Chapters and Other Publications — Thomas Lloyd, M.D., Ph.D.
Click on the sign to list the book chapters and other publications by year. Then click on the link for details of that publication.
2023
- Lloyd TE, de Visser M. Diagnosis of inclusion body myositis. In: Christopher-Stine L, Lundberg I, editors. The myositis handbook: An inclusive guide to the inflammatory myopathies. New Delhi: Jaypee Medical Publishers; 2023. (in press).
<2021
- Sullivan JS, Lloyd TE, Sumner CJ. Hereditary channelopathies caused by TRPV4 mutations. In: Koschak A, Weiss N, editors. Pathologies of calcium channels. 2nd ed. Berlin: Springer Verlag; 2014.
- Lloyd TE, Chaudhry V. Management of hereditary neuropathies. In: Bertorini T, editor. Neuromuscular disorders: Management and therapy. Philadelphia: Elsevier; 2010.
- Lloyd TE, Greenberg B, Aldrich E. Stroke. In: Nilsson K, Paccini J, editors. Osler medical handbook. 2nd ed. Philadelphia: Mosby; 2006.
- Lloyd TE, Bellen HJ. Genetic analysis of neurotransmitter release in mice and humans. In: Bellen HJ, editor. Neurotransmitter release. Oxford Univ Press; 1999.