The following pages link to Lafora disease
External toolsShowing 50 items.
View (previous 50 | next 50) (20 | 50 | 100 | 250 | 500)- Myoclonic epilepsy (links | edit)
- List of ICD-9 codes 240–279: endocrine, nutritional and metabolic diseases, and immunity disorders (links | edit)
- Infantile epileptic spasms syndrome (links | edit)
- List of neuroscientists (links | edit)
- Hypsarrhythmia (links | edit)
- Postictal state (links | edit)
- List of MeSH codes (C16) (links | edit)
- List of MeSH codes (C10) (links | edit)
- MERRF syndrome (links | edit)
- Seizure types (links | edit)
- Epilepsy Society (links | edit)
- Pyruvate carboxylase deficiency (links | edit)
- Abdominal epilepsy (links | edit)
- Dravet syndrome (links | edit)
- Childhood absence epilepsy (links | edit)
- Benign familial neonatal seizures (links | edit)
- Idiopathic generalized epilepsy (links | edit)
- Hyperoxaluria (links | edit)
- Todd's paresis (links | edit)
- Unverricht–Lundborg disease (links | edit)
- Sucrose intolerance (links | edit)
- Epilepsy Foundation (links | edit)
- Generalized epilepsy (links | edit)
- Triosephosphate isomerase deficiency (links | edit)
- Epilepsy Action Australia (links | edit)
- Laforin (links | edit)
- Galactokinase deficiency (links | edit)
- Aldolase A deficiency (links | edit)
- Glycogen storage disease type VI (links | edit)
- Renal glycosuria (links | edit)
- Pentosuria (links | edit)
- Galactose epimerase deficiency (links | edit)
- Essential fructosuria (links | edit)
- Galactose-1-phosphate uridylyltransferase deficiency (links | edit)
- Generalized tonic–clonic seizure (links | edit)
- Complex partial status epilepticus (links | edit)
- Lafora's disease (redirect page) (links | edit)
- List of eponymous diseases (links | edit)
- Talk:Lafora's disease (links | edit)
- User:PriceDL/List of all WikiProject Medicine articles (links | edit)
- User:CFCF/sandbox/46 (links | edit)
- Misplaced Pages:Version 1.0 Editorial Team/Medicine articles by quality log (links | edit)
- Misplaced Pages:Version 1.0 Editorial Team/Dermatology articles by quality log (links | edit)
- Misplaced Pages:WikiProject Medicine/Dermatology task force/Articles created (links | edit)
- Misplaced Pages:WikiProject Medicine/Lists of pages/Articles (links | edit)
- Misplaced Pages:WikiProject Medicine/Lists of pages/NA-, ???-importance medicine articles (links | edit)
- Misplaced Pages:WikiProject Medicine/Popular pages En 2013b (links | edit)
- Progressive myoclonus epilepsy (links | edit)
- Glucose-galactose malabsorption (links | edit)
- Ramsay Hunt syndrome type 1 (links | edit)
- Ohtahara syndrome (links | edit)
- Mitochondrial pyruvate carrier 2 (links | edit)
- Monocarboxylate transporter 1 (links | edit)
- Primary hyperoxaluria (links | edit)
- Dentatorubral–pallidoluysian atrophy (links | edit)
- Hexokinase deficiency (links | edit)
- Galactosemic cataract (links | edit)
- Glycogen storage disease type IX (links | edit)
- Inborn errors of carbohydrate metabolism (links | edit)
- List of skin conditions (links | edit)