PI
paola imbrici
University of Bari Aldo Moro
Research areas: Biochemistry, Genetics and Molecular Biology · Molecular Biology · Ion channel regulation and function · Cardiac electrophysiology and arrhythmias · Ion Transport and Channel Regulation
0000-0001-9140-5350
Employment
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University of Bari Researcher2012 - Present
Education
Projects & Funding
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Advanced diagnostics and innovative procedures for diagnosis and therapy in striated muscle channelopathies Ministry of Health2011 - 2015
Publications (63)
- Empagliflozin in Lafora disease: A first‐in‐human 6‐month pilot study with electroclinical and FDG‐PET findings Save
- A Novel KCNA1 Variant in a Patient With Tremor and Autism Spectrum Disorder Causes Mixed LOF/GOF Defects of Kv1.1 Channels Save
- Expanding the phenotypic spectrum of CACNA1A‐related developmental and epileptic encephalopathy in adults Save
- State-of-the-Art Research and New Pharmacological Perspectives on Renal Involvement in Duchenne Muscular Dystrophy: A Narrative Review Save
- Selenoprotein N and SEPN1-Related Myopathies: Mechanisms, Models, and Therapeutic Perspectives Save
- From Symptomatic Therapies to Disease-Modifying Approaches for Neuronal Sodium Channel Disorders Save
- Towards development of Nav1.7 channel modulators for pain treatment: A comparison of mexiletine effect in two cell models by automated patch clamp Save
- Empagliflozin Repurposing for Lafora Disease: A Pilot Clinical Trial and Preclinical Investigation of Novel Therapeutic Targets Save
- Retrospective Clinical Investigation into the Association Between Abnormal Blood Clotting, Oral Anticoagulant Therapy, and Medium-Term Mortality in a Cohort of COVID-19 Patients Save
- Dapagliflozin ameliorates Lafora disease phenotype in a zebrafish model Save
- Retrospective Clinical Investigation Into the Association Between Abnormal Blood Clotting, Oral Anticoagulant Therapy and Medium-Term Mortality in a Cohort of COVID 19 Patients Save
- The importance of combining multiple genetic techniques to define recessive forms of myotonia congenita Save
- Therapeutic Approaches to Tuberous Sclerosis Complex: From Available Therapies to Promising Drug Targets Save
- The Biallelic Inheritance of Two Novel SCN1A Variants Results in Developmental and Epileptic Encephalopathy Responsive to Levetiracetam Save
- Pleiotropic Effects of Direct Oral Anticoagulants in Chronic Heart Failure and Atrial Fibrillation: Machine Learning Analysis Save
- Brugada Syndrome: More than a Monogenic Channelopathy Save
- Biophysical Aspects of Neurodegenerative and Neurodevelopmental Disorders Involving Endo-/Lysosomal CLC Cl−/H+ Antiporters Save
- Small Molecules Targeting Kidney ClC-K Chloride Channels: Applications in Rare Tubulopathies and Common Cardiovascular Diseases Save
- Sarcoplasmic Reticulum Ca2+ Buffer Proteins: A Focus on the Yet-To-Be-Explored Role of Sarcalumenin in Skeletal Muscle Health and Disease Save
- Blockers of Skeletal Muscle Nav1.4 Channels: From Therapy of Myotonic Syndrome to Molecular Determinants of Pharmacological Action and Back Save