CATALOGO DEI PRODOTTI DELLA RICERCA

ANTONIAZZI, Franco
 Distribuzione geografica
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Continente #
NA - Nord America 11.508
EU - Europa 9.412
AS - Asia 6.917
SA - Sud America 957
AF - Africa 121
OC - Oceania 41
Continente sconosciuto - Info sul continente non disponibili 14
Totale 28.970
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Nazione #
US - Stati Uniti d'America 11.332
SG - Singapore 2.727
GB - Regno Unito 2.560
CN - Cina 2.324
IT - Italia 1.564
DE - Germania 901
SE - Svezia 822
BR - Brasile 817
RU - Federazione Russa 751
HK - Hong Kong 738
FR - Francia 709
FI - Finlandia 697
IE - Irlanda 694
VN - Vietnam 283
UA - Ucraina 244
KR - Corea 215
ID - Indonesia 103
NL - Olanda 101
TR - Turchia 94
CA - Canada 91
JP - Giappone 89
IN - India 84
BE - Belgio 74
AT - Austria 53
PL - Polonia 50
ES - Italia 46
MX - Messico 44
AR - Argentina 43
BD - Bangladesh 37
AU - Australia 36
ZA - Sudafrica 28
EC - Ecuador 26
IR - Iran 25
PK - Pakistan 25
IQ - Iraq 24
MA - Marocco 24
CH - Svizzera 21
PE - Perù 16
TG - Togo 16
UZ - Uzbekistan 16
AE - Emirati Arabi Uniti 15
CO - Colombia 15
EG - Egitto 13
NO - Norvegia 13
SA - Arabia Saudita 13
CL - Cile 12
LT - Lituania 12
PH - Filippine 12
TW - Taiwan 12
LV - Lettonia 11
PY - Paraguay 11
CZ - Repubblica Ceca 10
NG - Nigeria 10
RO - Romania 10
IL - Israele 9
KE - Kenya 9
MY - Malesia 9
PT - Portogallo 9
VE - Venezuela 9
AZ - Azerbaigian 8
GR - Grecia 8
JM - Giamaica 8
JO - Giordania 8
BG - Bulgaria 7
DK - Danimarca 7
KG - Kirghizistan 7
PA - Panama 7
EU - Europa 6
HU - Ungheria 6
MD - Moldavia 6
TN - Tunisia 6
A2 - ???statistics.table.value.countryCode.A2??? 5
AL - Albania 5
DO - Repubblica Dominicana 5
DZ - Algeria 5
LB - Libano 5
NZ - Nuova Zelanda 5
OM - Oman 5
BO - Bolivia 4
EE - Estonia 4
HR - Croazia 4
NI - Nicaragua 4
SV - El Salvador 4
TH - Thailandia 4
CI - Costa d'Avorio 3
CR - Costa Rica 3
KW - Kuwait 3
LK - Sri Lanka 3
MK - Macedonia 3
NP - Nepal 3
SK - Slovacchia (Repubblica Slovacca) 3
UY - Uruguay 3
XK - ???statistics.table.value.countryCode.XK??? 3
AM - Armenia 2
AO - Angola 2
BS - Bahamas 2
CU - Cuba 2
GT - Guatemala 2
KZ - Kazakistan 2
LA - Repubblica Popolare Democratica del Laos 2
Totale 28.942
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Città #
Southend 2.119
Jacksonville 1.828
Chandler 1.530
Singapore 1.349
Dallas 1.188
Woodbridge 848
Hong Kong 727
Ashburn 691
Dublin 686
Ann Arbor 588
Verona 452
Beijing 386
Houston 376
Wilmington 276
Princeton 266
Lawrence 265
New York 228
Los Angeles 218
Nanjing 193
Jinan 190
Munich 169
Shenyang 152
Helsinki 148
Sindelfingen 137
Buffalo 136
Milan 129
Hebei 109
Lancaster 98
The Dalles 95
Turku 92
Tianjin 87
Jakarta 86
Dong Ket 82
Boardman 79
Changsha 76
Tokyo 76
São Paulo 71
Columbus 70
Brussels 69
Nanchang 68
Seoul 64
Zhengzhou 61
Bologna 60
Ningbo 59
Guangzhou 58
Santa Clara 56
Council Bluffs 55
Redondo Beach 55
Hangzhou 53
Haikou 49
Jiaxing 47
Seattle 46
Taiyuan 46
Ho Chi Minh City 44
San Francisco 44
Rome 43
Nuremberg 40
Taizhou 40
Frankfurt am Main 38
Redmond 36
Norwalk 34
Moscow 33
Vienna 33
London 32
Düsseldorf 30
Auburn Hills 29
Hanoi 28
Lappeenranta 28
Toronto 27
Rio de Janeiro 26
Fairfield 25
Redwood City 25
Turin 23
Warsaw 23
Fuzhou 22
Lanzhou 22
Boston 21
Brooklyn 21
Washington 21
Amsterdam 20
Dearborn 20
Stockholm 19
Falls Church 18
Phoenix 18
Brasília 17
Meda 17
Naples 17
Lomé 16
Mexico City 16
Tashkent 16
Chennai 15
Detroit 15
Kent 15
Madrid 15
Saint Louis 15
Belo Horizonte 14
Edinburgh 14
Johannesburg 14
Melbourne 14
Montreal 14
Totale 18.269
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Nome #
