Ronen Spiegel

4PUBLICATIONS
1CO-AUTHORS
Electronic and magnetic properties of condensed matter; superconductivityNeurology and neuromuscular diseasesMetabolic medicineEpigenetics (incl. genome methylation and epigenomics)
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Publications (4)

|Jul 03, 2024
Primary CoQ10 deficiency: treatable heterogeneous group of disorders.

Ronen Spiegel

|Feb 28, 2024
Lack of mitochondrial complex I assembly factor NDUFAF2 results in a distinctive infantile-onset brainstem neurodegenerative disease with early lethality.

Firas Abu Hanna, Yoav Zehavi, Eran Cohen-Barak

|Feb 22, 2022
Molybdenum cofactor deficiency: A natural history.

Ronen Spiegel, Bernd C Schwahn, Liza Squires

|Jan 20, 2021
A novel de novo heterozygous pathogenic variant in the SDHA gene results in childhood onset bilateral optic atrophy and cognitive impairment.

Yoav Zehavi, Ann Saada, Haneen Jabaly-Habib

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Frequent Collaborators

1 joint publications

Firas Abu Hanna