CINECA IRIS Institutional Research Information System

CETANI, FILOMENA
 Distribuzione geografica
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Continente #
NA - Nord America 11.630
AS - Asia 6.033
EU - Europa 3.834
SA - Sud America 960
AF - Africa 339
OC - Oceania 7
Continente sconosciuto - Info sul continente non disponibili 6
Totale 22.809
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Nazione #
US - Stati Uniti d'America 11.309
SG - Singapore 1.867
CN - Cina 1.600
IT - Italia 1.111
HK - Hong Kong 1.091
BR - Brasile 794
SE - Svezia 598
VN - Vietnam 583
DE - Germania 391
BG - Bulgaria 331
AT - Austria 250
GB - Regno Unito 236
CA - Canada 225
TR - Turchia 218
FR - Francia 211
RU - Federazione Russa 163
FI - Finlandia 158
IN - India 156
UA - Ucraina 153
CI - Costa d'Avorio 141
KR - Corea 98
JP - Giappone 82
CH - Svizzera 67
BD - Bangladesh 60
AR - Argentina 54
MX - Messico 41
NL - Olanda 40
SA - Arabia Saudita 39
SN - Senegal 39
IQ - Iraq 37
ZA - Sudafrica 37
UZ - Uzbekistan 34
ID - Indonesia 33
NG - Nigeria 30
PK - Pakistan 30
EC - Ecuador 28
MA - Marocco 28
PL - Polonia 28
CO - Colombia 22
BE - Belgio 21
VE - Venezuela 21
KE - Kenya 19
ES - Italia 17
EG - Egitto 14
JO - Giordania 13
CL - Cile 11
CZ - Repubblica Ceca 11
JM - Giamaica 10
PH - Filippine 9
PY - Paraguay 9
UY - Uruguay 9
AE - Emirati Arabi Uniti 8
ET - Etiopia 8
IL - Israele 8
PS - Palestinian Territory 8
CR - Costa Rica 7
DZ - Algeria 7
KZ - Kazakistan 7
NP - Nepal 7
AZ - Azerbaigian 6
DO - Repubblica Dominicana 6
LT - Lituania 6
PE - Perù 6
BO - Bolivia 5
EU - Europa 5
HN - Honduras 5
LB - Libano 5
NI - Nicaragua 5
RS - Serbia 5
TT - Trinidad e Tobago 5
AL - Albania 4
AU - Australia 4
BJ - Benin 4
DK - Danimarca 4
GE - Georgia 4
IE - Irlanda 4
KG - Kirghizistan 4
LV - Lettonia 4
OM - Oman 4
RO - Romania 4
BB - Barbados 3
MY - Malesia 3
NZ - Nuova Zelanda 3
PT - Portogallo 3
SY - Repubblica araba siriana 3
TH - Thailandia 3
TN - Tunisia 3
BH - Bahrain 2
BS - Bahamas 2
CG - Congo 2
CY - Cipro 2
GT - Guatemala 2
HU - Ungheria 2
MK - Macedonia 2
MN - Mongolia 2
PA - Panama 2
PR - Porto Rico 2
QA - Qatar 2
SI - Slovenia 2
SK - Slovacchia (Repubblica Slovacca) 2
Totale 22.783
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Città #
Woodbridge 1.231
Ashburn 1.193
Singapore 990
Hong Kong 974
Fairfield 895
Ann Arbor 717
Dallas 639
Santa Clara 629
Chandler 597
Houston 583
San Jose 551
Seattle 374
Shanghai 364
Beijing 343
Milan 339
Sofia 329
Wilmington 326
Cambridge 318
New York 253
Vienna 217
Boardman 181
Jacksonville 168
Los Angeles 167
Ottawa 154
Serra 154
Ho Chi Minh City 151
Princeton 149
Abidjan 141
Lawrence 141
Medford 128
Hefei 124
Lauterbourg 124
Hanoi 115
Nanjing 109
Florence 102
Munich 101
Seoul 94
Izmir 90
Tokyo 81
Buffalo 78
Istanbul 78
Des Moines 74
Redondo Beach 63
São Paulo 63
San Diego 61
Frankfurt am Main 58
Piscataway 55
Council Bluffs 54
London 54
Bern 53
Dong Ket 50
Lancaster 45
Helsinki 42
Rome 42
Pisa 41
Dakar 39
Dearborn 37
Jüchen 32
Nanchang 32
Orem 31
Tashkent 31
Turku 31
Columbus 30
Hyderabad 29
Chicago 28
Lagos 28
Redwood City 27
Da Nang 25
Rio de Janeiro 25
The Dalles 25
Boulder 24
Düsseldorf 23
Fuzhou 22
Phoenix 22
Montreal 21
Norwalk 21
Shenyang 21
Brussels 19
Johannesburg 19
Changsha 18
Kent 18
Brooklyn 17
Guangzhou 17
Kunming 17
Nairobi 17
Ankara 16
Belo Horizonte 16
Bremen 16
Chennai 16
Hebei 16
Ogden 16
Toronto 16
Washington 16
Atlanta 15
Baltimore 15
Dhaka 15
Nuremberg 15
San Francisco 15
Warsaw 15
Baghdad 14
Totale 16.225
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Nome #
A quick intraoperative parathyroid hormone assay in the surgical management of patients with primary hyperparathyroidism: a study of 206 consecutive cases 246
Somatostatin analogues do not affect calcium metabolism in patients with acromegaly and primary hyperparathyroidism due to MEN 1-Like syndrome 239
