CASSIO, ALESSANDRA
 Distribuzione geografica
Continente #
NA - Nord America 4.835
AS - Asia 4.460
EU - Europa 3.719
AF - Africa 330
SA - Sud America 306
OC - Oceania 7
Continente sconosciuto - Info sul continente non disponibili 5
Totale 13.662
Nazione #
US - Stati Uniti d'America 4.777
SG - Singapore 1.350
CN - Cina 1.316
GB - Regno Unito 969
VN - Vietnam 776
IT - Italia 551
DE - Germania 535
SE - Svezia 410
HK - Hong Kong 372
UA - Ucraina 262
RU - Federazione Russa 248
IN - India 241
BR - Brasile 220
FR - Francia 188
IE - Irlanda 153
KR - Corea 147
CI - Costa d'Avorio 100
JP - Giappone 91
ZA - Sudafrica 84
NL - Olanda 72
FI - Finlandia 62
EE - Estonia 55
NG - Nigeria 55
TG - Togo 52
BG - Bulgaria 45
AR - Argentina 44
CH - Svizzera 44
TR - Turchia 35
CA - Canada 34
ID - Indonesia 33
SC - Seychelles 22
BE - Belgio 21
AT - Austria 20
JO - Giordania 20
PL - Polonia 20
IR - Iran 17
MX - Messico 17
ES - Italia 16
LT - Lituania 13
CL - Cile 12
CZ - Repubblica Ceca 12
EC - Ecuador 12
TW - Taiwan 12
GR - Grecia 11
BD - Bangladesh 8
TH - Thailandia 8
EG - Egitto 6
KZ - Kazakistan 6
AU - Australia 5
PY - Paraguay 5
UY - Uruguay 5
CO - Colombia 4
LB - Libano 4
PH - Filippine 4
SK - Slovacchia (Repubblica Slovacca) 4
DK - Danimarca 3
EU - Europa 3
IQ - Iraq 3
MA - Marocco 3
A2 - ???statistics.table.value.countryCode.A2??? 2
AE - Emirati Arabi Uniti 2
DO - Repubblica Dominicana 2
HR - Croazia 2
KH - Cambogia 2
OM - Oman 2
PK - Pakistan 2
SN - Senegal 2
SY - Repubblica araba siriana 2
VE - Venezuela 2
BB - Barbados 1
BO - Bolivia 1
CR - Costa Rica 1
CY - Cipro 1
DJ - Gibuti 1
DZ - Algeria 1
ET - Etiopia 1
GH - Ghana 1
GT - Guatemala 1
HU - Ungheria 1
IL - Israele 1
JM - Giamaica 1
KE - Kenya 1
KG - Kirghizistan 1
KI - Kiribati 1
KW - Kuwait 1
LU - Lussemburgo 1
MY - Malesia 1
NZ - Nuova Zelanda 1
PA - Panama 1
PE - Perù 1
SA - Arabia Saudita 1
SM - San Marino 1
TN - Tunisia 1
UZ - Uzbekistan 1
Totale 13.662
Città #
Singapore 926
Southend 845
Ashburn 523
Chandler 408
Fairfield 401
Hong Kong 365
Dong Ket 292
Santa Clara 274
Hefei 269
Princeton 214
Wilmington 213
Woodbridge 195
Houston 182
Beijing 180
Jacksonville 175
Seattle 170
Ann Arbor 166
Cambridge 150
Dublin 150
Boardman 123
Ho Chi Minh City 119
Seoul 111
Abidjan 100
Hanoi 96
Bologna 95
Nanjing 89
Westminster 88
Los Angeles 85
Tokyo 83
Berlin 79
Padova 79
Abeokuta 55
Lomé 52
Saint Petersburg 46
Turin 46
Munich 43
Sofia 43
Jinan 42
Shenyang 42
Medford 40
Buffalo 39
Mülheim 39
Helsinki 36
Milan 35
San Diego 35
Changsha 33
Redondo Beach 32
Frankfurt am Main 30
Dallas 29
Olalla 28
Bengaluru 27
Bern 27
Shanghai 27
Jiaxing 26
Nanchang 26
Tianjin 23
Denver 22
Guangzhou 22
Jakarta 21
New York 21
Amman 20
Nuremberg 20
Hangzhou 19
Hebei 19
Norwalk 19
São Paulo 19
Brussels 18
Phoenix 18
Redmond 18
Dearborn 17
Des Moines 17
Mahé 17
Zhengzhou 16
Chicago 15
Haiphong 14
Montreal 14
Parma 14
Ankara 13
The Dalles 13
Council Bluffs 12
Da Nang 12
London 12
Ningbo 12
Turku 12
Düsseldorf 11
Haikou 11
Naples 11
Quận Bình Thạnh 11
Rome 11
Taizhou 11
Verona 11
Prague 10
Boydton 9
Brooklyn 9
Falkenstein 9
Moscow 9
Mountain View 9
Taiyuan 9
Talas 9
Warsaw 9
Totale 8.771
Nome #
Central precocious puberty:short-term comparative data of treatment with monthly or long-acting thre months depot triptorelin 319
Screening e diagnosi dell’iperplasia surrenale congenita: dalle vecchie alle nuove tecnologie. 283
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 254
A new DAX1 gene mutation associated with congenital adrenal hypoplasia and hypogonadotropic hypogonadism 239
Active and total ghrelin concentrations in the newborn 215
Reproductive outcome in girls with congenital and acquired autoimmune thyroid pathology 190
Analysis of the TSHR gene in patients with isolated hyperthyrotropinemia 183
Long-term clinical significance of thyroid autoimmunity in children with celiac disease. 177
Il nodulo tiroideo in età pediatrica:problemi di interesse chirurgico 177
Normative Basal Values of Hormones and Proteins of Gonadal and Adrenal Functions from Birth to Adulthood 167
46, XX DSD due to androgen excess in monogenic disorders of steroidogenesis: Genetic, biochemical, and clinical features 167
Comparison between Liquid and Tablet Formulations of Levothyroxine in the Initial Treatment of Congenital Hypothyroidism 166
Characteristics of a nationwide cohort of patients presenting with isolated hypogonadotropic hypogonadism (IHH) 166
Diagnostic features of thyroid nodules in pediatrics 165
