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SaveEBF3-related neurodevelopment disorder affecting an individual of Singaporean Arab and Malay origin: case report and review of the literature
Ramalingam, Chitra Gangadaran; Lim, Jiin Ying; Goh, Jeannette; Kam, Sylvia; Law, Hai Yang; Mislan, Nur Afiqah Binte Mohd; Ng, Ivy; Thomas, Terrence Gerard Sundram; Lim, Weng Khong; Mascarenhas, Sandra Sylvia; Jamuar, Saumya Shekhar Share Save Share Save International consensus definitions for infection-triggered encephalopathy syndromesSakuma, Hiroshi; Thomas, Terrence; Debinski, Carly; Eyre, Michael; Han, Velda X.; Jones, Hannah F.; Kawano, Go; Lee, Vanessa W.; Malone, Stephen; Matsuishi, Toyojiro; Mohammad, Shekeeb S.; Mori, Takayuki; Nishida, Hiroya; Nosadini, Margherita; Takanashi, Jun-ichi; Mizuguchi, Masashi; Lim, Ming; Dale, Russell C. Share Save Defining the Clinicoradiologic Syndrome of SARS-CoV-2 Acute Necrotizing Encephalopathy: A Systematic Review and 3 New Pediatric CasesLee, Vanessa W.; Kam, Kai Qian; Mohamed, Ahmad R.; Musa, Husna; Anandakrishnan, Poorani; Shen, Qingtang; Palazzo, Alexander F.; Dale, Russell C.; Lim, Ming; Thomas, Terrence Share Save CSF neopterin and quinolinic acid are biomarkers of neuroinflammation and neurotoxicity in FIRES and other infection-triggered encephalopathy syndromesDale, Russell C.; Thomas, Terrence; Patel, Shrujna; Han, Velda X.; Kothur, Kavitha; Troedson, Christopher; Gupta, Sachin; Gill, Deepak; Malone, Stephen; Waak, Michaela; Calvert, Sophie; Subramanian, Gopinath; Andrews, P. Ian; Kandula, Tejaswi; Menezes, Manoj P.; Ardern-Holmes, Simone; Mohammad, Shekeeb; Bandodkar, Sushil; Yan, Jingya Share Save International Consensus Recommendations for the Treatment of Pediatric NMDAR Antibody EncephalitisNosadini, Margherita; Thomas, Terrence; Eyre, Michael; Anlar, Banu; Armangue, Thais; Benseler, Susanne M.; Cellucci, Tania; Deiva, Kumaran; Gallentine, William; Gombolay, Grace; Gorman, Mark P.; Hacohen, Yael; Jiang, Yuwu; Lim, Byung Chan; Muscal, Eyal; Ndondo, Alvin; Neuteboom, Rinze; Rostasy, Kevin; Sakuma, Hiroshi; Sharma, Suvasini; Tenembaum, Silvia Noemi; Van Mater, Heather Ann; Wells, Elizabeth; Wickstrom, Ronny; Yeshokumar, Anusha K.; Irani, Sarosh R.; Dalmau, Josep; Lim, Ming; Dale, Russell C. Share Save Neurology of COVID-19 in Singapore (vol 418, 117118, 2020)Koh, Jasmine Shimin; De Silva, Deidre Anne; Quek, Amy May Lin; Chiew, Hui Jin; Tu, Tian Ming; Seet, Christopher Ying Hao; Hoe, Rebecca Hui Min; Saini, Monica; Hui, Andrew Che-Fai; Angon, Jasmyn; Ker, Justin Ruixin; Yong, Ming Hui; Goh, Yihui; Yu, Wai-Yung; Lim, Tchoyoson Choie Cheio; Tan, Benjamin Yong Qiang; Ng, Kay Wei Ping; Yeo, Leonard Leong Litt; Pang, Yu Zhi; Prakash, Kumar M.; Ahmad, Aftab; Thomas, Terrence; Lye, David Chien Boon; Tan, Kevin; Umapathi, Thirugnanam Share Save Neurology of COVID-19 in SingaporeKoh, Jasmine Shimin; De Silva, Deidre