SFERA Archivio dei prodotti della Ricerca dell'Università di Ferrara

CALZOLARI, Elisa
 Distribuzione geografica
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Continente #
NA - Nord America 4.493
EU - Europa 3.669
AS - Asia 1.767
SA - Sud America 237
AF - Africa 27
OC - Oceania 5
Totale 10.198
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Nazione #
US - Stati Uniti d'America 4.399
IT - Italia 2.180
CN - Cina 652
SG - Singapore 637
DE - Germania 457
UA - Ucraina 289
BR - Brasile 206
HK - Hong Kong 183
GB - Regno Unito 176
TR - Turchia 132
FI - Finlandia 120
NL - Olanda 106
SE - Svezia 92
RU - Federazione Russa 85
CA - Canada 59
FR - Francia 37
BE - Belgio 35
VN - Vietnam 33
MX - Messico 30
TH - Thailandia 25
IN - India 24
ES - Italia 22
JP - Giappone 20
ZA - Sudafrica 18
BD - Bangladesh 17
PL - Polonia 17
IR - Iran 11
CZ - Repubblica Ceca 10
AR - Argentina 8
CH - Svizzera 8
AT - Austria 7
IE - Irlanda 7
LT - Lituania 7
CL - Cile 5
ID - Indonesia 5
PT - Portogallo 5
PY - Paraguay 5
AU - Australia 4
EC - Ecuador 4
IQ - Iraq 4
KZ - Kazakistan 4
VE - Venezuela 4
AE - Emirati Arabi Uniti 3
CO - Colombia 3
JO - Giordania 3
SA - Arabia Saudita 3
ET - Etiopia 2
GR - Grecia 2
HU - Ungheria 2
KE - Kenya 2
MA - Marocco 2
MD - Moldavia 2
AZ - Azerbaigian 1
BB - Barbados 1
BO - Bolivia 1
BY - Bielorussia 1
CI - Costa d'Avorio 1
CR - Costa Rica 1
DZ - Algeria 1
HN - Honduras 1
KG - Kirghizistan 1
KR - Corea 1
LK - Sri Lanka 1
MK - Macedonia 1
MY - Malesia 1
NG - Nigeria 1
NP - Nepal 1
NZ - Nuova Zelanda 1
PA - Panama 1
PH - Filippine 1
PK - Pakistan 1
PS - Palestinian Territory 1
QA - Qatar 1
RO - Romania 1
TT - Trinidad e Tobago 1
UY - Uruguay 1
UZ - Uzbekistan 1
Totale 10.198
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Città #
Woodbridge 458
Fairfield 439
Ashburn 424
Singapore 366
Houston 272
Chandler 264
Beijing 259
Ann Arbor 258
Jacksonville 257
Milan 209
Santa Clara 188
Hong Kong 182
Seattle 173
Cambridge 166
Wilmington 163
Rome 158
Los Angeles 96
Munich 93
Izmir 81
Nanjing 78
Naples 74
New York 57
Dallas 54
Princeton 51
Buffalo 45
Boardman 42
Turin 42
Falkenstein 38
Addison 36
San Diego 36
Turku 36
Catania 34
Palermo 34
Shanghai 34
Brussels 33
Bari 30
Florence 30
Helsinki 29
Hefei 26
San Mateo 26
Bangkok 25
Bremen 25
São Paulo 25
London 23
Mexico City 23
Shenyang 23
Verona 23
Brescia 21
Tianjin 21
Toronto 20
Falls Church 19
Hebei 18
Padova 18
Tokyo 18
Bologna 17
Chicago 17
Redwood City 16
Brooklyn 14
Carbonera 14
Ho Chi Minh City 14
Montreal 14
Nanchang 14
The Dalles 14
Ottawa 13
Venice 13
Dearborn 12
Ferrara 12
Johannesburg 12
Warsaw 12
Changsha 11
Chennai 11
Philadelphia 11
Boston 10
Groningen 10
Jiaxing 10
Messina 10
Salerno 10
Denver 9
Iesi 9
Nola 9
Washington 9
Atlanta 8
Genoa 8
Mountain View 8
Trieste 8
Vicenza 8
Caserta 7
Frankfurt am Main 7
Hanoi 7
Jinan 7
Kunming 7
Modena 7
Olomouc 7
Pescara 7
Secaucus 7
Sesto San Giovanni 7
Stockholm 7
Ardabil 6
Auburn Hills 6
Bergamo 6
Totale 6.135
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Nome #
Mutazione Q283P nel gene HFE in un eterozigote C282Y affetto da emocromatosi. 1.519
Genetica della labiopalatoschisi non sindromica: ruolo di polimorfismi del metabolismo dei folati e dell’omocisteina. 877
Associazione tra il polimorfismo c.66A>G del gene MTRR e la palatoschisi non-sindromica. 250
Trisomy 15 mosaicism owing to familial reciprocal translocation t(1;15): Implication for prenatal diagnosis 237
In vitro short-term test evaluation of catecholestrogens genotoxicity 220
FISH screening for subtelomeric rearrangements in 219 patients with idiopathic mental retardation and normal karyotype. 202
Characterization of a deleted Y chromosome in a male with Turner stigmata 197
G.P.12.06 A comprehensive molecular characterisation of dystrophinopathies 191
Mole maker phenotype: possible narrowing of the candidate region. 188
Intronic breakpoint definition and transcription analysis in DMD/BMD patients with deletion/duplication at the 5′ mutation hot spot of the dystrophin gene 187
Occurrence of Del(GIB6-D13S1830) mutation in Italian non-syndromic hearing loss patients carrying a single GJB2 mutated allele 186
Psychiatric disorder in a familial 15;18 translocation and sublocalization of myelin basic protein of 18q22.3 181
Transthyretin RNA profiling in livers from transplanted patients affected by familial amyloidotic polyneuropathy, and identification of a dual transcription start point 180
