Notice by Bohan, Timothy Patrick, Bolt, Jodie Lynn, Donnelly, Joseph Herbert, Engel, Murray, Fishman, Marvin A., Frank, Yitzchak, Graf, William David, Johnston, Michael V., Mandelbaum, David Ezra, Mantovani, John F., Miller, Geoffrey, Mintz, Mark Ivan, Painter, Michael J., Patterson, Marc Clayton, Pavlakis, Steven George, Percy, Alan K., Pietrucha, Dorothy M., Rapin, Isabelle, Schneider, Sanford, Taylor, Donald A., Trauner, Doris A., Trommer, Barbara Lois, Turner, Robert Pearce, Wollack, Jan Brian, Bilynsky, Roman Oleh, Kugler, Steven Lloyd, Kuntz, Nancy L., Rodriguez, Diana Leticia, Schubert, Romaine S., Selman, Jay E., Shevell, Michael, Swisher, Charles N.

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Notice by Bohan, Timothy Patrick, Bolt, Jodie Lynn, Donnelly, Joseph Herbert, Engel, Murray, Fishman, Marvin A., Frank, Yitzchak, Graf, William David, Johnston, Michael V., Mandelbaum, David Ezra, Mantovani, John F., Miller, Geoffrey, Mintz, Mark Ivan, Painter, Michael J., Patterson, Marc Clayton, Pavlakis, Steven George, Percy, Alan K., Pietrucha, Dorothy M., Rapin, Isabelle, Schneider, Sanford, Taylor, Donald A., Trauner, Doris A., Trommer, Barbara Lois, Turner, Robert Pearce, Wollack, Jan Brian, Bilynsky, Roman Oleh, Kugler, Steven Lloyd, Kuntz, Nancy L., Rodriguez, Diana Leticia, Schubert, Romaine S., Selman, Jay E., Shevell, Michael, Swisher, Charles N.

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Recommendations for the detection and diagnosis of Niemann-Pick disease type C: An update by Patterson, Marc C, Clayton, Peter, Gissen, Paul, Anheim, Mathieu, Bauer, Peter, Bonnot, Olivier, Dardis, Andrea, Dionisi-Vici, Carlo, Klünemann, Hans-Hermann, Latour, Philippe, Lourenço, Charles M, Ory, Daniel S, Parker, Alasdair, Pocoví, Miguel, Strupp, Michael, Vanier, Marie T, Walterfang, Mark, Marquardt, Thorsten

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Lathosterolosis: A Relatively Mild Case with Cataracts and Learning Difficulties by Anderson, R., Rust, S., Ashworth, J., Clayton-Smith, J., Taylor, R. L., Clayton, P. T., Morris, A. A. M.

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Normal Neurodevelopmental Outcomes in PNPO Deficiency: A Case Series and Literature Review by Hatch, J., Coman, D., Clayton, P., Mills, P., Calvert, S., Webster, R. I., Riney, Kate

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Seizures Due to a KCNQ2 Mutation: Treatment with Vitamin B6 by Reid, Emma S., Williams, Hywel, Stabej, Polona Le Quesne, James, Chela, Ocaka, Louise, Bacchelli, Chiara, Footitt, Emma J., Boyd, Stewart, Cleary, Maureen A., Mills, Philippa B., Clayton, Peter T.

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Normal Cerebrospinal Fluid Pyridoxal 5′-Phosphate Level in a PNPO-Deficient Patient with Neonatal-Onset Epileptic Encephalopathy by Levtova, Alina, Camuzeaux, Stephane, Laberge, Anne-Marie, Allard, Pierre, Brunel-Guitton, Catherine, Diadori, Paola, Rossignol, Elsa, Hyland, Keith, Clayton, Peter T., Mills, Philippa B., Mitchell, Grant A.

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PNPO Deficiency and Cirrhosis: Expanding the Clinical Phenotype? by Coman, D., Lewindon, P., Clayton, P., Riney, K.

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Coenzyme Q10 and Pyridoxal Phosphate Deficiency Is a Common Feature in Mucopolysaccharidosis Type III by Yubero, Dèlia, Montero, Raquel, O’Callaghan, Mar, Pineda, Mercè, Meavilla, Silvia, Delgadillo, Veronica, Sierra, Cristina, Altimira, Laura, Navas, Plácido, Pope, Simon, Oppenheim, Marcus, Neergheen, Viruna, Ghosh, Arunabha, Mills, Phillipa, Clayton, Peter, Footitt, Emma, Cleary, Maureen, Hargreaves, Iain, Jones, Simon A., Heales, Simon, Artuch, Rafael

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