136 related articles for article (PubMed ID: 7449803)
1. 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]
2. Successful treatment of familial idiopathic lipid storage myopathy with L-carnitine and modified lipid diet.
Snyder TM; Little BW; Roman-Campos G; McQuillen JB
Neurology; 1982 Oct; 32(10):1106-15. PubMed ID: 6889698
[TBL] [Abstract][Full Text] [Related]
3. Carnitine deficiency myopathy.
Vaisrub S
JAMA; 1973 Jul; 225(2):165-6. PubMed ID: 4740280
[No Abstract] [Full Text] [Related]
4. Successful treatment of pure myopathy, associated with complex I deficiency, with riboflavin and carnitine.
Bernsen PL; Gabreëls FJ; Ruitenbeek W; Sengers RC; Stadhouders AM; Renier WO
Arch Neurol; 1991 Mar; 48(3):334-8. PubMed ID: 1900413
[TBL] [Abstract][Full Text] [Related]
5. 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]
6. Carnitine deficiency of human skeletal muscle with associated lipid storage myopathy: a new syndrome.
Engel AG; Angelini C
Science; 1973 Mar; 179(4076):899-902. PubMed ID: 4687787
[TBL] [Abstract][Full Text] [Related]
7. [Clinical, morphological and biochemical studies on muscle carnitine deficiency (author's transl)].
Pongratz D; Hübner G; Deufel T; Wieland O; Pongratz E; Liphardt R
Klin Wochenschr; 1979 Sep; 57(18):927-36. PubMed ID: 502358
[TBL] [Abstract][Full Text] [Related]
8. 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]
9. Successful carnitine treatment in two siblings having lipid storage myopathy with hypertrophic cardiomyopathy.
Matsuishi T; Hirata K; Terasawa K; Kato H; Yoshino M; Ohtaki E; Hirose F; Nonaka I; Sugiyama N; Ohta K
Neuropediatrics; 1985 Feb; 16(1):6-12. PubMed ID: 3974805
[TBL] [Abstract][Full Text] [Related]
10. Lipid storage myopathy in familial hyperlipoproteinemia.
Kinoshita M; Wakata N
Arch Neurol; 1984 May; 41(5):551-4. PubMed ID: 6721723
[TBL] [Abstract][Full Text] [Related]
11. Lipid storage myopathy: successful treatment with propranolol.
Martyn C; Jellinek EH; Webb JN
Br Med J (Clin Res Ed); 1981 Jun; 282(6281):1997-9. PubMed ID: 6788163
[TBL] [Abstract][Full Text] [Related]
12. Infantile lipid storage myopathy with nocturnal hypoventilation shows abnormal low-affinity muscle carnitine uptake in vitro.
Vergani L; Angelini C
Neuromuscul Disord; 1999 Jul; 9(5):320-2. PubMed ID: 10407853
[TBL] [Abstract][Full Text] [Related]
13. [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]
14. Hepatitis-associated lipid storage myopathy.
Patten BM; Shabot JM; Alperin J; Dodson RF
Ann Intern Med; 1977 Oct; 87(4):417-21. PubMed ID: 907240
[TBL] [Abstract][Full Text] [Related]
15. Infantile idiopathic myopathic carnitine deficiency: treatment with L-carnitine.
Shapira Y; Glick B; Harel S; Vattin JJ; Gutman A
Pediatr Neurol; 1993; 9(1):35-8. PubMed ID: 8452598
[TBL] [Abstract][Full Text] [Related]
16. [Lipid myopathy: a heterogenic familial case].
Kuntzer T; Robert D; Cox J; Meier C; Schwartz A; Guelpa G; Pfister CE
Schweiz Med Wochenschr; 1987 Dec; 117(50):2027-9. PubMed ID: 3433086
[TBL] [Abstract][Full Text] [Related]
17. [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]
18. 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]
19. 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]
20. Fatal lipid storage myopathy with deficiency of cytochrome-c-oxidase and carnitine. A contribution to the combined cytochemical-finestructural identification of cytochrome-c-oxidase in longterm frozen muscle.
Müller-Höcker J; Pongratz D; Deufel T; Trijbels JM; Endres W; Hübner G
Virchows Arch A Pathol Anat Histopathol; 1983; 399(1):11-23. PubMed ID: 6298999
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]