The parent and family impact of CLN3 disease: an observational survey-based study von Schulz, Angela, Patel, Nita, Brudvig, Jon J, Stehr, Frank, Weimer, Jill M, Augustine, Erika F

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Classification and Natural History of the Neuronal Ceroid Lipofuscinoses von Mink, Jonathan W., Augustine, Erika F., Adams, Heather R., Marshall, Frederick J., Kwon, Jennifer M.

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Sex Differences in Clinical Features of Early, Treated Parkinson's Disease von Augustine, Erika F, Pérez, Adriana, Dhall, Rohit, Umeh, Chizoba C, Videnovic, Aleksandar, Cambi, Franca, Wills, Anne-Marie A, Elm, Jordan J, Zweig, Richard M, Shulman, Lisa M, Nance, Martha A, Bainbridge, Jacquelyn, Suchowersky, Oksana

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Assessing the integrity of auditory sensory memory processing in CLN3 disease (Juvenile Neuronal Ceroid Lipofuscinosis (Batten disease)): an auditory evoked potential study of the... von Brima, Tufikameni, Freedman, Edward G, Prinsloo, Kevin D, Augustine, Erika F, Adams, Heather R, Wang, Kuan Hong, Mink, Jonathan W, Shaw, Luke H, Mantel, Emma P, Foxe, John J

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N-of-1 Studies in an Era of Precision Medicine von Augustine, Erika F, Yu, Timothy W, Finkel, Richard S

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The Psychiatric Care of Children and Young Adults With Neurodegenerative Diseases von Hauptman, Aaron J., Augustine, Erika F., Brown, Heather B.

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Utilizing the Un-Meeting model to advance innovative translational and team science von Augustine, Erika F, Steele, Scott J, McIntosh, Scott, Sugarwala, Laura, White, Robert J, Yousefi-Nooraie, Reza, Zand, Martin S, Ossip, Deborah J

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Clinical Trials in Rare Disease: Challenges and Opportunities von Augustine, Erika F., Adams, Heather R., Mink, Jonathan W.

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No sex differences in use of dopaminergic medication in early Parkinson disease in the US and Canada - baseline findings of a multicenter trial von Umeh, Chizoba C, Pérez, Adriana, Augustine, Erika F, Dhall, Rohit, Dewey, Jr, Richard B, Mari, Zoltan, Simon, David K, Wills, Anne-Marie A, Christine, Chadwick W, Schneider, Jay S, Suchowersky, Oksana

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A human model of Batten disease shows role of CLN3 in phagocytosis at the photoreceptor–RPE interface von Tang, Cynthia, Han, Jimin, Dalvi, Sonal, Manian, Kannan, Winschel, Lauren, Volland, Stefanie, Soto, Celia A., Galloway, Chad A., Spencer, Whitney, Roll, Michael, Milliner, Caroline, Bonilha, Vera L., Johnson, Tyler B., Latchney, Lisa, Weimer, Jill M., Augustine, Erika F., Mink, Jonathan W., Gullapalli, Vamsi K., Chung, Mina, Williams, David S., Singh, Ruchira

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Un-Meetings as tools for translational idea generation: A semantic content analysis of an Opioid Crisis Un-Meeting von Yousefi Nooraie, Reza, White, Robert J, Steele, Scott, Augustine, Erika F, Ossip, Deborah J, Zand, Martin S

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Challenges of Phenotype-Genotype Correlations in Rare Diseases von Masten, Margaux C, Augustine, Erika F, Mink, Jonathan W

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The state-of-the-art of N-of-1 therapies and the IRDiRC N-of-1 development roadmap von Jonker, Anneliene H., Tataru, Elena-Alexandra, Graessner, Holm, Dimmock, David, Jaffe, Adam, Baynam, Gareth, Davies, James, Mitkus, Shruti, Iliach, Oxana, Horgan, Rich, Augustine, Erika F., Bateman-House, Alison, Pasmooij, Anna Maria Gerdina, Yu, Tim, Synofzik, Matthis, Douville, Julie, Lapteva, Larissa, Brooks, Philip John, O’Connor, Daniel, Aartsma-Rus, Annemieke

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Recognizing and Responding to the Needs of Future Child and Adult Neurology Care Through the Evolution of Residency Training von McArthur, Justin Charles, Augustine, Erika F., Carmichael, S. Thomas, Ferriero, Donna M., Jensen, Frances E., Jeste, Shafali S., Jordan, Lori C., Llinas, Rafael H., Schlaggar, Bradley L., Sun, Lisa R., Pomeroy, Scott L.

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The Care Continuum: An Evolving Model for Care and Research in Rare Diseases von Augustine, Erika F, Dorsey, E Ray, Saltonstall, Peter L

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Experimental Neurotherapeutics: Surfing the Tidal Wave of New Opportunities von Reoma, Lauren B., Busza, Ania, Mouradian, M. Maral, Kaufmann, Petra, Augustine, Erika F., Frank, Samuel, Sutula, Thomas P., Cole, Andrew J., Fitter, Heather D., Meurer, William, Nath, Avindra, Griggs, Robert C.

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The CLN3 Disease Staging System: A new tool for clinical research in Batten disease von Masten, Margaux C., Williams, Justin D., Vermilion, Jennifer, Adams, Heather R., Vierhile, Amy, Collins, Alyssa, Marshall, Frederick J., Augustine, Erika F., Mink, Jonathan W.

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Clinical pearls and scientific advancement: Reconciling tradition with new knowledge von Augustine, Erika F, Gilbert, Donald L

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Delineation of the movement disorders associated with FOXG1 mutations von Papandreou, Apostolos, Schneider, Ruth B, Augustine, Erika F, Ng, Joanne, Mankad, Kshitij, Meyer, Esther, McTague, Amy, Ngoh, Adeline, Hemingway, Cheryl, Robinson, Robert, Varadkar, Sophia M, Kinali, Maria, Salpietro, Vincenzo, OʼDriscoll, Margaret C, Basheer, S Nigel, Webster, Richard I, Mohammad, Shekeeb S, Pula, Shpresa, McGowan, Marian, Trump, Natalie, Jenkins, Lucy, Elmslie, Frances, Scott, Richard H, Hurst, Jane A, Perez-Duenas, Belen, Paciorkowski, Alexander R, Kurian, Manju A

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Management of CLN1 Disease: International Clinical Consensus von Augustine, Erika F., Adams, Heather R., de los Reyes, Emily, Drago, Kristen, Frazier, Margie, Guelbert, Norberto, Laine, Minna, Levin, Tanya, Mink, Jonathan W., Nickel, Miriam, Peifer, Danielle, Schulz, Angela, Simonati, Alessandro, Topcu, Meral, Turunen, Joni A., Williams, Ruth, Wirrell, Elaine C., King, Sharon

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