Showing results (161-170 of 176) with videos related to
Sort By:
Pageof 18
American Journal of Human Genetics|March 31, 2015
Loss-of-function alanyl-tRNA synthetase mutations cause an autosomal-recessive early-onset epileptic encephalopathy with persistent myelination defectCas Simons, Laurie B Griffin, Guy Helman, et al.HGG Advances|October 1, 2025
Bi-allelic variants in BCAT1 impair mitochondrial function and are associated with a candidate neurometabolic disorderBrianna L DiSanza, Giulia S Porcari, Livia Sertori Finoti, et al.Journal of the American College of Radiology : JACR|May 6, 2017
ACR Appropriateness Criteria® Cerebrovascular Disease, Michael B Salmela, Shabnam Mortazavi, et al.Brain : a Journal of Neurology|July 26, 2024
Prenatal assessment of brain malformations on neuroimaging: an expert panel reviewIvana Pogledic, Kshitij Mankad, Mariasavina Severino, et al.Journal of the American College of Radiology : JACR|May 7, 2020
ACR Appropriateness Criteria® Cerebrovascular Disease-Child, Richard L Robertson, Susan Palasis, et al.Journal of the American College of Radiology : JACR|May 7, 2020
ACR Appropriateness Criteria® Head Trauma-Child, Maura E Ryan, Sumit Pruthi, et al.Journal of the American College of Radiology : JACR|November 27, 2022
ACR Appropriateness Criteria® Ataxia-Child, Rupa Radhakrishnan, Lindsey A G Shea, et al.AJNR. American Journal of Neuroradiology|August 17, 2023
Dandy-Walker Phenotype with Brainstem Involvement: 2 Distinct Subgroups with Different PrognosisC A P F Alves, J Sidpra, A Manteghinejad, et al.Journal of the American College of Radiology : JACR|May 6, 2019
ACR Appropriateness Criteria® Suspected Spine Trauma-Child, Nadja Kadom, Susan Palasis, et al.Neurology. Genetics|September 25, 2025
Deep Intronic SVA_E Insertion Identified as the Most Common Pathogenic Variant Associated With Canavan Disease: A Diagnostic Blind SpotCarlos A Dominguez Gonzalez, Katrina M Bell, Ramakrishnan Rajagopalan, et al.Pageof 18