VERCELLI, Liliana
 Distribuzione geografica
Continente #
NA - Nord America 2.066
EU - Europa 1.704
AS - Asia 541
AF - Africa 20
Continente sconosciuto - Info sul continente non disponibili 9
SA - Sud America 8
OC - Oceania 6
Totale 4.354
Nazione #
US - Stati Uniti d'America 2.039
DK - Danimarca 553
CN - Cina 342
IT - Italia 309
IE - Irlanda 181
SE - Svezia 166
AT - Austria 156
FR - Francia 100
SG - Singapore 79
FI - Finlandia 68
UA - Ucraina 35
DE - Germania 34
GB - Regno Unito 28
KR - Corea 27
VN - Vietnam 24
CA - Canada 23
IN - India 23
BE - Belgio 16
KE - Kenya 15
HK - Hong Kong 12
NL - Olanda 12
GR - Grecia 10
PL - Polonia 10
EU - Europa 9
IL - Israele 7
JP - Giappone 7
TR - Turchia 7
AU - Australia 5
BR - Brasile 5
RO - Romania 4
RU - Federazione Russa 4
AL - Albania 3
PR - Porto Rico 3
SN - Senegal 3
TW - Taiwan 3
CH - Svizzera 2
CY - Cipro 2
CZ - Repubblica Ceca 2
HU - Ungheria 2
LK - Sri Lanka 2
PT - Portogallo 2
SK - Slovacchia (Repubblica Slovacca) 2
UZ - Uzbekistan 2
BD - Bangladesh 1
BG - Bulgaria 1
CL - Cile 1
CO - Colombia 1
EC - Ecuador 1
EG - Egitto 1
ES - Italia 1
IR - Iran 1
KZ - Kazakistan 1
LI - Liechtenstein 1
MN - Mongolia 1
MX - Messico 1
NO - Norvegia 1
NZ - Nuova Zelanda 1
SI - Slovenia 1
TN - Tunisia 1
Totale 4.354
Città #
Ann Arbor 528
Chandler 263
Beijing 196
Dublin 180
Vienna 154
Torino 138
Nyköping 102
Fairfield 73
Houston 73
Villeurbanne 71
Wilmington 70
Ashburn 69
Medford 63
Singapore 58
Princeton 55
Dearborn 54
Hangzhou 36
Jacksonville 34
Redwood City 29
Woodbridge 24
Seattle 23
Cambridge 18
Padova 16
Brussels 15
Hebei 15
Dong Ket 14
Boardman 12
Boston 12
Toronto 11
Turin 11
Hefei 10
Los Angeles 10
Norwalk 10
Shanghai 10
Hong Kong 9
Warsaw 9
Duncan 8
Guangzhou 8
Orange 8
Pisa 8
Philadelphia 7
Pinerolo 7
San Diego 7
Athens 6
Chengdu 6
Guiyang 6
Jinan 6
Kunming 6
Milan 6
Munich 6
New York 6
Verona 6
Bergamo 5
Nanjing 5
Bologna 4
Edinburgh 4
Houten 4
London 4
Nanchang 4
Nutley 4
San Mateo 4
Santa Clara 4
Casamarciano 3
Central District 3
Dallas 3
Helsinki 3
Kocaeli 3
Montréal 3
Moose Jaw 3
Pune 3
Rome 3
Suzhou 3
Tel Aviv 3
Washington 3
Atlanta 2
Auburn Hills 2
Banská Štiavnica 2
Bitonto 2
Brent 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
Guapé 2
Jerusalem 2
Konya 2
Lachine 2
Lanzo 2
Lisbon 2
Melbourne 2
Nicosia 2
Nuremberg 2
Totale 2.712
Nome #
Intrathecal administration of nusinersen in adult and adolescent patients with spinal muscular atrophy and scoliosis: Transforaminal versus conventional approach 253
Role of autophagy in an asymptomatic young woman with late-onset glycogen storage disease type 2 (GSD2). 224
Mutation analysis of CHCHD2 and CHCHD10 in Italian patients with mitochondrial myopathy 193
Measuring quality of life impairment in skeletal muscle channelopathies. 184
Phenotypic heterogeneity of the 8344A>G mtDNA "MERRF" mutation. 182
Symptomatic heterozygous patients in late-onset glycogen storage disease type 2. 181
Screening for later-onset Pompe's disease in patients with paucisymptomatic hyperCKemia. 178
LMNA-associated myopathies: the Italian experience in a large cohort of patients. 176
Clinical and molecular cross-sectional study of a cohort of adult type III spinal muscular atrophy patients: clues from a biomarker study. 175
MYH7-related myopathies: Clinical, histopathological and imaging findings in a cohort of Italian patients 173
Large scale genotype-phenotype analyses indicate that novel prognostic tools are required for families with facioscapulohumeral muscular dystrophy. 160
Myoclonus in mitochondrial disorders. 158
The m.3243A>G mitochondrial DNA mutation and related phenotypes. A matter of gender? 150
Muscle biopsy study in ten cases of lamin a/c mutation with different phenotypes. 121
Multifactorial analysis of muscle involvement in twenty cases of laminopathies with different phenotypes 106
Muscular involvement in Whipple's disease with gastrointestinal sparing 104
Necrotizing myopathies: the experience of the center for neuromuscular disease in Turin. 96
