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Publications by Feizel Alsiddiq
Pathogenic Mutations in ARX, CDKL5 and STXBP1 Genes Are Not Associated With the Early-Onset Epileptic Encephalopathy in Malaysian Pediatric Patients: A Pilot Study
Neuroscience Research Notes
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Early-Onset Epileptic Encephalopathy and Severe Developmental Delay in an Association With De Novo Double Mutations in NF1 and MAGEL2
Epilepsia Open
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SCN2A-Related Early-Onset Epileptic Encephalopathy Responsive to Phenobarbital
Journal of Pediatric Epilepsy
Early-Onset Epileptic Encephalopathy Caused by Gain-Of-Function Mutations in the Voltage Sensor of Kv7.2 and Kv7.3 Potassium Channel Subunits
Journal of Neuroscience
Neuroscience
Mutations in the Potassium Channel Subunit KCNE1 Are Associated With Early-Onset Familial Atrial Fibrillation
BMC Medical Genetics
Genetics
The Prognostic Value of Neurofilament Levels in Patients With Sepsis-Associated Encephalopathy – A Prospective, Pilot Observational Study
PLoS ONE
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G396(P) Is Infantile Laryngomalacia Associated With Early Onset Adenotonsillar Hypertrophy: A Retrospective Pilot Study
Archives of Disease in Childhood
Child Health
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Perinatology
De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy With Contractures, Macrocephaly, and Dyskinesias
American Journal of Human Genetics
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Re-Annotation of 191 Developmental and Epileptic Encephalopathy-Associated Genes Unmasks De Novo Variants in SCN1A
npj Genomic Medicine
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Molecular Biology
PINK1, Parkin, and DJ-1 Mutations in Italian Patients With Early-Onset Parkinsonism
European Journal of Human Genetics
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