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7. [Lipid metabolism disorder in skeletal musculature (carnitine palmitoyltransferase deficiency) and paroxysmal myoglobinuria]. Aver'ianov IuN; Aleksandrovskaia TN; Kal'nova LI; Morozova EA; Shaldaeva VV Zh Nevropatol Psikhiatr Im S S Korsakova; 1980; 80(11):1623-8. PubMed ID: 6935889 [TBL] [Abstract][Full Text] [Related]
8. Fatal systemic carnitine deficiency with lipid storage in skeletal muscle, heart, liver and kidney. Boudin G; Mikol J; Guillard A; Engel AG J Neurol Sci; 1976 Dec; 30(2-3):313-25. PubMed ID: 187738 [TBL] [Abstract][Full Text] [Related]
9. [Primary cardiomyopathy in children with lipid infiltration of the myocardium and skeletal muscles and demonstration of a palmityl-carnitine transferase deficiency. Apropos of 4 cases]. Normand J; Carrier H; Berthillier G; Bozio A; Jocteur-Monrozier D; André M; Joffre B Arch Mal Coeur Vaiss; 1979 May; 72(5):529-35. PubMed ID: 115406 [TBL] [Abstract][Full Text] [Related]
11. Disorders of lipid metabolism in muscle. Di Mauro S; Trevisan C; Hays A Muscle Nerve; 1980; 3(5):369-88. PubMed ID: 7421873 [TBL] [Abstract][Full Text] [Related]
12. Fatal lipid storage myopathy in an infant: case report and autopsy findings. Esiri MM; Bower BD; Ross BD J Neurol Sci; 1979 Mar; 41(1):93-100. PubMed ID: 438846 [TBL] [Abstract][Full Text] [Related]
13. Lipid storage myopathy associated with recurrent Reye syndrome-like attacks, but with a normal carnitine level. Matsuishi T; Yuge K; Aramaki S; Yoshino M; Yoshida I; Yamashita F Brain Dev; 1988; 10(2):125-9. PubMed ID: 3389475 [TBL] [Abstract][Full Text] [Related]
15. Familial carnitine deficiency. A fatal case and subclinical state in a sister. Scholte HR; Meijer AE; van Wijngaarden GK; Leenders KL J Neurol Sci; 1979 Jun; 42(1):87-101. PubMed ID: 156248 [TBL] [Abstract][Full Text] [Related]
16. Carnitine palmitoyltransferase II deficiency with normal carnitine palmitoyltransferase I in skeletal muscle and leucocytes. Scholte HR; Jennekens FG; Bouvy JJ J Neurol Sci; 1979 Jan; 40(1):39-51. PubMed ID: 762593 [TBL] [Abstract][Full Text] [Related]
18. Fatal cases of lipid storage myopathy with carnitine deficiency. Cornelio F; Di Donato S; Peluchetti D; Bizze A; Bertagnolio B; D'Angelo A; Wiesmann U J Neurol Neurosurg Psychiatry; 1977 Feb; 40(2):170-8. PubMed ID: 194020 [TBL] [Abstract][Full Text] [Related]
19. A case report of Carnitine Palmitoyltransferase deficiency type II. Singh R; Rabi Atul Adawiyah M Med J Malaysia; 2022 Jan; 77(1):98-100. PubMed ID: 35087004 [TBL] [Abstract][Full Text] [Related]
20. Defect in fatty acid oxidation: laboratory and pathologic findings in a patient. Tonsgard JH; Stephens JK; Rhead WJ; Penn D; Horwitz AL; Kirschner BS; Whitington PF; Berger S; Tripp ME Pediatr Neurol; 1991; 7(2):125-30. PubMed ID: 2059253 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]