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Archives of Neurology|September 1, 1982
Incomplete palmitate oxidation. Possible source of human myopathyJ B Shumate, M H Brooke, J E Carroll, et al.
Neurology|December 1, 1981
Riboflavin-responsive lipid myopathy and carnitine deficiencyJ E Carroll, J B Shumate, M H Brooke, et al.
Muscle & Nerve|March 1, 1982
Palmitate oxidation in human muscle: comparison to CPT and carnitineJ B Shumate, J E Carroll, M H Brooke, et al.
Archives of Neurology|February 1, 1986
'Dystrophic' lipid myopathy in two sistersJ E Carroll, M H Brooke, A Villadiego, et al.
Muscle & Nerve|March 1, 1978
Biochemical and physiologic consequences of carnitine palmityltransferase deficiencyJ E Carroll, M H Brooke, D C DeVivo, et al.
Metabolism: Clinical and Experimental|June 1, 1979
Fasting as a provocative test in neuromuscular diseasesJ E Carroll, D C DeVivo, M H Brooke, et al.
Lancet (London, England)|March 30, 1985
National Post-Perinatal Infant Mortality and Cot Death Study, Scotland 1981-82G C Arneil, H Brooke, A A Gibson, et al.
The American Journal of Physiology|January 1, 1980
Contractile, biochemical, and histochemical properties of thyrotoxic rat soleus muscleR H Fitts, W W Winder, M H Brooke, et al.
Neurology|June 1, 1987
McArdle's disease with myoadenylate deaminase deficiency: observations in a combined enzyme deficiencyS L Heller, K K Kaiser, G J Planer, et al.
Lancet (London, England)|September 18, 1982
Post-perinatal infant mortality in Glasgow 1979-81G C Arneil, H Brooke, A A Gibson, et al.
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