Complete recovery in a severe case of anti-ssa positive necrotizing myopathy after rituximab therapy 91
A young boy with a new mutation in lamin A/C gene responsive to treatment with ACHE inhibitors 90
A peculiar case of LGMD with rimmed vacuoles 90
Clinicopathological features and disease course in three patients with focal myositis 87
La distrofia muscolare oculo-faringea: caratteristiche cliniche e genetiche 84
A case of to treatment with piridostigmine bromide: a new phenotype? 84
New pharmacotherapies for genetic neuromuscular disorders: opportunities and challenges 82
Clinical expression of facioscapulohumeral muscular dystrophy in carriers of 1-3 D4Z4 reduced alleles: experience of the FSHD Italian National Registry 78
Late-onset glycogen storage disease type II: therapeutical indications in a subset of paucisymptomatic patients with a single mutation 78
MC ARDLE DISEASE (GLYCOGENOSIS TYPE 5): LONG TERM FOLLOW UP IN A SMALL COHORT OF ITALIAN PATIENTS 73
Young girl with relapsing- remitting hyperCKemia and limb·girdle weakness in the last ten years. 63
Differential diagnosis of vacuolar muscle biopsies: use of p62, LC3 and LAMP2 immunohistochemistry 61
A novel clinical tool to classify facioscapulohumeral muscular dystrophy phenotypes 60
The genetic basis of undiagnosed muscular dystrophies and myopathies 58
Unusual symptoms and pathology in a woman with myofibrillar myopathy. 56
"Mitochondrial neuropathies": A survey from the large cohort of the Italian Network 52
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 47
A 5-year clinical follow-up study from the Italian National Registry for FSHD 47
LOPED study: Looking for an early diagnosis in a late-onset Pompe disease high-risk population 43
Redefining phenotypes associated with mitochondrial DNA single deletion 41
Revisiting mitochondrial ocular myopathies: a study from the Italian Network 37
Interpretation of the epigenetic signature of facioscapulohumeral muscular dystrophy in light of genotype-phenotype studies 37
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 37
Interpreting genetic variants in titin in patients with muscle disorders 36
Cytokine Profile in Striated Muscle Laminopathies: New Promising Biomarkers for Disease Prediction 35
Copy number variants account for a tiny fraction of undiagnosed myopathic patients 34
Clinical and Molecular Spectrum of Myotonia and Periodic Paralyses Associated With Mutations in SCN4A in a Large Cohort of Italian Patients 29
Elevated tgf b2 serum levels in emery-dreifuss muscular dystrophy: Implications for myocyte and tenocyte differentiation and fibrogenic processes 27
Lipomatosis incidence and characteristics in an Italian cohort of mitochondrial patients 18
Longitudinal evaluation of SMN levels as biomarker for spinal muscular atrophy: Results of a phase IIb double-blind study of salbutamol 17
microRNAs as biomarkers in Pompe disease 16
Phenotypic Variability Among Patients With D4Z4 Reduced Allele Facioscapulohumeral Muscular Dystrophy 16
Response to a letter to the editor 15
Large genotype–phenotype study in carriers of D4Z4 borderline alleles provides guidance for facioscapulohumeral muscular dystrophy diagnosis 14
Muscle pain in mitochondrial diseases: a picture from the Italian network 12
Adults living with Duchenne muscular dystrophy: old and new challenges in a cohort of 19 patients in their third to fifth decade 4
Distribution of Exonic Variants in Glycogen Synthesis and Catabolism Genes in Late Onset Pompe Disease (LOPD) 2
Totale 4.565
Categoria #
all - tutte 12.386
article - articoli 0
book - libri 0
conference - conferenze 2.966
curatela - curatele 0
other - altro 0
patent - brevetti 0
selected - selezionate 0
volume - volumi 0
Totale 15.352


Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2019/2020904 0 0 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
2022/2023858 75 106 21 86 64 218 53 45 94 33 45 18
2023/2024333 36 68 18 15 25 47 10 11 3 27 27 46
2024/202555 6 40 9 0 0 0 0 0 0 0 0 0
Totale 4.565