IRIS
CALABRESE, Giuseppe
 Distribuzione geografica
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Continente #
NA - Nord America 5.120
EU - Europa 4.409
AS - Asia 3.998
SA - Sud America 373
AF - Africa 39
Continente sconosciuto - Info sul continente non disponibili 6
OC - Oceania 5
Totale 13.950
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Nazione #
US - Stati Uniti d'America 5.032
SG - Singapore 1.438
CN - Cina 1.344
UA - Ucraina 770
IT - Italia 635
IE - Irlanda 567
GB - Regno Unito 561
SE - Svezia 506
DE - Germania 483
TR - Turchia 479
FR - Francia 404
IN - India 391
BR - Brasile 317
VN - Vietnam 200
FI - Finlandia 177
RU - Federazione Russa 134
CA - Canada 54
AT - Austria 40
MX - Messico 24
ZA - Sudafrica 24
PL - Polonia 23
JP - Giappone 21
AR - Argentina 19
BD - Bangladesh 19
CZ - Repubblica Ceca 19
HK - Hong Kong 18
BE - Belgio 17
KR - Corea 16
NL - Olanda 16
RO - Romania 15
IL - Israele 12
ES - Italia 10
GR - Grecia 10
IR - Iran 10
LT - Lituania 10
EC - Ecuador 9
IQ - Iraq 9
VE - Venezuela 9
EU - Europa 6
AU - Australia 5
CL - Cile 5
ID - Indonesia 5
PE - Perù 5
UZ - Uzbekistan 5
KE - Kenya 4
MY - Malesia 4
PK - Pakistan 4
PY - Paraguay 4
TW - Taiwan 4
DO - Repubblica Dominicana 3
DZ - Algeria 3
MD - Moldavia 3
OM - Oman 3
SA - Arabia Saudita 3
AE - Emirati Arabi Uniti 2
AZ - Azerbaigian 2
CO - Colombia 2
CR - Costa Rica 2
DK - Danimarca 2
EG - Egitto 2
GD - Grenada 2
NO - Norvegia 2
NP - Nepal 2
RS - Serbia 2
UY - Uruguay 2
BB - Barbados 1
BH - Bahrain 1
CH - Svizzera 1
ET - Etiopia 1
GE - Georgia 1
GY - Guiana 1
HN - Honduras 1
JO - Giordania 1
KZ - Kazakistan 1
LB - Libano 1
MA - Marocco 1
MK - Macedonia 1
SC - Seychelles 1
SK - Slovacchia (Repubblica Slovacca) 1
SN - Senegal 1
SY - Repubblica araba siriana 1
TG - Togo 1
TH - Thailandia 1
TN - Tunisia 1
TT - Trinidad e Tobago 1
Totale 13.950
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Città #
Singapore 946
Jacksonville 811
Chandler 692
Dublin 564
Southend 449
Beijing 360
Ashburn 322
Princeton 291
Izmir 263
Dallas 256
Nanjing 243
Dearborn 179
Los Angeles 178
Wilmington 157
The Dalles 137
Cambridge 135
Chieti 123
Tongling 109
Munich 103
Nanchang 99
Santa Clara 95
Grafing 92
Boardman 91
Buffalo 87
Dong Ket 75
Ann Arbor 72
Altamura 71
New York 56
Woodbridge 50
Hebei 49
Kunming 49
Shenyang 48
Tianjin 47
Pescara 46
Ho Chi Minh City 40
Helsinki 36
Vienna 36
Washington 33
Jiaxing 31
Rome 31
Hanoi 30
Jinan 28
São Paulo 28
Redondo Beach 27
Hangzhou 26
Brooklyn 25
Grevenbroich 25
Tokyo 21
Augusta 20
Chicago 20
Council Bluffs 20
Hefei 20
Johannesburg 19
Düsseldorf 18
Kocaeli 18
Montreal 18
Brno 17
Hong Kong 17
Norwalk 17
Guangzhou 16
Ningbo 16
San Francisco 16
Seoul 16
Stockholm 16
Denver 15
San Mateo 15
Toronto 15
Warsaw 15
Zhengzhou 15
Changsha 14
Auburn Hills 13
Brussels 13
Lanzhou 13
Atlanta 12
Boston 12
London 12
Phoenix 12
Campinas 11
Mexico City 11
Poplar 11
Rio de Janeiro 11
Brasília 10
Houston 10
Seattle 10
Bangalore 9
Chennai 9
Leawood 9
Manchester 9
Orem 9
Changchun 8
Milan 8
Montesilvano Marina 8
Mumbai 8
Orange 8
Ardabil 7
Atessa 7
Charlotte 7
Moscow 7
Querétaro 7
Teramo 7
Totale 8.423
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Nome #
16p13.3 microduplication syndrome: A new characteristic case without intellectual disability 178
16q22.1 microdeletion detected by array-CGH in a family with mental retardation and lobular breast cancer. 176
A new case of Yq microdeletion transmitted from a normal father to two infertile sons. 165
Zinc sulfate supplementation improves thyroid function in hypozincemic Down children 160
Widening of a Y-chromosome interval 6 deletion transmitted from a father to his infertile son accounts for an oligozoospermia critical region distal to RBM1 and DAZ genes 155
Discovering a familial Xp11.4 microduplication: Does the mother matter? 144
A new case of partial 2p trisomy due to de novo interstitial duplication 2p21-22. 142
Lack of correlation between elevated maternal serum hCG during second-trimester biochemical screening and fetal congenital anomaly. 137
Yq Microdeletion in a Patient with VACTERL Association and Shawl Scrotum with Bifid Scrotum: A Real Pathogenetic Association or a Coincidence? 136
A new case of pure partial 7q duplication 134
Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis 133
A cytogenetic survey of 13 patients with acute lymphocytic leukemia (ALL). 132
[Chromosome anomalies and Waldenström's macroglobulinemia]. 129
Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment. 128
C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy 127
Amenorrhoea in a girl with pericentric inversion of chromosome 11. 126
