Thomas Voit

发表

Entwicklung und Überprüfung von Kausalhypothesen: Gestaltungsoptionen für einen Analyseprozess zur Fundierung betrieblicher Ziel- und Kennzahlensysteme durch Kausalhypothesen am Beispiel des Performance-Managements

Thomas Voit, 2010 .

Gamification als Change-Management-Methode im Prozessmanagement

Thomas Voit, T. Voit, 2015, HMD Praxis der Wirtschaftsinformatik.

Long-term microdystrophin gene therapy is effective in a canine model of Duchenne muscular dystrophy

Thomas Voit, Jean-Yves Hogrel, Laurent Servais, 2017, Nature Communications.

The EuroBioBank Network: 10 years of hands-on experience of collaborative, transnational biobanking for rare diseases

Francesco Muntoni, Hanns Lochmüller, Alessandra Renieri, 2014, European Journal of Human Genetics.

G Protein-Coupled Receptor-Dependent Development of Human Frontal Cortex

William B. Dobyns, A. James Barkovich, Bernard S. Chang, 2004, Science.

Respiratory function assessment and intervention in neuromuscular disorders

Thomas Voit, Christian Dohna-Schwake, T. Voit, 2005, Current opinion in neurology.

NMR imaging estimates of muscle volume and intramuscular fat infiltration in the thigh: variations with muscle, gender, and age

Noura Azzabou, Jamie S. McPhee, Thomas Voit, 2015, AGE.

tRNA splicing endonuclease mutations cause pontocerebellar hypoplasia

Ingeborg Krägeloh-Mann, Francesco Muntoni, Peter Nürnberg, 2008, Nature Genetics.

Manual segmentation of individual muscles of the quadriceps femoris using MRI: A reappraisal

David Reversat, Noura Azzabou, Thomas Voit, 2014, Journal of magnetic resonance imaging : JMRI.

Mutations in INPP5K Cause a Form of Congenital Muscular Dystrophy Overlapping Marinesco-Sjögren Syndrome and Dystroglycanopathy

Isabella Moroni, Thomas Voit, Hamid Galehdari, 2017, American journal of human genetics.

Bilateral frontoparietal polymicrogyria: Clinical and radiological features in 10 families with linkage to chromosome 16

P Ellen Grant, Thomas Voit, William B Dobyns, 2003, Annals of neurology.

ISPD loss-of-function mutations disrupt dystroglycan O-mannosylation and cause Walker-Warburg syndrome

Francesco Muntoni, William B. Dobyns, Stanley F. Nelson, 2012, Nature Genetics.

Longitudinal ambulatory measurements of gait abnormality in dystrophin-deficient dogs

Eric Barrey, Thomas Voit, Jean-Yves Hogrel, 2011, BMC musculoskeletal disorders.

A Movement Monitor Based on Magneto-Inertial Sensors for Non-Ambulant Patients with Duchenne Muscular Dystrophy: A Pilot Study in Controlled Environment

Thomas Voit, David Vissière, Jean-Yves Hogrel, 2016, PloS one.

Mutation screening of the N‐myc downstream‐regulated gene 1 (NDRG1) in patients with Charcot‐Marie‐Tooth Disease

Hanns Lochmüller, Thomas Voit, P K Thomas, 2003, Human mutation.