Rikard Blunck

11PUBLICATIONS
20CO-AUTHORS
Neurology and neuromuscular diseasesStructure and dynamics of materialsGene expression (incl. microarray and other genome-wide approaches)Computational statisticsElectrical circuits and systems
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Publications (11)

|Aug 29, 2024
KCNG4 Genetic Variant Linked to Migraine Prevents Expression of KCNB1.

Gabriel Lacroix, Shreyas Bhat, Zerghona Shafia

|Oct 25, 2022
Characterising ion channel structure and dynamics using fluorescence spectroscopy techniques.

Shreyas Bhat, Rikard Blunck

|Jul 28, 2022
Clinical and Functional Study of a De Novo Variant in the PVP Motif of Kv1.1 Channel Associated with Epilepsy, Developmental Delay and Ataxia.

Giorgia Dinoi, Michael Morin, Elena Conte

|Sep 28, 2021
A Novel KCNA2 Variant in a Patient with Non-Progressive Congenital Ataxia and Epilepsy: Functional Characterization and Sensitivity to 4-Aminopyridine.

Paola Imbrici, Elena Conte, Rikard Blunck

|Jul 02, 2021
Functional Characterization of Two Novel Mutations in SCN5A Associated with Brugada Syndrome Identified in Italian Patients.

Cristina Balla, Elena Conte, Rita Selvatici

|Jan 20, 2021
Musculoskeletal Features without Ataxia Associated with a Novel de novo Mutation in KCNA1 Impairing the Voltage Sensitivity of Kv1.1 Channel.

Paola Imbrici, Andrea Accogli, Rikard Blunck

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Frequent Collaborators

4 joint publications

Paola Imbrici

3 joint publications

Annamaria De Luca

2 joint publications

Shreyas Bhat

2 joint publications

Maria Cristina D'Adamo