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Journal of Immunology (Baltimore, Md. : 1950)|June 1, 2014
The thyroxine-containing thyroglobulin peptide (aa 2549-2560) is a target epitope in iodide-accelerated spontaneous autoimmune thyroiditisPanayota Kolypetri, Karen Carayanniotis, Shofiur Rahman, et al.
Molecular Biology Reports|April 29, 2024
Two case reports of a novel missense mutation in the PNPLA6 gene in two siblings with chorioretinal dystrophy, hypogonadotropic hypogonadism, and cerebellar ataxiaAndreas Liampas, Paschalis Nicolaou, Christina Votsi, et al.
Clinical Infectious Diseases : an Official Publication of the Infectious Diseases Society of America|September 1, 1992
Infections due to Nocardia transvalensis: clinical spectrum and antimicrobial therapyM M McNeil, J M Brown, P R Georghiou, et al.
Plos One|December 17, 2021
Equivalence of the GeneXpert System and GeneXpert Omni System for tuberculosis and rifampicin resistance detectionSophia B Georghiou, Riccardo Alagna, Daniela M Cirillo, et al.
Bioresource Technology|March 10, 2006
Cellulose, hemicelluloses, lignin and ash content of some organic materials and their suitability for use as paper pulp supplementsC Ververis, K Georghiou, D Danielidis, et al.
The Annals of Thoracic Surgery|August 7, 2003
Pulmonary inflammatory myofibroblastic tumor invading the left atriumMarius Berman, Georgios P Georghiou, Tommy Schonfeld, et al.
American Journal of Medical Genetics|December 1, 1992
New hereditary malformation syndrome of unusual facial appearance, skeletal deformities, and musculoskeletal and sensory defectsL T Middleton, V Anastasiades, K Panayidou, et al.
The Journal of Heart Valve Disease|December 9, 2003
Double-valve Libman-Sacks endocarditis: an entity that demands special considerationGeorgios P Georghiou, Yaron Shapira, Tamara Drozd, et al.
Plos One|April 6, 2012
Evaluation of genetic mutations associated with Mycobacterium tuberculosis resistance to amikacin, kanamycin and capreomycin: a systematic reviewSophia B Georghiou, Marisa Magana, Richard S Garfein, et al.
BMJ Case Reports|June 21, 2011
Complete deletion of the aprataxin gene: ataxia with oculomotor apraxia type 1 with severe phenotype and cognitive deficitGrace Yoon, Robyn Westmacott, Lynn Macmillan, et al.
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