Zobrazeno 1 - 10
of 23
pro vyhledávání: '"Teik-Beng Khoo"'
Autor:
Vanessa Wan Mun Lee, Teik Beng Khoo, Che Zubaidah Binti Che Daud, Kartikasalwah Binti Abdul Latif
Publikováno v:
Annals of Child Neurology, Vol 30, Iss 2, Pp 70-74 (2022)
Externí odkaz:
https://doaj.org/article/31c18b7011f14307a982090967347465
Autor:
Lip-Yuen Teng, Dianah Abd Hadi, Poorani Anandakrishnan, Sumitha Murugesu, Teik-Beng Khoo, Ahmad Rithauddin Mohamed
Publikováno v:
Brain and Development. 44:499-511
Geniospasm is a rare and generally benign movement disorder of the chin yet with potentially debilitating complications. Due to its rarity, previous literature was limited to only case reports or series with critical knowledge gap on its natural hist
Autor:
Lip‐Yuen Teng, Vanessa Wan‐Mun Lee, Sumitha Murugesu, Jun‐Xiong Lee, Nur Sakinah Ibrahim, Mohd Fatahudin Ishak, Ahmad Rithauddin Mohamed, Teik‐Beng Khoo
Publikováno v:
Epilepsia. 63:2011-2023
This study was undertaken to determine the hemoglobin A1c (HbA1c) and modified glucose-ketone index (mGKI) in children on different types of ketogenic diet (KD) for treatment of drug-resistant epilepsy, with attempts to evaluate their relationships w
Publikováno v:
Brain and Development. 44:44-49
Background Ferric chelate reductase 1 like (FRRS1L) encephalopathy is a rare cause of developmental and epileptic encephalopathy. Only a few cases have been reported thus far and seizures tend to be drug refractory. We report an additional case to hi
Publikováno v:
Journal of Pediatric Genetics.
Congenital myasthenic syndrome (CMS) is an uncommon inherited neuromuscular junction disease. The clinical presentation of this disorder is diverse. Typically patients with this disorder present with early-onset swallowing difficulty and apnea in inf
Autor:
Ahmad Rithauddin Mohamed, Choong Yi Fong, Teik Beng Khoo, Rui Lun Ng, Ann Nie Kong, Ching Ching Ng, Thiyagar Nadarajaw, Muhammad Yazid Jalaludin
Publikováno v:
Seizure. 79:103-111
Children with epilepsy (CWE) are at risk of vitamin D deficiency. Single nucleotide polymorphisms (SNPs) affecting the vitamin D pathway are potentially important risk factors for serum 25-hydroxyvitamin D [25(OH)D] concentration. The aims of our stu
Publikováno v:
Spinal Cord. 58:1030-1036
Cross-sectional study. To determine the prevalence and potential risk factors of vitamin D deficiency and insufficiency among Malaysian children with spina bifida. Four Malaysian tertiary hospitals. Children with spina bifida were assessed for potent
Autor:
Satomi Mitsuhashi, Atsushi Takata, Lip H Moey, Takeshi Mizuguchi, Mitsuko Nakashima, Satoko Miyatake, Noriko Miyake, Hirotomo Saitsu, Naomichi Matsumoto, Gaik S Ch'ng, Teik-Beng Khoo
Publikováno v:
Journal of Human Genetics. 64:347-350
We report the second case of early infantile epileptic encephalopathy (EIEE) arising from a homozygous truncating variant of NECAP1. The boy developed infantile-onset tonic-clonic and tonic seizures, then spasms in clusters. His electroencephalogram
Publikováno v:
Epilepsybehavior : EB. 111
Purpose Self-management is crucial in the management of chronic diseases. However, information is limited on medication self-management among parents of children with epilepsy. This study aimed to assess medication self-management among parents of ch
Autor:
Bih-Hwa Ching1 chingbihhwa@yahoo.com, Teik-Beng Khoo1
Publikováno v:
Neurology Asia. Sep2017, Vol. 22 Issue 3, p243-252. 10p.