Zanoteli E - Search Results

1

A Study of a Cohort of X-Linked Myotubular Myopathy at the Clinical, Histologic, and Genetic Levels.

Abath Neto O, Silva MR, Martins Cde A, Oliveira Ade S, Reed UC, Biancalana V, Pesquero JB, Laporte J, Zanoteli E. Abath Neto O, et al. Among authors: zanoteli e. Pediatr Neurol. 2016 May;58:107-12. doi: 10.1016/j.pediatrneurol.2016.01.023. Epub 2016 Feb 6. Pediatr Neurol. 2016. PMID: 26995067

2

Nebulin expression in patients with nemaline myopathy.

Gurgel-Giannetti J, Reed U, Bang ML, Pelin K, Donner K, Marie SK, Carvalho M, Fireman MA, Zanoteli E, Oliveira AS, Zatz M, Wallgren-Pettersson C, Labeit S, Vainzof M. Gurgel-Giannetti J, et al. Among authors: zanoteli e. Neuromuscul Disord. 2001 Mar;11(2):154-62. doi: 10.1016/s0960-8966(00)00177-2. Neuromuscul Disord. 2001. PMID: 11257471

3

Rod distribution and muscle fiber type modification in the progression of nemaline myopathy.

Gurgel-Giannetti J, Reed UC, Marie SK, Zanoteli E, Fireman MA, Oliveira AS, Werneck LC, Beggs AH, Zatz M, Vainzof M. Gurgel-Giannetti J, et al. Among authors: zanoteli e. J Child Neurol. 2003 Mar;18(3):235-40. doi: 10.1177/08830738030180031501. J Child Neurol. 2003. PMID: 12731651

4

Deletion of both MTM1 and MTMR1 genes in a boy with myotubular myopathy.

Zanoteli E, Laporte J, Rocha JC, Kretz C, Oliveira AS, Mandel JL, Perez AB, Gabbai AA, Buj-Bello A. Zanoteli E, et al. Am J Med Genet A. 2005 Apr 30;134(3):338-40. doi: 10.1002/ajmg.a.30574. Am J Med Genet A. 2005. PMID: 15690409 No abstract available.

5

A novel PtdIns3P and PtdIns(3,5)P2 phosphatase with an inactivating variant in centronuclear myopathy.

Tosch V, Rohde HM, Tronchère H, Zanoteli E, Monroy N, Kretz C, Dondaine N, Payrastre B, Mandel JL, Laporte J. Tosch V, et al. Among authors: zanoteli e. Hum Mol Genet. 2006 Nov 1;15(21):3098-106. doi: 10.1093/hmg/ddl250. Epub 2006 Sep 28. Hum Mol Genet. 2006. PMID: 17008356

6

Comparison of motor strength and function in patients with Duchenne muscular dystrophy with or without steroid therapy.

Parreira SL, Resende MB, Zanoteli E, Carvalho MS, Marie SK, Reed UC. Parreira SL, et al. Among authors: zanoteli e. Arq Neuropsiquiatr. 2010 Oct;68(5):683-8. doi: 10.1590/s0004-282x2010000500002. Arq Neuropsiquiatr. 2010. PMID: 21049175 Free article.

7

Duchenne muscular dystrophy: quality of life among 95 patients evaluated using the Life Satisfaction Index for Adolescents.

Simon VA, Resende MB, Simon MA, Zanoteli E, Reed UC. Simon VA, et al. Among authors: zanoteli e. Arq Neuropsiquiatr. 2011 Feb;69(1):19-22. doi: 10.1590/s0004-282x2011000100005. Arq Neuropsiquiatr. 2011. PMID: 21359417 Free article.

8

Evaluation of muscle strength and motor abilities in children with type II and III spinal muscle atrophy treated with valproic acid.

Darbar IA, Plaggert PG, Resende MB, Zanoteli E, Reed UC. Darbar IA, et al. Among authors: zanoteli e. BMC Neurol. 2011 Mar 24;11:36. doi: 10.1186/1471-2377-11-36. BMC Neurol. 2011. PMID: 21435220 Free PMC article. Clinical Trial.

9

Necklace fibers as histopathological marker in a patient with severe form of X-linked myotubular myopathy.

Gurgel-Giannetti J, Zanoteli E, de Castro Concentino EL, Abath Neto O, Pesquero JB, Reed UC, Vainzof M. Gurgel-Giannetti J, et al. Among authors: zanoteli e. Neuromuscul Disord. 2012 Jun;22(6):541-5. doi: 10.1016/j.nmd.2011.12.005. Epub 2012 Jan 20. Neuromuscul Disord. 2012. PMID: 22264517

10

Motor function measure scale, steroid therapy and patients with Duchenne muscular dystrophy.

Silva EC, Machado DL, Resende MB, Silva RF, Zanoteli E, Reed UC. Silva EC, et al. Among authors: zanoteli e. Arq Neuropsiquiatr. 2012 Mar;70(3):191-5. doi: 10.1590/s0004-282x2012000300007. Arq Neuropsiquiatr. 2012. PMID: 22392111 Free article.

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