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Rapamycin and its analogues (rapalogs) for Tuberous Sclerosis Complex-associated tumors: a systematic review on non-randomized studies using meta-analysis

Orphanet journal of rare diseases, 2015-08, Vol.10 (1), p.95, Article 95

2015

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Histone deacetylase inhibitors as potential treatment for spinal muscular atrophy

Genetics and molecular biology, 2013-01, Vol.36 (3), p.299-307

2013

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Transcript, methylation and molecular docking analyses of the effects of HDAC inhibitors, SAHA and Dacinostat, on SMN2 expression in fibroblasts of SMA patients

Journal of human genetics, 2016-09, Vol.61 (9), p.823-830

2016

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Combination of Multiple Ligation-Dependent Probe Amplification and Illumina MiSeq Amplicon Sequencing for TSC1 / TSC2 Gene Analyses in Patients with Tuberous Sclerosis Complex

The Journal of molecular diagnostics : JMD, 2017-03, Vol.19 (2), p.265-276

2017

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Two Novel Gross Deletions of TSC2 in Malaysian Patients with Tuberous Sclerosis Complex and TSC2/PKD1 Contiguous Deletion Syndrome

Japanese journal of clinical oncology, 2014-05, Vol.44 (5), p.506-511

2014

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Macrodactyly and poliosis in tuberous sclerosis complex

Japanese journal of clinical oncology, 2014-11, Vol.44 (11), p.1130-1130

2014

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Biochemical profiling to predict disease severity in metachromatic leukodystrophy

Molecular genetics and metabolism, 2010-02, Vol.99 (2), p.142-148

2010

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

Brain & development (Tokyo. 1979), 2009-01, Vol.31 (1), p.42-45

2009

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Does Nondisclosure of Genetic Paternity Status Constitute a Breach of Ethics?: Commentary on “The Dilemma of Revealing Sensitive Information on Paternity Status in Arabian Social and Cultural Contexts” by Abdallah A. Adlan and Henk A. M. J. ten Have

Journal of bioethical inquiry, 2012-12, Vol.9 (4), p.413-414

Zabidi-Hussin, Z. A. M. H.

2012

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Rapamycin and rapalogs for tuberous sclerosis complex

Cochrane database of systematic reviews, 2016-07, Vol.7 (7), p.CD011272

2016

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

Molecular genetics and metabolism, 2011-07, Vol.103 (3), p.303-304

2011

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

Indian journal of medical research (New Delhi, India : 1994), 2012, Vol.135, p.31

2012

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Mutation Spectrum of Dystrophin Gene in Malaysian Patients with Duchenne/Becker Muscular Dystrophy

Journal of neurogenetics, 2013-06, Vol.27 (1-2), p.11-15

2013

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Brain–immune–gut benefits with early life supplementation of milk fat globule membrane

JGH open, 2022-07, Vol.6 (7), p.454-461

2022

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Does nondisclosure of genetic paternity status constitute a breach of ethics? Commentary on 'The dilemma of revealing sensitive information on paternity status in Arabian social and cultural contexts' by Abdallah A. Adlan and Henk A.M.J. ten Have

Journal of bioethical inquiry, 2012-12, Vol.9 (4), p.413-414

Zabidi-Hussin, Z. A. M. H

2012

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Practical way of creating differential diagnoses through an expanded VITAMINSABCDEK mnemonic

Advances in medical education and practice, 2016, Vol.7 (Issue 1), p.247-248

Zabidi-Hussin, Zabidi A

2016

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Deletion Analysis of SMN1 Exon 7 Alone May Be Necessary and Sufficient for the Diagnosis of Spinal Muscular Atrophy

Journal of neurogenetics, 2011-03, Vol.25 (1-2), p.15-16

2011

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

Brain & development (Tokyo. 1979), 2010-05, Vol.32 (5), p.385-389, Article 385

2010

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Challenges in clinical research in Malaysia

Medical journal of Malaysia, 2007-10, Vol.62 (4), p.275-277

Zabidi-Hussin, Z A M H

2007

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Tuberous sclerosis complex: a review with a study of eight cases

Medical journal of Malaysia, 1994-12, Vol.49 (4), p.375-384

1994

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Beyond medical school - time to re-look?

The Malaysian journal of medical sciences, 2000-07, Vol.7 (2), p.1-2

Hussin, Z A

2000

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Effects of Mg substitution on the structural and magnetic properties of Coo.sNi0.5xMgxFe2O4 nanoparticle ferrites

中国物理B：英文版, 2016 (4), p.358-364

R M Rosnan Z Othaman R Hussin Ali A Ati Alireza Samavati Shadab Dabagh samad Zare

2016

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Pharmacokinetic interpretation of some antibiotics in camels

Archives internationales de pharmacodynamie et de thérapie, 1983-02, Vol.261 (2), p.186

1983

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Metal oxide nanofluids in electronic cooling: a review

Journal of materials science. Materials in electronics, 2020-03, Vol.31 (6), p.4381-4398

2020

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Amorphous silicon thin-film: Behaviour of light-induced degradation

Renewable & sustainable energy reviews, 2015-03, Vol.43, p.388-402

2015

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Rapamycin and its analogues (rapalogs) for Tuberous Sclerosis Complex-associated tumors: a systematic review on non-randomized studies using meta-analysis

Histone deacetylase inhibitors as potential treatment for spinal muscular atrophy

Transcript, methylation and molecular docking analyses of the effects of HDAC inhibitors, SAHA and Dacinostat, on SMN2 expression in fibroblasts of SMA patients

Combination of Multiple Ligation-Dependent Probe Amplification and Illumina MiSeq Amplicon Sequencing for TSC1 / TSC2 Gene Analyses in Patients with Tuberous Sclerosis Complex

Two Novel Gross Deletions of TSC2 in Malaysian Patients with Tuberous Sclerosis Complex and TSC2/PKD1 Contiguous Deletion Syndrome

Macrodactyly and poliosis in tuberous sclerosis complex

Biochemical profiling to predict disease severity in metachromatic leukodystrophy

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

Does Nondisclosure of Genetic Paternity Status Constitute a Breach of Ethics?: Commentary on “The Dilemma of Revealing Sensitive Information on Paternity Status in Arabian Social and Cultural Contexts” by Abdallah A. Adlan and Henk A. M. J. ten Have

Rapamycin and rapalogs for tuberous sclerosis complex

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

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

Mutation Spectrum of Dystrophin Gene in Malaysian Patients with Duchenne/Becker Muscular Dystrophy

Brain–immune–gut benefits with early life supplementation of milk fat globule membrane

Does nondisclosure of genetic paternity status constitute a breach of ethics? Commentary on 'The dilemma of revealing sensitive information on paternity status in Arabian social and cultural contexts' by Abdallah A. Adlan and Henk A.M.J. ten Have

Practical way of creating differential diagnoses through an expanded VITAMINSABCDEK mnemonic

Deletion Analysis of SMN1 Exon 7 Alone May Be Necessary and Sufficient for the Diagnosis of Spinal Muscular Atrophy

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

Challenges in clinical research in Malaysia

Tuberous sclerosis complex: a review with a study of eight cases

Beyond medical school - time to re-look?

Effects of Mg substitution on the structural and magnetic properties of Coo.sNi0.5xMgxFe2O4 nanoparticle ferrites

Pharmacokinetic interpretation of some antibiotics in camels

Metal oxide nanofluids in electronic cooling: a review

Amorphous silicon thin-film: Behaviour of light-induced degradation

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