SFERA Archivio dei prodotti della Ricerca dell'Università di Ferrara

CALZOLARI, Elisa
 Distribuzione geografica
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Continente #
NA - Nord America 5.180
EU - Europa 4.013
AS - Asia 2.746
SA - Sud America 344
AF - Africa 61
OC - Oceania 10
Totale 12.354
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Nazione #
US - Stati Uniti d'America 5.059
IT - Italia 2.344
SG - Singapore 1.039
CN - Cina 706
DE - Germania 469
VN - Vietnam 337
UA - Ucraina 295
BR - Brasile 261
HK - Hong Kong 204
GB - Regno Unito 199
TR - Turchia 151
FI - Finlandia 137
NL - Olanda 124
SE - Svezia 96
RU - Federazione Russa 94
FR - Francia 90
IN - India 68
CA - Canada 67
JP - Giappone 57
MX - Messico 40
BE - Belgio 36
BD - Bangladesh 31
TH - Thailandia 26
ZA - Sudafrica 26
ES - Italia 25
AR - Argentina 23
IQ - Iraq 22
PL - Polonia 19
EC - Ecuador 15
LT - Lituania 15
ID - Indonesia 14
CO - Colombia 12
IR - Iran 12
CZ - Repubblica Ceca 11
SA - Arabia Saudita 11
CL - Cile 10
IE - Irlanda 10
PY - Paraguay 9
VE - Venezuela 9
AU - Australia 8
CH - Svizzera 8
JO - Giordania 8
UZ - Uzbekistan 8
AE - Emirati Arabi Uniti 7
AT - Austria 7
KE - Kenya 7
PH - Filippine 7
ET - Etiopia 6
PK - Pakistan 6
PT - Portogallo 6
KZ - Kazakistan 5
MA - Marocco 5
TN - Tunisia 5
BY - Bielorussia 4
GR - Grecia 4
MY - Malesia 4
AL - Albania 3
CR - Costa Rica 3
DO - Repubblica Dominicana 3
EG - Egitto 3
GE - Georgia 3
HU - Ungheria 3
OM - Oman 3
PS - Palestinian Territory 3
RS - Serbia 3
UY - Uruguay 3
AZ - Azerbaigian 2
DZ - Algeria 2
GA - Gabon 2
JM - Giamaica 2
KG - Kirghizistan 2
LV - Lettonia 2
MD - Moldavia 2
NG - Nigeria 2
NP - Nepal 2
QA - Qatar 2
RO - Romania 2
SY - Repubblica araba siriana 2
TT - Trinidad e Tobago 2
BB - Barbados 1
BG - Bulgaria 1
BO - Bolivia 1
BW - Botswana 1
CI - Costa d'Avorio 1
DM - Dominica 1
FJ - Figi 1
GY - Guiana 1
HN - Honduras 1
HR - Croazia 1
KH - Cambogia 1
KR - Corea 1
LK - Sri Lanka 1
ME - Montenegro 1
MK - Macedonia 1
MN - Mongolia 1
NZ - Nuova Zelanda 1
PA - Panama 1
SK - Slovacchia (Repubblica Slovacca) 1
TG - Togo 1
Totale 12.354
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Città #
Singapore 687
Ashburn 582
Woodbridge 458
Fairfield 439
San Jose 319
Beijing 273
Houston 272
Chandler 264
Ann Arbor 258
Jacksonville 257
Milan 224
Hong Kong 200
Santa Clara 194
Seattle 174
Rome 168
Cambridge 166
Wilmington 163
Los Angeles 112
Ho Chi Minh City 108
Munich 95
Izmir 82
Hanoi 79
Nanjing 79
Naples 78
New York 65
Dallas 56
Tokyo 54
Princeton 51
Buffalo 49
Helsinki 44
Boardman 42
Turin 42
Lauterbourg 40
The Dalles 39
Falkenstein 38
Addison 36
San Diego 36
Turku 36
Palermo 35
Brussels 34
Catania 34
Shanghai 34
Bari 31
Orem 31
Florence 30
London 30
São Paulo 30
Hefei 26
San Mateo 26
Bangkok 25
Bremen 25
Da Nang 25
Mexico City 25
Bologna 23
Shenyang 23
Verona 23
Tianjin 22
Brescia 21
Toronto 21
Montreal 20
Chennai 19
Falls Church 19
Chicago 18
Hebei 18
Padova 18
Brooklyn 17
Denver 17
Johannesburg 17
Redwood City 16
Carbonera 14
Nanchang 14
Ottawa 14
Warsaw 14
Haiphong 13
Venice 13
Baghdad 12
Dearborn 12
Ferrara 12
Boston 11
Changsha 11
Frankfurt am Main 11
Philadelphia 11
Stockholm 11
Atlanta 10
Groningen 10
Jiaxing 10
Messina 10
Phoenix 10
Salerno 10
Washington 10
Genoa 9
Iesi 9
Modena 9
Nola 9
Hải Dương 8
Manchester 8
Mountain View 8
Reggio Emilia 8
Tashkent 8
Trieste 8
Totale 7.439
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Nome #
Mutazione Q283P nel gene HFE in un eterozigote C282Y affetto da emocromatosi. 1.621
Genetica della labiopalatoschisi non sindromica: ruolo di polimorfismi del metabolismo dei folati e dell’omocisteina. 994
Associazione tra il polimorfismo c.66A>G del gene MTRR e la palatoschisi non-sindromica. 320
Trisomy 15 mosaicism owing to familial reciprocal translocation t(1;15): Implication for prenatal diagnosis 294
In vitro short-term test evaluation of catecholestrogens genotoxicity 270
FISH screening for subtelomeric rearrangements in 219 patients with idiopathic mental retardation and normal karyotype. 252
Characterization of a deleted Y chromosome in a male with Turner stigmata 251
G.P.12.06 A comprehensive molecular characterisation of dystrophinopathies 244
Intronic breakpoint definition and transcription analysis in DMD/BMD patients with deletion/duplication at the 5′ mutation hot spot of the dystrophin gene 239
Mole maker phenotype: possible narrowing of the candidate region. 225
Occurrence of Del(GIB6-D13S1830) mutation in Italian non-syndromic hearing loss patients carrying a single GJB2 mutated allele 224
Transthyretin RNA profiling in livers from transplanted patients affected by familial amyloidotic polyneuropathy, and identification of a dual transcription start point 223
