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Teguh Haryo Sasongko

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M Marini; Hisahide Nishio; M Ravichandran; Teguh Haryo Sasongko; Mohd S Watihayati; Z A M H Zabidi-Hussin; Ali Atif; F Hayati; Bin Alwi Zilfalil
Allele-specific PCR for a cost-effective & time-efficient diagnostic screening of spinal muscular atrophy.
Abdul Qawee Rani; A B Razak Salmi; Teguh Haryo Sasongko; Yasuhiro Takeshima; Mariko Yagi; Z A M H Zabidi-Hussin; Bin Alwi Zilfalil; Hiroyuki Awano; Tomoko Lee; Rusdy Ghazali Malueka; Masafumi Matsuo
Two closely spaced nonsense mutations in the DMD gene in a Malaysian family.
Teguh Haryo Sasongko; Bin Alwi Zilfalil; Zamh Zabidi-Hussin
Deletion analysis of SMN1 exon 7 alone may be necessary and sufficient for the diagnosis of spinal muscular atrophy.

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2012: M Marini; Hisahide Nishio; M Ravichandran; Teguh Haryo Sasongko; Mohd S Watihayati; Z A M H Zabidi-Hussin; Ali Atif; F Hayati; Bin Alwi Zilfalil
Allele-specific PCR for a cost-effective & time-efficient diagnostic screening of spinal muscular atrophy.
The Indian journal of medical research 2012;135():31-5.
2011: Abdul Qawee Rani; A B Razak Salmi; Teguh Haryo Sasongko; Yasuhiro Takeshima; Mariko Yagi; Z A M H Zabidi-Hussin; Bin Alwi Zilfalil; Hiroyuki Awano; Tomoko Lee; Rusdy Ghazali Malueka; Masafumi Matsuo
Two closely spaced nonsense mutations in the DMD gene in a Malaysian family.
Molecular genetics and metabolism 2011;103(3):303-4.
2011: Teguh Haryo Sasongko; Bin Alwi Zilfalil; Zamh Zabidi-Hussin
Deletion analysis of SMN1 exon 7 alone may be necessary and sufficient for the diagnosis of spinal muscular atrophy.
Journal of neurogenetics 2011;25(1-2):15-6.
2010: Teguh Haryo Sasongko; Surini Yusoff; Ali Atif; Hayati Fatemeh; Abdulqawee Rani; Marzuki Marini; Che Badariah Ab Aziz; Z A M H Zabidi-Hussin; Hisahide Nishio; Bin Alwi Zilfalil
Screening of the LIX1 gene in Japanese and Malaysian patients with SMA and/or SMA-like disorder.
Brain & development 2010;32(5):385-9.
2008: Van Khanh Tran; Teguh Haryo Sasongko; Dang Diem Hong; Nguyen Thi Hoan; Vu Chi Dung; Myeong Jin Lee; Yasuhiro Takeshima; Masafumi Matsuo; Hisahide Nishio
SMN2 and NAIP gene dosages in Vietnamese patients with spinal muscular atrophy.
Pediatrics international : official journal of the Japan Pediatric Society 2008;50(3):346-51.
2008: Ahmad Hamim Sadewa; Teguh Haryo Sasongko; Myeong J Lee; Kazunari Daikoku; Akiyo Yamamoto; Takemi Yamasaki; Shigenori Tanaka; Masafumi Matsuo; Hisahide Nishio
Germ-line mutation of KCNQ2, p.R213W, in a Japanese family with benign familial neonatal convulsion.
Pediatrics international : official journal of the Japan Pediatric Society 2008;50(2):167-71.
2008: Teguh Haryo Sasongko; S Yusoff; Myeong Jin Lee; Eri Nishioka; Masafumi Matsuo; Hisahide Nishio
Hypomutability at the polyadenine tract in SMN intron 3 shows the invariability of the a-SMN protein structure.
Annals of human genetics 2008;72(Pt 2):288-91.
2008: Teguh Haryo Sasongko; Mari Wataya-Kaneda; Keiko Koterazawa; Surini Yusoff; Indra Sari Kusuma Harahap; Myeong Jin Lee; Masafumi Matsuo; Hisahide Nishio
Novel mutations in 21 patients with tuberous sclerosis complex and variation of tandem splice-acceptor sites in TSC1 exon 14.
The Kobe journal of medical sciences 2008;54(1):E73-81.
2007: Tomohiro Kotani; Retno Sutomo; Teguh Haryo Sasongko; Ahmad Hamim Sadewa; Toshinori Minato; Emiko Fujii; Shoichi Endo; Myeong Jin Lee; Hitoshi Ayaki; Yosuke Harada; Masafumi Matsuo; Hisahide Nishio
A novel mutation at the N-terminal of SMN Tudor domain inhibits its interaction with target proteins.
Journal of neurology 2007;254(5):624-30.
2007: Ahmad Hamim Sadewa; Yosuke Harada; Teguh Haryo Sasongko; Masafumi Matsuo; Hisahide Nishio
C117T variant in the SMN1 gene found in the Japanese population.
Pediatrics international : official journal of the Japan Pediatric Society 2007;49(1):8-10.
2007: Teguh Haryo Sasongko; Ahmad Hamim Sadewa; Myeong Jin Lee; Keiko Koterazawa; Hisahide Nishio
Nonsense mutations of the ZFHX1B gene in two Japanese girls with Mowat-Wilson syndrome.
The Kobe journal of medical sciences 2007;53(4):157-62.
2005: Teguh Haryo Sasongko; Ahmad Hamim Sadewa; Pungky Ardani Kusuma; Martua Parlindungan Damanik; Myeong Jin Lee; Hitoshi Ayaki; Kandai Nozu; Akinobu Goto; Masafumi Matsuo; Hisahide Nishio
ACE gene polymorphism in children with nephrotic syndrome in the Indonesian population.
The Kobe journal of medical sciences 2005;51(3-4):41-7.