Works by Ahmad-Annuar, Azlina

Results: 44

Association study of MCCC1/LAMP3 and DGKQ variants with Parkinson's disease in patients of Malay ancestry.
Published in:
Neurological Sciences, 2021, v. 42, n. 10, p. 4203, doi. 10.1007/s10072-021-05056-x
By:
- Lim, Jia Lun;
- Ng, Ebonne Yulin;
- Lim, Shen-Yang;
- Tan, Ai Huey;
- Abdul-Aziz, Zariah;
- Ibrahim, Khairul Azmi;
- Gopalai, Aroma Agape;
- Tay, Yi Wen;
- Vijayanathan, Yuganthini;
- Toh, Tzi Shin;
- Lim, Soo Kun;
- Bee, Ping-Chong;
- Puvanarajah, Santhi Datuk;
- Viswanathan, Shanthi;
- Looi, Irene;
- Lim, Thien Thien;
- Eow, Gaik Bee;
- Cheah, Wee Kooi;
- Tan, Eng-King;
- Ahmad-Annuar, Azlina
Publication type:
Article
LRRK2 N551K and R1398H variants are protective in Malays and Chinese in Malaysia: A case–control association study for Parkinson's disease.
Published in:
Molecular Genetics & Genomic Medicine, 2019, v. 7, n. 11, p. N.PAG, doi. 10.1002/mgg3.604
By:
- Gopalai, Aroma Agape;
- Lim, Jia Lun;
- Li, Hui‐Hua;
- Zhao, Yi;
- Lim, Thien Thien;
- Eow, Gaik B.;
- Puvanarajah, Santhi;
- Viswanathan, Shanthi;
- Norlinah, Mohamed Ibrahim;
- Abdul Aziz, Zariah;
- Lim, Soo Kun;
- Tan, Chong Tin;
- Tan, Ai Huey;
- Lim, Shen‐Yang;
- Tan, Eng‐King;
- Ahmad Annuar, Azlina
Publication type:
Article
Association of LRRK2 Haplotype With Age at Onset in Parkinson Disease.
Published in:
JAMA Neurology, 2018, v. 75, n. 1, p. 127, doi. 10.1001/jamaneurol.2017.3363
By:
- Xiao, Bin;
- Deng, Xiao;
- Ng, Ebonne Yu-Lin;
- Allen, John Carson;
- Lim, Shen-Yang;
- Ahmad-Annuar, Azlina;
- Tan, Eng-King
Publication type:
Article
A Perspective on the Role of microRNA-128 Regulation in Mental and Behavioral Disorders.
Published in:
Frontiers in Cellular Neuroscience, 2015, v. 9, p. 1, doi. 10.3389/fncel.2015.00465
By:
- Ai-Sze Ching;
- Ahmad-Annuar, Azlina
Publication type:
Article
A case of rapidly progressive amyotrophic lateral sclerosis associated with SOD1 mutation (p.D126H variant) following COVID-19 vaccination.
Published in:
Neurology Asia, 2024, v. 29, n. 4, p. 1171, doi. 10.54029/2024shv
By:
- Chen Fei Ng;
- Shahrizaila, Nortina;
- Ahmad-Annuar, Azlina;
- Edgar, Suzanna;
- Hui Jan Tan;
- Remli, Rabani
Publication type:
Article
Rare homozygous PRKN exon 7 duplication in a Ibanese patient from Northwestern Borneo with young onset Parkinson's disease.
Published in:
Neurology Asia, 2022, v. 27, n. 2, p. 515, doi. 10.54029/2022frs
By:
- Siaw Cheng Wong;
- Zhun Foo Tan;
- Yi-Wen Tay;
- Wan Chung Law;
- Ahmad-Annuar, Azlina;
- Ai Huey Tan;
- Shen-Yang Lim
Publication type:
Article
Parkinson's disease with homozygous PINK1 p.Leu489Pro mutations in two Indian sisters.
