Tiina A. Tyni

Stenbackinkatu 11, PL 281
Helsinki, 00029, Finland

Last Updated: 09/26/2026

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Found 17 publications

Moyamoya angiopathy: radiological follow-up findings in Finnish patients.

Moyamoya angiopathy: radiological follow-up findings in Finnish patients.

Journal: Journal of neurology

Published: January 20, 2020

Erratum to "Peripheral neuropathy in patients with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency - A follow-up EMG study of 12 patients" [Eur J Paediatr Neuro 20 (2016) 38-44].

Erratum to "Peripheral neuropathy in patients with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency - A follow-up EMG study of 12 patients" [Eur J Paediatr Neuro 20 (2016) 38-44].

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society

Published: January 16, 2019

Moyamoya angiopathy: long-term follow-up study in a Finnish population.

Moyamoya angiopathy: long-term follow-up study in a Finnish population.

Journal: Journal of neurology

Published: October 11, 2018

Genetic Basis of Severe Childhood-Onset Cardiomyopathies.

Genetic Basis of Severe Childhood-Onset Cardiomyopathies.

Journal: Journal of the American College of Cardiology

Published: February 13, 2018

Patient with multiple acyl-CoA dehydrogenation deficiency disease and FLAD1 mutations benefits from riboflavin therapy.

Patient with multiple acyl-CoA dehydrogenation deficiency disease and FLAD1 mutations benefits from riboflavin therapy.

Journal: Neuromuscular disorders : NMD

Published: September 28, 2016

Moyamoya vasculopathy - Patient demographics and characteristics in the Finnish population.

Moyamoya vasculopathy - Patient demographics and characteristics in the Finnish population.

Journal: International journal of stroke : official journal of the International Stroke Society

Published: September 15, 2016

Riboflavin-Responsive and -Non-responsive Mutations in FAD Synthase Cause Multiple Acyl-CoA Dehydrogenase and Combined Respiratory-Chain Deficiency.

Riboflavin-Responsive and -Non-responsive Mutations in FAD Synthase Cause Multiple Acyl-CoA Dehydrogenase and Combined Respiratory-Chain Deficiency.

Journal: American journal of human genetics

Published: January 22, 2016

Earlier diagnosis and strict diets improve the survival rate and clinical course of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

Earlier diagnosis and strict diets improve the survival rate and clinical course of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

Journal: Acta paediatrica (Oslo, Norway : 1992)

Published: June 05, 2015

Patient-Specific Induced Pluripotent Stem Cell-Derived RPE Cells: Understanding the Pathogenesis of Retinopathy in Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency.

Patient-Specific Induced Pluripotent Stem Cell-Derived RPE Cells: Understanding the Pathogenesis of Retinopathy in Long-Chain 3-Hydroxyacyl-CoA Dehydrogenase Deficiency.

Journal: Investigative ophthalmology & visual science

Published: May 30, 2015

The rare Costello variant HRAS c.173C>T (p.T58I) with severe neonatal hypertrophic cardiomyopathy.

The rare Costello variant HRAS c.173C>T (p.T58I) with severe neonatal hypertrophic cardiomyopathy.

Journal: American journal of medical genetics. Part A

Published: May 09, 2015

Peripheral neuropathy in patients with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency - A follow-up EMG study of 12 patients.

Peripheral neuropathy in patients with long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency - A follow-up EMG study of 12 patients.

Journal: European journal of paediatric neurology : EJPN : official journal of the European Paediatric Neurology Society

Published: April 18, 2015

Fetal left ventricular noncompaction cardiomyopathy and fatal outcome due to complete deficiency of mitochondrial trifunctional protein.

Fetal left ventricular noncompaction cardiomyopathy and fatal outcome due to complete deficiency of mitochondrial trifunctional protein.

Journal: European journal of pediatrics

Published: February 20, 2015

Showing 1-12 of 17

Last Updated: 09/26/2026