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Flemming Wibrand Selected Research

Flemming Wibrand Research Topics

Disease

4Mitochondrial Myopathies (Mitochondrial Myopathy)
12/2019 - 12/2006
3Fabry Disease (Fabry's Disease)
01/2022 - 11/2011
3Muscular Diseases (Myopathy)
10/2017 - 02/2014
2Lysosomal Storage Diseases (Lysosomal Storage Disease)
11/2022 - 12/2017
2Mitochondrial Encephalomyopathies (Mitochondrial Encephalomyopathy)
01/2022 - 03/2007
2Lipoma (Lipomata)
10/2021 - 12/2017
2Leber Hereditary Optic Atrophy (Leber's Hereditary Optic Neuropathy)
01/2016 - 02/2013
2Mitochondrial Diseases (Mitochondrial Disease)
06/2010 - 01/2006
1Rare Diseases (Rare Disease)
01/2023
1Atrophy
11/2022
1Muscle Weakness
11/2022
1Ataxia (Dyssynergia)
10/2021
1Inborn Genetic Diseases (Disease, Hereditary)
07/2021
1Medium chain acyl CoA dehydrogenase deficiency
10/2020
1Inborn Errors Metabolism (Inborn Errors of Metabolism)
12/2019
1Globoid Cell Leukodystrophy (Krabbe Disease)
03/2019
1Hyperplasia
01/2018
1Tyrosinemias (Tyrosinemia)
01/2018
1Type 2 Diabetes Mellitus (MODY)
01/2018
1Liver Diseases (Liver Disease)
01/2018
1Non-alcoholic Fatty Liver Disease
01/2018
1Ophthalmoplegia (External Ophthalmoplegia)
10/2017
1Spinocerebellar Ataxias (Spinocerebellar Ataxia)
01/2017
1Methylmalonic acidemia
03/2016
1Succinate-Coa Ligase Deficiency
03/2016
1Myoglobinuria
01/2016
1Seizures (Absence Seizure)
01/2016
1Rhabdomyolysis
01/2016
1Muscle Hypotonia (Hypotonia)
01/2016
1Brain Diseases (Brain Disorder)
01/2016
1alpha-Mannosidosis
06/2015
1Obesity
03/2015
1Cytochrome-c Oxidase Deficiency
03/2015
1Intellectual Disability (Idiocy)
01/2015
1Gout
01/2015
1Lesch-Nyhan Syndrome (Choreoathetosis Self Mutilation Hyperuricemia Syndrome)
01/2015
1Nephrolithiasis
01/2015
1Respiratory Insufficiency (Respiratory Failure)
01/2014
1Recurrent Myoglobinuria
05/2013
1Neuropathy ataxia and retinitis pigmentosa
02/2013
1Leigh Disease (Leigh's Disease)
02/2013
1Mucolipidoses (Sialidosis)
01/2012
1Fatal Infantile Lactic Acidosis
08/2007
1Diabetes Mellitus
12/2006
1Hearing Loss (Hearing Impairment)
12/2006
1Hypoxia (Hypoxemia)
04/2005
1Stroke (Strokes)
10/2003
1MELAS Syndrome (Syndrome, MELAS)
10/2003
1Mitochondrial encephalopathy
10/2003
1Lactic Acidosis
10/2003

Drug/Important Bio-Agent (IBA)

10Mitochondrial DNA (mtDNA)IBA
12/2019 - 10/2003
8EnzymesIBA
01/2022 - 05/2010
3GalactosidasesIBA
11/2022 - 11/2011
3Lactic Acid (Lactate)FDA LinkGeneric
01/2016 - 12/2006
2Proteins (Proteins, Gene)FDA Link
01/2023 - 12/2019
2Biomarkers (Surrogate Marker)IBA
07/2021 - 12/2019
2AntioxidantsIBA
10/2020 - 06/2010
2Fatty Acids (Saturated Fatty Acids)IBA
10/2020 - 06/2010
2Acyl Coenzyme A (Acyl CoA)IBA
12/2019 - 06/2010
2Oxidoreductases (Dehydrogenase)IBA
12/2019 - 06/2010
2Coenzyme A (CoA)IBA
12/2019 - 06/2010
2Glucose (Dextrose)FDA LinkGeneric
01/2018 - 04/2005
1Glu Transfer RNAIBA
10/2021
1Acyl-CoA Dehydrogenase (Medium-Chain Acyl-Coenzyme A Dehydrogenase)IBA
10/2020
1Thioctic Acid (Lipoic Acid)IBA
10/2020
1Transfer RNA (tRNA)IBA
12/2019
1GalactosylceramidaseIBA
03/2019
1Glucagon (Glukagon)FDA Link
01/2018
1Amino AcidsFDA Link
01/2018
1nitisinone (Orfadin)FDA Link
01/2018
1succinylacetoneIBA
01/2018
1CholesterolIBA
01/2018
1Branched-Chain Amino AcidsIBA
01/2018
1alpha-Galactosidase (Beano)IBA
12/2017
1m-AAA proteasesIBA
01/2017
1Succinate-CoA Ligases (Succinyl Coenzyme A Synthetases)IBA
03/2016
1alpha-Mannosidase (LAMAN)IBA
06/2015
1Electron Transport Complex IV (Cytochrome c Oxidase)IBA
03/2015
1Hypoxanthine Phosphoribosyltransferase (Hypoxanthine Guanine Phosphoribosyltransferase)IBA
01/2015
1Met Transfer RNAIBA
01/2015
1Uric Acid (Urate)IBA
01/2015
1Lys Transfer RNAIBA
02/2014
1Mitochondrial Proton-Translocating ATPases (Mitochondrial ATP Synthase)IBA
02/2013
1Phosphotransferases (Kinase)IBA
01/2012
1Succinic Acid (Succinate)IBA
08/2007
1Coenzyme A Ligases (Acid-Thiol Ligases)IBA
08/2007
1Methylmalonic AcidIBA
03/2007
1Oxygen (Dioxygen)IBA
12/2006
1TaurineFDA Link
01/2006
1BromidesIBA
04/2005
1HypoxanthineIBA
04/2005
1Leu Transfer RNAIBA
10/2003

Therapy/Procedure

1Glycemic Control
01/2018