SFERA Archivio dei prodotti della Ricerca dell'Università di Ferrara

CALZOLARI, Elisa
 Distribuzione geografica
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Continente #
NA - Nord America 3.970
EU - Europa 3.332
AS - Asia 1.086
SA - Sud America 156
AF - Africa 14
OC - Oceania 6
Totale 8.564
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Nazione #
US - Stati Uniti d'America 3.925
IT - Italia 2.031
CN - Cina 436
SG - Singapore 417
DE - Germania 385
UA - Ucraina 292
GB - Regno Unito 160
BR - Brasile 143
TR - Turchia 130
FI - Finlandia 117
SE - Svezia 93
NL - Olanda 82
RU - Federazione Russa 46
CA - Canada 37
BE - Belgio 35
FR - Francia 28
TH - Thailandia 25
HK - Hong Kong 19
IR - Iran 11
JP - Giappone 11
CZ - Repubblica Ceca 10
PL - Polonia 9
ZA - Sudafrica 9
BD - Bangladesh 8
CH - Svizzera 8
IN - India 8
IE - Irlanda 7
ES - Italia 6
LT - Lituania 6
AU - Australia 5
AT - Austria 4
KZ - Kazakistan 4
MX - Messico 4
PT - Portogallo 4
AR - Argentina 3
VE - Venezuela 3
CL - Cile 2
CO - Colombia 2
GR - Grecia 2
HU - Ungheria 2
ID - Indonesia 2
IQ - Iraq 2
JO - Giordania 2
MA - Marocco 2
MD - Moldavia 2
MN - Mongolia 2
AE - Emirati Arabi Uniti 1
BB - Barbados 1
BO - Bolivia 1
BY - Bielorussia 1
CR - Costa Rica 1
DZ - Algeria 1
HN - Honduras 1
KE - Kenya 1
KG - Kirghizistan 1
LK - Sri Lanka 1
MK - Macedonia 1
NG - Nigeria 1
NP - Nepal 1
NZ - Nuova Zelanda 1
PK - Pakistan 1
PS - Palestinian Territory 1
PY - Paraguay 1
QA - Qatar 1
RO - Romania 1
SA - Arabia Saudita 1
TT - Trinidad e Tobago 1
UY - Uruguay 1
UZ - Uzbekistan 1
Totale 8.564
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Città #
Woodbridge 461
Fairfield 439
Ashburn 282
Chandler 266
Houston 266
Jacksonville 263
Ann Arbor 258
Singapore 218
Milan 204
Santa Clara 184
Seattle 173
Cambridge 167
Wilmington 166
Beijing 152
Rome 149
Izmir 82
Nanjing 79
Naples 71
Princeton 52
Munich 44
Boardman 43
Turin 42
Los Angeles 39
Addison 37
New York 37
San Diego 36
Shanghai 34
Brussels 33
Turku 33
Catania 31
Palermo 31
Bari 30
Florence 30
Helsinki 28
San Mateo 26
Bangkok 25
Bremen 25
Shenyang 23
Brescia 21
Tianjin 21
Falkenstein 20
London 20
Falls Church 19
Verona 19
Hebei 18
Hong Kong 18
Padova 18
Bologna 16
Redwood City 16
Nanchang 15
Toronto 15
Carbonera 14
Dearborn 14
The Dalles 14
Ferrara 13
Ottawa 13
Venice 13
Philadelphia 11
São Paulo 11
Changsha 10
Jiaxing 10
Messina 10
Salerno 10
Iesi 9
Nola 9
Tokyo 9
Mountain View 8
Trieste 8
Vicenza 8
Washington 8
Auburn Hills 7
Caserta 7
Genoa 7
Jinan 7
Kunming 7
Modena 7
Olomouc 7
Pescara 7
Sesto San Giovanni 7
Ardabil 6
Bergamo 6
Frankfurt am Main 6
Groningen 6
Guangzhou 6
Leawood 6
Molfetta 6
Pavia 6
Warsaw 6
Zhengzhou 6
Alba 5
Cerignola 5
Chicago 5
Des Moines 5
Indiana 5
Parma 5
Arese 4
Augusta 4
Bagnatica 4
Bosisio Parini 4
Brooklyn 4
Totale 5.170
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Nome #
Mutazione Q283P nel gene HFE in un eterozigote C282Y affetto da emocromatosi. 1.404
Genetica della labiopalatoschisi non sindromica: ruolo di polimorfismi del metabolismo dei folati e dell’omocisteina. 773
Associazione tra il polimorfismo c.66A>G del gene MTRR e la palatoschisi non-sindromica. 206
Trisomy 15 mosaicism owing to familial reciprocal translocation t(1;15): Implication for prenatal diagnosis 198
In vitro short-term test evaluation of catecholestrogens genotoxicity 183
Occurrence of del(GIB6-D13S1830) mutation in Italian non-syndromic hearing loss patients carrying a single GJB2 mutated allele. 166
FISH screening for subtelomeric rearrangements in 219 patients with idiopathic mental retardation and normal karyotype. 164
Psychiatric disorder in a familial 15;18 translocation and sublocalization of myelin basic protein of 18q22.3 154
Characterization of a deleted Y chromosome in a male with Turner stigmata 153
Transthyretin RNA profiling in livers from transplanted patients affected by familial amyloidotic polyneuropathy, and identification of a dual transcription start point. 152
Mole maker phenotype: possible narrowing of the candidate region. 151
Intronic breakpoint definition and transcription analysis in DMD/BMD patients with deletion/duplication at the 5′ mutation hot spot of the dystrophin gene 145
G.P.12.06 A comprehensive molecular characterisation of dystrophinopathies 144
Commercial kit-based diagnosis is not enough for prenatal testing of beta-thalassemia: pitfalls in diagnostic mutation analysis raises the need for reference laboratories 140
