Early-life pulmonary arterial hypertension with subsequent development of diffuse pulmonary arteriovenous malformations in hereditary haemorrhagic telangiectasia type 1 von Mache, C J, Gamillscheg, A, Popper, H H, Haworth, S G

Volltext

Importance of environmental transmission in cases of EHEC O157 causing hemolytic uremic syndrome von GRIF, K, ORTH, D, LEDERER, I, BERGHOLD, C, ROEDL, S, MACHE, C. J, DIERICH, M. P, WÜRZNER, R

Volltext

Echo-enhanced color doppler cystosonography of vesicoureteral reflux in children: Improvement by stimulated acoustic emission von RICCABONA, M, MACHE, C. J, LINDBICHLER, F

Volltext

FK 506 and Successful Pregnancy in a Patient After Renal Transplantation von Resch, B, Mache, C.J, Windhager, T, Holzer, H, Leitner, G, Müller, W

Volltext

Severe chorea with positive anti-basal ganglia antibodies after herpesencephalitis von Marschitz, I, Rödl, S, Gruber-Sedlmayr, U, Church, A, Giovannoni, G, Zobel, G, Mache, C J, Raith, J, Plecko, B

Volltext

Autosomal dominant familial Mediterranean fever-like syndrome von MACHE, C. J, GORIUP, U, FISCHEL-GHODSIAN, N, CHEN, X, SCHWINGSHANDL, J

Volltext

Functional analyses indicate a pathogenic role of factor H autoantibodies in atypical haemolytic uraemic syndrome von Strobel, Stefanie, Hoyer, Peter F., Mache, Christoph J., Sulyok, Endre, Liu, Wei-shih, Richter, Heiko, Oppermann, Martin, Zipfel, Peter F., Józsi, Mihály

Volltext

Infants Requiring Maintenance Dialysis: Outcomes of Hemodialysis and Peritoneal Dialysis von Vidal, Enrico, MD, PhD, van Stralen, Karlijn J., PhD, Chesnaye, Nicholas C., MSc, Bonthuis, Marjolein, PhD, Holmberg, Christer, MD, Zurowska, Aleksandra, MD, Trivelli, Antonella, MD, Da Silva, José Eduardo Esteves, MD, Herthelius, Maria, MD, Adams, Brigitte, MD, Bjerre, Anna, MD, PhD, Jankauskiene, Augustina, MD, PhD, Miteva, Polina, MD, Emirova, Khadizha, MD, Bayazit, Aysun K., MD, Mache, Christoph J., MD, Sánchez-Moreno, Ana, MD, Harambat, Jérôme, MD, PhD, Groothoff, Jaap W., MD, PhD, Jager, Kitty J., MD, PhD, Schaefer, Franz, MD, Verrina, Enrico, MD

Volltext

Functional characterization of GATA3 mutations causing the hypoparathyroidism-deafness-renal (HDR) dysplasia syndrome: insight into mechanisms of DNA binding by the GATA3 transcrip... von Ali, Asif, Christie, Paul T., Grigorieva, Irina V., Harding, Brian, Van Esch, Hilde, Ahmed, S. Faisal, Bitner-Glindzicz, Maria, Blind, Eberhard, Bloch, Catherine, Christin, Patricia, Clayton, Peter, Gecz, Jozef, Gilbert-Dussardier, Brigitte, Guillen-Navarro, Encarna, Hackett, Anna, Halac, Isil, Hendy, Geoffrey N., Lalloo, Fiona, Mache, Christoph J., Mughal, Zulf, Ong, Albert C.M., Rinat, Choni, Shaw, Nicholas, Smithson, Sarah F., Tolmie, John, Weill, Jacques, Nesbit, M. Andrew, Thakker, Rajesh V.

Volltext

Prothrombin fragment 1+2 during oral anticoagulation in congenital nephrotic syndrome von Mache, C J, Muntean, W, Resch, B, Ring, E

Volltext

Successful treatment of chronic recurrent multifocal osteomyelitis with tumor necrosis factor-α blockage von DEUTSCHMANN, Andrea, MACHE, Christoph J, BODO, Koppany, ZEBEDIN, Doris, RING, Ekkehard

Volltext

Transforming growth factor-β receptor mutations and pulmonary arterial hypertension in childhood von HARRISON, Rachel E, BERGER, Rolf, HAWORTH, Sheila G, TULLOH, Robert, MACHE, Christoph J, MORRELL, Nicholas W, ALDRED, Micheala A, TREMBATH, Richard C

Volltext

Familial hemophagocytic lymphohistiocytosis associated with disseminated T-cell lymphoma : a report of two siblings von MACHE, C. J, SLAVC, I, SCHMID, C, HOEFLER, G, URBAN, C. E, SCHWINGER, W, WINTER, E, HULLA, W, ZENZ, W, HOLTER, W

Volltext

Undifferentiated (embryonal) sarcoma of the liver in childhood. Successful combined‐modality therapy in four patients von Urban, Christian E., Mache, Christoph J., Schwinger, Wolfgang, Riccabona, Michael, Pakisch, Brigitte, Ranner, Gerhard, Schimpl, GÜNther, Brandesky, Gernot, Messner, Heimo, Pobegen, Walter, Becker, Hans, Grienberger, Heinz

Volltext

PAEDIATRIC NEPHROLOGY von Vidal, E., Van Stralen, K. J., Schaefer, F., Adams, B., Bjerre, A., Dusunsel, R., Emirova, K. M., Esteves Da Silva, J. E., Herthelius, M., Holmberg, C., Jankauskiene, A., Mache, C. J., Miteva, P., Sanchez-Moreno, A., Trivelli, A., Zurowska, A., Groothoff, J. W., Jager, K., Verrina, E., Basu, B., Pandey, R., Mondal, N., Melhem, N., Shroff, R., Samyn, M., Van'T Hoff, W.

Volltext

1003 Plasmapheresis in Treatment of Pediatric Patients with Neurological Deseases: 10 Years Experience von Rödl, S, Marschitz, I, Mache, C J, Gruber-Sedlmayr, U, Plecko, B, Zobel, G

Volltext

1004 Rescue Treatment with Hemodiafiltration in Infants with End-Stage Renal Failure After Complications on Peritoneal Dialyses von Rödl, S, Marschitz, I, Mache, C J, Koestenberger, M, Madler, G, Rehak, T, Zobel, G

Volltext

1005 One Year Clinical Experience with the Prismaflex Hf 20 Set in Four Infants von Rödl, S, Marschitz, I, Mache, C J, Koestenberger, M, Madler, G, Rehak, T, Zobel, G

Volltext

Adoptive Immunotransfer with Viable Donor Mononuclear Cells for Recurrent Chronic Myelogenous Leukemia After Allogeneic Bone Marrow Transplantation in Two Children von Schwinger, W., Urban, C., Mache, C. J., Resch, B., Lackner, H., Höfler, G., Beham-Schmid, C., Gilli, R., Wagner, K., Haas, O. A., Lion, T.

Volltext

Ultrasound and MRI findings in a case of childhood amyloid goiter von Mache, C J, Schwingshandl, J, Riccabona, M, Ranner, G, Ring, E, Fock, C, Ratschek, M, Malle, E, Borkenstein, M H

Volltext