Author spotlight
Oliver Sacks
Phenotypic convergence of Menkes and Wilson disease November 17, 2016
Mitochondrial cytopathy with common MELAS mutation presenting as multiple system atrophy mimic November 17, 2016
De novo FGF12 mutation in 2 patients with neonatal-onset epilepsy November 10, 2016
Novel HSPB1 mutation causes both motor neuronopathy and distal myopathy October 31, 2016
Copy number analysis reveals a novel multiexon deletion of the COLQ gene in congenital myasthenia October 31, 2016
Germline and somatic mutations in the MTOR gene in focal cortical dysplasia and epilepsy October 31, 2016
FHF1 (FGF12) epileptic encephalopathy October 28, 2016
SORL1 mutations in early- and late-onset Alzheimer disease October 26, 2016
Peripheral neuropathy in patients with CPEO associated with single and multiple mtDNA deletions October 19, 2016
Heterozygous mutations in HSD17B4 cause juvenile peroxisomal D-bifunctional protein deficiency October 18, 2016
Epidermolysis bullosa simplex with muscular dystrophy associated with PLEC deletion mutation October 11, 2016
Muscle involvement in limb-girdle muscular dystrophy with GMPPB deficiency (LGMD2T) October 11, 2016
Oliver Sacks
Cases
Worldwide collaboration
November 29, 2016 Download Podcast
Dr. Adam Numis interviews Dr. David Gloss about his AAN Practice Advisory paper on the utility of EEG theta/beta power ratio in attention deficit hyperactivity disorder diagnosis. Dr. Ilena George is reading our e-Pearl of the week about hemiplegic migraine. In the next part of the podcast, Dr. Alberto Espay interviews Dr. Steven Frucht on the topic of how to approach myoclonus.