M. Breithaupt

Health professions and risk of sporadic Creutzfeldt-Jakob disease, 1965 to 2010.

C. V. van Duijn, I. Zerr, A. Molesworth, 2012, Euro surveillance : bulletin Europeen sur les maladies transmissibles = European communicable disease bulletin.

Current Essentials in Inflammatory Myopathies

Jens Schmidt, M. Breithaupt, 2013, EMJ Neurology.

Genetic prion disease with codon 196 PRNP mutation: clinical and pathological findings

H. Kretzschmar, D. Varges, I. Zerr, 2011, Neurobiology of Aging.

Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease

C. Begue, R. G. Will, J. P. Brandel, 2009, Brain : a journal of neurology.

Explorer Updated clinical diagnostic criteria for sporadic Creutzfeldt-Jakob disease

G. Jansen, K. Kallenberg, P. Smith, 2016 .

Diagnosis of Prion Disease: Conventional Approaches

I. Zerr, J. Gawinecka, K. Stoeck, 2013 .

Treatment strategies for inclusion body myositis

Jens Schmidt, M. Breithaupt, 2014 .

Doxycycline in early CJD: a double-blinded randomised phase II and observational study

Tim Friede, Walter J Schulz-Schaeffer, T. Friede, 2016, Journal of Neurology, Neurosurgery & Psychiatry.

Intensity of human prion disease surveillance predicts observed disease incidence

C. Masters, H. Budka, G. Jansen, 2013, Journal of Neurology, Neurosurgery & Psychiatry.

In-Frame Insertion Mutation in the SPG11 Gene Causes Autosomal Recessive Spastic Paraplegia with Thin Corpus Callosum “In A” Turkish Family with Late Age of Onset of the Phenotype

I. Zerr, S. Mosalaganti, M. Shoukier, 2015 .

Update on Treatment of Inclusion Body Myositis

Jens Schmidt, M. Breithaupt, 2013, Current Rheumatology Reports.

Magnetic Resonance Imaging in E200K and V210I Mutations of the Prion Protein Gene

K. Kallenberg, H. Kretzschmar, I. Zerr, 2013, Alzheimer disease and associated disorders.