Similar articles

• Carnitine palmityl transferase deficiency: myoglobinuria and respiratory failure.

  Bertorini T, Yeh YY, Trevisan C, Stadlan E, Sabesin S, DiMauro S. Bertorini T, et al. Neurology. 1980 Mar;30(3):263-71. doi: 10.1212/wnl.30.3.263. Neurology. 1980. PMID: 7189025
• Combined partial deficiency of muscle carnitine palmitoyltransferase and carnitine with autosomal dominant inheritance.

  Ionasescu V, Hug G, Hoppel C. Ionasescu V, et al. J Neurol Neurosurg Psychiatry. 1980 Aug;43(8):679-82. doi: 10.1136/jnnp.43.8.679. J Neurol Neurosurg Psychiatry. 1980. PMID: 7431028 Free PMC article.
• [Lipid metabolism disorder in skeletal musculature (carnitine palmitoyltransferase deficiency) and paroxysmal myoglobinuria].

  Aver'ianov IuN, Aleksandrovskaia TN, Kal'nova LI, Morozova EA, Shaldaeva VV. Aver'ianov IuN, et al. Zh Nevropatol Psikhiatr Im S S Korsakova. 1980;80(11):1623-8. Zh Nevropatol Psikhiatr Im S S Korsakova. 1980. PMID: 6935889 Russian.
• [Intolerance to exercise caused by carnitine palmitoyltransferase deficiency].

  Desnuelle C, Pellissier JF, de Barsy T, Serratrice G. Desnuelle C, et al. Rev Neurol (Paris). 1990;146(3):231-4. Rev Neurol (Paris). 1990. PMID: 2184487 Review. French.
• [Changes in carnitine metabolism. A case report about probable partial deficiency of muscle carnitine palmitoyltransferase].

  De Prà M, Oberti F, De Benedittis A. De Prà M, et al. Pediatr Med Chir. 1990 Jul-Aug;12(4):397-403. Pediatr Med Chir. 1990. PMID: 2075107 Review. Italian.