Maria Arvio

8PUBLICATIONS
7CO-AUTHORS
Neurology and neuromuscular diseasesTraditional Chinese medicine and treatmentsMedical mycologyPersonality and individual differencesPsychology of ageing
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Publications (8)

|Feb 23, 2023
Manifestations of Intellectual Disability, Dystonia, and Parkinson's Disease in an Adult Patient with ARX Gene Mutation c.558_560dup p.(Pro187dup).

Maria Arvio, Jaana Lähdetie, Hannu Koivu

|Nov 14, 2022
Medicine use in people with intellectual disabilities: a Finnish nationwide register study.

F Nurminen, H Rättö, M Arvio

|Aug 30, 2021
Report of a novel missense mutation in the MECP2 gene in a middle-aged man with intellectual disability syndrome.

Maria Arvio, Maria Haanpää, Pia Pohjola

|Aug 09, 2021
Neurocognitive follow-up in adult siblings with Phelan-McDermid syndrome due to a novel SHANK3 splicing site mutation.

Minna Kankuri-Tammilehto, Oili Sauna-Aho, Maria Arvio

|May 01, 2021
Screening of dementia indicating signs in adults with intellectual disabilities.

Maria Arvio, Nina Bjelogrlic-Laakso

|Nov 17, 2020
Adult phenotype of the homozygous missense mutation c.655G>A, p.Gly219Arg in SLC13A5: A case report.

Maria Arvio, Jaana Lähdetie

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Frequent Collaborators

1 joint publications

F Nurminen

1 joint publications

Jozef Gecz

1 joint publications

Cheryl Shoubridge

1 joint publications

Minna Kankuri-Tammilehto