Growth hormone and early treatment. 268
Disturbi respiratori del sonno in bambini affetti da acondroplasia 252
Snoring in a cohort of obese children: association with palate position and nocturnal desaturations 232
Un insolito caso di ipercalcemia associato a una mutazione del gene RET. 222
A base substitution at IVS-19 3'-end splice junction causes exon 20 skipping in pro alpha 2(I) collagen mRNA and produces mild osteogenesis imperfecta 219
Apparent Mineralocorticoid Excess by a Novel Mutation and Epigenetic Modulation by HSD11B2 Promoter Methylation 201
A base substitution at IVS-19 3' splice junction causes exon 20 skipping in pro alpha 2(I) collagen mRNA and produces mild osteogenesis imperfecta 178
A de novo G to T transversion in a pro-alpha 1(I) collagen gene for a moderate case of osteogenesis imperfecta. Substitution of cysteine for glycine 178 in the triple helical domain 176
A novel splicing mutation in FKBP10 causing osteogenesis imperfecta with a possible mineralization defect 171
Diagnostic pitfalls in the assessment of congenital hypopituitarism. 168
[OP.6A.07] SLEEP DISORDERED BREATHING IS ASSOCIATED WITH BLOOD PRESSURE AND CAROTID ARTERIAL STIFFNESS IN A SAMPLE OF OBESE CHILDREN 165
A Novel Splicing Mutation in FKBP10 in a patient with a moderate Osteogenesis Imperfecta histologically classificable as type VI 160
Age at Menarche (MA) in chronic diseases: celiac disease (CD), insulin-dependent diabetes (T1DM) and growth hormone deficiency (GHD). 160
La pubertà precoce 158
Sviluppo puberale e fertilità nei soggetti con deficit combinato di ormone della crescita e gonadotropine 156
Analysis of the d3-growth hormone receptor polymorphism in large cohorts of small, appropriate and large for gestational age newborns. 156
SLEEP-DISORDERED BREATHING IN CHILDREN WITH RECURRENT WHEEZING/ASTHMA: A SINGLE CENTRE STUDY 153
Lack of expression of SERPINF1, the gene coding for pigment epithelium derived factor, causes progressively deforming Osteogenesis Imperfecta with normal type I collagen 151
Type VI Osteogenesis imperfecta: effect of plasma transfusion on bone metabolism 145
Treatment with neridronate in children and adolescents with osteogenesis imperfecta: Data from open-label, not controlled, three-year Italian study 145
Isochromosome Yp in a boy with Hypogonadotropic Hypogonadism, Gynaecomastia and short stature 144
A novel de novo partial xq duplication in a girl with short stature, nonverbal learning disability and diminished ovarian reserve - effect of growth hormone treatment and fertility preservation strategies: a case report and up-to-date review 144
Effetti del trattamento con GH sui Biomarker Auxologici e Metabolici: Esperienza della Clinica pediatrica, Università di Verona 143
Etiology and age incidence of precocious puberty in girls: a multicentric study 143
Bone development during GH and GnRH analog treatment 142
A potential role of RUNX2- RUNT domain in modulating the expression of genes involved in bone metastases: an in vitro study with melanoma cells 142
21-Hydroxylase-Deficient congenital adrenal hyperplasia classic form therapy knowledge and management: targeted educational intervention for paediatricians 142
Effects of COVID-19 lockdown on lifestyle behaviors in children with obesity: Longitudinal study update 142
Defects of SERPINF1 cause progressively deforming recessive osteogenesis imperfecta with normal Collagen I 141
Idiopathic Juvenile Osteoporosis: Clinical Experience from a Single Centre and Screening of LRP5 and LRP6 Genes 140
A surprising Case of Premature Thelarche after an anti-fungal therapy 137
