VALLI, ROBERTO VINCENZO ORESTE
 Distribuzione geografica
Continente #
AS - Asia 103
NA - Nord America 89
EU - Europa 83
SA - Sud America 23
AF - Africa 5
Totale 303
Nazione #
US - Stati Uniti d'America 87
CN - Cina 48
SG - Singapore 24
IE - Irlanda 21
RU - Federazione Russa 21
BR - Brasile 16
IT - Italia 16
DE - Germania 14
HK - Hong Kong 14
VN - Vietnam 13
EC - Ecuador 4
FI - Finlandia 3
AR - Argentina 2
CA - Canada 2
GB - Regno Unito 2
IN - India 2
MA - Marocco 2
PL - Polonia 2
AT - Austria 1
CI - Costa d'Avorio 1
CO - Colombia 1
EG - Egitto 1
FR - Francia 1
JP - Giappone 1
LB - Libano 1
SE - Svezia 1
TN - Tunisia 1
UA - Ucraina 1
Totale 303
Città #
Dallas 27
Dublin 21
Hong Kong 14
Singapore 12
Beijing 10
Munich 10
Chandler 8
Nanjing 8
Ho Chi Minh City 7
Pavia 6
Ashburn 4
Milan 4
New York 4
Redondo Beach 4
Tianjin 4
Boardman 3
Los Angeles 3
Wilmington 3
Belo Horizonte 2
Brooklyn 2
Falkenstein 2
Frankfurt am Main 2
Hangzhou 2
Hanoi 2
Helsinki 2
Lawrence 2
Montreal 2
Moscow 2
Nanchang 2
Princeton 2
Quito 2
Rivignano 2
Santa Clara 2
Shanghai 2
Shenyang 2
Abidjan 1
Al Maḩallah al Kubrá 1
Atlanta 1
Augusta 1
Biên Hòa 1
Brasília 1
Camden 1
Changsha 1
Chicago 1
Chongqing 1
Curitiba 1
Curvelo 1
Córdoba 1
Delhi 1
Dezhou 1
Goiânia 1
Guayaquil 1
Haikou 1
Hebei 1
Indaiatuba 1
Jacksonville 1
Jinan 1
Kyiv 1
London 1
Longyan 1
Maceió 1
Machala 1
Medford 1
Niterói 1
Osório 1
Philadelphia 1
Pune 1
Quận Bảy 1
Reston 1
Rio Bonito 1
Rio de Janeiro 1
Salvador 1
San Juan 1
Santiago de Cali 1
Sorriso 1
São Félix do Xingu Municipality 1
São João de Meriti 1
Tangier 1
The Dalles 1
Thái Nguyên 1
Tokyo 1
Tunis 1
Turku 1
Warsaw 1
Wroclaw 1
Wuhu 1
Zhoukou 1
Totale 238
Nome #
Case Report: Heterozygous Germline Variant in EIF6 Additional to Biallelic SBDS Pathogenic Variants in a Patient With Ribosomopathy Shwachman-Diamond Syndrome 87
Whole exome sequencing discloses heterozygous variants in the DNAJC21 and EFL1 genes but not in SRP54 in 6 out of 16 patients with Shwachman-Diamond Syndrome carrying biallelic SBDS mutations 80
Shwachman-Diamond syndrome: diagnosis, pathogenesis and prognosis 80
Shwachman‐Diamond syndrome with clonal interstitial deletion of the long arm of chromosome 20 in bone marrow: haematological features, prognosis and genomic instability 33
Pleomorphic Parotid Adenoma in a Child Affected with Cri du Chat Syndrome: Clinical, Cytogenetic, and Molecular Analysis 31
Totale 311
Categoria #
all - tutte 1.456
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 1.456


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/20213 0 0 0 0 0 0 1 1 1 0 0 0
2021/202210 0 0 0 0 3 0 0 0 1 1 1 4
2022/202339 2 3 5 3 2 1 0 1 21 0 1 0
2023/202415 3 1 1 0 3 4 0 1 0 1 0 1
2024/202587 3 4 0 1 2 3 4 8 27 4 7 24
2025/2026124 16 25 29 29 22 3 0 0 0 0 0 0
Totale 311