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Targeting deregulated AMPK/mTORC1 pathways improves muscle function in myotonic dystrophy type I

The Journal of clinical investigation, 2017-02, Vol.127 (2), p.549-563

2017

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Global Deprivation of Brain-Derived Neurotrophic Factor in the CNS Reveals an Area-Specific Requirement for Dendritic Growth

The Journal of neuroscience, 2010-02, Vol.30 (5), p.1739-1749

2010

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Improved Muscle Function in Duchenne Muscular Dystrophy through L-Arginine and Metformin: An Investigator-Initiated, Open-Label, Single-Center, Proof-Of-Concept-Study

PloS one, 2016-01, Vol.11 (1), p.e0147634-e0147634

2016

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An essential role of MAG in mediating axon–myelin attachment in Charcot–Marie–Tooth 1A disease

Neurobiology of disease, 2013-01, Vol.49, p.221-231

2013

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The Raft-Associated Protein MAL Is Required for Maintenance of Proper Axon-Glia Interactions in the Central Nervous System

The Journal of cell biology, 2004-08, Vol.166 (5), p.731-742

2004

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IgM deposits on skin nerves in anti-myelin-associated glycoprotein neuropathy

Annals of neurology, 2005-02, Vol.57 (2), p.180-187

2005

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Identification of Plant-derived Alkaloids with Therapeutic Potential for Myotonic Dystrophy Type I

The Journal of biological chemistry, 2016-08, Vol.291 (33), p.17165-17177

2016

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Proteasome inhibitors increase missense mutated dysferlin in patients with muscular dystrophy

Science translational medicine, 2014-08, Vol.6 (250), p.250ra112

2014

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Confocal microscopic localization of anti-myelin-associated glycoprotein autoantibodies in a patient with peripheral neuropathy initially lacking a detectable IgM gammopathy

Acta neuropathologica, 1998-05, Vol.95 (5), p.540-546

1998

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Paraproteinaemic Neuropathies

Brain pathology (Zurich, Switzerland), 1999-04, Vol.9 (2), p.361-368

1999

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Immunoglobulin M Deposition in Cutaneous Nerves of Anti-Myelin-Associated Glycoprotein Polyneuropathy Patients Correlates With Axonal Degeneration

Journal of neuropathology and experimental neurology, 2009-02, Vol.68 (2), p.148-158

2009

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Caspr3 and Caspr4, Two Novel Members of the Caspr Family Are Expressed in the Nervous System and Interact with PDZ Domains

Molecular and cellular neuroscience, 2002-06, Vol.20 (2), p.283-297

2002

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Unraveling the differential expression of the two isoforms of myelin-associated glycoprotein in a mouse expressing GFP-tagged S-MAG specifically regulated and targeted into the different myelin compartments

Molecular and cellular neuroscience, 2006-04, Vol.31 (4), p.613-627

2006

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Allograft inflammatory factor-1: A pathogenetic factor for vasculitic neuropathy

Muscle & nerve, 2008-10, Vol.38 (4), p.1272-1279

2008

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Motor neuropathy in porphobilinogen deaminase-deficient mice imitates the peripheral neuropathy of human acute porphyria

The Journal of clinical investigation, 1999-04, Vol.103 (8), p.1127-1134

1999

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Characterisation of autoantibodies to peripheral myelin protein 22 in patients with hereditary and acquired neuropathies

Journal of neuroimmunology, 2000-05, Vol.104 (2), p.155-163

2000

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Matrix metalloproteinases-9 and -2 in secondary vasculitic neuropathies

Acta neuropathologica, 2003, Vol.105 (1), p.37-42

2003

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Microheterogeneity of anti-myelin-associated glycoprotein antibodies

Journal of the neurological sciences, 2003-03, Vol.207 (1), p.43-49

2003

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Anti-MAG IgM penetration into myelinated fibers correlates with the extent of myelin widening

Muscle & nerve, 1999-08, Vol.22 (8), p.1030-1037

1999

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Gene dosage effects in hereditary peripheral neuropathy. Expression of peripheral myelin protein 22 in Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies nerve biopsies

