Hendrik Milting

university hospital of the ruhr university bochum

Germany

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Articles (7)

Year:

2024

Year:

2023

Year:

2022

Year:

2022

Year:

2022

Year:

2022

Year:

2021

Collaborators (6)

Oskar Sierka

Medical University of Silesia

POLAND

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Matthias Vorgerd

GERMANY

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Karin Klingel

Head of Cardiopathology/Infection Pathology

University Hospital

GERMANY

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Peter van der Ven

University of Bonn

GERMANY

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Sabine Klaassen

GERMANY

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Misagh Piran

GERMANY

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Hendrik Milting

Research Interests

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Articles (7)

Risk factors association with transcriptional activity of metalloproteinase 9 (MMP-9) and tissue inhibitor of metalloproteinases 1 (TIMP-1) genes in patients with heart failure.

Novel Filamin C Myofibrillar Myopathy Variants Cause Different Pathomechanisms and Alterations in Protein Quality Systems

Left Ventricular Non-Compaction Cardiomyopathy-Still More Questions than Answers

Pathogenic Variants in Cardiomyopathy Disorder Genes Underlie Pediatric Myocarditis—Further Impact of Heterozygous Immune Disorder Gene Variants?

Cardiac Muscle Training—A New Way of Recognizing and Supporting Recovery for LVAD Patients in the Pediatric Population

Compound Heterozygous <i>FKTN</i> Variants in a Patient with Dilated Cardiomyopathy Led to an Aberrant α-Dystroglycan Pattern

The Desmin Mutation <i>DES</i>-c.735G>C Causes Severe Restrictive Cardiomyopathy by Inducing In-Frame Skipping of Exon-3

Collaborators (6)

Oskar Sierka

Matthias Vorgerd

Karin Klingel

Peter van der Ven

Sabine Klaassen

Misagh Piran

Make your next move.

Hendrik Milting

Research Interests

Explore related searches

Contact this professor

Articles (7)

Risk factors association with transcriptional activity of metalloproteinase 9 (MMP-9) and tissue inhibitor of metalloproteinases 1 (TIMP-1) genes in patients with heart failure.

Novel Filamin C Myofibrillar Myopathy Variants Cause Different Pathomechanisms and Alterations in Protein Quality Systems

Left Ventricular Non-Compaction Cardiomyopathy-Still More Questions than Answers

Pathogenic Variants in Cardiomyopathy Disorder Genes Underlie Pediatric Myocarditis—Further Impact of Heterozygous Immune Disorder Gene Variants?

Cardiac Muscle Training—A New Way of Recognizing and Supporting Recovery for LVAD Patients in the Pediatric Population

Compound Heterozygous <i>FKTN</i> Variants in a Patient with Dilated Cardiomyopathy Led to an Aberrant α-Dystroglycan Pattern

The Desmin Mutation <i>DES</i>-c.735G&gt;C Causes Severe Restrictive Cardiomyopathy by Inducing In-Frame Skipping of Exon-3

Collaborators (6)

Oskar Sierka

Matthias Vorgerd

Karin Klingel

Peter van der Ven

Sabine Klaassen

Misagh Piran

Make your next move.

The Desmin Mutation <i>DES</i>-c.735G>C Causes Severe Restrictive Cardiomyopathy by Inducing In-Frame Skipping of Exon-3