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

Author/Creator Udd, B

1. EXOME SEQUENCING IN THREE FAMILIES WITH CYTOPLASMIC BODY MYOPATHY WITH EARLY RESPIRATORY FAILURE. (29th November 2012)

Authors:: Chinnery, P; Pfeffer, G; Griffin, H; Elliott, H; Barresi, R; Straub, V; Udd, B; Horvath, R; Dick, D
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 83(2012)Supplement 2
Page Start:: A22
Record Type:: Journal Article
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2. Laing early onset distal myopathy: slow myosin defect with variable abnormalities on muscle biopsy. Issue 2 (15th August 2005)

Authors:: Lamont, P J; Udd, B; Mastaglia, F L; de Visser, M; Hedera, P; Voit, T; Bridges, L R; Fabian, V; Rozemuller, A; Laing, N G
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 77:Issue 2(2006)
Page Start:: 208
Record Type:: Journal Article
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3. Limb-girdle type muscular dystrophy in a large family with distal myopathy: homozygous manifestation of a dominant gene?. Issue 6 (June 1992)

Authors:: Udd, B
Journal:: Journal of medical genetics
Issue:: Volume 29:Issue 6(1992)
Page Start:: 383
Record Type:: Journal Article
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4. Myopathies caused by homozygous titin mutations: limb-girdle muscular dystrophy 2J and variations of phenotype. Issue 11 (22nd June 2010)

Authors:: Pénisson-Besnier, I; Hackman, P; Suominen, T; Sarparanta, J; Huovinen, S; Richard-Crémieux, I; Udd, B
Journal:: Journal of neurology, neurosurgery and psychiatry
Issue:: Volume 81:Issue 11(2010)
Page Start:: 1200
Record Type:: Journal Article
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5. P03 The use of BRUM1 resequencing microarray to identify mutations in patients with neonatal cholestasis. (16th November 2010)

Authors:: Hartley, J; Bruce, C; Brown, R; McKay, K; Bauman, U; Sturm, E; Udd, B; Mckiernan, P; McMullen, D; Mansson, J; McDonald, F; Maher, E; Knisely, A; Hendriksz, C; Kelly, D; Gissen, P
Journal:: Gut
Issue:: Volume 59(2010)Supplement 2
Page Start:: A12
Record Type:: Journal Article
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