Aminoacylase I deficiency: A novel inborn error of metabolism von Van Coster, R.N., Gerlo, E.A., Giardina, T.G., Engelke, U.F., Smet, J.E., De Praeter, C.M., Meersschaut, V.A., De Meirleir, L.J., Seneca, S.H., Devreese, B., Leroy, J.G., Herga, S., Perrier, J.P., Wevers, R.A., Lissens, W.

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A Novel Disorder Caused by Defective Biosynthesis of N-Linked Oligosaccharides Due to Glucosidase I Deficiency von De Praeter, Claudine M., Gerwig, Gerrit J., Bause, Ernst, Nuytinck, Lieve K., Vliegenthart, Johannes F.G., Breuer, Wilhelm, Kamerling, Johannis P., Espeel, Marc F., Martin, Jean-Jacques R., De Paepe, Anne M., Chan, Nora Wen Chun, Dacremont, Georges A., Van Coster, Rudy N.

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Fungal intracranial aneurysm in a child with familial chronic mucocutaneous candidiasis von LOEYS, B. L, VAN COSTER, R. N, DEFREYNE, L. R, LEROY, J. G

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Prenatal diagnosis of pyruvate carboxylase deficiency by direct measurement of catalytic activity on chorionic villi samples von Van Coster, R. N., Janssens, S., Misson, J.-P., Verloes, A., Leroy, J. G.

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Neurocutaneous Melanosis Presenting with Intracranial Amelanotic Melanoma von Vanzieleghem, Bart D, Lemmerling, Marc M, Van Coster, Rudy N

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Dominant Inheritance of Sialuria, an Inborn Error of Feedback Inhibition von Leroy, Jules G., Seppala, Raili, Huizing, Marjan, Dacremont, George, De Simpel, Helena, Van Coster, Rudy N., Orvisky, Edwin, Krasnewich, Donna M., Gahl, William A.

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Processing of N-linked carbohydrate chains in a patient with glucosidase I deficiency (CDG type IIb) von Völker, Christof, De Praeter, Claudine M., Hardt, Birgit, Breuer, Willi, Kalz-Füller, Burga, Van Coster, Rudy N., Bause, Ernst

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MRI findings in a neonate with cerebellar agenesis von Van Coster, Rudy N, De Praeter, Claudine M, Vanhaesebrouck, Piet J, Leroy, Jules G

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Pyruvate carboxylase deficiency : a benign variant with normal development von VAN COSTER, R. N, FERNHOFF, P. M, DE VIVO, D. C

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Pyruvate dehydrogenase deficiency: Molecular basis for intrafamilial heterogeneity von Fujii, Tatsuya, Van Coster, Rudy N., Old, Susan E., Medori, Rosella, Winter, Susan, Gubits, Ruth M., Matthews, Paul M., Brown, Ruth M., Brown, Garry K., Dahl, Hans-Henrik M., De Vivo, Darryl C.

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Myopathy in very-long-chain acyl-CoA dehydrogenase deficiency: clinical and biochemical differences with the fatal cardiac phenotype von Scholte, H.R., Van Coster, R.N.A., de Jonge, P.C., Poorthuis, B.J.H.M., Jeneson, J.A.L., Andresen, B.S., Gregersen, N., de Klerk, J.B.C., Busch, H.F.M.

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A family with X-linked dominant Charcot–Marie–Tooth caused by a connexin32 mutation von Verhelst, Helene E, Lofgren, Ann, Van Coster, Rudy N

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Fibrotic eye muscles, Axenfeld anomaly, flat face, and mild developmental retardation: A new example of the Chitty syndrome von Van Daele, Sabine G., Van Coster, Rudy N., Meire, Françoise, Smets, Anne M., Leroy, Jules G.

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Pyruvate Carboxylase Deficiency: A Benign Variant with Normal Development von VAN COSTER, R. N., FERNHOFF, P. M., DE VIVO, D. C.

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A human immune dysregulation syndrome characterized by severe hyperinflammation with a homozygous nonsense Roquin-1 mutation von Tavernier, S. J., Athanasopoulos, V., Verloo, P., Behrens, G., Staal, J., Bogaert, D. J., Naesens, L., De Bruyne, M., Van Gassen, S., Parthoens, E., Ellyard, J., Cappello, J., Morris, L. X., Van Gorp, H., Van Isterdael, G., Saeys, Y., Lamkanfi, M., Schelstraete, P., Dehoorne, J., Bordon, V., Van Coster, R., Lambrecht, B. N., Menten, B., Beyaert, R., Vinuesa, C. G., Heissmeyer, V., Dullaers, M., Haerynck, F.

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A Population of Fast Radio Bursts at Cosmological Distances von Thornton, D., Steppers, B., Bailes, M., Barsdell, B., Bates, S., Bhat, N. D. R., Burgay, M., Burke-Spolaor, S., Champion, D. J., Coster, P., D'Amico, N., Jameson, A., Johnston, S., Keith, M., Kramer, M., Levin, L., Milia, S., Ng, C., Possenti, A., van Straten, W.

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Author Correction: A human immune dysregulation syndrome characterized by severe hyperinflammation with a homozygous nonsense Roquin-1 mutation von Tavernier, S. J., Athanasopoulos, V., Verloo, P., Behrens, G., Staal, J., Bogaert, D. J., Naesens, L., De Bruyne, M., Van Gassen, S., Parthoens, E., Ellyard, J., Cappello, J., Morris, L. X., Van Gorp, H., Van Isterdael, G., Saeys, Y., Lamkanfi, M., Schelstraete, P., Dehoorne, J., Bordon, V., Van Coster, R., Lambrecht, B. N., Menten, B., Beyaert, R., Vinuesa, C. G., Heissmeyer, V., Dullaers, M., Haerynck, F.

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The High Time Resolution Universe Pulsar Survey -VIII. The Galactic millisecond pulsar population von Levin, L., Bailes, M., Barsdell, B. R., Bates, S. D., Bhat, N. D. R., Burgay, M., Burke-Spolaor, S., Champion, D. J., Coster, P., D'Amico, N., Jameson, A., Johnston, S., Keith, M. J., Kramer, M., Milia, S., Ng, C., Possenti, A., Stappers, B., Thornton, D., van Straten, W.

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The High Time Resolution Universe pulsar survey - X. Discovery of four millisecond pulsars and updated timing solutions of a further 12 von Ng, C., Bailes, M., Bates, S. D., Bhat, N. D. R., Burgay, M., Burke-Spolaor, S., Champion, D. J., Coster, P., Johnston, S., Keith, M. J., Kramer, M., Levin, L., Petroff, E., Possenti, A., Stappers, B. W., van Straten, W., Thornton, D., Tiburzi, C., Bassa, C. G., Freire, P. C. C., Guillemot, L., Lyne, A. G., Tauris, T. M., Shannon, R. M., Wex, N.

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Addition of infliximab compared with addition of sulfasalazine and hydroxychloroquine to methotrexate in patients with early rheumatoid arthritis (Swefot trial): 1-year results of... von van Vollenhoven, RF, Dr, Ernestam, S, MD, Geborek, P, MD, Petersson, IF, MD, Cöster, L, MD, Waltbrand, E, MD, Zickert, A, MD, Theander, J, MD, Thörner, Å, MD, Hellström, H, MD, Teleman, A, MD, Dackhammar, C, MD, Akre, F, MD, Forslind, K, MD, Ljung, L, MD, Oding, R, MD, Chatzidionysiou, A, MD, Wörnert, M, RN, Bratt, J, MD

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