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Acidosis during reoxygenation has an early detrimental effect on neuronal metabolic activity

Pediatric research, 2005-04, Vol.57 (4), p.488-493

2005

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Acylcarnitine profiles in mitochondrial myopathies

Neuromuscular disorders : NMD, 2015-10, Vol.25, p.S203-S203

2015

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Aerobic training is safe and improves exercise capacity in patients with mitochondrial myopathy

Brain (London, England : 1878), 2006-12, Vol.129 (12), p.3402-3412

2006

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CLPB Variants Associated with Autosomal-Recessive Mitochondrial Disorder with Cataract, Neutropenia, Epilepsy, and Methylglutaconic Aciduria

American journal of human genetics, 2015-02, Vol.96 (2), p.258-265

2015

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Correction: Systematic cascade screening in the Danish Fabry Disease Centre: 20 years of a national single-centre experience

PloS one, 2023-06, Vol.18 (6), p.e0287268-e0287268

2023

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Deficiency of the ¿ Subunit of Succinate-Coenzyme A Ligase Causes Fatal Infantile Lactic Acidosis with Mitochondrial DNA Depletion

American journal of human genetics, 2007-08, Vol.81 (2), p.383-387

2007

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Effect of aerobic training in patients with spinal and bulbar muscular atrophy (Kennedy disease)

Neurology, 2009-01, Vol.72 (4), p.317-323

2009

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Enzyme replacement therapy for alpha-mannosidosis: 12 months follow-up of a single centre, randomised, multiple dose study

Journal of inherited metabolic disease, 2013-11, Vol.36 (6), p.1015-1024

2013

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Four novel PDHA1 mutations in pyruvate dehydrogenase deficiency

Journal of inherited metabolic disease, 2009-12, Vol.32 (Suppl 1), p.235-239

2009

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G.P.115 Recurrent myoglobinuria and deranged acyl-carnitines due to mutation of the COII gene of mtDNA

Neuromuscular disorders : NMD, 2012-10, Vol.22 (9), p.890-890

2012

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G.P.55 - Acylcarnitine profiles in mitochondrial myopathies

Neuromuscular disorders : NMD, 2015-10, Vol.25, p.S203-S203

2015

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Hypertrichosis in patients with SURF1 mutations

American journal of medical genetics. Part A, 2005-11, Vol.138A (4), p.384-388

2005

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Impaired energy metabolism and abnormal muscle histology in mut- methylmalonic aciduria

Neurology, 2005-09, Vol.65 (6), p.931-933

2005

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Lactate transport in isolated mouse muscles studied with a tracer technique-kinetics, stereospecificity, pH dependency and maximal capacity

Acta physiologica Scandinavica, 1989-09, Vol.137 (1), p.33-39

1989

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Lactate transport studied in sarcolemmal giant vesicles from rats: effect of training

American journal of physiology: endocrinology and metabolism, 1993-02, Vol.264 (2), p.E156-E160

1993

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Lactate transport studied in sarcolemmal giant vesicles from rats : effect of training

American journal of physiology: endocrinology and metabolism, 1993-02, Vol.27 (2), p.E156-E160

1993

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A microplate-based enzymatic assay for the simultaneous determination of phenylalanine and tyrosine in serum

Clinica chimica acta, 2004-09, Vol.347 (1), p.89-96

Wibrand, Flemming

2004

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Mitochondrial encephalomyopathy with elevated methylmalonic acid is caused by SUCLA2 mutations

Brain (London, England : 1878), 2007-03, Vol.130 (3), p.853-861

2007

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An mtDNA mutation, 14453G-->A, in the NADH dehydrogenase subunit 6 associated with severe MELAS syndrome

European journal of human genetics : EJHG, 2001-10, Vol.9 (10), p.805-809

2001

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Multiple mtDNA deletions with features of MNGIE

Neurology, 2002-09, Vol.59 (6), p.926-929

2002

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Multisystem disorder associated with a missense mutation in the mitochondrial cytochrome b gene

Annals of neurology, 2001-10, Vol.50 (4), p.540-543

2001

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Opening of Glibenclamide-Sensitive K+Channels in Follicular Cells Promotes Xenopus Oocyte Maturation

Proceedings of the National Academy of Sciences - PNAS, 1992-06, Vol.89 (11), p.5133-5137

1992

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Opening of glibenclamide-sensitive K super(+) channels in follicular cells promotes Xenopus) oocyte maturation

Proceedings of the National Academy of Sciences - PNAS, 1992-01, Vol.89 (11), p.5133-5137

1992

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P361 Acylcarnitine profiles in patients with mitochondrial myopathy under different physiological conditions

Neuromuscular disorders : NMD, 2023-10, Vol.33, p.S185-S186

2023

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Reconstitution of the lactate carrier from rat skeletal-muscle sarcolemma

Biochemical journal, 1994-04, Vol.299 (2), p.533-537

1994

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Acidosis during reoxygenation has an early detrimental effect on neuronal metabolic activity

Acylcarnitine profiles in mitochondrial myopathies

Aerobic training is safe and improves exercise capacity in patients with mitochondrial myopathy

CLPB Variants Associated with Autosomal-Recessive Mitochondrial Disorder with Cataract, Neutropenia, Epilepsy, and Methylglutaconic Aciduria

Correction: Systematic cascade screening in the Danish Fabry Disease Centre: 20 years of a national single-centre experience

Deficiency of the ¿ Subunit of Succinate-Coenzyme A Ligase Causes Fatal Infantile Lactic Acidosis with Mitochondrial DNA Depletion

Effect of aerobic training in patients with spinal and bulbar muscular atrophy (Kennedy disease)

Enzyme replacement therapy for alpha-mannosidosis: 12 months follow-up of a single centre, randomised, multiple dose study

Four novel PDHA1 mutations in pyruvate dehydrogenase deficiency

G.P.115 Recurrent myoglobinuria and deranged acyl-carnitines due to mutation of the COII gene of mtDNA

G.P.55 - Acylcarnitine profiles in mitochondrial myopathies

Hypertrichosis in patients with SURF1 mutations

Impaired energy metabolism and abnormal muscle histology in mut- methylmalonic aciduria

Lactate transport in isolated mouse muscles studied with a tracer technique-kinetics, stereospecificity, pH dependency and maximal capacity

Lactate transport studied in sarcolemmal giant vesicles from rats: effect of training

Lactate transport studied in sarcolemmal giant vesicles from rats : effect of training

A microplate-based enzymatic assay for the simultaneous determination of phenylalanine and tyrosine in serum

Mitochondrial encephalomyopathy with elevated methylmalonic acid is caused by SUCLA2 mutations

An mtDNA mutation, 14453G-->A, in the NADH dehydrogenase subunit 6 associated with severe MELAS syndrome

Multiple mtDNA deletions with features of MNGIE

Multisystem disorder associated with a missense mutation in the mitochondrial cytochrome b gene

Opening of Glibenclamide-Sensitive K+Channels in Follicular Cells Promotes Xenopus Oocyte Maturation

Opening of glibenclamide-sensitive K super(+) channels in follicular cells promotes Xenopus) oocyte maturation

P361 Acylcarnitine profiles in patients with mitochondrial myopathy under different physiological conditions

Reconstitution of the lactate carrier from rat skeletal-muscle sarcolemma

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