PARMEGGIANI, Giulia
 Distribuzione geografica
Continente #
NA - Nord America 549
EU - Europa 135
AS - Asia 86
SA - Sud America 2
Continente sconosciuto - Info sul continente non disponibili 1
Totale 773
Nazione #
US - Stati Uniti d'America 547
CN - Cina 45
IT - Italia 37
SG - Singapore 31
DE - Germania 30
GB - Regno Unito 22
UA - Ucraina 16
SE - Svezia 9
FI - Finlandia 8
TR - Turchia 7
BE - Belgio 5
CZ - Repubblica Ceca 3
CA - Canada 2
HU - Ungheria 2
VN - Vietnam 2
BR - Brasile 1
BY - Bielorussia 1
CL - Cile 1
EU - Europa 1
IN - India 1
LI - Liechtenstein 1
LT - Lituania 1
Totale 773
Città #
Fairfield 86
Chandler 52
Houston 46
Woodbridge 45
Ashburn 42
Ann Arbor 37
Seattle 31
Singapore 28
Santa Clara 27
Jacksonville 22
Cambridge 21
Wilmington 15
New York 14
Beijing 12
Shanghai 10
Munich 9
Ferrara 7
Milan 7
Nanjing 7
Princeton 7
Boardman 6
Izmir 6
London 6
Los Angeles 6
San Diego 6
Bremen 5
Brussels 5
Helsinki 4
Nanchang 4
Pisa 4
Bologna 2
Brno 2
Budapest 2
Changsha 2
Des Moines 2
Frankfurt am Main 2
Jiaxing 2
Padova 2
Trento 2
Addison 1
Dearborn 1
Falls Church 1
Foggia 1
Hanoi 1
Hebei 1
Ho Chi Minh City 1
Hyderabad 1
Lappeenranta 1
Minsk 1
Nantong 1
Ningbo 1
Orange 1
Ottawa 1
Prague 1
San Mateo 1
São Paulo 1
Tappahannock 1
Tianjin 1
Toronto 1
Vaduz 1
Verdellino 1
Yellow Springs 1
Zhengzhou 1
Totale 619
Nome #
Double Interstitial Deletion of the Long Arm of Chromosome 6 in a Patient with Pierre Robin Sequence, Dysmorphisms, and Severe Developmental Delay 131
Mutation Load of Multiple Ion Channel Gene Mutations in Brugada Syndrome 128
Genetic counseling for women referred for advanced maternal age: a telegenetic approach 119
A Family with γ-Thalassemia and High Hb A2 Levels 118
Prenatal genetic counseling referrals for advanced maternal age: still room for improvement. 117
A New 3p14.2 Microdeletion in a Patient with Intellectual Disability and Language Impairment: Case Report and Review of the Literature 98
Expanding the clinical spectrum of recessive truncating mutations of KLHL7 to a Bohring-Opitz-like phenotype 58
SCN5A mutation is associated with a higher Shanghai Score in patients with type 1 Brugada ECG pattern 20
Totale 789
Categoria #
all - tutte 4.471
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 4.471


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202084 0 0 0 0 0 0 18 18 17 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
2024/2025107 4 8 18 12 38 27 0 0 0 0 0 0
Totale 789