Zabidi-Hussin Z - Search Results

1

Rapamycin and rapalogs for tuberous sclerosis complex.

Sasongko TH, Ismail NF, Zabidi-Hussin Z. Sasongko TH, et al. Among authors: zabidi hussin z. Cochrane Database Syst Rev. 2016 Jul 13;7(7):CD011272. doi: 10.1002/14651858.CD011272.pub2. Cochrane Database Syst Rev. 2016. Update in: Cochrane Database Syst Rev. 2023 Jul 11;7:CD011272. doi: 10.1002/14651858.CD011272.pub3 PMID: 27409709 Free PMC article. Updated. Review.

2

Combination of SMN2 copy number and NAIP deletion predicts disease severity in spinal muscular atrophy.

Watihayati MS, Fatemeh H, Marini M, Atif AB, Zahiruddin WM, Sasongko TH, Tang TH, Zabidi-Hussin ZA, Nishio H, Zilfalil BA. Watihayati MS, et al. Brain Dev. 2009 Jan;31(1):42-5. doi: 10.1016/j.braindev.2008.08.012. Epub 2008 Oct 7. Brain Dev. 2009. PMID: 18842367

3

Screening of the LIX1 gene in Japanese and Malaysian patients with SMA and/or SMA-like disorder.

Sasongko TH, Gunadi, Yusoff S, Atif AB, Fatemeh H, Rani A, Marini M, Ab Aziz CB, Zabidi-Hussin ZA, Nishio H, Zilfalil BA. Sasongko TH, et al. Brain Dev. 2010 May;32(5):385-9. doi: 10.1016/j.braindev.2009.06.008. Epub 2009 Aug 6. Brain Dev. 2010. PMID: 19664890

4

Deletion analysis of SMN1 exon 7 alone may be necessary and sufficient for the diagnosis of spinal muscular atrophy.

Sasongko TH, Gunadi, Zilfalil BA, Zabidi-Hussin Z. Sasongko TH, et al. J Neurogenet. 2011 Mar;25(1-2):15-6. doi: 10.3109/01677063.2011.559561. Epub 2011 Feb 22. J Neurogenet. 2011. PMID: 21338334

5

Two closely spaced nonsense mutations in the DMD gene in a Malaysian family.

Rani AQ, Malueka RG, Sasongko TH, Awano H, Lee T, Yagi M, Zilfalil BA, Salmi AB, Takeshima Y, Zabidi-Hussin ZA, Matsuo M. Rani AQ, et al. Mol Genet Metab. 2011 Jul;103(3):303-4. doi: 10.1016/j.ymgme.2011.04.002. Epub 2011 Apr 8. Mol Genet Metab. 2011. PMID: 21514860

6

Allele-specific PCR for a cost-effective & time-efficient diagnostic screening of spinal muscular atrophy.

Marini M, Sasongko TH, Watihayati MS, Atif AB, Hayati F; Gunadi; Zabidi-Hussin ZA, Ravichandran M, Nishio H, Zilfalil BA. Marini M, et al. Indian J Med Res. 2012;135(1):31-5. doi: 10.4103/0971-5916.93421. Indian J Med Res. 2012. PMID: 22382180 Free PMC article.

7

Mutation spectrum of dystrophin gene in malaysian patients with Duchenne/Becker muscular dystrophy.

Rani AQ, Sasongko TH, Sulong S, Bunyan D, Salmi AR, Zilfalil BA, Matsuo M, Zabidi-Hussin ZA. Rani AQ, et al. J Neurogenet. 2013 Jun;27(1-2):11-5. doi: 10.3109/01677063.2012.762580. Epub 2013 Feb 26. J Neurogenet. 2013. PMID: 23438214

8

Histone deacetylase inhibitors as potential treatment for spinal muscular atrophy.

Mohseni J, Zabidi-Hussin ZA, Sasongko TH. Mohseni J, et al. Genet Mol Biol. 2013 Sep;36(3):299-307. doi: 10.1590/S1415-47572013000300001. Epub 2013 Aug 30. Genet Mol Biol. 2013. PMID: 24130434 Free PMC article. Review.

9

Two novel gross deletions of TSC2 in Malaysian patients with tuberous sclerosis complex and TSC2/PKD1 contiguous deletion syndrome.

Ismail NF, Nik Abdul Malik NM, Mohseni J, Rani AM, Hayati F, Salmi AR, Narazah MY, Zabidi-Hussin ZA, Silawati AR, Keng WT, Ngu LH, Sasongko TH. Ismail NF, et al. Jpn J Clin Oncol. 2014 May;44(5):506-11. doi: 10.1093/jjco/hyu024. Epub 2014 Mar 30. Jpn J Clin Oncol. 2014. PMID: 24683199

10

Macrodactyly and poliosis in tuberous sclerosis complex.

Sasongko TH, Ismail NF, Nik Mohd Ariff NA, Zabidi-Hussin ZA. Sasongko TH, et al. Jpn J Clin Oncol. 2014 Nov;44(11):1130. doi: 10.1093/jjco/hyu157. Epub 2014 Oct 15. Jpn J Clin Oncol. 2014. PMID: 25320338 No abstract available.

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