Hakutulokset - Fang-Hoffmann, Junmin

Medium-Chain Acyl-CoA Dehydrogenase Deficiency: Evaluation of Genotype-Phenotype Correlation in Patients Detected by Newborn Screening Tekijä Gramer, Gwendolyn, Haege, Gisela, Fang-Hoffmann, Junmin, Hoffmann, Georg F., Bartram, Claus R., Hinderhofer, Katrin, Burgard, Peter, Lindner, Martin

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Implementing a tracking system for confirmatory diagnostic results after positive newborn screening for cystic fibrosis—implications for process quality and patient care Tekijä Gramer, Gwendolyn, Brockow, Inken, Labitzke, Christiane, Fang-Hoffmann, Junmin, Beivers, Andreas, Feyh, Patrik, Hoffmann, Georg F., Nennstiel, Uta, Sommerburg, Olaf

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Efficacy and outcome of expanded newborn screening for metabolic diseases - Report of 10 years from South-West Germany * Tekijä Lindner, Martin, Gramer, Gwendolyn, Haege, Gisela, Fang-Hoffmann, Junmin, Schwab, Karl O, Tacke, Uta, Trefz, Friedrich K, Mengel, Eugen, Wendel, Udo, Leichsenring, Michael, Burgard, Peter, Hoffmann, Georg F

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Newborn Screening for Vitamin B(6) Non-responsive Classical Homocystinuria: Systematical Evaluation of a Two-Tier Strategy Tekijä Okun, Jürgen G., Gan-Schreier, Hongying, Ben-Omran, Tawfeq, Schmidt, Kathrin V., Fang-Hoffmann, Junmin, Gramer, Gwendolyn, Abdoh, Ghassan, Shahbeck, Noora, Al Rifai, Hilal, Al Khal, Abdul Latif, Haege, Gisela, Chiang, Chuan-Chi, Kasper, David C., Wilcken, Bridget, Burgard, Peter, Hoffmann, Georg F.

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