SANDONA', DORIANNA

SANDONA', DORIANNA  

Dipartimento di Scienze Biomediche - DSB  

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Titolo Data di pubblicazione Autori Rivista Serie Titolo libro
1st International Workshop on Clinical trial readiness for sarcoglycanopathies 15-16 November 2016, Evry, France 2017 PEGORARO, ELENAGORECKI, DARIUSZ , CEZARYSANDONA', DORIANNASEMPLICINI, CLAUDIO + NEUROMUSCULAR DISORDERS - -
A CFTR Corrector For The Teatment Of Genetic Disorders Affecting Striated Muscle 2018 Sandonà DoriannaSacchetto RobertaBianchini ElisaVolpe PompeoMascarello Francesco + - - -
A single cell complementation class is common to several cases of Cytochrome c Oxidase defective Leigh's syndrome 1997 SANDONA', DORIANNAZEVIANI M. + HUMAN MOLECULAR GENETICS - -
A single point mutation (E166Q) prevents dicyclohexylcarbodiimide binding to the photosystem II subunit CP29 1997 SANDONA', DORIANNA + FEBS LETTERS - -
A STRUCTURAL INVESTIGATION OF THE CENTRAL CHLOROPHYLL A BINDING SITES IN THE MINOR PHOTOSYSTEM II ANTENNA PROTEIN, LHCB4 2002 SANDONA', DORIANNA + BIOCHEMISTRY - -
Adaptation of Mouse Skeletal Muscle to Long-Term Microgravity in the MDS Mission 2012 SANDONA', DORIANNABIANCHINI, ELISACICILIOT, STEFANODANIELI, DANIELAGERMINARIO, ELENAPICARD, ANNE ALEIDA + PLOS ONE - -
Advanced therapeutic approaches in sarcoglycanopathies 2024 Scano M.Benetollo A.Dalla Barba F.Sandona D. CURRENT OPINION IN PHARMACOLOGY - -
Age-dependent changes of signaling pathways of muscles from α-sarcoglycan-deficient mice 2008 GERMINARIO, ELENASANDONA', DORIANNADANIELI, DANIELA + - - -
An Automated Low-Cost Swim Tunnel for Measuring Swimming Performance in Fish 2021 Sandona D. + ZEBRAFISH - -
Analysis of some optical properties of a native and reconstituted photosystem II antenna complex, CP29: Pigment binding sites can be occupied by chlorophyll a or chlorophyll b and determine spectral forms 1997 SANDONA', DORIANNA + BIOCHEMISTRY - -
ATP as a first messanger controlling excitation-transcription coupling of skeletal muscle 2006 SANDONA', DORIANNAGERMINARIO, ELENADANIELI, DANIELA + - - abstract book
Biological markers of oxidative stress in mitochondrial myopathies with progressive external ophthalmoplegia. 1991 RIZZUTO, ROSARIOSANDONA', DORIANNA + JOURNAL OF THE NEUROLOGICAL SCIENCES - -
Brody Disease: A Novel Potential Therapeutic Approach for This Rare Human Disease 2022 AKYUREK, EYLEM EMEKBIANCHINI, ELISASANDONÀ, DORIANNASACCHETTO, ROBERTA. + - - Journal of Neuromuscular Diseases Abstracts of the 17th International Congress on Neuromuscular Diseases (ICNMD 2022)
Brody Disease: A Novel Zebrafish Animal Model to Test Potential Therapeutic Approach for This Rare Human Disease 2023 AKYUREK, EYLEM EMEKDALLA BARBA, FRANCESCOCAROTTI, MARCELLOFONSATTI, ELISAVETTORI, ANDREASANDONA, DORIANNASACCHETTO, ROBERTA + - - 12th European Zebrafish Meeting
Brody Disease: Utilizing a Novel Zebrafish Animal Model for Exploring Potential Therapeutic Strategies for this Rare Human Condition 2024 AKYUREK, EYLEM EMEKDALLA BARBA, FRANCESCOCAROTTI, MARCELLOFONSATTI, ELISAVETTORI, ANDREASANDONÀ, DORIANNASACCHETTO ROBERTA + - - 8°International Congress of Myology
C17 corrector for the treatment of sarcoglycanopathy: preliminary ADME studies 2022 Alberto BenetolloMartina ScanoSofia ParrasiaLucia BiasuttoFrancesco Dalla BarbaPaola CaccinMarcello CarottiDorianna Sandonà - - National Ph.D. Meeting, Salerno, Italy 24-26 March 2022
Calcium overload of dystrophic muscle may depend on the high expression level of P2X7 receptor 2001 SANDONA', DORIANNATARRICONE, ELENAMARTINELLO, TIZIANA + BIOPHYSICAL JOURNAL - -
CATTLE CONGENITAL PSEUDOMYOTONIA AS ANIMAL MODEL: WHEN DIAPHRAGM MUSCLE CAN MAKE THE DIFFERENCE 2023 AKYUREK, EYLEM EMEKBIANCHINI, ELISASANDONÀ, DORIANNASACCHETTO ROBERTA + - - 76°Convegno SISVET Società Italiana delle Scienze Veterinarie
CFTR corrector C17 is effective in muscular dystrophy, in vivo proof of concept in LGMDR3 2022 Martina ScanoAlberto BenetolloLeonardo NogaraMichela BondìFrancesco Dalla BarbaMichela SoardiAkyurek Eylem EmekPaola CaccinMarcello CarottiRoberta SacchettoBert BlaauwDorianna Sandonà + HUMAN MOLECULAR GENETICS - -
CFTR correctors for the treatment of type 2D Limb Girdle Muscular Dystrophy 2016 Marcello CarottiElisa BianchiniChiara FecchioRoberta SacchettoDorianna Sandonà + - - Convegno Monotematico SIF: Rare Diseases and Orphan Drugs: from genes to personalized medicine