Ohcanbohtosat - Kruer, Michael C

The Neuropathology of Neurodegeneration with Brain Iron Accumulation Dahkki Kruer, Michael C.

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Neurodegeneration with brain iron accumulation: a diagnostic algorithm Dahkki Kruer, Michael C., Boddaert, Nathalie

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Newly Characterized Forms of Neurodegeneration with Brain Iron Accumulation Dahkki Doorn, Joshua M., Kruer, Michael C.

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Prospects for stem cell therapy in Neuronal Ceroid Lipofuscinosis Dahkki Kruer, Michael C., Pearce, David A., Orchard, Paul J., Steiner, Robert D.

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Variability in Cerebral Palsy Diagnosis Dahkki Aravamuthan, Bhooma R., Fehlings, Darcy, Shetty, Sheetal, Fahey, Michael, Gilbert, Laura, Tilton, Ann, Kruer, Michael C.

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Cataplexy in Patients Harboring the KCNMA1 p.N999S Mutation Dahkki Heim, Jennifer, Vemuri, Anusha, Lewis, Sara, Guida, Brandon, Troester, Matthew, Keros, Sotirios, Meredith, Andrea, Kruer, Michael C.

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Dystonia in ATP2B3-associated X-linked Spinocerebellar Ataxia Dahkki Feyma, Timothy, Ramsey, Keri, Huentelman, Matthew J., Craig, David W., Padilla-Lopez, Sergio, Narayanan, Vinodh, Kruer, Michael C.

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Aggressive Course in Encephalitis With Opsoclonus, Ataxia, Chorea, and Seizures: The First Pediatric Case of γ-Aminobutyric Acid Type B Receptor Autoimmunity Dahkki Kruer, Michael C., Hoeftberger, Romana, Lim, Kit Yeng, Coryell, Jason C., Svoboda, Melissa D., Woltjer, Randall L., Dalmau, Josep

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Lisdexamfetamine Therapy in Paroxysmal Non‐kinesigenic Dyskinesia Associated with the KCNMA1‐N999S Variant Dahkki Keros, Sotirios, Heim, Jennifer, Hakami, Wejdan, Zohar‐Dayan, Efrat, Ben‐Zeev, Bruria, Grinspan, Zach, Kruer, Michael C., Meredith, Andrea L.

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Novel histopathologic findings in molecularly-confirmed pantothenate kinase-associated neurodegeneration Dahkki Kruer, Michael C., Hiken, Mark, Gregory, Allison, Malandrini, Alessandro, Clark, David, Hogarth, Penny, Grafe, Marjorie, Hayflick, Susan J., Woltjer, Randall L.

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Lessons from a pair of siblings with BPAN Dahkki Zarate, Yuri A, Jones, Julie R, Jones, Melanie A, Millan, Francisca, Juusola, Jane, Vertino-Bell, Annette, Schaefer, G Bradley, Kruer, Michael C

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Lessons from a pair of siblings with BPAN Dahkki Zarate, Yuri A, Jones, Julie R, Jones, Melanie A, Millan, Francisca, Juusola, Jane, Vertino-Bell, Annette, Schaefer, G Bradley, Kruer, Michael C

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Insights From Genetic Studies of Cerebral Palsy Dahkki Lewis, Sara A., Shetty, Sheetal, Wilson, Bryce A., Huang, Aris J., Jin, Sheng Chih, Smithers-Sheedy, Hayley, Fahey, Michael C., Kruer, Michael C.

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Recessive COL4A2 Mutation Leads to Intellectual Disability, Epilepsy, and Spastic Cerebral Palsy Dahkki Bakhtiari, Somayeh, Tafakhori, Abbas, Jin, Sheng Chih, Guida, Brandon S., Alehabib, Elham, Firouzbadi, Saghar, Bilguvar, Kaya, Fahey, Michael C., Darvish, Hossein, Kruer, Michael C.

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Is Resting State Functional MRI Effective Connectivity in Movement Disorders Helpful? A Focused Review Across Lifespan and Disease Dahkki Sussman, Bethany L., Wyckoff, Sarah N., Heim, Jennifer, Wilfong, Angus A., Adelson, P. David, Kruer, Michael C., Gonzalez, Maria Jose, Boerwinkle, Varina L.

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Identification of Somatic Chromosomal Abnormalities in Hypothalamic Hamartoma Tissue at the GLI3 Locus Dahkki Craig, David W., Itty, Abraham, Panganiban, Corrie, Szelinger, Szabolcs, Kruer, Michael C., Sekar, Aswin, Reiman, David, Narayanan, Vinodh, Stephan, Dietrich A., Kerrigan, John F.

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Analysis of ATP13A2 in large neurodegeneration with brain iron accumulation (NBIA) and dystonia-parkinsonism cohorts Dahkki Kruer, Michael C., Paudel, Reema, Wagoner, Wendy, Sanford, Lynn, Kara, Eleanna, Gregory, Allison, Foltynie, Tom, Lees, Andrew, Bhatia, Kailash, Hardy, John, Hayflick, Susan J., Houlden, Henry

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Variant recurrence confirms the existence of a FBXO31‐related spastic‐dystonic cerebral palsy syndrome Dahkki Dzinovic, Ivana, Škorvánek, Matej, Pavelekova, Petra, Zhao, Chen, Keren, Boris, Whalen, Sandra, Bakhtiari, Somayeh, Chih Jin, Sheng, Kruer, Michael C., Jech, Robert, Winkelmann, Juliane, Zech, Michael

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Identification of disease causing loci using an array-based genotyping approach on pooled DNA Dahkki Craig, David W, Huentelman, Matthew J, Hu-Lince, Diane, Zismann, Victoria L, Kruer, Michael C, Lee, Anne M, Puffenberger, Erik G, Pearson, John M, Stephan, Dietrich A

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C19orf12 mutation leads to Karak pallido-pyramidal syndrome Dahkki Kruer, Michael C., Salih, Mustafa A., Mooney, Catherine, Alzahrani, Jawahir, Elmalik, Salah A., Kabiraj, Mohammad M., Khan, Arif O., Paudel, Reema, Houlden, Henry, Azzedine, Hamid, Alkuraya, Fowzan

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