TUPLER, Rossella
 Distribuzione geografica
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Continente #
NA - Nord America 2.759
EU - Europa 729
AS - Asia 234
OC - Oceania 74
SA - Sud America 33
AF - Africa 15
Totale 3.844
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Nazione #
US - Stati Uniti d'America 2.724
IT - Italia 207
FR - Francia 106
GB - Regno Unito 96
CN - Cina 86
AU - Australia 74
DE - Germania 69
ES - Italia 55
JP - Giappone 43
NL - Olanda 37
CA - Canada 31
SE - Svezia 29
VN - Vietnam 24
RU - Federazione Russa 19
CL - Cile 17
IN - India 17
FI - Finlandia 15
BE - Belgio 14
ZA - Sudafrica 13
HK - Hong Kong 12
AE - Emirati Arabi Uniti 11
KR - Corea 11
PL - Polonia 11
AT - Austria 10
CZ - Repubblica Ceca 9
LT - Lituania 9
BR - Brasile 8
TR - Turchia 8
UA - Ucraina 8
IE - Irlanda 7
CH - Svizzera 6
AR - Argentina 5
ID - Indonesia 5
GR - Grecia 4
IR - Iran 4
MX - Messico 4
PT - Portogallo 4
CO - Colombia 3
HU - Ungheria 3
DK - Danimarca 2
HR - Croazia 2
IL - Israele 2
LU - Lussemburgo 2
PH - Filippine 2
RO - Romania 2
BY - Bielorussia 1
CY - Cipro 1
EE - Estonia 1
GH - Ghana 1
IQ - Iraq 1
KZ - Kazakistan 1
MA - Marocco 1
MT - Malta 1
MY - Malesia 1
PK - Pakistan 1
QA - Qatar 1
SG - Singapore 1
TH - Thailandia 1
TW - Taiwan 1
Totale 3.844
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Città #
Fairfield 441
Ashburn 257
Houston 226
Woodbridge 201
Seattle 184
Santa Cruz 156
Cambridge 130
Wilmington 116
Buffalo 103
Ann Arbor 84
San Diego 62
Des Moines 42
Beijing 33
Modena 33
Mountain View 33
Dong Ket 22
Madrid 22
Chicago 21
Rome 21
Boardman 20
New York 20
Stockholm 19
Los Angeles 18
Las Vegas 17
London 16
Shanghai 16
Clearwater 12
Riva 12
Bremen 11
Helsinki 11
Muizenberg 11
Munich 11
Paris 11
Southend 10
Dallas 9
Fuzhou 9
Mercer Island 9
Milan 9
Wuhan 9
Frattamaggiore 8
Glasgow 8
Lake Forest 8
Norristown 8
Ottawa 8
Santiago 8
Valley Stream 8
Bengaluru 7
Bologna 7
Boston 7
Liverpool 7
Salsomaggiore Terme 7
San Francisco 7
Seoul 7
Toronto 7
Central District 6
Council Bluffs 6
East Rockaway 6
Henderson 6
Napoli 6
Saint Petersburg 6
Buenos Aires 5
Calgary 5
Dublin 5
Mailly-le-Chateau 5
Melbourne 5
Mettendorf 5
Pavia 5
Phoenix 5
Portland 5
Sheffield 5
Turin 5
Vilnius 5
Yokohama 5
Badajoz 4
Baltimore 4
Bergamo 4
Cedar Knolls 4
Columbus 4
Flushing 4
Frankfurt am Main 4
Rochester 4
Rosciano 4
Shenyang 4
Silver Spring 4
Sävsjö 4
Warsaw 4
Alexandria 3
Amsterdam 3
Berlin 3
Brescia 3
Hangzhou 3
Hilversum 3
Hiroshima 3
Markham 3
Massa Marittima 3
Morayfield 3
Newark 3
Nice 3
Nijmegen 3
Old Bridge 3
Totale 2.754
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Nome #
Early onset facioscapulohumeral dystrophy - a systematic review using individual patient data, file e31e124d-1046-987f-e053-3705fe0a095a 861
Cochlear Dysfunction Is a Frequent Feature of Facioscapulohumeral Muscular Dystrophy Type 1 (FSHD1), file e31e124e-f2cc-987f-e053-3705fe0a095a 255
225th ENMC international workshop:: A global FSHD registry framework, 18–20 November 2016, Heemskerk, The Netherlands, file e31e124d-1044-987f-e053-3705fe0a095a 252
A 5-year clinical follow-up study from the Italian National Registry for FSHD, file e31e124e-88b7-987f-e053-3705fe0a095a 234
Clinical expression of facioscapulohumeral muscular dystrophy in carriers of 1-3 D4Z4 reduced alleles: experience of the FSHD Italian National Registry, file e31e124b-6ba7-987f-e053-3705fe0a095a 213
Facioscapulohumeral muscular dystrophy: more complex than it appears, file e31e124a-f0f5-987f-e053-3705fe0a095a 188
An integrated approach in a case of facioscapulohumeral dystrophy, file e31e124a-f0f6-987f-e053-3705fe0a095a 162
Large scale genotype-phenotype analyses indicate that novel prognostic tools are required for families with facioscapulohumeral muscular dystrophy., file e31e124b-6bde-987f-e053-3705fe0a095a 151
A novel clinical tool to classify facioscapulohumeral muscular dystrophy phenotypes, file e31e124f-09f7-987f-e053-3705fe0a095a 147
FHL1 reduces dystrophy in transgenic mice overexpressing FSHD muscular dystrophy region gene 1 (FRG1), file e31e124a-f0f3-987f-e053-3705fe0a095a 141
Large scale population analysis challenges the current criteria for the molecular diagnosis of fascioscapulohumeral muscular dystrophy (FSHD), file e31e124b-6c46-987f-e053-3705fe0a095a 132
Aberrant Compartment Formation by HSPB2 Mislocalizes Lamin A and Compromises Nuclear Integrity and Function, file e31e124e-1747-987f-e053-3705fe0a095a 126
