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Head & Neck|April 25, 2024
Evaluating the impact of the degree of extranodal extension on outcomes in locally advanced oral cavity cancerAnirudh Yalamanchali, Christopher Griffith, Chandana A Reddy, et al.Oral Oncology|April 20, 2021
TORS elective lingual tonsillectomy has less acute morbidity than therapeutic base of tongue TORSMihir R Patel, Lauren Ottenstein, Martha Ryan, et al.Health Technology Assessment (Winchester, England)|October 16, 2023
Helping pregnant smokers quit: a multi-centre randomised controlled trial of electronic cigarettes versus nicotine replacement therapyDunja Przulj, Francesca Pesola, Katie Myers Smith, et al.Human Mutation|July 23, 2022
Characterization of a possible founder synonymous variant in TECTA in multiple individuals with autosomal recessive hearing lossRobert Chen, Maria Alejandra Diaz-Miranda, Erfan Aref-Eshghi, et al.Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc|August 11, 2023
DNA Methylation Profiling Distinguishes Adamantinoma-Like Ewing Sarcoma From Conventional Ewing SarcomaKaren J Fritchie, Baptiste Ameline, Vanghelita Andrei, et al.Journal of Child Neurology|September 15, 2020
Boricua Founder Variant in FRRS1L Causes Epileptic Encephalopathy With Hyperkinetic MovementsImane Abdelmoumen, Sandra Jimenez, Ignacio Valencia, et al.Nature Communications|October 2, 2020
Author Correction: NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular diseasePaige B Martin, Yu Kigoshi-Tansho, Roger B Sher, et al.Nature Communications|September 16, 2020
NEMF mutations that impair ribosome-associated quality control are associated with neuromuscular diseasePaige B Martin, Yu Kigoshi-Tansho, Roger B Sher, et al.American Journal of Human Genetics|June 20, 2020
De Novo Variants in CNOT1, a Central Component of the CCR4-NOT Complex Involved in Gene Expression and RNA and Protein Stability, Cause Neurodevelopmental DelayLisenka E L M Vissers, Sreehari Kalvakuri, Elke de Boer, et al.American Journal of Human Genetics|April 8, 2022
Germline variants in tumor suppressor FBXW7 lead to impaired ubiquitination and a neurodevelopmental syndromeSarah E M Stephenson, Gregory Costain, Laura E R Blok, et al.Pageof 3