Maria Arvio
Publications 
2 of 3
- Cognition in adults with Williams syndrome — A 20-year follow-up study (2019)
- Molecular Genetics and Genomic Medicine
(A1 Refereed original research article in a scientific journal) - Heterozygous loss of function of IQSEC2/Iqsec2 leads to increased activated Arf6 and severe neurocognitive seizure phenotype in females (2019)
- Life Science Alliance
(A1 Refereed original research article in a scientific journal) - Kehitysvammaisen henkilön kipu (2019)
- Kipuviesti
(D1 Article in a professional journal) - Sähköhoito saattaa vähentää väkivaltaista käytöstä kehitysvammaisilla autismikirjon potilailla (2019)
- Duodecim
(D1 Article in a professional journal) - Two middle-aged women with the Finnish variant of muscle-eye-brain disease (MEB) (2019)
- American Journal of Medical Genetics Part A
(A1 Refereed original research article in a scientific journal) - A 69-year-old woman with Coffin-Siris syndrome (2018)
- American Journal of Medical Genetics Part A
(A1 Refereed original research article in a scientific journal) - Intellectual disability in patients with epilepsy with eyelid myoclonias (2018)
- SAGE Open Medical Case Reports
(A1 Refereed original research article in a scientific journal) - Kehitysvammaisen muistisairauksien arviointiin tarvitaan oma työkalu (2018)
- Lääkärilehti
(D1 Article in a professional journal) - Kehitysvamma on elinikäinen (2018)
- Duodecim
(A2 Refereed review article in a scientific journal ) - Signs indicating dementia in Down, Williams and Fragile X syndromes (2018)
- Molecular Genetics and Genomic Medicine
(A1 Refereed original research article in a scientific journal)
UTU Research Portal