Published in:
Neurology Asia, 2021, v. 26, n. 1, p. 167
By:
- Shen-Yang Lim;
- Ahmad-Annuar, Azlina;
- Lohmann, Katja;
- Ai Huey Tan;
- Yi Wen Tay;
- Jia Lun Lim;
- Ramli, Norlisah;
- Pei Chiek Teh;
- Kuppusamy, Rishikesan;
- Chong Tin Tan;
- Khean Jin Goh;
- Viswanathan, Shanthi;
- Bauer, Peter;
- Rolfs, Arndt;
- Klein, Christine
Publication type:
Article
Clinical phenotype of Parkinson's disease with a homozygous PRKN p.Cys441Arg mutation.
Published in:
Neurology Asia, 2021, v. 26, n. 1, p. 161
By:
- Shen-Yang Lim;
- Ahmad-Annuar, Azlina;
- Lohmann, Katja;
- Ai Huey Tan;
- Yi Wen Tay;
- Jia Lun Lim;
- Kai Bin Lim;
- Lei Cheng Lit;
- Bauer, Peter;
- Rolfs, Arndt;
- Klein, Christine
Publication type:
Article
Maternal intake of dietary virgin coconut oil modifies essential fatty acids and causes low body weight and spiky fur in mice.
Published in:
BMC Complementary & Alternative Medicine, 2017, v. 17, p. 1, doi. 10.1186/s12906-017-1600-z
By:
- Gunasekaran, Renuka;
- Shaker, Mohammed Rafid;
- Mohd-Zin, Siti Waheeda;
- Abdullah, Aminah;
- Ahmad-Annuar, Azlina;
- Abdul-Aziz, Noraishah Mydin
Publication type:
Article
Missense Mutation of Brain Derived Neurotrophic Factor (BDNF) Alters Neurocognitive Performance in Patients with Mild Traumatic Brain Injury: A Longitudinal Study.
Published in:
PLoS ONE, 2016, v. 11, n. 7, p. 1, doi. 10.1371/journal.pone.0158838
By:
- Narayanan, Vairavan;
- Veeramuthu, Vigneswaran;
- Ahmad-Annuar, Azlina;
- Ramli, Norlisah;
- Waran, Vicknes;
- Chinna, Karuthan;
- Bondi, Mark William;
- Delano-Wood, Lisa;
- Ganesan, Dharmendra
Publication type:
Article
Identification of the genomic mutation in Epha4<sup> rb-2J/rb-2J</sup> mice.
Published in:
Genome, 2016, v. 59, n. 7, p. 439, doi. 10.1139/gen-2015-0142
By:
- Mohd-Zin, Siti W.;
- Abdullah, Nor-Linda;
- Abdullah, Aminah;
- Greene, Nicholas D.E.;
- Cheah, Pike-See;
- Ling, King-Hwa;
- Yusof, Hadri;
- Marwan, Ahmed I.;
- Williams, Sarah M.;
- York, Kerri T.;
- Ahmad-Annuar, Azlina;
- Abdul-Aziz, Noraishah M.;
- Cristescu, M.E.
Publication type:
Article
Congenital myasthenic syndrome due to novel CHAT mutations in an ethnic kadazandusun family.
Published in:
2016
By:
- Tan, Joo‐San;
- Ambang, Tomica;
- Ahmad‐Annuar, Azlina;
- Rajahram, Giri Shan;
- Wong, Kum Thong;
- Goh, Khean Jin
Publication type:
journal article
X-linked Charcot-Marie-Tooth disease predominates in a cohort of multiethnic Malaysian patients.
Published in:
Muscle & Nerve, 2014, v. 49, n. 2, p. 198, doi. 10.1002/mus.23892
By:
- Shahrizaila, Nortina;
- Samulong, Sarimah;
- Tey, Shelisa;
- Suan, Liaw Chiew;
- Meng, Lao Kah;
- Goh, Khean Jin;
- Ahmad‐Annuar, Azlina
Publication type:
Article
A family with 2 X-linked disorders: Charcot-Marie-Tooth disease and hemophilia A.
