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Dystrophin‐deficient cardiomyocytes are abnormally vulnerable to mechanical stress‐induced contractile failure and injury

The FASEB journal, 2001-07, Vol.15 (9), p.1655-1657

2001

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Phosphorylase re-expression, increase in the force of contraction and decreased fatigue following notexin-induced muscle damage and regeneration in the ovine model of McArdle disease

Neuromuscular disorders : NMD, 2014-02, Vol.24 (2), p.167-177

2014

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Dystrophic phenotype of canine X-linked muscular dystrophy is mitigated by adenovirus-mediated utrophin gene transfer

Gene therapy, 2003-05, Vol.10 (9), p.750-757

2003

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The route of administration is a major determinant of the transduction efficiency of rat tissues by adenoviral recombinants

Gene therapy, 1995-03, Vol.2 (2), p.107

1995

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Distribution and threshold expression of the tRNA(Lys) mutation in skeletal muscle of patients with myoclonic epilepsy and ragged-red fibers (MERRF)

American journal of human genetics, 1992-12, Vol.51 (6), p.1187-1200

1992

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Muscle-Specific Overexpression of the Adenovirus Primary Receptor CAR Overcomes Low Efficiency of Gene Transfer to Mature Skeletal Muscle

Journal of Virology, 2001-05, Vol.75 (9), p.4276-4282

2001

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Ultrasound Increases Plasmid-Mediated Gene Transfer to Dystrophic Muscles without Collateral Damage

Molecular therapy, 2002-11, Vol.6 (5), p.687-693

2002

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When running a stop sign may be a good thing

Annals of neurology, 2001-06, Vol.49 (6), p.693-694

2001

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Emergence of early region 1-containing replication-competent adenovirus in stocks of replication-defective adenovirus recombinants (delta E1 + delta E3) during multiple passages in 293 cells

Human gene therapy, 1994-12, Vol.5 (12), p.1485-1491

1994

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Adenovirus and adeno-associated virus-mediated delivery of human myophosphorylase cDNA and LacZ cDNA to muscle in the ovine model of McArdle’s disease: Expression and re-expression of glycogen phosphorylase

Neuromuscular disorders : NMD, 2008-03, Vol.18 (3), p.248-258

2008

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Effects of aerobic training in patients with mitochondrial myopathies

Neurology, 1998-04, Vol.50 (4), p.1055-1060

1998

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Short-term dichloroacetate treatment improves indices of cerebral metabolism in patients with mitochondrial disorders

Neurology, 1995-06, Vol.45 (6), p.1193-1198

1995

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Viral hide-and-seek in sporadic ALS: a new challenge

Neurology, 2000-01, Vol.54 (1), p.6-6

2000

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Localization and Quantitation of the Chromosome 6-Encoded Dystrophin-Related Protein in Normal and Pathological Human Muscle

Journal of neuropathology and experimental neurology, 1993-03, Vol.52 (2), p.119-128

1993

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Prevention of the dystrophic phenotype in dystrophin/utrophin-deficient muscle following adenovirus-mediated transfer of a utrophin minigene

Gene therapy, 2000-02, Vol.7 (3), p.201-204

2000

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The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy

Nature genetics, 2001-09, Vol.29 (1), p.83-87

2001

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Proton MR spectroscopic characterization of differences in regional brain metabolic abnormalities in mitochondrial encephalomyopathies

Neurology, 1993-12, Vol.43 (12), p.2484-2484

1993

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Expression of immunoreactive major histocompatibility complex products in human skeletal muscles

Annals of neurology, 1988-01, Vol.23 (1), p.64-72

1988

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Challenges for the genetic screening in dysferlin deficiency--report of an instructive case and review of the literature

Clinical neuropathology, 2008-09, Vol.27 (5), p.289-294

2008

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Transient immunosuppression by FK506 permits a sustained high-level dystrophin expression after adenovirus-mediated dystrophin minigene transfer to skeletal muscles of adult dystrophic (mdx) mice

