Research for Rare - Research for rare diseases

mitoNET – Network for Mitochondrial Diseases

The principal goal of mitoNET is to establish a network of clinical centres in order to improve health care for patients with mitochondrial diseases. Steps to achieve this are:
• Buildup of a nationwide network of neurological and paediatric departments for recruitment and phenotyping of patients, setup a of a web-based register, and conduction of longitudinal studies.
• Comprehensive collection and storage of biological materials including DNA, RNA and myoblasts, providing aliquots to researchers within and outside of the net.
• Enhancing the range of diagnostic tools, including new assays to quantify mitochondrial proteins and dynamics, high-throughput genotyping, a systems approach and advanced brain imaging.
• in vitro investigations of novel treatments, including an approach to improve OXPHOS deficiency by fibrate-induction of peroxisome proliferator-activated receptor pathways and an approach to identify mechanisms behind and strategies against propagation of mtDNA mutations.
• Increased collaboration of basic researchers to boost synergy effects, interdisciplinary cooperation and training initiatives.
• Increased public and professional awareness.

Projekte
Kontakt
Sprecher des mitoNET
Prof. Dr. med. Thomas Klopstock
University of Munich Department of Neurology,
Friedrich-Baur-Institute
Ziemssenstr. 1a
80336 München
Tel: 089-4400 57400
E-Mail: thomas.klopstock@med.uni-muenchen.de

Koordinationsbüro:
Dr. Boriana Büchner
Tel: 089-4400 57421
Boriana.Buechner@med.uni-muenchen.de
Website: www.mitonet.org

Publications