Marzio Bellan
Publications by Year
Research Areas
Mitochondrial Function and Pathology, Metabolism and Genetic Disorders, ATP Synthase and ATPases Research, Cell death mechanisms and regulation, Retinal and Optic Conditions
Most-Cited Works
- → Gastrointestinal Dysmotility in Mitochondrial Neurogastrointestinal Encephalomyopathy Is Caused by Mitochondrial DNA Depletion(2008)115 cited
- → POLG mutations causing ophthalmoplegia, sensorimotor polyneuropathy, ataxia, and deafness(2004)91 cited
- → Mitochondrial Optic Neuropathies: How Two Genomes may Kill the Same Cell Type?(2007)77 cited
- → Mitochondrial Neurogastrointestinal Encephalomyopathy: Evidence of Mitochondrial DNA Depletion in the Small Intestine(2006)69 cited
- → Mitochondrial DNA nucleotide changes C14482G and C14482A in the ND6 gene are pathogenic for Leber's hereditary optic neuropathy(2002)52 cited
- → Myelin, mitochondria, and autoimmunity(2008)16 cited
- → Ocular findings in mitochondrial neurogastrointestinal encephalomyopathy: a case report(2004)15 cited
- → Premotor antidepressants use differs according to Parkinson's disease subtype: A cohort study(2021)3 cited
- RETINAL NERVE FIBER LAYER CHANGES IN UNAFFECTED MATERNAL RELATIVES OF PATIENTS WITH LEBER’S HEREDITARY OPTIC NEUROPATHY(2004)
- A new case of Sando syndrome and retinitis pigmentosa with novel combination of compound heterozygous POLG mutations.(2006)