Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
7R01NS033999-04
Application #
2669053
Study Section
Special Emphasis Panel (ZRG1-NEUC (01))
Program Officer
Oliver, Eugene J
Project Start
1995-04-01
Project End
1999-02-28
Budget Start
1998-01-01
Budget End
1998-02-28
Support Year
4
Fiscal Year
1997
Total Cost
Indirect Cost
Name
Scottish Rite Children's Medical Center
Department
Type
DUNS #
City
Atlanta
State
GA
Country
United States
Zip Code
30342
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

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