IRIS
CALABRESE, Giuseppe
 Distribuzione geografica
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Continente #
NA - Nord America 6.198
EU - Europa 4.851
AS - Asia 4.725
SA - Sud America 435
AF - Africa 62
Continente sconosciuto - Info sul continente non disponibili 6
OC - Oceania 6
Totale 16.283
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Nazione #
US - Stati Uniti d'America 6.087
SG - Singapore 1.727
CN - Cina 1.408
UA - Ucraina 774
IT - Italia 655
GB - Regno Unito 569
IE - Irlanda 568
RU - Federazione Russa 513
SE - Svezia 510
DE - Germania 486
TR - Turchia 482
VN - Vietnam 423
IN - India 414
FR - Francia 409
BR - Brasile 355
FI - Finlandia 177
CA - Canada 61
HK - Hong Kong 44
AT - Austria 40
MX - Messico 34
BD - Bangladesh 33
JP - Giappone 31
IQ - Iraq 30
ZA - Sudafrica 28
PL - Polonia 26
AR - Argentina 25
NL - Olanda 22
CZ - Repubblica Ceca 20
BE - Belgio 18
KR - Corea 16
VE - Venezuela 16
RO - Romania 15
IL - Israele 14
PK - Pakistan 14
LT - Lituania 13
EC - Ecuador 12
ES - Italia 12
GR - Grecia 10
IR - Iran 10
ID - Indonesia 9
SA - Arabia Saudita 9
CL - Cile 7
CO - Colombia 7
KE - Kenya 7
MY - Malesia 7
UZ - Uzbekistan 7
AU - Australia 6
EU - Europa 6
OM - Oman 6
PH - Filippine 6
AZ - Azerbaigian 5
PE - Perù 5
DO - Repubblica Dominicana 4
EG - Egitto 4
JO - Giordania 4
LB - Libano 4
PY - Paraguay 4
SY - Repubblica araba siriana 4
TN - Tunisia 4
TW - Taiwan 4
DZ - Algeria 3
JM - Giamaica 3
MA - Marocco 3
MD - Moldavia 3
NP - Nepal 3
UY - Uruguay 3
AE - Emirati Arabi Uniti 2
CH - Svizzera 2
CR - Costa Rica 2
DK - Danimarca 2
ET - Etiopia 2
GD - Grenada 2
MU - Mauritius 2
NO - Norvegia 2
RS - Serbia 2
SN - Senegal 2
TH - Thailandia 2
AL - Albania 1
BB - Barbados 1
BH - Bahrain 1
BW - Botswana 1
CG - Congo 1
CI - Costa d'Avorio 1
GE - Georgia 1
GT - Guatemala 1
GY - Guiana 1
HN - Honduras 1
KG - Kirghizistan 1
KW - Kuwait 1
KZ - Kazakistan 1
LK - Sri Lanka 1
LY - Libia 1
MK - Macedonia 1
NG - Nigeria 1
PA - Panama 1
QA - Qatar 1
SC - Seychelles 1
SK - Slovacchia (Repubblica Slovacca) 1
TG - Togo 1
TT - Trinidad e Tobago 1
Totale 16.283
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Città #
Singapore 1.123
Jacksonville 811
San Jose 712
Chandler 692
Dublin 565
Southend 449
Ashburn 445
Beijing 363
Princeton 291
Izmir 263
Dallas 257
Nanjing 243
Los Angeles 197
Dearborn 179
Wilmington 157
The Dalles 137
Cambridge 135
Chieti 125
Ho Chi Minh City 119
Tongling 109
Santa Clara 105
Munich 103
Nanchang 99
Boardman 92
Grafing 92
Buffalo 87
Hanoi 78
Dong Ket 75
Ann Arbor 72
Altamura 71
New York 65
Moscow 54
Pescara 51
Woodbridge 50
Hebei 49
Kunming 49
Shenyang 48
Tianjin 47
Orem 37
São Paulo 37
Helsinki 36
Hong Kong 36
Vienna 36
Rome 33
Washington 33
Jiaxing 31
Tokyo 29
Council Bluffs 28
Jinan 28
Redondo Beach 27
Brooklyn 26
Hangzhou 26
Grevenbroich 25
Montreal 23
Atlanta 21
Johannesburg 21
Augusta 20
Chicago 20
Hefei 20
Stockholm 20
Düsseldorf 18
Kocaeli 18
Warsaw 18
Brno 17
Haiphong 17
Norwalk 17
Toronto 17
Chennai 16
Denver 16
Guangzhou 16
Ningbo 16
San Francisco 16
Seoul 16
San Mateo 15
Zhengzhou 15
Changsha 14
London 14
Mexico City 14
Phoenix 14
Poplar 14
Auburn Hills 13
Boston 13
Brussels 13
Lanzhou 13
Baghdad 12
Houston 12
Rio de Janeiro 12
Campinas 11
Manchester 11
Milan 11
Brasília 10
Mumbai 10
Seattle 10
Bangalore 9
Leawood 9
Amsterdam 8
Biên Hòa 8
Can Tho 8
Changchun 8
Da Nang 8
Totale 9.799
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Nome #
16p13.3 microduplication syndrome: A new characteristic case without intellectual disability 210
16q22.1 microdeletion detected by array-CGH in a family with mental retardation and lobular breast cancer. 198
A new case of Yq microdeletion transmitted from a normal father to two infertile sons. 179
Zinc sulfate supplementation improves thyroid function in hypozincemic Down children 176
A new case of partial 2p trisomy due to de novo interstitial duplication 2p21-22. 173
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 169
Sequential combined test, second trimester maternal serum markers, and circulating fetal cells to select women for invasive prenatal diagnosis 169
Yq Microdeletion in a Patient with VACTERL Association and Shawl Scrotum with Bifid Scrotum: A Real Pathogenetic Association or a Coincidence? 165
Discovering a familial Xp11.4 microduplication: Does the mother matter? 162
A new case of pure partial 7q duplication 156
Lack of correlation between elevated maternal serum hCG during second-trimester biochemical screening and fetal congenital anomaly. 155
A woman with an apparent non mosaic 45,X , delivered a 45,X,der(X) liveborne female 153
