PARMEGGIANI, Giulia
 Distribuzione geografica
Continente #
NA - Nord America 564
EU - Europa 148
AS - Asia 134
SA - Sud America 18
AF - Africa 3
Continente sconosciuto - Info sul continente non disponibili 1
Totale 868
Nazione #
US - Stati Uniti d'America 562
SG - Singapore 74
CN - Cina 45
IT - Italia 40
DE - Germania 33
GB - Regno Unito 22
BR - Brasile 17
UA - Ucraina 16
SE - Svezia 9
FI - Finlandia 8
TR - Turchia 7
BE - Belgio 5
RU - Federazione Russa 5
CZ - Repubblica Ceca 3
CA - Canada 2
HK - Hong Kong 2
HU - Ungheria 2
VN - Vietnam 2
ZA - Sudafrica 2
AT - Austria 1
BD - Bangladesh 1
BY - Bielorussia 1
CL - Cile 1
CY - Cipro 1
EU - Europa 1
IN - India 1
LA - Repubblica Popolare Democratica del Laos 1
LI - Liechtenstein 1
LT - Lituania 1
NL - Olanda 1
TN - Tunisia 1
Totale 868
Città #
Fairfield 86
Chandler 52
Houston 46
Woodbridge 45
Ashburn 42
Ann Arbor 37
Seattle 31
Singapore 31
Santa Clara 27
Jacksonville 22
Cambridge 21
Wilmington 15
New York 14
Beijing 12
Los Angeles 10
Shanghai 10
Munich 9
Ferrara 7
Milan 7
Nanjing 7
Princeton 7
Boardman 6
Izmir 6
London 6
San Diego 6
Bremen 5
Brussels 5
Helsinki 4
Nanchang 4
Pisa 4
Council Bluffs 3
Bologna 2
Brno 2
Budapest 2
Changsha 2
Des Moines 2
Frankfurt am Main 2
Giugliano in Campania 2
Hong Kong 2
Jiaxing 2
Padova 2
São Paulo 2
Trento 2
Aceguá 1
Addison 1
Belo Horizonte 1
Bom Despacho 1
Brasília 1
Cachoeirinha 1
Carapicuíba 1
Curitiba 1
Dearborn 1
Falls Church 1
Fidenza 1
Foggia 1
Goiânia 1
Hanoi 1
Hebei 1
Ho Chi Minh City 1
Hyderabad 1
Itapira 1
Lappeenranta 1
Lorena 1
Minsk 1
Nantong 1
Nicosia 1
Ningbo 1
Nuremberg 1
Orange 1
Ottawa 1
Parauapebas 1
Prague 1
Pretoria 1
San Mateo 1
Santo André 1
São Miguel do Oeste 1
Tappahannock 1
The Dalles 1
Tianjin 1
Toronto 1
Tunis 1
Uruará 1
Vaduz 1
Verdellino 1
Vienna 1
Vientiane 1
Várzea da Palma 1
Yellow Springs 1
Zhengzhou 1
Totale 657
Nome #
Double Interstitial Deletion of the Long Arm of Chromosome 6 in a Patient with Pierre Robin Sequence, Dysmorphisms, and Severe Developmental Delay 143
Mutation Load of Multiple Ion Channel Gene Mutations in Brugada Syndrome 139
A Family with γ-Thalassemia and High Hb A2 Levels 133
Genetic counseling for women referred for advanced maternal age: a telegenetic approach 132
Prenatal genetic counseling referrals for advanced maternal age: still room for improvement. 126
A New 3p14.2 Microdeletion in a Patient with Intellectual Disability and Language Impairment: Case Report and Review of the Literature 109
Expanding the clinical spectrum of recessive truncating mutations of KLHL7 to a Bohring-Opitz-like phenotype 72
SCN5A mutation is associated with a higher Shanghai Score in patients with type 1 Brugada ECG pattern 30
Totale 884
Categoria #
all - tutte 5.125
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 5.125


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202031 0 0 0 0 0 0 0 0 0 19 9 3
2020/202180 5 5 9 8 5 7 3 9 1 9 10 9
2021/202274 5 1 0 4 9 7 1 10 1 6 3 27
2022/2023114 9 15 3 19 15 16 9 7 18 0 2 1
2023/202461 7 4 3 0 3 19 2 5 1 1 4 12
2024/2025202 4 8 18 12 38 27 11 13 60 11 0 0
Totale 884