Mutation analysis of the MECP2 gene in British and Italian Rett syndrome females 176
A two-locus model for non-syndromic congenital dysplasia of the hip (CDH) 176
Nonhomologous Robertsonian translocations (NHRTs) and uniparental disomy (UPD) risk: An Italian multicentric prenatal survey 174
Commercial kit-based diagnosis is not enough for prenatal testing of beta-thalassemia: pitfalls in diagnostic mutation analysis raises the need for reference laboratories 170
Exclusion of COL2A1 and VDR as Developmental Dysplasia of the Hip Genes 169
Analisi del polimorfismo IVS2+4T>C del gene HFE in soggetti con sovraccarico di ferro. 168
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 165
EUROCAT and orofacial clefts: The epidemiology of orofacial clefts in 30 european regions 163
Prenatal genetic counseling referrals for advanced maternal age: still room for improvement. 161
Exploring the clinical and epidemiological complexity of GJB2-linked deafness 160
Genomic definition of a pure intronic dystrophin deletion responsible for an XLDC splicing mutation: In vitro mimicking and antisense modulation of the splicing abnormality 158
Prenatal diagnosis of a de novo satellited chromosome 18 (18ps) associated with 18p deletion 157
Epidemiology of cleft palate in Europe: Implications for genetic research 156
Clinical anophthalmos in a family 153
CHARACTERIZATION OF THE PSEUDOGENIC REGION OF VON WILLEBRAND FACTOR BY MOLECULAR CLONING AND "IN SITU" HYBRIDIZATION 145
Prenatal diagnosis of a complete mole coexisting with a dichorionic twin pregnancy: Case report 142
Progress in understanding GJB2-linked deafness 139
Comparison of two statistical techniques for the surveillance of birth defects through a Monte Carlo simulation 137
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Screening of mutations in the CFTR gene in 1195 couples entering assisted reproduction technique programs. 127
null 125
Association between the c.66A>G variant in the Methionine Synthase reductase and nonsyndromic cleft palate. 123
Localization of cloned human DNA sequences and analysis of chromosomal alteration by in situ hybridization 122
Cloning and chromosome localization of the gene for the methenyltratrahydrofolate-synthetase 120
Analisi dei genotipi ed aplotipi HFE nella popolazione Ferrarese 117
Inferences on the inheritance of congenital anomalies from temporal and spatial patterns of occurrence 112
Schisi facciale e genetica dei folati 106
Frequenze genotipiche ed aplotipiche HFE nella popolazione della Provincia di Ferrara 106
Cytogenetic and array CGH characterization of an intrachromosomal complex rearrangement of 4q in a patient with a 4q-phenotype. 103
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null 99
Una nuova mutazione del gene HFE in un eterozigote C282Y con emocromatosi. 98
Biosensor technology for real-time detection of the cystic fibrosis W1282X mutation in CFTR 95
G.P.3.02 In vivo biodistribution of non-viral systems for oligoribonucleotides delivery 92
null 92
Mental retardation (MR) and coagulation factor XI deficiency in two first cousins once removed: a new X-linked syndrome? 92
null 91
null 91
Epidemiologia e genetica delle schisi orofacciali 84
null 78
Cystathionine beta-synthase c.844ins68 gene variant and non-syndromic cleft lip and palate. 78
CHARACTERIZATION OF THE PSEUDOGENIC AND GENIC HOMOLOGOUS REGIONS OF VON WILLEBRAND FACTOR 76
Genomic and transcription studies as diagnostic tools for a prenatal detection of X-linked dilated cardiomyopathy due to a dystrophin gene mutation. 75
Congenital heart defects: 15 Years of experience of the Emilia-Romagna Registry (Italy) 66
Idiopathic central retinal vein occlusion in a thrombophilic patient with the heterozygous 20210 G/A prothrombin genotype 62
Are omphalocele and neural tube defects related congenital anomalies?: Data from 21 registries in Europe (EUROCAT) 53
Multiple exon skipping and RNA circularisation contribute to the severe phenotypic expression of exon 5 dystrophin deletion. 50
Totale 10.248
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Categoria #
all - tutte 37.349
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 659
Totale 38.008
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021481 0 0 0 0 31 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
2025/20261.664 425 161 370 477 231 0 0 0 0 0 0 0
Totale 10.248