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The Journal of Clinical Investigation|March 11, 2006
Disease-associated mutations affect intracellular traffic and paracellular Mg2+ transport function of Claudin-16P Jaya Kausalya, Salah Amasheh, Dorothee Günzel, et al.
Pediatric Nephrology (Berlin, Germany)|May 18, 2020
Stiripentol fails to lower plasma oxalate in a dialysis-dependent PH1 patientCaroline Kempf, Anja Pfau, Johannes Holle, et al.
Pediatric Nephrology (Berlin, Germany)|September 22, 2018
Outcome of membranoproliferative glomerulonephritis and C3-glomerulopathy in children and adolescentsJohannes Holle, Lena Berenberg-Goßler, Kaiyin Wu, et al.
Methods in Molecular Biology (Clifton, N.J.)|November 1, 2015
Reconstruction of Protein Networks Using Reverse-Phase Protein Array DataSilvia von der Heyde, Johanna Sonntag, Frank Kramer, et al.
BMC Medical Informatics and Decision Making|October 2, 2025
Cross- & multi-lingual medication detection: a transformer-based analysisLisa Raithel, Johann Frei, Philippe Thomas, et al.
Seminars in Thrombosis and Hemostasis|September 25, 2010
The autoimmune disease DEAP-hemolytic uremic syndromeChristine Skerka, Peter F Zipfel, Dominik Müller, et al.
Blood Purification|September 19, 2019
Single-Pass Albumin Dialysis in the Treatment of Children with Liver FailureJohannes Holle, Alexander Gratopp, Sophie Balmer, et al.
Pediatric Nephrology (Berlin, Germany)|March 12, 2004
NPHS2 mutation associated with recurrence of proteinuria after transplantationHeiko Billing, Dominik Müller, Rainer Ruf, et al.
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