Published in:
Muscle & Nerve, 2012, v. 46, n. 3, p. 454, doi. 10.1002/mus.23346
By:
- Shahrizaila, Nortina;
- Goh, Khean Jin;
- Ahmad-Annuar, Azlina;
- Chaudhry, Rabia;
- Ly, Carolyn;
- Ryan, Monique M.;
- Nicholson, Garth;
- Kennerson, Marina
Publication type:
Article
Using global team science to identify genetic parkinson's disease worldwide.
Published in:
2019
By:
- Vollstedt, Eva‐Juliane;
- Kasten, Meike;
- Klein, Christine;
- Aasly, Jan;
- Adler, Charles;
- Ahmad‐Annuar, Azlina;
- Albanese, Alberto;
- Alcalay, Roy N.;
- Al‐Mubarak, Bashayer;
- Alvarez, Victoria;
- Andree‐Muñoz, Brennie;
- Annesi, Grazia;
- Appel‐Cresswell, Silke;
- Arkadir, David;
- Armasu, Sebastian;
- Barber, Thomas R.;
- Bardien, Soraya;
- Barkhuizen, Melinda;
- Barrett, Matthew J.;
- Başak, A. Nazlı
Publication type:
Editorial
Quantitative magnetic resonance imaging and radiogenomic biomarkers for glioma characterisation: a systematic review.
Published in:
British Journal of Radiology, 2018, v. 91, n. 1092, p. N.PAG, doi. 10.1259/bjr.20170930
By:
- Seow, Pohchoo;
- Wong, Jeannie Hsiu Ding;
- Ahmad-Annuar, Azlina;
- Mahajan, Abhishek;
- Abdullah, Nor Aniza;
- Ramli, Norlisah
Publication type:
Article
ATXN2 polyglutamine intermediate repeats length expansions in Malaysian patients with amyotrophic lateral sclerosis (ALS)
Published in:
Neurogenetics, 2025, v. 26, n. 1, p. 1, doi. 10.1007/s10048-024-00798-0
By:
- Edgar, Suzanna;
- Zulhairy-Liong, Nurul Angelyn;
- Ellis, Melina;
- Trivedi, Shuchi;
- Zhu, Danqing;
- Odongo, Jeffrey Ochieng;
- Goh, Khean-Jin;
- Capelle, David Paul;
- Shahrizaila, Nortina;
- Kennerson, Marina L.;
- Ahmad-Annuar, Azlina
Publication type:
Article
Linkage analysis and whole exome sequencing reveals AHNAK2 as a novel genetic cause for autosomal recessive CMT in a Malaysian family.
Published in:
Neurogenetics, 2019, v. 20, n. 3, p. 117, doi. 10.1007/s10048-019-00576-3
By:
- Tey, Shelisa;
- Shahrizaila, Nortina;
- Drew, Alexander P.;
- Samulong, Sarimah;
- Goh, Khean-Jin;
- Battaloglu, Esra;
- Atkinson, Derek;
- Parman, Yesim;
- Jordanova, Albena;
- Chung, Ki Wha;
- Choi, Byung-Ok;
- Li, Yi-Chung;
- Auer-Grumbach, Michaela;
- Nicholson, Garth A.;
- Kennerson, Marina L.;
- Ahmad-Annuar, Azlina
Publication type:
Article
Analysis of dynein intermediate chains, light intermediate chains and light chains in a cohort of hereditary peripheral neuropathies.
Published in:
Neurogenetics, 2014, v. 15, n. 4, p. 229, doi. 10.1007/s10048-014-0414-0
By:
- Tey, Shelisa;
- Ahmad-Annuar, Azlina;
- Drew, Alexander;
- Shahrizaila, Nortina;
- Nicholson, Garth;
- Kennerson, Marina
Publication type:
Article
Genetic Testing for Parkinson's Disease and Movement Disorders in Less Privileged Areas: Barriers and Opportunities.
Published in:
Movement Disorders Clinical Practice, 2024, v. 11, n. 1, p. 14, doi. 10.1002/mdc3.13903
By:
- Tan, Ai Huey;
- Cornejo‐Olivas, Mario;
- Okubadejo, Njideka;
- Pal, Pramod Kumar;
- Saranza, Gerard;
- Saffie‐Awad, Paula;
- Ahmad‐Annuar, Azlina;
- Schumacher‐Schuh, Artur F.;
- Okeng'o, Kigocha;
- Mata, Ignacio F.;
- Gatto, Emilia M.;
- Lim, Shen‐Yang
Publication type:
Article
COVID‐19 pandemic: Lessons learned for undergraduate research training.
