| scholarly article | Q13442814 |
| P356 | DOI | 10.1136/JNNP.39.11.1114 |
| P953 | full work available at URL | https://europepmc.org/articles/PMC1083312 |
| https://europepmc.org/articles/PMC1083312?pdf=render | ||
| P932 | PMC publication ID | 1083312 |
| P698 | PubMed publication ID | 1011021 |
| P5875 | ResearchGate publication ID | 22143998 |
| P2093 | author name string | H. Isaacs | |
| J. J. Heffron | |||
| A. Pickering | |||
| M. Badenhorst | |||
| P2860 | cites work | Protein measurement with the Folin phenol reagent | Q20900776 |
| A mitochondrial carnitine acylcarnitine translocase system | Q35072156 | ||
| The syndrome of 'continuous muscle-fibre activity' cured: further studies | Q37103800 | ||
| A disorder of muscle lipid metabolism and myoglobinuria. Absence of carnitine palmityl transferase | Q39727955 | ||
| Hereditary carnitine deficiency of muscle | Q39727985 | ||
| Idiopathic cardiomyopathy and skeletal muscle abnormality | Q39966022 | ||
| Luft's disease. Further biochemical and ultrastructural studies of skeletal muscle in the second case | Q42449142 | ||
| Carnitine Deficiency of Human Skeletal Muscle with Associated Lipid Storage Myopathy: A New Syndrome | Q44097276 | ||
| Carnitine and the Twins | Q45032184 | ||
| Two childhood myopathies with abnormal mitochondria. I. Megaconial myopathy. II. Pleoconial myopathy | Q51238390 | ||
| THE DISTRIBUTION OF CARNITINE, ACETYLCARNITINE, AND CARNITINE ACETYLTRANSFERASE IN RAT TISSUES | Q51252072 | ||
| Myopathy associated with abnormal lipid metabolism in skeletal muscle | Q55847298 | ||
| Neutral-lipid storage disease: a new disorder of lipid metabolism | Q57971906 | ||
| Serum carnitine. An index of muscle destruction in man | Q69475445 | ||
| Autophagic glycogenosis of late onset with mitochondrial abnormalities: light and electron microscopic observations | Q69869570 | ||
| Lipid storage myopathy responsive to prednisone | Q70410732 | ||
| Carnitine palmityltransferase. Location of two enzymatic activities in rat liver mitochondria | Q70447423 | ||
| A Skeletal-Muscle Disorder Associated with Intermittent Symptoms and a Possible Defect of Lipid Metabolism | Q71425473 | ||
| Carnitine depletion in the choline-deficient state | Q72326261 | ||
| The familial occurrence of fat containing vacuoles in the leukocytes diagnosed in two brothers suffering from dystrophia musculorum progressiva (ERB.). | Q73236252 | ||
| LONG-CHAIN CARNITINE ACYLTRANSFERASE AND THE ROLE OF ACYLCARNITINE DERIVATIVES IN THE CATALYTIC INCREASE OF FATTY ACID OXIDATION INDUCED BY CARNITINE | Q76852241 | ||
| Evolution and content of vacuoles in primary hypokalemic periodic paralysis | Q93694342 | ||
| A myopathy associated with lipid storage | Q93724729 | ||
| P433 | issue | 11 | |
| P407 | language of work or name | English | Q1860 |
| P921 | main subject | lipid metabolism | Q2792936 |
| P304 | page(s) | 1114-1123 | |
| P577 | publication date | 1976-11-01 | |
| P1433 | published in | Journal of Neurology, Neurosurgery and Psychiatry | Q1599804 |
| P1476 | title | Weakness associated with the pathological presence of lipid in skeletal muscle: a detailed study of a patient with carnitine deficiencey | |
| P478 | volume | 39 |
| Q51877455 | "Carnitine deficient" myopathy and cardiomyopathy with fatal outcome |
| Q72613965 | A hereditary case of lipid storage myopathy with carnitine deficiency. Ultrastructural observation of muscle tissue in parents |
| Q33584380 | Autosomal recessive lipid storage myopathy (probable carnitine deficiency) |
| Q39764040 | Clinical varieties of carnitine and carnitine palmitoyltransferase deficiency |
| Q48214254 | Further studies of mitochondrial and lipid storage myopathies |
| Q42107345 | Lipid storage myopathy: successful treatment with propranolol |
| Q66842525 | Metabolic Myopathies |
| Q39501840 | Muscular carnitine synthesis and palmitate metabolism in vitro |
| Q69714913 | Type II fiber myolysis in a patient with hypocarnitinemia |
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