Ambulatory clinical parameters and sleep respiratory events in a group of obese children unselected for respiratory problems 137
The Runt domain of RUNX2 induces the migration of melanoma cells to bone 137
Bone mineral metabolism in girls with precocious puberty during gonadotrophin-releasing hormone agonist treatment 135
Altered bone metabolism in children infected with human immunodeficiency virus. 135
Worldwide Interest in Vitamin D, Negative Effects on Kidneys, and Bone Density: Analysis of Google Trends Data 133
idiopathic Central Precocious Puberty (ICPP) and Maternal Attachment Security 133
SNORING IN OBESE CHILDREN AND ITS CLINICAL SIGNIFICANCE IN AMBULATORY SETTING 133
Growth Hormone in Combination with Bisphosphonate Treatment in Osteogenesis Imperfecta. 130
Hypercalciuria and renal function and in children affected by osteogenesis imperfecta 130
Lung Function in Women with Idiopathic Central Precocious Puberty: A Pilot Study
 130
Runx2 stimulates neoangiogenesis through the Runt domain in melanoma 129
Tumore del testicolo a cellule di Leydig 128
Hypovitaminosis D and nocturnal hypertension in obese children: an interesting link. 128
3-hydroxyacyl-coenzyme a dehydrogenase deficiency: identification of a new mutation causing hyperinsulinemic hypoketotic hypoglycemia, altered organic acids and acylcarnitines concentrations. 127
The recurrent causal mutation for osteogenesis imperfecta type V occurs at a highly methylated CpG dinucleotide within the IFITM5 gene 126
Oftalmopatia nella malattia di Basedow infantile 125
How to cope with a severe skeletal dysplasia 125
SLEEP RESPIRATORY EVENTS AND CLINICAL PARAMETERS AND IN A GROUP OF OBESE CHILDREN 125
Clinical pitfalls in the diagnosis of segmental overgrowth syndromes: a child with the c.2740G > A mutation in PIK3CA gene 125
45,X/46,X,i(Yp): Importance of Assessment and Support during Puberty and Adolescence 124
A strange picture of karyotype and good response to higher dosage of GH 123
Cantú syndrome: A new case and evolution of clinical conditions during first 2-year follow-up 122
[Acceleration of pubertal development] 122
Clinical and radiographic delineation of odontochondrodysplasia 122
Osteogenesis imperfecta. 122
Significant association among growing pains, vitamin D supplementation, and bone mineral status: results from a pilot cohort study. 122
Individual fatty acids in erythrocyte membranes are associated with several features of the metabolic syndrome in obese children 122
Graves' ophthalmopathy evolution studied by MRI during childhood and adolescence. 121
Sleep-disordered breathing is associated with blood pressure and carotid arterial stiffness in obese children 121
Short stature: an ordinary sign for an unordinary diagnosis 121
Osteogenesi Imperfetta 120
Possible role of CYP450 Generated Omega-3/Omega-6 PUFA metabolites in the modulation of blood pressure and vascular function in obese children 120
Molecular screening in OI patients at Verona reference center: typical mutations 119
Osteogenesis Imperfecta: clinical, biochemical and molecular findings 119
Bone mineral status in children with growing pains: a pilot study 119
Effects of COVID-19 Lockdown on Lifestyle Behaviors in Children with Obesity Living in Verona, Italy: A Longitudinal Study 119
The SHOX Gene and The Short Stature. Roundtable On Diagnosis and Treatment of Short Stature Due To SHOX Haploinsufficiency: How Genetics, Radiology And Anthropometry Can Help The Pediatrician in The Diagnostic Process Padova 118
New Insights into the Runt Domain of RUNX2 in Melanoma Cell Proliferation and Migration 118
Osteogenesis Imperfecta: Practical treatment guidelines 116
