The consequences of extended newborn screening programmes: Do we know who needs treatment? von Wilcken, B.

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Recent advances in newborn screening von Wilcken, B.

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Glutaric aciduria type I: outcome following detection by newborn screening von Bijarnia, S., Wiley, V., Carpenter, K., Christodoulou, J., Ellaway, C. J., Wilcken, B.

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Selection of Reference Genes for Quantitative Real-time PCR Analysis in Canine Mammary Tumors Using the GeNorm Algorithm von Etschmann, B, Wilcken, B, Stoevesand, K, Schulenburg, A. von der, Sterner-Kock, A

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Guideline for the diagnosis and management of glutaryl‐CoA dehydrogenase deficiency (glutaric aciduria type I) von Kölker, S., Christensen, E., Leonard, J. V., Greenberg, C. R., Burlina, A. B., Burlina, A. P., Dixon, M., Duran, M., Goodman, S. I., Koeller, D. M., Müller, E., Naughten, E. R., Neumaier‐Probst, E., Okun, J. G., Kyllerman, M., Surtees, R. A., Wilcken, B., Hoffmann, G. F., Burgard, P.

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Geographical and ethnic variation of the 677C>T allele of 5,10 methylenetetrahydrofolate reductase (MTHFR): findings from over 7000 newborns from 16 areas world wide von Wilcken, B, Bamforth, F, Li, Z, Zhu, H, Ritvanen, A, Redlund, M, Stoll, C, Alembik, Y, Dott, B, Czeizel, A E, Gelman-Kohan, Z, Scarano, G, Bianca, S, Ettore, G, Tenconi, R, Bellato, S, Scala, I, Mutchinick, O M, López, M A, de Walle, H, Hofstra, R, Joutchenko, L, Kavteladze, L, Bermejo, E, Martínez-Frías, M L, Gallagher, M, Erickson, J D, Vollset, S E, Mastroiacovo, P, Andria, G, Botto, L D

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The natural history of vascular disease in homocystinuria and the effects of treatment von Wilcken, D. E. L., Wilcken, B.

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Rare diseases and the assessment of intervention: What sorts of clinical trials can we use? von Wilcken, B.

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Mapping spatial and field dependence of magnetic domain memory by soft X-ray speckle metrology von Chesnel, K., Nelson, J., Wilcken, B., Kevan, S. D.

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3-Methylglutaconic aciduria type I redefined: A syndrome with late-onset leukoencephalopathy von WORTMANN, S. B, KREMER, B. H, WILCKEN, B, CRUYSBERG, J. R, DAS, A. M, MORAVA, E, WEVERS, R. A, GRAHAM, A, WILLEMSEN, M. A, LOUPATTY, F. J, HOGG, S. L, ENGELKE, U. F, KLUIJTMANS, L. A, WANDERS, R. J, ILLSINGER, S

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Contiguous gene deletion syndrome in a female with ornithine transcarbamylase deficiency von Balasubramaniam, S., Rudduck, C., Bennetts, B., Peters, G., Wilcken, B., Ellaway, C.

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n of 1 trial for an ornithine transcarbamylase deficiency carrier von Hackett, A., Gillard, J., Wilcken, B.

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Screening Newborns for Inborn Errors of Metabolism by Tandem Mass Spectrometry von Wilcken, Bridget, Wiley, Veronica, Hammond, Judith, Carpenter, Kevin

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Newborn screening with tandem mass spectrometry: 12 months' experience in NSW Australia von Wiley, V, Carpenter, K, Wilcken, B

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Vascular Complications of Severe Hyperhomocysteinemia in Patients with Homocystinuria Due to Cystathionine β-Synthase Deficiency: Effects of Homocysteine-Lowering Therapy von YAP, SUFIN, NAUGHTEN, EILEEN R., WILCKEN, BRIDGET, WILCKEN, DAVID E.L., BOERS, GODFRIED H.J.

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Evaluation of newborn screening for medium chain acyl-CoA dehydrogenase deficiency in 275 000 babies von Carpenter, K, Wiley, V, Sim, K G, Heath, D, Wilcken, B

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Non-Ketotic Hyperglycinemia is usually not detectable by tandem mass spectrometry newborn screening von Tan, E.S., Wiley, V., Carpenter, K., Wilcken, B.

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Newborn screening may fail to identify intermediate forms of maple syrup urine disease von Bhattacharya, K., Khalili, V., Wiley, V., Carpenter, K., Wilcken, B.

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Newborn screening for cystic fibrosis: Techniques and strategies von Wilcken, Bridget

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Intron-8 polythymidine sequence in Australasian individuals with CF mutations R117H and R117C von Massie, R.J.H, Poplawski, N, Wilcken, B, Goldblatt, J, Byrnes, C, Robertson, C

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