113 related articles for article (PubMed ID: 1476782)
1. Bicarnesine-treated carnitine deficient myopathy: clinico-chemical investigations.
László A; Klujber L; Svékus A
Acta Paediatr Hung; 1992; 32(3):235-9. PubMed ID: 1476782
[TBL] [Abstract][Full Text] [Related]
2. [Carnitine-deficient myopathy successfully treated with bicarnesine; clinico-chemical and muscle morphology studies].
László A; Klujber L; Svékus A
Orv Hetil; 1986 Mar; 127(13):777-9. PubMed ID: 3703543
[No Abstract] [Full Text] [Related]
3. [Lipidic myopathy with severe cardiomyopathy caused by a generalized carnitine deficiency. Favourable course during carnitine hydrochloride treatment].
Morand P; Despert F; Carrier HN; Saudubray BM; Fardeau M; Romieux B; Fauchier C; Combe P
Arch Mal Coeur Vaiss; 1979 May; 72(5):536-44. PubMed ID: 115407
[TBL] [Abstract][Full Text] [Related]
4. Primary carnitine deficiency in a male adult.
Karmaniolas K; Ioannidis P; Liatis S; Dalamanga M; Papalambros T; Migdalis I
J Med; 2002; 33(1-4):105-10. PubMed ID: 12939109
[TBL] [Abstract][Full Text] [Related]
5. A case history of myopathic carnitine deficiency benefited by glucocorticoids and L-carnitine supplementation.
Howard LJ; Beckerman AH
Drug Nutr Interact; 1985; 3(4):191-6. PubMed ID: 4064927
[TBL] [Abstract][Full Text] [Related]
6. Effects of L-carnitine supplementation on muscular symptoms in hemodialyzed patients.
Sakurauchi Y; Matsumoto Y; Shinzato T; Takai I; Nakamura Y; Sato M; Nakai S; Miwa M; Morita H; Miwa T; Amano I; Maeda K
Am J Kidney Dis; 1998 Aug; 32(2):258-64. PubMed ID: 9708610
[TBL] [Abstract][Full Text] [Related]
7. Primary carnitine deficiency: adult onset lipid storage myopathy with a mild clinical course.
Vielhaber S; Feistner H; Weis J; Kreuder J; Sailer M; Schröder JM; Kunz WS
J Clin Neurosci; 2004 Nov; 11(8):919-24. PubMed ID: 15519880
[TBL] [Abstract][Full Text] [Related]
8. Carnitine deficiency of skeletal muscle: report of a treated case.
Angelini C; Lücke S; Cantarutti F
Neurology; 1976 Jul; 26(7):633-7. PubMed ID: 945511
[TBL] [Abstract][Full Text] [Related]
9. Successful carnitine treatment in a non-carnitine-deficient lipid storage myopathy.
Sengers RC; Bakkeren JA; Trijbels JM; Stadhouders AM; Egberink GJ; ter Laak HJ; Jaspar HJ
Eur J Pediatr; 1980 Dec; 135(2):205-9. PubMed ID: 7449803
[TBL] [Abstract][Full Text] [Related]
10. [Carnitine deficiency myopathy (author's transl)].
Jerusalem F
Nervenarzt; 1980 May; 51(5):266-71. PubMed ID: 7007897
[No Abstract] [Full Text] [Related]
11. Nearly fatal muscle carnitine deficiency with full recovery after replacement therapy.
Prockop LD; Engel WK; Shug AL
Neurology; 1983 Dec; 33(12):1629-31. PubMed ID: 6685837
[TBL] [Abstract][Full Text] [Related]
12. [Carnitine in normal subjects and in pathology].
Odièvre M
Arch Fr Pediatr; 1984 Dec; 41(10):721-6. PubMed ID: 6398040
[No Abstract] [Full Text] [Related]
13. Carnitine deficiency associated with long-term pivampicillin treatment: the effect of a replacement therapy regime.
Rose SJ; Stokes TC; Patel S; Cooper MB; Betteridge DJ; Payne JE
Postgrad Med J; 1992 Nov; 68(805):932-4. PubMed ID: 1494519
[TBL] [Abstract][Full Text] [Related]
14. The syndrome of carnitine deficiency.
Di Donato S; Cornelio F
Riv Patol Nerv Ment; 1976 Aug; 97(4):181-5. PubMed ID: 1032033
[TBL] [Abstract][Full Text] [Related]
15. Primary systemic carnitine deficiency: a Turkish case with a novel homozygous SLC22A5 mutation and 14 years follow-up.
Yilmaz BS; Kor D; Mungan NO; Erdem S; Ceylaner S
J Pediatr Endocrinol Metab; 2015 Sep; 28(9-10):1179-81. PubMed ID: 26030785
[TBL] [Abstract][Full Text] [Related]
16. L-carnitine: its therapeutic potential.
DiPalma JR
Am Fam Physician; 1986 Dec; 34(6):127-30. PubMed ID: 3788753
[No Abstract] [Full Text] [Related]
17. Carnitine metabolism and deficiency syndromes.
Rebouche CJ; Engel AG
Mayo Clin Proc; 1983 Aug; 58(8):533-40. PubMed ID: 6348429
[TBL] [Abstract][Full Text] [Related]
18. [Carnitine-deficient cardiomyopathy].
Kádár K; Melegh B; Szendrei E; Herczegfalvi A
Orv Hetil; 1994 Feb; 135(9):473-4. PubMed ID: 8139852
[TBL] [Abstract][Full Text] [Related]
19. Sodium valproate -- induced skeletal myopathy.
Kasturi L; Sawant SP
Indian J Pediatr; 2005 Mar; 72(3):243-4. PubMed ID: 15812121
[TBL] [Abstract][Full Text] [Related]
20. Dominantly inherited megalencephaly, muscle weakness, and myoliposis: a carnitine-deficient myopathy within the spectrum of the Ruvalcaba-Myhre-Smith syndrome.
Powell BR; Budden SS; Buist NR
J Pediatr; 1993 Jul; 123(1):70-5. PubMed ID: 8320628
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]
