Shoffner, J M (2001) Molecular analysis of oxidative phosphorylation diseases for detection of mitochondrial DNA mutations. Curr Protoc Hum Genet Chapter 9:Unit 9.9
|
Shoffner, J M (2001) An introduction: oxidative phosphorylation diseases. Semin Neurol 21:237-50
|
Shoffner, J M (2000) Mitochondrial myopathy diagnosis. Neurol Clin 18:105-23
|
Shoffner, J M (1999) Oxidative phosphorylation disease diagnosis. Ann N Y Acad Sci 893:42-60
|
Shoffner, J M (1999) Oxidative phosphorylation disease diagnosis. Semin Neurol 19:341-51
|
Shoffner, J M (1997) Oxidative phosphorylation defects and Alzheimer's disease. Neurogenetics 1:13-9
|
Sorkin, J A; Shoffner, J M; Grossniklaus, H E et al. (1997) Strabismus and mitochondrial defects in chronic progressive external ophthalmoplegia. Am J Ophthalmol 123:235-42
|
North, K; Korson, M S; Krawiecki, N et al. (1996) Oxidative phosphorylation defect associated with primary adrenal insufficiency. J Pediatr 128:688-92
|
Gebhart, S S; Shoffner, J M; Koontz, D et al. (1996) Insulin resistance associated with maternally inherited diabetes and deafness. Metabolism 45:526-31
|
Shoffner, J M (1996) Maternal inheritance and the evaluation of oxidative phosphorylation diseases. Lancet 348:1283-8
|
Showing the most recent 10 out of 11 publications