Current perspectives in the study of human mitochondriopathies
Author:
Affiliation:
1. Neurology DepartmentSt Vincent's Hospital41 Victoria ParadeFitzroyVIC3065
2. Department of BiochemistryMonash UniversityWellington RoadClaytonVIC3168
3. Muscle LaboratoryRoyal Children's HospitalFlemington RoadParkvilleVIC3052
Publisher
AMPCo
Subject
General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.5694/j.1326-5377.1988.tb120480.x
Reference29 articles.
1. A CASE OF SEVERE HYPERMETABOLISM OF NONTHYROID ORIGIN WITH A DEFECT IN THE MAINTENANCE OF MITOCHONDRIAL RESPIRATORY CONTROL: A CORRELATED CLINICAL, BIOCHEMICAL, AND MORPHOLOGICAL STUDY
2. TWO CHILDHOOD MYOPATHIES WITH ABNORMAL MITOCHONDRIA
3. Oculocraniosomatic Neuromuscular Disease With "Ragged-Red" Fibers
4. CLINICAL FEATURES OF MITOCHONDRIAL MYOPATHY
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2. Ophthalmic Involvement in Myo-neuro-gastrointestinal Encephalopathy Syndrome;American Journal of Ophthalmology;1992-09
3. Adult-onset mitochondrial myopathy.;Postgraduate Medical Journal;1992-03-01
4. Polymyalgia rheumatica and mitochondrial myopathy: Clinicopathologic and biochemical studies in five cases;The American Journal of Medicine;1992-02
5. MITOCHONDRIAL DNA MUTATIONS AS AN IMPORTANT CONTRIBUTOR TO AGEING AND DEGENERATIVE DISEASES;The Lancet;1989-03
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