Skip to main page content
Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

My NCBI Filters
Text availability
Article attribute
Article type
Publication date

Search Results

11 results
Filters applied: . Clear all Results are displayed in a computed author sort order. Results by year timeline is unavailable
Page 1
Meiotic breakpoint mapping of a proposed X linked visual loss susceptibility locus in Leber's hereditary optic neuropathy.
Handoko HY, Wirapati PJ, Sudoyo HA, Sitepu M, Marzuki S. Handoko HY, et al. Among authors: sudoyo ha. J Med Genet. 1998 Aug;35(8):668-71. doi: 10.1136/jmg.35.8.668. J Med Genet. 1998. PMID: 9719375 Free PMC article.
Molecular genetics of Leber's hereditary optic neuropathy: study of a six-generation family from Western Australia.
Sudoyo H, Marzuki S, Mastaglia F, Carroll W. Sudoyo H, et al. J Neurol Sci. 1992 Mar;108(1):7-17. doi: 10.1016/0022-510x(92)90181-j. J Neurol Sci. 1992. PMID: 1352537
Update in molecular genetics: mitochondrial energy transduction disorders.
Marzuki S, Sudoyo H, Lertrit P. Marzuki S, et al. Southeast Asian J Trop Med Public Health. 1995;26 Suppl 1:155-61. Southeast Asian J Trop Med Public Health. 1995. PMID: 8629096 Review. No abstract available.
Leber's hereditary optic neuropathy in Indonesia: two families with the mtDNA 11778G>A and 14484T>C mutations.
Sudoyo H, Sitepu M, Malik S, Poesponegoro HD, Marzuki S. Sudoyo H, et al. Hum Mutat. 1998;Suppl 1:S271-4. doi: 10.1002/humu.1380110186. Hum Mutat. 1998. PMID: 9452107 No abstract available.
Microphotometric analysis of NADH-tetrazolium reductase deficiency in fibroblasts of patients with Leber hereditary optic neuropathy.
Malik S, Sudoyo H, Marzuki S. Malik S, et al. J Inherit Metab Dis. 2000 Nov;23(7):730-44. doi: 10.1023/a:1005687031531. J Inherit Metab Dis. 2000. PMID: 11117434
Evidence for the de novo regeneration of the pattern of the length heteroplasmy associated with the T16189C variant in the control (D-loop) region of mitochondrial DNA.
Malik S, Sudoyo H, Pramoonjago P, Sukarna T, Darwis D, Marzuki S. Malik S, et al. J Hum Genet. 2002;47(3):122-30. doi: 10.1007/s100380200013. J Hum Genet. 2002. PMID: 11950064
Nuclear mitochondrial interplay in the modulation of the homopolymeric tract length heteroplasmy in the control (D-loop) region of the mitochondrial DNA.
Malik S, Sudoyo H, Pramoonjago P, Suryadi H, Sukarna T, Njunting M, Sahiratmadja E, Marzuki S. Malik S, et al. Hum Genet. 2002 May;110(5):402-11. doi: 10.1007/s00439-002-0717-3. Epub 2002 Apr 4. Hum Genet. 2002. PMID: 12073009
Asian-specific mtDNA backgrounds associated with the primary G11778A mutation of Leber's hereditary optic neuropathy.
Sudoyo H, Suryadi H, Lertrit P, Pramoonjago P, Lyrawati D, Marzuki S. Sudoyo H, et al. J Hum Genet. 2002;47(11):594-604. doi: 10.1007/s100380200091. J Hum Genet. 2002. PMID: 12436196
Nonsyndromic sensorineural deafness associated with the A1555G mutation in the mitochondrial small subunit ribosomal RNA in a Balinese family.
Malik S, Sudoyo H, Sasmono T, Winata S, Arhya IN, Pramoonjago P, Sudana W, Marzuki S. Malik S, et al. J Hum Genet. 2003;48(3):119-24. doi: 10.1007/s100380300018. J Hum Genet. 2003. PMID: 12624722
Human genome diversity and disease on the island Southeast Asia.
Marzuki S, Sudoyo H, Suryadi H, Setianingsih I, Pramoonjago P. Marzuki S, et al. Adv Exp Med Biol. 2003;531:3-18. doi: 10.1007/978-1-4615-0059-9_1. Adv Exp Med Biol. 2003. PMID: 12916777 Review. No abstract available.
11 results
You have reached the last page of results. A maximum of 10,000 results are available.
Jump to page