Published in:
Biochemistry & Molecular Biology Education, 2022, v. 50, n. 5, p. 476, doi. 10.1002/bmb.21665
By:
- Ibrahim, Kamariah;
- Ahmad‐Annuar, Azlina
Publication type:
Article
Improved inherited peripheral neuropathy genetic diagnosis by whole-exome sequencing.
Published in:
Molecular Genetics & Genomic Medicine, 2015, v. 3, n. 2, p. 143, doi. 10.1002/mgg3.126
By:
- Drew, Alexander P.;
- Zhu, Danqing;
- Kidambi, Aditi;
- Ly, Carolyn;
- Tey, Shelisa;
- Brewer, Megan H.;
- Ahmad‐Annuar, Azlina;
- Nicholson, Garth A.;
- Kennerson, Marina L.
Publication type:
Article
Multistep modeling applied to a Malaysian ALS registry.
Published in:
2025
By:
- Capelle, David Paul;
- Sabirin, Wafa;
- Zulhairy-Liong, Nurul Angelyn;
- Edgar, Suzanna;
- Goh, Khean-Jin;
- Ahmad-Annuar, Azlina;
- Shahrizaila, Nortina
Publication type:
Report
Clinical Outcomes After Ventriculo-Peritoneal Shunting in Patients With Classic vs. Complex NPH.
Published in:
Frontiers in Neurology, 2022, v. 13, p. 1, doi. 10.3389/fneur.2022.868000
By:
- Eng Tah Goh;
- Christine Lock;
- Audrey Jia Luan Tan;
- Bee Ling Tan;
- Sai Liang;
- Pillay, Robin;
- Kumar, Sumeet;
- Ahmad-Annuar, Azlina;
- Narayanan, Vairavan;
- Kwok, Janell;
- Yi Jayne Tan;
- Adeline SL Ng;
- Eng King Tan;
- Zofia Czosnyka;
- Czosnyka, Marek;
- Pickard, John D.;
- Keong, Nicole C.
Publication type:
Article
Glucocerebrosidase (GBA) gene variants in a multi-ethnic Asian cohort with Parkinson's disease: mutational spectrum and clinical features.
Published in:
Journal of Neural Transmission, 2022, v. 129, n. 1, p. 37, doi. 10.1007/s00702-021-02421-0
By:
- Lim, Jia Lun;
- Lohmann, Katja;
- Tan, Ai Huey;
- Tay, Yi Wen;
- Ibrahim, Khairul Azmi;
- Abdul Aziz, Zariah;
- Mawardi, Ahmad Shahir;
- Puvanarajah, Santhi Datuk;
- Lim, Thien Thien;
- Looi, Irene;
- Ooi, Joshua Chin Ern;
- Chia, Yuen Kang;
- Muthusamy, Kalai Arasu;
- Bauer, Peter;
- Rolfs, Arndt;
- Klein, Christine;
- Ahmad-Annuar, Azlina;
- Lim, Shen-Yang
Publication type:
Article
Signaling across the synapse: a role for Wnt and Dishevelled in presynaptic assembly and neurotransmitter release.
Published in:
Journal of Cell Biology, 2006, v. 174, n. 1, p. 127, doi. 10.1083/jcb.200511054
By:
- Ahmad-Annuar, Azlina;
- Ciani, Lorenza;
- Simeonidis, Iordanis;
- Herreros, Judit;
- Fredj, Naila Ben;
- Rosso, Silvana B.;
- Hall, Anita;
- Brickley, Stephen;
- Salinas, Patricia C.
Publication type:
Article
Spina Bifida: Pathogenesis, Mechanisms, and Genes in Mice and Humans.
