SFERA Archivio dei prodotti della Ricerca dell'Università di Ferrara

CALZOLARI, Elisa
 Distribuzione geografica
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Continente #
NA - Nord America 4.598
EU - Europa 3.734
AS - Asia 2.077
SA - Sud America 251
AF - Africa 33
OC - Oceania 5
Totale 10.698
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Nazione #
US - Stati Uniti d'America 4.497
IT - Italia 2.219
SG - Singapore 846
CN - Cina 660
DE - Germania 459
UA - Ucraina 290
BR - Brasile 214
HK - Hong Kong 185
GB - Regno Unito 184
TR - Turchia 133
FI - Finlandia 120
NL - Olanda 108
VN - Vietnam 99
SE - Svezia 94
RU - Federazione Russa 86
CA - Canada 61
FR - Francia 40
BE - Belgio 35
MX - Messico 33
IN - India 29
TH - Thailandia 25
JP - Giappone 23
ES - Italia 22
ZA - Sudafrica 21
BD - Bangladesh 17
PL - Polonia 17
ID - Indonesia 13
IR - Iran 12
AR - Argentina 11
CZ - Repubblica Ceca 10
LT - Lituania 10
CH - Svizzera 8
AT - Austria 7
IE - Irlanda 7
IQ - Iraq 6
PY - Paraguay 6
CL - Cile 5
EC - Ecuador 5
PT - Portogallo 5
VE - Venezuela 5
AE - Emirati Arabi Uniti 4
AU - Australia 4
JO - Giordania 4
KZ - Kazakistan 4
BY - Bielorussia 3
CO - Colombia 3
HU - Ungheria 3
SA - Arabia Saudita 3
CR - Costa Rica 2
ET - Etiopia 2
GA - Gabon 2
GR - Grecia 2
KE - Kenya 2
MA - Marocco 2
MD - Moldavia 2
MY - Malesia 2
PK - Pakistan 2
PS - Palestinian Territory 2
AL - Albania 1
AZ - Azerbaigian 1
BB - Barbados 1
BO - Bolivia 1
CI - Costa d'Avorio 1
DO - Repubblica Dominicana 1
DZ - Algeria 1
EG - Egitto 1
HN - Honduras 1
KG - Kirghizistan 1
KR - Corea 1
LK - Sri Lanka 1
MK - Macedonia 1
NG - Nigeria 1
NP - Nepal 1
NZ - Nuova Zelanda 1
PA - Panama 1
PH - Filippine 1
QA - Qatar 1
RO - Romania 1
TT - Trinidad e Tobago 1
UY - Uruguay 1
UZ - Uzbekistan 1
Totale 10.698
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Città #
Singapore 504
Ashburn 467
Woodbridge 458
Fairfield 439
Houston 272
Chandler 264
Beijing 262
Ann Arbor 258
Jacksonville 257
Milan 214
Santa Clara 189
Hong Kong 184
Seattle 174
Cambridge 166
Wilmington 163
Rome 161
Los Angeles 103
Munich 95
Izmir 81
Nanjing 78
Naples 74
New York 60
Dallas 54
Princeton 51
Buffalo 48
Boardman 42
Turin 42
Falkenstein 38
Addison 36
San Diego 36
Turku 36
Catania 34
Palermo 34
Shanghai 34
Brussels 33
Bari 31
Ho Chi Minh City 31
Florence 30
Helsinki 29
London 27
São Paulo 27
Hanoi 26
Hefei 26
San Mateo 26
Bangkok 25
Bremen 25
Mexico City 24
Shenyang 23
Verona 23
Bologna 22
Brescia 21
Tianjin 21
Tokyo 21
The Dalles 20
Toronto 20
Falls Church 19
Hebei 18
Padova 18
Chicago 17
Brooklyn 16
Montreal 16
Redwood City 16
Denver 15
Carbonera 14
Nanchang 14
Johannesburg 13
Ottawa 13
Venice 13
Chennai 12
Dearborn 12
Ferrara 12
Warsaw 12
Changsha 11
Philadelphia 11
Boston 10
Groningen 10
Jiaxing 10
Messina 10
Salerno 10
Iesi 9
Nola 9
Stockholm 9
Washington 9
Atlanta 8
Genoa 8
Mountain View 8
Orem 8
Phoenix 8
Trieste 8
Vicenza 8
Caserta 7
Da Nang 7
Frankfurt am Main 7
Jinan 7
Kunming 7
Modena 7
Olomouc 7
Pescara 7
Secaucus 7
Sesto San Giovanni 7
Totale 6.423
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Nome #
Mutazione Q283P nel gene HFE in un eterozigote C282Y affetto da emocromatosi. 1.542
Genetica della labiopalatoschisi non sindromica: ruolo di polimorfismi del metabolismo dei folati e dell’omocisteina. 896
Associazione tra il polimorfismo c.66A>G del gene MTRR e la palatoschisi non-sindromica. 270
Trisomy 15 mosaicism owing to familial reciprocal translocation t(1;15): Implication for prenatal diagnosis 246
In vitro short-term test evaluation of catecholestrogens genotoxicity 231
FISH screening for subtelomeric rearrangements in 219 patients with idiopathic mental retardation and normal karyotype. 211
Characterization of a deleted Y chromosome in a male with Turner stigmata 207
Intronic breakpoint definition and transcription analysis in DMD/BMD patients with deletion/duplication at the 5′ mutation hot spot of the dystrophin gene 201
G.P.12.06 A comprehensive molecular characterisation of dystrophinopathies 201
Mole maker phenotype: possible narrowing of the candidate region. 197
Occurrence of Del(GIB6-D13S1830) mutation in Italian non-syndromic hearing loss patients carrying a single GJB2 mutated allele 196
Transthyretin RNA profiling in livers from transplanted patients affected by familial amyloidotic polyneuropathy, and identification of a dual transcription start point 190
Mutation analysis of the MECP2 gene in British and Italian Rett syndrome females 188
