A M Lund - JoVE Visualize

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Journal of Neuroscience Research|June 16, 2004

On the neurotoxicity of glutaric, 3-hydroxyglutaric, and trans-glutaconic acids in glutaric acidemia type 1T M Lund, E Christensen, A S Kristensen, et al.

Zentralblatt Fur Veterinarmedizin. Reihe A|March 1, 1994

Osteogenesis imperfecta in Holstein-Friesian calvesJ S Agerholm, A M Lund, B Bloch, et al.

Journal of Inherited Metabolic Disease|September 16, 2003

What is the role of medium-chain triglycerides in the management of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency?A M Lund, M A Dixon, P Vreken, et al.

Journal of Inherited Metabolic Disease|September 16, 2003

Plasma and erythrocyte fatty acid concentrations in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiencyA M Lund, M A Dixon, P Vreken, et al.

JIMD Reports|July 18, 2025

Human D-Lactate Dehydrogenase Deficiency: A Case Report in a Young BoyT B Sloth, M C Ørngreen, J Ek, et al.

Human Reproduction (Oxford, England)|June 8, 2007

Preserved fertility in a non-mosaic Klinefelter patient with a mutation in the fibroblast growth factor receptor 3 gene: case reportA Juul, L Aksglaede, A M Lund, et al.

Neurology|November 25, 2010

Brain N-acetylaspartate levels correlate with motor function in metachromatic leukodystrophyC i Dali, L G Hanson, N W Barton, et al.

Journal of Inherited Metabolic Disease|May 29, 2015

Cognitive profile and activities of daily living: 35 patients with alpha-mannosidosisL Borgwardt, A M Thuesen, K J Olsen, et al.

Molecular Genetics and Metabolism|February 23, 2019

Recognition of alpha-mannosidosis in paediatric and adult patients: Presentation of a diagnostic algorithm from an international working groupN Guffon, A Tylki-Szymanska, L Borgwardt, et al.

The Journal of Clinical Endocrinology and Metabolism|February 22, 2013

Patients with medium-chain acyl-coenzyme a dehydrogenase deficiency have impaired oxidation of fat during exercise but no effect of L-carnitine supplementationK L Madsen, N Preisler, M C Orngreen, et al.

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Showing results (31-40 of 53) with videos related to

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Pageof 6

Journal of Neuroscience Research|June 16, 2004

On the neurotoxicity of glutaric, 3-hydroxyglutaric, and trans-glutaconic acids in glutaric acidemia type 1T M Lund, E Christensen, A S Kristensen, et al.

Zentralblatt Fur Veterinarmedizin. Reihe A|March 1, 1994

Osteogenesis imperfecta in Holstein-Friesian calvesJ S Agerholm, A M Lund, B Bloch, et al.

Journal of Inherited Metabolic Disease|September 16, 2003

What is the role of medium-chain triglycerides in the management of long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency?A M Lund, M A Dixon, P Vreken, et al.

Journal of Inherited Metabolic Disease|September 16, 2003

Plasma and erythrocyte fatty acid concentrations in long-chain 3-hydroxyacyl-CoA dehydrogenase deficiencyA M Lund, M A Dixon, P Vreken, et al.

JIMD Reports|July 18, 2025

Human D-Lactate Dehydrogenase Deficiency: A Case Report in a Young BoyT B Sloth, M C Ørngreen, J Ek, et al.

Human Reproduction (Oxford, England)|June 8, 2007

Preserved fertility in a non-mosaic Klinefelter patient with a mutation in the fibroblast growth factor receptor 3 gene: case reportA Juul, L Aksglaede, A M Lund, et al.

Neurology|November 25, 2010

Brain N-acetylaspartate levels correlate with motor function in metachromatic leukodystrophyC i Dali, L G Hanson, N W Barton, et al.

Journal of Inherited Metabolic Disease|May 29, 2015

Cognitive profile and activities of daily living: 35 patients with alpha-mannosidosisL Borgwardt, A M Thuesen, K J Olsen, et al.

Molecular Genetics and Metabolism|February 23, 2019

Recognition of alpha-mannosidosis in paediatric and adult patients: Presentation of a diagnostic algorithm from an international working groupN Guffon, A Tylki-Szymanska, L Borgwardt, et al.

The Journal of Clinical Endocrinology and Metabolism|February 22, 2013

Patients with medium-chain acyl-coenzyme a dehydrogenase deficiency have impaired oxidation of fat during exercise but no effect of L-carnitine supplementationK L Madsen, N Preisler, M C Orngreen, et al.

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