Identification of multiple transcribed sequences from the spinal muscular atrophy region on human chromosome 125
Clustering of Y chromosome deletions in subinterval E of interval 6 supports the existence of an oligozoospermia critical region outside the DAZ gene 125
Screening of mutations in the CFTR gene in 1195 couples entering assisted reproduction technique programs 124
A woman with an apparent non mosaic 45,X , delivered a 45,X,der(X) liveborne female 124
Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis. 123
A peptidase gene in chromosome 8q is disrupted by a balanced translocation in a duane syndrome patient 123
X/Y translocation in a family with Leri-Weill dyschondrosteosis 122
A newborne with ring chromosome 10, aganglionic megacolon, and renal hypoplasia. 122
Therapeutic potential of hAECs for early Achilles tendon defect repair through regeneration 119
A new case of mosaicism for invdup(15) duplicated for Prader-Willi/Angelman syndrome critical region (PWACR) in an adult healthy man. 119
Concerns about using Zn supplementation in Down's syndrome (DS) children. 118
Deletion 18p11.32p11.31 in a Child with Global Developmental Delay and Atypical, Drug-Resistant Absence Seizures 118
I nuovi orizzonti della diagnosi prenatale 117
A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11 117
AluI and HaeIII restriction enzyme banding patterns of Macaca fuscata and Cercopithecus aethiops sabaeus chromosomes. 117
De novo 9q33 microdeletion identified by array-comparative genomic hybridization in a foetus with sex reversal and congenital heart defects. 117
Characterization of novel genes in AZF regions 116
Routine fluorescence in situ hybridization analysis for detection of BCR-ABL rearrangement in myeloproliferative disorders 115
SHOX mutations detected by FISH and direct sequencing in patients with short stature 113
A case of triploidy detected by crosstrimester test. 113
[Cytogenetic study of 201 subjects with altered reproductive fitness]. 113
UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome 112
Human homologue sequences to the drosophila dishevelled segment-polarity gene are deleted in the Di George Syndrome 112
Assignment of the -arrestin 1 gene (ARBB1) to human chromosome 11q13 111
Comparison of methods for the detection of in situ restriction enzyme - nick translation using fluorochromes and confocal microscopy 110
Identification of deletions and duplications of the DMD gene in affected males and carrier females by multiple ligation probe amplification (MLPA). 110
Identification and characterization of different SHOX gene deletions in patients with Leri-Weill dyschondrosteosys by MLPA assay 110
Cytogenetic survey of benign prostate hyperplasia 109
Isolation of osteogenic progenitors from human amniotic fluid using a single step culture protocol. 107
A new case of chronic myelogenous leukemia with 14q+ marker and review of the literature. 106
Array-CGH characterization of a de novo t(X;Y)(p22;q11) in a female with short stature and mental retardation. 106
Non-invasive prenatal screening: a 20-year experience in Italy 105
Spectral karyotyping (SKY) refinement of a complex karyotype with t(20;21) in a Ph-positive CML patient submitted to peripheral blood stem cell transplantation 104
Assignment of TACSTD1 (alias TROP1, M4S1) to human chromosome 2p21 and refinement of mapping of TACSTD2 (alias TROP2, M1S1) to human chromosome 1p32 by in situ hybridization 104
A Mosaic Ring Chromosome 21 in a Patient with Mild Intellectual Disability not Evidenced by Array-Cgh 104
INOSITIDE-SPECIFIC PHOSPHOLIPASE Cbeta1 GENE DELETION IN THE PROGRESSION OF MYELODYSPLASTIC SYNDROME TO ACUTE MYELOID LEUKEMIA 103
Assignment of the hexokinase type 3 gene (HK3) to human chromosome band 5q35.3 by somatic cell hybrids and in situ hybridization 102
Identification in chromosome 8q11 of a region of homology with the g1 amplicon of the Y chromosome and functional analysis of the BEYLA gene. 101
Complex translocation of the Ph chromosome and Ph negative in CML arise from similar mechanisms as evidenced by FISH analysis 101
Array-CGH characterization of a prenatally detected de novo 46,X,der(Y)t(X;Y)(p22.3;q11.2) in a male fetus 100
Fluorescence in situ hybridization analysis of minimal residual disease and the relevance of the der(9) deletion in imatinib-treated patients with chronic myeloid leukemia. 99
Aneuploidy screening using circulating fetal cells in maternal blood by dual-probe FISH protocol: A prospective feasibility study on a series of 172 pregnant women 99
