ID - Indonesia 38
TH - Thailandia 34
BD - Bangladesh 32
ES - Italia 32
MX - Messico 29
AT - Austria 26
PL - Polonia 24
TW - Taiwan 24
BE - Belgio 22
JO - Giordania 22
SC - Seychelles 22
IR - Iran 17
CL - Cile 16
IQ - Iraq 16
GR - Grecia 15
AU - Australia 14
LT - Lituania 13
CZ - Repubblica Ceca 12
EC - Ecuador 12
MA - Marocco 11
CO - Colombia 10
SA - Arabia Saudita 10
PK - Pakistan 9
KZ - Kazakistan 8
PT - Portogallo 8
LB - Libano 7
CR - Costa Rica 6
PE - Perù 6
TN - Tunisia 6
BO - Bolivia 5
ET - Etiopia 5
HU - Ungheria 5
OM - Oman 5
PY - Paraguay 5
SK - Slovacchia (Repubblica Slovacca) 5
SY - Repubblica araba siriana 5
UY - Uruguay 5
GH - Ghana 4
KE - Kenya 4
RO - Romania 4
DK - Danimarca 3
DO - Repubblica Dominicana 3
EU - Europa 3
JM - Giamaica 3
MY - Malesia 3
PA - Panama 3
PS - Palestinian Territory 3
VE - Venezuela 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AE - Emirati Arabi Uniti 2
DZ - Algeria 2
GT - Guatemala 2
HR - Croazia 2
KH - Cambogia 2
LY - Libia 2
NP - Nepal 2
RS - Serbia 2
SN - Senegal 2
UZ - Uzbekistan 2
AL - Albania 1
AO - Angola 1
AZ - Azerbaigian 1
BB - Barbados 1
BF - Burkina Faso 1
CY - Cipro 1
DJ - Gibuti 1
IL - Israele 1
KG - Kirghizistan 1
KI - Kiribati 1
Totale 16.727
Salva come PNG Salva come JPEG
Città #
Singapore 1.081
Southend 845
Ashburn 623
San Jose 445
Chandler 408
Fairfield 401
Hong Kong 389
Ho Chi Minh City 340
Hanoi 296
Dong Ket 292
Santa Clara 287
Hefei 269
Princeton 214
Wilmington 213
Woodbridge 195
Beijing 183
Houston 183
Jacksonville 175
Seattle 170
Dublin 168
Ann Arbor 166
Cambridge 150
Boardman 123
Lauterbourg 122
Tokyo 112
Seoul 111
Bologna 109
Los Angeles 107
Abidjan 100
Nanjing 92
Westminster 91
Berlin 79
Padova 79
Helsinki 78
Abeokuta 55
Council Bluffs 55
Haiphong 55
Lomé 53
Turin 47
Saint Petersburg 46
Buffalo 43
Da Nang 43
Munich 43
Shenyang 43
Sofia 43
Jinan 42
New York 41
Dallas 40
Medford 40
Milan 40
Frankfurt am Main 39
Mülheim 39
Shanghai 39
Changsha 36
Hangzhou 35
San Diego 35
Guangzhou 34
Redondo Beach 32
Bengaluru 28
Montreal 28
Olalla 28
Bern 27
Jiaxing 26
Nanchang 26
Denver 25
Tianjin 25
Chicago 24
São Paulo 24
Amman 22
Phoenix 22
Jakarta 21
Nuremberg 21
Brussels 19
Des Moines 19
Hebei 19
Norwalk 19
The Dalles 19
Redmond 18
Zhengzhou 18
Dearborn 17
Mahé 17
Ankara 16
Cairo 16
Chengdu 16
London 16
Rome 15
Parma 14
Ningbo 13
Quận Bình Thạnh 13
Thái Bình 13
Biên Hòa 12
Hải Dương 12
Kav 12
Naples 12
Turku 12
Zurich 12
Atlanta 11
Brooklyn 11
Düsseldorf 11
Haikou 11
Totale 10.474
Salva come PNG Salva come JPEG
Nome #
Congenital Hypothyroidism: A 2020-2021 Consensus Guidelines Update-An ENDO-European Reference Network Initiative Endorsed by the European Society for Pediatric Endocrinology and the European Society for Endocrinology 654
Central precocious puberty:short-term comparative data of treatment with monthly or long-acting thre months depot triptorelin 362
Screening e diagnosi dell’iperplasia surrenale congenita: dalle vecchie alle nuove tecnologie. 314
A new DAX1 gene mutation associated with congenital adrenal hypoplasia and hypogonadotropic hypogonadism 257
psychological and behavioural aspects in children and adolescents with congenital hypothyroidism diagnosed by neonatal screening:comparison between parents' and children's perceptions 247
Active and total ghrelin concentrations in the newborn 237
Reproductive outcome in girls with congenital and acquired autoimmune thyroid pathology 216
46, XX DSD due to androgen excess in monogenic disorders of steroidogenesis: Genetic, biochemical, and clinical features 207
Long-term clinical significance of thyroid autoimmunity in children with celiac disease. 204
