Showing results (31-40 of 48) with videos related to

Sort By:
Pageof 5
American Journal of Therapeutics|July 24, 2012
Hormonal secretion and quality of life in Nelson syndrome and Cushing disease after long acting repeatable octreotide: a short series and updateAlejandro L Arregger, Estela M L Cardoso, Olga B Sandoval, et al.
Journal of Inherited Metabolic Disease|April 22, 2009
Early-onset hyperargininaemia: a severe disorder?M Schiff, J-F Benoist, M L Cardoso, et al.
Journal of Inherited Metabolic Disease|December 18, 2007
Incidence of 3-hydroxy-3-methylglutaryl-coenzyme A lyase (HL) deficiency in Brazil, South AmericaC R Vargas, A Sitta, G Schmitt, et al.
International Endodontic Journal|August 14, 2015
Suboptimal push-out bond strengths of calcium silicate-based sealersD S Oliveira, M L Cardoso, T F Queiroz, et al.
Clinical Genetics|March 21, 2013
Living with inborn errors of cholesterol biosynthesis: lessons from adult patientsM L Cardoso, M Barbosa, D Serra, et al.
Molecular Genetics and Metabolism|August 17, 2004
The E37X is a common HMGCL mutation in Portuguese patients with 3-hydroxy-3-methylglutaric CoA lyase deficiencyM L Cardoso, M R Rodrigues, E Leão, et al.
Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|July 28, 2010
Salivary testosterone for the diagnosis of androgen deficiency in end-stage renal diseaseEstela M L Cardoso, Liliana N Contreras, Elida G Tumilasci, et al.
Journal of Inherited Metabolic Disease|October 17, 2006
Mutational spectrum of classical galactosaemia in Spain and PortugalL Gort, M D Boleda, L Tyfield, et al.
Pageof 5