NEJM -- Table of Contents (May 18 1989, 320 [20])

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Mitochondrial DNA deletions in progressive external ophthalmoplegia and Kearns-Sayre syndrome
C. T. Moraes and Others
Abstract

A mitochondrial DNA mutation as a cause of Leber's hereditary optic neuropathy
G. Singh, M. T. Lott, and D. C. Wallace
Abstract

Treatment of cyclic neutropenia with granulocyte colony-stimulating factor
W. P. Hammond, T. H. Price, L. M. Souza, and D. C. Dale
Abstract

Assessing acid-base status in circulatory failure. Differences between arterial and central venous blood
H. J. Adrogue and Others
Abstract

Bronchial hyperresponsiveness to methacholine in patients with impaired left ventricular function
L. R. Cabanes and Others
Abstract

The biology of osteoarthritis
D. Hamerman

A defect in mitochondrial electron-transport activity (NADH-coenzyme Q oxidoreductase) in Leber's hereditary optic neuropathy
W. D. Parker, C. A. Oley, and J. K. Parks

Weekly clinicopathological exercises. Case 20-1989. A 33-year-old woman with exertional dyspnea and Raynaud's phenomenon

The mitochondrial genome--breaking the magic circle
A. E. Harding

Treatment of a marrow stem-cell disorder with granulocyte colony-stimulating factor
P. J. Quesenberry

The clinical implications of venous carbon dioxide tension
H. L. Bleich

Cardiac asthma--a fresh look at an old wheeze
A. P. Fishman

Women in medical education

Exposure of health care workers to the blood of patients infected with the human immunodeficiency virus

Ursodeoxycholic acid and gallstones during weight loss

Alcohol-induced injury to the liver
G. A. Rao and E. C. Larkin

Superior limbic keratoconjunctivitis apparently related to particulate material from a ventilation system
R. Corona and J. L. Abraham

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