Human Genome Epidemiology Literature Finder
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Records 1 - 3 (of 3 Records) |
| Query Trace: Bruxism and COMT[original query] |
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| Single nucleotide polymorphisms in dopamine receptor D2 are associated with bruxism and its circadian phenotypes in children. Cranio : the journal of craniomandibular practice 2019 12 40 (2): 152-159. Scariot Rafaela, Brunet Leonardo, Olsson Bernardo, Palinkas Marcelo, Regalo Simone Cecilio Hallak, Rebellato Nelson Luis Barbosa, Brancher João Armando, Torres Carolina Paes, Diaz-Serrano Kranya Victoria, Küchler Erika Calvano, Zielak João Ces |
| Genetic basis of sleep bruxism and sleep apnea-response to a medical puzzle. Scientific reports 2020 May 10 (1): 7497. Wieckiewicz Mieszko, Bogunia-Kubik Katarzyna, Mazur Grzegorz, Danel Dariusz, Smardz Joanna, Wojakowska Anna, Poreba Rafal, Dratwa Marta, Chaszczewska-Markowska Monika, Winocur Efraim, Emodi-Perlman Alona, Martynowicz Hele |
| Bruxism Throughout the Lifespan and Variants in MMP2, MMP9 and COMT. Journal of personalized medicine 2020 5 10 (2): . Vieira Alexandre R, Scariot Rafaela, Gerber Jennifer T, Arid Juliana, Küchler Erika C, Sebastiani Aline M, Palinkas Marcelo, Díaz-Serrano Kranya V, Torres Carolina P, Regalo Simone C H, Nelson-Filho Paulo, Bussaneli Diego G, Deeley Kathleen, Modesto Adria |
- Page last reviewed:Feb 1, 2024
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