Search Results - Gallus, G.N.

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  1. 1
    Homozygosity for P.Cys183ser mutation in Notch3 gene may influence the severity of clinical presentation? Report of an Italian family

    Homozygosity for P.Cys183ser mutation in Notch3 gene may influence the severity of clinical presentation? Report of an Italian family by Bianchi, S, Rufa, A, Vinciguerra, C, Gallus, G.N, Federico, A

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  2. 2
    Three new mutations in CSF1R gene in 3 Italian patients with hereditary diffuse leukoencephalopathy with axonal spheroids

    Three new mutations in CSF1R gene in 3 Italian patients with hereditary diffuse leukoencephalopathy with axonal spheroids by Di Donato, I, Bianchi, S, Taglia, I, Gallus, G.N, Stabile, C, Battisti, C, Rufa, A, Dotti, M.T, Federico, A

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  3. 3
    Two new heterozygous mutations of Htra1 gene in a Caucasian patient affected by CARASIL

    Two new heterozygous mutations of Htra1 gene in a Caucasian patient affected by CARASIL by Bianchi, S, Di Palma, C, Gallus, G.N, Taglia, I, Poggiani, A, Rosini, F, Cerase, A, Rufa, A, Muresanu, D, Dotti, M.T

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  4. 4
    Chronic progressive external ophthalmoplegia: A new heteroplasmic tRNALeu(CUN) mutation of mitochondrial DNA

    Chronic progressive external ophthalmoplegia: A new heteroplasmic tRNALeu(CUN) mutation of mitochondrial DNA by Cardaioli, E, Da Pozzo, P, Malfatti, E, Gallus, G.N, Rubegni, A, Malandrini, A, Gaudiano, C, Guidi, L, Serni, G, Berti, G, Dotti, M.T, Federico, A

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  5. 5
    Genotype-phenotype and OCT correlations in Autosomal Dominant Optic Atrophy related to OPA1 gene mutations: Report of 13 Italian families

    Genotype-phenotype and OCT correlations in Autosomal Dominant Optic Atrophy related to OPA1 gene mutations: Report of 13 Italian families by Pretegiani, E., Rosini, F., Rufa, A., Gallus, G.N., Cardaioli, E., Da Pozzo, P., Bianchi, S., Serchi, V., Collura, M., Franceschini, R., Bianchi Marzoli, S., Dotti, M.T., Federico, A.

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  6. 6
    Chronic progressive external ophthalmoplegia: A new heteroplasmic tRNA Leu(CUN) mutation of mitochondrial DNA

    Chronic progressive external ophthalmoplegia: A new heteroplasmic tRNA Leu(CUN) mutation of mitochondrial DNA by Cardaioli, E., Da Pozzo, P., Malfatti, E., Gallus, G.N., Rubegni, A., Malandrini, A., Gaudiano, C., Guidi, L., Serni, G., Berti, G., Dotti, M.T., Federico, A.

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