Published in:
Scientifica, 2017, p. 1, doi. 10.1155/2017/5364827
By:
- Mohd-Zin, Siti W.;
- Marwan, Ahmed I.;
- Abou Chaar, Mohamad K.;
- Ahmad-Annuar, Azlina;
- Abdul-Aziz, Noraishah M.
Publication type:
Article
Rapid-Onset Dystonia-Parkinsonism in a Chinese Girl with a De Novo ATP1A3 c.2267G>A (p.R756H) Genetic Mutation.
Published in:
Movement Disorders Clinical Practice, 2015, v. 2, n. 1, p. 74, doi. 10.1002/mdc3.12122
By:
- Tan, Ai Huey;
- Ozelius, Laurie J.;
- Brashear, Allison;
- Lang, Anthony E.;
- Ahmad‐Annuar, Azlina;
- Tan, Chong Tin;
- Lim, Shen‐Yang
Publication type:
Article
Establishing an online resource to facilitate global collaboration and inclusion of underrepresented populations: Experience from the MJFF Global Genetic Parkinson's Disease Project.
Published in:
PLoS ONE, 2023, v. 18, n. 10, p. 1, doi. 10.1371/journal.pone.0292180
By:
- Vollstedt, Eva-Juliane;
- Madoev, Harutyun;
- Aasly, Anna;
- Ahmad-Annuar, Azlina;
- Al-Mubarak, Bashayer;
- Alcalay, Roy N.;
- Alvarez, Victoria;
- Amorin, Ignacio;
- Annesi, Grazia;
- Arkadir, David;
- Bardien, Soraya;
- Barker, Roger A.;
- Barkhuizen, Melinda;
- Basak, A. Nazli;
- Bonifati, Vincenzo;
- Boon, Agnita;
- Brighina, Laura;
- Brockmann, Kathrin;
- Carmine Belin, Andrea;
- Carr, Jonathan
Publication type:
Article
Genome-wide association study of Parkinson's disease in East Asians.
Published in:
Human Molecular Genetics, 2017, v. 26, n. 1, p. 226, doi. 10.1093/hmg/ddw379
By:
- Jia Nee Foo;
- Tan, Louis C.;
- Irwan, Ishak D.;
- Wing-Lok Au;
- Hui Qi Low;
- Prakash, Kumar-M.;
- Ahmad-Annuar, Azlina;
- Jinxin Bei;
- Chan, Anne Y. Y.;
- Chiung Mei Chen;
- Yi-Chun Chen;
- Sun Ju Chung;
- Hao Deng;
- Shen-Yang Lim;
- Mok, Vincent;
- Hao Pang;
- Zhong Pei;
- Rong Peng;
- Hui-Fang Shang;
- Kyuyoung Song
Publication type:
Article
Analysis of non-synonymous-coding variants of Parkinson's disease-related pathogenic and susceptibility genes in East Asian populations.
Published in:
Human Molecular Genetics, 2014, v. 23, n. 14, p. 3891, doi. 10.1093/hmg/ddu086
By:
- Foo, Jia Nee;
- Tan, Louis C.;
- Liany, Herty;
- Koh, Tat Hung;
- Irwan, Ishak D.;
- Ng, Yen Yek;
- Ahmad-Annuar, Azlina;
- Au, Wing-Lok;
- Aung, Tin;
- Chan, Anne Y.Y.;
- Chong, Siow-Ann;
- Chung, Sun Ju;
- Jung, Yusun;
- Khor, Chiea Chuen;
- Kim, Juyeon;
- Lee, Jimmy;
- Lim, Shen-Yang;
- Mok, Vincent;
- Prakash, Kumar-M.;
- Song, Kyuyoung
Publication type:
Article
Improved spinal cord gray matter morphology induced by Spirulina platensis following spinal cord injury in rat models.
Published in:
Ultrastructural Pathology, 2020, v. 44, n. 4-6, p. 359, doi. 10.1080/01913123.2020.1792597
By:
- Abdullahi, Dauda;
- Ahmad Annuar, Azlina;
- Sanusi, Junedah
Publication type:
Article
Neuroprotective potential of Spirulina platensis on lesioned spinal cord corticospinal tract under experimental conditions in rat models.
