Skip to main content Accessibility help

We use cookies to distinguish you from other users and to provide you with a better experience on our websites. Close this message to accept cookies or find out how to manage your cookie settings.

Close cookie message
×
Hostname: page-component-77c89778f8-cnmwb Total loading time: 0 Render date: 2024-07-19T11:50:54.879Z Has data issue: false hasContentIssue false

Chapter 3 - Clinical Approach in Adults

from Section 1 - Introduction to Mitochondrial Medicine

Published online by Cambridge University Press:  28 April 2018

By
Michael J. Keogh ,
Hannah E. Steele  and
Patrick F. Chinnery
Edited by
Patrick F. Chinnery  and
Michael J. Keogh
Patrick F. Chinnery
Affiliation:
University of Cambridge
Michael J. Keogh
Affiliation:
University of Newcastle upon Tyne
Get access

Summary

A summary is not available for this content so a preview has been provided. Please use the Get access link above for information on how to access this content.
Image of the first page of this content. For PDF version, please use the ‘Save PDF’ preceeding this image.'
Type
Chapter
Information
Clinical Mitochondrial Medicine , pp. 22 - 38
Publisher: Cambridge University Press
Print publication year: 2018

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Chinnery, PF. Inheritance of mitochondrial disorders. Mitochondrion 2002; 2(1–2): 149–155.Google Scholar
Cree, LM, Samuels, DC, Chinnery, PF. The inheritance of pathogenic mitochondrial DNA mutations. Biochimica et biophysica acta 2009; 1792(12): 1097–1102.Google Scholar
McFarland, R, Taylor, RW, Turnbull, DM. The neurology of mitochondrial DNA disease. The Lancet Neurology 2002; 1(6): 343–351.Google Scholar
Kullar, PJ, Quail, J, Lindsey, P, et al. Both mitochondrial DNA and mitonuclear gene mutations cause hearing loss through cochlear dysfunction. Brain: A Journal of Neurology 2016; 139(Pt. 6): e33.CrossRefGoogle ScholarPubMed
Schaefer, AM, Walker, M, Turnbull, DM, Taylor, RW. Endocrine disorders in mitochondrial disease. Molecular and Cellular Endocrinology 2013; 379(1–2): 2–11.Google Scholar
DiMauro, S, Hirano, M. Mitochondrial DNA deletion syndromes. In Pagon, RA, Adam, MP, Ardinger, HH, et al., eds. GeneReviews(R). Seattle (WA); 2011.Google Scholar
Taylor, RW, Schaefer, AM, Barron, MJ, McFarland, R, Turnbull, DM. The diagnosis of mitochondrial muscle disease. Neuromuscular Disorders: NMD 2004; 14(4): 237–245.CrossRefGoogle ScholarPubMed

Save book to Kindle

To save this book to your Kindle, first ensure coreplatform@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×