Minetti C - Search Results

1

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: minetti c. Neuromuscul Disord. 1991;1(3):195-200. doi: 10.1016/0960-8966(91)90024-m. Neuromuscul Disord. 1991. PMID: 1822794

2

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. Eur J Pediatr. 1993 Oct;152(10):848-51. doi: 10.1007/BF02073385. Eur J Pediatr. 1993. PMID: 8223790

3

Dystrophin at the plasma membrane of human muscle fibers shows a costameric localization.

Minetti C, Beltrame F, Marcenaro G, Bonilla E. Minetti C, et al. Neuromuscul Disord. 1992;2(2):99-109. doi: 10.1016/0960-8966(92)90041-4. Neuromuscul Disord. 1992. PMID: 1422204

4

Immunologic study of vinculin in Duchenne muscular dystrophy.

Minetti C, Tanji K, Bonilla E. Minetti C, et al. Neurology. 1992 Sep;42(9):1751-4. doi: 10.1212/wnl.42.9.1751. Neurology. 1992. PMID: 1513465

5

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. Neurology. 1991 Aug;41(8):1288-92. doi: 10.1212/wnl.41.8.1288. Neurology. 1991. PMID: 1714059

6

[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: minetti c. Minerva Pediatr. 1991 Mar;43(3):67-70. Minerva Pediatr. 1991. PMID: 1870528 Italian. No abstract available.

7

Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): clinical, biochemical, and genetic features of an autosomal recessive mitochondrial disorder.

Hirano M, Silvestri G, Blake DM, Lombes A, Minetti C, Bonilla E, Hays AP, Lovelace RE, Butler I, Bertorini TE, et al. Hirano M, et al. Among authors: minetti c. Neurology. 1994 Apr;44(4):721-7. doi: 10.1212/wnl.44.4.721. Neurology. 1994. PMID: 8164833

8

Abnormalities in the expression of beta-spectrin in Duchenne muscular dystrophy.

Minetti C, Tanji K, Rippa PG, Morreale G, Cordone G, Bonilla E. Minetti C, et al. Neurology. 1994 Jun;44(6):1149-53. doi: 10.1212/wnl.44.6.1149. Neurology. 1994. PMID: 8208414

9

Carrier detection of Duchenne and Becker muscular dystrophy using muscle dystrophin immunohistochemistry.

Oliveira AS, Gabbai AA, Schmidt B, Kiyomoto BH, Lima JG, Minetti C, Bonilla E. Oliveira AS, et al. Among authors: minetti c. Arq Neuropsiquiatr. 1992 Dec;50(4):478-85. doi: 10.1590/s0004-282x1992000400010. Arq Neuropsiquiatr. 1992. PMID: 1309152

10

Acute quadriplegic myopathy: a complication of treatment with steroids, nondepolarizing blocking agents, or both.

Hirano M, Ott BR, Raps EC, Minetti C, Lennihan L, Libbey NP, Bonilla E, Hays AP. Hirano M, et al. Among authors: minetti c. Neurology. 1992 Nov;42(11):2082-7. doi: 10.1212/wnl.42.11.2082. Neurology. 1992. PMID: 1436516

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