René I F M de Coo

8PUBLICATIONS
72CO-AUTHORS
Microelectromechanical systems (MEMS)Cell and nuclear divisionMetabolic medicineNeurology and neuromuscular diseasesMedical devices
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Publications (8)

|May 27, 2025
MCT8 Deficiency in Females.

Stefan Groeneweg, Ferdy S van Geest, Floor van der Most

|Oct 24, 2023
A Delphi Survey Study to Formulate Statements on the Treatability of Inherited Metabolic Disorders to Decide on Eligibility for Newborn Screening.

Abigail Veldman, M B Gea Kiewiet, Dineke Westra

|Feb 21, 2022
Neurodegenerative and functional signatures of the cerebellar cortex in m.3243A > G patients.

Roy A M Haast, Irenaeus F M De Coo, Dimo Ivanov

|Jul 08, 2020
Using urine to diagnose large-scale mtDNA deletions in adult patients.

Kristin N Varhaug, Gonzalo S Nido, Irenaeus de Coo

|Mar 27, 2019
Leigh syndrome caused by mutations in MTFMT is associated with a better prognosis.

Hannah Hayhurst, Irenaeus F M de Coo, Dorota Piekutowska-Abramczuk

|Feb 15, 2018
Genetic defects in mtDNA-encoded protein translation cause pediatric, mitochondrial cardiomyopathy with early-onset brain disease.

Rick Kamps, Radek Szklarczyk, Tom E Theunissen

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Frequent Collaborators

1 joint publications

Marije E C Meuwissen

1 joint publications

Rachel Schot

1 joint publications

Sofija Buta

1 joint publications

Sigrid Tinschert