Jong M. Rho

Acetoacetate, acetone, and dibenzylamine (a contaminant in l-(+)-beta-hydroxybutyrate) exhibit direct anticonvulsant actions in vivo.

Ictal EEG patterns in band heterotopia.

Clinical and electrographic features of epileptic spasms persisting beyond the second year of life.

Age-dependent differences in flurothyl-induced c-fos and c-jun mRNA expression in the mouse brain.

Molecular biology and ontogeny of gamma-aminobutyric acid (GABA) receptors in the mammalian central nervous system.

Calorie restriction and ketogenic diet diminish neuronal excitability in rat dentate gyrus in vivo.

Intravenous immunoglobulin as adjunctive therapy for juvenile spasms.

Voltage-dependent block of N-methyl-D-aspartate receptors by the novel anticonvulsant dibenzylamine, a bioactive constituent of L-(+)-beta-hydroxybutyrate.

The ketogenic diet increases mitochondrial uncoupling protein levels and activity.

Molecular biology and ontogeny of glutamate receptors in the mammalian central nervous system.

Basic science behind the catastrophic epilepsies.

A cDNA microarray analysis of gene expression profiles in rat hippocampus following a ketogenic diet.

Lack of long-term histopathologic changes in brain and skeletal muscle of mice treated with a ketogenic diet.

Clinical experience with zonisamide monotherapy and adjunctive therapy in children with epilepsy at a tertiary care referral center.

Electrophysiological properties of human hypothalamic hamartomas.

Impaired motor control in patients with benign focal epilepsy of childhood.

Anticonvulsant mechanisms of the ketogenic diet.

Ketone bodies are protective against oxidative stress in neocortical neurons.

Electrophysiological properties and subunit composition of GABAA receptors in patients with gelastic seizures and hypothalamic hamartoma.

The ketogenic diet: stoking the powerhouse of the cell.

Hypothalamic hamartoma: basic mechanisms of intrinsic epileptogenesis.

Do seizures affect the developing brain? Lessons from the laboratory.

Substantia(ting) ketone body effects on neuronal excitability.

GABAA receptor-mediated activation of L-type calcium channels induces neuronal excitation in surgically resected human hypothalamic hamartomas.

Fasting is neuroprotective following traumatic brain injury.

The ketogenic diet and epilepsy.

Can reducing sugar retard kindling?

Oxidative impairment of hippocampal long-term potentiation involves activation of protein phosphatase 2A and is prevented by ketone bodies.

GABA(A) receptor-mediated excitation in dissociated neurons from human hypothalamic hamartomas.

Optimal clinical management of children receiving the ketogenic diet: recommendations of the International Ketogenic Diet Study Group.

The neuroprotective properties of calorie restriction, the ketogenic diet, and ketone bodies.

Bicarbonate contributes to GABAA receptor-mediated neuronal excitation in surgically resected human hypothalamic hamartomas.

Epilepsia. Ketogenic diet and treatments. Introduction/perspectives.

UCP-mediated free fatty acid uncoupling of isolated cortical mitochondria from fasted animals: correlations to dietary modulations.

The ketogenic diet in a pill: is this possible?

Ketogenic diets: evidence for short- and long-term efficacy.

Arresting a seizure by dropping a little Acid.

Ketogenic diet treatment abolishes seizure periodicity and improves diurnal rhythmicity in epileptic Kcna1-null mice.

Reversible lamotrigine-induced neurobehavioral disturbances in children with epilepsy.

Ketogenic diets: an update for child neurologists.

Anticonvulsant effects of the selective melatonin receptor agonist ramelteon.

Ketones prevent synaptic dysfunction induced by mitochondrial respiratory complex inhibitors.

A "happy" toddler presenting with sudden, life-threatening seizures.

The ketogenic diet reverses gene expression patterns and reduces reactive oxygen species levels when used as an adjuvant therapy for glioma.

Another Look at Early GABAergic Neurotransmission: Maybe It's Not So Exciting After All!

How does altered metabolism lead to seizure control? Partially filling the knowledge gap.

Pediatric neuropharmacotherapeutics. Introduction.

L-Type calcium channel blockade reduces network activity in human epileptic hypothalamic hamartoma tissue.

Pediatric stroke.

Ketogenic diet in the treatment of seizures associated with hypothalamic hamartomas.

The ketogenic diet: what has science taught us?

Adenosine: a fundamental factor formed from Fatty feasts for fighting fits?

The ketogenic diet as a treatment paradigm for diverse neurological disorders.

The ketogenic diet is an effective adjuvant to radiation therapy for the treatment of malignant glioma.

Inflammation-mediated memory dysfunction and effects of a ketogenic diet in a murine model of multiple sclerosis.

Finding a better drug for epilepsy: antiepileptogenesis targets.

Sweets Are BAD for Seizures.

Unilateral Foot Drop as an Initial Presentation of a Brain Tumor in a Child.

Loss of the Kv1.1 potassium channel promotes pathologic sharp waves and high frequency oscillations in in vitro hippocampal slices.

High dose folic acid supplementation of rats alters synaptic transmission and seizure susceptibility in offspring.

Ketogenic diet improves core symptoms of autism in BTBR mice.

Ketogenic Diets, Mitochondria and Neurological Diseases.

Inorganic polyphosphate regulates neuronal excitability through modulation of voltage-gated channels.