Emil Ylikallio
Helsinki, Finland
Last Updated: 09/26/2026
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Found 42 publications
Metabolic costs and trade-offs of hypermetabolism in human motor neurons with ATP synthase deficiency.
Journal: Communications biology
Published: March 21, 2025
Dose-dependent CHCHD10 dysregulation dictates motor neuron disease severity and alters creatine metabolism.
Journal: Acta neuropathologica communications
Published: February 21, 2025
Variants in tropomyosins TPM2 and TPM3 causing muscle hypertonia.
Journal: Neuromuscular disorders : NMD
Published: September 21, 2023
Lowered oxidative capacity in spinal muscular atrophy, Jokela type; comparison with mitochondrial muscle disease.
Journal: Frontiers in neurology
Published: August 15, 2023
Structural insights into Charcot-Marie-Tooth disease-linked mutations in human GDAP1.
Journal: FEBS open bio
Published: February 28, 2022
Neurofilament Light Regulates Axon Caliber, Synaptic Activity, and Organelle Trafficking in Cultured Human Motor Neurons.
Journal: Frontiers in cell and developmental biology
Published: November 22, 2021
Serum Creatine, Not Neurofilament Light, Is Elevated in CHCHD10-Linked Spinal Muscular Atrophy.
Journal: Frontiers in neurology
Published: October 12, 2021
Threshold of heteroplasmic truncating MT-ATP6 mutation in reprogramming, Notch hyperactivation and motor neuron metabolism.
Journal: Human molecular genetics
Published: August 05, 2021
Bi-allelic loss-of-function OBSCN variants predispose individuals to severe recurrent rhabdomyolysis.
Journal: Brain : a journal of neurology
Published: June 04, 2021
Last Updated: 09/26/2026