CRIS Current Research Information System

CASSIO, ALESSANDRA
 Distribuzione geografica
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Continente #
NA - Nord America 6.593
AS - Asia 6.139
EU - Europa 4.190
AF - Africa 420
SA - Sud America 407
Continente sconosciuto - Info sul continente non disponibili 295
OC - Oceania 16
Totale 18.060
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Nazione #
US - Stati Uniti d'America 6.429
VN - Vietnam 1.614
SG - Singapore 1.553
CN - Cina 1.545
GB - Regno Unito 1.012
IT - Italia 690
DE - Germania 546
HK - Hong Kong 436
SE - Svezia 412
FR - Francia 318
IN - India 284
BR - Brasile 270
UA - Ucraina 266
RU - Federazione Russa 246
IE - Irlanda 174
KR - Corea 162
JP - Giappone 139
FI - Finlandia 104
ZA - Sudafrica 103
CI - Costa d'Avorio 100
NL - Olanda 87
BD - Bangladesh 76
CA - Canada 76
AR - Argentina 58
NG - Nigeria 58
TR - Turchia 56
EE - Estonia 55
TG - Togo 53
CH - Svizzera 50
PH - Filippine 46
BG - Bulgaria 45
ID - Indonesia 44
EG - Egitto 42
ES - Italia 36
TH - Thailandia 34
MX - Messico 32
AT - Austria 26
TW - Taiwan 26
PL - Polonia 24
SC - Seychelles 23
BE - Belgio 22
JO - Giordania 22
CO - Colombia 19
CL - Cile 17
IR - Iran 17
IQ - Iraq 16
GR - Grecia 15
AU - Australia 14
LT - Lituania 14
EC - Ecuador 13
CZ - Repubblica Ceca 11
MA - Marocco 11
SA - Arabia Saudita 11
JM - Giamaica 10
KZ - Kazakistan 9
PK - Pakistan 9
PT - Portogallo 9
CR - Costa Rica 8
PE - Perù 8
LB - Libano 7
VE - Venezuela 7
HN - Honduras 6
NI - Nicaragua 6
TN - Tunisia 6
BO - Bolivia 5
ET - Etiopia 5
GT - Guatemala 5
HU - Ungheria 5
KE - Kenya 5
OM - Oman 5
PY - Paraguay 5
SK - Slovacchia (Repubblica Slovacca) 5
SY - Repubblica araba siriana 5
UY - Uruguay 5
GH - Ghana 4
MY - Malesia 4
RO - Romania 4
AE - Emirati Arabi Uniti 3
DK - Danimarca 3
DO - Repubblica Dominicana 3
EU - Europa 3
PA - Panama 3
PS - Palestinian Territory 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AG - Antigua e Barbuda 2
AL - Albania 2
CY - Cipro 2
DZ - Algeria 2
GD - Grenada 2
HR - Croazia 2
KH - Cambogia 2
LY - Libia 2
PR - Porto Rico 2
RS - Serbia 2
SN - Senegal 2
SV - El Salvador 2
TT - Trinidad e Tobago 2
UZ - Uzbekistan 2
XK - ???statistics.table.value.countryCode.XK??? 2
AO - Angola 1
Totale 17.750
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Città #
Singapore 1.102
Southend 836
Ashburn 679
San Jose 558
Chandler 408
Hong Kong 402
Fairfield 400
Ho Chi Minh City 342
Santa Clara 309
Hanoi 294
Dong Ket 292
Hefei 269
Council Bluffs 246
Wilmington 214
Princeton 212
Woodbridge 196
Beijing 188
Houston 184
Jacksonville 176
Dublin 170
Seattle 170
Ann Arbor 166
Cambridge 149
Boardman 123
Lauterbourg 121
Los Angeles 118
Bologna 111
Seoul 111
Tokyo 111
Abidjan 100
Nanjing 92
Westminster 90
Berlin 78
Helsinki 78
Padova 78
Abeokuta 55
Haiphong 54
Lomé 53
Dallas 51
New York 51
Buffalo 49
Turin 48
Milan 46
Saint Petersburg 45
Da Nang 43
Munich 43
Sofia 43
Jinan 42
Shenyang 41
Shanghai 40
Frankfurt am Main 39
Medford 39
Mülheim 39
São Paulo 39
San Diego 36
Changsha 35
Chicago 35
Guangzhou 34
Hangzhou 34
Redondo Beach 32
Denver 30
Montreal 29
Bengaluru 28
Phoenix 28
Bern 27
Olalla 27
Nanchang 26
Jiaxing 25
Tianjin 25
Nuremberg 23
Amman 22
Jakarta 22
Des Moines 20
Rome 20
The Dalles 20
Brussels 19
Hebei 19
Norwalk 19
London 18
Redmond 18
Zhengzhou 18
Dearborn 17
Mahé 17
Ankara 16
Cairo 16
Chengdu 16
San Francisco 16
Brooklyn 15
Naples 15
Atlanta 14
Parma 14
Ningbo 13
Quận Bình Thạnh 13
Thái Bình 13
Biên Hòa 12
Hải Dương 12
Kav 12
Miami 12
Spartanburg 12
Talas 12
Totale 10.989
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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 740
