Chapters and Other Publications — Thomas Lloyd, M.D., Ph.D.

Click on the Expand plus sign sign to list the book chapters and other publications by year. Then click on the link for details of that publication.

2023

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  • 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

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  • 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.