RIGUZZI, PIETRO
 Distribuzione geografica
Continente #
NA - Nord America 101
EU - Europa 88
AS - Asia 69
SA - Sud America 25
AF - Africa 7
Totale 290
Nazione #
US - Stati Uniti d'America 98
SG - Singapore 43
IT - Italia 38
BR - Brasile 22
DE - Germania 17
FI - Finlandia 10
CN - Cina 8
HK - Hong Kong 8
IN - India 5
NL - Olanda 5
CZ - Repubblica Ceca 4
GB - Regno Unito 3
RU - Federazione Russa 3
SE - Svezia 3
BD - Bangladesh 2
FR - Francia 2
AR - Argentina 1
AT - Austria 1
CM - Camerun 1
CO - Colombia 1
ES - Italia 1
ET - Etiopia 1
GA - Gabon 1
HN - Honduras 1
IR - Iran 1
JM - Giamaica 1
KE - Kenya 1
KZ - Kazakistan 1
NA - Namibia 1
NI - Nicaragua 1
PL - Polonia 1
PY - Paraguay 1
SN - Senegal 1
TN - Tunisia 1
TR - Turchia 1
Totale 290
Città #
Singapore 32
Fairfield 16
Munich 13
Santa Clara 13
Padova 11
Turku 9
Hong Kong 8
Milan 8
Ashburn 6
Boardman 5
Olomouc 4
Cambridge 3
Chennai 3
Rome 3
Woodbridge 3
Ann Arbor 2
Beijing 2
Chandler 2
Charlotte 2
Chicago 2
Des Moines 2
Houston 2
London 2
Medford 2
Prato 2
Princeton 2
Rio de Janeiro 2
Addis Ababa 1
Asunción 1
Bogotá 1
Brasília 1
Bytom 1
Cambuí 1
Covina 1
Curtarolo 1
Dakar 1
Dhaka 1
El Progreso 1
Elk Grove Village 1
Falkenstein 1
Fayetteville 1
Forest City 1
Fort Wayne 1
Frankfurt am Main 1
Garanhuns 1
Helsinki 1
Istanbul 1
Jaraguá 1
Jardim 1
Kingston 1
Kostanay 1
Lanús 1
Leeds 1
Libreville 1
Los Angeles 1
Madrid 1
Magé 1
Managua 1
Mangaratiba 1
Manhuaçu 1
Mogi das Cruzes 1
Montello 1
Nairobi 1
Ogden 1
Ourinhos 1
Padua 1
Panambi 1
Petrópolis 1
Poção de Pedras 1
Queens 1
Raleigh 1
Rankin 1
Ribeirão Preto 1
Rio Brilhante 1
Roxbury 1
San Diego 1
Santa Vitória do Palmar 1
Seattle 1
São José do Rio Preto 1
São Paulo 1
Tehran 1
Tunis 1
Vicenza 1
Votuporanga 1
Windhoek 1
Xaxim 1
Totale 220
Nome #
Next-generation sequencing application to investigate skeletal muscle channelopathies in a large cohort of Italian patients 56
The IAAM LTBP4 Haplotype is Protective Against Dystrophin-Deficient Cardiomyopathy 52
null 42
Focal epilepsy followed by rapidly progressive frontotemporal dementia: a rare manifestation of VCP mutation 35
Natural history of Becker muscular dystrophy: DMD gene mutations predict clinical severity 33
Continuitiy of care with ataluren in Duchenne Muscular Dystrophy patients with nonsense mutations after loss of ambulation. Personal experience 32
Transition and management of patients with Duchenne Muscular Dystrophy: a narrative review based on Italian experts' opinion and real-world experience 22
Deep characterization of females with heterozygous Duchenne muscular dystrophy mutations 15
Robotic Thymectomy for Myasthenia Gravis: Analysis of the Surgical and Neurological Outcomes After a 20 Years' Experience 13
Encephalopathy as unique manifestation of Sjogren's syndrome: Expanding the spectrum of steroid-responsive encephalopathy 9
Totale 309
Categoria #
all - tutte 1.489
article - articoli 1.489
book - libri 0
conference - conferenze 0
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 2.978


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2020/202113 0 0 0 0 0 0 0 0 0 0 0 13
2021/202228 6 1 1 1 1 6 1 0 0 5 1 5
2022/20238 2 0 0 0 1 2 0 1 1 0 1 0
2023/202424 0 1 2 2 0 1 2 0 3 7 3 3
2024/2025236 4 21 10 5 31 5 29 15 7 15 56 38
Totale 309