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Teguh Haryo Sasongko
Teguh Haryo Sasongko
International Medical University, School of Medicine. Associate Professor.
在 imu.edu.my 的电子邮件经过验证 - 首页
标题
引用次数
引用次数
年份
Rapamycin and rapalogs for tuberous sclerosis complex
TH Sasongko, NFD Ismail, Z Zabidi‐Hussin
Cochrane Database of Systematic Reviews, 2016
90*2016
Combination of SMN2 copy number and NAIP deletion predicts disease severity in spinal muscular atrophy
MS Watihayati, H Fatemeh, M Marini, AB Atif, WM Zahiruddin, ...
Brain and Development 31 (1), 42-45, 2009
672009
Combination of SMN2 copy number and NAIP deletion predicts disease severity in spinal muscular atrophy
MS Watihayati, H Fatemeh, M Marini, AB Atif, WM Zahiruddin, ...
Brain and Development 31 (1), 42-45, 2009
672009
Histone deacetylase inhibitors as potential treatment for spinal muscular atrophy
J Mohseni, Z Zabidi-Hussin, TH Sasongko
Genetics and molecular biology 36 (3), 299-307, 2013
612013
Angiotensin‐converting enzyme (ACE) inhibitors for proteinuria and microalbuminuria in people with sickle cell disease
TH Sasongko, S Nagalla
Cochrane Database of Systematic Reviews, 2021
492021
A novel mutation at the N-terminal of SMN Tudor domain inhibits its interaction with target proteins
T Kotani, R Sutomo, TH Sasongko, AH Sadewa, T Minato, E Fujii, S Endo, ...
Journal of neurology 254 (5), 624, 2007
492007
DNA methylation: an epigenetic insight into type 2 diabetes mellitus
F Alam, A Islam, S Hua Gan, M Mohamed, T Haryo Sasongko
Current pharmaceutical design 22 (28), 4398-4419, 2016
412016
Analysis of sequence variations in low-density lipoprotein receptor gene among Malaysian patients with familial hypercholesterolemia
A Al-Khateeb, MK Zahri, MS Mohamed, TH Sasongko, S Ibrahim, Z Yusof, ...
BMC medical genetics 12, 1-11, 2011
412011
SMN2 and NAIP gene dosages in Vietnamese patients with spinal muscular atrophy
VK Tran, TH Sasongko, DD Hong, NT Hoan, VC Dung, MJ Lee, Gunadi, ...
Pediatrics International 50 (3), 346-351, 2008
382008
Germ‐line mutation of KCNQ2, p.R213W, in a Japanese family with benign familial neonatal convulsion
AH Sadewa, TH Sasongko, Gunadi, MJ Lee, K Daikoku, A Yamamoto, ...
Pediatrics International 50 (2), 167-171, 2008
302008
Natural products towards the discovery of potential future antithrombotic drugs
MA Islam, F Alam, I Khalil, T Haryo Sasongko, S Hua Gan
Current pharmaceutical design 22 (20), 2926-2946, 2016
292016
In silico analyses and cytotoxicity study of asiaticoside and asiatic acid from malaysian plant as potential mTOR inhibitors
NN Zulkipli, R Zakaria, I Long, SF Abdullah, EF Muhammad, HA Wahab, ...
Molecules 25 (17), 3991, 2020
272020
ACE gene polymorphism in children with nephrotic syndrome in the Indonesian population
TH Sasongko, AH Sadewa, PA Kusuma, MP Damanik, MJ Lee, H Ayaki, ...
KOBE JOURNAL OF MEDICAL SCIENCES 51 (3/4), 41, 2005
272005
Antiphospholipid antibody-mediated thrombotic mechanisms in antiphospholipid syndrome: towards pathophysiology-based treatment
A Islam, F Alam, T Haryo Sasongko, S Hua Gan
Current pharmaceutical design 22 (28), 4451-4469, 2016
262016
Antiphospholipid antibodies in epilepsy: A systematic review and meta-analysis
MA Islam, F Alam, C Cavestro, C Calcii, TH Sasongko, RA Levy, SH Gan
Autoimmunity reviews 17 (8), 755-767, 2018
252018
Rapamycin and its analogues (rapalogs) for Tuberous Sclerosis Complex-associated tumors: a systematic review on non-randomized studies using meta-analysis
TH Sasongko, NFD Ismail, NMA Nik Abdul Malik, Z Zabidi-Hussin
Orphanet journal of rare diseases 10, 1-11, 2015
242015
‘Non-criteria’neurologic manifestations of antiphospholipid syndrome: a hidden kingdom to be discovered
A Islam, F Alam, M Amjad Kamal, K Keng Wong, T Haryo Sasongko, ...
CNS & Neurological Disorders-Drug Targets (Formerly Current Drug Targets-CNS …, 2016
232016
Type 2 diabetes mellitus and Alzheimer’s disease: bridging the pathophysiology and management
F Alam, A Islam, T Haryo Sasongko, S Hua Gan
Current pharmaceutical design 22 (28), 4430-4442, 2016
222016
Permissibility of prenatal diagnosis and abortion for fetuses with severe genetic disorder: type 1 spinal muscular atrophy
TH Sasongko, AR Salmi, BA Zilfalil, MA Albar, ZA Mohd Hussin
Annals of Saudi medicine 30 (6), 427-431, 2010
202010
Mutation Spectrum of Dystrophin Gene in Malaysian Patients with Duchenne/Becker Muscular Dystrophy
AQ Rani, TH Sasongko, S Sulong, D Bunyan, AR Salmi, BA Zilfalil, ...
Journal of Neurogenetics 27 (1-2), 11-15, 2013
182013
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