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Proceedings. IEEE International Symposium on Biomedical Imaging|September 4, 2020
LEARNING TO DETECT BRAIN LESIONS FROM NOISY ANNOTATIONSDavood Karimi, Jurriaan M Peters, Abdelhakim Ouaalam, et al.Clinical Endocrinology|February 10, 2015
Postoperative follow-up of Cushing's disease using cortisol, desmopressin and coupled dexamethasone-desmopressin tests: a head-to-head comparisonPauline Le Marc'hadour, Marie Muller, Frederique Albarel, et al.Molecular Autism|January 29, 2021
Cross-level analysis of molecular and neurobehavioral function in a prospective series of patients with germline heterozygous PTEN mutations with and without autismThomas W Frazier, Ritika Jaini, Robyn M Busch, et al.American Journal of Medical Genetics. Part A|May 20, 2004
Unusual features in a patient with neurofibromatosis type 1: multiple subcutaneous lipomas, a juvenile polyp in ascending colon, congenital intrahepatic portosystemic venous shunt, and horseshoe kidneyCagatay Oktenli, Davut Gul, M Salih Deveci, et al.Journal of Autism and Developmental Disorders|February 17, 2021
Brief Report: Role of Parent-Reported Executive Functioning and Anxiety in Insistence on Sameness in Individuals with Germline PTEN MutationsMirko Uljarević, Thomas W Frazier, Gaëlle Rached, et al.Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology|February 13, 2013
Implementation of universal microsatellite instability and immunohistochemistry screening for diagnosing lynch syndrome in a large academic medical centerBrandie Heald, Thomas Plesec, Xiuli Liu, et al.Plos One|April 18, 2023
Microbiomic profiles of bile in patients with benign and malignant pancreaticobiliary diseaseShyam K Poudel, Roshan Padmanabhan, Heloni Dave, et al.American Journal of Medical Genetics. Part A|August 23, 2021
Toward better characterization of restricted and repetitive behaviors in individuals with germline heterozygous PTEN mutationsMirko Uljarević, Thomas W Frazier, Gaëlle Rached, et al.Endocrine-Related Cancer|May 26, 2018
65 YEARS OF THE DOUBLE HELIX: Genetics informs precision practice in the diagnosis and management of pheochromocytomaHartmut P Neumann, William F Young, Tobias Krauss, et al.Human Molecular Genetics|December 25, 2016
Germline compound heterozygous poly-glutamine deletion in USF3 may be involved in predisposition to heritable and sporadic epithelial thyroid carcinomaYing Ni, Spencer Seballos, Benjamin Fletcher, et al.Pageof 59