Published in:
Ultrastructural Pathology, 2019, v. 43, n. 6, p. 273, doi. 10.1080/01913123.2019.1695693
By:
- Abdullahi, Dauda;
- Ahmad Annuar, Azlina;
- Sanusi, Junedah
Publication type:
Article
A mixed method study on the impact of living with spinal muscular atrophy in Malaysia from patients' and caregivers' perspectives.
Published in:
2022
By:
- Ch'ng, Gaik Siew;
- Koh, Karina;
- Ahmad-Annuar, Azlina;
- Taib, Fahisham;
- Koh, Cha Ling;
- Lim, Edmund Soon Chin
Publication type:
journal article
Deregulation of microRNAs in blood and skeletal muscles of myotonic dystrophy type 1 patients.
Published in:
2017
By:
- Ambrose, Kathlin K.;
- Ishak, Taufik;
- Lay-Hoong Lian;
- Khean-Jin Goh;
- Kum-Thong Wong;
- Ahmad-Annuar, Azlina;
- Meow-Keong Thong;
- Lian, Lay-Hoong;
- Goh, Khean-Jin;
- Wong, Kum-Thong;
- Thong, Meow-Keong
Publication type:
journal article
Clinical and functional evidence for the pathogenicity of the LRRK2 p.Arg1067Gln variant.
Published in:
NPJ Parkinson's Disease, 2025, v. 11, n. 1, p. 1, doi. 10.1038/s41531-025-00884-6
By:
- Lim, Shen-Yang;
- Toh, Tzi Shin;
- Hor, Jia Wei;
- Lim, Jia Lun;
- Lit, Lei Cheng;
- Ahmad-Annuar, Azlina;
- Tay, Yi Wen;
- Foo, Jia Nee;
- Ng, Ebonne Yulin;
- Muthusamy, Kalai Arasu;
- Mohamed Ibrahim, Norlinah;
- Ibrahim, Khairul Azmi;
- Tan, Louis Chew Seng;
- Zulkefli, Jannah;
- Khairul Anuar, Anis Nadhirah;
- Black, Kirsten;
- Lis, Pawel;
- Xie, Fei;
- Cen, Zhidong;
- Lim, Kai Shi
Publication type:
Article
LRRK2 G2385R and R1628P Mutations Are Associated with an Increased Risk of Parkinson's Disease in the Malaysian Population.
Published in:
BioMed Research International, 2014, v. 2014, p. 1, doi. 10.1155/2014/867321
By:
- Gopalai, Aroma Agape;
- Shen-Yang Lim;
- Jing Yi Chua;
- Shelisa Tey;
- Thien Thien Lim;
- Ibrahim, Norlinah Mohamed;
- Ai Huey Tan;
- Gaik Bee Eow;
- Aziz, Zariah Abdul;
- Puvanarajah, Santhi Datuk;
- Viswanathan, Shanthi;
- Looi, Irene;
- Soo Kun Lim;
- Li Ping Tan;
- Yip Boon Chong;
- Chong Tin Tan;
- Yi Zhao;
- E. K. Tan;
- Ahmad-Annuar, Azlina
Publication type:
Article
Editorial: Genetic and molecular diversity in Parkinson’s disease.
Published in:
Frontiers in Aging Neuroscience, 2022, v. 14, p. 1, doi. 10.3389/fnagi.2022.1094914
By:
- Abdul Murad, Nor Azian;
- Sulaiman, Siti Aishah;
- Ahmad-Annuar, Azlina;
- Ibrahim, Norlinah Mohamed;
- Mohamed, Wael;
- Md Rani, Shahrul Azmin;
- Kin Ying Mok
Publication type:
Article
PARK16 is associated with PD in the Malaysian population.
