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American Journal of Transplantation : Official Journal of the American Society of Transplantation and the American Society of Transplant Surgeons|January 16, 2007
Intravenous iloprost: a new therapeutic option for patients with post-transplant distal limb syndrome (PTDLS)F-P Tillmann, M Jäger, D Blondin, et al.
American Heart Journal|November 1, 1982
Effects of antiarrhythmic surgery on late ventricular potentials recorded by precordial signal averaging in patients with ventricular tachycardiaG Breithardt, L Seipel, J Ostermeyer, et al.
American Journal of Medical Genetics. Part A|May 15, 2009
The Xp contiguous deletion syndrome and autismMarwan Shinawi, Ankita Patel, Prisana Panichkul, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|January 1, 1992
Human cytomegalovirus in rejected kidney grafts; detection by polymerase chain reactionJ Markovic-Lipkovski, C A Müller, G Engler-Blum, et al.
The Clinical Investigator|June 1, 1994
Primary systemic amyloidosis leading to advanced renal and cardiac involvement in a 30-year old manI Spyridopoulos, U Helber, W Voelker, et al.
Human Genetics|September 1, 1996
Yeast artificial chromosome mapping of the cystinosis locus on chromosome 17p by fluorescence in situ hybridizationI Stec, U Peters, E Harms, et al.
Journal of Child Neurology|June 26, 2025
Sleep Problems and Clinical Severity in Rett SyndromeSarika U Peters, Cary Fu, Althea Robinson Shelton, et al.
Pflugers Archiv : European Journal of Physiology|November 3, 1998
Effect of extracellular pH on the myo-inositol transporter SMIT expressed in Xenopus oocytesJ Matskevitch, C A Wagner, T Risler, et al.
Clinical Nephrology|September 1, 1993
Daily subcutaneous administration of recombinant human erythropoietin (rhEPO) in peritoneal dialysis patients: a European dose-response studyB Faller, A Slingeneyer, M Waller, et al.
BMC Medical Genetics|February 14, 2006
Coarctation of the aorta and mild to moderate developmental delay in a child with a de novo deletion of chromosome 15(q21.1q22.2)Seema R Lalani, Trilochan Sahoo, Merideth E Sanders, et al.
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