Comparison between Liquid and Tablet Formulations of Levothyroxine in the Initial Treatment of Congenital Hypothyroidism 202
Analysis of the TSHR gene in patients with isolated hyperthyrotropinemia 199
A New Homozygous CACNB2 Mutation has Functional Relevance and Supports a Role for Calcium Channels in Autism Spectrum Disorder 196
Il nodulo tiroideo in età pediatrica:problemi di interesse chirurgico 193
Final Height Related to Growth Hormone Levels (Stimulated and Physiological) Evaluated in Short Children Before and After Growth Hormone Therapy 192
Diagnosis and Successful Intrauterine Treatment of Fetal Goiter: A Case Report 192
Normative Basal Values of Hormones and Proteins of Gonadal and Adrenal Functions from Birth to Adulthood 188
Cystathionine Beta-Synthase Deficiency: Three Consecutive Cases Detected in 40 Days by Newborn Screening in Emilia Romagna (Italy) and a Comprehensive Review of the Literature 187
Characteristics of a nationwide cohort of patients presenting with isolated hypogonadotropic hypogonadism (IHH) 186
Carnitine longitudinal pattern in preterm infants <1800 g body weight: a case–control study 185
Diagnostic features of thyroid nodules in pediatrics 184
Thyroid status in children and adolescents after bone marrow transplantation(BMT) with and without total body irradiation (TBI)conditioning 180
Thyrotropin-stimulating hormone receptor gene analysis in pediatric patients with non-autoimmune subclinical hypothyroidism 180
X-linked hypophosphatemic rickets: An Italian experts' opinion survey 179
Two Novel Missense mutations in the GnRHR Gene in Two Siblings with Isolated Hypogonadotropic Hypogonadism 178
Final height and Pubertal development in congenital hypothyroidism before and after neonatal screening programs. 177
Autoimmune polyglandular syndrome type III after haploidentical hematopoietic stem cell transplantation in a child with acute myeloid leukemia. 176
A Case of Acrodermatitis Dysmetabolica in a Child Affected by Citrullinemia Type I: When Early Diagnosis and Timely Treatment Are Not Enough 174
Down Syndrome and thyroid dysfunction: longitudinal follow-up 0-10 years 174
Copy number determination of hypothyroidism genes by MLPA analysis in patients with hypothyroidism and thyroid hypoplasia 173
Hashimoto encepahlopathy in an adolescent boy. 170
Levothyroxine treatment in pediatric benign thyroid nodules 169
Congenital hypothyroidism (CH): the re-evaluation of diagnosis in CH patients with in situ gland identified by newborn screening 168
La pubertà normale e la pubertà precoce centrale. 163
Thyroid neoplasms after head and neck irradiation (RT) in childhood cancer survivors 162
Beta-ketothiolase (T2) deficiency detected with newborn screening (NBS) 158
Comparison between Liquid and Tablet Formulations in the Treatment of Congenital Hypothyroidism up to 3 Years of Age: The First Italian Study 156
Futuro endocrino a lungo termine nella pubertà precoce centrale trattata e non trattata (PPC). 156
Clinical relevance of short-chain acyl-CoA dehydrogenase (SCAD) deficiency: Exploring the role of new variants including the first SCAD-disease-causing allele carrying a synonymous mutation 156
Auxological and endocrine findings in narcolepsy type 1: seventeen-year follow-up from a pediatric endocrinology center 155
Implicating factors in the increase in cases of central precocious puberty (CPP) during the COVID-19 pandemic: Experience of a tertiary centre of pediatric endocrinology and review of the literature 155
Influence of gender and pubertal stage at diagnosis on growth outcome in childhood thyrotoxicosis: results of a collaborative study. 155
