BATTINI, ROBERTA
 Distribuzione geografica
Continente #
NA - Nord America 143
EU - Europa 81
AS - Asia 25
SA - Sud America 3
AF - Africa 1
Totale 253
Nazione #
US - Stati Uniti d'America 141
IT - Italia 44
SE - Svezia 13
SG - Singapore 13
IN - India 7
BG - Bulgaria 6
FI - Finlandia 5
FR - Francia 4
BR - Brasile 3
CN - Cina 3
DE - Germania 3
GB - Regno Unito 3
CA - Canada 1
CH - Svizzera 1
IE - Irlanda 1
JM - Giamaica 1
JP - Giappone 1
LA - Repubblica Popolare Democratica del Laos 1
TG - Togo 1
UA - Ucraina 1
Totale 253
Città #
Fairfield 20
Chandler 18
Ashburn 15
Rome 8
Wilmington 8
Ann Arbor 6
Sofia 6
Woodbridge 6
Seattle 5
Genoa 4
Princeton 4
San Paolo di Civitate 4
Singapore 4
Torre del Greco 4
Asciano 3
Cambridge 3
Helsinki 3
Houston 3
Lawrence 3
Millbury 3
Reggio Nell'emilia 3
Bremen 2
Campinas 2
Duncan 2
Lappeenranta 2
Mori 2
Naples 2
New York 2
Paris 2
San Diego 2
San Gregorio da Sassola 2
Santa Maria La Carita 2
Beijing 1
Boardman 1
Boston 1
Buffalo 1
Cannock 1
Dublin 1
Edinburgh 1
Ficarazzi 1
Florence 1
Hefei 1
Lomé 1
Los Angeles 1
Mannheim 1
Pisa 1
Pune 1
Renens 1
Shenyang 1
St Louis 1
São Paulo 1
Tokyo 1
Toronto 1
Vientiane 1
Totale 177
Nome #
CEP290 mutations are frequently identified in the oculo-renal form of Joubert syndrome-related disorders 70
Monoallelic KIF1A‑related disorders: a multicenter cross sectional study and systematic literature review 48
New pathogenic variants in COQ4 cause ataxia and neurodevelopmental disorder without detectable CoQ10 deficiency in muscle or skin fibroblasts 39
null 23
6 minute walk test in Duchenne MD patients with different mutations: 12 month changes 21
Aromatic L-amino Acid Decarboxylase (AADC) deficiency: results from an Italian modified Delphi consensus 16
Expanding Phenotype of Poirier-Bienvenu Syndrome: New Evidence from an Italian Multicentrical Cohort of Patients 15
Bi-allelic genetic variants in the translational GTPases GTPBP1 and GTPBP2 cause a distinct identical neurodevelopmental syndrome 14
Long-term neurological and psychiatric outcomes in patients with aromatic l-amino acid decarboxylase deficiency 13
MKS3/TMEM67 mutations are a major cause of COACH syndrome, a joubert syndrome related disorder with liver involvement 12
Suitability of North Star Ambulatory Assessment in young boys with Duchenne muscular dystrophy 8
Identification of Potential Clusters of Signs and Symptoms to Prioritize Patients’ Eligibility for AADCd Screening by 3-OMD Testing: An Italian Delphi Consensus 6
Totale 285
Categoria #
all - tutte 1.572
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 1.572


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202030 0 0 0 2 4 4 4 7 4 3 2 0
2020/202128 2 0 3 0 0 0 0 6 4 5 2 6
2021/202257 0 1 2 2 3 3 1 6 6 4 21 8
2022/202388 7 11 1 13 8 8 3 11 7 6 9 4
2023/202478 3 6 0 10 6 10 10 7 0 10 7 9
2024/20254 4 0 0 0 0 0 0 0 0 0 0 0
Totale 285