Clinical profile of juvenile primary hyperparathyroidism: a prospective study 229
Surgery or surveillance for mild asymptomatic primary hyperparathyroidism: a prospective, randomized clinical trial 227
Parathyroid Carcinoma and Adenoma Co-existing in One Patient: Case Report and Comparative Proteomic Analysis 225
First evidence of TRPV5 and TRPV6 channels in human parathyroid glands: possible involvement in neoplastic transformation. 217
A reappraisal of the Rb1 gene abnormalities in the diagnosis of parathyroid cancer 215
Assays of TSH-receptor antibodies in 576 patients with various thyroid disorders: their incidence, significance and clinical usefulness 207
A new mutation of the MEN1 gene in an italian kindred with multiple endocrine neoplasia type 1 207
Beta-catenin activation is not involved in sporadic parathyroid carcinomas and adenomas 206
A proteomic approach to study parathyroid glands 205
Evaluation of formalin-fixed paraffin-embedded tissues in the proteomic analysis of parathyroid glands. 203
Morphometric vertebral fractures in postmenopausal women with primary hyperparathyroidism 202
Autoantibodies against type I interferons as an additional diagnostic criterion for autoimmune polyendocrine syndrome type I 198
Non-surgical management of primary hyperparathyroidism 198
Cinacalcet efficacy in patients with moderately severe primary hyperparathyroidism according to the European Medicine Agency prescription labeling. 197
Hereditary hypercalcemia caused by a homozygous pathogenic variant in the cyp24a1 gene: A case report and review of the literature 193
The thyroperoxidase doublet is not produced by alternative splicing 191
Six novel MEN1 gene mutations in sporadic parathyroid tumors 188
A patient with MEN1 and end‑stage chronic kidney disease due to Alport syndrome: Decision making on the eligibility of transplantation 187
TSH receptor antibodies do not alter the function of gonadotropin receptors stably expressed in eukaryotic cells 186
Calcium-sensing receptor gene polymorphism is not associated with bone mineral density in Italian postmenopausal women 184
Persistent primary hyperparathyroidism caused by an ectopic adenoma in the piriform sinus: case report and review of the literature 183
Mapping thyroid peroxidase epitopes using recombinant protein fragments 183
Post-surgical follow-up of differentiated thyroid cancer. 183
Differential effects of NaCl concentration on the constitutive activity of the thyrotropin and the luteinizing hormone/chorionic gonadotropin receptors 182
Different somatic alterations of the HRPT2 gene in a patient with recurrent sporadic primary hyperparathyroidism carrying an HRPT2 germline mutation 182
Whole exome sequencing in familial isolated primary hyperparathyroidism 180
Calcium-sensing receptor gene polymorphisms in primary hyperparathyroidism 179
Exome analysis of a large family with Familial Isolated Primary Hyperparathyroidism (FIHP) and multiple cancers. 179
Risk factors for renal calcifications and determinants of hypercalciuria in patients with chronic, post-surgical hypoparathyroidism 176
Familial hypocalciuric hypercalcemia type 1 due to a novel homozygous mutation of the calcium-sensing receptor gene 174
A New MEN2 Syndrome with Clinical Features of Both MEN2A and MEN2B Associated with a New RET Germline Deletion 174
a novel germline mutation of men 1 gene in a patient with acromegaly and multiple endocrine tumors 173
Genetic analysis of the MEN1 gene and HPRT2 locus in two Italian kindreds with familial isolated 172
No evidence for mutations in the calcium-sensing receptor gene in sporadic parathyroid adenomas 171
Clinical presentation and management of patients with primary hyperparathyroidism in Italy 171
European Expert Consensus on Practical Management of Specific Aspects of Parathyroid Disorders in Adults and in Pregnancy: Recommendations of the ESE Educational Program of Parathyroid Disorders 170
