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Scotton, Chiara
84
results:
Search for persons
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Format
Online (84)
Mediatypes
Articles (Online) (21)
OpenAccess-fulltext (63)
Languages
english (68)
italian (3)
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1
Impact of intermittently scanned continuous glucose monitor..:
Franceschi, Roberto
;
Scotton, Chiara
;
Leonardi, Letizia
...
Acta Diabetologica. 59 (2022) 7 - p. 911-919 , 2022
Link:
https://doi.org/10.1007/..
?
2
Circadian Genes as Exploratory Biomarkers in DMD: Results F..:
Rossi, Rachele
;
Falzarano, Maria Sofia
;
Osman, Hana
...
Frontiers in Physiology. 12 (2021) - p. , 2021
Link:
https://doi.org/10.3389/..
?
3
TCTEX1D1 is a genetic modifier of disease progression in Du..:
CINRG Investigators
;
Spitali, Pietro
;
Zaharieva, Irina
...
European Journal of Human Genetics. 28 (2020) 6 - p. 815-825 , 2020
Link:
https://doi.org/10.1038/..
?
4
Homozygous Recessive Versican Missense Variation Is Associa..:
Bigoni, Stefania
;
Neri, Marcella
;
Scotton, Chiara
...
Frontiers in Genetics. 9 (2019) - p. , 2019
Link:
https://doi.org/10.3389/..
?
5
Report of a novel ATP7A mutation causing distal motor neuro..:
Gualandi, Francesca
;
Sette, Elisabetta
;
Fortunato, Fernanda
...
Neuromuscular Disorders. 29 (2019) 10 - p. 776-785 , 2019
Link:
https://doi.org/10.1016/..
?
6
Transcriptional and epigenetic analyses of the DMD locus re..:
Gherardi, Samuele
;
Bovolenta, Matteo
;
Passarelli, Chiara
...
Biochimica et Biophysica Acta (BBA) - Gene Regulatory Mechanisms. 1860 (2017) 11 - p. 1138-1147 , 2017
Link:
https://doi.org/10.1016/..
?
7
Recessive mutations inMSTO1cause mitochondrial dynamics imp..:
Nasca, Alessia
;
Scotton, Chiara
;
Zaharieva, Irina
...
Human Mutation. 38 (2017) 8 - p. 970-977 , 2017
Link:
https://doi.org/10.1002/..
?
8
Complex phenotypes associated with STIM1 mutations in both ..:
Harris, Elizabeth
;
Burki, Umar
;
Marini-Bettolo, Chiara
...
Neuromuscular Disorders. 27 (2017) 9 - p. 861-872 , 2017
Link:
https://doi.org/10.1016/..
?
9
The Popeye Domain Containing Genes and Their Function in St..:
Schindler, Roland
;
Scotton, Chiara
;
French, Vanessa
..
Journal of Cardiovascular Development and Disease. 3 (2016) 2 - p. 22 , 2016
Link:
https://doi.org/10.3390/..
?
10
Duchenne Muscular Dystrophy: From Diagnosis to Therapy:
Falzarano, Maria
;
Scotton, Chiara
;
Passarelli, Chiara
.
Molecules. 20 (2015) 10 - p. 18168-18184 , 2015
Link:
https://doi.org/10.3390/..
?
11
Paternal germline mosaicism in collagen VI related myopathi..:
Armaroli, Annarita
;
Trabanelli, Cecilia
;
Scotton, Chiara
...
European Journal of Paediatric Neurology. 19 (2015) 5 - p. 533-536 , 2015
Link:
https://doi.org/10.1016/..
?
12
Biomarkers in rare neuromuscular diseases:
Scotton, Chiara
;
Passarelli, Chiara
;
Neri, Marcella
.
Experimental Cell Research. 325 (2014) 1 - p. 44-49 , 2014
Link:
https://doi.org/10.1016/..
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13
Muscle Proteomics Reveals Novel Insights into the Pathophys..:
De Palma, Sara
;
Capitanio, Daniele
;
Vasso, Michele
...
Journal of Proteome Research. 13 (2014) 11 - p. 5022-5030 , 2014
Link:
https://doi.org/10.1021/..
?
14
SERCA1 protein expression in muscle of patients with Brody ..:
Guglielmi, Valeria
;
Vattemi, Gaetano
;
Gualandi, Francesca
...
Molecular Genetics and Metabolism. 110 (2013) 1-2 - p. 162-169 , 2013
Link:
https://doi.org/10.1016/..
?
15
Exome sequencing in a family with intellectual disability, ..:
Zanni, Ginevra
;
Scotton, Chiara
;
Passarelli, Chiara
...
neurogenetics. 14 (2013) 3-4 - p. 247-250 , 2013
Link:
https://doi.org/10.1007/..
1-15