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Mostrati risultati da 1 a 20 di 273
Titolo Data di pubblicazione Autore(i) File
Becker muscular dystrophy or spinal muscular atrophy?--Dystrophin studies resolve conflicting results of electromyography and muscle biopsy. 1-gen-1991 Mcdonald, Td; Medori, R; Younger, Ds; Chang, Hw; Minetti, Carlo; Uncini, A; Bonilla, E; Hays, Ap; Lovelace, Re
[The defect in muscular glucose-6-phosphate dehydrogenase]. 1-gen-1991 Bado, M; Minetti, Carlo; Mallamaci, L; Bresolin, N; Leveratto, L; Iester, A; Cordone, G.
Progressive depletion of fast alpha-actinin-positive muscle fibers in Duchenne muscular dystrophy. 1-gen-1991 Minetti, Carlo; Ricci, E; Bonilla, E.
[Infantile dermatomyositis. Clinical aspects and prospective treatments]. 1-gen-1991 Cordone, G; Buoncompagni, A; Ciccone, O; Minetti, Carlo; Fasce, L; Scribanis, R; De Langlade, E.
[Congenital myopathies]. 1-gen-1991 Cordone, G; Bado, M; Minetti, Carlo
[Clinical,manifestations of the myopathies due to deletions/mutations of the dystrophin gene]. 1-gen-1991 Bonilla, E; Minetti, Carlo; Chang, Hw; Medori, R; Cordone, G; Di Mauro, S.
Dystrophin deficiency in young girls with sporadic myopathy and normal karyotype. 1-gen-1991 Minetti, Carlo; Chang, Hw; Medori, R; Prelle, A; Moggio, M; Johnsen, Sd; Bonilla, E.
Dystrophinopathy in isolated cases of myopathy in females. 1-gen-1992 Hoffman, Ep; Arahata, K; Minetti, Carlo; Bonilla, E; Rowland, Lp
Dystrophin at the plasma membrane of human muscle fibers shows a costameric localization. 1-gen-1992 Minetti, Carlo; Beltrame, Francesco; Marcenaro, G; Bonilla, E.
Acute quadriplegic myopathy: a complication of treatment with steroids, nondepolarizing blocking agents, or both. 1-gen-1992 Hirano, M; Ott, Br; Raps, Ec; Minetti, Carlo; Lennihan, L; Libbey, Np; Bonilla, E; Hays, Ap
Carrier detection of Duchenne and Becker muscular dystrophy using muscle dystrophin immunohistochemistry. 1-gen-1992 Oliveira, As; Gabbai, Aa; Schmidt, B; Kiyomoto, Bh; Lima, Jg; Minetti, Carlo; Bonilla, E.
Mosaic expression of dystrophin in carriers of Becker's muscular dystrophy and the X-linked syndrome of myalgia and cramps. 1-gen-1992 Minetti, Carlo; Bonilla, E.
Immunologic study of vinculin in Duchenne muscular dystrophy. 1-gen-1992 Minetti, Carlo; Tanji, K; Bonilla, E.
Caveolinopathies 1-gen-1993 Bruno, C; Sotgia, F; Gazzerro, E; Minetti, Carlo; Lisanti, Mp
Dystrophinopathy in two young boys with exercise-induced cramps and myoglobinuria. 1-gen-1993 Minetti, Carlo; Tanji, K; Chang, Hw; Medori, R; Cordone, G; Dimauro, S; Bonilla, E.
Abnormalities in the expression of beta-spectrin in Duchenne muscular dystrophy. 1-gen-1994 Minetti, Carlo; Tanji, K; Rippa, Pg; Morreale, G; Cordone, G; Bonilla, E.
Mitochondrial neurogastrointestinal encephalomyopathy (MNGIE): clinical, biochemical, and genetic features of an autosomal recessive mitochondrial disorder. 1-gen-1994 Hirano, M; Silvestri, G; Blake, Dm; Lombes, A; Minetti, Carlo; Bonilla, E; Hays, Ap; Lovelace, Re; Butler, I; Bertorini, Te
[Muscle phosphorylase deficiency in childhood. A case report]. 1-gen-1994 Bruno, C; Iester, A; Bado, M; Morreale, G; Broda, P; Minetti, Carlo; Cordone, A; Cordone, G.
[Early myoclonic encephalopathy and spinal muscular atrophy type I]. 1-gen-1995 Bado, M; Bruno, C; Morreale, G; Parisi, F; Minetti, Carlo; Cordone, G.
Disruption of muscle basal lamina in congenital muscular dystrophy with merosin deficiency. 1-gen-1996 Minetti, Carlo; Bado, M; Morreale, G; Pedemonte, M; Cordone, G.
Mostrati risultati da 1 a 20 di 273
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