Publications by authors named "Surini Yusoff"

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Psychometric Validation of the Malay Version of the Emotional Abuse Questionnaire (EAQ-M).
Muhammad Khairul Amri Yusoff, Fahisham Taib, Surini Yusoff, Nurul Jannah Ambak

Malays J Med Sci· June 2025

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Clinical predictors of acute kidney injury in children with acute post-streptococcal glomerulonephritis: a tertiary centre experience.
Wan Adlina Wan Yusof, Najib Majdi Yaacob, Ariffin Nasir, Surini Yusoff, Mohamad Ikram Ilias

Singapore Med J· January 2025

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The Validity and Reliability of Malay Version Child Exposure to Domestic Violence Scale.
Tina Azreen Norazman, Surini Yusoff, Hanif Mohd Niza Nizal, Fahisham Taib

Malays J Med Sci· August 2023

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High allele frequency of CYP2C9*3 (rs1057910) in a Negrito's subtribe population in Malaysia; Aboriginal people of Jahai.
Rasmaizatul Akma Rosdi, Narazah Mohd Yusoff, Rusli Ismail, Tan Soo Choon, Mohamed Saleem, Surini Yusoff

Ann Hum Biol· September 2016

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High resolution melting analysis of the NR1I3 genetic variants: Is there an association with neonatal hyperbilirubinemia?
Tian Pei Cheung, Hans Van Rostenberghe, Rosliza Ismail, Noor Namirah Nawawi, Nurul Amierah Abdullah, Narazah Mohd Yusoff, Surini Yusoff

Gene· December 2015

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Trinucleotide insertion in the SMN2 promoter may not be related to the clinical phenotype of SMA.
Nur Imma Fatimah Harahap, Atsuko Takeuchi, Surini Yusoff, Koji Tominaga, Takeshi Okinaga

Brain Dev· August 2015

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Guidelines for nucleic acid detection and analysis in hematological disorders.
Rosline Hassan, Azlan Husin, Sarina Sulong, Surini Yusoff, Muhammad Farid Johan

Malays J Pathol· August 2015

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The first Malay database toward the ethnic-specific target molecular variation.
Hashim Halim-Fikri, Ali Etemad, Ahmad Zubaidi Abdul Latif, Amir Feisal Merican, Atif Amin Baig, Shafini Mohamed Yusoff, Surini Yusoff

BMC Res Notes· April 2015

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Multiplex amplification refractory mutation system (MARMS) for the detection of β-globin gene mutations among the transfusion-dependent β-thalassemia Malay patients in Kelantan, Northeast of Peninsular Malaysia.
Sarifah Hanafi, Rosline Hassan, Rosnah Bahar, Wan Zaidah Abdullah, Muhammad Farid Johan, Surini Yusoff, Narazah Yusoff

Am J Blood Res· September 2014

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Acetaminophen administration in a patient with Gilbert's syndrome.
Taku Nakagawa, Takeo Mure, Surini Yusoff, Eiichi Ono, Indra Sari Kusuma Harahap

Pediatr Int· December 2012

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Full-length sequence of mouse acupuncture-induced 1-L (aig1l) gene including its transcriptional start site.
Mika Ohta, Aki Sugano, Shuji Goto, Surini Yusoff, Yushi Hirota

Evid Based Complement Alternat Med· August 2012

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Herbal Medicine Containing Licorice May Be Contraindicated for a Patient with an HSD11B2 Mutation.
Indra Sari Kusuma Harahap, Naoko Sasaki, Gunadi, Surini Yusoff, Myeong Jin Lee

Evid Based Complement Alternat Med· August 2012

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Valproic acid increases SMN2 expression and modulates SF2/ASF and hnRNPA1 expression in SMA fibroblast cell lines.
Indra Sari Kusuma Harahap, Toshio Saito, Lai Poh San, Naoko Sasaki, Gunadi, Surini Yusoff

Brain Dev· March 2012

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A homozygous mutation in UGT1A1 exon 5 may be responsible for persistent hyperbilirubinemia in a Japanese girl with Gilbert's syndrome.
Taku Nakagawa, Takeo Mure, Surini Yusoff, Eiichi Ono, Indra Sari Kusuma Harahap

Kobe J Med Sci· July 2011

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Generalized epilepsy with febrile seizures plus (GEFS+) spectrum: clinical manifestations and SCN1A mutations in Indonesian patients.
Elisabeth Siti Herini, Gunadi, Indra Sari Kusuma Harahap, Surini Yusoff, Satoru Morikawa

Epilepsy Res· June 2010

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Screening of the LIX1 gene in Japanese and Malaysian patients with SMA and/or SMA-like disorder.
Teguh Haryo Sasongko, Gunadi, Surini Yusoff, Amin Baig Atif, Hayati Fatemeh

Brain Dev· May 2010

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Novel SCN1A mutations in Indonesian patients with severe myoclonic epilepsy in infancy.
Elisabeth Siti Herini, Gunadi, Marjan J A van Kempen, Surini Yusoff, Sutaryo

Pediatr Int· April 2010

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A polymorphic mutation, c.-3279T>G, in the UGT1A1 promoter is a risk factor for neonatal jaundice in the Malay population.
Surini Yusoff, Atsuko Takeuchi, Chitose Ashi, Masako Tsukada, Nur H Ma'amor, Narazah M Yusoff

Pediatr Res· April 2010

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Novel mutations in 21 patients with tuberous sclerosis complex and variation of tandem splice-acceptor sites in TSC1 exon 14.
Teguh Haryo Sasongko, Mari Wataya-Kaneda, Keiko Koterazawa, Gunadi, Surini Yusoff

Kobe J Med Sci· May 2008

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Evaluation of mutation effects on UGT1A1 activity toward 17beta-estradiol using liquid chromatography-tandem mass spectrometry.
Keiko Wada, Atsuko Takeuchi, Kayoko Saiki, Retno Sutomo, Hans Van Rostenberghe, Narazah Mohd Yusoff, Surini Yusoff

J Chromatogr B Analyt Technol Biomed Life Sci· June 2006

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Frequencies of A(TA)7TAA, G71R, and G493R mutations of the UGT1A1 gene in the Malaysian population.
Surini Yusoff, Hans Van Rostenberghe, Narazah M Yusoff, Norlelawati A Talib, Noraida Ramli

Biol Neonate· May 2006

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