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You searched for: Author/Creator Soldovieri, Maria Virginia

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1. A novel homozygous KCNQ3 loss‐of‐function variant causes non‐syndromic intellectual disability and neonatal‐onset pharmacodependent epilepsy. Issue 3 (11th August 2019)

2. A novel KCNQ3 mutation in familial epilepsy with focal seizures and intellectual disability. (19th December 2014)

4. Autism and developmental disability caused by KCNQ3 gain‐of‐function variants. Issue 2 (26th June 2019)

5. De novo gain‐of‐function variants in KCNT2 as a novel cause of developmental and epileptic encephalopathy. Issue 6 (27th July 2018)

7. Effects of natural and synthetic isothiocyanate-based H2S-releasers against chemotherapy-induced neuropathic pain: Role of Kv7 potassium channels. (15th July 2017)

8. Expression and function of Kv7.4 channels in rat cardiac mitochondria: possible targets for cardioprotection. Issue 1 (29th December 2015)

9. Gabapentin treatment in a patient with KCNQ2 developmental epileptic encephalopathy. (October 2020)

10. Infantile spasms and encephalopathy without preceding neonatal seizures caused by KCNQ2 R198Q, a gain‐of‐function variant. (9th November 2016)