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Author/Creator Woodward, Cathy E

1. Distal myopathy with cachexia: an unrecognised phenotype caused by dominantly-inherited mitochondrial polymerase γ mutations. Issue 1 (29th August 2012)

Authors:
Pitceathly, Robert D S; Tomlinson, Susan E; Hargreaves, Iain; Bhardwaj, Nisha; Holton, Janice L; Morrow, Jasper M; Evans, Julie; Smith, Conrad; Fratter, Carl; Woodward, Cathy E; Sweeney, Mary G; Rahman, Shamima; Hanna, Michael G
Journal:
Journal of neurology, neurosurgery and psychiatry
Issue:
Volume 84:Issue 1(2013)
Page Start:
107
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

2. Kearns–Sayre syndrome caused by defective R1/p53R2 assembly. Issue 9 (4th March 2011)

Authors:
Pitceathly, Robert D S; Fassone, Elisa; Taanman, Jan-Willem; Sadowski, Michael; Fratter, Carl; Mudanohwo, Ese E; Woodward, Cathy E; Sweeney, Mary G; Holton, Janice L; Hanna, Michael G; Rahman, Shamima
Journal:
Journal of medical genetics
Issue:
Volume 48:Issue 9(2011)
Page Start:
610
Record Type:
Journal Article
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Available online (eLD content is only available in our Reading Rooms) ↗

3. Primary mitochondrial diseases increase susceptibility to bipolar affective disorder. Issue 8 (11th June 2020)

Authors:
Colasanti, Alessandro; Bugiardini, Enrico; Amawi, Sami; Poole, Olivia V; Skorupinska, Iwona; Skorupinska, Mariola; Germain, Louise; Kozyra, Damian; Holmes, Sarah; James, Natalie; Woodward, Cathy E; Quinlivan, Rosaline; Young, Allan H; Hanna, Michael G; Pitceathly, Robert D S
Journal:
Journal of neurology, neurosurgery and psychiatry
Issue:
Volume 91:Issue 8(2020)
Page Start:
892
Record Type:
Journal Article
View Content:
Available online (eLD content is only available in our Reading Rooms) ↗