Teguh Haryo Sasongko

Summary

Publications

  1. ncbi request reprint ACE gene polymorphism in children with nephrotic syndrome in the Indonesian population
    Teguh Haryo Sasongko
    Division of Public Health, Kobe University Graduate School of Medicine
    Kobe J Med Sci 51:41-7. 2005
  2. doi request reprint Angiotensin-converting enzyme (ACE) inhibitors for proteinuria and microalbuminuria in people with sickle cell disease
    Teguh H Sasongko
    Human Genome Center, School of Medical Sciences, Universiti Sains Malaysia, Kota Bharu, Malaysia
    Cochrane Database Syst Rev 3:CD009191. 2013
  3. pmc Analysis of sequence variations in low-density lipoprotein receptor gene among Malaysian patients with familial hypercholesterolemia
    Alyaa Al-Khateeb
    Human Genome Centre, School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia
    BMC Med Genet 12:40. 2011
  4. ncbi request reprint Nonsense mutations of the ZFHX1B gene in two Japanese girls with Mowat-Wilson syndrome
    Teguh Haryo Sasongko
    Department of Public Health, Kobe University Graduate School of Medicine
    Kobe J Med Sci 53:157-62. 2007
  5. doi request reprint Deletion analysis of SMN1 exon 7 alone may be necessary and sufficient for the diagnosis of spinal muscular atrophy
    Teguh Haryo Sasongko
    Human Genome Center, School of Medical Sciences, Universiti Sains Malaysia, USM Health Campus, Kelantan, Malaysia
    J Neurogenet 25:15-6. 2011
  6. ncbi request reprint Novel mutations in 21 patients with tuberous sclerosis complex and variation of tandem splice-acceptor sites in TSC1 exon 14
    Teguh Haryo Sasongko
    Department of Genetic Epidemiology, Graduate School of Medicine, Kobe University, Japan
    Kobe J Med Sci 54:E73-81. 2008
  7. doi request reprint Screening of the LIX1 gene in Japanese and Malaysian patients with SMA and/or SMA-like disorder
    Teguh Haryo Sasongko
    Human Genome Center, School of Medical Sciences, Universiti Sains Malaysia, Kota Bharu, Kelantan, Malaysia
    Brain Dev 32:385-9. 2010
  8. doi request reprint Combination of SMN2 copy number and NAIP deletion predicts disease severity in spinal muscular atrophy
    Mohd Shamshudin Watihayati
    Human Genome Center, School of Medical Sciences, Health Campus, Universiti Sains Malaysia, 16150 Kubang Kerian, Kota Bharu, Kelantan, Malaysia
    Brain Dev 31:42-5. 2009
  9. doi request reprint SMN2 and NAIP gene dosages in Vietnamese patients with spinal muscular atrophy
    Van Khanh Tran
    Department of Pediatrics, Graduate School of Medicine, Kobe University, Japan
    Pediatr Int 50:346-51. 2008
  10. ncbi request reprint A novel mutation at the N-terminal of SMN Tudor domain inhibits its interaction with target proteins
    Tomohiro Kotani
    Dept of Public Health, Kobe University Graduate School of Medicine, 7 5 1 Kusunoki cho, Chuo Ku, Kobe, 650 0017, Japan
    J Neurol 254:624-30. 2007