Parathyroid expression of calcium-sensing receptor protein and in vivo parathyroid hormone-Ca(2+) set-point in patients with primary hyperparathyroidism 170
CDC73 mutational status and loss of parafibromin in the outcome of parathyroid cancer. 170
Evidences for an allelic variant of the human LC/CG receptor rather than a gene duplication: functional comparison of wild-type and variant receptors 169
SAT-393 Cognitive Function Evaluation in an Italian Cohort of Patients with Post-Operative Hypoparathyroidism 167
A Novel Mutation in the Calcium Sensing Receptor Gene in an Italian Family Affected by Autosomal Dominant Hypocalcemia 166
Identification and functional characterization of loss-of-function mutations of the calcium-sensing receptor in four Italian kindreds with familial hypocalciuric hypercalcemia 165
Development of an algorithm to predict serum vitamin D levels using a simple questionnaire based on sunlight exposure 165
Patient with monoclonal gammopathy, thyrotoxicosis, pretibial myxedema and thyroid-associated ophthalmopathy; demonstration of direct binding of autoantibodies to the thyrotropin receptor 164
Update on parathyroid carcinoma 163
Functional characteristics of a variant thyrotropin receptor 162
The impact of thyroidectomy on parathyroid glands:a biochemical and clinical profile 162
Loss of p27 expression is associated with MEN1 gene mutations in sporadic parathyroid adenomas 162
Correction to: Whole exome sequencing in familial isolated primary hyperparathyroidism 161
Should parafibromin staining replace HRTP2 gene analysis as an additional tool for histologic diagnosis of parathyroid carcinoma? 161
Parafibromin as a tool for the diagnosis of parathyroid tumors 160
Oncogenic mutations in thyroid adenoma: methodological criteria 159
Efficacy and safety of long-term management of patients with chronic post-surgical hypoparathyroidism 159
Multiple endocrine neoplasia type 1: analysis of germline MEN1 mutations in the Italian multicenter MEN1 patient database 159
Familial hypocalciuric hypercalcemia associated with a novel homozygous loss-of-function mutation, E671D, of the calcium-sensing receptor gene 158
Parathyroid carcinoma 156
A large functioning parathyroid lipoadenoma 156
Mutational and large deletion study of genes implicated in hereditary forms of primary hyperparathyroidism and correlation with clinical features 156
Activating Antibodies to the Calcium-sensing Receptor in Immunotherapy-induced Hypoparathyroidism 156
Genetic and clinical features of multiple endocrine neoplasia types 1 and 2 155
Identification and functional characterization of loss-of-function mutations of the calcium-sensing receptor in four Italian kindreds with familial hypocalciuric hypercalcemia 154
Do the heterozygous carriers of a CYP24A1 mutation display a different biochemical phenotype than wild types? 154
Familial hyperparathyroidism: surgical outcome after 30 years of follow-up in three families with germline HRPT2 mutations 153
Rare diseases in clinical endocrinology: A taxonomic classification system 152
Fenotipo misto MEN2A/MEN2B da nuova mutazione germinale di RET: prima descrizione clinico-genetica e iconografia 152
Performance in Behavioral Testing in an Animal Model of Post-Surgical Hypoparathyroidism 151
Microvessel density in human normal and neoplastic parathyroids 150
The impact of thyroidectomy on parathyroid glands: a biochemical and clinical profile 149
Familial parathyroid hyperplasia:is there a place for minimally invasive surgery?Description of the first treated case 149
HypoparaNet: A Database of Chronic Hypoparathyroidism Based on Expert Medical-Surgical Centers in Italy 149
Two Italian kindreds with familial hypocalciuric hypercalcaemia caused by loss-of-function mutations in the calcium-sensing receptor (CaR) gene: functional characterization of a novel CaR missense mutation 148
