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Publications by Stephanie Mei Ling See
Lafora Disease in a Malaysian With a Rare Mutation in the EPM2A Gene
Seizure : the journal of the British Epilepsy Association
Medicine
Neurology
Related publications
NHLRC1repeat Expansion in Two Beagles With Lafora Disease
Journal of Small Animal Practice
Small Animals
Rare LPL Gene Missense Mutation in an Infant With Hypertriglyceridemia
Journal of Clinical Laboratory Analysis
Allergy
Immunology
Biochemistry
Public Health
Medical Laboratory Technology
Clinical Biochemistry
Hematology
Microbiology
Environmental
Occupational Health
Variant Alzheimer Disease With Spastic Paraparesis: A Rare Presenilin-1 Mutation
Canadian Journal of Neurological Sciences
Medicine
Neurology
Rare Genetic Creutzfeldt-Jakob Disease With E196A Mutation: A Case Report
Prion
Biochemistry
Molecular Neuroscience
Infectious Diseases
Cell Biology
Cellular
A Novel Mutation of the Ceruloplasmin Gene in a Patient With Heteroallelic Ceruloplasmin Gene Mutation (HypoCPGM)
Tohoku Journal of Experimental Medicine
Biochemistry
Medicine
Genetics
Molecular Biology
Wide Range of Disease Onset in a Family With Alzheimer Disease and a His163Tyr Mutation in the Presenilin-1 Gene
Archives of Neurology
A Rare Truncating Mutation in ADH1C (G78Stop) Shows Significant Association With Parkinson Disease in a Large International Sample
Archives of Neurology
PTG Depletion Removes Lafora Bodies and Rescues the Fatal Epilepsy of Lafora Disease
PLoS Genetics
Evolution
Ecology
Genetics
Molecular Biology
Cancer Research
Systematics
Behavior
Musculoskeletal Melioidosis in a Malaysian Return Driver With Chronic Osteomyelitis – A Rare Case Report
International Journal of Current Microbiology and Applied Sciences
