Search Page
Filters
Search Results
440 results
Results are displayed in a computed author sort order.
The Publication Date timeline is not available.
Page 1
Mitochondrial encephalomyopathies: biochemical approach.
Rev Neurol (Paris). 1991;147(6-7):443-9.
Rev Neurol (Paris). 1991.
PMID: 1660180
Review.
Localization of mitochondrial DNA in normal and pathological muscle using immunological probes: a new approach to the study of mitochondrial myopathies.
J Neurol Sci. 1991 Sep;105(1):88-92. doi: 10.1016/0022-510x(91)90123-o.
J Neurol Sci. 1991.
PMID: 1665507
Free article.
mtDNA depletion with variable tissue expression: a novel genetic abnormality in mitochondrial diseases.
Am J Hum Genet. 1991 Mar;48(3):492-501.
Am J Hum Genet. 1991.
PMID: 1998336
Free PMC article.
Mitochondrial encephalomyopathies.
Neurol Clin. 1990 Aug;8(3):483-506.
Neurol Clin. 1990.
PMID: 2170831
Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome.
N Engl J Med. 1989 May 18;320(20):1293-9. doi: 10.1056/NEJM198905183202001.
N Engl J Med. 1989.
PMID: 2541333
Mitochondrial encephalomyopathies.
Rev Neurol (Paris). 1989;145(10):671-89.
Rev Neurol (Paris). 1989.
PMID: 2682927
Review.
Mitochondrial myopathies.
J Inherit Metab Dis. 1987;10 Suppl 1:113-28. doi: 10.1007/BF01812852.
J Inherit Metab Dis. 1987.
PMID: 2824920
Review.
Molecular defects in cytochrome oxidase in mitochondrial diseases.
J Bioenerg Biomembr. 1988 Jun;20(3):353-64. doi: 10.1007/BF00769637.
J Bioenerg Biomembr. 1988.
PMID: 2841309
Review.
Deletions of mitochondrial DNA in Kearns-Sayre syndrome.
Neurology. 1988 Sep;38(9):1339-46. doi: 10.1212/wnl.38.9.1339.
Neurology. 1988.
PMID: 3412580
Cite