Ugo I - Search Results

1

Dystrophin levels as low as 30% are sufficient to avoid muscular dystrophy in the human.

Neri M, Torelli S, Brown S, Ugo I, Sabatelli P, Merlini L, Spitali P, Rimessi P, Gualandi F, Sewry C, Ferlini A, Muntoni F. Neri M, et al. Among authors: ugo i. Neuromuscul Disord. 2007 Dec;17(11-12):913-8. doi: 10.1016/j.nmd.2007.07.005. Epub 2007 Sep 7. Neuromuscul Disord. 2007. PMID: 17826093

2

Abnormalities in alpha-dystroglycan expression in MDC1C and LGMD2I muscular dystrophies.

Brown SC, Torelli S, Brockington M, Yuva Y, Jimenez C, Feng L, Anderson L, Ugo I, Kroger S, Bushby K, Voit T, Sewry C, Muntoni F. Brown SC, et al. Among authors: ugo i. Am J Pathol. 2004 Feb;164(2):727-37. doi: 10.1016/s0002-9440(10)63160-4. Am J Pathol. 2004. PMID: 14742276 Free PMC article.

3

Syncoilin upregulation in muscle of patients with neuromuscular disease.

Brown SC, Torelli S, Ugo I, De Biasia F, Howman EV, Poon E, Britton J, Davies KE, Muntoni F. Brown SC, et al. Among authors: ugo i. Muscle Nerve. 2005 Dec;32(6):715-25. doi: 10.1002/mus.20431. Muscle Nerve. 2005. PMID: 16124004

4

Late onset and very mild course of Xp21 Becker type muscular dystrophy.

Bosone I, Bortolotto S, Mongini T, Doriguzzi C, Chiadò-Piat L, Ugo I, Mutani R, Palmucci L. Bosone I, et al. Among authors: ugo i. Clin Neuropathol. 2001 Sep-Oct;20(5):196-9. Clin Neuropathol. 2001. PMID: 11594504

5

Unusual clinical expression of dystrophinopathy in a female, mimicking a congenital myopathy.

Palmucci L, Doriguzzi C, Mongini T, Chiadò-Piat L, Ugo I. Palmucci L, et al. Among authors: ugo i. Eur Neurol. 1999;42(4):221-4. doi: 10.1159/000008111. Eur Neurol. 1999. PMID: 10567819

6

Variable histological expression of dystrophinopathy in two females.

Doriguzzi C, Palmucci L, Mongini T, Chiadò-Piat L, Saggiorato C, Ugo I, Hoffman EP. Doriguzzi C, et al. Among authors: ugo i. Acta Neuropathol. 1999 Jun;97(6):657-60. doi: 10.1007/s004010051043. Acta Neuropathol. 1999. PMID: 10378386

7

Muscle apoptosis in humans occurs in normal and denervated muscle, but not in myotonic dystrophy, dystrophinopathies or inflammatory disease.

Migheli A, Mongini T, Doriguzzi C, Chiadò-Piat L, Piva R, Ugo I, Palmucci L. Migheli A, et al. Among authors: ugo i. Neurogenetics. 1997 Sep;1(2):81-7. doi: 10.1007/s100480050012. Neurogenetics. 1997. PMID: 10732808

8

A new polymorphism, g119A>G, in the integrin alpha 7 (ITGA7) gene.

Pirulli D, Zezlina S, Vatta L, Di Stefano P, Boniotto M, Tarone G, Mongini T, Ugo I, Palmucci L, Amoroso A, Crovella S. Pirulli D, et al. Among authors: ugo i. Hum Mutat. 2000 Aug;16(2):180. doi: 10.1002/1098-1004(200008)16:2<180::AID-HUMU18>3.0.CO;2-D. Hum Mutat. 2000. PMID: 10923047 No abstract available.

9

Localization of diazepam-binding inhibitor-related peptides and peripheral type benzodiazepine receptors in the frog adrenal gland.

Lesouhaitier O, Feuilloley M, Lihrmann I, Ugo I, Fasolo A, Tonon MC, Vaudry H. Lesouhaitier O, et al. Among authors: ugo i. Cell Tissue Res. 1996 Mar;283(3):403-12. doi: 10.1007/s004410050551. Cell Tissue Res. 1996. PMID: 8593670

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