PALAZZO, VIVIANA
 Distribuzione geografica
Continente #
NA - Nord America 390
EU - Europa 272
AS - Asia 55
Continente sconosciuto - Info sul continente non disponibili 1
Totale 718
Nazione #
US - Stati Uniti d'America 387
IT - Italia 103
IE - Irlanda 60
SE - Svezia 47
HK - Hong Kong 36
PL - Polonia 18
FI - Finlandia 9
CN - Cina 8
GB - Regno Unito 7
BE - Belgio 6
CH - Svizzera 6
DE - Germania 5
ES - Italia 4
FR - Francia 4
JO - Giordania 4
CA - Canada 3
VN - Vietnam 2
EU - Europa 1
ID - Indonesia 1
IL - Israele 1
IN - India 1
IR - Iran 1
RO - Romania 1
RU - Federazione Russa 1
SG - Singapore 1
UA - Ucraina 1
Totale 718
Città #
Dublin 60
Chandler 43
Florence 28
Fairfield 24
Hong Kong 22
Woodbridge 22
Ashburn 21
Warsaw 18
Princeton 17
Altamura 16
Cambridge 16
Ann Arbor 15
Lawrence 15
Houston 14
Buffalo 13
Boston 11
Milan 11
Seattle 11
Wilmington 9
Beijing 6
Bern 6
Brussels 6
New York 6
Boardman 5
Rome 5
Barcelona 4
Bremen 4
Genoa 4
Medford 4
Paris 4
San Diego 4
Norwalk 3
Poggio a Caiano 3
Redwood City 3
Cagliari 2
Dallas 2
Dong Ket 2
Falls Church 2
Toronto 2
Trento 2
Andover 1
Arezzo 1
Bologna 1
Campi Bisenzio 1
Chennai 1
Chieti 1
Duncan 1
Ferrara 1
Hangzhou 1
Herzliya 1
Jacksonville 1
Kashan 1
Modena 1
Moscow 1
Naples 1
Ottawa 1
San Casciano in Val di Pesa 1
Scandicci 1
Singapore 1
Tappahannock 1
Washington 1
Totale 486
Nome #
NGS e malattie renali: aspetti clinici e molecolari delle acidosi tubulari renali 109
The genetic and clinical spectrum of a large cohort of patients with distal renal tubular acidosis 103
Molecular characterization of paediatric glioneuronal tumours with neuropil-like islands: a genome-wide copy number analysis. 79
Therapeutic implications of novel mutations of the RFX6 gene associated with early-onset diabetes 68
Chiari 1 malformation and exome sequencing in 51 trios: the emerging role of rare missense variants in chromatin remodeling genes 68
Noninvasive Prenatal Diagnosis in a Family at Risk for Fraser Syndrome 47
Severe Obesity Associated with Severe Hyperinsulinism and T2D in a Family with Mutation in SH2B1 Gene 45
Studio clinico e molecolare di famiglie italiane affette da displasia ectodermica: analisi dei geni ED1, EDAR ed EDARADD 44
A Clinical Workflow for Cost-Saving High-Rate Diagnosis of Genetic Kidney Diseases 37
[A child with severe growth delay and renal cysts] 33
TOWARD THE GENETIC BASIS OF OESOPHAGEAL ATRESIA: CLINICAL AND MOLECULAR STUDY BY NEXT GENERATION SEQUENCING 30
MOLECULAR CHARACTERIZATION OF PEDIATRIC GLIONEURONAL TUMOR WITH NEUROPIL-LIKE ISLANDS: A GENOME-WIDE COPY NUMBER ANALYSIS 29
Leopard-like retinopathy and severe early-onset portal hypertension expand the phenotype of KARS1-related syndrome: a case report 25
The promise and challenge of high throughput sequencing to discover genes involved in Medullary Sponge Kidney disease 24
Totale 741
Categoria #
all - tutte 2.369
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 2.369


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201945 0 0 0 0 0 0 0 1 0 6 9 29
2019/202088 22 18 3 4 5 3 8 5 5 8 3 4
2020/202191 2 6 1 15 6 12 5 6 8 20 5 5
2021/202275 2 9 0 4 0 4 2 7 1 3 15 28
2022/2023287 24 46 11 18 18 43 38 10 45 6 18 10
2023/202498 5 13 18 8 4 16 4 30 0 0 0 0
Totale 741