Presence of cystic fibrosis-related diabetes mellitus is tightly linked to poor lung function in patients with cystic fibrosis: Data from the European Epidemiologic Registry of Cys... von Koch, C., Rainisio, M., Madessani, U., Harms, H.K., Hodson, M.E., Mastella, G., McKenzie, S.G., Navarro, J., Strandvik, B.

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Does Optimal Egg Size Vary with Demographic Stage Because of a Physiological Constraint? von Bowden, R. M., Harms, H. K., Paitz, R. T., Janzen, F. J.

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Diversity of the basic defect of homozygous CFTR mutation genotypes in humans von Stanke, F, Ballmann, M, Bronsveld, I, Dörk, T, Gallati, S, Laabs, U, Derichs, N, Ritzka, M, Posselt, H-G, Harms, H K, Griese, M, Blau, H, Mastella, G, Bijman, J, Veeze, H, Tümmler, B

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Allergic bronchopulmonary aspergillosis in cystic fibrosis. A European epidemiological study von Mastella, G., Rainisio, M., Harms, H.K, Hodson, M.E, Koch, C, Navarro, J, Strandvik, B, McKenzie, S.G, The Investigators Of The Epidemiologic Registry of Cystic Fibrosis, On Behalf Of

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Factors associated with poor pulmonary function: cross-sectional analysis of data from the ERCF von Navarro, J, Rainisio, M, Harms, H.K, Hodson, M.E, Koch, C, Mastella, G, Strandvik, B, McKenzie, S.G

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European Epidemiologic Registry of Cystic Fibrosis (ERCF): Comparison of major disease manifestations between patients with different classes of mutations von Koch, C., Cuppens, H., Rainisio, M., Madessani, U., Harms, H.K., Hodson, M.E., Mastella, G., Navarro, J., Strandvik, B., McKenzie, S.G.

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Dornase alfa in the treatment of cystic fibrosis in Europe: A report from the Epidemiologic Registry of Cystic Fibrosis von Hodson, M.E., McKenzie, S., Harms, H.K., Koch, C., Mastella, G., Navarro, J., Strandvik, B.

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Carbohydrate-deficient glycoprotein syndrome type Ib. Phosphomannose isomerase deficiency and mannose therapy von Niehues, R, Hasilik, M, Alton, G, Körner, C, Schiebe-Sukumar, M, Koch, H G, Zimmer, K P, Wu, R, Harms, E, Reiter, K, von Figura, K, Freeze, H H, Harms, H K, Marquardt, T

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Adenovirus infection in cystic fibrosis patients : implications for the use of adenoviral vectors for gene transfer von ROSENECKER, J, HARMS, K.-H, BERTELE, R. M, POHL-KOPPE, A, MUTIUS, E. V, ADAM, D, NICOLAI, T

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Oral mannose therapy persistently corrects the severe clinical symptoms and biochemical abnormalities of phosphomannose isomerase deficiency von Harms, HK, Zimmer, K-P, Kurnik, K, Bertele-Harms, RM, Weidinger, S, Reiter, K

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Allergic bronchopulmonary aspergillosis in cystic fibrosis von Mastella, G, Rainisio, M, Harms, H K, Hodson, M E, Koch, C, Navarro, J, Strandvik, B, McKenzie, S G

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Age and Season Impact Resource Allocation to Eggs and Nesting Behavior in the Painted Turtle von Harms, Heidi K., Paitz, Ryan T., Bowden, Rachel M., Janzen, Fredric J.

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Geographic distribution and origin of CFTR mutations in Germany von TÜMMLER, B, STORRS, T, RUTJES, J, SCHNEPPENHEIM, R, BAUER, I, BREUEL, K, STUHRMANN, M, SCHMIDTKE, J, LINDNER, M, EIGEL, A, HORST, J, KAISER, R, DZIADEK, V, LENTZE, M. J, SCHMIDT, K, VON DER HARDT, H, ESTIVILL, X, DÖRK, T, MEITINGER, T, GOLLA, A, BERTELE-HARMS, R. M, HARMS, H. K, SCHRÖDER, E, CLASS, A

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Mycoserological study of the treatment of paediatric cystic fibrosis patients with Saccharomyces boulardii (Saccharomyces cerevisiae Hansen CBS 5926) von Müller, J., Remus, N., Harms, K. H.

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Correlation of IgE antibody titer to Aspergillus fumigatus with decreased lung function in cystic fibrosis von Nicolai, Thomas, Arleth, Sissi, Spaeth, Anne, Bertele-Harms, Rose-Marie, Harms, H. Karsten

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Enzyme-Substitution Therapy with the Yeast Saccharomyces cerevisiae in Congenital Sucrase-Isomaltase Deficiency von Harms, Hinrich-Karsten, Bertele-Harms, Rose-Marie, Bruer-Kleis, Dorothea

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Genetic determination of diabetes mellitus in patients with cystic fibrosis von Rosenecker, Joseph, Eichler, Irmgard, Kühn, Ludwig, Harms, Hinrich K., von der Hardt, Horst

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A reliable screening test for childhood celiac disease: fluorescent immunosorbent test for gliadin antibodies. A prospective multicenter study von Bürgin-Wolff, A, Bertele, R M, Berger, R, Gaze, H, Harms, H K, Just, M, Khanna, S, Schürmann, K, Signer, E, Tomovic, D

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EARLY ALLOGRAFT REJECTION IN CHILDREN AFTER LIVER TRANSPLANTATION IS ASSOCIATED WITH PERIPHERAL AND GRAFT EOSINOPHILIA von Lang, Th, Stangl, M., Kappler, M., Harms, K. H., Rau, H. G., Cox, K. L.

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Calcium metabolism and cystic fibrosis: mitochondrial abnormalities suggest a modification of the mitochondrial membrane von VON RUECKEL, A. A, BERTELE, R, HARMS, H. K

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