Gene therapy, 1996-08, Vol.3 (8), p.706

1996

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Short-term aerobic training response in chronic myopathies

Muscle & nerve, 1999-09, Vol.22 (9), p.1239-1243

1999

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Localization of coxsackie virus and adenovirus receptor (CAR) in normal and regenerating human muscle

Neuromuscular disorders : NMD, 2005-08, Vol.15 (8), p.541-548

2005

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Muscle Pain, Fatigue, and Mitochondriopathies

The New England journal of medicine, 1999-09, Vol.341 (14), p.1077-1078

1999

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Lariat branch point mutation in the dysferlin gene with mild limb-girdle muscular dystrophy

Neurology, 2006-04, Vol.66 (7), p.1114-1116

2006

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Adenovirus-mediated dystrophin minigene transfer improves muscle strength in adult dystrophic (MDX) mice

Gene therapy, 1998, Vol.5 (3), p.369-379

1998

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Dystrophin‐deficient cardiomyocytes are abnormally vulnerable to mechanical stress‐induced contractile failure and injury

Phosphorylase re-expression, increase in the force of contraction and decreased fatigue following notexin-induced muscle damage and regeneration in the ovine model of McArdle disease

Dystrophic phenotype of canine X-linked muscular dystrophy is mitigated by adenovirus-mediated utrophin gene transfer

The route of administration is a major determinant of the transduction efficiency of rat tissues by adenoviral recombinants

Distribution and threshold expression of the tRNA(Lys) mutation in skeletal muscle of patients with myoclonic epilepsy and ragged-red fibers (MERRF)

Muscle-Specific Overexpression of the Adenovirus Primary Receptor CAR Overcomes Low Efficiency of Gene Transfer to Mature Skeletal Muscle

Ultrasound Increases Plasmid-Mediated Gene Transfer to Dystrophic Muscles without Collateral Damage

When running a stop sign may be a good thing

Emergence of early region 1-containing replication-competent adenovirus in stocks of replication-defective adenovirus recombinants (delta E1 + delta E3) during multiple passages in 293 cells

Adenovirus and adeno-associated virus-mediated delivery of human myophosphorylase cDNA and LacZ cDNA to muscle in the ovine model of McArdle’s disease: Expression and re-expression of glycogen phosphorylase

Effects of aerobic training in patients with mitochondrial myopathies

Short-term dichloroacetate treatment improves indices of cerebral metabolism in patients with mitochondrial disorders

Viral hide-and-seek in sporadic ALS: a new challenge

Localization and Quantitation of the Chromosome 6-Encoded Dystrophin-Related Protein in Normal and Pathological Human Muscle

Prevention of the dystrophic phenotype in dystrophin/utrophin-deficient muscle following adenovirus-mediated transfer of a utrophin minigene

The UDP-N-acetylglucosamine 2-epimerase/N-acetylmannosamine kinase gene is mutated in recessive hereditary inclusion body myopathy

Proton MR spectroscopic characterization of differences in regional brain metabolic abnormalities in mitochondrial encephalomyopathies

Expression of immunoreactive major histocompatibility complex products in human skeletal muscles

Challenges for the genetic screening in dysferlin deficiency--report of an instructive case and review of the literature

Transient immunosuppression by FK506 permits a sustained high-level dystrophin expression after adenovirus-mediated dystrophin minigene transfer to skeletal muscles of adult dystrophic (mdx) mice

Short-term aerobic training response in chronic myopathies

Localization of coxsackie virus and adenovirus receptor (CAR) in normal and regenerating human muscle

Muscle Pain, Fatigue, and Mitochondriopathies

Lariat branch point mutation in the dysferlin gene with mild limb-girdle muscular dystrophy

Adenovirus-mediated dystrophin minigene transfer improves muscle strength in adult dystrophic (MDX) mice

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