A cytogenetic survey of 13 patients with acute lymphocytic leukemia (ALL). 152
C677T mutation in the 5,10-MTHFR gene and risk of Down syndrome in Italy 152
[Chromosome anomalies and Waldenström's macroglobulinemia]. 151
Mosaic 7q31 deletion involving FOXP2 gene associated with language impairment. 146
A peptidase gene in chromosome 8q is disrupted by a balanced translocation in a duane syndrome patient 144
Identification of multiple transcribed sequences from the spinal muscular atrophy region on human chromosome 142
A newborne with ring chromosome 10, aganglionic megacolon, and renal hypoplasia. 142
Amenorrhoea in a girl with pericentric inversion of chromosome 11. 142
Non-invasive prenatal screening: a 20-year experience in Italy 142
Identification of 14 rare marker chromosomes and derivatives by spectral karyotyping in prenatal and postnatal diagnosis. 141
Screening of mutations in the CFTR gene in 1195 couples entering assisted reproduction technique programs 140
[Cytogenetic study of 201 subjects with altered reproductive fitness]. 139
X/Y translocation in a family with Leri-Weill dyschondrosteosis 138
Clustering of Y chromosome deletions in subinterval E of interval 6 supports the existence of an oligozoospermia critical region outside the DAZ gene 137
AluI and HaeIII restriction enzyme banding patterns of Macaca fuscata and Cercopithecus aethiops sabaeus chromosomes. 137
A quarter of men with idiopathic oligo-azoospermia display chromosomal abnormalities and microdeletions of different types in interval 6 of Yq11 136
Deletion 18p11.32p11.31 in a Child with Global Developmental Delay and Atypical, Drug-Resistant Absence Seizures 136
A new case of mosaicism for invdup(15) duplicated for Prader-Willi/Angelman syndrome critical region (PWACR) in an adult healthy man. 136
I nuovi orizzonti della diagnosi prenatale 135
Concerns about using Zn supplementation in Down's syndrome (DS) children. 134
Therapeutic potential of hAECs for early Achilles tendon defect repair through regeneration 134
UFD1L, a developmentally expressed ubiquitination gene, is deleted in CATCH 22 syndrome 132
Identification of deletions and duplications of the DMD gene in affected males and carrier females by multiple ligation probe amplification (MLPA). 132
Routine fluorescence in situ hybridization analysis for detection of BCR-ABL rearrangement in myeloproliferative disorders 132
A case of triploidy detected by crosstrimester test. 131
De novo 9q33 microdeletion identified by array-comparative genomic hybridization in a foetus with sex reversal and congenital heart defects. 130
Characterization of novel genes in AZF regions 129
Human homologue sequences to the drosophila dishevelled segment-polarity gene are deleted in the Di George Syndrome 128
Cytogenetic survey of benign prostate hyperplasia 128
Identification and characterization of different SHOX gene deletions in patients with Leri-Weill dyschondrosteosys by MLPA assay 128
A Mosaic Ring Chromosome 21 in a Patient with Mild Intellectual Disability not Evidenced by Array-Cgh 127
Array-CGH characterization of a de novo t(X;Y)(p22;q11) in a female with short stature and mental retardation. 126
A new case of chronic myelogenous leukemia with 14q+ marker and review of the literature. 125
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 124
SHOX mutations detected by FISH and direct sequencing in patients with short stature 124
Assignment of the -arrestin 1 gene (ARBB1) to human chromosome 11q13 124
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 123
Comparison of methods for the detection of in situ restriction enzyme - nick translation using fluorochromes and confocal microscopy 122
Array-CGH characterization of a prenatally detected de novo 46,X,der(Y)t(X;Y)(p22.3;q11.2) in a male fetus 121
Isolation of osteogenic progenitors from human amniotic fluid using a single step culture protocol. 120
Complex translocation of the Ph chromosome and Ph negative in CML arise from similar mechanisms as evidenced by FISH analysis 120
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 119
INOSITIDE-SPECIFIC PHOSPHOLIPASE Cbeta1 GENE DELETION IN THE PROGRESSION OF MYELODYSPLASTIC SYNDROME TO ACUTE MYELOID LEUKEMIA 118
[Cytogenetic study of 140 patients with changes in sexual features]. 116
Clinical-Grade Expanded Regulatory T Cells Are Enriched with Highly Suppressive Cells Producing IL-10, Granzyme B, and IL-35 116
Identification in chromosome 8q11 of a region of homology with the g1 amplicon of the Y chromosome and functional analysis of the BEYLA gene. 115
Duplication Xp22.2 and pseudoisodicentricYq detected by FISH and PCR in a sterile male 115
