Precipitous Deterioration of Motor Function, Cognition, and Behavior
JAMA Neurol 74:591-596, Fernandez-Fournier, M.,et al, 2017
Heterozygous de-Novo Mutations in ATP1A3 in Patients with Alternating Hemiplegia of Childhood:A Whole-Exome Sequencing Gene-Identification Study
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Late onset autism and anti-NMDA-receptor encephalitis
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Clinicopath Conf, Rapid-Onset-Dystonia-Parkinsonism Due to a Mutation in the ATP1A3 Gene
NEJM 362:2213-2219, Case 17-2010, 2010
Anterior Opercular Syndrome, Caused by Herpes Simplex Encephalitis
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Acute Pseudobulbar Mutism with Good Functional Recovery
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Congenital Bilateral Perisylvian Syndrome:Study of 31 Patients
Lancet 341:608-612, Kuzniecky,R.,et al, 1993
Primary Lateral Sclerosis, Clin Features, Neuropath & Dx Criteria
Brain 115:495-520, Pringle,C.E.,et al, 1992
Dysphagia, Speech Disorders and Centrotemporal Spikes-Waves
Arch Francaises De Pediatrie 47:115-117, Boulloche,J.,et al, 1990
Chronic Progressive Spinobulbar Spasticity, A Rare Form of Primary Lateral Sclerosis
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Diagnosis of Treatable Wilson's Disease
NEJM 298:1347, Cartwright,G.E., 1978
Neuromuscular Disease in Primary Hyperparathyroidism
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