Publications by authors named "Heli Helander"

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A Novel Homozygous Variant in 2 Cases of Spastic Ataxia Type 2.
Katariina Granath, Salla M Kangas, Sanna Huhtaniska, Maria Suo-Palosaari, Veli-Pekka Ronkainen, Heli Helander

Neurol Genet· December 2025

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Phenotypic Heterogeneity in Genetic and Acquired Pediatric Cerebellar Disorders.
Katariina Granath, Sanna Huhtaniska, Juulia Ellonen, Tytti Pokka, Salla M Kangas, Heli Helander

Mov Disord· September 2025

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Serum HMGB1 in febrile seizures.
Maria K Hautala, Kirsi H Mikkonen, Tytti M L Pokka, Sirpa K Rannikko, Ulla V Koskela, Heli M Helander

Epilepsy Res· July 2024

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Evidence for the additivity of rare and common variant burden throughout the spectrum of intellectual disability.
Lea Urpa, Mitja I Kurki, Elisa Rahikkala, Eija Hämäläinen, Veikko Salomaa, Heli Helander

Eur J Hum Genet· May 2024

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Recurrent febrile seizures and serum cytokines: a controlled follow-up study.
Maria K Hautala, Heli M Helander, Tytti M-L Pokka, Ulla V Koskela, Heikki M J Rantala

Pediatr Res· May 2023

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Starting a DBS service for children: It's not the latitude but the attitude - Establishment of the paediatric DBS centre in Northern Finland.
Maija Lahtinen, Heli Helander, Päivi Vieira, Johanna Uusimaa, Jani Katisko

Eur J Paediatr Neurol· January 2022

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Respiratory viruses and febrile response in children with febrile seizures: A cohort study and embedded case-control study.
Maria Hautala, Jukka Arvila, Tytti Pokka, Kirsi Mikkonen, Ulla Koskela, Heli Helander

Seizure· January 2021

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Contribution of rare and common variants to intellectual disability in a sub-isolate of Northern Finland.
Mitja I Kurki, Elmo Saarentaus, Olli Pietiläinen, Padhraig Gormley, Dennis Lal, Heli Helander

Nat Commun· January 2019

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Intractable Epilepsy due to MTR Deficiency: Importance of Homocysteine Analysis.
Jonna Komulainen-Ebrahim, Eemeli Saastamoinen, Elisa Rahikkala, Heli Helander, Reetta Hinttala

Neuropediatrics· December 2017

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Does Botulinum Toxin A Treatment Enhance the Walking Pattern in Idiopathic Toe-Walking?
Heli Sätilä, Anneli Beilmann, Päivi Olsén, Heli Helander, Mari Eskelinen

Neuropediatrics· June 2016

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The MELAS mutations 3946 and 3949 perturb the critical structure in a conserved loop of the ND1 subunit of mitochondrial complex I.
Marko Kervinen, Reetta Hinttala, Heli M Helander, Sari Kurki, Johanna Uusimaa

Hum Mol Genet· September 2006

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