Thyroid status in children and adolescents after bone marrow transplantation(BMT) with and without total body irradiation (TBI)conditioning 164
A new homozygous CACNB2 mutation has functional relevance and supports a role for calcium channels in autism spectrum disorder. 164
Final Height Related to Growth Hormone Levels (Stimulated and Physiological) Evaluated in Short Children Before and After Growth Hormone Therapy 163
psychological and behavioural aspects in children and adolescents with congenital hypothyroidism diagnosed by neonatal screening:comparison between parents' and children's perceptions 161
Diagnosis and Successful Intrauterine Treatment of Fetal Goiter: A Case Report 160
Autoimmune polyglandular syndrome type III after haploidentical hematopoietic stem cell transplantation in a child with acute myeloid leukemia. 160
Final height and Pubertal development in congenital hypothyroidism before and after neonatal screening programs. 154
Thyrotropin-stimulating hormone receptor gene analysis in pediatric patients with non-autoimmune subclinical hypothyroidism 154
Two Novel Missense mutations in the GnRHR Gene in Two Siblings with Isolated Hypogonadotropic Hypogonadism 153
Levothyroxine treatment in pediatric benign thyroid nodules 149
X-linked hypophosphatemic rickets: An Italian experts' opinion survey 149
Carnitine longitudinal pattern in preterm infants <1800 g body weight: a case–control study 146
La pubertà normale e la pubertà precoce centrale. 145
Down Syndrome and thyroid dysfunction: longitudinal follow-up 0-10 years 145
Thyroid neoplasms after head and neck irradiation (RT) in childhood cancer survivors 144
Copy number determination of hypothyroidism genes by MLPA analysis in patients with hypothyroidism and thyroid hypoplasia 144
Influence of gender and pubertal stage at diagnosis on growth outcome in childhood thyrotoxicosis: results of a collaborative study. 142
Congenital hypothyroidism (CH): the re-evaluation of diagnosis in CH patients with in situ gland identified by newborn screening 142
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 141
Central Precocious Puberty: Treatment with Triptorelin 11.25 mg 140
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 139
Acute suppurative thyroiditis in childhood: spontaneous closure of sinus pyriform fistola may occur even very early. 137
Più sicurezza per il neonato: lo screening metabolico allargato 136
Futuro endocrino a lungo termine nella pubertà precoce centrale trattata e non trattata (PPC). 136
Beta-ketothiolase (T2) deficiency detected with newborn screening (NBS) 133
NKX2.1-Related Disorders: a novel mutation with mild clinical presentation. 133
A Case of Acrodermatitis Dysmetabolica in a Child Affected by Citrullinemia Type I: When Early Diagnosis and Timely Treatment Are Not Enough 131
Reproductive outcome in patients treated and not treated for idiopathic early puberty: long-term results of a randomized trial in adults. 131
Fanconi-Bickel syndrome: a mild form associated with GLUT2 mutation 130
Valutazione della funzionalità tiroidea nei pazienti irradiati per neoplasie insorte in età pediatrica. 128
Behavioural and emotional aspects in children with early-treated congenital hypothyroidism 128
Prospective evaluation of the natural course of idiopathic subclinical hypothyroidism in childhood and adolescence. 126
Subclinical hypothyroidism in children and adolescents: a wide range of clinical, biochemical, and genetic factors involved. 125
High risk of congenital hypothyroidism in multiple pregnancies. 125
Relationships between thyroid function and autoimmunity with metabolic derangement at the onset of type 1 diabetes: A cross-sectional and longitudinal study 125
Thyroid Enlargement from Newborn to Adolescent 125
CYP21 genotype, adult height, and pubertal development in 55 patients treated for 21-hydroxylase deficiency. 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). 125
The impact of maternal thyroid disorders on neonatal screening for congenital hypothyroidism (CH): a regional experience 124
Current knowledge on endocrine disrupting chemicals (EDCs) from animal biology to humans, from pregnancy to adulthood: Highlights from a national italian meeting 124
Maternal PKU: Defining phenylalanine tolerance and its variation during pregnancy, according to genetic background 123
Auxological and endocrine findings in narcolepsy type 1: seventeen-year follow-up from a pediatric endocrinology center 122
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 120
Prevalence and follow-up of thyroid disfunction at type 1 diabetes mellitus (T!DM) onset in pediatric population 119