NKX2.1-Related Disorders: a novel mutation with mild clinical presentation. 154
Relationships between thyroid function and autoimmunity with metabolic derangement at the onset of type 1 diabetes: A cross-sectional and longitudinal study 153
Acute suppurative thyroiditis in childhood: spontaneous closure of sinus pyriform fistola may occur even very early. 152
Central Precocious Puberty: Treatment with Triptorelin 11.25 mg 151
Prospective evaluation of the natural course of idiopathic subclinical hypothyroidism in childhood and adolescence. 151
Fanconi-Bickel syndrome: a mild form associated with GLUT2 mutation 150
Più sicurezza per il neonato: lo screening metabolico allargato 146
Maternal PKU: Defining phenylalanine tolerance and its variation during pregnancy, according to genetic background 146
Due casi falsi negativi con forma classica allo screening neonatale per la sindrome adreno-genitale congenita della Regione Emilia-Romagna (1980-83, 1991-2003). 146
CYP21 genotype, adult height, and pubertal development in 55 patients treated for 21-hydroxylase deficiency. 145
Current knowledge on endocrine disrupting chemicals (EDCs) from animal biology to humans, from pregnancy to adulthood: Highlights from a national italian meeting 145
High risk of congenital hypothyroidism in multiple pregnancies. 144
Height outcome and pubertal development in CYP21 genotyped CAH male patients 144
Reproductive outcome in patients treated and not treated for idiopathic early puberty: long-term results of a randomized trial in adults. 144
The impact of maternal thyroid disorders on neonatal screening for congenital hypothyroidism (CH): a regional experience 142
Thyroid Enlargement from Newborn to Adolescent 142
Valutazione della funzionalità tiroidea nei pazienti irradiati per neoplasie insorte in età pediatrica. 141
Behavioural and emotional aspects in children with early-treated congenital hypothyroidism 141
Congenital hypothyroidism due to defects of thyroid development and mild increase of TSH at screening: data from the Italian National Registry of infants with congenital hypothyroidism 141
Prevalence and follow-up of thyroid disfunction at type 1 diabetes mellitus (T!DM) onset in pediatric population 140
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) 140
Prevalence and ultrasound patterns of testicular adrenal rest tumors in adults with congenital adrenal hyperplasia 138
Thyroid nodules and cancer in children and adolescents affected by autoimmune thyroiditis 136
Incidence of congenital hypothyroidism in the Autonomous Province of Bolzano: benefit of increased iodine intake. 135
Subclinical hypothyroidism in children and adolescents: a wide range of clinical, biochemical, and genetic factors involved. 133
Child Neurology: A Case Series of Heterogeneous Neuropsychiatric Symptoms and Outcome in Very Early-Onset Narcolepsy Type 1 132
Acute suppurative thyroiditis: prevalence and natural history in an Italian pediatric population 130
European Society for Paediatric Endocrinology consensus guidelines on screening, diagnosis, and management of congenital hypothyroidism. 130
Stochastic epigenetic mutations as possible explanation for phenotypical discordance among twins with congenital hypothyroidism 129
Mutational and functional studies on NR5A1 gene in 46,XY disorders of sex development: identification of six novel loss of function mutations 128
TSHR gene analysis in paediatric subjects with NASH (non autoimmune subclinical hypothyroidism) not selected by neonatal screening 127
Fertility in adult females with congenital hypothyroidism (CH) diagnosed by neonatal screening 126