Central precocious puberty:short-term comparative data of treatment with monthly or long-acting thre months depot triptorelin 392
Screening e diagnosi dell’iperplasia surrenale congenita: dalle vecchie alle nuove tecnologie. 328
A new DAX1 gene mutation associated with congenital adrenal hypoplasia and hypogonadotropic hypogonadism 264
psychological and behavioural aspects in children and adolescents with congenital hypothyroidism diagnosed by neonatal screening:comparison between parents' and children's perceptions 253
Active and total ghrelin concentrations in the newborn 243
Reproductive outcome in girls with congenital and acquired autoimmune thyroid pathology 225
46, XX DSD due to androgen excess in monogenic disorders of steroidogenesis: Genetic, biochemical, and clinical features 214
Comparison between Liquid and Tablet Formulations of Levothyroxine in the Initial Treatment of Congenital Hypothyroidism 213
Analysis of the TSHR gene in patients with isolated hyperthyrotropinemia 211
Long-term clinical significance of thyroid autoimmunity in children with celiac disease. 211
Final Height Related to Growth Hormone Levels (Stimulated and Physiological) Evaluated in Short Children Before and After Growth Hormone Therapy 208
A New Homozygous CACNB2 Mutation has Functional Relevance and Supports a Role for Calcium Channels in Autism Spectrum Disorder 204
Diagnosis and Successful Intrauterine Treatment of Fetal Goiter: A Case Report 201
Normative Basal Values of Hormones and Proteins of Gonadal and Adrenal Functions from Birth to Adulthood 200
Il nodulo tiroideo in età pediatrica:problemi di interesse chirurgico 197
Carnitine longitudinal pattern in preterm infants <1800 g body weight: a case–control study 197
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 195
High risk of congenital hypothyroidism in multiple pregnancies. 195
X-linked hypophosphatemic rickets: An Italian experts' opinion survey 193
Thyroid status in children and adolescents after bone marrow transplantation(BMT) with and without total body irradiation (TBI)conditioning 192
Characteristics of a nationwide cohort of patients presenting with isolated hypogonadotropic hypogonadism (IHH) 192
Diagnostic features of thyroid nodules in pediatrics 189
Thyrotropin-stimulating hormone receptor gene analysis in pediatric patients with non-autoimmune subclinical hypothyroidism 186
Two Novel Missense mutations in the GnRHR Gene in Two Siblings with Isolated Hypogonadotropic Hypogonadism 185
Final height and Pubertal development in congenital hypothyroidism before and after neonatal screening programs. 185
La pubertà normale e la pubertà precoce centrale. 184
Autoimmune polyglandular syndrome type III after haploidentical hematopoietic stem cell transplantation in a child with acute myeloid leukemia. 182
Copy number determination of hypothyroidism genes by MLPA analysis in patients with hypothyroidism and thyroid hypoplasia 182
Down Syndrome and thyroid dysfunction: longitudinal follow-up 0-10 years 182
A Case of Acrodermatitis Dysmetabolica in a Child Affected by Citrullinemia Type I: When Early Diagnosis and Timely Treatment Are Not Enough 181
Hashimoto encepahlopathy in an adolescent boy. 179
Congenital hypothyroidism (CH): the re-evaluation of diagnosis in CH patients with in situ gland identified by newborn screening 176
Thyroid neoplasms after head and neck irradiation (RT) in childhood cancer survivors 175
Comparison between Liquid and Tablet Formulations in the Treatment of Congenital Hypothyroidism up to 3 Years of Age: The First Italian Study 173
Levothyroxine treatment in pediatric benign thyroid nodules 172
