High Risk of Reading Disability and Speech Sound Disorder in Rolandic Epilepsy Families: Case–Control Study by Clarke, Tara, Strug, Lisa J., Murphy, Peregrine L., Bali, Bhavna, Carvalho, Janessa, Foster, Suzanne, Tremont, Geoffrey, Gagnon, Bernadine R., Dorta, Nelson, Pal, Deb K.

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Autosomal Dominant Inheritance of Centrotemporal Sharp Waves in Rolandic Epilepsy Families by Bali, Bhavna, Kull, Lewis L., Strug, Lisa J., Clarke, Tara, Murphy, Peregrine L., Akman, Cigdem I., Greenberg, David A., Pal, Deb K.

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An autosomal dominant genetically heterogeneous variant of rolandic epilepsy and speech disorder by Kugler, Steven L., Bali, Bhavna, Lieberman, Philip, Strug, Lisa, Gagnon, Bernadine, Murphy, Peregrine L., Clarke, Tara, Greenberg, David A., Pal, Deb K.

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Incidence and predictors of PEG placement in ALS/MND by Albert, Steven M, Murphy, Peregrine L, Del Bene, Maura, Rowland, Lewis P, Mitsumoto, Hiroshi

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Prospective study of palliative care in ALS: choice, timing, outcomes by Albert, Steven M., Murphy, Peregrine L., Del Bene, Maura L., Rowland, L.P.

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Lipoidal corneal degeneration in aged falcons by Moore, Bret A, Paul‐Murphy, Joanne R, Adamson, Kathleen L, Dubielzig, Richard R, Kern, Thomas, Gonzales, Ben J, Wolff, Peregrine, Murphy, Christopher J

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