Medori R - Search Results

1

Dystrophinopathy in two young boys with exercise-induced cramps and myoglobinuria.

Minetti C, Tanji K, Chang HW, Medori R, Cordone G, DiMauro S, Bonilla E. Minetti C, et al. Among authors: medori r. Eur J Pediatr. 1993 Oct;152(10):848-51. doi: 10.1007/BF02073385. Eur J Pediatr. 1993. PMID: 8223790

2

Dystrophin deficiency in young girls with sporadic myopathy and normal karyotype.

Minetti C, Chang HW, Medori R, Prelle A, Moggio M, Johnsen SD, Bonilla E. Minetti C, et al. Among authors: medori r. Neurology. 1991 Aug;41(8):1288-92. doi: 10.1212/wnl.41.8.1288. Neurology. 1991. PMID: 1714059

3

Becker muscular dystrophy or spinal muscular atrophy?--Dystrophin studies resolve conflicting results of electromyography and muscle biopsy.

McDonald TD, Medori R, Younger DS, Chang HW, Minetti C, Uncini A, Bonilla E, Hays AP, Lovelace RE. McDonald TD, et al. Among authors: medori r. Neuromuscul Disord. 1991;1(3):195-200. doi: 10.1016/0960-8966(91)90024-m. Neuromuscul Disord. 1991. PMID: 1822794

4

Partial dystrophin deficiency in monozygous twin carriers of the Duchenne gene discordant for clinical myopathy.

Bonilla E, Younger DS, Chang HW, Tantravahi U, Miranda AF, Medori R, DiMauro S, Warburton D, Rowland LP. Bonilla E, et al. Among authors: medori r. Neurology. 1990 Aug;40(8):1267-70. doi: 10.1212/wnl.40.8.1267. Neurology. 1990. PMID: 2199849

5

[Clinical,manifestations of the myopathies due to deletions/mutations of the dystrophin gene].

Bonilla E, Minetti C, Chang HW, Medori R, Cordone G, Di Mauro S. Bonilla E, et al. Among authors: medori r. Minerva Pediatr. 1991 Mar;43(3):67-70. Minerva Pediatr. 1991. PMID: 1870528 Italian. No abstract available.

6

Dystrophin deficiency in a case of congenital myopathy.

Prelle A, Medori R, Moggio M, Chan HW, Gallanti A, Scarlato G, Bonilla E. Prelle A, et al. Among authors: medori r. J Neurol. 1992 Feb;239(2):76-8. doi: 10.1007/BF00862976. J Neurol. 1992. PMID: 1552307

7

MELAS syndrome: characteristic migrainous and epileptic features and maternal transmission.

Montagna P, Gallassi R, Medori R, Govoni E, Zeviani M, Di Mauro S, Lugaresi E, Andermann F. Montagna P, et al. Among authors: medori r. Neurology. 1988 May;38(5):751-4. doi: 10.1212/wnl.38.5.751. Neurology. 1988. PMID: 3362373

8

Genetic abnormalities in Duchenne and Becker dystrophies: clinical correlations.

Medori R, Brooke MH, Waterston RH. Medori R, et al. Neurology. 1989 Apr;39(4):461-5. doi: 10.1212/wnl.39.4.461. Neurology. 1989. PMID: 2648185

9

Two dissimilar brothers with Becker's dystrophy have an identical genetic defect.

Medori R, Brooke MH, Waterston RH. Medori R, et al. Neurology. 1989 Nov;39(11):1493-6. doi: 10.1212/wnl.39.11.1493. Neurology. 1989. PMID: 2682349

10

Pyruvate dehydrogenase deficiency: molecular basis for intrafamilial heterogeneity.

Fujii T, Van Coster RN, Old SE, Medori R, Winter S, Gubits RM, Matthews PM, Brown RM, Brown GK, Dahl HH, et al. Fujii T, et al. Among authors: medori r. Ann Neurol. 1994 Jul;36(1):83-9. doi: 10.1002/ana.410360116. Ann Neurol. 1994. PMID: 8024267

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