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 172
Auxological and endocrine findings in narcolepsy type 1: seventeen-year follow-up from a pediatric endocrinology center 171
Futuro endocrino a lungo termine nella pubertà precoce centrale trattata e non trattata (PPC). 166
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 164
Beta-ketothiolase (T2) deficiency detected with newborn screening (NBS) 164
Influence of gender and pubertal stage at diagnosis on growth outcome in childhood thyrotoxicosis: results of a collaborative study. 162
Central Precocious Puberty: Treatment with Triptorelin 11.25 mg 161
NKX2.1-Related Disorders: a novel mutation with mild clinical presentation. 159
Acute suppurative thyroiditis in childhood: spontaneous closure of sinus pyriform fistola may occur even very early. 157
Fanconi-Bickel syndrome: a mild form associated with GLUT2 mutation 157
Relationships between thyroid function and autoimmunity with metabolic derangement at the onset of type 1 diabetes: A cross-sectional and longitudinal study 157
Current knowledge on endocrine disrupting chemicals (EDCs) from animal biology to humans, from pregnancy to adulthood: Highlights from a national italian meeting 157
Prospective evaluation of the natural course of idiopathic subclinical hypothyroidism in childhood and adolescence. 156
Prevalence and ultrasound patterns of testicular adrenal rest tumors in adults with congenital adrenal hyperplasia 156
Maternal PKU: Defining phenylalanine tolerance and its variation during pregnancy, according to genetic background 154
Più sicurezza per il neonato: lo screening metabolico allargato 153
Due casi falsi negativi con forma classica allo screening neonatale per la sindrome adreno-genitale congenita della Regione Emilia-Romagna (1980-83, 1991-2003). 153
CYP21 genotype, adult height, and pubertal development in 55 patients treated for 21-hydroxylase deficiency. 152
The impact of maternal thyroid disorders on neonatal screening for congenital hypothyroidism (CH): a regional experience 151
Height outcome and pubertal development in CYP21 genotyped CAH male patients 149
Reproductive outcome in patients treated and not treated for idiopathic early puberty: long-term results of a randomized trial in adults. 149
Valutazione della funzionalità tiroidea nei pazienti irradiati per neoplasie insorte in età pediatrica. 148
Prevalence and follow-up of thyroid disfunction at type 1 diabetes mellitus (T!DM) onset in pediatric population 147
Behavioural and emotional aspects in children with early-treated congenital hypothyroidism 147
Thyroid Enlargement from Newborn to Adolescent 147
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 145
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) 145
Incidence of congenital hypothyroidism in the Autonomous Province of Bolzano: benefit of increased iodine intake. 142
Acute suppurative thyroiditis: prevalence and natural history in an Italian pediatric population 140
Subclinical hypothyroidism in children and adolescents: a wide range of clinical, biochemical, and genetic factors involved. 140
Thyroid nodules and cancer in children and adolescents affected by autoimmune thyroiditis 140
Fertility in adult females with congenital hypothyroidism (CH) diagnosed by neonatal screening 139
Child Neurology: A Case Series of Heterogeneous Neuropsychiatric Symptoms and Outcome in Very Early-Onset Narcolepsy Type 1 139
Mutational and functional studies on NR5A1 gene in 46,XY disorders of sex development: identification of six novel loss of function mutations 136
European Society for Paediatric Endocrinology consensus guidelines on screening, diagnosis, and management of congenital hypothyroidism. 135