Psychiatric disorder in a familial 15;18 translocation and sublocalization of myelin basic protein of 18q22.3 188
A two-locus model for non-syndromic congenital dysplasia of the hip (CDH) 187
Nonhomologous Robertsonian translocations (NHRTs) and uniparental disomy (UPD) risk: An Italian multicentric prenatal survey 182
Prenatal genetic counseling referrals for advanced maternal age: still room for improvement. 179
Commercial kit-based diagnosis is not enough for prenatal testing of beta-thalassemia: pitfalls in diagnostic mutation analysis raises the need for reference laboratories 179
Analisi del polimorfismo IVS2+4T>C del gene HFE in soggetti con sovraccarico di ferro. 178
EUROCAT and orofacial clefts: The epidemiology of orofacial clefts in 30 european regions 176
Exclusion of COL2A1 and VDR as Developmental Dysplasia of the Hip Genes 176
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 175
Exploring the clinical and epidemiological complexity of GJB2-linked deafness 167
Prenatal diagnosis of a de novo satellited chromosome 18 (18ps) associated with 18p deletion 167
Epidemiology of cleft palate in Europe: Implications for genetic research 165
Clinical anophthalmos in a family 164
Genomic definition of a pure intronic dystrophin deletion responsible for an XLDC splicing mutation: In vitro mimicking and antisense modulation of the splicing abnormality 162
CHARACTERIZATION OF THE PSEUDOGENIC REGION OF VON WILLEBRAND FACTOR BY MOLECULAR CLONING AND "IN SITU" HYBRIDIZATION 154
Comparison of two statistical techniques for the surveillance of birth defects through a Monte Carlo simulation 149
Prenatal diagnosis of a complete mole coexisting with a dichorionic twin pregnancy: Case report 147
Progress in understanding GJB2-linked deafness 141
Association between the c.66A>G variant in the Methionine Synthase reductase and nonsyndromic cleft palate. 134
Screening of mutations in the CFTR gene in 1195 couples entering assisted reproduction technique programs. 132
null 131
Localization of cloned human DNA sequences and analysis of chromosomal alteration by in situ hybridization 130
Cloning and chromosome localization of the gene for the methenyltratrahydrofolate-synthetase 129
null 125
Analisi dei genotipi ed aplotipi HFE nella popolazione Ferrarese 124
Frequenze genotipiche ed aplotipiche HFE nella popolazione della Provincia di Ferrara 117
Inferences on the inheritance of congenital anomalies from temporal and spatial patterns of occurrence 114
Cytogenetic and array CGH characterization of an intrachromosomal complex rearrangement of 4q in a patient with a 4q-phenotype. 113
Schisi facciale e genetica dei folati 111
G.P.3.02 In vivo biodistribution of non-viral systems for oligoribonucleotides delivery 106
Biosensor technology for real-time detection of the cystic fibrosis W1282X mutation in CFTR 104
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null 99
Una nuova mutazione del gene HFE in un eterozigote C282Y con emocromatosi. 98
Mental retardation (MR) and coagulation factor XI deficiency in two first cousins once removed: a new X-linked syndrome? 94
Cystathionine beta-synthase c.844ins68 gene variant and non-syndromic cleft lip and palate. 94
Epidemiologia e genetica delle schisi orofacciali 94
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CHARACTERIZATION OF THE PSEUDOGENIC AND GENIC HOMOLOGOUS REGIONS OF VON WILLEBRAND FACTOR 86
Genomic and transcription studies as diagnostic tools for a prenatal detection of X-linked dilated cardiomyopathy due to a dystrophin gene mutation. 86
null 78
Congenital heart defects: 15 Years of experience of the Emilia-Romagna Registry (Italy) 76
Idiopathic central retinal vein occlusion in a thrombophilic patient with the heterozygous 20210 G/A prothrombin genotype 70
Are omphalocele and neural tube defects related congenital anomalies?: Data from 21 registries in Europe (EUROCAT) 63
Multiple exon skipping and RNA circularisation contribute to the severe phenotypic expression of exon 5 dystrophin deletion. 54
Totale 10.748
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Categoria #
all - tutte 38.534
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 683
Totale 39.217
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021450 0 0 0 0 0 67 28 77 11 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
2025/20262.164 425 161 370 477 648 83 0 0 0 0 0 0
Totale 10.748