Leigh Syndrome Latest Advances

Can early diagnosis of Leigh syndrome impact prognosis?

Journal: Expert review of neurotherapeutics

Published: September 08, 2026

An optimized "hypoxia in a pill" regimen reverses neurodegenerative disease phenotypes in multiple preclinical models.

Journal: bioRxiv : the preprint server for biology

Published: July 10, 2026

Navigating the Mitochondrial Maze: A Case Report of Emergent Cesarean Delivery After Labor Induction in a Patient With Leigh Syndrome.

Journal: A&A practice

Published: June 10, 2026

TTC19-related mitochondrial disease: A characteristic neuroimaging signature?

Journal: Molecular genetics and metabolism

Published: June 02, 2026

Disease-mutations perturb proton transfer reactions in respiratory complex I.

Journal: Biochimica et biophysica acta. Bioenergetics

Published: May 27, 2026

MyD88 deficiency modestly attenuates disease in a Leigh syndrome mouse model while enrofloxacin accelerates disease.

Journal: bioRxiv : the preprint server for biology

Published: May 25, 2026

When LHON Mimics Demyelination: Area Postrema Syndrome in Biallelic DNAJC30 Variants.

Journal: Journal of clinical medicine

Published: May 13, 2026

SLIRP differentially modulates RNA binding of pathogenic LRPPRC variants.

Journal: NAR molecular medicine

Published: May 04, 2026

β-ureidopropionase deficiency mimicking Leigh syndrome associated with methylmalonic aciduria.

Journal: BMJ case reports

Published: May 04, 2026

COX14 Variants Are Associated With Mitochondrial Complex IV Deficiency Nuclear Type 10 (MC4DN10).

Journal: American journal of medical genetics. Part A

Published: May 01, 2026

Cardiac Tamponade After Late Central Venous Catheter Dislodgement in Two Pediatric Patients-A Rare but Potentially Fatal Complication.

Journal: Children (Basel, Switzerland)

Published: April 29, 2026

Perianesthetic Complications in Genetic Mitochondrial Disease: A Review of Case Reports.

Journal: Paediatric anaesthesia

Published: April 22, 2026

Leigh Syndrome Latest Advances

Find the Latest Research About Leigh Syndrome

Can early diagnosis of Leigh syndrome impact prognosis?

Can early diagnosis of Leigh syndrome impact prognosis?

An optimized "hypoxia in a pill" regimen reverses neurodegenerative disease phenotypes in multiple preclinical models.

An optimized "hypoxia in a pill" regimen reverses neurodegenerative disease phenotypes in multiple preclinical models.

Navigating the Mitochondrial Maze: A Case Report of Emergent Cesarean Delivery After Labor Induction in a Patient With Leigh Syndrome.

Navigating the Mitochondrial Maze: A Case Report of Emergent Cesarean Delivery After Labor Induction in a Patient With Leigh Syndrome.

TTC19-related mitochondrial disease: A characteristic neuroimaging signature?

TTC19-related mitochondrial disease: A characteristic neuroimaging signature?

Disease-mutations perturb proton transfer reactions in respiratory complex I.

Disease-mutations perturb proton transfer reactions in respiratory complex I.

MyD88 deficiency modestly attenuates disease in a Leigh syndrome mouse model while enrofloxacin accelerates disease.

MyD88 deficiency modestly attenuates disease in a Leigh syndrome mouse model while enrofloxacin accelerates disease.

When LHON Mimics Demyelination: Area Postrema Syndrome in Biallelic DNAJC30 Variants.

When LHON Mimics Demyelination: Area Postrema Syndrome in Biallelic DNAJC30 Variants.

SLIRP differentially modulates RNA binding of pathogenic LRPPRC variants.

SLIRP differentially modulates RNA binding of pathogenic LRPPRC variants.

β-ureidopropionase deficiency mimicking Leigh syndrome associated with methylmalonic aciduria.

β-ureidopropionase deficiency mimicking Leigh syndrome associated with methylmalonic aciduria.

COX14 Variants Are Associated With Mitochondrial Complex IV Deficiency Nuclear Type 10 (MC4DN10).

COX14 Variants Are Associated With Mitochondrial Complex IV Deficiency Nuclear Type 10 (MC4DN10).

Cardiac Tamponade After Late Central Venous Catheter Dislodgement in Two Pediatric Patients-A Rare but Potentially Fatal Complication.

Cardiac Tamponade After Late Central Venous Catheter Dislodgement in Two Pediatric Patients-A Rare but Potentially Fatal Complication.

Perianesthetic Complications in Genetic Mitochondrial Disease: A Review of Case Reports.

Perianesthetic Complications in Genetic Mitochondrial Disease: A Review of Case Reports.