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"Epilepsy," familial adult "myoclonic," 3
Did you mean "Epilepsy," familial adult "mayoclinic," 3?
- ... Undlien DE, Brodtkorb E. SCN1A mutation screening in adult patients with Lennox-Gastaut syndrome features. Epilepsy Behav. 2009 Nov;16(3):555-7. doi: 10.1016/j.yebeh.2009. ...
- Curing the Epilepsies: The Promise of Research
(National Institute of Neurological Disorders and Stroke)
Epilepsy/Statistics and Research ... Epilepsy ... National Institute of Neurological Disorders and Stroke ... Request free mailed brochure ... From the National Institutes ... - ... s mother (maternal inheritance). DRPLA Haw River syndrome Myoclonic epilepsy ... Pericak-Vance MA, Vance JM. The Haw River syndrome: dentatorubropallidoluysian atrophy (DRPLA) in an African-American family. Nat Genet. 1994 Aug;7(4):521-4. ...
- ... disease often develop seizures and uncontrollable muscle jerks (myoclonic epilepsy), a decline in intellectual function (dementia), problems with ... with no history of the disorder in their family. Adult neuronal ceroid lipofuscinosis Ceroid lipofuscinosis, neuronal, 4B, autosomal ...
- Movement Disorders/Specifics ... Movement Disorders ... Multiple Sclerosis/Related Issues ... Multiple Sclerosis ... National Institute of Neurological Disorders and Stroke
- ... also have features of another mitochondrial disorder called myoclonic epilepsy with ragged-red fibers (MERRF); these additional features ... the MT-TH gene have features of both myoclonic epilepsy with ragged-red fibers (MERRF) and MELAS. The ...
- Seizures/Start Here ... Seizures ... Epilepsy/Start Here ... Epilepsy ... Epilepsy is a chronic brain disorder in which groups of nerve cells, or neurons, in the brain sometimes ...
- Absence Seizure (Petit Mal Seizure) (Mayo Foundation for Medical Education and Research)Seizures/Specifics ... Seizures ... Mayo Foundation for Medical Education and Research