IRIS
PASQUALI, FRANCESCO
 Distribuzione geografica
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Continente #
NA - Nord America 371
EU - Europa 258
AS - Asia 225
AF - Africa 2
OC - Oceania 2
Continente sconosciuto - Info sul continente non disponibili 1
SA - Sud America 1
Totale 860
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Nazione #
US - Stati Uniti d'America 370
CN - Cina 194
IE - Irlanda 110
FI - Finlandia 42
UA - Ucraina 37
DE - Germania 27
SG - Singapore 20
SE - Svezia 14
IT - Italia 12
GB - Regno Unito 8
JP - Giappone 3
TR - Turchia 3
AU - Australia 2
FR - Francia 2
IN - India 2
RU - Federazione Russa 2
AR - Argentina 1
BD - Bangladesh 1
BE - Belgio 1
CA - Canada 1
EU - Europa 1
ID - Indonesia 1
LV - Lettonia 1
MU - Mauritius 1
NL - Olanda 1
PL - Polonia 1
SA - Arabia Saudita 1
TN - Tunisia 1
Totale 860
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Città #
Dublin 110
Chandler 99
Jacksonville 60
Nanjing 52
Beijing 31
New York 30
Ashburn 22
Boardman 21
Shenyang 21
Helsinki 16
Wilmington 16
Lawrence 14
Medford 14
Nanchang 14
Princeton 14
Changsha 13
Singapore 13
Tianjin 13
Shanghai 11
Hebei 10
Hangzhou 9
Jiaxing 9
Milan 3
Pavia 3
Tokyo 3
Verona 3
Fairfield 2
Falls Church 2
Jinan 2
Munich 2
Ningbo 2
Berlin 1
Brussels 1
Canberra 1
Delhi 1
Dhaka 1
Guangzhou 1
Gunzenhausen 1
London 1
Norwalk 1
Nova Milanese 1
Novokuznetsk 1
Pune 1
Riyadh 1
Seattle 1
Sydney 1
Toronto 1
Tunis 1
Warsaw 1
Washington 1
Zhengzhou 1
Totale 654
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Nome #
Familial platelet disorder with propensity to acute myelogenous leukemia: Genetic heterogeneity and progression to leukemia via acquisition of clonal chromosome anomalies 78
Constitutional trisomy 8 as first mutation in multistep carcinogenesis: clinical, cytogenetic and molecular data on three cases 75
Duplication of the short arm of chromosome 9. Analysis of five cases. 66
The 9p- deletion syndrome. A patient with a 45,XX,-9,-15,+t(9/15) constitution due to maternal 3:1 meiotic disjunction. 65
Translocation t(2;12)(p25;21q) classè d'abord comme 2/X. 65
Chromosome instability in cultured lymphocytes of patients with ovarian or uterine cancer. 64
Due anomalie "non-random" nelle leucemie mieloidi acute: t(8:21), t(15;17). 64
Chromosome abnormalities and male sterility 55
Gene dosage effect for glucuronidase (GUSB) in monosomy 7 cells of patients with myelopriliferative disorders 53
Gene dosage effect in acquired monosomy 7: distinct behaviour of beta-glucuronidase and phosphoserine phosphatase 49
Roberts syndrome: phenotypic variation, cytogenetic definition and heterozygote detection. 49
Five unusual karyotypes in Down's syndrome 47
Bone marrow failure may be caused by chromosome anomalies exerting effects on RUNX1T1 gene 47
Trisomy 8 in myelodysplasia and acute leukemia is constitutional in 15-20% of cases. 46
Case Report: Heterozygous Germline Variant in EIF6 Additional to Biallelic SBDS Pathogenic Variants in a Patient With Ribosomopathy Shwachman-Diamond Syndrome 32
The frequent and clinically benign anomalies of chromosomes 7 and 20 in Shwachman-diamond syndrome may be subject to further clonal variations 13
Totale 868
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Categoria #
all - tutte 3.436
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 3.436
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202060 0 0 0 0 0 8 3 7 0 17 25 0
2020/202172 8 6 2 7 0 9 0 14 2 13 9 2
2021/202273 0 0 0 1 3 3 1 5 3 0 10 47
2022/2023276 27 28 6 13 37 23 0 13 122 1 6 0
2023/2024114 22 9 2 3 9 44 4 4 0 1 8 8
2024/202541 12 17 1 8 3 0 0 0 0 0 0 0
Totale 868