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Correction: Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry.
PLoS One. 2015 Aug 31;10(8):e0137370. doi: 10.1371/journal.pone.0137370. eCollection 2015.
PLoS One. 2015.
PMID: 26322789
Free PMC article.
No abstract available.
Alternating Hemiplegia of Childhood: Retrospective Genetic Study and Genotype-Phenotype Correlations in 187 Subjects from the US AHCF Registry.
Viollet L, Glusman G, Murphy KJ, Newcomb TM, Reyna SP, Sweney M, Nelson B, Andermann F, Andermann E, Acsadi G, Barbano RL, Brown C, Brunkow ME, Chugani HT, Cheyette SR, Collins A, DeBrosse SD, Galas D, Friedman J, Hood L, Huff C, Jorde LB, King MD, LaSalle B, Leventer RJ, Lewelt AJ, Massart MB, Mérida MR 2nd, Ptáček LJ, Roach JC, Rust RS, Renault F, Sanger TD, Sotero de Menezes MA, Tennyson R, Uldall P, Zhang Y, Zupanc M, Xin W, Silver K, Swoboda KJ.
Viollet L, et al. Among authors: cheyette sr.
PLoS One. 2015 May 21;10(5):e0127045. doi: 10.1371/journal.pone.0127045. eCollection 2015.
PLoS One. 2015.
PMID: 25996915
Free PMC article.
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Lamotrigine-induced tic disorder: report of five pediatric cases.
Sotero de Menezes MA, Rho JM, Murphy P, Cheyette S.
Sotero de Menezes MA, et al.
Epilepsia. 2000 Jul;41(7):862-7. doi: 10.1111/j.1528-1157.2000.tb00254.x.
Epilepsia. 2000.
PMID: 10897158
Free article.
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Encephalitis lethargica: lessons for contemporary neuropsychiatry.
Cheyette SR, Cummings JL.
Cheyette SR, et al.
J Neuropsychiatry Clin Neurosci. 1995 Spring;7(2):125-34. doi: 10.1176/jnp.7.2.125.
J Neuropsychiatry Clin Neurosci. 1995.
PMID: 7626955
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Agenesis of the mesencephalon and metencephalon with cerebellar hypoplasia: putative mutation in the EN2 gene--report of 2 cases in early infancy.
Sarnat HB, Benjamin DR, Siebert JR, Kletter GB, Cheyette SR.
Sarnat HB, et al. Among authors: cheyette sr.
Pediatr Dev Pathol. 2002 Jan-Feb;5(1):54-68. doi: 10.1007/s10024-001-0103-5.
Pediatr Dev Pathol. 2002.
PMID: 11815869
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