Neurology, 1997-12, Vol.49 (6), p.1635-1640

1997

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RESEARCH REPORT: Normal expression of myelin protein zero with frame-shift mutation correlates with mild phenotype

Journal of the peripheral nervous system, 2006-03, Vol.11 (1), p.61-66

2006

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Normal expression of myelin protein zero with frame-shift mutation correlates with mild phenotype

Journal of the peripheral nervous system, 2006-03, Vol.11 (1), p.61-66

2006

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Reciprocal expression of myelin-associated glycoprotein splice variants in the adult human peripheral and central nervous systems

Brain research. Molecular brain research., 1997-12, Vol.52 (2), p.299-306

1997

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Predictors for efficacy of percutaneous mitral valve repair using the MitraClip system: the results of the MitraSwiss registry

Heart (British Cardiac Society), 2013-07, Vol.99 (14), p.1034-1040

2013

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Comprehensive vasodilatation in women with acute heart failure: Novel insights from the GALACTIC randomized controlled trial

European journal of heart failure, 2023-12, Vol.25 (12), p.2218-2229

2023

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Targeting deregulated AMPK/mTORC1 pathways improves muscle function in myotonic dystrophy type I

Global Deprivation of Brain-Derived Neurotrophic Factor in the CNS Reveals an Area-Specific Requirement for Dendritic Growth

Improved Muscle Function in Duchenne Muscular Dystrophy through L-Arginine and Metformin: An Investigator-Initiated, Open-Label, Single-Center, Proof-Of-Concept-Study

An essential role of MAG in mediating axon–myelin attachment in Charcot–Marie–Tooth 1A disease

The Raft-Associated Protein MAL Is Required for Maintenance of Proper Axon-Glia Interactions in the Central Nervous System

IgM deposits on skin nerves in anti-myelin-associated glycoprotein neuropathy

Identification of Plant-derived Alkaloids with Therapeutic Potential for Myotonic Dystrophy Type I

Proteasome inhibitors increase missense mutated dysferlin in patients with muscular dystrophy

Confocal microscopic localization of anti-myelin-associated glycoprotein autoantibodies in a patient with peripheral neuropathy initially lacking a detectable IgM gammopathy

Paraproteinaemic Neuropathies

Immunoglobulin M Deposition in Cutaneous Nerves of Anti-Myelin-Associated Glycoprotein Polyneuropathy Patients Correlates With Axonal Degeneration

Caspr3 and Caspr4, Two Novel Members of the Caspr Family Are Expressed in the Nervous System and Interact with PDZ Domains

Unraveling the differential expression of the two isoforms of myelin-associated glycoprotein in a mouse expressing GFP-tagged S-MAG specifically regulated and targeted into the different myelin compartments

Allograft inflammatory factor-1: A pathogenetic factor for vasculitic neuropathy

Motor neuropathy in porphobilinogen deaminase-deficient mice imitates the peripheral neuropathy of human acute porphyria

Characterisation of autoantibodies to peripheral myelin protein 22 in patients with hereditary and acquired neuropathies

Matrix metalloproteinases-9 and -2 in secondary vasculitic neuropathies

Microheterogeneity of anti-myelin-associated glycoprotein antibodies

Anti-MAG IgM penetration into myelinated fibers correlates with the extent of myelin widening

Gene dosage effects in hereditary peripheral neuropathy. Expression of peripheral myelin protein 22 in Charcot-Marie-Tooth disease type 1A and hereditary neuropathy with liability to pressure palsies nerve biopsies

RESEARCH REPORT: Normal expression of myelin protein zero with frame-shift mutation correlates with mild phenotype

Normal expression of myelin protein zero with frame-shift mutation correlates with mild phenotype

Reciprocal expression of myelin-associated glycoprotein splice variants in the adult human peripheral and central nervous systems

Predictors for efficacy of percutaneous mitral valve repair using the MitraClip system: the results of the MitraSwiss registry

Comprehensive vasodilatation in women with acute heart failure: Novel insights from the GALACTIC randomized controlled trial

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