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List of works by Teguh Haryo Sasongko

'Non-Criteria' Neurologic Manifestations of Antiphospholipid Syndrome: A Hidden Kingdom to be Discovered.

scientific article published on 20 September 2016

A novel mutation at the N-terminal of SMN Tudor domain inhibits its interaction with target proteins

scientific article published on 06 April 2007

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

scientific article published in January 2012

Analysis of sequence variations in low-density lipoprotein receptor gene among Malaysian patients with familial hypercholesterolemia

scientific article

Angiotensin-converting enzyme (ACE) inhibitors for proteinuria and microalbuminuria in people with sickle cell disease

scientific article (publication date: 4 June 2015)

Angiotensin-converting enzyme (ACE) inhibitors for proteinuria and microalbuminuria in people with sickle cell disease

scientific article (publication date: 28 March 2013)

Antiphospholipid Antibody-Mediated Thrombotic Mechanisms in Antiphospholipid Syndrome: Towards Pathophysiology-Based Treatment

scientific article published on 27 May 2016

Antiphospholipid antibodies in epilepsy: A systematic review and meta-analysis

scientific article published on 06 June 2018

Antiplatelet and anticoagulant agents for preventing recurrence of peripheral vascular thrombosis in patients with Antiphospholipid syndrome

scientific article

C117T variant in the SMN1 gene found in the Japanese population.

scientific article published in February 2007

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

scientific article

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

scientific article

DNA Methylation: An Epigenetic Insight into Type 2 Diabetes Mellitus

scientific article published on 27 May 2016

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

scientific article published on 22 February 2011

Germ-line mutation of KCNQ2, p.R213W, in a Japanese family with benign familial neonatal convulsion.

scientific article

Histone deacetylase inhibitors as potential treatment for spinal muscular atrophy

scientific article

Hypomutability at the polyadenine tract in SMN intron 3 shows the invariability of the a-SMN protein structure.

scientific article

MERCI: a useful systematic 'aide memoir' to help clinicians teach ethics

scientific article published in December 2009

Macrodactyly and poliosis in tuberous sclerosis complex

scientific article published on 15 October 2014

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

scientific article published on 26 February 2013

Nomenclature Confusion in Deletion Mutations Involving Repetitive Nucleotides: A Lesson from HBB Gene Codon 35 (-C) vs. Codon 36 (-C).

scientific article published on 6 August 2015

Novel complex re-arrangement of ARG1 commonly shared by unrelated patients with hyperargininemia

scientific article published on 5 October 2013

Permissibility of prenatal diagnosis and abortion for fetuses with severe genetic disorder: type 1 spinal muscular atrophy

scientific article

Placebo Controlled Trials: Interests of Subjects versus Interests of Drug Regulators.

scientific article published on 18 August 2017

Presence of Anticardiolipin Antibodies in Patients with Dementia: A Systematic Review and Meta-Analysis

scientific article published on 2 August 2017

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

scientific article

Rapamycin and rapalogs for tuberous sclerosis complex

scientific article

SMN2 and NAIP gene dosages in Vietnamese patients with spinal muscular atrophy.

scientific article published in June 2008

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

scientific article

Social and Communicative Functions of Informed Consent Forms in East Asia and Beyond.

scientific article published on 20 July 2017

Therapeutic Suppression of Nonsense Mutation: An Emerging Target in Multiple Diseases and Thrombotic Disorders.

scientific article published on 22 November 2016

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

scientific article published on 2 June 2016

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

scientific article published on 08 April 2011

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

scientific article published on 30 March 2014

Type 2 Diabetes Mellitus and Alzheimer's Disease: Bridging the Pathophysiology and Management

scientific article published on 27 May 2016

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