Alina Ivaniuk 🇺🇦(@AlinaIvaniuk) 's Twitter Profileg
Alina Ivaniuk 🇺🇦

@AlinaIvaniuk

🇺🇦 adult neurologist | 🇺🇸 research fellow @ClevelandClinic➡PGY0 @MayoFL_NeuroRes |⭐@yesILAE Vice-Chair | 🧠🧬epilepsy & genetics | 🙋‍♀️ tweets are my own

ID:1335892604236468226

calendar_today07-12-2020 10:23:18

232 Tweets

275 Followers

216 Following

Christian Bosselmann(@cmbosselmann) 's Twitter Profile Photo

Really proud of this collaborative effort to establish strong genotype-phenotype relationships and treatment guidance for SCN8A-related chronic and episodic ataxia. Fantastic effort by Hang Lyu, Yuanyuan Liu, and the Tübingen-Dianalund dream team.

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Shruti Agashe(@shruti_agashe1) 's Twitter Profile Photo

Published recently - IFCN and its Clinical Neurophysiology journals Our findings show that ICH during sEEG may be under reported in literature however despite ICH most patients have a favorable outcome. Electrographic clues during sEEG could alert the reader about the possibility of ICH.

Published recently - @ClinicalNeuroph Our findings show that ICH during sEEG may be under reported in literature however despite ICH most patients have a favorable outcome. Electrographic clues during sEEG could alert the reader about the possibility of ICH.
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Alina Ivaniuk 🇺🇦(@AlinaIvaniuk) 's Twitter Profile Photo

Being mentored by Dennis Lal is an honor and blessing – not every mentor will cover their mentees’ presentation. has a pleasure of having him on the stage for Nth time 🔥
📢Stay tuned for the results of our huge epilepsy gene cataloging effort - paper is on the horizon!

Being mentored by @LalDennis is an honor and blessing – not every mentor will cover their mentees’ presentation. #IEC2023 has a pleasure of having him on the stage for Nth time 🔥 📢Stay tuned for the results of our huge epilepsy gene cataloging effort - paper is on the horizon!
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Alina Ivaniuk 🇺🇦(@AlinaIvaniuk) 's Twitter Profile Photo

Honored to represent the community that granted me numerous friends and contributed so much to shaping my career and humbled to have been supported by my colleagues. Such an exciting new chapter with my yesILAE family! 🙏

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Alessandra Rossi(@AleRossiNeuro) 's Twitter Profile Photo

A really original genetic study of its kind, presented by Katrine M Johannesen, shows the broad phenotypic spectrum of GABRA3 related disorders can be explained by sex and function effect of the variants. ILAE Rikke S. Møller Philip K. Ahring

A really original genetic study of its kind, presented by @Katrine92658231, shows the broad phenotypic spectrum of GABRA3 related disorders can be explained by sex and function effect of the #GABRA3 variants. @IlaeWeb #ILAE #IEC2023 @FiladelfiaGene1 @Philip_K_Ahring
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Ana Mingorance(@CNSdrughunter) 's Twitter Profile Photo

Deep phenotyping of a cohort of more than 50 kids with syndrome in the ENVISION study from Encoded Therapeutics sees no correlation between seizure burden and developmental / behavioral outcomes. That’s why we need more treatments!

Great talk at

Deep phenotyping of a cohort of more than 50 kids with #Dravet syndrome in the ENVISION study from Encoded Therapeutics sees no correlation between seizure burden and developmental / behavioral outcomes. That’s why we need more treatments! Great talk at #IEC2023
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Alina Ivaniuk 🇺🇦(@AlinaIvaniuk) 's Twitter Profile Photo

New preprint from our group! Looking at genes with similar structure can facilitate interpretation of genetic variants – check out to find out how! 👇👇👇

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Jaiver Macea(@j_maceaortiz) 's Twitter Profile Photo

Are you a basic/translational scientist aiming to improve the translational efficiency of preclinical research in ?
ILAE R&I Task Force created a survey to assess the gaps. yesILAE Society for Neuroscience (SfN) Ángel Aledo-Serrano Sebastian Ortiz, MD Alina Ivaniuk 🇺🇦 surveymonkey.co.uk/r/research_and…)

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ILAE(@IlaeWeb) 's Twitter Profile Photo

is pleased to announce the Genetic Literacy in Epilepsy Series! The goal is to provide a concise, accessible resource on advances in for busy clinicians who can then apply this knowledge to help patients.
Read now: ilae.org/genetic-litera…
Wiley Neuro

#ILAE is pleased to announce the Genetic Literacy in Epilepsy Series! The goal is to provide a concise, accessible resource on advances in #epilepsy #genetics for busy clinicians who can then apply this knowledge to help patients. Read now: ilae.org/genetic-litera… @WileyNeuro
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yesILAE(@yesILAE) 's Twitter Profile Photo

📢 YES Asia&Oceania team announces a series of weekly webinars on stereoEEG with one of the world's leading experts Dr. Aileen McGonigal!
💡Interested? Register here - the link will come shortly before the webinars. Topics in the 1st comment 👇tinyurl.com/2p8p3tep
ILAE

📢 YES Asia&Oceania team announces a series of weekly webinars on stereoEEG with one of the world's leading experts Dr. Aileen McGonigal! 💡Interested? Register here - the link will come shortly before the webinars. Topics in the 1st comment 👇tinyurl.com/2p8p3tep @IlaeWeb
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Stéphanie Baulac(@BaulacS) 's Twitter Profile Photo

New study from our lab 🧬: using trace tissue from SEEG electrodes, we detected somatic mutations in mTOR pathway genes, causing epilepsies due to focal cortical dysplasia. 👉Potential link between mutation load to epileptic activity & improved diagnostic. Sara Baldassari

New study from our lab 🧬: using trace tissue from SEEG electrodes, we detected somatic mutations in mTOR pathway genes, causing epilepsies due to focal cortical dysplasia. 👉Potential link between mutation load to epileptic activity & improved diagnostic. @SaraBaldassari4
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Dennis Lal(@LalDennis) 's Twitter Profile Photo

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New pre-print research from the team on deficiency disorder ( ) & potential cardiovascular involvement! Using natural language processing, our team around Alina Ivaniuk 🇺🇦 @team identified tachycardia as a significant association with CDD (OR 4.2). Interpretation is…

1/2 New pre-print research from the team on #CDKL5 deficiency disorder (#CDD) & potential cardiovascular involvement! Using natural language processing, our team around @AlinaIvaniuk @team identified tachycardia as a significant association with CDD (OR 4.2). Interpretation is…
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Diana Le Duc(@Diana_Le_Duc) 's Twitter Profile Photo

Our paper on the importance of rare genetic variation for epilepsies has just been published. If you are interested in how variants that occur in general population impact epilepsy phenotypes check our work at lnkd.in/e3YgzbHk. This was a huge collaborative effort.

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