Published in:
American Journal of Medical Genetics. Part B: Neuropsychiatric Genetics, 2016, v. 171B, n. 6, p. 839, doi. 10.1002/ajmg.b.32454
By:
- Gopalai, Aroma Agape;
- Ahmad‐Annuar, Azlina;
- Li, Hui‐Hua;
- Zhao, Yi;
- Lim, Shen‐Yang;
- Tan, Ai Huey;
- Lim, Thien Thein;
- Eow, Gaik Bee;
- Santhi, Puvanarajah;
- Shanthi, Viswanathan;
- Norlinah, Mohamed Ibrahim;
- Aziz, Zariah Abdul;
- Lim, Soo Kun;
- Tan, Chong Tin;
- Tan, Eng‐King
Publication type:
Article
Cranial neural tube defect after trimethoprim exposure.
Published in:
BMC Research Notes, 2018, v. 11, n. 1, p. N.PAG, doi. 10.1186/s13104-018-3593-1
By:
- Abdullah, Nor Linda;
- Gunasekaran, Renuka;
- Mohd-Zin, Siti Waheeda;
- Lim, Bee-Hui;
- Maniam, Pramila;
- Mohd-Salleh, Anis Shuhada;
- Thong, Meow-Keong;
- Chik, Zamri;
- Nordin, Noreena;
- Omar, Zaliha;
- Engkasan, Julia Patrick;
- Ganesan, Dharmendra;
- Aiezzah, Zakaria Nurul;
- Ahmad-Annuar, Azlina;
- Abdul-Aziz, Noraishah Mydin
Publication type:
Article
Ala97Ser mutation is common among ethnic Chinese Malaysians with transthyretin familial amyloid polyneuropathy.
Published in:
2019
By:
- Low, Soon Chai;
- Tan, Cheng Yin;
- Md Sari, Nor Ashikin;
- Ahmad-Annuar, Azlina;
- Wong, Kum Thong;
- Lin, Kon-Ping;
- Shahrizaila, Nortina;
- Tan, Chong Tin;
- Goh, Khean Jin
Publication type:
Letter
Identification of Genetic Variants in Progressive Supranuclear Palsy in Southeast Asia.
Published in:
Movement Disorders, 2024, v. 39, n. 10, p. 1829, doi. 10.1002/mds.29932
By:
- Ng, Adeline Su Lyn;
- Tan, Ai Huey;
- Tan, Yi Jayne;
- Lim, Jia Lun;
- Lian, Michelle Mulan;
- Dy Closas, Alfand Marl;
- Ahmad‐Annuar, Azlina;
- Viswanathan, Shanthi;
- Chia, Yuen Kang;
- Foo, Jia Nee;
- Lim, Weng Khong;
- Tan, Eng‐King;
- Lim, Shen‐Yang
Publication type:
Article
Underrepresented Populations in Parkinson's Genetics Research: Current Landscape and Future Directions.
Published in:
Movement Disorders, 2022, v. 37, n. 8, p. 1593, doi. 10.1002/mds.29126
By:
- Schumacher‐Schuh, Artur Francisco;
- Bieger, Andrei;
- Okunoye, Olaitan;
- Mok, Kin Ying;
- Lim, Shen‐Yang;
- Bardien, Soraya;
- Ahmad‐Annuar, Azlina;
- Santos‐Lobato, Bruno Lopes;
- Strelow, Matheus Zschornack;
- Salama, Mohamed;
- Rao, Shilpa C.;
- Zewde, Yared Zenebe;
- Dindayal, Saiesha;
- Azar, Jihan;
- Prashanth, Lingappa Kukkle;
- Rajan, Roopa;
- Noyce, Alastair J.;
- Okubadejo, Njideka;
- Rizig, Mie;
- Lesage, Suzanne
Publication type:
Article
Clinical Phenotype of LRRK2 R1441C in 2 Chinese Sisters.
Published in:
Neurodegenerative Diseases, 2020, v. 20, n. 1, p. 39, doi. 10.1159/000508131
By:
- Lim, Shen-Yang;
- Lim, Jia Lun;
- Ahmad-Annuar, Azlina;
- Lohmann, Katja;
- Tan, Ai Huey;
- Lim, Kai Bin;
- Tay, Yi Wen;
- Shing, Yee Lee;
- Muthusamy, Kalai Arasu;
- Bauer, Peter;
- Rolfs, Arndt;
- Klein, Christine
Publication type:
Article