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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.Brain & Development|June 1, 1997
L-2-Hydroxyglutaric aciduria: clinical, biochemical and magnetic resonance imaging in six Portuguese pediatric patientsC Barbot, I Fineza, L Diogo, 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.Molecular and Biochemical Parasitology|August 27, 1998
Conservation of genetic linkage between heat shock protein 100 and glycosylphosphatidylinositol-specific phospholipase C in Trypanosoma brucei and Trypanosoma cruziM B Redpath, N Carnall, H Webb, 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