Newborn screening importance in detection of asymptomatic forms of epimerase deficiency galactosemia (EDG) 125
Congenital Adrenal Hyperplasias Presenting in the Newborn and Young Infant 125
Hemophagocytic lymphohistiocytosis and lysinuric protein intolerance:case report 123
Molecular characterization to predict tetrahydrobiopterin (BH4) responsiveness in phenylalanine hydroxylase (PAH) deficiency 123
Peculiarities of Graves' disease in children and adolescents with Down's syndrome 122
AutoimmunePolyendocrinopathyCandidiasisEctodermalDystrophy Syndrome(APECED) clinical and molecular features in three patients from southernItaly. 122
Risk factors for congenital hypothyroidism: results of a population case-control study (1997-2003). 120
Hypothalamic-pituitary function in 22 subjects with pediatric-onset Langerhans cell histiocytosis 118
Serum thyrotropin concentration in children with isolated thyroid nodules. 117
Epidemiology of congenital hypothyroidism: what can be deduced from the Italian registry of infants with congenital hypothyroidism. 113
The Italian National register of infants with congenital hypothyroidism: twenty years of surveillance and study of congenital hypothyroidism. 111
Thyroid function in children and adolescents with Hashimoto's thyroiditis after l-thyroxine discontinuation. 111
Multiple factors influencing the incidence of congenital hypothyroidism detected by neonatal screening 110
A Frequent Oligogenic Involvement in Congenital Hypothyroidism 110
Endocrinopatie 108
Thyroid autoimmunity in children with celiac disease: longitudinal long-term follow-up 107
Neonatal Screening for Congenital Hypothyroidism: What Can We Learn from Discordant Twins 107
Effect of initial levothyroxine dose on neurodevelopmental and growth outcomes in children with congenital hypothyroidism 106
Clinical Management of Hypothyroidism in pregnancy. The actions. 103
Extreme hyperosmolarity and severe ketoacidosis in a child with type 1 diabetes mellitus at onset safely treated with current guidelines 102
Adolescents with severe obesity show a higher cardiovascular (CV) risk than those with type 1 diabetes: a study with skin advanced glycation end products and intima media thickness evaluation. Acta Diabetol. 2020 Nov;57(11):1297-1305. doi: 10.1007/s00592-020-01537-1. Epub 2020 Jun 5. PMID: 32504306 101
Influence of Hashimoto thyroiditis on the development of thyroid nodules and cancer in children and adolescents 98
Autoimmune-Polyendocrinopathy-Candidiasis-Ectodermal- Dystrophy (APECED) in Calabria: clinical, immunological and genetic patterns. 96
Ruolo degli androgeni e dei mineralcorticoidi sulla crescita fetale. 95
Rare PHEX intron variant causes complete and severe phenotype in a family with hypophosphatemic rickets: a case report 91
Testicular Adrenal Rest Tumors in Congenital Adrenal Hyperplasia: Study of a Cohort of Patients from a Single Italian Center 88
doi:10.1186/1824-7288-40-S1-A16 Iodine deficiency in pregnancy. Italian Journal of Pediatrics 2014 40(Suppl 1):A16. 88
Totale 15.758
Salva come PNG Salva come JPEG
Categoria #
all - tutte 43.052
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 43.052
Salva come PNG Salva come JPEG


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021495 0 0 0 0 0 0 0 0 0 0 79 416
2021/20221.686 215 59 108 128 155 110 27 123 66 63 338 294
2022/20231.977 175 292 96 228 166 143 65 110 356 55 181 110
2023/2024582 49 103 39 77 47 72 29 34 18 54 42 18
2024/20252.449 106 381 162 239 362 116 128 58 21 128 141 607
2025/20266.224 532 591 511 449 701 404 753 495 1.130 501 157 0
Totale 17.026