Tumor volume as a predictor of survival in advanced laryngeal cancer treated with total laryngectomy.

Autor: Hanubal KS; College of Medicine, University of Florida, Gainesville, Florida, USA., Galochkina Z; Division of Quantitative Sciences, University of Florida Health Cancer Center, Gainesville, Florida, USA., Lee JH; Division of Quantitative Sciences, University of Florida Health Cancer Center, Gainesville, Florida, USA.; Department of Biostatistics, University of Florida, Gainesville, Florida, USA., List MA; College of Medicine, University of Florida, Gainesville, Florida, USA., Massini TC; Department of Radiology, University of Florida, Gainesville, Florida, USA., Conrad D; Department of Otolaryngology, University of Florida, Gainesville, Florida, USA., Hughley B; Department of Otolaryngology, University of Florida, Gainesville, Florida, USA., Danan D; Department of Otolaryngology, University of Florida, Gainesville, Florida, USA., DeJesus R; Department of Radiology, University of Florida, Gainesville, Florida, USA., Hitchcock K; Department of Radiation Oncology, University of Florida, Gainesville, Florida, USA.; University of Florida Health Cancer Center, Gainesville, Florida, USA., Nichols S; College of Medicine, University of Florida, Gainesville, Florida, USA., Mendenhall W; Department of Radiation Oncology, University of Florida, Gainesville, Florida, USA.; University of Florida Health Cancer Center, Gainesville, Florida, USA., Dziegielewski PT; Department of Otolaryngology, University of Florida, Gainesville, Florida, USA.; University of Florida Health Cancer Center, Gainesville, Florida, USA.

Publikováno v: Head & neck [Head Neck] 2023 Jun; Vol. 45 (6), pp. 1376-1388. Date of Electronic Publication: 2023 Apr 03.

Variants in EXOSC9 Disrupt the RNA Exosome and Result in Cerebellar Atrophy with Spinal Motor Neuronopathy.

Autor: Burns DT; Wellcome Trust Centre for Mitochondrial Research, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne NE1 3BZ, UK., Donkervoort S; Neuromuscular and Neurogenetic Disorders of Childhood Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA., Müller JS; Wellcome Trust Centre for Mitochondrial Research, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne NE1 3BZ, UK., Knierim E; Department of Neuropediatrics and NeuroCure Clinical Research Center, Charité-Universitätsmedizin, Charitéplatz 1, 10117 Berlin, Germany., Bharucha-Goebel D; Neuromuscular and Neurogenetic Disorders of Childhood Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA; Division of Neurology, Children's National Medical Center, Washington, DC 20010, USA., Faqeih EA; Section of Medical Genetics, Department of Pediatric Subspecialties, Children's Specialized Hospital, King Fahad Medical City, Riyadh, Saudi Arabia., Bell SK; Division of Pediatric Neurology, Department of Pediatrics, University of Florida College of Medicine, Gainesville, FL 32610, USA., AlFaifi AY; Section of Medical Genetics, Department of Pediatric Subspecialties, Children's Specialized Hospital, King Fahad Medical City, Riyadh, Saudi Arabia., Monies D; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia., Millan F; GeneDx, Gaithersburg, MD 20877, USA., Retterer K; GeneDx, Gaithersburg, MD 20877, USA., Dyack S; Departments of Pediatrics and Medicine, Dalhousie University, Halifax, NS B3H 4R2, Canada., MacKay S; Maritime Medical Genetics Service, IWK Health Centre, Halifax, NS B3K 6R8, Canada., Morales-Gonzalez S; Department of Neuropediatrics and NeuroCure Clinical Research Center, Charité-Universitätsmedizin, Charitéplatz 1, 10117 Berlin, Germany., Giunta M; Wellcome Trust Centre for Mitochondrial Research, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne NE1 3BZ, UK., Munro B; Wellcome Trust Centre for Mitochondrial Research, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne NE1 3BZ, UK., Hudson G; Wellcome Trust Centre for Mitochondrial Research, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne NE1 3BZ, UK., Scavina M; Division of Neurology, Nemours/DuPont Hospital for Children, Wilmington, DE 19803, USA., Baker L; Division of Genetics, Nemours/DuPont Hospital for Children, Wilmington, DE 19803, USA., Massini TC; Department of Radiology, University of Florida College of Medicine, Gainesville, FL 32610, USA., Lek M; Center for Mendelian Genomics, Program in Medical and Population Genetics, Broad Institute of MIT and Harvard, Cambridge, MA 01242, USA., Hu Y; Neuromuscular and Neurogenetic Disorders of Childhood Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA., Ezzo D; Neuromuscular and Neurogenetic Disorders of Childhood Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA., AlKuraya FS; Department of Genetics, King Faisal Specialist Hospital and Research Center, Riyadh, Saudi Arabia., Kang PB; Division of Pediatric Neurology, Department of Pediatrics, University of Florida College of Medicine, Gainesville, FL 32610, USA., Griffin H; Wellcome Trust Centre for Mitochondrial Research, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne NE1 3BZ, UK., Foley AR; Neuromuscular and Neurogenetic Disorders of Childhood Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA., Schuelke M; Department of Neuropediatrics and NeuroCure Clinical Research Center, Charité-Universitätsmedizin, Charitéplatz 1, 10117 Berlin, Germany., Horvath R; Wellcome Trust Centre for Mitochondrial Research, Institute of Genetic Medicine, Newcastle University, Newcastle upon Tyne NE1 3BZ, UK. Electronic address: rita.horvath@ncl.ac.uk., Bönnemann CG; Neuromuscular and Neurogenetic Disorders of Childhood Section, National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, MD 20892, USA.

Publikováno v: American journal of human genetics [Am J Hum Genet] 2018 May 03; Vol. 102 (5), pp. 858-873.