Neurodegeneration with brain iron accumulation

le Gregory, Allison, Hayflick, Susan J.
Foilsithe 2005

Genetics of Neurodegeneration with Brain Iron Accumulation

le Gregory, Allison, Hayflick, Susan J.
Foilsithe in Curr Neurol Neurosci Rep (2011)

Metabolism and energy requirements in pantothenate kinase-associated neurodegeneration

le Williams, Sarah, Gregory, Allison, Hogarth, Penelope, Hayflick, Susan J., Gillingham, Melanie B.
Foilsithe in Mol Genet Metab (2013)

Brain MRI Pattern Recognition in Neurodegeneration With Brain Iron Accumulation

le Lee, Jae-Hyeok, Yun, Ji Young, Gregory, Allison, Hogarth, Penelope, Hayflick, Susan J.
Foilsithe in Front Neurol (2020)

WDR45 Mutation in Atypical Rett Syndrome with Brain Iron Accumulation

le Crisp, Sarah J., Meyer, Esther, Gregory, Allison, Archer, Hayley, Hayflick, Susan, Kurian, Manju A., de Silva, Rajith
Foilsithe in Mov Disord Clin Pract (2015)

In vivo regulatory phosphorylation of the phosphoenolpyruvate carboxylase AtPPC1 in phosphate-starved Arabidopsis thaliana

le Gregory, Allison L., Hurley, Brenden A., Tran, Hue T., Valentine, Alexander J., She, Yi-Min, Knowles, Vicki L., Plaxton, William C.
Foilsithe 2009

Clinical records organized and optimized for clinical integration and clinical decision making

le Vanderbilt, Allison A., Jain, Samay, Mayer, Sallie D., Gregory, Allison A., Ryan, Mark H., Bradner, Melissa K., Baugh, Reginald F.
Foilsithe in Int J Med Educ (2016)

A new NBIA patient from Turkey with homozygous C19ORF12 mutation

le Kasapkara, Çloğdem Seher, Tümer, Leyla, Gregory, Allison, Ezgü, Fatih, İnci, Aslı, Derinkuyu, Betül Emine, Fox, Rachel, Rogers, Caleb, Hayflick, Susan
Foilsithe in Acta Neurol Belg (2018)

Novel histopathologic findings in molecularly-confirmed pantothenate kinase-associated neurodegeneration

le Kruer, Michael C., Hiken, Mark, Gregory, Allison, Malandrini, Alessandro, Clark, David, Hogarth, Penny, Grafe, Marjorie, Hayflick, Susan J., Woltjer, Randall L.
Foilsithe 2011

Neuro-Ophthalmologic and Electroretinographic Findings in Pantothenate Kinase-Associated Neurodegeneration (formerly Hallervorden-Spatz Syndrome)

le Egan, Robert A., Weleber, Richard G., Hogarth, Penelope, Gregory, Allison, Coryell, Jason, Westaway, Shawn K., Gitschier, Jane, Das, Soma, Hayflick, Susan J.
Foilsithe 2005

Analysis of ATP13A2 in large neurodegeneration with brain iron accumulation (NBIA) and dystonia-parkinsonism cohorts

le 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
Foilsithe 2012

Alterations of Red Cell Membrane Properties in Nneuroacanthocytosis

le Siegl, Claudia, Hamminger, Patricia, Jank, Herbert, Ahting, Uwe, Bader, Benedikt, Danek, Adrian, Gregory, Allison, Hartig, Monika, Hayflick, Susan, Hermann, Andreas, Prokisch, Holger, Sammler, Esther M., Yapici, Zuhal, Prohaska, Rainer, Salzer, Ulrich
Foilsithe 2013

Correction: Alterations of Red Cell Membrane Properties in Neuroacanthocytosis

le Siegl, Claudia, Hamminger, Patricia, Jank, Herbert, Ahting, Uwe, Bader, Benedikt, Danek, Adrian, Gregory, Allison, Hartig, Monika, Hayflick, Susan, Hermann, Andreas, Prokisch, Holger, Sammler, Esther M., Yapici, Zuhal, Prohaska, Rainer, Salzer, Ulrich
Foilsithe 2013

Defective FA2H Leads to a Novel Form of Neurodegeneration with Brain Iron Accumulation (NBIA)

le Kruer, Michael C., Paisán-Ruiz, Coro, Boddaert, Nathalie, Yoon, Moon Y., Hama, Hiroko, Gregory, Allison, Malandrini, Alessandro, Woltjer, Randall L., Munnich, Arnold, Gobin, Stephanie, Polster, Brenda J., Palmeri, Silvia, Edvardson, Simon, Hardy, John, Houlden, Henry, Hayflick, Susan J.
Foilsithe in Ann Neurol (2010)