Congenital Adrenal Hyperplasias Presenting in the Newborn and Young Infant 134
Newborn screening importance in detection of asymptomatic forms of epimerase deficiency galactosemia (EDG) 133
Stochastic epigenetic mutations as possible explanation for phenotypical discordance among twins with congenital hypothyroidism 132
TSHR gene analysis in paediatric subjects with NASH (non autoimmune subclinical hypothyroidism) not selected by neonatal screening 132
Molecular characterization to predict tetrahydrobiopterin (BH4) responsiveness in phenylalanine hydroxylase (PAH) deficiency 131
Hemophagocytic lymphohistiocytosis and lysinuric protein intolerance:case report 130
AutoimmunePolyendocrinopathyCandidiasisEctodermalDystrophy Syndrome(APECED) clinical and molecular features in three patients from southernItaly. 128
Peculiarities of Graves' disease in children and adolescents with Down's syndrome 127
Hypothalamic-pituitary function in 22 subjects with pediatric-onset Langerhans cell histiocytosis 126
Epidemiology of congenital hypothyroidism: what can be deduced from the Italian registry of infants with congenital hypothyroidism. 126
Risk factors for congenital hypothyroidism: results of a population case-control study (1997-2003). 126
Serum thyrotropin concentration in children with isolated thyroid nodules. 121
Clinical Management of Hypothyroidism in pregnancy. The actions. 120
A Frequent Oligogenic Involvement in Congenital Hypothyroidism 119
Thyroid function in children and adolescents with Hashimoto's thyroiditis after l-thyroxine discontinuation. 119
Multiple factors influencing the incidence of congenital hypothyroidism detected by neonatal screening 118
Neonatal Screening for Congenital Hypothyroidism: What Can We Learn from Discordant Twins 116
Effect of initial levothyroxine dose on neurodevelopmental and growth outcomes in children with congenital hypothyroidism 114
Endocrinopatie 113
Thyroid autoimmunity in children with celiac disease: longitudinal long-term follow-up 113
The Italian National register of infants with congenital hypothyroidism: twenty years of surveillance and study of congenital hypothyroidism. 113
Ruolo degli androgeni e dei mineralcorticoidi sulla crescita fetale. 112
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 109
Extreme hyperosmolarity and severe ketoacidosis in a child with type 1 diabetes mellitus at onset safely treated with current guidelines 108
Influence of Hashimoto thyroiditis on the development of thyroid nodules and cancer in children and adolescents 103
Autoimmune-Polyendocrinopathy-Candidiasis-Ectodermal- Dystrophy (APECED) in Calabria: clinical, immunological and genetic patterns. 99
Current Loss-Of-Function Mutations in The Thyrotropin Receptor Gene: When to Investigate, Clinical Effects, and Treatment. 95
Rare PHEX intron variant causes complete and severe phenotype in a family with hypophosphatemic rickets: a case report 94
Testicular Adrenal Rest Tumors in Congenital Adrenal Hyperplasia: Study of a Cohort of Patients from a Single Italian Center 93
Totale 16.713
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Categoria #
all - tutte 47.978
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 47.978
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.402 0 0 108 127 154 109 27 121 66 63 338 289
2022/20231.970 174 289 96 227 166 143 64 109 356 55 181 110
2023/2024580 49 103 39 77 47 71 29 34 17 54 42 18
2024/20252.437 104 379 162 237 359 114 128 58 21 128 141 606
2025/20266.496 531 590 508 449 698 400 745 491 1.125 496 272 191
2026/2027815 112 201 502 0 0 0 0 0 0 0 0 0
Totale 18.060