Anne; Quek, Amy May Lin; Chiew, Hui Jin; Tu, Tian Ming; Seet, Christopher Ying Hao; Hoe, Rebecca Hui Min; Saini, Monica; Hui, Andrew Che-Fai; Angon, Jasmyn; Ker, Justin Ruixin; Yong, Ming Hui; Goh, Yihui; Yu, Wai-Yung; Lim, Tchoyoson Choie Cheio; Tan, Benjamin Yong Qiang; Ng, Kay Wei Ping; Yeo, Leonard Leong Litt; Pang, Yu Zhi; Prakash, Kumar M.; Ahmad, Aftab; Thomas, Terrence; Lye, David Chien Boon; Tan, Kevin; Umapathi, Thirugnanam Share Save Loss-of-function mutations in UDP-Glucose 6-Dehydrogenase cause recessive developmental epileptic encephalopathyHengel, Holger; Bosso-Lefevre, Celia; Grady, George; Szenker-Ravi, Emmanuelle; Li, Hankun; Pierce, Sarah; Lebigot, Elise; Tan, Thong-Teck; Eio, Michelle Y.; Narayanan, Gunaseelan; Utami, Kagistia Hana; Yau, Monica; Handal, Nader; Deigendesch, Werner; Keimer, Reinhard; Marzouqa, Hiyam M.; Gunay-Aygun, Meral; Muriello, Michael J.; Verhelst, Helene; Weckhuysen, Sarah; Mahida, Sonal; Naidu, Sakkubai; Thomas, Terrence G.; Lim, Jiin Ying; Tan, Ee Shien; Haye, Damien; Willemsen, Michel A. A. P.; Oegema, Renske; Mitchell, Wendy G.; Pierson, Tyler Mark; Andrews, Marisa V.; Willing, Marcia C.; Rodan, Lance H.; Barakat, Tahsin Stefan; van Slegtenhorst, Marjon; Gavrilova, Ralitza H.; Martinelli, Diego; Gilboa, Tal; Tamim, Abdullah M.; Hashem, Mais O.; AlSayed, Moeenaldeen D.; Abdulrahim, Maha M.; Al-Owain, Mohammed; Awaji, Ali; Mahmoud, Adel A. H.; Faqeih, Eissa A.; Al Asmari, Ali; Algain, Sulwan M.; Jad, Lamyaa A.; Aldhalaan, Hesham M.; Helbig, Ingo; Koolen, David A.; Riess, Angelika; Kraegeloh-Mann, Ingeborg; Bauer, Peter; Gulsuner, Suleyman; Stamberger, Hannah; Ng, Alvin Yu Jin; Tang, Sha; Tohari, Sumanty; Keren, Boris; Schultz-Rogers, Laura E.; Klee, Eric W.; Barresi, Sabina; Tartaglia, Marco; Mor-Shaked, Hagar; Maddirevula, Sateesh; Begtrup, Amber; Telegrafi, Aida; Pfundt, Rolph; Schuele, Rebecca; Ciruna, Brian; Bonnard, Carine; Pouladi, Mahmoud A.; Stewart, James C.; Claridge-Chang, Adam; Lefeber, Dirk J.; Alkuraya, Fowzan S.; Mathuru, Ajay S.; Venkatesh, Byrappa; Barycki, Joseph J.; Simpson, Melanie A.; Jamuar, Saumya S.; Schoels, Ludger; Reversade, Bruno Share Save Share Save Share Save Share Save Rapid-Onset Obesity With Hypothalamic Dysfunction, Hypoventilation, and Autonomic Dysregulation (ROHHAD) Syndrome May Have a Hypothalamus-Periaqueductal Gray LocalizationChow, Cristelle; Fortier, Marielle Valerie; Das, Lena; Menon, Anuradha P.; Vasanwala, Rashida; Lam, Joyce C. M.; Ng, Zhi Min; Ling, Simon Robert; Chan, Derrick W. S.; Choong, Chew Thye; Liew, Wendy K. M.; Thomas, Terrence Share Save Share Save Two mutations in the HSN2 gene explain the high prevalence of HSAN2 in French CanadiansRoddier, K; Thomas, T; Marleau, G; Gagnon, AM; Dicaire, MJ; St-Denis, A; Gosselin, I; Sarrazin, AM; Larbrisseau, A; Lambert, M; Vanasse, M; Gaudet, D; Rouleau, GA; Brais, B Share Save 
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