Recurrent vomiting and acute renal failure after HUS: Question von Holder, M., Bald, M., Leichter, H.E.

Volltext

Need for Long-term Follow-up in Enterohemorrhagic Escherichia coli—Associated Hemolytic Uremic Syndrome Due to Late-Emerging Sequelae von Karch, Helga, Rosales, Alejandra, Hofer, Johannes, Zimmerhackl, Lothar-Bernd, Jungraithmayr, Therese C., Riedl, Magdalena, Giner, Thomas, Strasak, Alexander, Orth-Höller, Dorothea, Würzner, Reinhard, Karch, Helge

Volltext

Mutation analysis of 18 nephronophthisis associated ciliopathy disease genes using a DNA pooling and next generation sequencing strategy von Otto, Edgar A, Ramaswami, Gokul, Janssen, Sabine, Chaki, Moumita, Allen, Susan J, Zhou, Weibin, Airik, Rannar, Hurd, Toby W, Ghosh, Amiya K, Wolf, Matthias T, Hoppe, Bernd, Neuhaus, Thomas J, Bockenhauer, Detlef, Milford, David V, Soliman, Neveen A, Antignac, Corinne, Saunier, Sophie, Johnson, Colin A, Hildebrandt, Friedhelm

Volltext

Rationale, design and objectives of ARegPKD, a European ARPKD registry study von Ebner, Kathrin, Feldkoetter, Markus, Ariceta, Gema, Bergmann, Carsten, Buettner, Reinhard, Doyon, Anke, Duzova, Ali, Goebel, Heike, Haffner, Dieter, Hero, Barbara, Hoppe, Bernd, Illig, Thomas, Jankauskiene, Augustina, Klopp, Norman, König, Jens, Litwin, Mieczyslaw, Mekahli, Djalila, Ranchin, Bruno, Sander, Anja, Testa, Sara, Weber, Lutz Thorsten, Wicher, Dorota, Yuzbasioglu, Ayse, Zerres, Klaus, Dötsch, Jörg, Schaefer, Franz, Liebau, Max Christoph

Volltext

Early diagnosis of bardet-biedl syndrome von FRALICK, R. A, LEICHTER, H. E, SHETH, K. J

Volltext

Recent Progress of the ARegPKD Registry Study on Autosomal Recessive Polycystic Kidney Disease von Ebner, Kathrin, Schaefer, Franz, Liebau, Max Christoph

Volltext

Reversal of Central Nervous System Involvement in Hemolytic Uremic Syndrome by Use of Plasma Exchanges von Sheth, Kumudchandra J., Leichter, Heinz E., Gill, Joan C., Baumgardt, Anne

Volltext

Peritoneal clearances with different dialysis regimens in children undergoing continuous cycling peritoneal dialysis von LEICHTER, H. E, SALUSKY, I. B, LILIEN, T. V, LAIDLAW, S, ALLIAPOULOS, J. C, HALL, T. L, FINE, R. N

Volltext

Hepatocellular injury in Streptococcus pnumoniae-associated hemolytic uremic syndrome in children von PAN, C. G, LEICHTER, H. E, WERLIN, S. L

Volltext

Pseudotumor cerebri with vision impairment in two children with renal transplantation von SHETH, K. J, KIVLIN, J. D, LEICHTER, H. E, PAN, C. G, MULTAUF, C

Volltext

Answer von Holder, M, Bald, M, Leichter, H E

Volltext

Recurrent vomiting and acute renal failure after HUS von Holder, M, Bald, M, Leichter, H E

Volltext

Short-course antithymocyte globulin for treatment of renal transplant rejection in children von LEICHTER, H. E, ETTENGER, R. B, JORDAN, S. C, SALUSKY, I. B, FINE, R. N

Volltext

Pediatric renal transplantation with mycophenolate mofetil-based immunosuppression without induction: Results after three years von JUNGRAITHMAYR, Therese, STASKEWITZ, Astrid, KLAUS, Günter, LEICHTER, Heinz E, MIHATSCH, Michael J, MICHALK, Dietrich V, MISSELWITZ, Joachim, PLANK, Christian, QUERFELD, Uwe, WEBER, Lutz T, WIESEL, Manfred, TÖNSHOFF, Burkhard, KIRSTE, Günter, ZIMMERHACKL, Lothar B, BÖSWALD, Michael, BULLA, Monika, BURGHARD, Rainer, DIPPELL, Jürgen, GREINER, Christel, HELMCHEN, Udo, KLARE, Bernd

Volltext

Racial incidence of hemolytic-uremic syndrome von Sheth, K J, Gill, J C, Havens, P L, Leichter, H E

Volltext

Increased renal echogenicity in a preterm neonate: Question von Bald, Martin, Holder, Martin, Zieger, Michael, Vochem, Matthias, Leichter, Heinz E.

Volltext

Acquired cystic kidney disease in children undergoing long-term dialysis von LEICHTER, K. E, DIETRICH, R, SALUSKY, I. B, FOLEY, J, COHEN, A. H, KANGARLOO, H, FINE, R. N

Volltext

Alport's syndrome and achalasia von Leichter, H E, Vargas, J, Cohen, A H, Ament, M, Salusky, I B

Volltext

Primary focal segmental glomerulosclerosis - Long-term outcome after pediatric renal transplantation von Jungraithmayr, Therese C., Bulla, Monika, Dippell, Jürgen, Greiner, Christel, Griebel, Martin, Leichter, Heinz E., Plank, Christian, Tönshoff, Burkhard, Weber, Lutz T., Zimmerhackl, Lothar B.

Volltext

Dent disease with compound heterozygous mutations leading to severe chronic renal failure in a female patient von Holder, Martin, Bald, Martin, Leichter, Heinz E, Ludwig, Michael

Volltext