Chiara Scotton

Ferrara, Italy

Last Updated: 09/26/2026

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Found 24 publications

Impact of intermittently scanned continuous glucose monitoring with alarms on sleep and metabolic outcomes in children and adolescents with type 1 diabetes.

Impact of intermittently scanned continuous glucose monitoring with alarms on sleep and metabolic outcomes in children and adolescents with type 1 diabetes.

Journal: Acta diabetologica

Published: December 29, 2021

Circadian Genes as Exploratory Biomarkers in DMD: Results From Both the mdx Mouse Model and Patients.

Circadian Genes as Exploratory Biomarkers in DMD: Results From Both the mdx Mouse Model and Patients.

Journal: Frontiers in physiology

Published: March 10, 2021

Corrigendum to: "Transcriptional and epigenetic analyses of the DMD locus reveal novel cis-acting DNA elements that govern muscle dystrophin expression". [Biochim. Biophys. Acta Gene Regul. Mech. 2017 Nov;1860(11):1138-1147.].

Corrigendum to: "Transcriptional and epigenetic analyses of the DMD locus reveal novel cis-acting DNA elements that govern muscle dystrophin expression". [Biochim. Biophys. Acta Gene Regul. Mech. 2017 Nov;1860(11):1138-1147.].

Journal: Biochimica et biophysica acta. Gene regulatory mechanisms

Published: November 04, 2020

Report of a novel ATP7A mutation causing distal motor neuropathy.

Report of a novel ATP7A mutation causing distal motor neuropathy.

Journal: Neuromuscular disorders : NMD

Published: April 17, 2019

TCTEX1D1 is a genetic modifier of disease progression in Duchenne muscular dystrophy.

TCTEX1D1 is a genetic modifier of disease progression in Duchenne muscular dystrophy.

Journal: European journal of human genetics : EJHG

Published: November 14, 2018

Homozygous Recessive Versican Missense Variation Is Associated With Early Teeth Loss in a Pakistani Family.

Homozygous Recessive Versican Missense Variation Is Associated With Early Teeth Loss in a Pakistani Family.

Journal: Frontiers in genetics

Published: July 25, 2018

Transcriptional and epigenetic analyses of the DMD locus reveal novel cis‑acting DNA elements that govern muscle dystrophin expression.

Transcriptional and epigenetic analyses of the DMD locus reveal novel cis‑acting DNA elements that govern muscle dystrophin expression.

Journal: Biochimica et biophysica acta. Gene regulatory mechanisms

Published: May 09, 2017

Complex phenotypes associated with STIM1 mutations in both coiled coil and EF-hand domains.

Complex phenotypes associated with STIM1 mutations in both coiled coil and EF-hand domains.

Journal: Neuromuscular disorders : NMD

Published: March 10, 2017

Recessive mutations in MSTO1 cause mitochondrial dynamics impairment, leading to myopathy and ataxia.

Recessive mutations in MSTO1 cause mitochondrial dynamics impairment, leading to myopathy and ataxia.

Journal: Human mutation

Published: November 16, 2016

Duchenne Muscular Dystrophy Myogenic Cells from Urine-Derived Stem Cells Recapitulate the Dystrophin Genotype and Phenotype.

Duchenne Muscular Dystrophy Myogenic Cells from Urine-Derived Stem Cells Recapitulate the Dystrophin Genotype and Phenotype.

Journal: Human gene therapy

Published: August 18, 2016

The Popeye Domain Containing Genes and their Function in Striated Muscle.

The Popeye Domain Containing Genes and their Function in Striated Muscle.

Journal: Journal of cardiovascular development and disease

Published: April 26, 2016

Duchenne Muscular Dystrophy: From Diagnosis to Therapy.

Duchenne Muscular Dystrophy: From Diagnosis to Therapy.

Journal: Molecules (Basel, Switzerland)

Published: July 20, 2015

Showing 1-12 of 24

Last Updated: 09/26/2026