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The Journal of Clinical Endocrinology and Metabolism|June 11, 2014
Common genetic variants in the glucocorticoid receptor and the 11β-hydroxysteroid dehydrogenase type 1 genes influence long-term cognitive impairments in patients with Cushing's syndrome in remissionOskar Ragnarsson, Camilla A M Glad, Peter Berglund, et al.Journal of Developmental and Behavioral Pediatrics : JDBP|October 7, 2021
Parent-Reported Social Skills in Children with Neurofibromatosis Type 1: Longitudinal Patterns and Relations with Attention and Cognitive FunctioningDanielle M Glad, Christina L Casnar, Brianna D Yund, et al.Biochemistry|October 4, 1994
Metabolic studies on Saccharomyces cerevisiae containing fused citrate synthase/malate dehydrogenaseC Lindbladh, R D Brodeur, W C Small, et al.Optics Letters|October 30, 2009
Time-resolved studies of stimulated emission from colloidal dye solutionsM Siddique, R R Alfano, G A Berger, et al.Journal of Pediatric Psychology|October 19, 2021
Longitudinal Investigation of Early Motor Development in Neurofibromatosis Type 1Sara K Pardej, Danielle M Glad, Christina L Casnar, et al.Child Neuropsychology : a Journal on Normal and Abnormal Development in Childhood and Adolescence|February 16, 2022
Patterns of performance of children with neurofibromatosis type 1 on the K-CPT and K-CPT 2Sara K Pardej, Danielle M Glad, Kristin M Lee, et al.European Journal of Endocrinology|September 15, 2017
MECHANISMS IN ENDOCRINOLOGY: Clinical and pharmacogenetic aspects of the growth hormone receptor polymorphismCesar L Boguszewski, Edna J L Barbosa, Per-Arne Svensson, et al.Scientific Reports|March 17, 2017
Reduced DNA methylation and psychopathology following endogenous hypercortisolism - a genome-wide studyCamilla A M Glad, Johanna C Andersson-Assarsson, Peter Berglund, et al.Biochemistry|October 4, 1994
Preparation and kinetic characterization of a fusion protein of yeast mitochondrial citrate synthase and malate dehydrogenaseC Lindbladh, M Rault, C Hagglund, et al.Journal of the Endocrine Society|December 22, 2017
Pseudoacromegaly: A Differential Diagnostic Problem for Acromegaly With a Genetic SolutionPer Dahlqvist, Rupert Spencer, Pedro Marques, et al.Pageof 17