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World Journal of Urology|November 30, 2005
Diagnosis and metaphylaxis of stone disease. Consensus concept of the National Working Committee on Stone Disease for the upcoming German Urolithiasis GuidelineM Straub, W L Strohmaier, W Berg, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|September 10, 2011
Autosomal dominant mutation in the signal peptide of renin in a kindred with anemia, hyperuricemia, and CKDBodo B Beck, Howard Trachtman, Michael Gitman, et al.
Journal of Molecular and Cellular Cardiology|September 1, 1996
Consequences of coronary occlusion on changes in regional interstitial myocardial neuropeptide Y and norepinephrine concentrationsP M Mertes, K el-Abbassi, Y Jaboin, et al.
Transplant Infectious Disease : an Official Journal of the Transplantation Society|April 11, 2012
Skin lesions, malaise, and heart failure in a renal transplant recipientC Kocher, S Segerer, A Schleich, et al.
Inorganic Chemistry|March 30, 2026
Pressure-Induced Reduction of Dicyanamide by Samarium(II) in a Coordination PolymerHannah B Wineinger, Tyler W Hines, Kacy N Mendoza, et al.
American Journal of Physiology. Lung Cellular and Molecular Physiology|October 22, 2002
Decreased alveolar oxygen induces lung inflammationC Madjdpour, U R Jewell, S Kneller, et al.
Inorganic Chemistry|March 10, 2025
Insights into the Complexation of Actinides by Diethylenetriaminepentaacetic Acid from Characterization of the Americium(III) ComplexBrian M Rotermund, Nicholas B Beck, Hannah B Wineinger, et al.
Autism : the International Journal of Research and Practice|December 14, 2021
Stakeholder informed development of the Emotion Awareness and Skills Enhancement team-based program (EASE-Teams)Kelly B Beck, Jessie B Northrup, Kaitlyn E Breitenfeldt, et al.
Glycobiology|August 31, 2024
Cosmc regulates O-glycan extension in murine hepatocytesRajindra P Aryal, Maxence Noel, Junwei Zeng, et al.
Stem Cell Research|November 13, 2019
Generation of an induced pluripotent stem cell line (CIMAi001-A) from a compound heterozygous Primary Hyperoxaluria Type I (PH1) patient carrying p.G170R and p.R122* mutations in the AGXT geneRebeca Martinez-Turrillas, Saray Rodriguez-Diaz, Paula Rodriguez-Marquez, et al.
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