GIUSTI, FRANCESCA
 Distribuzione geografica
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Continente #
NA - Nord America 3.090
EU - Europa 2.558
AS - Asia 439
Continente sconosciuto - Info sul continente non disponibili 2
SA - Sud America 2
AF - Africa 1
OC - Oceania 1
Totale 6.093
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Nazione #
US - Stati Uniti d'America 3.087
PL - Polonia 1.586
IT - Italia 300
SE - Svezia 238
IE - Irlanda 234
HK - Hong Kong 221
CN - Cina 100
FI - Finlandia 43
GB - Regno Unito 41
FR - Francia 36
VN - Vietnam 34
JO - Giordania 33
BE - Belgio 23
DE - Germania 21
IN - India 18
SG - Singapore 13
CH - Svizzera 12
TR - Turchia 12
ES - Italia 6
NL - Olanda 5
RU - Federazione Russa 5
UA - Ucraina 5
KR - Corea 4
CA - Canada 3
BR - Brasile 2
EU - Europa 2
IR - Iran 2
AT - Austria 1
AU - Australia 1
HR - Croazia 1
IL - Israele 1
MU - Mauritius 1
MY - Malesia 1
RO - Romania 1
Totale 6.093
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Città #
Warsaw 1.586
Fairfield 536
Chandler 287
Ashburn 278
Woodbridge 243
Dublin 234
Seattle 224
Cambridge 217
Houston 197
Ann Arbor 169
Hong Kong 167
Wilmington 167
Lawrence 84
Altamura 79
Princeton 70
Beijing 68
Boston 47
Florence 47
Buffalo 35
Medford 31
San Diego 30
Shanghai 26
Boardman 25
Dong Ket 24
Brussels 21
New York 20
Phoenix 16
Pune 14
Andover 13
Bern 12
Falls Church 12
Norwalk 12
Kent 11
Jacksonville 10
Paris 10
Izmir 8
Renton 8
Singapore 8
Lyon 7
Rome 7
Hillsboro 6
Salerno 6
West Jordan 6
Langhorne 5
Naples 5
Albany 4
Barcelona 4
Redmond 4
Turin 4
Washington 4
Bari 3
Duncan 3
Rhenen 3
Tappahannock 3
Toronto 3
Castelliri 2
Cedar Knolls 2
Delhi 2
Falkenstein 2
Fortaleza 2
Grand Ridge 2
Guangzhou 2
Helsinki 2
Kilburn 2
Leawood 2
London 2
Madrid 2
Manchester 2
Milan 2
Montescaglioso 2
Moscow 2
Redwood City 2
Richmond 2
San Mateo 2
Seoul 2
Southwark 2
Tampa 2
Taranto 2
Utrecht 2
Wuhan 2
Acton 1
Aversa 1
Baltimore 1
Cagliari 1
Casièr 1
Cento 1
Como 1
Cutrofiano 1
Deiva Marina 1
Düsseldorf 1
Ferrara 1
Gallarate 1
Hounslow 1
Isfahan 1
Jerusalem 1
Kuala Lumpur 1
Laurel 1
Lommel 1
Los Angeles 1
Messina 1
Totale 5.193
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Nome #
The negative feedback-loop between the oncomir Mir-24-1 and menin modulates the Men1 tumorigenesis by mimicking the "Knudson's second hit". 229
Natural History of MEN1 GEP-NET: Single-Center Experience After a Long Follow-Up. 226
Multiple endocrine neoplasia syndrome type 1: institution, management, and data analysis of a nationwide multicenter patient database 225
Management impact: effects on quality of life and prognosis in MEN1 220
Thyroid cancer: current molecular perspectives. 209
Molecular genetics in primary hyperparathyroidism: the role of genetic tests in differential diagnosis, disease prevention strategy, and therapeutic planning. A 2017 update 203
MEN1 in children and adolescents: Data from patients of a regional referral center for hereditary endocrine tumors 198
Prevalence of osteoporosis in the Italian population and main risk factors: results of BoneTour Campaign. 192
Correction of vitamin D status by calcidiol: pharmacokinetic profile, safety, and biochemical effects on bone and mineral metabolism of daily and weekly dosage regimens 189
Correction to: Multiple endocrine neoplasia type 1: analysis of germline MEN1 mutations in the Italian multicenter MEN1 patient database. 183
The LARO-MEN1 study: a longitudinal clinical experience with octreotide Long-Acting Release in patients with Multiple Endocrine Neoplasia type 1 Syndrome 182
