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Susana Teijeira Selected Research

Myosins (Myosin)

4/2011A novel MYH7 mutation links congenital fiber type disproportion and myosin storage myopathy.

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Susana Teijeira Research Topics

Disease

2Fabry Disease (Fabry's Disease)
10/2018 - 02/2006
2Glycogen Storage Disease Type V (McArdle's Disease)
12/2011 - 07/2004
2Muscular Diseases (Myopathy)
04/2011 - 02/2002
2Muscular Dystrophies (Muscular Dystrophy)
11/2009 - 01/2009
1Frontotemporal Dementia (Semantic Dementia)
01/2020
1Amyotrophic Lateral Sclerosis (Lou Gehrig's Disease)
01/2020
1Recurrent Myoglobinuria
03/2012
1Congenital Structural Myopathies (Centronuclear Myopathy)
04/2011
1Myosin Storage Myopathy
04/2011
1Lafora Disease
02/2010
1Inborn Genetic Diseases (Disease, Hereditary)
02/2010
1Duchenne Muscular Dystrophy (Muscular Dystrophy, Becker)
11/2009
1Limb-Girdle Muscular Dystrophies (Limb-Girdle Muscular Dystrophy)
11/2009
1Distal Myopathies (Distal Muscular Dystrophy)
01/2009
1Angiokeratoma
02/2006
1Glycogen Storage Disease (Glycogenosis)
07/2004
1Myotonic Dystrophy (Dystrophia Myotonica)
04/2003
1Glycogen Storage Disease Type II (Pompe's Disease)
02/2002

Drug/Important Bio-Agent (IBA)

3Proteins (Proteins, Gene)FDA Link
01/2020 - 01/2009
2Nonsense Codon (Nonsense Mutation)IBA
12/2011 - 02/2002
1DipeptidesIBA
01/2020
1Aligeron (AS 2)IBA
10/2018
1GalactosidasesIBA
10/2018
1Creatine Kinase (Creatine Phosphokinase)IBA
03/2012
1Myosin Heavy Chains (Myosin Heavy Chain)IBA
04/2011
1Myosins (Myosin)IBA
04/2011
1polyglucosanIBA
02/2010
1Prostaglandins BIBA
02/2010
1DystrophinIBA
11/2009
1Caveolin 3IBA
01/2009
1EnzymesIBA
02/2006
1ceramide trihexosideIBA
02/2006
1Muscle Form Glycogen Phosphorylase (Myophosphorylase)IBA
07/2004
1Electron Transport Complex III (Coenzyme Q-Cytochrome-c Reductase)IBA
04/2003
1AsparagineIBA
02/2002
1alpha-Glucosidases (Acid Maltase)IBA
02/2002
1AcidsIBA
02/2002
1GlycogenIBA
02/2002