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Practical Approach to Longitudinal Neurologic Care of Adults With X-Linked Adrenoleukodystrophy and Adrenomyeloneuropathy Kornbluh, Alexandra B.; Baldwin, Aaron; Fatemi, Ali; Vanderver, Adeline; Adang, Laura A.; Van Haren, Keith; Sampson, Jacinda; Eichler, Florian S.; Sadjadi, Reza; Engelen, Marc; Orthmann-Murphy, Jennifer L. Share Save
Consensus guidelines for the monitoring and management of metachromatic leukodystrophy in the United States Adang, Laura A.; Bonkowsky, Joshua L.; Boelens, Jaap Jan; Mallack, Eric; Ahrens-Nicklas, Rebecca; Bernat, John A.; Bley, Annette; Burton, Barbara; Darling, Alejandra; Eichler, Florian; Eklund, Erik; Emrick, Lisa; Escolar, Maria; Fatemi, Ali; Fraser, Jamie L.; Gaviglio, Amy; Keller, Stephanie; Patterson, Marc C.; Orchard, Paul; Orthmann-Murphy, Jennifer; Santoro, Jonathan D.; Schoels, Ludger; Sevin, Caroline; Srivastava, Isha N.; Rajan, Deepa; Rubin, Jennifer P.; Van Haren, Keith; Wasserstein, Melissa; Zerem, Ayelet; Fumagalli, Francesca; Laugwitz, Lucia; Vanderver, Adeline Share Save
Disparities in Genetic Testing for Neurologic Disorders Baldwin, Aaron; Copeland, Juliette; Azage, Meron; Dratch, Laynie; Johnson, Kelsey; Paul, Rachel A.; Amado, Defne A.; Baer, Michael; Deik, Andres; Elman, Lauren B.; Guo, Michael; Hamedani, Ali G.; Irwin, David J.; Lasker, Aaron; Orthmann-Murphy, Jennifer; Quinn, Colin C.; Tropea, Thomas F.; Scherer, Steven S.; Shinohara, Russell T.; Hamilton, Roy H.; Ellis, Colin A. Share Save
A Prospective Natural History Study of Patients with Adult-Onset Leukoencephalopathy with Axonal Spheroids and Pigmented Glia (ALSP) Rajagovindan, Raj; Matys, Benjamin; Finger, Elizabeth; Gelfand, Jeffrey; Isaacson, Stuart; Koehler, Wolfgang; Kumar, Rajeev; Lynch, David; Orthmann-Murphy, Jennifer; Schoels, Ludger; Wolf, Nicole; Meier, Andreas; Papapetropoulos, Spyridon; Wszolek, Zbigniew Share Save
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Diagnosis and management of glycogen storage disease type IV, including adult polyglucosan body disease: A clinical practice resource Koch, Rebecca L.; Soler-Alfonso, Claudia; Kiely, Bridget T.; Asai, Akihiro; Smith, Ariana L.; Bali, Deeksha S.; Kang, Peter B.; Landstrom, Andrew P.; Akman, H. Orhan; Burrow, T. Andrew; Orthmann-Murphy, Jennifer L.; Goldman, Deberah S.; Pendyal, Surekha; El-Gharbawy, Areeg H.; Austin, Stephanie L.; Case, Laura E.; Schiffmann, Raphael; Hirano, Michio; Kishnani, Priya S. Share Save
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Lineage tracing reveals dynamic changes in oligodendrocyte precursor cells following cuprizone-induced demyelination Baxi, Emily G.; DeBruin, Joseph; Jin, Jing; Strasburger, Hayley J.; Smith, Matthew D.; Orthmann-Murphy, Jennifer L.; Schott, Jason T.; Fairchild, Amanda N.; Bergles, Dwight E.; Calabresi, Peter A. Share Save
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Hereditary spastic paraplegia is a novel phenotype for GJA12/GJC2 mutations Orthmann-Murphy, Jennifer L.; Salsano, Ettore; Abrams, Charles K.; Bizzi, Alberto; Uziel, Graziella; Freidin, Mona M.; Lamantea, Eleonora; Zeviani, Massimo; Scherer, Steven S.; Pareyson, Davide Share Save
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