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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.
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