Bittner, Reginald E.

Mutant glycosyltransferase and altered glycosylation of α-dystroglycan in the myodystrophy mouse

Grewal, P. K., Holzfeind, P. J., Bittner, R. E., & Hewitt, J. E. (2001) · Nature Genetics

Muscle Physiology and DisordersGlycosylation and Glycoproteins Research

Cited by 301

Mutations in FKBP14 cause a variant of Ehlers-Danlos syndrome with progressive kyphoscoliosis, myopathy, and hearing loss

Baumann, M., Giunta, C., Krabichler, B., Rüschendorf, F., Zoppi, N., Colombi, M., Bittner, R. E., Quijano-Roy, S., Muntoni, F., Cirak, S., et al. (2012) · The American Journal of Human Genetics

Connective tissue disorders researchGenomics and Rare Diseases

Cited by 162

Dysferlin Is a New Marker for Leaky Brain Blood Vessels in Multiple Sclerosis

Hochmeister, S., Grundtner, R., Bauer, J., Engelhardt, B., Lyck, R., Gordon, G., Korosec, T., Kutzelnigg, A., Berger, J. J., Bradl, M., et al. (2006) · Journal of Neuropathology and Experimental Neurology

Multiple Sclerosis Research StudiesBarrier Structure and Function Studies

Cited by 160

Effects of Oral Creatine Supplementation in a Patient with MELAS Phenotype and Associated Nephropathy

Barisic, N., Bernert, G., Ipsiroglu, O., Stromberger, C., Müller, T., Gruber, S., Prayer, D., Moser, E., Bittner, R. E., & Stöckler-Ipsiroglu, S. (2002) · Neuropediatrics

Metabolism and Genetic DisordersMuscle metabolism and nutrition

Cited by 66