VERCELLI, Liliana
 Distribuzione geografica
Continente #
NA - Nord America 2.036
EU - Europa 1.703
AS - Asia 450
AF - Africa 19
Continente sconosciuto - Info sul continente non disponibili 9
OC - Oceania 6
SA - Sud America 5
Totale 4.228
Nazione #
US - Stati Uniti d'America 2.010
DK - Danimarca 553
CN - Cina 331
IT - Italia 291
IE - Irlanda 190
SE - Svezia 166
AT - Austria 156
FR - Francia 98
FI - Finlandia 67
BE - Belgio 35
UA - Ucraina 35
DE - Germania 34
KR - Corea 27
GB - Regno Unito 25
VN - Vietnam 24
CA - Canada 23
IN - India 23
KE - Kenya 15
NL - Olanda 12
HK - Hong Kong 10
PL - Polonia 10
EU - Europa 9
GR - Grecia 8
IL - Israele 7
JP - Giappone 7
TR - Turchia 7
AU - Australia 5
RO - Romania 4
RU - Federazione Russa 4
AL - Albania 3
PR - Porto Rico 3
SN - Senegal 3
TW - Taiwan 3
BR - Brasile 2
CH - Svizzera 2
CY - Cipro 2
HU - Ungheria 2
LK - Sri Lanka 2
PT - Portogallo 2
UZ - Uzbekistan 2
BD - Bangladesh 1
BG - Bulgaria 1
CL - Cile 1
CO - Colombia 1
CZ - Repubblica Ceca 1
EC - Ecuador 1
EG - Egitto 1
ES - Italia 1
IR - Iran 1
KZ - Kazakistan 1
LI - Liechtenstein 1
MN - Mongolia 1
NO - Norvegia 1
NZ - Nuova Zelanda 1
SG - Singapore 1
SI - Slovenia 1
Totale 4.228
Città #
Ann Arbor 528
Chandler 263
Beijing 193
Dublin 189
Vienna 154
Torino 138
Nyköping 102
Fairfield 73
Houston 73
Villeurbanne 71
Wilmington 70
Ashburn 67
Medford 63
Princeton 55
Dearborn 54
Hangzhou 36
Brussels 34
Jacksonville 34
Redwood City 29
Woodbridge 24
Seattle 23
Cambridge 18
Padova 16
Hebei 15
Dong Ket 14
Boardman 12
Boston 12
Toronto 11
Hefei 10
Norwalk 10
Shanghai 10
Warsaw 9
Duncan 8
Orange 8
Pisa 8
Turin 8
Hong Kong 7
Philadelphia 7
Pinerolo 7
San Diego 7
Guiyang 6
Jinan 6
Kunming 6
Milan 6
Munich 6
Verona 6
Chengdu 5
London 5
Nanjing 5
New York 5
Athens 4
Bologna 4
Edinburgh 4
Guangzhou 4
Houten 4
Nanchang 4
Nutley 4
San Mateo 4
Casamarciano 3
Central District 3
Dallas 3
Kocaeli 3
Montréal 3
Moose Jaw 3
Pune 3
Rome 3
Suzhou 3
Tel Aviv 3
Washington 3
Atlanta 2
Auburn Hills 2
Bitonto 2
Carmichael 2
Caserta 2
Changsha 2
Citta 2
Cormeilles-en-Parisis 2
Deer Park 2
Dehiwala 2
Delhi 2
Falls Church 2
Farsta 2
Fuzhou 2
Giv‘atayim 2
Helsinki 2
Jerusalem 2
Konya 2
Lachine 2
Lanzo 2
Lisbon 2
Melbourne 2
Nicosia 2
Palermo 2
Paris 2
Pompei 2
Reading 2
Romagnano Sesia 2
Seoul 2
Taipei 2
Tirana 2
Totale 2.653
Nome #
Intrathecal administration of nusinersen in adult and adolescent patients with spinal muscular atrophy and scoliosis: Transforaminal versus conventional approach 237
Role of autophagy in an asymptomatic young woman with late-onset glycogen storage disease type 2 (GSD2). 216
Mutation analysis of CHCHD2 and CHCHD10 in Italian patients with mitochondrial myopathy 186
Measuring quality of life impairment in skeletal muscle channelopathies. 183
Phenotypic heterogeneity of the 8344A>G mtDNA "MERRF" mutation. 182
Symptomatic heterozygous patients in late-onset glycogen storage disease type 2. 180
LMNA-associated myopathies: the Italian experience in a large cohort of patients. 175
Clinical and molecular cross-sectional study of a cohort of adult type III spinal muscular atrophy patients: clues from a biomarker study. 174
Screening for later-onset Pompe's disease in patients with paucisymptomatic hyperCKemia. 171
MYH7-related myopathies: Clinical, histopathological and imaging findings in a cohort of Italian patients 169
Myoclonus in mitochondrial disorders. 155
Large scale genotype-phenotype analyses indicate that novel prognostic tools are required for families with facioscapulohumeral muscular dystrophy. 155
The m.3243A>G mitochondrial DNA mutation and related phenotypes. A matter of gender? 148
Muscle biopsy study in ten cases of lamin a/c mutation with different phenotypes. 123
Muscular involvement in Whipple's disease with gastrointestinal sparing 103
Multifactorial analysis of muscle involvement in twenty cases of laminopathies with different phenotypes 102
Necrotizing myopathies: the experience of the center for neuromuscular disease in Turin. 96