Clinical guidelines for the prevention and treatment of osteoporosis: summary statements and recommendations from the Italian Society for Orthopaedics and Traumatology 165
Calcium Intake in Bone Health: A Focus on Calcium-Rich Mineral Waters 160
When Parathyroidectomy Should Be Indicated or Postponed in Adolescents With MEN1-Related Primary Hyperparathyroidism 157
Total and Subtotal Parathyroidectomy in Young Patients With Multiple Endocrine Neoplasia Type 1-Related Primary Hyperparathyroidism: Potential Post-surgical Benefits and Complications 151
A novel germline inactivating mutation in the CASR gene in an Italian kindred affected by familial hypocalciuric hypercalcemia. 141
Characterization of a novel CDC73 gene mutation in a hyperparathyrodism-jaw tumor patient affected by parathyroid carcinoma in the absence of somatic loss of heterozygosity. 135
Multiple endocrine neoplasia type 1: extensive analysis of a large database of Florentine patients 125
Blomstrand’s chondrodysplasia 120
Germline mutations in MEN1 and BRCA1 genes in a woman with familial multiple endocrine neoplasia type 1 and inherited breast-ovarian cancer syndromes: a case report. 110
Genetic predictors of skeletal outcomes in healthy fertile women: The Bonturno Study. 106
Multiple endocrine neoplasia type 1 (MEN1): not only inherited endocrine tumors. 106
Multiple endocrine neoplasia type 1: analysis of germline MEN1 mutations in the Italian multicenter MEN1 patient database 101
Common susceptibility alleles and SQSTM1 mutations predict disease extent and severity in a multinational study of patients with Paget's disease. 100
Hereditary hyperparathyroidism syndromes. 94
DNA-based test: when and why to apply it to primary hyperparathyroidism clinical phenotypes 87
Correction of vitamin D status by calcidiol: pharmacokinetic profile, safety, and biochemical effects on bone and mineral metabolism of daily and weekly dosage regimens: response to comments by Chen et al. 85
Genetic test in multiple endocrine neoplasia type 1 syndrome: An evolving story. 84
Human Preosteoblastic Cell Culture from a Patient with Severe Tumoral Calcinosis-Hyperphosphatemia Due to a New GALNT3 Gene Mutation: Study of In Vitro Mineralization. 83
Osteonecrosis of the Jaw In A Patient With Rheumatoid Artritis Treated With An Oral Aminobisphosphonate: A Clinical Case Report 79
Cinacalcet therapy in patients affected by primary hyperparathyroidism associated to Multiple Endocrine Neoplasia Syndrome type 1 (MEN1) 78
Calcolosi renale recidivante: una nnuova mutazione del gene codificante il recettore del calcio( CASR) 75
Un particolare caso di iperparatiroidismo primitivo giovanile 70
Osteonecrosis of the jaw in a patient with rheumatoid artritis treated with an oral aminobisphosphonate: a clinical case report. 68
Molecular diagnosis of parathyroid carcinoma: a reality in the near future. 67
Prevalence of Osteoporosis and Risk Factors For Bone Demineralization In Italy: First Results From the Firmo Study 62
A heterozygous frameshift mutation in exon 1 of CDKN1B gene in a patient affected by MEN4 syndrome. 60
CYP19 and ESR1 gene polymorphisms: response of the bone mineral density in post-menopausal women to hormonal replacement therapy 59
Gastroenteropancreatic Neuroendocrine Tumors in Multiple Endocrine Neoplasia Type 1 58
Variazioni molecolari del gene codificante la fosfatasi alcalina: correlazione con la massa ossea (BMD) e i markers biochimici di turnover osseo 58
Sarcomatoid carcinoma of the kidney in a MEN1 patient: Case report and genetic profile. 57
Primary hyperparathyroidism in multiple endocrine neoplasia type 1: when to perform surgery? 56
