Human Genome Epidemiology Literature Finder
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Records 1 - 4 (of 4 Records) |
| Query Trace: Migraine with Aura and SCN1A[original query] |
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| Genetic studies of Polish migraine patients: screening for causative mutations in four migraine-associated genes. Human genomics 2016 10 (1): 3. Domitrz Izabela, Kosiorek Michalina, ?ekanowski Cezary, Kami?ska An |
| Analysis of Genetic Variants in SCN1A, SCN2A, KCNK18, TRPA1 and STX1A as a Possible Marker of Migraine. Current genomics 2020 Apr 21 (3): 224-236. Kowalska Marta, Prendecki Micha?, Kapelusiak-Pielok Magdalena, Grzelak Teresa, ?agan-J?drzejczyk Urszula, Wiszniewska Ma?gorzata, Kozubski Wojciech, Dorszewska Jolan |
| Higher burden of rare frameshift indels in genes related to synaptic transmission separate familial hemiplegic migraine from common types of migraine. Journal of medical genetics 2020 1 57 (9): 610-616. Rasmussen Andreas Hoiberg, Olofsson Isa, Chalmer Mona Ameri, Olesen Jes, Hansen Thomas Folkma |
| Efficacy of galcanezumab in proline-rich transmembrane protein 2 (PRRT2)-associated familial hemiplegic migraine: A case series. Headache 2024 9 . Costanza Sottani, Giulia Di Lazzaro, Paolo Calabresi, Maria Grazia Pomponi, Francesco Danilo Tiziano, Anna Rita Bentivoglio, Serenella Servidei, Catello Vollo |
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