Anders Paetau, MD PhD
Affiliations: | Pathology | University of Helsinki, Helsingfors, Finland |
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"Anders Paetau"Bio:
HAARTMAN INST/UNIV HELSINKI
PATHOLOGY DEPT
PO BOX 21
HAARTMANINKATU 3
Helsinki 00014 Finland
Mean distance: 106866
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Publications
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| Rönkkö J, Molchanova S, Revah-Politi A, et al. (2020) Dominant mutations in ITPR3 cause Charcot-Marie-Tooth disease. Annals of Clinical and Translational Neurology |
| Kantonen J, Mahzabin S, Mäyränpää MI, et al. (2020) Neuropathologic features of four autopsied COVID-19 patients. Brain Pathology |
| Raunio A, Kaivola K, Tuimala J, et al. (2019) Lewy-related pathology exhibits two anatomically and genetically distinct progression patterns: a population-based study of Finns aged 85. Acta Neuropathologica. 138: 771-782 |
| Kuuluvainen L, Kaivola K, Mönkäre S, et al. (2019) Oligogenic basis of sporadic ALS: The example of p.Ala90Val mutation. Neurology. Genetics. 5: e335 |
| Sainio MT, Välipakka S, Rinaldi B, et al. (2018) Recessive PYROXD1 mutations cause adult-onset limb-girdle-type muscular dystrophy. Journal of Neurology |
| Pasanen P, Myllykangas L, Pöyhönen M, et al. (2018) Genetics of dementia in a Finnish cohort. European Journal of Human Genetics : Ejhg |
| Ignatenko O, Chilov D, Paetau I, et al. (2018) Loss of mtDNA activates astrocytes and leads to spongiotic encephalopathy. Nature Communications. 9: 70 |
| Auranen M, Paetau A, Piirilä P, et al. (2017) Patient with multiple acyl-CoA dehydrogenation deficiency disease and FLAD1 mutations benefits from riboflavin therapy. Neuromuscular Disorders. 27: 581-584 |
| Anttonen AK, Laari A, Kousi M, et al. (2017) ZNHIT3 is defective in PEHO syndrome, a severe encephalopathy with cerebellar granule neuron loss. Brain : a Journal of Neurology |
| Ritvonen E, Pitkänen E, Karppinen A, et al. (2017) Impact of AIP and inhibitory G protein alpha 2 proteins on clinical features of sporadic GH-secreting pituitary adenomas. European Journal of Endocrinology. 176: 243-252 |