Identification of genomic deletions spanning the PCDH19 gene in two unrelated girls with intellectual disability and seizures von Vincent, AK, Noor, A, Janson, A, Minassian, BA, Ayub, M, Vincent, JB, Morel, CF

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Lafora disease: Current biology and therapeutic approaches von Mitra, S., Gumusgoz, E., Minassian, B.A.

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Progressive myoclonus epilepsy with polyglucosans (Lafora disease): Evidence for a third locus von CHAN, E. M, OMER, S, AHMED, M, BRIDGES, L. R, BENNETT, C, SCHERER, S. W, MINASSIAN, B. A

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Genetic diagnosis in Lafora disease : Genotype-phenotype correlations and diagnostic pitfalls von LOHI, H, TURNBULL, J, ZHAO, X. C, PULLENAYEGUM, S, IANZANO, L, YAHYAOUI, M, MIKATI, M. A, FRANCESCHETTI, S, ZARA, F, MINASSIAN, B. A

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Mutation spectrum and predicted function of laforin in Lafora's progressive myoclonus epilepsy von MINASSIAN, B. A, IANZANO, L, MELOCHE, M, ANDERMANN, E, ROULEAU, G. A, DELGADO-ESCUETA, A. V, SCHERER, S. W

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Genetic mapping of a new Lafora progressive myoclonus epilepsy locus (EPM2B) on 6p22 von Chan, E M, Bulman, D E, Paterson, A D, Turnbull, J, Andermann, E, Andermann, F, Rouleau, G A, Delgado-Escueta, A V, Scherer, S W, Minassian, B A

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Skin biopsy in Lafora disease: Genotype-phenotype correlations and diagnostic pitfalls von ANDRADE, D. M, ACKERLEY, C. A, MINETT, T. S. C, TEIVE, H. A. G, BOHLEGA, S, SCHERER, S. W, MINASSIAN, B. A

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Magnetoencephalographic localization in pediatric epilepsy surgery: Comparison with invasive intracranial electroencephalography von Minassian, Berge A., Otsubo, Hiroshi, Weiss, Shelly, Elliott, Irene, Rutka, James T., Snead III, O. Carter

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FINE-MAPPING THE GENE FOR X-LINKED MYOPATHY WITH EXCESSIVE AUTOPHAGY von MUNTEANU, I, RAMACHANDRAN, N, MNATZAKANIAN, G. N, VILLANOVA, M, FARDEAU, M, LEVY, N, KISSEL, J. T, MINASSIAN, B. A

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Non-coding VMA21 deletions cause X-linked Myopathy with Excessive Autophagy von Ruggieri, A, Ramachandran, N, Wang, P, Haan, E, Kneebone, C, Manavis, J, Morandi, L, Moroni, I, Blumbergs, P, Mora, M, Minassian, B.A

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NHLRC1 repeat expansion in two beagles with Lafora disease von Hajek, I., Kettner, F., Simerdova, V., Rusbridge, C., Wang, P., Minassian, B. A., Palus, V.

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Lafora disease: a case report, pathologic and genetic study von Harirchian, M H, Shandiz, E Esmailee, Turnbull, J, Minassian, B A, Shahsiah, R

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Angelman syndrome: Correlations between epilepsy phenotypes and genotypes von Minassian, Berge A., Delorey, Timothy M., Olsen, Richard W., Philippart, Michel, Bronstein, Yuri, Zhang, Quanwei, Guerrini, Renzo, van Ness, Paul, Livet, Marie O., Delgado-Escueta, Antonio V.

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Nonepileptic visual hallucinations in Lafora disease von ANDRADE, D. M, DEL CAMPO, J. M, MORO, E, MINASSIAN, B. A, WENNBERG, R. A

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Narrowing in on the causative defect of an intriguing X-linked myopathy with excessive autophagy von MINASSIAN, B. A, AIYAR, R, KALIMO, H, ALIC, S, BANWELL, B, VILLANOVA, M, FARDEAU, M, MANDELL, J. W, JUEL, V. C, RAFII, M, AURANEN, M

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Lafora’s disease: towards a clinical, pathologic, and molecular synthesis von Minassian, Berge A

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Electrophysiology extends the phenotypic spectrum of X-linked myopathy with excessive autophagy von MUNTEANU, I, ACKERLEY, C. A, MNATZAKANIAN, G. N, KISSEL, J. T, MINASSIAN, B. A

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LAFORA BODIES IN SKELETAL MUSCLE ARE FIBER TYPE SPECIFIC von TURNBULL, J, GIRARD, J.-M, PENCEA, N, ZHAO, X, GRAHAM, T. E, WANG, P, ACKERLEY, C. A, MINASSIAN, B. A

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EEG in asymptomatic relatives of idiopathic epilepsy; a prospective study von Duaa, BM, Boelman, C, Brunga, L, Minassian, BA, Andrade, D

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Identification of new and common mutations in the EPM2A gene in Lafora disease von MINASSIAN, B. A, IANZANO, L, DELGADO-ESCUETA, A. V, SCHERER, S. W

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