Nils-Göran Larsson

Papers authored by Nils-Göran Larsson

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1995 M�rH Tulinius, Massoud Houshmand, Nils-G�ran Larsson

, Elisabeth Holme, Anders Oldfors, Eva Holmberg, Jan Wahlstr�m

De novo mutation in the mitochondrial ATP synthase subunit 6 gene (T8993G) with rapid segregation resulting in Leigh syndrome in the offspring

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Anders Oldfors, Elisabeth Holme, M�r Tulinius, Nils-G�ran Larsson

Tissue distribution and disease manifestations of the tRNALys A�G(8344) mitochondrial DNA mutation in a case of myoclonus epilepsy and ragged red fibres

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Anders Oldfors, Ali-Reza Moslemi, Ing-Marie Fyhr, Elisabeth Holme, Nils-Göran Larsson

, Christopher Lindberg

Mitochondrial DNA Deletions in Muscle Fibers in Inclusion Body Myositis:

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Elisabeth Holme, Már H. Tulinius, Nils-Göran Larrson, N. G. Larsson

, Anders Oldfors

Inheritance and expression of mitochondrial DNA point mutations

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Erik Walum, Gun Eriksson, Anders Peterson, Elisabeth Holme, Nils-Göran Larsson

, Charlotta Eriksson, Wael El-Shamy

Use of Primary Cultures and Continuous Cell Lines to Study Effects on Astrocytic Regulatory Functions

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Nils-G�ran Larsson

, Mar H. Tulinius, Elisabeth Holme, Anders Oldfors

Pathogenetic aspects of the A8344G mutation of mitochondrial DNA associated with MERRF syndrome and multiple symmetric lipomas

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1994 Már H. Tulinius, Anders Oldfors, Elisabeth Holme, Nils-G�ran Larsson

, Massoud Houshmand, Per Fahleson, Lars Sigström, Lars Sigstr�m, Bengt Kristiansson

Atypical presentation of multisystem disorders in two girls with mitochondrial DNA deletions

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N. G. Larsson

, A. Oldfors, E. Holme, D. A. Clayton

Low Levels of Mitochondrial Transcription Factor A in Mitochondrial DNA Depletion

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Massoud Houshmand, Nils-Göran Larsson

, Elisabeth Holme, Anders Oldfors, Már H. Tulinius, Oluf Andersen

Automatic sequencing of mitochondrial tRNA genes in patients with mitochondrial encephalomyopathy

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1993 E. Holme, Ng G. Larsson

, A. Oldfors, M. Tulinius, P. Sahlin, G. Stenman

Multiple symmetric lipomas with high levels of mtDNA with the tRNA(Lys) A-->G(8344) mutation as the only manifestation of disease in a carrier of myoclonus epilepsy and ragged-red fibers (MERRF) syndrome.

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Anders Oldfors, Nils-Göran Larsson

, Christopher Lindberg, Elisabeth Holme

Mitochondrial DNA deletions in inclusion body myositis

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1992 Elisabeth Holme, Joachim Greter, Carl-Eric Jacobson, Nils-Göran Larsson

, Sven Lindstedt, Karl Olof Nilsson, Anders Oldfors, Már Tulinius

Mitochondrial ATP-Synthase Deficiency in a Child with 3-Methylglutaconic Aciduria

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Ng G. Larsson

, Mh H. Tulinius, E. Holme, A. Oldfors, O. Andersen, J. Wahlström, J. Aasly

Segregation and manifestations of the mtDNA tRNA(Lys) A-->G(8344) mutation of myoclonus epilepsy and ragged-red fibers (MERRF) syndrome.

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Nils-Göran Larsson

, Elisabeth Holme

Multiple short direct repeats associated with single mtDNA deletions

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Anders Oldfors, Nils-Göran Larsson

, Elisabeth Holme, Már Tulinius, Bernhard Kadenbach, Martin Droste

Mitochondrial DNA deletions and cytochrome c oxidase deficiency in muscle fibres

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Ng G. Larsson

, Hg G. Eiken, H. Boman, E. Holme, A. Oldfors, Mh H. Tulinius

Lack of transmission of deleted mtDNA from a woman with Kearns-Sayre syndrome to her child.

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1991 Nils-Göran Larsson

, Oluf Andersen, Elisabeth Holme, Anders Oldfors, Jan Wahlström

Leber's hereditary optic neuropathy and complex I deficiency in muscle

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Már H. Tulinius, Elisabeth Holme, Bengt Kristiansson, Nils-Göran Larsson

, Anders Oldfors

Mitochondrial encephalomyopathies in childhood. II. Clinical manifestations and syndromes

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Már H. Tulinius, Elisabeth Holme, Bengt Kristiansson, Nils-Göran Larsson

, Anders Oldfors

Mitochondrial encephalomyopathies in childhood. I. Biochemical and morphologic investigations

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1990 A. Oldfors, I.-M. Fyhr, E. Holme, N.-G. Larsson

, M. Tulinius

Neuropathology in Kearns-Sayre syndrome

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Papers authored by Nils-Göran Larsson