Haplotype analysis of two pairs of unrelated Italian families affected by Paget's disease of bone, exhibiting different geographical origins and two different mutations of p62/sequestosomel gene, supports the evidence for common founders. 51
Fracture unit: a (possible) model of implementation in Italy. 51
Soft tissue postraumatic calcifications associated with a new FGF23 gene mutation: clinicopathological and molecular genetic study 50
Multiple Endocrine Neoplasia Type 1 50
A New Fgf23 Gene Polymorphism: Possible Role In the Pathogenesis of the Development of Extraskeletal Calcifications? 49
Efficacy of Cinacalcet Therapy In Patients Affected By Primary Hyperparathyroidism Associated To Multiple Endocrine Neoplasia Syndrome Type 1 (men1): Preliminary Results of the Florentine Study 49
THE EFFECTS OF RH-PTH (1-34) ON BONE METABOLISM IN HYPOPARATHYROID PATIENTS 49
Carcinoma mammario e osteoporosi: risultati preliminari di uno studio fiorentino 47
Construction of a database for the evaluation and the clinical management of patients with breast cancer treated with antiestrogens and/or aromatase inhibitors. 46
Un nuovo caso di sclerosi ossea: osteopochilosi 43
CALCIFICATIONS IN DERMATOMYOSITIS: A CLINICAL CASE WITH AN ALTERATION OF PHOSPHATE HOMEOSTASIS, CARRIER OF A NEW FGF23 GENE MUTATION 40
[Left laparoscopic adrenalectomy for pheochromocytoma in MEN 2B: case report]. 40
Prevalenza dell'osteoporosi e dei principale fattori di rischio nella popolazione italiana: risultiati del BOne tour 2012 38
Osteogenesis Imperfecta: Realization of A Multidisciplinar Network To Improve Information, Expertise and Resources 37
Genotype-Phenotype Correlation Analyses in an Italian MEN1 Series. MEN1 Gene Mutational Performed at the Center for Hereditary Endocrine Tumors of Florence 37
A NOVEL TISSUE-NONSPECIFIC ISOENZYME OF ALKALINE PHOSPHATASE (TNSALP) MUTATION IN ADULT PATIENT WITH LOW BONE MASS AND MUSCULOSKELETAL SYMPTOMS 35
ALPL genotypes in patients with atypical femur fractures or other biochemical and clinical signs of hypophosphatasia 34
Tricho-rhino-phalangeal syndrome: role of different methods of measuring bone density 33
Association between vitamin D and bisphenol A levels in an elderly Italian population: results from the InCHIANTI study 32
Circulating MicroRNAs as Biomarkers of Osteoporosis and Fragility Fractures 28
Genetic Determinants of inherited endocrine tumors: do they have a direct role in bone metabolism regulation and osteoporosis? 26
RETROSPECTIVE COHORT STUDY OF PATIENTS AFFECTED BY CHRONIC HYPOPARATHYROIDISM 19
Endocrine sequelae of hematopoietic stem cell transplantation: Effects on mineral homeostasis and bone metabolism 16
Calcifediol: mechanisms of action 15
Oxidative Stress and Inflammation in Osteoporosis: Molecular Mechanisms Involved and the Relationship with microRNAs 11
Pancreatic neuroendocrine tumors in MEN1 patients: difference in post-operative complications and tumor progression between major and minimal pancreatic surgeries 9
Calcifediol: Why, When, How Much? 6
High frequency of heterozygous rare variants of the SLC34A1 and SLC9A3R1 genes in patients with atypical femur fracture 3
Totale 6.157
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Categoria #
all - tutte 15.721
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 15.721
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019446 0 0 0 0 0 0 0 0 0 0 243 203
2019/20201.610 122 132 66 108 220 170 169 190 159 110 139 25
2020/2021959 73 102 23 109 50 87 58 139 84 132 48 54
2021/2022453 15 41 30 21 23 15 21 38 18 28 74 129
2022/20231.178 117 265 39 86 83 200 140 58 134 11 23 22
2023/2024560 12 50 80 22 23 81 35 216 10 14 17 0
Totale 6.157