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Neuromuscular Disorders : NMD|January 26, 2019
Dominantly inherited distal nemaline/cap myopathy caused by a large deletion in the nebulin geneKirsi J Kiiski, Vilma-Lotta Lehtokari, Anna K Vihola, et al.
JAMA Psychiatry|November 15, 2023
Neighborhood Disadvantage and Autism Spectrum Disorder in a Population With Health InsuranceXin Yu, Md Mostafijur Rahman, Sarah A Carter, et al.
BMC Medicine|June 11, 2026
Ambient pollution components and sources are associated with hippocampal architecture and memory in pre-adolescentsMichael A Rosario, Kirthana Sukumaran, Katherine L Bottenhorn, et al.
Biology of Blood and Marrow Transplantation : Journal of the American Society for Blood and Marrow Transplantation|May 15, 2001
Marrow transplants from unrelated donors for patients with aplastic anemia: minimum effective dose of total body irradiationH J Deeg, I D Amylon, R E Harris, et al.
Cancer|July 3, 2023
A phase 2 study of neoadjuvant chemotherapy plus durvalumab in resectable locally advanced head and neck squamous cell carcinomaShetal A Patel, Michael K Gibson, Allison Deal, et al.
American Journal of Human Genetics|August 5, 2005
Mitochondrial DNA polymerase W748S mutation: a common cause of autosomal recessive ataxia with ancient European originAnna H Hakonen, Silja Heiskanen, Vesa Juvonen, et al.
Head & Neck|December 17, 2018
Shoulder symptoms and quality of life impact of limited neck dissection after de-intensified chemoradiotherapy: Secondary analysis of two prospective trialsKyle Wang, Dominic H Moon, Robert J Amdur, et al.
Clinical Pharmacology and Therapeutics|April 7, 2022
Innovative Randomized Phase I Study and Dosing Regimen Selection to Accelerate and Inform Pivotal COVID-19 Trial of NirmatrelvirRavi Shankar P Singh, Sima S Toussi, Frances Hackman, et al.
Scientific Reports|July 9, 2024
Molecular characterization of the salivary adenoid cystic carcinoma immune landscape by anatomic subsitesJason Tasoulas, Travis P Schrank, Harish Bharambe, et al.
Annals of Neurology|January 8, 2014
Atypical phenotypes in titinopathies explained by second titin mutationsAnni Evilä, Anna Vihola, Jaakko Sarparanta, et al.
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