Nonhomologous Robertsonian translocations (NHRTs) and uniparental disomy (UPD) risk: an Italian multicentric prenatal survey. 138
Mutation analysis of the MECP2 gene in British and Italian Rett syndrome females. 137
Genomic definition of a pure intronic dystrophin deletion responsible for an XLDC splicing mutation: In vitro mimicking and antisense modulation of the splicing abnormality 136
A two-locus model for non-syndromic congenital dysplasia of the hip (CDH) 135
Analisi del polimorfismo IVS2+4T>C del gene HFE in soggetti con sovraccarico di ferro. 132
Epidemiology of cleft palate in Europe: implications for genetic research. 132
Prenatal genetic counseling referrals for advanced maternal age: still room for improvement. 132
null 131
EUROCAT and orofacial clefts: The epidemiology of orofacial clefts in 30 european regions 130
Prenatal diagnosis of a de novo satellited chromosome 18 (18ps) associated with 18p deletion 130
Exclusion of COL2A1 and VDR as Developmental Dysplasia of the Hip Genes 130
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 129
null 125
Clinical anophthalmos in a family 125
CHARACTERIZATION OF THE PSEUDOGENIC REGION OF VON WILLEBRAND FACTOR BY MOLECULAR CLONING AND "IN SITU" HYBRIDIZATION 123
Prenatal diagnosis of a complete mole coexisting with a dichorionic twin pregnancy: case report. 123
Comparison of two statistical techniques for the surveillance of birth defects through a Monte Carlo simulation 123
Exploring the clinical and epidemiological complexity of GJB2-linked deafness. 120
Progress in understanding GJB2-linked deafness 112
Screening of mutations in the CFTR gene in 1195 couples entering assisted reproduction technique programs. 109
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Cloning and chromosome localization of the gene for the methenyltratrahydrofolate-synthetase 94
Localization of cloned human DNA sequences and analysis of chromosomal alterations by in situ hybridization. 94
Association between the c.66A>G variant in the Methionine Synthase reductase and nonsyndromic cleft palate. 94
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Analisi dei genotipi ed aplotipi HFE nella popolazione Ferrarese 90
Inferences on the inheritance of congenital anomalies from temporal and spatial patterns of occurrence 87
Schisi facciale e genetica dei folati 82
Frequenze genotipiche ed aplotipiche HFE nella popolazione della Provincia di Ferrara 82
Genomic organization and expression of the MTHFS gene 80
null 78
Una nuova mutazione del gene HFE in un eterozigote C282Y con emocromatosi. 75
Cytogenetic and array CGH characterization of an intrachromosomal complex rearrangement of 4q in a patient with a 4q-phenotype. 73
Epidemiologia e genetica delle schisi orofacciali 69
Mental retardation (MR) and coagulation factor XI deficiency in two first cousins once removed: a new X-linked syndrome? 68
Biosensor technology for real-time detection of the cystic fibrosis W1282X mutation in CFTR 63
Genomic and transcription studies as diagnostic tools for a prenatal detection of X-linked dilated cardiomyopathy due to a dystrophin gene mutation. 53
CHARACTERIZATION OF THE PSEUDOGENIC AND GENIC HOMOLOGOUS REGIONS OF VON WILLEBRAND FACTOR 50
Cystathionine beta-synthase c.844ins68 gene variant and non-syndromic cleft lip and palate. 50
G.P.3.02 In vivo biodistribution of non-viral systems for oligoribonucleotides delivery 47
Congenital heart defects: 15 Years of experience of the Emilia-Romagna Registry (Italy) 37
Idiopathic central retinal vein occlusion in a thrombophilic patient with the heterozygous 20210 G/A prothrombin genotype 35
Are omphalocele and neural tube defects related congenital anomalies?: Data from 21 registries in Europe (EUROCAT) 28
Multiple exon skipping and RNA circularisation contribute to the severe phenotypic expression of exon 5 dystrophin deletion. 27
Totale 8.614
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Categoria #
all - tutte 32.014
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 552
Totale 32.566
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202031 0 0 0 0 0 0 0 0 0 0 0 31
2020/2021753 71 72 38 85 31 68 28 78 11 86 129 56
2021/2022789 32 64 86 41 46 35 46 33 32 54 69 251
2022/2023858 63 89 34 96 119 97 57 81 99 22 57 44
2023/2024949 80 69 53 32 65 116 70 59 56 92 94 163
2024/20252.211 126 123 167 199 262 192 105 100 299 185 287 166
Totale 8.614