Ricci, Martina
 Distribuzione geografica
Continente #
EU - Europa 341
NA - Nord America 285
AS - Asia 65
AF - Africa 2
OC - Oceania 1
SA - Sud America 1
Totale 695
Nazione #
US - Stati Uniti d'America 283
IT - Italia 116
IE - Irlanda 68
SE - Svezia 39
PL - Polonia 27
SG - Singapore 27
DE - Germania 22
FR - Francia 18
CN - Cina 14
CZ - Repubblica Ceca 14
FI - Finlandia 10
RU - Federazione Russa 10
IN - India 7
GB - Regno Unito 6
NL - Olanda 4
KR - Corea 3
TR - Turchia 3
BE - Belgio 2
CH - Svizzera 2
CI - Costa d'Avorio 2
HK - Hong Kong 2
IR - Iran 2
JP - Giappone 2
PK - Pakistan 2
AE - Emirati Arabi Uniti 1
AT - Austria 1
AU - Australia 1
BR - Brasile 1
CA - Canada 1
IL - Israele 1
NO - Norvegia 1
PA - Panama 1
RS - Serbia 1
VN - Vietnam 1
Totale 695
Città #
Dublin 66
Chandler 53
Ashburn 46
Rome 42
New York 28
Warsaw 26
Milan 20
Singapore 15
Brno 13
Houston 10
Fairfield 9
Helsinki 8
Marseille 8
Wilmington 8
Chicago 7
Boardman 6
Boston 6
Bremen 6
Princeton 6
Seattle 6
Beijing 5
Woodbridge 5
Moscow 4
Palermo 4
Trieste 4
Amsterdam 3
Ann Arbor 3
Caorle 3
Grottaferrata 3
Munich 3
Paris 3
Pune 3
Ronciglione 3
San Mateo 3
Seoul 3
Washington 3
Abidjan 2
Bengaluru 2
Busto Arsizio 2
Cagliari 2
Chino 2
Ciserano 2
Frankfurt am Main 2
Hong Kong 2
Jacksonville 2
Kazan' 2
Liège 2
London 2
Los Angeles 2
Mainz 2
Maple Shade Township 2
Monza 2
Padova 2
Redwood City 2
Ronchis 2
Salò 2
Sandston 2
Valence 2
Bern 1
Brisbane 1
Cambridge 1
Capoterra 1
Casarano 1
Civitavecchia 1
Dearborn 1
Dong Ket 1
Dubai 1
Genoa 1
Gunzenhausen 1
Hefei 1
Hounslow 1
Jarrow 1
Kensington 1
Kragujevac 1
Krakow 1
Lappeenranta 1
Leawood 1
Lugano 1
Mantova 1
Naaldwijk 1
Nova Iguaçu 1
Prague 1
Ranica 1
San Diego 1
Sant'Agostino 1
Shanghai 1
Springfield 1
Toronto 1
Vienna 1
Zanjan 1
Totale 520
Nome #
Prevalence and predictor factors of respiratory impairment in a large cohort of patients with Myotonic Dystrophy type 1 (DM1): A retrospective, cross sectional study 136
Prevalence of Spinal Muscular Atrophy in the Era of Disease-Modifying Therapies: An Italian Nationwide Survey 77
Neurological assessment of newborns with spinal muscular atrophy identified through neonatal screening 73
Longitudinal Cognitive Assessment in Low-Risk Very Preterm Infants 58
Nusinersen efficacy data for 24-month in type 2 and 3 spinal muscular atrophy 55
Onasemnogene abeparvovec in spinal muscular atrophy: predictors of efficacy and safety in naïve patients with spinal muscular atrophy and following switch from other therapies 53
A Longitudinal Follow-Up Study of Intellectual Function in Duchenne Muscular Dystrophy over Age: Is It Really Stable? 35
Early neurological assessment and long-term neuromotor outcomes in late preterm infants: A critical review 32
Reply to the letter entitled “Predictors of respiratory impairment in patients with myotonic dystrophy type 1” 31
Hereditary Hyperekplexia: A New Family and a Systematic Review of GLRA1 Gene-Related Phenotypes 31
A Longitudinal Follow-Up Study of Intellectual Function in Duchenne Muscular Dystrophy over Age: Is It Really Stable? 24
Longitudinal Analysis of PUL 2.0 Domains in Ambulant and Non-Ambulant Duchenne Muscular Dystrophy Patients: How do they Change in Relation to Functional Ability? 21
Early neurological signs in infants identified through neonatal screening for SMA: do they predict outcome? 18
Long term follow-up of scoliosis progression in type II SMA patients 18
Prevalence of Spinal Muscular Atrophy in the Era of Disease-Modifying Therapies: An Italian Nationwide Survey 17
Assessing Prevalence and Characteristics of Oro-bulbar Involvement in Children and Adults with SMA Type 2 and 3 Using a Multimodal Approach 13
Can the CHOP-INTEND be used as An Outcome Measure in the First Months of Age? Implications for Clinical Trials and Real World Data 11
Longitudinal Analysis of PUL 2.0 Domains in Ambulant and Non-Ambulant Duchenne Muscular Dystrophy Patients: How do they Change in Relation to Functional Ability? 7
Prevalence of Spinal Muscular Atrophy in the Era of Disease-Modifying Therapies: An Italian Nationwide Survey 5
Communicative development inventory in type 1 and presymptomatic infants with spinal muscular atrophy: a cohort study 5
A Longitudinal Follow-Up Study of Intellectual Function in Duchenne Muscular Dystrophy over Age: Is It Really Stable? 5
Totale 725
Categoria #
all - tutte 4.494
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 4.494


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/202017 0 1 1 0 1 2 0 0 1 1 8 2
2020/202158 4 4 6 2 13 3 12 0 4 7 2 1
2021/202244 3 0 0 6 0 2 0 2 1 4 7 19
2022/2023222 21 23 9 15 18 13 23 28 18 6 19 29
2023/2024363 11 55 18 21 18 53 50 11 8 21 53 44
2024/202520 16 4 0 0 0 0 0 0 0 0 0 0
Totale 725