The many shades of enhancement: timing of post-gadolinium images strongly influences the scoring of juvenile idiopathic arthritis wrist involvement on MRI von Rieter, Jasper F. M. M., de Horatio, Laura Tanturri, Nusman, Charlotte M., Müller, Lil-Sofie Ording, Hemke, Robert, Avenarius, Derk F. M., van Rossum, Marion A. J., Malattia, Clara, Maas, Mario, Rosendahl, Karen

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A novel deletion involving the connexin-30 gene, del(GJB6-d13s1854), found in trans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impai... von del Castillo, F J, Rodríguez-Ballesteros, M, Álvarez, A, Hutchin, T, Leonardi, E, de Oliveira, C A, Azaiez, H, Brownstein, Z, Avenarius, M R, Marlin, S, Pandya, A, Shahin, H, Siemering, K R, Weil, D, Wuyts, W, Aguirre, L A, Martín, Y, Moreno-Pelayo, M A, Villamar, M, Avraham, K B, Dahl, H-H M, Kanaan, M, Nance, W E, Petit, C, Smith, R J H, Van Camp, G, Sartorato, E L, Murgia, A, Moreno, F, del Castillo, I

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Pediatric whole-body magnetic resonance imaging: comparison of STIR and T2 Dixon sequences in the detection and grading of high signal bone marrow changes von Zadig, P., von Brandis, E., Ording Müller, L. S., Tanturri de Horatio, L., Rosendahl, K., Avenarius, D. F. M.

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OTOF mutations revealed by genetic analysis of hearing loss families including a potential temperature sensitive auditory neuropathy allele von Varga, R, Avenarius, M R, Kelley, P M, Keats, B J, Berlin, C I, Hood, L J, Morlet, T G, Brashears, S M, Starr, A, Cohn, E S, Smith, R J H, Kimberling, W J

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Automated segmentation of magnetic resonance bone marrow signal: a feasibility study von von Brandis, Elisabeth, Jenssen, Håvard B., Avenarius, Derk F. M., Bjørnerud, Atle, Flatø, Berit, Tomterstad, Anders H., Lilleby, Vibke, Rosendahl, Karen, Sakinis, Tomas, Zadig, Pia K. K., Müller, Lil-Sofie Ording

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The paediatric wrist revisited—findings of bony depressions in healthy children on radiographs compared to MRI von Avenarius, Derk M. F., Ording Müller, Lil-Sofie, Eldevik, Petter, Owens, Catherine M., Rosendahl, Karen

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Erosion or normal variant? 4-year MRI follow-up of the wrists in healthy children von Avenarius, Derk F. M., Ording Müller, Lil-Sofie, Rosendahl, Karen

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Correction to: Automated segmentation of magnetic resonance bone marrow signal: a feasibility study von von Brandis, Elisabeth, Jenssen, Håvard B., Avenarius, Derk F. M., Bjørnerud, Atle, Flatø, Berit, Tomterstad, Anders H., Lilleby, Vibke, Rosendahl, Karen, Sakinis, Tomas, Zadig, Pia K. K., Müller, Lil-Sofie Ording

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Whole body magnetic resonance imaging in healthy children and adolescents: Bone marrow appearances of the appendicular skeleton von Zadig, Pia K, von Brandis, Elisabeth, Flatø, Berit, Ording Müller, Lil-Sofie, Nordal, Ellen B, de Horatio, Laura Tanturri, Rosendahl, Karen, Avenarius, Derk F M

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Whole body magnetic resonance imaging in healthy children and adolescents. Bone marrow appearances of the axial skeleton von von Brandis, Elisabeth, Zadig, Pia K., Avenarius, Derk F.M., Flatø, Berit, Kristian Knudsen, Per, Lilleby, Vibke, Nguyen, Bac, Rosendahl, Karen, Ording Müller, Lil-Sofie

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Joint Fluid, Bone Marrow Edemalike Changes, and Ganglion Cysts in the Pediatric Wrist: Features That May Mimic Pathologic Abnormalities-Follow-Up of a Healthy Cohort von Avenarius, Derk F M, Ording Müller, Lil-Sofie, Rosendahl, Karen

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Whole-body MRI in children and adolescents: Can T2-weighted Dixon fat-only images replace standard T1-weighted images in the assessment of bone marrow? von Tanturri de Horatio, Laura, Zadig, Pia K., von Brandis, Elisabeth, Ording Müller, Lil-Sofie, Rosendahl, Karen, Avenarius, Derk F.M.

