164 related articles for article (PubMed ID: 6661102)
1. [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
[TBL] [Abstract][Full Text] [Related]
2. Carnitine palmityl transferase deficiency: myoglobinuria and respiratory failure.
Bertorini T; Yeh YY; Trevisan C; Stadlan E; Sabesin S; DiMauro S
Neurology; 1980 Mar; 30(3):263-71. PubMed ID: 7189025
[TBL] [Abstract][Full Text] [Related]
3. Carnitine-palmityl-transferase deficiency.
Cumming WJ; Hardy M; Hudgson P; Walls J
J Neurol Sci; 1976 Dec; 30(2-3):247-58. PubMed ID: 187736
[TBL] [Abstract][Full Text] [Related]
4. Heterogeneity of carnitine-palmitoyltransferase deficiency.
Di Donato S; Castiglione A; Rimoldi M; Cornelio F; Vendemia F; Cardace G; Bertagnolio B
J Neurol Sci; 1981 May; 50(2):207-15. PubMed ID: 7229666
[TBL] [Abstract][Full Text] [Related]
5. 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
[TBL] [Abstract][Full Text] [Related]
6. [Recurrent paroxysmal myoglobinuria with acute renal insufficiency caused by muscular carnitine (palmitoyltransferase deficiency. A case].
Meunier J; Perrot D; Bret M; Pissere-Meunier J; Bouletreau P; Pasquier J; Carrier H; Berthillier G
Nouv Presse Med; 1982 Sep; 11(37):2767-71. PubMed ID: 7145668
[TBL] [Abstract][Full Text] [Related]
7. Recurrent myoglobinuria due to muscle carnitine palmityl transferase deficiency.
Reza MJ; Kar NC; Pearson CM; Kark RA
Ann Intern Med; 1978 May; 88(5):610-5. PubMed ID: 646243
[TBL] [Abstract][Full Text] [Related]
8. Increased serum lactate dehydrogenase isoenzyme 1 and "flipped" LD-1/LD-2 ratio in myopathy associated with partial carnitine palmitoyltransferase deficiency.
Moses GC; Henderson AR
Clin Chem; 1987 Nov; 33(11):2111-3. PubMed ID: 3677386
[TBL] [Abstract][Full Text] [Related]
9. [Muscular carnitine-palmityl-transferase deficiency].
Rumpf KW; Kaiser H; Goebel HH; Wagner HA; Ullmann B; DiMauro S; Scheler F
Dtsch Med Wochenschr; 1983 Jul; 108(27):1058-61. PubMed ID: 6861647
[TBL] [Abstract][Full Text] [Related]
10. Cold induced rhabdomyolysis in carnitine palmyityl transferase deficiency.
Brownell AK; Severson DL; Thompson CD; Fletcher T
Can J Neurol Sci; 1979 Aug; 6(3):367-70. PubMed ID: 487329
[TBL] [Abstract][Full Text] [Related]
11. [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]
12. Recurrent myoglobinuria and muscle carnitine palmityltransferase deficiency.
Herman J; Nadler HL
J Pediatr; 1977 Aug; 91(2):247-50. PubMed ID: 874682
[TBL] [Abstract][Full Text] [Related]
13. Biochemical and physiologic consequences of carnitine palmityltransferase deficiency.
Carroll JE; Brooke MH; DeVivo DC; Kaiser KK; Hagberg JM
Muscle Nerve; 1978; 1(2):103-10. PubMed ID: 750917
[TBL] [Abstract][Full Text] [Related]
14. 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
[TBL] [Abstract][Full Text] [Related]
15. Combined partial deficiency of muscle carnitine palmitoyltransferase and carnitine with autosomal dominant inheritance.
Ionasescu V; Hug G; Hoppel C
J Neurol Neurosurg Psychiatry; 1980 Aug; 43(8):679-82. PubMed ID: 7431028
[TBL] [Abstract][Full Text] [Related]
16. Myoglobinuria in carnitine palmityltransferase deficiency.
Rowett D
Int Urol Nephrol; 1982; 14(3):285-91. PubMed ID: 7161012
[TBL] [Abstract][Full Text] [Related]
17. Partial muscle carnitine palmitoyltransferase-A deficiency. Rhabdomyolysis associated with transiently decreased muscle carnitine content after ibuprofen therapy.
Ross NS; Hoppel CL
JAMA; 1987 Jan; 257(1):62-5. PubMed ID: 3783904
[TBL] [Abstract][Full Text] [Related]
18. [Intolerance to exercise caused by carnitine palmitoyltransferase deficiency].
Desnuelle C; Pellissier JF; de Barsy T; Serratrice G
Rev Neurol (Paris); 1990; 146(3):231-4. PubMed ID: 2184487
[TBL] [Abstract][Full Text] [Related]
19. Clinical varieties of carnitine and carnitine palmitoyltransferase deficiency.
Angelini C; Trevisan C; Isaya G; Pegolo G; Vergani L
Clin Biochem; 1987 Feb; 20(1):1-7. PubMed ID: 3552320
[TBL] [Abstract][Full Text] [Related]
20. Muscle Carnitine Palmitoyltransferase II Deficiency: A Review of Enzymatic Controversy and Clinical Features.
Lehmann D; Motlagh L; Robaa D; Zierz S
Int J Mol Sci; 2017 Jan; 18(1):. PubMed ID: 28054946
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]