GRAZIANI, LUDOVICO
 Distribuzione geografica
Continente #
AS - Asia 187
NA - Nord America 112
EU - Europa 60
SA - Sud America 30
AF - Africa 1
Totale 390
Nazione #
US - Stati Uniti d'America 109
SG - Singapore 86
HK - Hong Kong 41
CN - Cina 32
BR - Brasile 22
IT - Italia 16
RU - Federazione Russa 15
VN - Vietnam 15
DE - Germania 7
JP - Giappone 7
NL - Olanda 5
AT - Austria 4
VE - Venezuela 4
GB - Regno Unito 3
AR - Argentina 2
ES - Italia 2
FI - Finlandia 2
IN - India 2
MX - Messico 2
PL - Polonia 2
AE - Emirati Arabi Uniti 1
BG - Bulgaria 1
CA - Canada 1
CO - Colombia 1
FR - Francia 1
ID - Indonesia 1
KG - Kirghizistan 1
PT - Portogallo 1
PY - Paraguay 1
SE - Svezia 1
TR - Turchia 1
ZA - Sudafrica 1
Totale 390
Città #
Singapore 56
Hong Kong 41
San Jose 26
Beijing 11
Ashburn 10
Los Angeles 7
Tokyo 7
Council Bluffs 6
Hanoi 5
Ho Chi Minh City 5
Rome 5
Caracas 4
Amsterdam 3
Frankfurt am Main 3
New York 3
Nuremberg 3
Redondo Beach 3
Santa Clara 3
Vienna 3
Curitiba 2
Haiphong 2
Helsinki 2
Mexico City 2
North Bergen 2
São Paulo 2
Zhengzhou 2
Ankara 1
Annapolis 1
Asunción 1
Banfield 1
Belo Horizonte 1
Bishkek 1
Blumenau 1
Boise 1
Buffalo 1
Campinas 1
Carteret 1
Chennai 1
Da Nang 1
Dallas 1
Des Moines 1
Fitzgerald 1
Frederico Westphalen 1
Greensboro 1
Guarulhos 1
Hangzhou 1
Houston 1
Hyderabad 1
Jakarta 1
Johannesburg 1
Jundiaí 1
Lombard 1
Londrina 1
Milan 1
Mogi das Cruzes 1
Moscow 1
Nova Iguaçu 1
Orem 1
Pelotas 1
Phoenix 1
Picos 1
Popayán 1
Poplar 1
Porto 1
Porto Alegre 1
Resistencia 1
Rio Negro 1
Rio das Ostras 1
Secaucus 1
Sofia 1
Stockholm 1
São Carlos 1
São João de Meriti 1
São Roque do Canaã 1
Thái Nguyên 1
Toronto 1
Verê 1
Warsaw 1
Weifang 1
Wroclaw 1
Wuxi 1
Totale 273
Nome #
WDFY3 Haploinsufficiency Is Associated With Autosomal Dominant Neurodevelopmental Disorders and Macrocephaly 93
Genetic Variability of SOX10-Related Disorders within an Italian Family: Straddling the Line between Kallmann and Waardenburg Syndrome 86
Co-Inheritance of Pathogenic Variants in PKD1 and PKD2 Genes Determined by Parental Segregation and De Novo Origin: A Case Report 65
Case report: A new de novo 6q21q22.1 interstitial deletion case in a girl with cerebellar vermis hypoplasia and developmental delay and literature review 64
A Novel COL4A5 Pathogenic Variant Joins the Dots in a Family with a Synchronous Diagnosis of Alport Syndrome and Polycystic Kidney Disease 58
Prenatal identification of a pathogenic maternal FGFR1 variant in two consecutive pregnancies with fetal forebrain malformations 42
Totale 408
Categoria #
all - tutte 1.498
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 1.498


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2024/2025187 0 63 10 4 6 15 14 3 15 38 14 5
2025/2026221 25 19 21 16 29 16 31 24 29 11 0 0
Totale 408