Mitochondrial anomalies in a Swiss family with autosomal dominant myoglobinuria
- 14 April 1997
- journal article
- Published by Wiley in American Journal of Medical Genetics
- Vol. 69 (4) , 365-369
- https://doi.org/10.1002/(sici)1096-8628(19970414)69:4<365::aid-ajmg6>3.0.co;2-k
Abstract
No abstract availableKeywords
This publication has 19 references indexed in Scilit:
- A microdeletion in cytochrome c oxidase (COX) subunit III associated with COX deficiency and recurrent myoglobinuriaNature Genetics, 1996
- [sup 123 I] beta-CIT/SPECT imaging demonstrates bilateral loss of dopamine transporters in hemi-Parkinson's diseaseNeurology, 1996
- Rhabdomyolysis Associated with Bacteremia Due to Streptococcus pneumoniae: Case Report and ReviewClinical Infectious Diseases, 1993
- Mitochondrial DNA mutations and disease: It's the quantity that countsNeuro-Ophthalmology, 1993
- The biochemistry of malignant hyperthermia: recent conceptsInternational Journal of Biochemistry, 1992
- Immunoquantitative Analysis of Human Carnitine Palmitoyltransferase I and II DefectsPediatric Research, 1990
- Stimulation of Muscle Protein Degradation and Prostaglandin E2Release by Leukocytic Pyrogen (Interleukin-1)New England Journal of Medicine, 1983
- Rhabdomyolysis Associated With Escherichia coli SepticemiaSouthern Medical Journal, 1980
- Myoglobinuria Associated with Influenza A InfectionAnnals of Internal Medicine, 1974
- Muscle Carnitine Palmityltransferase Deficiency and MyoglobinuriaScience, 1973