IRIS
PASSAMANO, Luigia
 Distribuzione geografica
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Continente #
EU - Europa 165
NA - Nord America 98
AS - Asia 33
SA - Sud America 1
Totale 297
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Nazione #
US - Stati Uniti d'America 98
IE - Irlanda 80
IT - Italia 32
CN - Cina 16
ES - Italia 15
SG - Singapore 14
GB - Regno Unito 12
DE - Germania 5
GR - Grecia 5
IS - Islanda 4
PT - Portogallo 4
UA - Ucraina 4
FI - Finlandia 2
VN - Vietnam 2
AR - Argentina 1
FR - Francia 1
KR - Corea 1
SE - Svezia 1
Totale 297
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Città #
Dublin 80
Santiago de Compostela 13
Jacksonville 8
Singapore 8
New York 6
Princeton 6
Roxbury 6
Cambridge 4
Milan 4
Beijing 3
Boardman 3
Chandler 3
Hebei 3
Wilmington 3
Woodbridge 3
Ashburn 2
Bremen 2
Cagliari 2
Castelfranco Emilia 2
Des Moines 2
Duncan 2
Ferrara 2
Ho Chi Minh City 2
Houston 2
Jinan 2
Madrid 2
Medford 2
Miami 2
Ovar 2
Parma 2
Shenyang 2
Tianjin 2
Trieste 2
Vila Nova de Gaia 2
Badia Polesine 1
Caserta 1
Haikou 1
Helsinki 1
Jiaxing 1
Lanzhou 1
Lappeenranta 1
Las Varillas 1
Los Angeles 1
Munich 1
Nanjing 1
Naples 1
Paris 1
Pomigliano d'Arco 1
Prineville 1
Rome 1
Seoul 1
Turin 1
Valenzano 1
Totale 210
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Nome #
P.P.6 02 Cardiac and respiratory involvement in autosomal recessive limb-girdle muscular dystrophies 41
Autosomal dominant Ullrich congenital muscular dystrophy due to a de novo mutation in COL6A3 gene. A case report 38
G.P.4.03 Mutations in the lamin A/C gene: An emergent cause of fatal arrhythmias in congenital muscular dystrophies 37
Nusinersen safety and effects on motor function in adult spinal muscular atrophy type 2 and 3 36
Estimating the impact of COVID-19 pandemic on services provided by Italian Neuromuscular Centers: an Italian Association of Myology survey of the acute phase 26
The Role of TRPM4 Gene Mutations in Causing Familial Progressive Cardiac Conduction Disease: A Further Contribution 26
Deletion of the Williams Beuren Syndrome Critical Region unmasks facioscapulohumeral muscular dystrophy 23
CLCN1 Molecular Characterization in 19 South-Italian Patients With Dominant and Recessive Type of Myotonia Congenita 23
Spectrum of Genetic Variants in the Dystrophin Gene: A Single Centre Retrospective Analysis of 750 Duchenne and Becker Patients from Southern Italy 16
Bi-Allelic DES Gene Variants Causing Autosomal Recessive Myofibrillar Myopathies Affecting Both Skeletal Muscles and Cardiac Function 15
Gender effect on onset, prevalence and surgical treatment of cataract in patients with Myotonic Dystrophy type 1 13
Adults with spinal muscular atrophy: a large-scale natural history study shows gender effect on disease 11
Xp21 contiguous gene deletion syndrome presenting as Duchenne muscular dystrophy and glycerol kinase deficiency associated with intellectual disability: case report and review literature 10
Gain and loss of upper limb abilities in Duchenne muscular dystrophy patients: A 24-month study 5
Totale 320
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Categoria #
all - tutte 2.090
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 2.090
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/20205 0 0 0 0 2 0 2 0 0 0 1 0
2020/202137 0 0 7 12 10 0 2 0 1 0 5 0
2021/202235 0 0 0 0 13 0 1 0 1 6 2 12
2022/2023107 8 0 2 0 8 2 16 0 64 1 3 3
2023/2024118 7 13 15 6 29 8 8 6 2 2 12 10
2024/20252 0 2 0 0 0 0 0 0 0 0 0 0
Totale 320