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Wyszukujesz frazę ""Madsen, Karen Lindhardt"" wg kryterium: Autor


Tytuł :
Impaired Fat Oxidation During Exercise in Long-Chain Acyl-CoA Dehydrogenase Deficiency Patients and Effect of IV-Glucose.
Autorzy :
Madsen KL; Department of Neurology, Copenhagen Neuromuscular Center, Rigshospitalet, Copenhagen, Denmark.
Stemmerik MG; Department of Neurology, Copenhagen Neuromuscular Center, Rigshospitalet, Copenhagen, Denmark.
Buch AE; Department of Neurology, Copenhagen Neuromuscular Center, Rigshospitalet, Copenhagen, Denmark.
Poulsen NS; Department of Neurology, Copenhagen Neuromuscular Center, Rigshospitalet, Copenhagen, Denmark.
Lund AM; Department of Pediatrics, Centre for Inherited Metabolic Diseases, Rigshospitalet, Copenhagen, Denmark.; Department of Clinical Genetics, Centre for Inherited Metabolic Diseases, Rigshospitalet, Copenhagen, Denmark.
Vissing J; Department of Neurology, Copenhagen Neuromuscular Center, Rigshospitalet, Copenhagen, Denmark.
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Źródło :
The Journal of clinical endocrinology and metabolism [J Clin Endocrinol Metab] 2019 Sep 01; Vol. 104 (9), pp. 3610-3613.
Typ publikacji :
Case Reports; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Exercise*
Cardiomyopathies/*complications
Fatty Acids/*metabolism
Glucose/*administration & dosage
Lipid Metabolism, Inborn Errors/*drug therapy
Mitochondrial Myopathies/*complications
Mitochondrial Trifunctional Protein/*deficiency
Muscle Weakness/*drug therapy
Muscle, Skeletal/*drug effects
Nervous System Diseases/*complications
Rhabdomyolysis/*complications
Adolescent ; Adult ; Case-Control Studies ; Female ; Follow-Up Studies ; Humans ; Lipid Metabolism, Inborn Errors/complications ; Lipid Metabolism, Inborn Errors/etiology ; Lipid Metabolism, Inborn Errors/pathology ; Male ; Muscle Weakness/etiology ; Muscle Weakness/pathology ; Muscle, Skeletal/pathology ; Oxidation-Reduction ; Prognosis ; Sweetening Agents/administration & dosage ; Young Adult
SCR Disease Name :
Trifunctional Protein Deficiency With Myopathy And Neuropathy
Czasopismo naukowe
Tytuł :
L-Carnitine Improves Skeletal Muscle Fat Oxidation in Primary Carnitine Deficiency.
Autorzy :
Madsen KL; Copenhagen Neuromuscular Center, Department of Neurology, Rigshospitalet, Copenhagen, Denmark.
Preisler N; Copenhagen Neuromuscular Center, Department of Neurology, Rigshospitalet, Copenhagen, Denmark.
Rasmussen J; Department of Internal Medicine, The National Hospital of the Faroe Islands, Tórshavn, Faroe Islands.
Hedermann G; Copenhagen Neuromuscular Center, Department of Neurology, Rigshospitalet, Copenhagen, Denmark.
Olesen JH; Centre for Inherited Metabolic Diseases, Department of Clinical Genetics, Rigshospitalet, Copenhagen, Denmark.
Lund AM; Centre for Inherited Metabolic Diseases, Department of Clinical Genetics, Rigshospitalet, Copenhagen, Denmark.
Vissing J; Copenhagen Neuromuscular Center, Department of Neurology, Rigshospitalet, Copenhagen, Denmark.
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Źródło :
The Journal of clinical endocrinology and metabolism [J Clin Endocrinol Metab] 2018 Dec 01; Vol. 103 (12), pp. 4580-4588.
Typ publikacji :
Clinical Trial; Journal Article; Research Support, Non-U.S. Gov't
MeSH Terms :
Cardiomyopathies/*drug therapy
Carnitine/*administration & dosage
Carnitine/*deficiency
Fatty Acids/*metabolism
Hyperammonemia/*drug therapy
Lipid Metabolism/*drug effects
Muscle, Skeletal/*metabolism
Muscular Diseases/*drug therapy
Adult ; Calorimetry, Indirect ; Carbohydrate Metabolism/drug effects ; Carbohydrate Metabolism/physiology ; Cardiomyopathies/genetics ; Cardiomyopathies/metabolism ; Carnitine/genetics ; Carnitine/metabolism ; Exercise/physiology ; Female ; Humans ; Hyperammonemia/genetics ; Hyperammonemia/metabolism ; Lipid Metabolism/physiology ; Male ; Middle Aged ; Muscle, Skeletal/drug effects ; Muscular Diseases/genetics ; Muscular Diseases/metabolism ; Oxidation-Reduction ; Solute Carrier Family 22 Member 5/genetics ; Treatment Outcome ; Young Adult
SCR Disease Name :
Systemic carnitine deficiency
Czasopismo naukowe
Tytuł :
Bezafibrate in skeletal muscle fatty acid oxidation disorders: a randomized clinical trial.
Autorzy :
Ørngreen MC; From the Neuromuscular Clinic and Research Unit (M.C.Ø, K.L.M., N.P., G.A., J.V.), Department of Neurology, Rigshospitalet, University of Copenhagen, Denmark; and Centre de Référence de pathologie neuromusculaire Paris-Est (P.L.), Groupe Hospitalier Pitié-Salpêtrière, Assistance Publique-Hôpitaux de Paris, France.
Madsen KL
Preisler N
Andersen G
Vissing J
Laforêt P
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Źródło :
Neurology [Neurology] 2014 Feb 18; Vol. 82 (7), pp. 607-13. Date of Electronic Publication: 2014 Jan 22.
Typ publikacji :
Journal Article; Randomized Controlled Trial; Research Support, Non-U.S. Gov't
MeSH Terms :
Acyl-CoA Dehydrogenase, Long-Chain/*deficiency
Bezafibrate/*pharmacology
Carnitine O-Palmitoyltransferase/*deficiency
Fatty Acids/*metabolism
Hypolipidemic Agents/*pharmacology
Lipid Metabolism, Inborn Errors/*drug therapy
Lipid Metabolism, Inborn Errors/*metabolism
Mitochondrial Diseases/*drug therapy
Mitochondrial Diseases/*metabolism
Muscle, Skeletal/*metabolism
Muscular Diseases/*drug therapy
Muscular Diseases/*metabolism
Acyl-CoA Dehydrogenase, Long-Chain/blood ; Acyl-CoA Dehydrogenase, Long-Chain/metabolism ; Adolescent ; Adult ; Aged ; Bezafibrate/administration & dosage ; Bezafibrate/blood ; Clinical Protocols ; Congenital Bone Marrow Failure Syndromes ; Cross-Over Studies ; Fatty Acids/blood ; Female ; Humans ; Hypolipidemic Agents/administration & dosage ; Hypolipidemic Agents/blood ; Lipid Metabolism, Inborn Errors/blood ; Lipid Metabolism, Inborn Errors/diagnosis ; Male ; Middle Aged ; Mitochondrial Diseases/blood ; Mitochondrial Diseases/diagnosis ; Muscle, Skeletal/drug effects ; Muscular Diseases/blood ; Muscular Diseases/diagnosis ; Treatment Outcome ; Young Adult
SCR Disease Name :
Carnitine Palmitoyltransferase II Deficiency, Late-Onset; VLCAD deficiency
Czasopismo naukowe

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