Search details
1.
De Novo Truncating Variants in the Last Exon of SEMA6B Cause Progressive Myoclonic Epilepsy.
Am J Hum Genet
; 106(4): 549-558, 2020 04 02.
Article
in English
| MEDLINE | ID: mdl-32169168
2.
Glycemic biomarkers in children with drug-resistant epilepsy on various types of ketogenic diet therapies: A cross-sectional study.
Epilepsia
; 63(8): 2011-2023, 2022 08.
Article
in English
| MEDLINE | ID: mdl-35527506
3.
Vitamin D deficiency and its risk factors in Malaysian children with epilepsy.
Epilepsia
; 57(8): 1271-9, 2016 08.
Article
in English
| MEDLINE | ID: mdl-27378185
4.
Severe and rare neurological manifestations following COVID-19 infection in children: A Malaysian tertiary centre experience.
Brain Dev
; 45(10): 547-553, 2023 Nov.
Article
in English
| MEDLINE | ID: mdl-37661525
5.
Management of status epilepticus in Malaysia: A national survey of current practice and treatment gap.
J Clin Neurosci
; 114: 25-31, 2023 Aug.
Article
in English
| MEDLINE | ID: mdl-37279626
6.
Geniospasm: A systematic review on natural history, prognosis, and treatment.
Brain Dev
; 44(8): 499-511, 2022 Sep.
Article
in English
| MEDLINE | ID: mdl-35672188
7.
Association of common genetic variants with vitamin D status in Malaysian children with epilepsy.
Seizure
; 79: 103-111, 2020 Jul.
Article
in English
| MEDLINE | ID: mdl-32464532
8.
Tumefactive demyelinating lesion and bilateral optic neuritis in a paediatric myelin oligodendrocyte glycoprotein antibody-associated disease.
BMJ Case Rep
; 16(12)2023 Dec 16.
Article
in English
| MEDLINE | ID: mdl-38103908
Results
1 -
8
de 8
1
Next >
>>