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HORNET: a packet-over-WDM multiple access metropolitan area ring network von Shrikhande, K.V., White, I.M., Wonglumsom, D., Gemelos, S.M., Rogge, M.S., Fukashiro, Y., Avenarius, M., Kazovsky, L.G.

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Experimental demonstration of an access point for HORNET-A packet-over-WDM multiple-access MAN von Wonglumsom, D., White, I.M., Shrikhande, K., Rogge, M.S., Gemelos, S.M., Fu-Tai An, Fukashiro, Y., Avenarius, M., Kazovsky, L.G.

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Evidence for a direct role of the disease modifier SCNM1 in splicing von Howell, Viive M., Jones, Julie M., Bergren, Sarah K., Li, Li, Billi, Allison C., Avenarius, Matthew R., Meisler, Miriam H.

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Avoidance of mechanical ventilation by surfactant treatment of spontaneously breathing preterm infants (AMV): an open-label, randomised, controlled trial von Göpel, Wolfgang, Prof, Kribs, Angela, MD, Ziegler, Andreas, Prof, Laux, Reinhard, MD, Hoehn, Thomas, Prof, Wieg, Christian, MD, Siegel, Jens, MD, Avenarius, Stefan, MD, von der Wense, Axel, MD, Vochem, Matthias, MD, Groneck, Peter, Prof, Weller, Ursula, MD, Möller, Jens, Prof, Härtel, Christoph, MD, Haller, Sebastian, MD, Roth, Bernhard, Prof, Herting, Egbert, Prof

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GJB2 mutations: Passage through Iran von Najmabadi, Hossein, Nishimura, Carla, Kahrizi, Kimia, Riazalhosseini, Yasser, Malekpour, Mahdi, Daneshi, Ahmad, Farhadi, Mohammad, Mohseni, Marzieh, Mahdieh, Nejat, Ebrahimi, Ahmad, Bazazzadegan, Niloofar, Naghavi, Anoosh, Avenarius, Matthew, Arzhangi, Sanaz, Smith, Richard J.H.

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Permissive hypercapnia in extremely low birthweight infants (PHELBI): a randomised controlled multicentre trial von Thome, Ulrich H, Prof, Genzel-Boroviczeny, Orsolya, Prof, Bohnhorst, Bettina, Prof, Schmid, Manuel, MD, Fuchs, Hans, MD, Rohde, Oliver, MD, Avenarius, Stefan, MD, Topf, Hans-Georg, MD, Zimmermann, Andrea, MD, Faas, Dirk, MD, Timme, Katharina, MD, Kleinlein, Barbara, MD, Buxmann, Horst, MD, Schenk, Wilfried, MD, Segerer, Hugo, Prof, Teig, Norbert, MD, Gebauer, Corinna, MD, Hentschel, Roland, Prof, Heckmann, Matthias, Prof, Schlösser, Rolf, Prof, Peters, Jochen, Prof, Rossi, Rainer, Prof, Rascher, Wolfgang, MD, Böttger, Ralf, MD, Seidenberg, Jürgen, MD, Hansen, Gesine, Prof, Zernickel, Maria, MSc, Alzen, Gerhard, Prof, Dreyhaupt, Jens, PhD, Muche, Rainer, PhD, Hummler, Helmut D, Prof

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Automated segmentation of magnetic resonance bone marrow signal: a feasibility study von von Brandis, Elisabeth, Jenssen, Håvard Bjørke, Avenarius, Derk Frederik Matthaus, Bjørnerud, Atle, Flatø, Berit, Tomterstad, Anders, Lilleby, Vibke, Rosendahl, Karen, Sakinis, Tomas, Zadig, Pia Karin Karlsen, Müller, Lil-Sofie Ording

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A novel deletion involving the connexin-30 gene, del(GJb6-d13s1854), found in frans with mutations in the GJB2 gene (connexin-26) in subjects with DFNB1 non-syndromic hearing impai... von DEL CASTILLO, F. J, RODRIGUEZ-BALLESTEROS, M, PANDYA, A, SHAHIN, H, SIEMERING, K. R, WEIL, D, WUYTS, W, AGUIRRE, L. A, MARTIN, Y, MORENO-PELAYO, M. A, VILLAMAR, M, AVRAHAM, K. B, ALVAREZ, A, DAHL, H.-H. M, KANAAN, M, NANCE, W. E, PETIT, C, SMITH, R. J. H, VAN CAMP, G, SARTORATO, E. L, MURGIA, A, MORENO, F, DEL CASTILLO, I, HUTCHIN, T, LEONARDI, E, DE OLIVEIRA, C. A, AZAIEZ, H, BROWNSTEIN, Z, AVENARIUS, M. R, MARLIN, S

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