KALANTARI, SILVIA
 Distribuzione geografica
Continente #
NA - Nord America 277
EU - Europa 188
AS - Asia 30
AF - Africa 2
Totale 497
Nazione #
US - Stati Uniti d'America 277
IT - Italia 91
SE - Svezia 30
IE - Irlanda 29
UA - Ucraina 16
CN - Cina 14
DE - Germania 9
FR - Francia 4
BE - Belgio 3
KR - Corea 3
PH - Filippine 3
SA - Arabia Saudita 3
GB - Regno Unito 2
MA - Marocco 2
NO - Norvegia 2
UZ - Uzbekistan 2
ES - Italia 1
HK - Hong Kong 1
IN - India 1
IR - Iran 1
MN - Mongolia 1
PL - Polonia 1
VN - Vietnam 1
Totale 497
Città #
Ann Arbor 64
Chandler 59
Dublin 29
Torino 22
Nyköping 11
Ashburn 9
Vestignè 8
Wilmington 8
Hangzhou 7
Medford 7
Turin 7
Jacksonville 6
Princeton 6
Beijing 5
Houston 4
Brussels 3
San Diego 3
Santa Marinella 3
Woodstock 3
Acqui Terme 2
Boston 2
Brescia 2
Böblingen 2
Capurso 2
Fairfield 2
Frankfurt am Main 2
Gironico al Piano 2
London 2
Magugpo Poblacion 2
Naples 2
New York 2
Norwalk 2
Piemonte 2
Pontedera 2
Putignano 2
San Mateo 2
Seoul 2
Upper Marlboro 2
Augusta 1
Bologna 1
Bra 1
Buffalo 1
Cambridge 1
Carignano 1
Fremont 1
Garessio 1
Giessen 1
Gunzenhausen 1
Hebei 1
Ilsan 1
Issogne 1
Kashan 1
Moncalieri 1
Napoli 1
Omegna 1
Oslo 1
Rivalta Di Torino 1
Seattle 1
Silver Spring 1
Stavanger 1
Ulan Bator 1
Warsaw 1
Totale 326
Nome #
Clinical exome sequencing is a powerful tool in the diagnostic flow of monogenic kidney diseases: an Italian experience 153
NOVEL AND KNOWN MUTATIONS IDENTIFIED BY CLINICAL EXOME SEQUENCING FOR THE DIAGNOSIS OF POLYCYSTIC KIDNEY DISEASE 100
USE OF CLINICAL EXOME SEQUENCING IN THE DIAGNOSTIC FLOW OF MONOGENIC KIDNEY DISEASES: THE PIEDMONT EXPERIENCE 93
Adult-onset CblC deficiency: a challenging diagnosis involving different adult clinical specialists 60
Kaposiform hemangioendothelioma further broadens the phenotype of PIK3CA-related overgrowth spectrum 44
A novel COLEC10 mutation in a child with 3MC syndrome 44
The role of genetic testing in the diagnostic workflow of pediatric patients with kidney diseases: the experience of a single institution 10
New case of syncytial giant-cell variant of hepatocellular carcinoma in a pediatric patient with HNF1B deficiency: does it fit with the syndrome? 8
Relevance of next generation sequencing (NGS) data re-analysis in the diagnosis of monogenic diseases leading to organ failure 5
Totale 517
Categoria #
all - tutte 1.913
article - articoli 0
book - libri 0
conference - conferenze 548
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 2.461


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202173 0 0 0 0 27 2 7 10 15 2 7 3
2021/2022202 8 1 4 16 19 18 25 19 18 29 25 20
2022/2023169 14 22 3 15 12 36 8 7 23 8 15 6
2023/202473 10 20 6 8 2 12 6 4 1 4 0 0
Totale 517