Chromosome mapping of the human arrestin (SAG), beta-arrestin 2 (ARRB2), and beta-adrenergic receptor kinase 2 (ADRBK2) genes. 115
Assignment of the hexokinase type 3 gene (HK3) to human chromosome band 5q35.3 by somatic cell hybrids and in situ hybridization 115
[Clinical and cytogenetic staging of chronic myeloid leukemia. Philadelphia positive]. 113
A genetic assessment of trisomy 21 in a patient with persistent truncus arteriosus who died 38 years ago. 112
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. 112
Fetal Translocation between chromosomes 2, 18, and 21 resolved by fish 111
Karyotype refinement in five patients with acute myeloid leukemia using spectral karyotyping 109
Delayed Diagnosis of Potocki-Shaffer Syndrome in a Woman with Multiple Exostoses and Mental Retardation 109
Sensitivity of cutaneous chronic myelomonocytic leukaemia lesions to hypomethylating treatment 109
Chromosome changes in 19 patients with Waldenström's macroglobulinemia. 108
Growth delay in Down syndrome and zinc sulphate supplementation 107
Comparison of combined, stepwise sequential, contingent, and integrated screening in 7292 high-risk pregnant women 106
Two newborns with chromosome 4 imbalances: deletion 4q33-->q35 and ring r(4)(pterq35.2-qter). 105
Prognostic value of atypical chromosomal changes during chronic myeloid leukemia. 104
Non-invasive early prenatal molecular diagnosis using retrieved transcervical trophoblast cells. 104
Short arm rearrangements of sex chromosomes with haploinsufficiency of the SHOX gene are associated with Leri-Weill dyschondrosteosis. 103
Genomic organization, physical mapping, and involvement in Yq microdeletions of the VCY2 (BPY 2) gene 103
Molecular studies in three patients with isodicentric Y chromosome 103
Philadelphia (Ph), 14q+ and 1q+ chromosomes in immunoblastic phase (Richter's syndrome) in a patient with T chronic lymphocytic leukaemia. 103
Correlation between apoptosis and TP53 status in osteosarcoma 101
The methylenetethrahydrofolate reductase (MTHFR) C677T polymorphism and male infertility in Italy. 101
Prenatal diagnosis using the triple test 101
Cytogenetics and acute non lymphocytic leukemia. 101
Effect of HpaII and MspI restriction endonucleases on chronic myelogenous leukemia chromosomes. Detection of CpG dinucleotide demethylation in situ. 101
Acquisition of i(8q) as an early event in malignant triton tumors 100
FISH analysis in detecting 9p duplication (p22p24) 100
Rhombencephalosynapsis in a severely polymalformed fetus with non-mosaic tetrasomy 9p, in intracytoplasmic-sperm-injection pregnancy. 100
Screening biochimici prenatali: l’esperienza del tri-test in 17.869 gravidanze della regione Abruzzo. 99
Narrowing the Duane syndrome critical region at chromosome 8q13 down to 40 kb 98
Detection of chromosomal aneuploidies in fetal cells isolated from maternal blood using single-chromosome dual-probe FISH analysis 98
Cytogenetic survey of sixty-one patients with preleukemic syndrome including myeloproliferative and myelodysplastic diseases. 97
Chromosome 11 rearrangements and specific MLL amplification revealed by spectral karyotyping in a patient with refractory anaemia with excess of blasts(RAEB)”. 96
P53 loss and point mutation are associated with suppression of apoptosis and progression of CML into myeloid blastic crisis 96
On chromosomal DNA modifications by chemical and physical treatment of C-bands. 96
Heterochromatic polymorphisms of chromosome 16 evidenced by Alu I endonuclease digestion in chronic myelogenous leukemia. 96
Cytogenetics in patients with chronic myelogenous leukemia treated with bone marrow transplantation. 96
The polymorphic polyglutamine repeat in the mitochondrial DNA polymerase γ gene is not associated with oligozoospermia 95
Molecular characterization of two extra marker chromosomes detected at prenatal diagnosis 94
Complex translocation involving Ph chromosome in a patient with typical chronic myelogenous leukemia. 94
De novo complex chromosome rearrangement detected by fluorescence in situ hybridization on amniotic fluid cells 93
Effectiveness of crosstrimester test in selecting high-risk pregnant women to undergo invasive prenatal diagnosis 93
Totale 12.443
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Categoria #
all - tutte 60.071
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 60.071
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/2021304 0 0 0 0 0 0 0 0 0 158 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
2025/20264.656 464 223 468 606 504 332 883 337 518 321 0 0
Totale 16.480