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by Meade, T and Sleight, P and Collins, R and Armitage, J and Parish, S and Barton, J and Bray, C and Wincott, E and Bowman, L and Clarke, R and Graham, I and Simpson, D and Warlow, C and Wilcken, D and Tobert, J and Musliner, T and Wilhelmsen, L and Doll, R and Fox, K.M and Hill, C and Sandercock, P and Peto, R and Webster, J and Jamieson, J and Nixon, A and Lackie, S and Thompson, J and Brown, M and Blackwood, S and Morgan, M and Rhoden, W and Saeed, B and Houghton, M and Nicholson, A and Simpson, C and Hoburn, B and Cooper, I and Gallivan, A and Pickerell, E and Hancock, J and Watkinson, J and Ryder, B and Jones, S and Burbridge, W and Kitchen, M and O'Leary, H and Verow, C and Meynell, L and Rollinson, L and Bain, S and Jones, A and Jewkes, C and Russon, C and Bateson, M and Gill, P and Nicol, J and Stansbie, D and Bayly, G and Andrews, G and Halestrap, M and Meredith, J and Best, R and Appleyard, D and Briggs, R and Wareing, H and Holmes, K and Holt, J and Kenyon, M and White, C and Khalifa, M and Newton, D and Wass, A and Watkinson, R and Creamer, J and Anderson, S and Bethell, A and Butler, C and Washington, M and Weston, E and Machin, J and Cleaver, K and Wray, R and Sinclair, J and Van Aalst, A and Been, M and Mattu, R and Bates, D and Burke, A and Gill, L and Walton, E and Cowley, M and Robson, H and Graham, A and Rose, G and Kerr, M and Mallinson, J and Peascod, B and Kalk, J and Scott, A and Donnelly, R and ... and The SEARCH Collaborative Group and SEARCH Collaborative Grp and SEARCH Collaborative Group and Sahlgrenska akademin and Institutionen för medicin, avdelningen för akut och kardiovaskulär medicin and Institute of Medicine, Department of Emergeny and Cardiovascular Medicine and Göteborgs universitet and Gothenburg University and Sahlgrenska Academy
The New England Journal of Medicine, ISSN 0028-4793, 08/2008, Volume 359, Issue 8, pp. 789 - 799
A genomewide screen of patients with myopathy who were taking high-dose simvastatin (80 mg per day) showed a strong association between myopathy and variants... 
POPULATION | TRIALS | MEDICINE, GENERAL & INTERNAL | METAANALYSIS | EFFICACY | SAFETY | WIDE ASSOCIATION | TRANSPORTING POLYPEPTIDE 1B1 | SIMVASTATIN | SINGLE NUCLEOTIDE POLYMORPHISMS | ATORVASTATIN | Simvastatin - therapeutic use | Simvastatin - adverse effects | Humans | Middle Aged | Diabetes Mellitus - drug therapy | Genotype | Male | Risk | Genetic Markers | Hydroxymethylglutaryl-CoA Reductase Inhibitors - pharmacokinetics | Organic Anion Transporters - genetics | Hydroxymethylglutaryl-CoA Reductase Inhibitors - adverse effects | Myocardial Infarction - drug therapy | Arterial Occlusive Diseases - drug therapy | Hydroxymethylglutaryl-CoA Reductase Inhibitors - therapeutic use | Female | Aged | Myocardial Infarction - prevention & control | Polymorphism, Single Nucleotide | Chromosomes, Human, Pair 12 | Muscular Diseases - chemically induced | Muscular Diseases - genetics | Solute Carrier Organic Anion Transporter Family Member 1b1 | Complications and side effects | Analysis | Muscle diseases | Genetic aspects | Dosage and administration | Single nucleotide polymorphisms | Risk factors | Statins | Drug therapy | Kinases | Drug dosages | Cholesterol | Index Medicus | Abridged Index Medicus | MEDICIN OCH HÄLSOVETENSKAP | Single Nucleotide | genetics | Arterial Occlusive Diseases | pharmacokinetics | Muscular Diseases | Hydroxymethylglutaryl-CoA Reductase Inhibitors | Chromosomes | MEDICAL AND HEALTH SCIENCES | Human | drug therapy | chemically induced | Simvastatin | prevention & control | Diabetes Mellitus | Myocardial Infarction | Pair 12 | Organic Anion Transporters | adverse effects | therapeutic use | Polymorphism
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Nature Medicine, ISSN 1078-8956, 07/2015, Volume 21, Issue 7, pp. 786 - 794
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European Heart Journal, ISSN 0195-668X, 05/2013, Volume 34, Issue 17, pp. 1279 - 1291
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1994, Neurological disease and therapy, ISBN 0824788249, Volume 25, xxvi, 608
Book
Annals of Neurology, ISSN 0364-5134, 07/2018, Volume 84, Issue 1, pp. 64 - 77
ObjectiveSpinocerebellar ataxia type 3 (SCA3), also known as Machado-Joseph disease, is the most common dominantly inherited ataxia. Despite advances in... 
PURKINJE NEURONS | ANDROGEN RECEPTOR | SPINAL MUSCULAR-ATROPHY | MACHADO-JOSEPH-DISEASE | MOUSE MODEL | POLYGLUTAMINE DISEASES | AUTOPHAGY | DYSFUNCTION | ANTISENSE OLIGONUCLEOTIDES | NEUROSCIENCES | NEURODEGENERATIVE DISEASES | CLINICAL NEUROLOGY | Action Potentials - genetics | Age Factors | Apoptosis - drug effects | Motor Activity - drug effects | Apoptosis - genetics | Male | Brain - metabolism | Oligonucleotides, Antisense - therapeutic use | Exploratory Behavior - drug effects | Ataxin-3 - chemistry | Female | Microfilament Proteins - metabolism | Purkinje Cells - drug effects | Action Potentials - drug effects | Gliosis - etiology | Disease Models, Animal | Machado-Joseph Disease - pathology | Calcium-Binding Proteins - metabolism | Gene Expression Regulation - genetics | Mice, Transgenic | Mutation - genetics | Brain - drug effects | Gene Expression Regulation - drug effects | Machado-Joseph Disease - drug therapy | Motor Activity - genetics | Animals | Machado-Joseph Disease - physiopathology | Gliosis - drug therapy | Mice | Purkinje Cells - pathology | RNA-Binding Proteins - metabolism | Ataxin-3 - genetics | Machado-Joseph Disease - genetics | Medical research | Therapy | Afterhyperpolarization | Medical treatment | Medical services | Transgenic mice | Clinical trials | Firing rate | Trinucleotide repeats | Motors | Antisense oligonucleotides | Polyglutamine diseases | Motor task performance | Hereditary diseases | Machado-Joseph disease | Ataxia | Biocompatibility | In vivo methods and tests | Trinucleotide repeat diseases
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Medicine (United States), ISSN 0025-7974, 2014, Volume 93, Issue 3, pp. 150 - 157
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Annals of the Rheumatic Diseases, ISSN 0003-4967, 07/2013, Volume 72, Issue 7, pp. 1217 - 1220
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