Yusoff NM - Search Results

1

High prevalence of Southeast Asian ovalocytosis in Malays with distal renal tubular acidosis.

Yusoff NM, Van Rostenberghe H, Shirakawa T, Nishiyama K, Amin N, Darus Z, Zainal N, Isa N, Nozu H, Matsuo M. Yusoff NM, et al. J Hum Genet. 2003;48(12):650-653. doi: 10.1007/s10038-003-0095-2. Epub 2003 Nov 15. J Hum Genet. 2003. PMID: 14618420

2

Molecular heterogeneity of glucose-6-phosphate dehydrogenase deficiency in Malays in Malaysia.

Yusoff NM, Shirakawa T, Nishiyama K, Ghazali S, Ee CK, Orita A, Abdullah WZ, Isa MN, Van Rostenberghe H, Matsuo M. Yusoff NM, et al. Int J Hematol. 2002 Aug;76(2):149-52. doi: 10.1007/BF02982577. Int J Hematol. 2002. PMID: 12215013

3

Screening for G71R mutation of the UGT1A1 gene in the Javanese-Indonesian and Malay-Malaysian populations.

Sutomo R, Talib NA, Yusoff NM, Van Rostenberghe H, Sadewa AH, Sunarti, Sofro AS, Yokoyama N, Lee MJ, Matsuo M, Nishio H. Sutomo R, et al. Among authors: yusoff nm. Pediatr Int. 2004 Oct;46(5):565-9. doi: 10.1111/j.1442-200x.2004.01959.x. Pediatr Int. 2004. PMID: 15491385

4

Glucose-6-phosphate dehydrogenase deficiency: molecular heterogeneity in southeast Asian countries.

Matsuo M, Nishiyama K, Shirakawa T, Padilla CD, San LP, Suryantoro P, Yusoff NM, Dao NT. Matsuo M, et al. Among authors: yusoff nm. Southeast Asian J Trop Med Public Health. 2003;34 Suppl 3:127-9. Southeast Asian J Trop Med Public Health. 2003. PMID: 15906715

5

G6PD Viangchan and G6PD Mediterranean are the main variants in G6PD deficiency in the Malay population of Malaysia.

Yusoff NM, Shirakawa T, Nishiyama K, Ee CK, Isa MN, Matsuo M. Yusoff NM, et al. Southeast Asian J Trop Med Public Health. 2003;34 Suppl 3:135-7. Southeast Asian J Trop Med Public Health. 2003. PMID: 15906717

6

Poor correlation between hemolysis and jaundice in glucose 6-phosphate dehydrogenase-deficient babies.

Jalloh S, Van Rostenberghe H, Yusoff NM, Ghazali S, Nik Ismail NZ, Matsuo M, Wahab NA, Nishio H. Jalloh S, et al. Among authors: yusoff nm. Pediatr Int. 2005 Jun;47(3):258-61. doi: 10.1111/j.1442-200x.2005.02052.x. Pediatr Int. 2005. PMID: 15910447

7

Frequencies of A(TA)7TAA, G71R, and G493R mutations of the UGT1A1 gene in the Malaysian population.

Yusoff S, Van Rostenberghe H, Yusoff NM, Talib NA, Ramli N, Ismail NZ, Ismail WP, Matsuo M, Nishio H. Yusoff S, et al. Among authors: yusoff nm. Biol Neonate. 2006;89(3):171-6. doi: 10.1159/000088844. Epub 2005 Oct 6. Biol Neonate. 2006. PMID: 16210851

8

Evaluation of mutation effects on UGT1A1 activity toward 17beta-estradiol using liquid chromatography-tandem mass spectrometry.

Wada K, Takeuchi A, Saiki K, Sutomo R, Van Rostenberghe H, Yusoff NM, Laosombat V, Sadewa AH, Talib NA, Yusoff S, Lee MJ, Ayaki H, Nakamura H, Matsuo M, Nishio H. Wada K, et al. Among authors: yusoff nm, yusoff s. J Chromatogr B Analyt Technol Biomed Life Sci. 2006 Jun 21;838(1):9-14. doi: 10.1016/j.jchromb.2006.01.030. Epub 2006 Feb 28. J Chromatogr B Analyt Technol Biomed Life Sci. 2006. PMID: 16504606

9

A polymorphic mutation, c.-3279T>G, in the UGT1A1 promoter is a risk factor for neonatal jaundice in the Malay population.

Yusoff S, Takeuchi A, Ashi C, Tsukada M, Ma'amor NH, Zilfalil BA, Yusoff NM, Nakamura T, Hirai M, Harahap IS, Gunadi, Lee MJ, Nishimura N, Takaoka Y, Morikawa S, Morioka I, Yokoyama N, Matsuo M, Nishio H, van Rostenberghe H. Yusoff S, et al. Among authors: yusoff nm. Pediatr Res. 2010 Apr;67(4):401-6. doi: 10.1203/PDR.0b013e3181d22f78. Pediatr Res. 2010. PMID: 20057336

10

The evolutionary origins of Southeast Asian Ovalocytosis.

Paquette AM, Harahap A, Laosombat V, Patnode JM, Satyagraha A, Sudoyo H, Thompson MK, Yusoff NM, Wilder JA. Paquette AM, et al. Among authors: yusoff nm. Infect Genet Evol. 2015 Aug;34:153-9. doi: 10.1016/j.meegid.2015.06.002. Epub 2015 Jun 3. Infect Genet Evol. 2015. PMID: 26047685

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