Neuro-ophthalmologic Manifestations of Mitochondrial DNA Disorders: Chronic Progressive External Ophthalmoplegia, Kearns-Sayre Syndrome, and Leber’s Hereditary Optic Neuropathy-Reference-Cited by-同舟云学术

Neuro-ophthalmologic Manifestations of Mitochondrial DNA Disorders: Chronic Progressive External Ophthalmoplegia, Kearns-Sayre Syndrome, and Leber’s Hereditary Optic Neuropathy

Published:1991-02 Issue:1 Volume:9 Page:147-161
ISSN:0733-8619
Container-title:Neurologic Clinics
language:en
Short-container-title:Neurologic Clinics

Author:

Kosmorsky Gregory,Johns Donald R.

Publisher

Elsevier BV

Subject

Clinical Neurology

Reference46 articles.

1. Sequence in organization of the human mitochondrial genome;Anderson;Nature,1981

2. Kearns-Sayre Syndrome;Bastiaensen;Remarks on the pathogenesis with reference to a case with dwarfism and calcification of the basal ganglia. Neurol Ophthal,1984

3. Lumping or splitting? “Ophthalmoplegia- plus” or Kearns-Sayres syndrome?;Berenberg;Ann Neurol,1977

4. Diabetes mellitus in Kearns-Sayre syndrome;Boltshauser;Am J Dis Child,1978

5. Myocardial ultrastructure and the development of atrioventricular block in Kearns-Sayres syndrome;Charles;Circulation,1981

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