Publications by authors named "Rosetta Marotta"

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Long-term screening for primary mitochondrial DNA variants associated with Leber hereditary optic neuropathy: incidence, penetrance and clinical features.
Rosetta Marotta, Judy Chin, Maria Chiotis, Neil Shuey, Steven J Collins

Mitochondrion· September 2020

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Late-adult onset Leigh syndrome.
Penelope McKelvie, Bernard Infeld, Rosetta Marotta, Judy Chin, David Thorburn

J Clin Neurosci· February 2012

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Novel single base pair COX III subunit deletion of mitochondrial DNA associated with rhabdomyolysis.
Rosetta Marotta, Judy Chin, Denise M Kirby, Maria Chiotis, Mark Cook

J Clin Neurosci· February 2011

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Association of the MELAS m.3243A>G mutation with myositis and the superiority of urine over muscle, blood and hair for mutation detection.
Rosetta Marotta, Katrina Reardon, Penny A McKelvie, Maria Chiotis, Judy Chin

J Clin Neurosci· September 2009

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Dominant inheritance of premature ovarian failure associated with mutant mitochondrial DNA polymerase gamma.
Alistair T Pagnamenta, Jan-Willem Taanman, Callum J Wilson, Neil E Anderson, Rosetta Marotta

Hum Reprod· October 2006

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DNA electroporation in vivo targets mature fibres in dystrophic mdx muscle.
Sharon H A Wong, Kym N Lowes, Anita F Quigley, Rosetta Marotta, Magdalena Kita

Neuromuscul Disord· October 2005

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Writer's cramp in an Australian pedigree with DYT1 dystonia.
Mehdi van den Bos, Rosetta Marotta, Sandra Goldup, Tim Chataway, Frank Firgaira

J Clin Neurosci· June 2004

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