Bone mass at final height in precocious puberty after gonadotropin-releasing hormone agonist with and without calcium supplementation. 116
Isochromosome Yp in a boy with Hypogonadotropic Hypogonadism, Gynaecomastia and short stature 116
Genotype in the diagnosis of 21-hydroxylase deficiency: who should undergo CYP21A2 analysis? 116
[Bone mass formation in childhood and risk of osteoporosis] 115
BISPHOSPHONATE TREATMENT IN INFANTS WITH SEVERE OSTEOGENESIS IMPERFECTA 115
Are children affected by osteogenesis imperfecta and treated with bisphosphonates at greater risk of osteonecrosis in jaws? 114
Bone Mineral status in children with growing pains: a pilot study 114
Early bisphosphonate treatment in infants with severe osteogenesis imperfecta. 114
Idiopathic Central Precocious Puberty (ICPP), Adulth lung function and Asthma 114
[Somatotropin function in term and premature newborns during the first month of life] 113
PEAK BONE MASS AND BODY COMPOSITION IN PRECOCIOUS PUBERTY AFTER GNRH AGONIST THERAPY WITH AND WITHOUT CALCIUM SUPPLEMENTATION 113
LH RESPONSE TO D-TRP-LHRH ANALOGUE IN EARLY DIAGNOSIS OF MALE DELAY OF PUBERTY 112
[Endocrine-gynecological problems in female adolescents] 112
GNRH analogue treatment and decrease of bone mass density (BMD) in a patient with osteogenesis imperfecta (OI) and central precocious puberty (CPP). 112
case of heterokaryotic monozygotic twins discordant for turner syndrome diagnosed with amniocentesis 112
Thyreoglobulin secretion in hypothyroidism infants 111
Influence of thyroid morphology on psychomotor development in patients with congenital hypothyroidism during 8 year follow-up 110
Children with premature pubarche: is an alterated neonatal 17-Ohp screening test a predictive factor? 110
[Delayed puberty] 109
Body composition after discontinuation of growth hormone (GH) in GH deficiency (GHD). 109
Positive effects of cyclic administration of intravenous neridronate in growing patients with osteogenesis imperfecta 109
Identification of a novel pax8 gene sequence variant in four members of the same family: from congenital hypothyroidism with thyroid hypoplasia to mild subclinical hypothyroidism 109
Fatty Acid Profile and Desaturase Activities in 7-10-Year-Old Children Attending Primary School in Verona South District: Association between Palmitoleic Acid, SCD-16, Indices of Adiposity, and Blood Pressure 109
Free urinary cortisol in obese children 108
[Normal pubertal development] 108
Use of the gonadotropin-releasing hormone agonist triptorelin in the diagnosis of delayed puberty in boys 108
CALCIUM SUPPLEMENTATION, OESTROGENS AND BONE DENSITY IN GNRHA TREATED PRECOCIOUS PUBERTY 108
Determination of thyroxine in the hair of newborns by radioimmunoassay with high-performance liquid chromatographic confirmation 108
Condrodisplasie e mucopolisaccaridosi. Fisipopatologia, Clinica e Terapia 108
Idiopathic juvenile osteoporosis and vitamin D insufficiency 108
Totale 13.417
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Categoria #
all - tutte 109.308
article - articoli 95.543
book - libri 0
conference - conferenze 10.244
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 3.521
Totale 218.616
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20211.884 0 0 0 264 349 276 57 193 196 70 276 203
2021/20222.032 184 596 26 153 57 45 26 126 59 56 193 511
2022/20234.480 339 449 413 721 398 1.025 56 261 559 42 156 61
2023/20242.876 108 215 283 306 325 373 231 178 26 235 388 208
2024/20256.392 392 485 262 1.136 307 228 337 306 853 380 550 1.156
2025/20263.580 1.166 792 1.427 195 0 0 0 0 0 0 0 0
Totale 29.271