IRIS
PASQUALI, FRANCESCO
 Distribuzione geografica
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Continente #
NA - Nord America 355
EU - Europa 256
AS - Asia 203
OC - Oceania 2
AF - Africa 1
Continente sconosciuto - Info sul continente non disponibili 1
SA - Sud America 1
Totale 819
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Nazione #
US - Stati Uniti d'America 354
CN - Cina 192
IE - Irlanda 110
FI - Finlandia 42
UA - Ucraina 37
DE - Germania 25
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
Totale 819
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Città #
Dublin 110
Chandler 99
Jacksonville 60
Nanjing 52
Beijing 31
New York 30
Ashburn 22
Shenyang 21
Helsinki 16
Wilmington 16
Lawrence 14
Medford 14
Nanchang 14
Princeton 14
Changsha 13
Tianjin 13
Hebei 10
Shanghai 10
Hangzhou 9
Jiaxing 9
Boardman 5
Milan 3
Pavia 3
Tokyo 3
Verona 3
Fairfield 2
Falls Church 2
Jinan 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
Warsaw 1
Washington 1
Zhengzhou 1
Totale 621
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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 73
Constitutional trisomy 8 as first mutation in multistep carcinogenesis: clinical, cytogenetic and molecular data on three cases 73
Duplication of the short arm of chromosome 9. Analysis of five cases. 64
The 9p- deletion syndrome. A patient with a 45,XX,-9,-15,+t(9/15) constitution due to maternal 3:1 meiotic disjunction. 63
Chromosome instability in cultured lymphocytes of patients with ovarian or uterine cancer. 62
Due anomalie "non-random" nelle leucemie mieloidi acute: t(8:21), t(15;17). 62
Translocation t(2;12)(p25;21q) classè d'abord comme 2/X. 62
Chromosome abnormalities and male sterility 53
Gene dosage effect for glucuronidase (GUSB) in monosomy 7 cells of patients with myelopriliferative disorders 50
Gene dosage effect in acquired monosomy 7: distinct behaviour of beta-glucuronidase and phosphoserine phosphatase 47
Roberts syndrome: phenotypic variation, cytogenetic definition and heterozygote detection. 47
Five unusual karyotypes in Down's syndrome 45
Bone marrow failure may be caused by chromosome anomalies exerting effects on RUNX1T1 gene 45
Trisomy 8 in myelodysplasia and acute leukemia is constitutional in 15-20% of cases. 44
Case Report: Heterozygous Germline Variant in EIF6 Additional to Biallelic SBDS Pathogenic Variants in a Patient With Ribosomopathy Shwachman-Diamond Syndrome 26
The frequent and clinically benign anomalies of chromosomes 7 and 20 in Shwachman-diamond syndrome may be subject to further clonal variations 11
Totale 827
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Categoria #
all - tutte 2.794
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 2.794
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020214 55 92 0 7 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
Totale 827