Height outcome and pubertal development in CYP21 genotyped CAH male patients 118
Acute suppurative thyroiditis: prevalence and natural history in an Italian pediatric population 117
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 116
European Society for Paediatric Endocrinology consensus guidelines on screening, diagnosis, and management of congenital hypothyroidism. 116
Thyroid nodules and cancer in children and adolescents affected by autoimmune thyroiditis 115
Incidence of congenital hypothyroidism in the Autonomous Province of Bolzano: benefit of increased iodine intake. 115
Stochastic epigenetic mutations as possible explanation for phenotypical discordance among twins with congenital hypothyroidism 114
Comparison between Liquid and Tablet Formulations in the Treatment of Congenital Hypothyroidism up to 3 Years of Age: The First Italian Study 114
AutoimmunePolyendocrinopathyCandidiasisEctodermalDystrophy Syndrome(APECED) clinical and molecular features in three patients from southernItaly. 112
Peculiarities of Graves' disease in children and adolescents with Down's syndrome 109
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) 108
Hypothalamic-pituitary function in 22 subjects with pediatric-onset Langerhans cell histiocytosis 105
Mutational and functional studies on NR5A1 gene in 46,XY disorders of sex development: identification of six novel loss of function mutations 105
Serum thyrotropin concentration in children with isolated thyroid nodules. 102
Risk factors for congenital hypothyroidism: results of a population case-control study (1997-2003). 102
Molecular characterization to predict tetrahydrobiopterin (BH4) responsiveness in phenylalanine hydroxylase (PAH) deficiency 102
Fertility in adult females with congenital hypothyroidism (CH) diagnosed by neonatal screening 101
Newborn screening importance in detection of asymptomatic forms of epimerase deficiency galactosemia (EDG) 101
Multiple factors influencing the incidence of congenital hypothyroidism detected by neonatal screening 99
Hemophagocytic lymphohistiocytosis and lysinuric protein intolerance:case report 99
TSHR gene analysis in paediatric subjects with NASH (non autoimmune subclinical hypothyroidism) not selected by neonatal screening 99
The Italian National register of infants with congenital hypothyroidism: twenty years of surveillance and study of congenital hypothyroidism. 98
A Frequent Oligogenic Involvement in Congenital Hypothyroidism 98
Hashimoto encepahlopathy in an adolescent boy. 97
Congenital Adrenal Hyperplasias Presenting in the Newborn and Young Infant 97
Epidemiology of congenital hypothyroidism: what can be deduced from the Italian registry of infants with congenital hypothyroidism. 96
Thyroid function in children and adolescents with Hashimoto's thyroiditis after l-thyroxine discontinuation. 96
Endocrinopatie 95
Thyroid autoimmunity in children with celiac disease: longitudinal long-term follow-up 93
Autoimmune-Polyendocrinopathy-Candidiasis-Ectodermal- Dystrophy (APECED) in Calabria: clinical, immunological and genetic patterns. 89
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 89
Clinical Management of Hypothyroidism in pregnancy. The actions. 85
Influence of Hashimoto thyroiditis on the development of thyroid nodules and cancer in children and adolescents 84
Neonatal Screening for Congenital Hypothyroidism: What Can We Learn from Discordant Twins 84
Prevalence and ultrasound patterns of testicular adrenal rest tumors in adults with congenital adrenal hyperplasia 84
Ruolo degli androgeni e dei mineralcorticoidi sulla crescita fetale. 83
Effect of initial levothyroxine dose on neurodevelopmental and growth outcomes in children with congenital hypothyroidism 82
Child Neurology: A Case Series of Heterogeneous Neuropsychiatric Symptoms and Outcome in Very Early-Onset Narcolepsy Type 1 82
Extreme hyperosmolarity and severe ketoacidosis in a child with type 1 diabetes mellitus at onset safely treated with current guidelines 81
null 77
Long term clinical history of an Italian cohort of infantile onset Pompe disease treated with enzyme replacement therapy 69
Biological clock and heredity in pubertal timing: what is new? 69
Totale 13.055
Categoria #
all - tutte 37.668
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 37.668


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021818 0 0 0 0 0 59 16 79 88 81 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
2025/20263.119 532 591 511 449 701 335 0 0 0 0 0 0
Totale 13.921