Fellow of The Academy of Medical Sciences, United Kingdom
His main research concerns Acetylcholine receptor, Myasthenia gravis, Immunology, Congenital myasthenic syndrome and Neuromuscular junction. His Acetylcholine receptor research is within the category of Internal medicine. His research in Myasthenia gravis intersects with topics in Arthrogryposis multiplex congenita and Antigen.
His research integrates issues of Odds ratio, Receptor, Allele frequency and Age of onset in his study of Immunology. David Beeson has researched Congenital myasthenic syndrome in several fields, including Surgery, Weakness and Neuromuscular transmission. His Neuromuscular junction study combines topics from a wide range of disciplines, such as DPAGT1, Bioinformatics and Cell biology.
The scientist’s investigation covers issues in Acetylcholine receptor, Congenital myasthenic syndrome, Myasthenia gravis, Neuromuscular junction and Immunology. David Beeson interconnects Molecular biology, Endocrinology and Protein subunit in the investigation of issues within Acetylcholine receptor. His biological study spans a wide range of topics, including DPAGT1, Pediatrics and Neuromuscular transmission.
His work focuses on many connections between Neuromuscular transmission and other disciplines, such as Weakness, that overlap with his field of interest in Ptosis. His work in Myasthenia gravis addresses subjects such as Antibody, which are connected to disciplines such as Virology. The various areas that he examines in his Neuromuscular junction study include Agrin, Synapse, Muscle weakness and Cell biology.
His primary scientific interests are in Neuromuscular junction, Acetylcholine receptor, Neuromuscular transmission, Congenital myasthenic syndrome and Myasthenia gravis. His Neuromuscular junction research is multidisciplinary, incorporating elements of Postsynaptic potential, Pyridostigmine, Muscle contraction, Cell biology and Synapse. David Beeson combines subjects such as Endocrinology and Motor neuron with his study of Acetylcholine receptor.
His Neuromuscular transmission research is multidisciplinary, relying on both Genetics, Ptosis, Phenotype, Acetylcholine and Weakness. The concepts of his Congenital myasthenic syndrome study are interwoven with issues in Missense mutation, Repetitive nerve stimulation, DPAGT1, Muscle weakness and Pediatrics. His Myasthenia gravis research entails a greater understanding of Immunology.
His primary areas of study are Neuromuscular transmission, Neuromuscular junction, Genetics, Acetylcholine receptor and Myasthenia gravis. His Neuromuscular transmission research is multidisciplinary, incorporating perspectives in Phenotype and Congenital myasthenic syndrome. His Congenital myasthenic syndrome research includes themes of Frameshift mutation, Terminal bouton, Weakness and Pathology.
His Neuromuscular junction research includes elements of Laminin, Glycosylation and Pyridostigmine. His work deals with themes such as Myotube differentiation and Cell biology, which intersect with Acetylcholine receptor. His Myasthenia gravis study incorporates themes from Autoantibody and Severity of illness.
This overview was generated by a machine learning system which analysed the scientist’s body of work. If you have any feedback, you can contact us here.
N-methyl-d-aspartate antibody encephalitis: temporal progression of clinical and paraclinical observations in a predominantly non-paraneoplastic disorder of both sexes
Sarosh R. Irani;Katarzyna Bera;Patrick Waters;Luigi Zuliani.
Brain (2010)
Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria.
Johannes N. Spelbrink;Fang Yuan Li;Valeria Tiranti;Kaisu Nikali.
Nature Genetics (2001)
IgG1 antibodies to acetylcholine receptors in 'seronegative' myasthenia gravis.
Maria Isabel Leite;Saiju Jacob;Stuart Viegas;Judy Cossins.
Brain (2008)
Detection and characterization of MuSK antibodies in seronegative myasthenia gravis
John McConville;Maria Elena Farrugia;David Beeson;Uday Kishore.
Annals of Neurology (2004)
Autoantibodies detected to expressed K+ channels are implicated in neuromyotonia.
Ian K. Hart;Caroline Waters;Angela Vincent;Claire Newland.
Annals of Neurology (1997)
Factors influencing success of clinical genome sequencing across a broad spectrum of disorders
Jenny C. Taylor;Jenny C. Taylor;Hilary C. Martin;Stefano Lise;John Broxholme.
Nature Genetics (2015)
Aquaporin-4 antibodies in neuromyelitis optica and longitudinally extensive transverse myelitis.
Patrick Waters;Sven Jarius;Edward Littleton;Maria Isabel Leite.
JAMA Neurology (2008)
Dok-7 Mutations Underlie a Neuromuscular Junction Synaptopathy
David Beeson;Osamu Higuchi;Jackie Palace;Judy Cossins.
Science (2006)
An IRF8-binding promoter variant and AIRE control CHRNA1 promiscuous expression in thymus
Matthieu Giraud;Richard Taubert;Claire Vandiedonck;Xiayi Ke.
Nature (2007)
Arthrogryposis multiplex congenita with maternal autoantibodies specific for a fetal antigen
A. Vincent;C. Newland;D. Beeson;S. Riemersma.
The Lancet (1995)
If you think any of the details on this page are incorrect, let us know.
We appreciate your kind effort to assist us to improve this page, it would be helpful providing us with as much detail as possible in the text box below:
University of Oxford
TU Dresden
University of Oxford
University of Freiburg
University College London
Nanyang Technological University
University of Oxford
University of Oxford
Newcastle University
University College London
Hasselt University
Otto-von-Guericke University Magdeburg
University of Hildesheim
Nokia (United States)
Harvard University
Indian Institute of Technology Kharagpur
Habley Medical Technology Corporation
University of Wisconsin–Madison
University of Pennsylvania
University of Tokyo
University of Waterloo
Imperial College London
Stanford University
University of California, San Francisco
University of New South Wales
Stanford University