165 related articles for article (PubMed ID: 8232675)
1. [Therapy of metabolic myopathies].
Reichmann H
Nervenarzt; 1993 Oct; 64(10):627-32. PubMed ID: 8232675
[TBL] [Abstract][Full Text] [Related]
2. [Diagnosis and therapy of mitochondrial diseases].
Pál E
Ideggyogy Sz; 2012 Jul; 65(7-8):229-37. PubMed ID: 23074842
[TBL] [Abstract][Full Text] [Related]
3. Neurological mitochondrial cytopathies.
Mehndiratta MM; Agarwal P; Tatke M; Krishnamurthy M
Neurol India; 2002 Jun; 50(2):162-7. PubMed ID: 12134180
[TBL] [Abstract][Full Text] [Related]
4. [Diagnosis and therapy of mitochondriopathies].
Sperl W
Wien Klin Wochenschr; 1997 Feb; 109(3):93-9. PubMed ID: 9139466
[TBL] [Abstract][Full Text] [Related]
5. [Neuroimaging of mitochondrial diseases].
Goto T; Momoi MY
Nihon Rinsho; 2002 Apr; 60 Suppl 4():236-9. PubMed ID: 12013855
[No Abstract] [Full Text] [Related]
6. Defects of beta-oxidation including carnitine deficiency.
Bartlett K; Pourfarzam M
Int Rev Neurobiol; 2002; 53():469-516. PubMed ID: 12512350
[No Abstract] [Full Text] [Related]
7. [Mitochondrial disease].
Miyabayashi S
Ryoikibetsu Shokogun Shirizu; 1994; (4):778-81. PubMed ID: 8007306
[No Abstract] [Full Text] [Related]
8. [MELAS: Mitochondrial Encephalomyopathy, Lactic Acidosis and Stroke-Like Episodes].
Murakami H; Ono K
Brain Nerve; 2017 Feb; 69(2):111-117. PubMed ID: 28202819
[TBL] [Abstract][Full Text] [Related]
9. Mitochondrial myopathies.
DiMauro S; Bonilla E; Zeviani M; Nakagawa M; DeVivo DC
Ann Neurol; 1985 Jun; 17(6):521-38. PubMed ID: 3927817
[TBL] [Abstract][Full Text] [Related]
10. [Hereditary metabolic muscular diseases caused by demonstrable enzyme defect].
Kuhn E
Dtsch Med Wochenschr; 1980 Oct; 105(42):1469-73. PubMed ID: 6450673
[No Abstract] [Full Text] [Related]
11. Exercise as a therapeutic strategy for primary mitochondrial cytopathies.
Tarnopolsky MA
J Child Neurol; 2014 Sep; 29(9):1225-34. PubMed ID: 25008908
[TBL] [Abstract][Full Text] [Related]
12. Variability of mitochondrial cytochemistry in human neuromuscular diseases.
Shah A; Sahgal V; Sahgal S; Subramani V; Kochar H
J Submicrosc Cytol Pathol; 1988 Apr; 20(2):287-95. PubMed ID: 3395968
[TBL] [Abstract][Full Text] [Related]
13. [Lipidic myopathies].
Muñoz-Blanco JL
Rev Neurol; 1998 Apr; 26 Suppl 1():S72-80. PubMed ID: 9810593
[TBL] [Abstract][Full Text] [Related]
14. Metabolic myopathies.
Bosch EP; Munsat TL
Med Clin North Am; 1979 Jul; 63(4):759-82. PubMed ID: 157414
[No Abstract] [Full Text] [Related]
15. Acute renal failure due to carnitine palmitoyltransferase II deficiency.
Uzel B; Altiparmak MR; Ataman R; Serdengeçti K
Neth J Med; 2003 Dec; 61(12):417-20. PubMed ID: 15025419
[TBL] [Abstract][Full Text] [Related]
16. Mitochondrial cytopathies.
Schmiedel J; Jackson S; Schäfer J; Reichmann H
J Neurol; 2003 Mar; 250(3):267-77. PubMed ID: 12638015
[TBL] [Abstract][Full Text] [Related]
17. Myopathies due to enzyme deficiencies.
Cornelio F; Di Donato S
J Neurol; 1985; 232(6):329-40. PubMed ID: 2934518
[TBL] [Abstract][Full Text] [Related]
18. Clinical manifestation of mitochondrial diseases.
Magner M; Kolářová H; Honzik T; Švandová I; Zeman J
Dev Period Med; 2015; 19(4):441-9. PubMed ID: 26982751
[TBL] [Abstract][Full Text] [Related]
19. [New approaches for the treatment of metabolic myopathies].
Laforêt P; Nicolino M; Eymard B
Rev Neurol (Paris); 2007 Oct; 163(10):930-5. PubMed ID: 18033029
[TBL] [Abstract][Full Text] [Related]
20. [Mitochondrial disease].
Goto Y
Ryoikibetsu Shokogun Shirizu; 2000; (29 Pt 4):496-502. PubMed ID: 11032007
[No Abstract] [Full Text] [Related]
[Next] [New Search]