Collaborators

  • Hitoshi Ayaki
  • Yasuhiro Takeshima
  • Keiko Koterazawa
  • Samir K Ballas
  • Mariko Yagi
  • Kandai Nozu
  • Dang Diem Hong
  • Masafumi Matsuo
  • Abdul Qawee Rani
  • Bin Alwi Zilfalil
  • Hisahide Nishio
  • Z A M H Zabidi-Hussin
  • Ahmad Hamim Sadewa
  • Jafar Mohseni
  • Alyaa Al-Khateeb
  • Mohd Shamshudin Watihayati
  • Van Khanh Tran
  • - Gunadi
  • Myeong Jin Lee
  • Tomohiro Kotani
  • Yosuke Harada
  • Syah Nor Iman Othman
  • Winnie Ong Peitee
  • Muzhirah Haniffa
  • Lock Hock Ngu
  • Che Abdul Razak
  • Fatemeh Hayati
  • Rowani Mohd Rawi
  • Chia Boon Hock
  • Sarina Sulong
  • David Bunyan
  • Abdul Razak Salmi
  • A B Razak Salmi
  • Suhairi Ibrahim
  • Mohd K Zahri
  • Hiroyuki Awano
  • Tomoko Lee
  • Zurkurnai Yusof
  • Bin A Zilfalil
  • Rusdy Ghazali Malueka
  • Mohd S Mohamed
  • Amin Baig Atif
  • Marzuki Marini
  • Wan Mohd Zahiruddin
  • Hayati Fatemeh
  • Thean Hock Tang
  • Nguyen Thi Hoan
  • Vu Chi Dung
  • Shoichi Endo
  • Retno Sutomo
  • Emiko Fujii
  • Toshinori Minato