A two-locus model for non-syndromic congenital dysplasia of the hip (CDH) 221
Mutation analysis of the MECP2 gene in British and Italian Rett syndrome females 217
Prenatal genetic counseling referrals for advanced maternal age: still room for improvement. 216
Analisi del polimorfismo IVS2+4T>C del gene HFE in soggetti con sovraccarico di ferro. 213
Commercial kit-based diagnosis is not enough for prenatal testing of beta-thalassemia: pitfalls in diagnostic mutation analysis raises the need for reference laboratories 210
EUROCAT and orofacial clefts: The epidemiology of orofacial clefts in 30 european regions 208
Psychiatric disorder in a familial 15;18 translocation and sublocalization of myelin basic protein of 18q22.3 208
Clinical anophthalmos in a family 207
Exclusion of COL2A1 and VDR as Developmental Dysplasia of the Hip Genes 204
Nonhomologous Robertsonian translocations (NHRTs) and uniparental disomy (UPD) risk: An Italian multicentric prenatal survey 203
MECP2 gene mutation analysis in the British and Italian Rett Syndrome patients: hot spot map of the most recurrent mutations and bioinformatic analysis of a new MECP2 conserved region 200
Exploring the clinical and epidemiological complexity of GJB2-linked deafness 197
Epidemiology of cleft palate in Europe: Implications for genetic research 195
Prenatal diagnosis of a de novo satellited chromosome 18 (18ps) associated with 18p deletion 194
Association between the c.66A>G variant in the Methionine Synthase reductase and nonsyndromic cleft palate. 185
CHARACTERIZATION OF THE PSEUDOGENIC REGION OF VON WILLEBRAND FACTOR BY MOLECULAR CLONING AND "IN SITU" HYBRIDIZATION 181
Genomic definition of a pure intronic dystrophin deletion responsible for an XLDC splicing mutation: In vitro mimicking and antisense modulation of the splicing abnormality 175
Prenatal diagnosis of a complete mole coexisting with a dichorionic twin pregnancy: Case report 171
Comparison of two statistical techniques for the surveillance of birth defects through a Monte Carlo simulation 167
Cloning and chromosome localization of the gene for the methenyltratrahydrofolate-synthetase 166
Localization of cloned human DNA sequences and analysis of chromosomal alteration by in situ hybridization 165
Progress in understanding GJB2-linked deafness 159
Analisi dei genotipi ed aplotipi HFE nella popolazione Ferrarese 157
Screening of mutations in the CFTR gene in 1195 couples entering assisted reproduction technique programs. 152
Frequenze genotipiche ed aplotipiche HFE nella popolazione della Provincia di Ferrara 149
G.P.3.02 In vivo biodistribution of non-viral systems for oligoribonucleotides delivery 143
Cytogenetic and array CGH characterization of an intrachromosomal complex rearrangement of 4q in a patient with a 4q-phenotype. 140
Biosensor technology for real-time detection of the cystic fibrosis W1282X mutation in CFTR 136
null 131
Schisi facciale e genetica dei folati 129
Inferences on the inheritance of congenital anomalies from temporal and spatial patterns of occurrence 129
Cystathionine beta-synthase c.844ins68 gene variant and non-syndromic cleft lip and palate. 128
null 125
Una nuova mutazione del gene HFE in un eterozigote C282Y con emocromatosi. 120
Epidemiologia e genetica delle schisi orofacciali 119
CHARACTERIZATION OF THE PSEUDOGENIC AND GENIC HOMOLOGOUS REGIONS OF VON WILLEBRAND FACTOR 118
Genomic and transcription studies as diagnostic tools for a prenatal detection of X-linked dilated cardiomyopathy due to a dystrophin gene mutation. 110
Mental retardation (MR) and coagulation factor XI deficiency in two first cousins once removed: a new X-linked syndrome? 107
null 100
Congenital heart defects: 15 Years of experience of the Emilia-Romagna Registry (Italy) 99
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Idiopathic central retinal vein occlusion in a thrombophilic patient with the heterozygous 20210 G/A prothrombin genotype 93
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Are omphalocele and neural tube defects related congenital anomalies?: Data from 21 registries in Europe (EUROCAT) 79
null 78
Multiple exon skipping and RNA circularisation contribute to the severe phenotypic expression of exon 5 dystrophin deletion. 71
Totale 12.405
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Categoria #
all - tutte 41.384
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 749
Totale 42.133
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021267 0 0 0 0 0 0 0 0 0 85 127 55
2021/2022779 32 63 86 39 45 34 46 33 32 54 67 248
2022/2023850 62 89 33 96 116 97 57 81 96 22 57 44
2023/2024945 79 69 53 32 65 116 70 59 56 92 92 162
2024/20252.245 126 123 166 199 259 189 104 100 299 183 284 213
2025/20263.821 425 161 370 477 648 285 558 206 369 322 0 0
Totale 12.405