A genetic assessment of trisomy 21 in a patient with persistent truncus arteriosus who died 38 years ago. 98
[Cytogenetic study of 140 patients with changes in sexual features]. 98
Fetal Translocation between chromosomes 2, 18, and 21 resolved by fish 97
Karyotype refinement in five patients with acute myeloid leukemia using spectral karyotyping 97
Chromosome mapping of the human arrestin (SAG), beta-arrestin 2 (ARRB2), and beta-adrenergic receptor kinase 2 (ADRBK2) genes. 96
Sensitivity of cutaneous chronic myelomonocytic leukaemia lesions to hypomethylating treatment 96
Chromosome changes in 19 patients with Waldenström's macroglobulinemia. 95
Delayed Diagnosis of Potocki-Shaffer Syndrome in a Woman with Multiple Exostoses and Mental Retardation 95
Duplication Xp22.2 and pseudoisodicentricYq detected by FISH and PCR in a sterile male 94
Clinical-Grade Expanded Regulatory T Cells Are Enriched with Highly Suppressive Cells Producing IL-10, Granzyme B, and IL-35 94
Comparison of combined, stepwise sequential, contingent, and integrated screening in 7292 high-risk pregnant women 93
Growth delay in Down syndrome and zinc sulphate supplementation 92
[Clinical and cytogenetic staging of chronic myeloid leukemia. Philadelphia positive]. 92
Short arm rearrangements of sex chromosomes with haploinsufficiency of the SHOX gene are associated with Leri-Weill dyschondrosteosis. 91
Molecular studies in three patients with isodicentric Y chromosome 91
Correlation between apoptosis and TP53 status in osteosarcoma 90
The methylenetethrahydrofolate reductase (MTHFR) C677T polymorphism and male infertility in Italy. 90
Philadelphia (Ph), 14q+ and 1q+ chromosomes in immunoblastic phase (Richter's syndrome) in a patient with T chronic lymphocytic leukaemia. 90
Non-invasive early prenatal molecular diagnosis using retrieved transcervical trophoblast cells. 90
Acquisition of i(8q) as an early event in malignant triton tumors 89
Prenatal diagnosis using the triple test 89
Genomic organization, physical mapping, and involvement in Yq microdeletions of the VCY2 (BPY 2) gene 89
Effect of HpaII and MspI restriction endonucleases on chronic myelogenous leukemia chromosomes. Detection of CpG dinucleotide demethylation in situ. 89
P53 loss and point mutation are associated with suppression of apoptosis and progression of CML into myeloid blastic crisis 87
Chromosome abnormalities in breast fibroadenomas 87
Rhombencephalosynapsis in a severely polymalformed fetus with non-mosaic tetrasomy 9p, in intracytoplasmic-sperm-injection pregnancy. 87
Two newborns with chromosome 4 imbalances: deletion 4q33-->q35 and ring r(4)(pterq35.2-qter). 86
Prognostic value of atypical chromosomal changes during chronic myeloid leukemia. 86
Cytogenetic survey of sixty-one patients with preleukemic syndrome including myeloproliferative and myelodysplastic diseases. 86
Complex translocation involving Ph chromosome in a patient with typical chronic myelogenous leukemia. 86
Detection of chromosomal aneuploidies in fetal cells isolated from maternal blood using single-chromosome dual-probe FISH analysis 86
FISH analysis in detecting 9p duplication (p22p24) 85
Narrowing the Duane syndrome critical region at chromosome 8q13 down to 40 kb 85
Effectiveness of crosstrimester test in selecting high-risk pregnant women to undergo invasive prenatal diagnosis 85
Molecular characterization of two extra marker chromosomes detected at prenatal diagnosis 85
Cytogenetics and acute non lymphocytic leukemia. 85
Screening biochimici prenatali: l’esperienza del tri-test in 17.869 gravidanze della regione Abruzzo. 84
Molecular characterization of an unusual variant t(15;17) detected in an APL patient 84
On chromosomal DNA modifications by chemical and physical treatment of C-bands. 83
Heterochromatic polymorphisms of chromosome 16 evidenced by Alu I endonuclease digestion in chronic myelogenous leukemia. 83
Cytogenetics in patients with chronic myelogenous leukemia treated with bone marrow transplantation. 83
Characterization of a new TSPY gene family member in Yq (TSPYq1). 82
Totale 10.767
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Categoria #
all - tutte 55.339
article - articoli 0
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 55.339
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021753 0 0 0 0 0 176 14 10 249 158 43 103
2021/2022618 24 8 3 83 61 96 5 55 32 6 68 177
2022/20232.120 160 281 144 223 210 433 121 176 262 18 48 44
2023/2024908 56 32 71 27 56 286 171 45 6 38 5 115
2024/20252.281 172 325 268 83 53 29 74 83 307 121 284 482
2025/20262.323 464 223 468 606 504 58 0 0 0 0 0 0
Totale 14.147