SFERA Archivio dei prodotti della Ricerca dell'Università di Ferrara

CALZOLARI, Elisa
 Distribuzione geografica
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Continente #
NA - Nord America 5.502
EU - Europa 4.111
AS - Asia 2.785
SA - Sud America 338
AF - Africa 61
Continente sconosciuto - Info sul continente non disponibili 54
OC - Oceania 10
Totale 12.861
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Nazione #
US - Stati Uniti d'America 5.362
IT - Italia 2.434
SG - Singapore 1.026
CN - Cina 706
DE - Germania 466
VN - Vietnam 328
UA - Ucraina 295
BR - Brasile 254
HK - Hong Kong 207
GB - Regno Unito 201
TR - Turchia 154
FI - Finlandia 137
NL - Olanda 135
SE - Svezia 97
RU - Federazione Russa 93
FR - Francia 89
BD - Bangladesh 88
CA - Canada 82
IN - India 66
JP - Giappone 58
MX - Messico 41
BE - Belgio 36
ES - Italia 26
TH - Thailandia 26
ZA - Sudafrica 26
AR - Argentina 22
IQ - Iraq 20
PL - Polonia 18
EC - Ecuador 15
ID - Indonesia 14
LT - Lituania 14
CO - Colombia 12
IR - Iran 12
CL - Cile 11
CZ - Repubblica Ceca 11
SA - Arabia Saudita 11
IE - Irlanda 10
PY - Paraguay 10
VE - Venezuela 9
AU - Australia 8
CH - Svizzera 8
JO - Giordania 8
PH - Filippine 8
AE - Emirati Arabi Uniti 7
AT - Austria 7
KE - Kenya 7
UZ - Uzbekistan 7
ET - Etiopia 6
PK - Pakistan 6
PT - Portogallo 6
KZ - Kazakistan 5
MA - Marocco 5
MY - Malesia 5
TN - Tunisia 5
BY - Bielorussia 4
CR - Costa Rica 4
HU - Ungheria 4
AL - Albania 3
EG - Egitto 3
GE - Georgia 3
GR - Grecia 3
JM - Giamaica 3
OM - Oman 3
PS - Palestinian Territory 3
RS - Serbia 3
AZ - Azerbaigian 2
DO - Repubblica Dominicana 2
DZ - Algeria 2
GA - Gabon 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
UY - Uruguay 2
BB - Barbados 1
BG - Bulgaria 1
BO - Bolivia 1
BW - Botswana 1
CI - Costa d'Avorio 1
DM - Dominica 1
FJ - Figi 1
GT - Guatemala 1
GY - Guiana 1
HN - Honduras 1
HR - Croazia 1
KH - Cambogia 1
KN - Saint Kitts e Nevis 1
KR - Corea 1
LK - Sri Lanka 1
ME - Montenegro 1
MK - Macedonia 1
MN - Mongolia 1
NZ - Nuova Zelanda 1
PA - Panama 1
PE - Perù 1
Totale 12.805
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Città #
Singapore 677
Ashburn 599
Woodbridge 458
Fairfield 439
San Jose 391
Houston 273
Beijing 272
Ann Arbor 258
Jacksonville 257
Chandler 256
Milan 230
Hong Kong 203
Santa Clara 203
Seattle 174
Rome 173
Cambridge 166
Wilmington 163
Los Angeles 123
Council Bluffs 109
Ho Chi Minh City 107
Munich 93
Naples 84
Izmir 82
Nanjing 79
Hanoi 77
New York 72
Dallas 61
Buffalo 55
Tokyo 55
Princeton 51
Helsinki 44
Turin 42
Boardman 41
Lauterbourg 39
Falkenstein 38
Addison 36
Palermo 36
San Diego 36
Turku 36
Shanghai 35
Brussels 34
Catania 34
Florence 32
The Dalles 32
Toronto 32
Bari 30
Orem 30
London 29
São Paulo 29
Bologna 28
Hefei 27
Mexico City 26
San Mateo 26
Bangkok 25
Bremen 25
Da Nang 24
Shenyang 23
Verona 23
Tianjin 22
Brescia 21
Brooklyn 21
Montreal 20
Chennai 19
Chicago 19
Falls Church 19
Hebei 18
Padova 18
Denver 17
Johannesburg 17
Redwood City 16
Venice 16
Carbonera 14
Nanchang 14
Ottawa 14
Boston 13
Warsaw 13
Dearborn 12
Ferrara 12
Groningen 12
Haiphong 12
Baghdad 11
Frankfurt am Main 11
Genoa 11
Philadelphia 11
Stockholm 11
Atlanta 10
Changsha 10
Jiaxing 10
Messina 10
Modena 10
Phoenix 10
Reggio Emilia 10
Salerno 10
Washington 10
Iesi 9
Nola 9
Charlotte 8
Hải Dương 8
Manchester 8
Mountain View 8
Totale 7.686
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Nome #
Mutazione Q283P nel gene HFE in un eterozigote C282Y affetto da emocromatosi. 1.697
Genetica della labiopalatoschisi non sindromica: ruolo di polimorfismi del metabolismo dei folati e dell’omocisteina. 1.028
Associazione tra il polimorfismo c.66A>G del gene MTRR e la palatoschisi non-sindromica. 363
Trisomy 15 mosaicism owing to familial reciprocal translocation t(1;15): Implication for prenatal diagnosis 305
In vitro short-term test evaluation of catecholestrogens genotoxicity 275
G.P.12.06 A comprehensive molecular characterisation of dystrophinopathies 272
Characterization of a deleted Y chromosome in a male with Turner stigmata 261
FISH screening for subtelomeric rearrangements in 219 patients with idiopathic mental retardation and normal karyotype. 258
Intronic breakpoint definition and transcription analysis in DMD/BMD patients with deletion/duplication at the 5′ mutation hot spot of the dystrophin gene 251
Transthyretin RNA profiling in livers from transplanted patients affected by familial amyloidotic polyneuropathy, and identification of a dual transcription start point 231
Mole maker phenotype: possible narrowing of the candidate region. 231
Occurrence of Del(GIB6-D13S1830) mutation in Italian non-syndromic hearing loss patients carrying a single GJB2 mutated allele 230
A two-locus model for non-syndromic congenital dysplasia of the hip (CDH) 230
