Bresolin N - Search Results

1

Variants in KIF1A gene in dominant and sporadic forms of hereditary spastic paraparesis.

Citterio A, Arnoldi A, Panzeri E, Merlini L, D'Angelo MG, Musumeci O, Toscano A, Bondi A, Martinuzzi A, Bresolin N, Bassi MT. Citterio A, et al. Among authors: bresolin n. J Neurol. 2015 Dec;262(12):2684-90. doi: 10.1007/s00415-015-7899-9. Epub 2015 Sep 26. J Neurol. 2015. PMID: 26410750 Free article.

2

Leber's hereditary optic neuropathy: genetic, biochemical, and phosphorus magnetic resonance spectroscopy study in an Italian family.

Cortelli P, Montagna P, Avoni P, Sangiorgi S, Bresolin N, Moggio M, Zaniol P, Mantovani V, Barboni P, Barbiroli B, et al. Cortelli P, et al. Among authors: bresolin n. Neurology. 1991 Aug;41(8):1211-5. doi: 10.1212/wnl.41.8.1211. Neurology. 1991. PMID: 1866007

3

Ryanodine receptor gene point mutation and malignant hyperthermia susceptibility.

Moroni I, Gonano EF, Comi GP, Tegazzin V, Prelle A, Bordoni A, Bresolin N, Scarlato G. Moroni I, et al. Among authors: bresolin n. J Neurol. 1995 Feb;242(3):127-33. doi: 10.1007/BF00936884. J Neurol. 1995. PMID: 7751854

4

Early-onset cerebellar ataxia, myoclonus and hypogonadism in a case of mitochondrial complex III deficiency treated with vitamins K3 and C.

Toscano A, Fazio MC, Vita G, Cannavó S, Bresolin N, Bet L, Prelle A, Barbiroli B, Iotti S, Zaniol P, et al. Toscano A, et al. Among authors: bresolin n. J Neurol. 1995 Mar;242(4):203-9. doi: 10.1007/BF00919592. J Neurol. 1995. PMID: 7798118

5

Muscle phosphoglycerate mutase (PGAM) deficiency in the first Caucasian patient: biochemistry, muscle culture and 31P-MR spectroscopy.

Vita G, Toscano A, Bresolin N, Meola G, Fortunato F, Baradello A, Barbiroli B, Frassineti C, Zaniol P, Messina C. Vita G, et al. Among authors: bresolin n. J Neurol. 1994 Mar;241(5):289-94. doi: 10.1007/BF00868435. J Neurol. 1994. PMID: 8006681

6

Clinical variability in Becker muscular dystrophy. Genetic, biochemical and immunohistochemical correlates.

Comi GP, Prelle A, Bresolin N, Moggio M, Bardoni A, Gallanti A, Vita G, Toscano A, Ferro MT, Bordoni A, et al. Comi GP, et al. Among authors: bresolin n. Brain. 1994 Feb;117 ( Pt 1):1-14. doi: 10.1093/brain/117.1.1-a. Brain. 1994. PMID: 8149204

7

Muscle mitochondria investigation in myotonic dystrophy.

Vita G, Toscano A, Prelle A, Bordoni A, Checcarelli N, Bresolin N, Baradello A, Messina C. Vita G, et al. Among authors: bresolin n. Eur Neurol. 1993;33(6):423-7. doi: 10.1159/000116987. Eur Neurol. 1993. PMID: 8307063

8

Bezafibrate-induced myopathy: no evidence for defects in muscle metabolism.

Vita G, Toscano A, Mileto G, Pitrone F, Ferrò MT, Gagliardi E, Bresolin N, Fortunato F, Messina C. Vita G, et al. Among authors: bresolin n. Eur Neurol. 1993;33(2):168-72. doi: 10.1159/000116927. Eur Neurol. 1993. PMID: 8467827

9

In vivo biolistic technique in control and mdx dystrophic mice.

Ausenda CD, Bresolin N, De Liso A, D'Angelo MG, Moggio M, Del Bo R, Gallanti A, Comi GP, Torrente Y, Bordoni A, Scarlato G. Ausenda CD, et al. Among authors: bresolin n. Muscle Nerve. 1996 Jul;19(7):912-4. doi: 10.1002/(SICI)1097-4598(199607)19:7<912::AID-MUS18>3.0.CO;2-K. Muscle Nerve. 1996. PMID: 8965850 No abstract available.

10

A novel mitochondrial tRNA(Ile) point mutation in chronic progressive external ophthalmoplegia.

Franceschina L, Salani S, Bordoni A, Sciacco M, Napoli L, Comi GP, Prelle A, Fortunato F, Hadjigeorgiou GM, Farina E, Bresolin N, D'Angelo MG, Scarlato G. Franceschina L, et al. Among authors: bresolin n. J Neurol. 1998 Nov;245(11):755-8. doi: 10.1007/s004150050283. J Neurol. 1998. PMID: 9808249 No abstract available.

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