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Matthias Vorgerd

Showing results (111-120 of 140) with videos related to

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Journal of Neurology|December 12, 2024
Assessing axonal pathology and disease progression in chronic inflammatory demyelinating polyneuropathy using corneal confocal microscopyRafael Klimas, Dietrich Sturm, Annika Altenborg, et al.
Cells|May 13, 2023
Novel Filamin C Myofibrillar Myopathy Variants Cause Different Pathomechanisms and Alterations in Protein Quality SystemsDominik Sellung, Lorena Heil, Nassam Daya, et al.
Molecular Neurobiology|January 24, 2023
A Homozygous PPP1R21 Splice Variant Associated with Severe Developmental Delay, Absence of Speech, and Muscle Weakness Leads to Activated Proteasome FunctionAndreas Hentschel, Nancy Meyer, Nicolai Kohlschmidt, et al.
Annals of Neurology|December 24, 2016
Proteomics of rimmed vacuoles define new risk allele in inclusion body myositisAnne-Katrin Güttsches, Stefen Brady, Kathryn Krause, et al.
Molecular Neurobiology|March 21, 2023
Correction: A Homozygous PPP1R21 Splice Variant Associated with Severe Developmental Delay, Absence of Speech, and Muscle Weakness Leads to Activated Proteasome FunctionAndreas Hentschel, Nancy Meyer, Nicolai Kohlschmidt, et al.
Skeletal Muscle|February 12, 2026
Unveiling FLNC variants: iPSC-derived myogenic cells as a model to study disease mechanismsNassam M Daya, Anne Schänzer, Andreas Hentschel, et al.
Human Molecular Genetics|October 17, 2015
Myofibrillar instability exacerbated by acute exercise in filaminopathyFrédéric Chevessier, Julia Schuld, Zacharias Orfanos, et al.
Neurology. Genetics|July 8, 2021
FLNC-Associated Myofibrillar Myopathy: New Clinical, Functional, and Proteomic DataRudolf Andre Kley, Yvonne Leber, Bertold Schrank, et al.
Molecular & Cellular Proteomics : MCP|November 2, 2012
A combined laser microdissection and mass spectrometry approach reveals new disease relevant proteins accumulating in aggregates of filaminopathy patientsRudolf A Kley, Alexandra Maerkens, Yvonne Leber, et al.
Orphanet Journal of Rare Diseases|October 15, 2020
Creation and implementation of a European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC registry)Tomàs Pinós, Antoni L Andreu, Claudio Bruno, et al.
Pageof 14

Showing results (111-120 of 140) with videos related to

Sort By:
Pageof 14
Journal of Neurology|December 12, 2024
Assessing axonal pathology and disease progression in chronic inflammatory demyelinating polyneuropathy using corneal confocal microscopyRafael Klimas, Dietrich Sturm, Annika Altenborg, et al.
Cells|May 13, 2023
Novel Filamin C Myofibrillar Myopathy Variants Cause Different Pathomechanisms and Alterations in Protein Quality SystemsDominik Sellung, Lorena Heil, Nassam Daya, et al.
Molecular Neurobiology|January 24, 2023
A Homozygous PPP1R21 Splice Variant Associated with Severe Developmental Delay, Absence of Speech, and Muscle Weakness Leads to Activated Proteasome FunctionAndreas Hentschel, Nancy Meyer, Nicolai Kohlschmidt, et al.
Annals of Neurology|December 24, 2016
Proteomics of rimmed vacuoles define new risk allele in inclusion body myositisAnne-Katrin Güttsches, Stefen Brady, Kathryn Krause, et al.
Molecular Neurobiology|March 21, 2023
Correction: A Homozygous PPP1R21 Splice Variant Associated with Severe Developmental Delay, Absence of Speech, and Muscle Weakness Leads to Activated Proteasome FunctionAndreas Hentschel, Nancy Meyer, Nicolai Kohlschmidt, et al.
Skeletal Muscle|February 12, 2026
Unveiling FLNC variants: iPSC-derived myogenic cells as a model to study disease mechanismsNassam M Daya, Anne Schänzer, Andreas Hentschel, et al.
Human Molecular Genetics|October 17, 2015
Myofibrillar instability exacerbated by acute exercise in filaminopathyFrédéric Chevessier, Julia Schuld, Zacharias Orfanos, et al.
Neurology. Genetics|July 8, 2021
FLNC-Associated Myofibrillar Myopathy: New Clinical, Functional, and Proteomic DataRudolf Andre Kley, Yvonne Leber, Bertold Schrank, et al.
Molecular & Cellular Proteomics : MCP|November 2, 2012
A combined laser microdissection and mass spectrometry approach reveals new disease relevant proteins accumulating in aggregates of filaminopathy patientsRudolf A Kley, Alexandra Maerkens, Yvonne Leber, et al.
Orphanet Journal of Rare Diseases|October 15, 2020
Creation and implementation of a European registry for patients with McArdle disease and other muscle glycogenoses (EUROMAC registry)Tomàs Pinós, Antoni L Andreu, Claudio Bruno, et al.
Pageof 14