Pallidal neuronal apolipoprotein E in pantothenate kinase-associated neurodegeneration recapitulates ischemic injury to the globuspallidus

le Woltjer, Randall L., Reese, Lindsay C., Richardson, Brian E., Tran, Huong, Green, Sarah, Pham, Thao, Chalupsky, Megan, Gabriel, Isabella, Light, Tyler, Sanford, Lynn, Jeong, Suh Y., Hamada, Jeffrey, Schwanemann, Leila K., Rogers, Caleb, Gregory, Allison, Hogarth, Penelope, Hayflick, Susan J.
Foilsithe in Mol Genet Metab (2015)

Magnetic resonance imaging pattern recognition in childhood bilateral basal ganglia disorders

le Mohammad, Shekeeb S, Angiti, Rajeshwar Reddy, Biggin, Andrew, Morales-Briceño, Hugo, Goetti, Robert, Perez-Dueñas, Belen, Gregory, Allison, Hogarth, Penelope, Ng, Joanne, Papandreou, Apostolos, Bhattacharya, Kaustuv, Rahman, Shamima, Prelog, Kristina, Webster, Richard I, Wassmer, Evangeline, Hayflick, Susan, Livingston, John, Kurian, Manju, Chong, W Kling, Dale, Russell C
Foilsithe in Brain Commun (2020)

New NBIA subtype: Genetic, clinical, pathologic, and radiographic features of MPAN

le Hogarth, Penelope, Gregory, Allison, Kruer, Michael C., Sanford, Lynn, Wagoner, Wendy, Natowicz, Marvin R., Egel, Robert T., Subramony, S.H., Goldman, Jennifer G., Berry-Kravis, Elizabeth, Foulds, Nicola C., Hammans, Simon R., Desguerre, Isabelle, Rodriguez, Diana, Wilson, Callum, Diedrich, Andrea, Green, Sarah, Tran, Huong, Reese, Lindsay, Woltjer, Randall L., Hayflick, Susan J.
Foilsithe 2013

4′‐Phosphopantetheine corrects CoA, iron, and dopamine metabolic defects in mammalian models of PKAN

le Jeong, Suh Young, Hogarth, Penelope, Placzek, Andrew, Gregory, Allison M, Fox, Rachel, Zhen, Dolly, Hamada, Jeffrey, van der Zwaag, Marianne, Lambrechts, Roald, Jin, Haihong, Nilsen, Aaron, Cobb, Jared, Pham, Thao, Gray, Nora, Ralle, Martina, Duffy, Megan, Schwanemann, Leila, Rai, Puneet, Freed, Alison, Wakeman, Katrina, Woltjer, Randall L, Sibon, Ody CM, Hayflick, Susan J
Foilsithe in EMBO Mol Med (2019)

Exome Sequence Reveals Mutations in CoA Synthase as a Cause of Neurodegeneration with Brain Iron Accumulation

le Dusi, Sabrina, Valletta, Lorella, Haack, Tobias B., Tsuchiya, Yugo, Venco, Paola, Pasqualato, Sebastiano, Goffrini, Paola, Tigano, Marco, Demchenko, Nikita, Wieland, Thomas, Schwarzmayr, Thomas, Strom, Tim M., Invernizzi, Federica, Garavaglia, Barbara, Gregory, Allison, Sanford, Lynn, Hamada, Jeffrey, Bettencourt, Conceição, Houlden, Henry, Chiapparini, Luisa, Zorzi, Giovanna, Kurian, Manju A., Nardocci, Nardo, Prokisch, Holger, Hayflick, Susan, Gout, Ivan, Tiranti, Valeria
Foilsithe 2014

PLA2G6, encoding a phospholipase A(2), is mutated in neurodegenerative disorders with high brain iron

le Morgan, Neil V, Westaway, Shawn K, Morton, Jenny E V, Gregory, Allison, Gissen, Paul, Sonek, Scott, Cangul, Hakan, Coryell, Jason, Canham, Natalie, Nardocci, Nardo, Zorzi, Giovanna, Pasha, Shanaz, Rodriguez, Diana, Desguerre, Isabelle, Mubaidin, Amar, Bertini, Enrico, Trembath, Richard C, Simonati, Alessandro, Schanen, Carolyn, Johnson, Colin A, Levinson, Barbara, Woods, C Geoffrey, Wilmot, Beth, Kramer, Patricia, Gitschier, Jane, Maher, Eamonn R, Hayflick, Susan J
Foilsithe 2006