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Diabetologia|December 29, 2011
Hepatic leptin signalling and subdiaphragmatic vagal efferents are not required for leptin-induced increases of plasma IGF binding protein-2 (IGFBP-2) in ob/ob miceJ Levi, F K Huynh, H C Denroche, et al.
Veterinary Journal (London, England : 1997)|April 25, 2026
Diabetic and overweight cats have altered gut microbial diversity and compositionSouvik Patra, Ursula H Neumann, Chantal J McMillan, et al.
Radiology|January 31, 2002
Pheochromocytomas: detection with 18F DOPA whole body PET--initial resultsStefan Hoegerle, Egbert Nitzsche, Carsten Altehoefer, et al.
The New England Journal of Medicine|September 28, 2007
Evidence of MEN-2 in the original description of classic pheochromocytomaHartmut P H Neumann, Alexander Vortmeyer, Dieter Schmidt, et al.
Central European Neurosurgery|March 16, 2010
Essentials and pitfalls in the treatment of CNS hemangioblastomas and von Hippel-Lindau diseaseS Gläsker, J H Klingler, K Müller, et al.
Malaria Journal|February 4, 2010
Optimized high gradient magnetic separation for isolation of Plasmodium-infected red blood cellsSebastian C Bhakdi, Annette Ottinger, Sangdao Somsri, et al.
World Journal of Surgery|February 3, 2018
Minimally Invasive Surgery (MIS) in Children and Adolescents with Pheochromocytomas and Retroperitoneal Paragangliomas: Experiences in 42 PatientsMartin K Walz, Laura D Iova, Judith Deimel, et al.
American Journal of Kidney Diseases : the Official Journal of the National Kidney Foundation|April 30, 2005
Chronic renal failure and proteinuria in adulthood: Fabry disease predominantly affecting the kidneysMarkus Cybulla, Ellen Schaefer, Susanne Wendt, et al.
Endocrinology|January 16, 2014
IGFBP2 is neither sufficient nor necessary for the physiological actions of leptin on glucose homeostasis in male ob/ob miceUrsula H Neumann, Sam Chen, Yuen Yi C Tam, et al.
Clinical Endocrinology|April 5, 2013
Testing new susceptibility genes in the cohort of apparently sporadic phaeochromocytoma/paraganglioma patients with clinical characteristics of hereditary syndromesMariola Pęczkowska, Aldona Kowalska, Jacek Sygut, et al.
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