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

Author/Creator Duno, M

1. Corticobasal and ataxia syndromes widen the spectrum of C9ORF72 hexanucleotide expansion disease. (19th April 2013)

Authors:: Lindquist, SG; Duno, M; Batbayli, M; Puschmann, A; Braendgaard, H; Mardosiene, S; Svenstrup, K; Pinborg, LH; Vestergaard, K; Hjermind, LE; Stokholm, J; Andersen, BB; Johannsen, P; Nielsen, JE
Journal:: Clinical genetics
Issue:: Volume 83:Number 3(2013:Mar.)
Page Start:: 279
Record Type:: Journal Article
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2. Corticobasal and ataxia syndromes widen the spectrum of C9ORF72 hexanucleotide expansion disease. (4th July 2012)

Authors:: Lindquist, SG; Duno, M; Batbayli, M; Puschmann, A; Braendgaard, H; Mardosiene, S; Svenstrup, K; Pinborg, LH; Vestergaard, K; Hjermind, LE; Stokholm, J; Andersen, BB; Johannsen, P; Nielsen, JE
Journal:: Clinical genetics
Issue:: Volume 83:Number 3(2013:Mar.)
Page Start:: 279
Record Type:: Journal Article
View Content:: Available online (eLD content is only available in our Reading Rooms) ↗

3. McArdle disease: a clinical review. Issue 11 (22nd September 2010)

Authors:: Quinlivan, R; Buckley, J; James, M; Twist, A; Ball, S; Duno, M; Vissing, J; Bruno, C; Cassandrini, D; Roberts, M; Winer, J; Rose, M; Sewry, C
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 81:Issue 11(2010)
Page Start:: 1182
Record Type:: Journal Article
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4. Mutations in PCDH21 cause autosomal recessive cone-rod dystrophy. Issue 10 (30th August 2010)

Authors:: Ostergaard, E; Batbayli, M; Duno, M; Vilhelmsen, K; Rosenberg, T
Journal:: Journal of medical genetics
Issue:: Volume 47:Issue 10(2010)
Page Start:: 665
Record Type:: Journal Article
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