Hakutulokset - Minassian, Berge

Post-modern therapeutic approaches for progressive myoclonus epilepsy Tekijä Minassian, Berge A.

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Efficacy and Tolerability of Perampanel in Ten Patients with Lafora Disease Tekijä Goldsmith, Danielle, Minassian, Berge A.

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Extraneurological sparing in long‐lived typical Lafora disease Tekijä Goldsmith, Danielle, Minassian, Berge A.

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From Genetic Testing to Precision Medicine in Epilepsy Tekijä Striano, Pasquale, Minassian, Berge A.

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LUBAC: a new player in polyglucosan body disease Tekijä Aboujaoude, Andrew, Minassian, Berge, Mitra, Sharmistha

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A Review of Targeted Therapies for Monogenic Epilepsy Syndromes Tekijä Zimmern, Vincent, Minassian, Berge, Korff, Christian

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Infantile spasms with periventricular nodular heterotopia, unbalanced chromosomal translocation 3p26.2 ‐10p15.1 and 6q22.31 duplication Tekijä Jones, Kevin, Weiss, Shelly K., Minassian, Berge

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Progressive Myoclonus Epilepsies: The Gene-Empowered Era Tekijä Minassian, Berge A., Striano, Pasquale, Avanzini, Giuliano

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The History of Progressive Myoclonus Epilepsies Tekijä Genton, Pierre, Striano, Pasquale, Minassian, Berge A.

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Lafora Disease: A Review of Molecular Mechanisms and Pathology Tekijä Verhalen, Brandy, Arnold, Susan, Minassian, Berge A.

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Lafora Disease: current biology and therapeutic approaches Tekijä Mitra, Sharmistha, Gumusgoz, Emrah, Minassian, Berge A.

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SUCLA2 Arg407Trp mutation can cause a nonprogressive movement disorder – deafness syndrome Tekijä Alkhater, Reem A., Ahonen, Saija, Minassian, Berge A.

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EPM2A in-frame deletion slows neurological decline in Lafora Disease Tekijä Lomax, Lysa Boissé, Verhalen, Brandy, Minassian, Berge A.

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Chromosome 12p Deletion Spanning the GRIN2B Gene Presenting With a Neurodevelopmental Phenotype: A Case Report and Review of Literature Tekijä Mishra, Navin, Kouzmitcheva, Elizabeth, Orsino, Angela, Minassian, Berge A.

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PI4K2A deficiency in an intellectual disability, epilepsy, myoclonus, akathisia syndrome Tekijä Alkhater, Reem A., Scherer, Stephen W., Minassian, Berge A., Walker, Susan

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Diabetes Mellitus in a Patient With Lafora Disease: Possible Links With Pancreatic β-Cell Dysfunction and Insulin Resistance Tekijä Nicolescu, Ramona C., Al-Khawaga, Sara, Minassian, Berge A., Hussain, Khalid

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Sexually Divergent Mortality and Partial Phenotypic Rescue After Gene Therapy in a Mouse Model of Dravet Syndrome Tekijä Niibori, Yosuke, Lee, Shiron J., Minassian, Berge A., Hampson, David R.

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Sensitive quantification of α-glucans in mouse tissues, cell cultures, and human cerebrospinal fluid Tekijä Nitschke, Silvia, Petković, Sara, Ahonen, Saija, Minassian, Berge A., Nitschke, Felix

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Ketogenic diet reduces Lafora bodies in murine Lafora disease Tekijä Israelian, Lori, Wang, Peixiang, Gabrielian, Shoghig, Zhao, Xiaochu, Minassian, Berge A.

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Fatal hepatic failure and pontine and extrapontine myelinolysis in XMEA Tekijä Ackerley, Cameron A., Cooper, Mary Anne, Munoz, David G., Minassian, Berge A.

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