340 related articles for article (PubMed ID: 7617396)
1. An unusual case of muscular limb-girdle dystrophy and mitochondrial myopathy.
Calore EE; Cavaliere MJ; Wakamatsu A; Perez NM; Maeda MY; Russo DH
Pathologica; 1994 Dec; 86(6):649-51. PubMed ID: 7617396
[TBL] [Abstract][Full Text] [Related]
2. Cytochrome c oxidase reaction improves histopathological assessment of zidovudine myopathy.
Chariot P; Monnet I; Gherardi R
Ann Neurol; 1993 Oct; 34(4):561-5. PubMed ID: 8215243
[TBL] [Abstract][Full Text] [Related]
3. [Mitochondrial anomalies in oculopharyngeal muscular dystrophy].
de Seze J; Pasquier F; Ruchoux MM; Hurtevent JF; Petit H
Rev Neurol (Paris); 1997 Jun; 153(5):335-8. PubMed ID: 9296168
[TBL] [Abstract][Full Text] [Related]
4. [Congenital nemaline myopathy with mitochondrial abnormalities. An adult case report].
Oya Y; Segawa M; Ogawa M; Goto Y; Nonaka I; Kawai M
Rinsho Shinkeigaku; 2000 May; 40(5):452-8. PubMed ID: 11002727
[TBL] [Abstract][Full Text] [Related]
5. Autosomal dominant limb girdle myopathy with ragged-red fibers and cardiomyopathy. A pedigree study by in vivo 31P-MR spectroscopy indicating a multisystem mitochondrial defect.
Fabrizi GM; Lodi R; D'Ettorre M; Malandrini A; Cavallaro T; Rimoldi M; Zaniol P; Barbiroli B; Guazzi G
J Neurol Sci; 1996 Apr; 137(1):20-7. PubMed ID: 9120483
[TBL] [Abstract][Full Text] [Related]
6. Episodic myoglobinuria in a primary gamma-sarcoglycanopathy.
Pena L; Kim K; Charrow J
Neuromuscul Disord; 2010 May; 20(5):337-9. PubMed ID: 20356742
[TBL] [Abstract][Full Text] [Related]
7. A novel FKRP gene mutation in a Taiwanese patient with limb-girdle muscular dystrophy 2I.
Lin YC; Murakami T; Hayashi YK; Nishino I; Nonaka I; Yuo CY; Jong YJ
Brain Dev; 2007 May; 29(4):234-8. PubMed ID: 17055682
[TBL] [Abstract][Full Text] [Related]
8. Adult onset limb-girdle type mitochondrial myopathy with a mitochondrial DNA np8291 A-to-G substitution.
Hirata K; Nakagawa M; Higuchi I; Hashimoto K; Hanada K; Takahashi K; Niiyama T; Izumi K; Sakoda S; Yamada H; Osame M
J Hum Genet; 1999; 44(3):210-4. PubMed ID: 10319590
[TBL] [Abstract][Full Text] [Related]
9. Limb girdle muscular dystrophy: description of a phenotype.
Stübgen JP
Muscle Nerve; 1994 Dec; 17(12):1449-55. PubMed ID: 7969245
[TBL] [Abstract][Full Text] [Related]
10. Differential diagnosis of limb girdle syndromes.
Ishpekova B; Milanov I
Electromyogr Clin Neurophysiol; 1996 Dec; 36(8):469-75. PubMed ID: 8985674
[TBL] [Abstract][Full Text] [Related]
11. Late-onset autosomal recessive limb-girdle muscular dystrophy with rimmed vacuoles.
Nakamura A; Yoshida K; Ikeda S
Clin Neurol Neurosurg; 2004 Mar; 106(2):122-8. PubMed ID: 15003303
[TBL] [Abstract][Full Text] [Related]
12. [Calpain-3 gene defect causing limb gird muscular dystrophy in a Hungarian family].
Horváth R; Walter MC; Lochmüller H; Hübner A; Karcagi V; Pikó H; Timár L; Komoly S
Ideggyogy Sz; 2005 Jan; 58(1-2):52-8. PubMed ID: 15884399
[TBL] [Abstract][Full Text] [Related]
13. Focal cytochrome c oxidase deficiency in various neuromuscular diseases.
Yamamoto M; Koga Y; Ohtaki E; Nonaka I
J Neurol Sci; 1989 Jun; 91(1-2):207-13. PubMed ID: 2545831
[TBL] [Abstract][Full Text] [Related]
14. [A female infant of mitochondrial myopathy with findings of active necrosis and regeneration of muscle fibers].
Nagaura T; Sumi K; Nonaka I
Rinsho Shinkeigaku; 1990 Apr; 30(4):432-8. PubMed ID: 2387114
[TBL] [Abstract][Full Text] [Related]
15. Expression of NCAM (neural cell adhesion molecule) in mitochondrial myopathy.
Heuss D; Engelhardt A; Göbel H; Neundörfer B
Clin Neuropathol; 1995; 14(6):331-6. PubMed ID: 8605739
[TBL] [Abstract][Full Text] [Related]
16. [Surgery for blepharoptosis in muscular dystrophy].
Mahler O; Milstein A; Pollack A; Hauben D
Harefuah; 2000 Dec; 139(11-12):434-7, 494. PubMed ID: 11341188
[TBL] [Abstract][Full Text] [Related]
17. Muscle regeneration in mitochondrial myopathies.
Krag TO; Hauerslev S; Jeppesen TD; Duno M; Vissing J
Mitochondrion; 2013 Mar; 13(2):63-70. PubMed ID: 23376095
[TBL] [Abstract][Full Text] [Related]
18. [A pedigree of autosomal dominant limb-girdle myopathy with rimmed vacuole formation].
Kishibayashi J; Sunohara N; Saito Y
Rinsho Shinkeigaku; 1997 Jul; 37(7):603-10. PubMed ID: 9396357
[TBL] [Abstract][Full Text] [Related]
19. The RAGE pathway in inflammatory myopathies and limb girdle muscular dystrophy.
Haslbeck KM; Friess U; Schleicher ED; Bierhaus A; Nawroth PP; Kirchner A; Pauli E; Neundörfer B; Heuss D
Acta Neuropathol; 2005 Sep; 110(3):247-54. PubMed ID: 15986224
[TBL] [Abstract][Full Text] [Related]
20. Muscle structural changes in mitochondrial myopathy relate to genotype.
Olsen DB; Langkilde AR; Ørngreen MC; Rostrup E; Schwartz M; Vissing J
J Neurol; 2003 Nov; 250(11):1328-34. PubMed ID: 14648149
[TBL] [Abstract][Full Text] [Related]
[Next] [New Search]