-
1
-
-
0002868319
-
Myoglobinuria
-
Engel AG, Franzini-Armstrong C, eds. New York: McGraw-Hill
-
Penn AS. Myoglobinuria. In: Engel AG, Franzini-Armstrong C, eds. Myology, vol 2. 2nd ed. New York: McGraw-Hill, 1994: 1679-1696.
-
(1994)
Myology, Vol 2. 2nd Ed.
, vol.2
, pp. 1679-1696
-
-
Penn, A.S.1
-
2
-
-
0000902925
-
Myopathies due to drugs, toxins, and nutritional deficiency
-
Engel AG, Franzini-Armstrong C, eds. 2nd ed. New York: McGraw-Hill
-
Victor M, Sieb JP. Myopathies due to drugs, toxins, and nutritional deficiency. In: Engel AG, Franzini-Armstrong C, eds. Myology, vol. 2. 2nd ed. New York: McGraw-Hill, 1994:1697-1725.
-
(1994)
Myology
, vol.2
, pp. 1697-1725
-
-
Victor, M.1
Sieb, J.P.2
-
3
-
-
0029978895
-
Muscle-nerve involvement in autosomal dominant progressive external ophthalmoplegia with hypogonadism
-
Melberg A, Lundberg PO, Henriksson KG, Olsson Y, Stålberg E. Muscle-nerve involvement in autosomal dominant progressive external ophthalmoplegia with hypogonadism. Muscle Nerve 1996;19:751-757.
-
(1996)
Muscle Nerve
, vol.19
, pp. 751-757
-
-
Melberg, A.1
Lundberg, P.O.2
Henriksson, K.G.3
Olsson, Y.4
Stålberg, E.5
-
4
-
-
0029821848
-
Anticipation of autosomal dominant progressive external ophthalmoplegia with hypogonadism
-
Melberg A, Arnell H, Dahl N, et al. Anticipation of autosomal dominant progressive external ophthalmoplegia with hypogonadism. Muscle Nerve 1996;19:1561-1569.
-
(1996)
Muscle Nerve
, vol.19
, pp. 1561-1569
-
-
Melberg, A.1
Arnell, H.2
Dahl, N.3
-
5
-
-
0029834809
-
Clonal expansion of mitochondrial DNA with multiple deletions in autosomal dominant progressive external ophthalmoplegia
-
Moslemi A-R, Melberg A, Holme E, Oldfors A. Clonal expansion of mitochondrial DNA with multiple deletions in autosomal dominant progressive external ophthalmoplegia. Ann Neurol 1996;40:707-713.
-
(1996)
Ann Neurol
, vol.40
, pp. 707-713
-
-
Moslemi, A.-R.1
Melberg, A.2
Holme, E.3
Oldfors, A.4
-
6
-
-
0025828342
-
Mitochondrial DNA deletions in inherited recurrent myoglobinuria
-
Ohno K, Tanaka M, Sahashi K, et al. Mitochondrial DNA deletions in inherited recurrent myoglobinuria. Ann Neurol 1991;29:364-369.
-
(1991)
Ann Neurol
, vol.29
, pp. 364-369
-
-
Ohno, K.1
Tanaka, M.2
Sahashi, K.3
-
7
-
-
0028229765
-
Multiple deletions of mitochondrial DNA in sporadic and atypical cases of encephalomyopathy
-
Checcarelli N, Prelle A, Moggio M, et al. Multiple deletions of mitochondrial DNA in sporadic and atypical cases of encephalomyopathy. J Neurol Sci 1994;123:74-79.
-
(1994)
J Neurol Sci
, vol.123
, pp. 74-79
-
-
Checcarelli, N.1
Prelle, A.2
Moggio, M.3
-
8
-
-
0141610413
-
Muscle coenzyme Q deficiency in familial mitochondrial encephalomyopathy
-
Ogasahara S, Engel AG, Frens D, Mack D. Muscle coenzyme Q deficiency in familial mitochondrial encephalomyopathy. Proc Natl Acad Sci USA 1989;86:2379-2382.
-
(1989)
Proc Natl Acad Sci USA
, vol.86
, pp. 2379-2382
-
-
Ogasahara, S.1
Engel, A.G.2
Frens, D.3
Mack, D.4
-
9
-
-
0030003760
-
A microdeletion in cytochrome c oxidase (COX) subunit III associated with COX deficiency and recurrent myoglobinuria
-
Keightley JA, Hoffbuhr KC, Burton MD, et al. A microdeletion in cytochrome c oxidase (COX) subunit III associated with COX deficiency and recurrent myoglobinuria. Nat Genet 1996; 12:410-416.
-
(1996)
Nat Genet
, vol.12
, pp. 410-416
-
-
Keightley, J.A.1
Hoffbuhr, K.C.2
Burton, M.D.3
-
10
-
-
0031056639
-
A novel mitochondrial tRNA phenylalanine mutation presenting with acute rhabdomyolysis
-
Chinnery PF, Johnson MA, Taylor RW, Lightowlers RN, Turnbull DM. A novel mitochondrial tRNA phenylalanine mutation presenting with acute rhabdomyolysis. Ann Neurol 1997;41:408-410.
-
(1997)
Ann Neurol
, vol.41
, pp. 408-410
-
-
Chinnery, P.F.1
Johnson, M.A.2
Taylor, R.W.3
Lightowlers, R.N.4
Turnbull, D.M.5
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