Large genotype-phenotype study in carriers of D4Z4 borderline alleles provides guidance for facioscapulohumeral muscular dystrophy diagnosis, file e31e124e-f2cd-987f-e053-3705fe0a095a 124
Modulation of Cell Death and Promotion of Chondrogenic Differentiation by Fas/FasL in Human Dental Pulp Stem Cells (hDPSCs), file e31e124e-3e50-987f-e053-3705fe0a095a 122
Does DNA Methylation Matter in FSHD?, file e31e124e-6cb1-987f-e053-3705fe0a095a 119
Interpretation of the epigenetic signature of facioscapulohumeral muscular dystrophy in light of genotype-phenotype studies, file e31e124e-72a5-987f-e053-3705fe0a095a 116
Deletion of the Williams Beuren syndrome critical region unmasks facioscapulohumeral muscular dystrophy, file e31e124e-648b-987f-e053-3705fe0a095a 98
The Italian National Registry for FSHD: an enhanced data integration and an analytics framework towards Smart Health Care and Precision Medicine for a rare disease, file e31e124f-c7d7-987f-e053-3705fe0a095a 94
Increased resistance towards fatigability in patients with facioscapulohumeral muscular dystrophy, file e31e124f-1f82-987f-e053-3705fe0a095a 86
The genetic basis of undiagnosed muscular dystrophies and myopathies, file e31e124f-50ee-987f-e053-3705fe0a095a 72
Early onset facioscapulohumeral dystrophy - a systematic review using individual patient data, file 99a964de-7ec7-412c-af6d-7afefee681b2 65
Muscle Fiber Conduction Velocity Correlates With the Age at Onset in Mild FSHD Cases, file e31e124f-8976-987f-e053-3705fe0a095a 59
Counseling and prenatal diagnosis in facioscapulohumeral muscular dystrophy: A retrospective study on a 13‐year multidisciplinary approach, file e31e1250-776d-987f-e053-3705fe0a095a 48
De novo variants and recombination at 4q35: hints for preimplantation genetic testing in facioscapulohumeral muscular dystrophy, file 1a0852e2-f9ea-4a8b-b4a9-960c3d1b07ad 13
Inappropriate gene activation in FSHD: A repressor complex binds a chromosomal repeat deleted in dystrophic muscle, file d695cc66-1762-4c66-96db-bcc0125253c7 12
A locus for migraine without aura maps on chromosome 14q21.2- q22.3., file 157398b2-feef-4ae4-8c1b-5001498d2acb 11
An Italian family affected by Nasu-Hakola disease with a novel genetic mutation in the trem 2 gene, file 6ef91b12-e6b0-43ae-8f9a-aacee82b108f 11
The FSHD jigsaw: are we placing the tiles in the right position?, file cee6a257-918d-4d22-842b-27310f365223 10
Using Cluster Analysis to Overcome the Limits of Traditional Phenotype-Genotype Correlations: The Example of RYR1-Related Myopathies, file e57feee6-6e7c-40fa-b403-c5d5a4e23e5a 10
Role of PD-L1 in licensing immunoregulatory function of dental pulp mesenchymal stem cells, file 804dfb19-d921-412b-b3c6-a88dbb009500 7
Physical activity practiced at a young age is associated with a less severe subsequent clinical presentation in facioscapulohumeral muscular dystrophy, file 3b812b2e-8a4d-4594-8ee1-66cb3f063606 6
Phenotypic Variability Among Patients With D4Z4 Reduced Allele Facioscapulohumeral Muscular Dystrophy, file 941f1dcf-cb33-4b77-9e4b-757ece61bf85 5
The MeCP2/YY1 interaction regulates ANT1 expression at 4q35: novel hints for Rett syndrome pathogenesis., file e31e124a-b1c6-987f-e053-3705fe0a095a 5
Rippling muscle disease and facioscapulohumeral dystrophy-like phenotype in a patient carrying heterozygous CAV3 T78M mutation and D4Z4 partial deletion: further evidence for “double trouble” overlapping syndromes, file 4f908c1f-5b63-404e-b0d8-84c79a2ca768 1
Factors predicting disease progression in C9ORF72 ALS patients, file 6622c03c-5c8c-4336-b55d-61dfdf32a0b8 1
Facioscapulohumeral muscular dystrophy in mice overexpressing FRG1, file e31e124a-966f-987f-e053-3705fe0a095a 1
The Italian FSHD registry: An enhanced data integration and analytics framework for smart health care, file e31e124d-6802-987f-e053-3705fe0a095a 1
Totale 3.959
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Categoria #
all - tutte 13.642
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 13.642
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Totale Lug Ago Sett Ott Nov Dic Gen Feb Mar Apr Mag Giu
2018/201985 0 0 0 0 0 0 0 0 0 0 49 36
2019/2020456 40 16 19 26 29 49 54 51 55 42 52 23
2020/20211.172 42 39 78 148 87 144 149 97 86 110 111 81
2021/20221.059 144 48 96 78 77 52 75 63 70 83 178 95
2022/2023696 35 37 159 87 56 84 30 31 77 29 52 19
2023/2024343 11 20 37 41 43 29 37 41 35 44 5 0
Totale 3.959