Daniel L. Hurst

ILAE classification of the epilepsies: Position paper of the ILAE Commission for Classification and Terminology

The French and North American phenotypes of pyruvate carboxylase deficiency, correlation with biotin containing protein by 3H-biotin incorporation, 35S-streptavidin labeling, and Northern blotting with a cloned cDNA probe.

Bcl-2 is an inner mitochondrial membrane protein that blocks programmed cell death

Sequential MRI, SPECT and PET in respiratory syncytial virus encephalitis

PHF8, a gene associated with cleft lip/palate and mental retardation, encodes for an Nε-dimethyl lysine demethylase

The genetic landscape of the epileptic encephalopathies of infancy and childhood

Pediatric Multiple Sclerosis

Causes of encephalitis and differences in their clinical presentations in England: a multicentre, population-based prospective study

Diagnostic criteria for multiple sclerosis: 2010 Revisions to the McDonald criteria

New hypotheses for the health-protective mechanisms of whole-grain cereals: what is beyond fibre?

Neurologic Complications in Children with Enterovirus 71 Infection

Varicella‐Zoster Virus: Atypical Presentations and Unusual Complications

X-linked mental retardation associated with cleft lip/palate maps to Xp11.3-q21.3

Human Coronaviruses and Other Respiratory Viruses: Underestimated Opportunistic Pathogens of the Central Nervous System?

Prevention of herpes zoster: recommendations of the Advisory Committee on Immunization Practices (ACIP).

Inheritable Biotin-Treatable Disorders and Associated Phenomena

Epidemiology of Severe Myoclonic Epilepsy of Infancy

Acute cerebellar swelling in varicella encephalitis

Phenotypic variation in biotinidase deficiency

Use of Modafinil in Spastic Cerebral Palsy

X-linked hypogonadism, gynecomastia, mental retardation, short stature, and obesity—a new syndrome