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2. [A case of mitochondrial myopathy in a family with oculo-pharyngeal myopathy]. Goas JY; Leroy JP; Mocquard Y; Rouhart F Rev Neurol (Paris); 1991; 147(6-7):536-7. PubMed ID: 1962060 [TBL] [Abstract][Full Text] [Related]
3. A familial mitochondrial myopathy with central defect in neural transmission. Barron SA; Heffner RR; Zwirecki R Arch Neurol; 1979 Sep; 36(9):553-6. PubMed ID: 224846 [TBL] [Abstract][Full Text] [Related]
4. [Mitochondrial myopathy of progressive external ophthalmoplegia]. Guo YP Zhonghua Bing Li Xue Za Zhi; 1992 Dec; 21(6):358-60. PubMed ID: 1299529 [TBL] [Abstract][Full Text] [Related]
5. A study of a myopathy presenting as idiopathic scoliosis. Multicore disease or mitochondrial myopathy? Fitzsimons RB; Tyer HD J Neurol Sci; 1980 Apr; 46(1):33-48. PubMed ID: 7373343 [TBL] [Abstract][Full Text] [Related]
6. Myopathies with abnormal mitochondria: a clinicopathologic classification. Kamieniecka Z; Schmalbruch H Muscle Nerve; 1978; 1(5):413-5. PubMed ID: 263980 [TBL] [Abstract][Full Text] [Related]
7. Familial multicore disease with focal loss of cross-striations and ophthalmoplegia. Swash M; Schwartz MS J Neurol Sci; 1981 Oct; 52(1):1-10. PubMed ID: 7299413 [TBL] [Abstract][Full Text] [Related]
8. Familial oculocranioskeletal neuromuscular disease with abnormal muscle mitochondria. Tamura K; Santa T; Kuroiwa Y Brain; 1974 Dec; 97(4):665-72. PubMed ID: 4154795 [No Abstract] [Full Text] [Related]
9. [Centronuclear myopathy with autosomal dominant inheritance(author's transl)]. Mortier W; Michaelis E; Becker J; Gerhard L Humangenetik; 1975; 27(3):199-215. PubMed ID: 1150240 [TBL] [Abstract][Full Text] [Related]
10. VCP myopathy: A family with unusual clinical manifestations. Guo X; Zhao Z; Shen H; Qi B; Li N; Hu J Muscle Nerve; 2019 Mar; 59(3):365-369. PubMed ID: 30488450 [TBL] [Abstract][Full Text] [Related]
15. Minicore myopathy with ophthalmoplegia caused by mutations in the ryanodine receptor type 1 gene. Jungbluth H; Zhou H; Hartley L; Halliger-Keller B; Messina S; Longman C; Brockington M; Robb SA; Straub V; Voit T; Swash M; Ferreiro A; Bydder G; Sewry CA; Müller C; Muntoni F Neurology; 2005 Dec; 65(12):1930-5. PubMed ID: 16380615 [TBL] [Abstract][Full Text] [Related]
16. Neonatal ophthalmoplegia with microfibers: a reversible myopathy? Hanson PA; Mastrianni AF; Post L Neurology; 1977 Oct; 27(10):974-80. PubMed ID: 561912 [TBL] [Abstract][Full Text] [Related]
17. [A new familial muscular disorder demonstrated by the intra-sarcoplasmic accumulation of a granulo-filamentous material which is dense on electron microscopy (author's transl)]. Fardeau M; Godet-Guillain J; Tome FM; Collin H; Gaudeau S; Boffety C; Vernant P Rev Neurol (Paris); 1978; 134(6-7):411-25. PubMed ID: 570292 [TBL] [Abstract][Full Text] [Related]
18. Dominantly inherited mitochondrial myopathy with multiple deletions of mitochondrial DNA: clinical, morphologic, and biochemical studies. Servidei S; Zeviani M; Manfredi G; Ricci E; Silvestri G; Bertini E; Gellera C; Di Mauro S; Di Donato S; Tonali P Neurology; 1991 Jul; 41(7):1053-9. PubMed ID: 2067633 [TBL] [Abstract][Full Text] [Related]
19. Mitochondrial myopathies. A clinico-pathological study of cases with and without extra-ocular muscle involvement. Mechler F; Mastaglia FL; Serena M; Jenkison M; Johnson MA; Fawcett PR; Hudgson P; Walton JN Aust N Z J Med; 1986 Apr; 16(2):185-92. PubMed ID: 3463270 [TBL] [Abstract][Full Text] [Related]
20. Familial myopathies with restricted distribution, facial weakness and inflammatory changes in affected muscles. Bacq M; Telerman-Toppet N; Coërs C J Neurol; 1985; 231(6):295-300. PubMed ID: 3973638 [TBL] [Abstract][Full Text] [Related] [Next] [New Search]