Loss of Perivascular Kir4.1 Potassium Channels in the Sclerotic Hippocampus of Patients With Mesial Temporal Lobe Epilepsy

Evidence that compromised K+ spatial buffering contributes to the epileptogenic effect of mutations in the human kir4.1 gene (KCNJ10)

(2011) Nadia Nabil Haj-Yasein et al.   GLIA

Monocarboxylate transporter 1 is deficient on microvessels in the human epileptogenic hippocampus

(2010) Fredrik Lauritzen et al.   NEUROBIOLOGY OF DISEASE

Calpains and Delayed Calcium Deregulation in Excitotoxicity

(2010) Inês M. Araújo et al.   NEUROCHEMICAL RESEARCH

Astrocytes and epilepsy

(2010) Nihal C. Lanerolle et al.   Neurotherapeutics

The neurobiology of the dystrophin-associated glycoprotein complex

(2009) Adrian Waite et al.   ANNALS OF MEDICINE

Variants of the genes encoding AQP4 and Kir4.1 are associated with subgroups of patients with temporal lobe epilepsy

(2009) Kjell Heuser et al.   EPILEPSY RESEARCH

Epilepsy, Ataxia, Sensorineural Deafness, Tubulopathy, andKCNJ10Mutations

(2009) Detlef Bockenhauer et al.   NEW ENGLAND JOURNAL OF MEDICINE

Seizures, sensorineural deafness, ataxia, mental retardation, and electrolyte imbalance (SeSAME syndrome) caused by mutations in KCNJ10

(2009) U. I. Scholl et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA