Leigh's Syndrome News and Research

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Researchers uncover cause of rare childhood neurodegenerative disease

Researchers uncover cause of rare childhood neurodegenerative disease

Study reveals how devastating mitochondrial diseases strike families without any previous history

Study reveals how devastating mitochondrial diseases strike families without any previous history

Pioneering IVF technique offers hope to families with inheritable mitochondrial disorders

Pioneering IVF technique offers hope to families with inheritable mitochondrial disorders

U of A researchers to study origin of Leigh's disease

U of A researchers to study origin of Leigh's disease

Scientists identify timing of major metabolic shift in developing neurons

Scientists identify timing of major metabolic shift in developing neurons

Rapamycin drug could target neural damage linked to Leigh syndrome

Rapamycin drug could target neural damage linked to Leigh syndrome

Salk researchers move one step closer to making cures for genetic diseases a reality

Salk researchers move one step closer to making cures for genetic diseases a reality

Edison's EPI-743 receives FDA orphan drug designation for treatment of Leigh syndrome

Edison's EPI-743 receives FDA orphan drug designation for treatment of Leigh syndrome

Edison Pharmaceuticals' EPI-743 granted orphan designation for Leigh syndrome in Japan

Edison Pharmaceuticals' EPI-743 granted orphan designation for Leigh syndrome in Japan

Transgenomic to provide genetic testing services for Raptor’s clinical trial

Transgenomic to provide genetic testing services for Raptor’s clinical trial

Edison Pharmaceuticals initiates Phase 2B/3 study of EPI-743 in children with Leigh syndrome

Edison Pharmaceuticals initiates Phase 2B/3 study of EPI-743 in children with Leigh syndrome

Edison's vatiquinone receives Orphan Status for treatment of Friedreich's ataxia

Edison's vatiquinone receives Orphan Status for treatment of Friedreich's ataxia

Researchers discover new gene mutations which cause devastating mitochondrial disorders

Researchers discover new gene mutations which cause devastating mitochondrial disorders

Study may lead to personalized treatments for mitochondrial energy disorders

Study may lead to personalized treatments for mitochondrial energy disorders

Data emphasise need for comprehensive analysis of mtDNA in mitochondrial disease patients

Data emphasise need for comprehensive analysis of mtDNA in mitochondrial disease patients

Positive results from Edison’s EPI-743 phase 2A study on Leigh Syndrome

Positive results from Edison’s EPI-743 phase 2A study on Leigh Syndrome

Edison receives EMA COMP orphan designation for EPI-743 to treat Leigh syndrome

Edison receives EMA COMP orphan designation for EPI-743 to treat Leigh syndrome

Researchers discover new genetic defect that can lead to Leigh syndrome

Researchers discover new genetic defect that can lead to Leigh syndrome

MHI researchers receive $4.8M as grants for genetics and genomic medicine research projects

MHI researchers receive $4.8M as grants for genetics and genomic medicine research projects

Researchers study about abnormal gene functioning in mitochondria

Researchers study about abnormal gene functioning in mitochondria