Impact of vitamin D deficiency on the clinical and biochemical phenotype in women with sporadic primary hyperparathyroidism 148
Increased Risk of Renal Complications in Patients with Chronic Postsurgical Hypoparathyroidism Treated with Conventional Therapy 148
Persistent Secondary Hyperparathyroidism and Vertebral Fractures in Kidney Transplantation: Role of Calcium-Sensing Receptor Polymorphisms and Vitamin D Deficiency 148
Functional characteristics of three new germline mutations of the thyrotropin receptor gene causing autosomal dominant toxic thyroid hyperplasia 146
Do Patients with Atypical Parathyroid Adenoma Need Close Follow-up? 146
Spontaneous short-term remission of primary hyperparathyroidism from infarction of a parathyroid adenoma 145
Hypercalciuria: its value as a predictive risk factor for nephrolithiasis in asymptomatic primary hyperparathyroidism? 145
Clinical practice. Primary hyperparathyroidism. 144
Molecular pathogenesis of primary hyperparathyroidism 144
Outcome of 309 patients with metastatic differentiated thyroid carcinoma treated with radioiodine 144
Novel association of MEN1 gene mutations with parathyroid carcinoma 144
Multiple endocrine neoplasia syndrome type 1: institution, management, and data analysis of a nationwide multicenter patient database 142
Acute severe primary hyperparathyroidism: spontaneous remission after 2 years follow-up 138
Aryl hydrocarbon receptor interacting protein (AIP) mutations occur rarely in sporadic parathyroid adenomas. 137
Gene expression profile in metastatic and non-metastatic parathyroid carcinoma 137
A novel mutation of the autoimmune regulator gene in an Italian kindred with autoimmune polyendocrinopathy-candidiasis-ectodermal dystrophy, acting in a dominant fashion and strongly cosegregating with hypothyroid autoimmune thyroiditis 136
OR07-05 Is Urinary Calcium the Only Predictor of Nephrolithiasis in Patients with Asymptomatic Primary Hyperparathyroidism? 136
Two Italian kindreds with familial hypocalciuric hypercalcemia caused by loss-of-function mutations in the calcium-sensing receptor (CaR) gene: Functional characterization of a novel CaR mutation 135
Genetic analysis of the TSH receptor gene in differentiated human thyroid carcinomas 135
Genetic analysis of the MEN1 gene and HRPT2 locus in two Italian kindreds with familial isolated hyperparathyroidism 134
Hypoparathyroidism and pseudohypoparathyroidism in pregnancy: an Italian retrospective observational study 133
High-intensity focused ultrasound as an alternative to the surgical approach in primary hyperparathyroidism: a preliminary experience 131
Primary hyperparathyroidism 131
The sulfaphenazole-sensitive pathway acts as a compensatory mechanism for impaired nitric oxide availability in patients with primary hyperparathyroidism. Effect of surgical treatment 130
Diagnostic, therapeutic and healthcare management protocols in parathyroid surgery: II Consensus Conference of the Italian Association of Endocrine Surgery Units (U.E.C. CLUB). 129
Identification and functional characterization of unreported loss-of-function mutations of the calcium-sensing receptor in italian kindreds with familial hypocalciuric hypercalcemia 128
TSH receptor and disease 127
Totale 16.665
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Categoria #
all - tutte 67.108
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 67.108
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/20221.465 17 58 37 79 281 232 46 69 89 57 105 395
2022/20232.123 253 268 171 144 249 287 16 170 393 8 137 27
2023/20241.402 179 154 203 84 192 216 72 36 12 11 82 161
2024/20255.025 13 164 91 245 537 471 395 315 483 601 571 1.139
2025/20266.153 516 794 819 593 587 497 808 326 352 474 221 166
2026/202799 99 0 0 0 0 0 0 0 0 0 0 0
Totale 23.056