KALANTARI, SILVIA
 Distribuzione geografica
Continente #
NA - Nord America 344
EU - Europa 219
AS - Asia 90
AF - Africa 3
Totale 656
Nazione #
US - Stati Uniti d'America 342
IT - Italia 112
SG - Singapore 46
SE - Svezia 30
IE - Irlanda 29
CN - Cina 22
UA - Ucraina 17
DE - Germania 9
FR - Francia 5
ID - Indonesia 4
BE - Belgio 3
CH - Svizzera 3
FI - Finlandia 3
KR - Corea 3
PH - Filippine 3
SA - Arabia Saudita 3
AE - Emirati Arabi Uniti 2
AT - Austria 2
CA - Canada 2
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
ZA - Sudafrica 1
Totale 656
Città #
Ann Arbor 64
Chandler 59
Singapore 40
Santa Clara 39
Dublin 29
Torino 22
Turin 14
Ashburn 11
Nyköping 11
Hangzhou 8
Vestignè 8
Wilmington 8
Beijing 7
Columbus 7
Medford 7
Jacksonville 6
Princeton 6
Houston 4
Jakarta 4
Brussels 3
Guangzhou 3
Helsinki 3
Parma 3
San Diego 3
Santa Marinella 3
Woodstock 3
Zurich 3
Acqui Terme 2
Bologna 2
Boston 2
Brescia 2
Böblingen 2
Calgary 2
Capurso 2
Dubai 2
Fairfield 2
Frankfurt am Main 2
Gironico al Piano 2
London 2
Magugpo Poblacion 2
Montegiorgio 2
Naples 2
New York 2
Norwalk 2
Piemonte 2
Pontedera 2
Putignano 2
Rimini 2
Rome 2
San Mateo 2
Seoul 2
Upper Marlboro 2
Augusta 1
Boardman 1
Bra 1
Buffalo 1
Cambridge 1
Carignano 1
Council Bluffs 1
Dallas 1
Fremont 1
Garessio 1
Giessen 1
Gunzenhausen 1
Hebei 1
Ilsan 1
Issogne 1
Johannesburg 1
Kashan 1
Los Angeles 1
Lviv 1
Moncalieri 1
Napoli 1
Omegna 1
Oslo 1
Rivalta Di Torino 1
Seattle 1
Shanghai 1
Silver Spring 1
Stavanger 1
Ulan Bator 1
Vienna 1
Warsaw 1
Totale 459
Nome #
Clinical exome sequencing is a powerful tool in the diagnostic flow of monogenic kidney diseases: an Italian experience 167
USE OF CLINICAL EXOME SEQUENCING IN THE DIAGNOSTIC FLOW OF MONOGENIC KIDNEY DISEASES: THE PIEDMONT EXPERIENCE 113
NOVEL AND KNOWN MUTATIONS IDENTIFIED BY CLINICAL EXOME SEQUENCING FOR THE DIAGNOSIS OF POLYCYSTIC KIDNEY DISEASE 103
Adult-onset CblC deficiency: a challenging diagnosis involving different adult clinical specialists 92
A novel COLEC10 mutation in a child with 3MC syndrome 68
Kaposiform hemangioendothelioma further broadens the phenotype of PIK3CA-related overgrowth spectrum 58
Relevance of next generation sequencing (NGS) data re-analysis in the diagnosis of monogenic diseases leading to organ failure 26
The role of genetic testing in the diagnostic workflow of pediatric patients with kidney diseases: the experience of a single institution 25
New case of syncytial giant-cell variant of hepatocellular carcinoma in a pediatric patient with HNF1B deficiency: does it fit with the syndrome? 24
Totale 676
Categoria #
all - tutte 3.144
article - articoli 0
book - libri 0
conference - conferenze 724
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 3.868


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
2023/2024102 10 20 6 8 2 12 6 4 1 7 10 16
2024/2025130 1 12 15 27 56 19 0 0 0 0 0 0
Totale 676