A Patient Case of Malan Syndrome Involving 19p13.2 Deletion of NFIX with Longitudinal Follow-Up and Future Prospectives von Makker, Simran, Gagnon, Bernadine R, Trew, Isabella, Mougios, Vivian, Hanna, Anne, Cale, Jessica M, McIntosh, Craig S

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High Risk of Reading Disability and Speech Sound Disorder in Rolandic Epilepsy Families: Case–Control Study von 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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Identification and Remediation of Phonological and Motor Errors in Acquired Sound Production Impairment von Buchwald, Adam, Gagnon, Bernadine, Miozzo, Michele

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An autosomal dominant genetically heterogeneous variant of rolandic epilepsy and speech disorder von 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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