Author/Creator: Müller-Höcker, J - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Müller-Höcker, J

1. A systematic mutation screen of 10 nuclear and 25 mitochondrial candidate genes in 21 patients with cytochrome c oxidase (COX) deficiency shows tRNA(Ser)(UCN) mutations in a subgroup with syndromal encephalopathy. Issue 11 (November 1998)

Authors:: Jaksch, M; Hofmann, S; Kleinle, S; Liechti-Gallati, S; Pongratz, D E; Müller-Höcker, J; Jedele, K B; Meitinger, T; Gerbitz, K D
Journal:: Journal of medical genetics
Issue:: Volume 35:Issue 11(1998)
Page Start:: 895
Record Type:: Journal Article
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2. A tRNAAla mutation causing mitochondrial myopathy clinically resembling myotonic dystrophy. Issue 10 (20th October 2003)

Authors:: Horváth, R; Lochmüller, H; Scharfe, C; Do, B H; Oefner, P J; Müller-Höcker, J; Schoser, B G; Pongratz, D; Auer, D P; Jaksch, M
Journal:: Journal of medical genetics
Issue:: Volume 40:Issue 10(2003)
Page Start:: 752
Record Type:: Journal Article
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3. Childhood onset mitochondrial myopathy and lactic acidosis caused by a stop mutation in the mitochondrial cytochrome c oxidase III gene. Issue 11 (1st November 2002)

Authors:: Horváth, R; Scharfe, C; Hoeltzenbein, M; Do, B H; Schröder, C; Warzok, R; Vogelgesang, S; Lochmüller, H; Müller-Höcker, J; Gerbitz, K D; Oefner, P J; Jaksch, M
Journal:: Journal of medical genetics
Issue:: Volume 39:Issue 11(2002)
Page Start:: 812
Record Type:: Journal Article
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4. Missense mutations of ACTA1 cause dominant congenital myopathy with cores. Issue 11 (1st November 2004)

Authors:: Kaindl, A M; Rüschendorf, F; Krause, S; Goebel, H-H; Koehler, K; Becker, C; Pongratz, D; Müller-Höcker, J; Nürnberg, P; Stoltenburg-Didinger, G; Lochmüller, H; Huebner, A
Journal:: Journal of medical genetics
Issue:: Volume 41:Issue 11(2004)
Page Start:: 842
Record Type:: Journal Article
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5. Paraneoplastic chronic intestinal pseudoobstruction as a rare complication of bronchial carcinoid. Issue 7 (July 1992)

Authors:: Gerl, A; Storck, M; Schalhorn, A; Müller-Höcker, J; Jauch, K W; Schildberg, F W; Wilmanns, W
Journal:: Gut
Issue:: Volume 33:Issue 7(1992)
Page Start:: 1000
Record Type:: Journal Article
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6. Spontaneous recovery of a childhood onset mitochondrial myopathy caused by a stop mutation in the mitochondrial cytochrome c oxidase III gene. Issue 6 (1st June 2004)

Authors:: Horváth, R; Lochmüller, H; Hoeltzenbein, M; Müller-Höcker, J; Schoser, B G; Pongratz, D; Jaksch, M
Journal:: Journal of medical genetics
Issue:: Volume 41:Issue 6(2004)
Page Start:: e75
Record Type:: Journal Article
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