Author/Creator: Storey, E - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Storey, E

1. 1005 HEALTH-RELATED QUALITY OF LIFE AND FUTURE RISK OF HEALTH OUTCOMES AMONG OLDER ADULTS LIVING IN AUSTRALIA AND THE UNITED STATES. (14th June 2022)

Authors:: Phyo, A Z Z; Ryan, J; Gonzalez-Chica, D; Stocks, N; Woods, R; Murray, A; Reid, C; Nelson, M; Tonkin, A; Storey, E; Gasevic, D; Orchard, ; Shah, R; Freak-Poli, R
Journal:: Age and ageing
Issue:: Volume 51(2022)Supplement 2
Page Start:
Record Type:: Journal Article
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2. A low symptomatic form of neurodegeneration in younger carriers of the FMR1 premutation, manifesting typical radiological changes. Issue 3 (5th December 2007)

Authors:: Loesch, D Z; Cook, M; Litewka, L; Gould, E; Churchyard, A; Tassone, F; Slater, H R; Storey, E
Journal:: Journal of medical genetics
Issue:: Volume 45:Issue 3(2008)
Page Start:: 179
Record Type:: Journal Article
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3. A new dominantly inherited pure cerebellar ataxia, SCA 30. Issue 4 (7th November 2008)

Authors:: Storey, E; Bahlo, M; Fahey, M; Sisson, O; Lueck, C J; Gardner, R J M
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 80:Issue 4(2009)
Page Start:: 408
Record Type:: Journal Article
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4. Early intervention for mild cognitive impairment: a randomised controlled trial. Issue 7 (29th March 2009)

Authors:: Kinsella, G J; Mullaly, E; Rand, E; Ong, B; Burton, C; Price, S; Phillips, M; Storey, E
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 80:Issue 7(2009)
Page Start:: 730
Record Type:: Journal Article
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5. Spinocerebellar ataxia type 14: study of a family with an exon 5 mutation in the PRKCG gene. Issue 12 (16th November 2005)

Authors:: Fahey, M C; Knight, M A; Shaw, J H; Gardner, R J McK; du Sart, D; Lockhart, P J; Delatycki, M B; Gates, P C; Storey, E
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 76:Issue 12(2005)
Page Start:: 1720
Record Type:: Journal Article
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