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Maria Alessandra Carluccio Selected Research

Mitochondrial DNA (mtDNA)

3/2017Complex I deficiency related to T10158C mutation ND3 gene: A further definition of the clinical spectrum.

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Maria Alessandra Carluccio Research Topics

Disease

1CADASIL
07/2017
1Cerebral Small Vessel Diseases
07/2017
1MELAS Syndrome (Syndrome, MELAS)
03/2017
1Leigh Disease (Leigh's Disease)
03/2017
1Oculopharyngeal Muscular Dystrophy
08/2012
1Minicore Myopathy with External Ophthalmoplegia
08/2012
1Myotonic Dystrophy (Dystrophia Myotonica)
08/2012
1Mitochondrial Myopathies (Mitochondrial Myopathy)
04/2011
1Deafness (Deaf Mutism)
04/2011
1Seizures (Absence Seizure)
04/2011
1Distal Myopathies (Distal Muscular Dystrophy)
04/2010

Drug/Important Bio-Agent (IBA)

1hydroxide ionIBA
07/2017
1Vitamin DFDA LinkGeneric
07/2017
1Mitochondrial DNA (mtDNA)IBA
03/2017
1Ryanodine Receptor Calcium Release Channel (Ryanodine Receptor)IBA
08/2012
1Ser Transfer RNAIBA
04/2011
1ConnectinIBA
04/2010