Detail Information

Publications14

  1. ncbi request reprint ACE gene polymorphism in children with nephrotic syndrome in the Indonesian population
    Teguh Haryo Sasongko
    Division of Public Health, Kobe University Graduate School of Medicine
    Kobe J Med Sci 51:41-7. 2005
    ..Additionally, we also analyzed relationship between each genotype and steroid sensitivity among the MCNS patients...
  2. doi request reprint Angiotensin-converting enzyme (ACE) inhibitors for proteinuria and microalbuminuria in people with sickle cell disease
    Teguh H Sasongko
    Human Genome Center, School of Medical Sciences, Universiti Sains Malaysia, Kota Bharu, Malaysia
    Cochrane Database Syst Rev 3:CD009191. 2013
    ..It is common practice to administer ACE inhibitors for sickle nephropathy due to their renoprotective properties; however, little is known about their effectiveness and safety in this setting...
  3. pmc Analysis of sequence variations in low-density lipoprotein receptor gene among Malaysian patients with familial hypercholesterolemia
    Alyaa Al-Khateeb
    Human Genome Centre, School of Medical Sciences, Universiti Sains Malaysia, Kubang Kerian, Kelantan, Malaysia
    BMC Med Genet 12:40. 2011
    ....
  4. ncbi request reprint Nonsense mutations of the ZFHX1B gene in two Japanese girls with Mowat-Wilson syndrome
    Teguh Haryo Sasongko
    Department of Public Health, Kobe University Graduate School of Medicine
    Kobe J Med Sci 53:157-62. 2007
    ..In conclusion, molecular genetic analysis of ZFHX1B is important for a definite diagnosis of MWS which has a wide phenotypic spectrum of congenital anomalies...
  5. doi request reprint Deletion analysis of SMN1 exon 7 alone may be necessary and sufficient for the diagnosis of spinal muscular atrophy
    Teguh Haryo Sasongko
    Human Genome Center, School of Medical Sciences, Universiti Sains Malaysia, USM Health Campus, Kelantan, Malaysia
    J Neurogenet 25:15-6. 2011
    ..Deletion analysis of SMN1 exon 7 alone may be necessary and sufficient for the diagnosis of SMA. It is based on sole contribution of survival motor neuron 1 (SMN1) exon 7 to SMA pathogenesis...
  6. ncbi request reprint Novel mutations in 21 patients with tuberous sclerosis complex and variation of tandem splice-acceptor sites in TSC1 exon 14
    Teguh Haryo Sasongko
    Department of Genetic Epidemiology, Graduate School of Medicine, Kobe University, Japan
    Kobe J Med Sci 54:E73-81. 2008
    ..In conclusion, we confirmed the diagnosis of all patients using mutation analysis and clarified that variation of the tandem splice-acceptor sites in TSC1 exon 14 does not cause a splicing abnormality...
  7. doi request reprint Screening of the LIX1 gene in Japanese and Malaysian patients with SMA and/or SMA-like disorder
    Teguh Haryo Sasongko
    Human Genome Center, School of Medical Sciences, Universiti Sains Malaysia, Kota Bharu, Kelantan, Malaysia
    Brain Dev 32:385-9. 2010
    ..Recently, mutation in the gene underlying cat SMA, limb expression 1 (LIX1), has been reported. Similarity in clinical and pathological features of cat and human SMA may give an insight into possible similarity of the genetic etiology...
  8. doi request reprint Combination of SMN2 copy number and NAIP deletion predicts disease severity in spinal muscular atrophy
    Mohd Shamshudin Watihayati
    Human Genome Center, School of Medical Sciences, Health Campus, Universiti Sains Malaysia, 16150 Kubang Kerian, Kota Bharu, Kelantan, Malaysia
    Brain Dev 31:42-5. 2009
    ..In conclusion, combining the analysis of deletion of NAIP with the assessment of SMN2 copy number increases the value of this tool in predicting the severity of SMA...
  9. doi request reprint SMN2 and NAIP gene dosages in Vietnamese patients with spinal muscular atrophy
    Van Khanh Tran
    Department of Pediatrics, Graduate School of Medicine, Kobe University, Japan
    Pediatr Int 50:346-51. 2008
    ..Gene dosage of SMN2 is associated with clinical severity of SMA. But the relationship between gene dosage of NAIP and clinical severity of SMA remains to be clarified, although complete deletion of NAIP is frequent in type I patients...
  10. ncbi request reprint A novel mutation at the N-terminal of SMN Tudor domain inhibits its interaction with target proteins
    Tomohiro Kotani
    Dept of Public Health, Kobe University Graduate School of Medicine, 7 5 1 Kusunoki cho, Chuo Ku, Kobe, 650 0017, Japan
    J Neurol 254:624-30. 2007
    ..In conclusion, we reported here that a novel mutation, W92S, in the Tudor domain affects the interaction of SMN with the target proteins...
  11. doi request reprint Mutation spectrum of dystrophin gene in malaysian patients with Duchenne/Becker muscular dystrophy
    Abdul Qawee Rani
    Human Genome Centre, School of Medical Sciences, Universiti Sains Malaysia, USM Health Campus, Kelantan, Malaysia
    J Neurogenet 27:11-5. 2013
    ..8%) are located in the distal hotspot. However, the frequency of the mutations in our patient varied as compared with those found in other populations...
  12. doi request reprint Two closely spaced nonsense mutations in the DMD gene in a Malaysian family
    Abdul Qawee Rani
    Human Genome Center, School of Medical Sciences, Universiti Sains Malaysia, Kelantan, Malaysia
    Mol Genet Metab 103:303-4. 2011
    ..249Q>X, respectively) were identified within exon 8. The proband's mother carried both mutations on one allele. Multiple mutations may explain the occasional discrepancies between genotype and phenotype in dystrophinopathy...
  13. ncbi request reprint C117T variant in the SMN1 gene found in the Japanese population
    Ahmad Hamim Sadewa
    Department of Public Health, Kobe Uniersity Graduate School of Medicine, Kusunoki cho, Kobe, Japan
    Pediatr Int 49:8-10. 2007
    ..It is still a question whether the variant is specific to the Caucasian population, and whether it is found only in SMN2. In order to address these questions, Japanese populations were screened for the presence of C117T in the SMN genes...
  14. doi request reprint Novel complex re-arrangement of ARG1 commonly shared by unrelated patients with hyperargininemia
    Jafar Mohseni
    Human Genome Center, School of Medical Sciences, Universiti Sains Malaysia, USM Health Campus, 16150 Kubang Kerian, Kelantan, Malaysia
    Gene 533:240-5. 2014
    ..Until now, some mutations were reported worldwide and none of them were of Southeast Asian origins. Furthermore, most reported mutations were point mutations and a few others deletions or insertions...