Novel mutations in human and mouse SCN4A implicate AMPK in myotonia and periodic paralysis.

Earth history. Low mid-Proterozoic atmospheric oxygen levels and the delayed rise of animals.

Surgical management of medically refractory epilepsy due to early childhood stroke.

A nonsense mutation in mouse Tardbp affects TDP43 alternative splicing activity and causes limb-clasping and body tone defects.

Pathogenic Parkinson's disease mutations across the functional domains of LRRK2 alter the autophagic/lysosomal response to starvation.

Rodent models of amyotrophic lateral sclerosis.

Overexpression of human wild-type FUS causes progressive motor neuron degeneration in an age- and dose-dependent fashion.

Widespread iron-rich conditions in the mid-Proterozoic ocean.

Pathogenic LRRK2 mutations do not alter gene expression in cell model systems or human brain tissue.

Is billboard advertising beneficial for healthcare organizations? An investigation of efficacy and acceptability to patients.

Centrotemporal sharp wave EEG trait in rolandic epilepsy maps to Elongator Protein Complex 4 (ELP4).

Recognition and management of pediatric seizures.

Subacute sclerosing panencephalitis with atypical features.

Field research in humanitarian medical programmes. Treatment of neuropathic pain in Sierra Leone.

Referrals to a secondary care dental clinic for anxious adult patients: implications for treatment.