A peculiar case of LGMD with rimmed vacuoles 92
A young boy with a new mutation in lamin A/C gene responsive to treatment with ACHE inhibitors 91
Complete recovery in a severe case of anti-ssa positive necrotizing myopathy after rituximab therapy 90
A case of to treatment with piridostigmine bromide: a new phenotype? 88
Clinicopathological features and disease course in three patients with focal myositis 85
La distrofia muscolare oculo-faringea: caratteristiche cliniche e genetiche 84
New pharmacotherapies for genetic neuromuscular disorders: opportunities and challenges 84
Late-onset glycogen storage disease type II: therapeutical indications in a subset of paucisymptomatic patients with a single mutation 74
MC ARDLE DISEASE (GLYCOGENOSIS TYPE 5): LONG TERM FOLLOW UP IN A SMALL COHORT OF ITALIAN PATIENTS 73
Clinical expression of facioscapulohumeral muscular dystrophy in carriers of 1-3 D4Z4 reduced alleles: experience of the FSHD Italian National Registry 72
Young girl with relapsing- remitting hyperCKemia and limb·girdle weakness in the last ten years. 64
Differential diagnosis of vacuolar muscle biopsies: use of p62, LC3 and LAMP2 immunohistochemistry 60
The genetic basis of undiagnosed muscular dystrophies and myopathies 56
A novel clinical tool to classify facioscapulohumeral muscular dystrophy phenotypes 56
Unusual symptoms and pathology in a woman with myofibrillar myopathy. 55
"Mitochondrial neuropathies": A survey from the large cohort of the Italian Network 48
A 5-year clinical follow-up study from the Italian National Registry for FSHD 45
Redefining phenotypes associated with mitochondrial DNA single deletion 41
The analysis of myotonia congenita mutations discloses functional clusters of amino acids within the CBS2 domain and the C-terminal peptide of the ClC-1 channel 41
LOPED study: Looking for an early diagnosis in a late-onset Pompe disease high-risk population 39
Revisiting mitochondrial ocular myopathies: a study from the Italian Network 36
Assessing the Role of Anti rh-GAA in Modulating Response to ERT in a Late-Onset Pompe Disease Cohort from the Italian GSDII Study Group 36
Interpretation of the epigenetic signature of facioscapulohumeral muscular dystrophy in light of genotype-phenotype studies 35
Interpreting genetic variants in titin in patients with muscle disorders 33
Cytokine Profile in Striated Muscle Laminopathies: New Promising Biomarkers for Disease Prediction 32
Copy number variants account for a tiny fraction of undiagnosed myopathic patients 31
Clinical and Molecular Spectrum of Myotonia and Periodic Paralyses Associated With Mutations in SCN4A in a Large Cohort of Italian Patients 27
Elevated tgf b2 serum levels in emery-dreifuss muscular dystrophy: Implications for myocyte and tenocyte differentiation and fibrogenic processes 23
Longitudinal evaluation of SMN levels as biomarker for spinal muscular atrophy: Results of a phase IIb double-blind study of salbutamol 15
Lipomatosis incidence and characteristics in an Italian cohort of mitochondrial patients 14
Phenotypic Variability Among Patients With D4Z4 Reduced Allele Facioscapulohumeral Muscular Dystrophy 14
Response to a letter to the editor 13
Large genotype–phenotype study in carriers of D4Z4 borderline alleles provides guidance for facioscapulohumeral muscular dystrophy diagnosis 13
microRNAs as biomarkers in Pompe disease 12
Muscle pain in mitochondrial diseases: a picture from the Italian network 10
Totale 4.437
Categoria #
all - tutte 10.428
article - articoli 0
book - libri 0
conference - conferenze 2.497
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 12.925


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/2019128 0 0 0 0 0 0 0 38 26 19 24 21
2019/2020917 7 6 43 130 77 120 111 79 80 109 82 73
2020/2021504 84 12 20 60 33 15 31 18 34 61 50 86
2021/2022979 83 66 73 86 80 91 76 70 57 16 149 132
2022/2023874 75 106 21 86 64 218 62 46 95 35 47 19
2023/2024244 42 70 19 18 29 47 10 9 0 0 0 0
Totale 4.437