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Kirshenbaum GS, Burgess CR, Dery N, Fahnestock M, Peever JH, Roder JC. “Attenuation of Mania-Like Behavior in Na(+), K(+)-ATPase α3 Mutant Mice by Prospective Therapies for Bipolar Disorder: Melatonin and Exercise.” Neuroscience (February 2014): 195-204.

Kirshenbaum GS, Clapcote SJ, Duffy S, Burgess CR, Petersen J, Jarowek KJ, Yucel YH, Cortez MA, Snead OC 3rd, Vilsen B, Peever, JH, Ralph MR, Roder JC. “Mania-like Behavior Induced by Genetic Dysfunction of the Neuron-specific Na+,K+-ATPase α3 Sodium Pump.” Proc Natl Acad Sci U S A. 2011 Nov 1; 108(44): 18144-18149.

Kirshenbaum GS, Clapcote SJ, Petersen J, Vilsen B, Ralph MR, Roder JC. “Genetic Suppression of Agrin Reduces Mania-Like Behavior in Na+, K+-ATPase a3 Mutant Mice.” Genes Brain and Behavior (June 2012): 436-443.

Ulate-Campos A, Fons C, Campistol J, Martorell L, Cancho-Cadela R, Eiris J, Lopez-Laso E, Pineda M, Sans A, Velazquez R. “Alternating Hemiplegia of Childhood: ATP1A3 Gene Analysis in 16 Patients.” Med Clin (Barc) April 23, 2014. (in Spanish)

Kirshenbaum GS, Dachtler J, Roder JC, Clapcote SJ. “Characterization of Cognitive Deficits in Mice with an Alternating Hemiplegia-linked Mutation.” Behavioral Neuroscience (2015): 822–831.

Ulate-Campos A, Fons C, Artuch R, Castejon E, Martorell L, Ozelius L, Pascual J, Campistol J. “Alternating Hemiplegia of Childhood with a De Novo Mutation in APT1A3 and Changes in SLC2A1 Responsive to Ketogenic Diet.” Pediatric Neurology (December 6, 2013).

Kirshenbaum GS, Dachtler J, Roder JC, Clapcote SJ. “Transgenic Rescue of Phenotypic Deficits in a Mouse Model of Alternating Hemiplegia of Childhood.” Neurogenetics (2016): 57–63.
Kirshenbaum, GS, Dawson, N, Mullins, JG, Johnston, TH, Drinkhill, MJ, Edwards, IJ, Fox SH, Pratt, JA, Brotchie, JM, Roder, JC, Clapcote, SJ. “Alternating Hemiplegia of Childhood-Related Neural and Behavioural Phenotypes in Na+K+-ATPase a3 Missense Mutant Mice.” PLos ONE 2013; 8(3).

Wei W, Zheng XF, Ruan DD, Gan YM, Zhang YP, Chen Y, Lin XF, Tang FQ, Luo JW, Li YF. Different phenotypes of neurological diseases, including alternating hemiplegia of childhood and rapid-onset dystonia-parkinsonism, caused by de novo ATP1A3 mutation in a family. Neurol Sci. 2022 Apr;43(4):2555-2563. Abstract: https://pubmed.ncbi.nlm.nih.gov/34783933/

Kirshenbaum GS, Idris NF, Dachtler J, Roder JC, Clapcote SJ. “Deficits in Social Behavioral Tests in a Mouse Model of Alternating Hemiplegia of Childhood.” J Neurogenet. 2016 Mar 30; 8(3): 42-49.

Weigand KM, Messchaert M, Swarts HG, Russel FG, Koenderink JB. “Alternating Hemiplegia of Childhood Mutations Have a Differential Effect on Na(+).K(+)-ATPase Activity and Ouabain Binding.” Biochim Biophys Acta (July 2014).