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 229
EUROCAT and orofacial clefts: The epidemiology of orofacial clefts in 30 european regions 222
Prenatal genetic counseling referrals for advanced maternal age: still room for improvement. 221
Mutation analysis of the MECP2 gene in British and Italian Rett syndrome females 220
Analisi del polimorfismo IVS2+4T>C del gene HFE in soggetti con sovraccarico di ferro. 220
Commercial kit-based diagnosis is not enough for prenatal testing of beta-thalassemia: pitfalls in diagnostic mutation analysis raises the need for reference laboratories 217
Exploring the clinical and epidemiological complexity of GJB2-linked deafness 216
Psychiatric disorder in a familial 15;18 translocation and sublocalization of myelin basic protein of 18q22.3 215
Clinical anophthalmos in a family 214
Exclusion of COL2A1 and VDR as Developmental Dysplasia of the Hip Genes 212
Nonhomologous Robertsonian translocations (NHRTs) and uniparental disomy (UPD) risk: An Italian multicentric prenatal survey 206
Epidemiology of cleft palate in Europe: Implications for genetic research 203
Prenatal diagnosis of a de novo satellited chromosome 18 (18ps) associated with 18p deletion 201
Association between the c.66A>G variant in the Methionine Synthase reductase and nonsyndromic cleft palate. 200
CHARACTERIZATION OF THE PSEUDOGENIC REGION OF VON WILLEBRAND FACTOR BY MOLECULAR CLONING AND "IN SITU" HYBRIDIZATION 192
Genomic definition of a pure intronic dystrophin deletion responsible for an XLDC splicing mutation: In vitro mimicking and antisense modulation of the splicing abnormality 178
Comparison of two statistical techniques for the surveillance of birth defects through a Monte Carlo simulation 177
Cloning and chromosome localization of the gene for the methenyltratrahydrofolate-synthetase 174
Prenatal diagnosis of a complete mole coexisting with a dichorionic twin pregnancy: Case report 173
Localization of cloned human DNA sequences and analysis of chromosomal alteration by in situ hybridization 171
Progress in understanding GJB2-linked deafness 168
Analisi dei genotipi ed aplotipi HFE nella popolazione Ferrarese 166
Frequenze genotipiche ed aplotipiche HFE nella popolazione della Provincia di Ferrara 159
Screening of mutations in the CFTR gene in 1195 couples entering assisted reproduction technique programs. 156
Biosensor technology for real-time detection of the cystic fibrosis W1282X mutation in CFTR 149
G.P.3.02 In vivo biodistribution of non-viral systems for oligoribonucleotides delivery 148
Schisi facciale e genetica dei folati 148
Cytogenetic and array CGH characterization of an intrachromosomal complex rearrangement of 4q in a patient with a 4q-phenotype. 148
Inferences on the inheritance of congenital anomalies from temporal and spatial patterns of occurrence 138
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Epidemiologia e genetica delle schisi orofacciali 126
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Una nuova mutazione del gene HFE in un eterozigote C282Y con emocromatosi. 125
CHARACTERIZATION OF THE PSEUDOGENIC AND GENIC HOMOLOGOUS REGIONS OF VON WILLEBRAND FACTOR 124
Genomic and transcription studies as diagnostic tools for a prenatal detection of X-linked dilated cardiomyopathy due to a dystrophin gene mutation. 119
Mental retardation (MR) and coagulation factor XI deficiency in two first cousins once removed: a new X-linked syndrome? 109
Congenital heart defects: 15 Years of experience of the Emilia-Romagna Registry (Italy) 106
Cystathionine beta-synthase c.844ins68 gene variant and non-syndromic cleft lip and palate 101
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Idiopathic central retinal vein occlusion in a thrombophilic patient with the heterozygous 20210 G/A prothrombin genotype 96
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Are omphalocele and neural tube defects related congenital anomalies?: Data from 21 registries in Europe (EUROCAT) 91
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Multiple exon skipping and RNA circularisation contribute to the severe phenotypic expression of exon 5 dystrophin deletion. 75
Totale 12.861
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Categoria #
all - tutte 45.204
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 868
Totale 46.072
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2021/2022747 0 63 86 39 45 34 46 33 32 54 67 248
2022/2023836 61 87 33 93 114 95 57 80 94 21 57 44
2023/2024938 79 69 52 32 64 114 70 59 56 92 90 161
2024/20252.215 123 122 164 197 257 186 104 99 294 180 280 209
2025/20264.088 419 158 361 471 634 279 541 200 364 374 213 74
2026/2027240 99 141 0 0 0 0 0 0 0 0 0 0
Totale 12.861