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Journal Abstract Search
142 related items for PubMed ID: 3825503
1. Familial combined deficiency of muscle carnitine and carnitine palmityl transferase (CPT). Skard Heier M, Dietrichson P, Landaas S. Acta Neurol Scand; 1986 Dec; 74(6):479-85. PubMed ID: 3825503 [Abstract] [Full Text] [Related]
3. [Myopathy due to carnitine palmitoyltransferase deficiency. Report of 2 cases with enzymatic analyses on muscle tissue]. Werneck LC, Boer CA, Papadimitriou A, Di Mauro S. Arq Neuropsiquiatr; 1983 Dec; 41(4):377-84. PubMed ID: 6661102 [Abstract] [Full Text] [Related]
4. Biochemical and physiologic consequences of carnitine palmityltransferase deficiency. Carroll JE, Brooke MH, DeVivo DC, Kaiser KK, Hagberg JM. Muscle Nerve; 1978 Dec; 1(2):103-10. PubMed ID: 750917 [Abstract] [Full Text] [Related]
5. Carnitine palmityl transferase deficiency: clinical variability, carrier detection, and autosomal-recessive inheritance. Angelini C, Freddo L, Battistella P, Bresolin N, Pierobon-Bormioli S, Armani M, Vergani L. Neurology; 1981 Jul; 31(7):883-6. PubMed ID: 7195512 [Abstract] [Full Text] [Related]