Orcesi S - Search Results

1

Response to carbamazepine of recessive-type myotonia congenita.

Berardinelli A, Gorni K, Orcesi S. Berardinelli A, et al. Among authors: orcesi s. Muscle Nerve. 2000 Jan;23(1):138-9. doi: 10.1002/(sici)1097-4598(200001)23:1<138::aid-mus23>3.0.co;2-4. Muscle Nerve. 2000. PMID: 10590422 No abstract available.

2

A multicenter, double-blind, randomized trial of deflazacort versus prednisone in Duchenne muscular dystrophy.

Bonifati MD, Ruzza G, Bonometto P, Berardinelli A, Gorni K, Orcesi S, Lanzi G, Angelini C. Bonifati MD, et al. Among authors: orcesi s. Muscle Nerve. 2000 Sep;23(9):1344-7. doi: 10.1002/1097-4598(200009)23:9<1344::aid-mus4>3.0.co;2-f. Muscle Nerve. 2000. PMID: 10951436 Clinical Trial.

3

AAEM news and comments.

Berardinelli A, Gorni K, Orcesi S. Berardinelli A, et al. Among authors: orcesi s. Muscle Nerve. 2000 Jan;23(1):142-6. Muscle Nerve. 2000. PMID: 10590423 No abstract available.

4

Dystrophinopathies: peculiar clinical and laboratory aspects.

Berardinelli A, Gorni K, Orcesi S, Tagliabue A, Uggetti C, Lanzi G. Berardinelli A, et al. Among authors: orcesi s. Funct Neurol. 2001;16(4 Suppl):255-62. Funct Neurol. 2001. PMID: 11996522 No abstract available.

5

Quantitative MR evaluation of body composition in patients with Duchenne muscular dystrophy.

Pichiecchio A, Uggetti C, Egitto MG, Berardinelli A, Orcesi S, Gorni KO, Zanardi C, Tagliabue A. Pichiecchio A, et al. Among authors: orcesi s. Eur Radiol. 2002 Nov;12(11):2704-9. doi: 10.1007/s00330-002-1392-4. Epub 2002 May 8. Eur Radiol. 2002. PMID: 12386760

6

Bilateral putaminal necrosis associated with the mitochondrial DNA A8344G myoclonus epilepsy with ragged red fibers (MERRF) mutation: an infantile case.

Orcesi S, Gorni K, Termine C, Uggetti C, Veggiotti P, Carrara F, Zeviani M, Berardinelli A, Lanzi G. Orcesi S, et al. J Child Neurol. 2006 Jan;21(1):79-82. doi: 10.1177/08830738060210010901. J Child Neurol. 2006. PMID: 16551460

7

A new self-report quality of life questionnaire for children with neuromuscular disorders: presentation of the instrument, rationale for its development, and some preliminary results.

Orcesi S, Ariaudo G, Mercuri E, Beghi E, Rezzani C, Balottin U; SOLE NMDs Study Group. Orcesi S, et al. J Child Neurol. 2014 Feb;29(2):167-81. doi: 10.1177/0883073813511859. Epub 2013 Dec 18. J Child Neurol. 2014. PMID: 24352162

8

New molecular findings in congenital myopathies due to selenoprotein N gene mutations.

Cagliani R, Fruguglietti ME, Berardinelli A, D'Angelo MG, Prelle A, Riva S, Napoli L, Gorni K, Orcesi S, Lamperti C, Pichiecchio A, Signaroldi E, Tupler R, Magri F, Govoni A, Corti S, Bresolin N, Moggio M, Comi GP. Cagliani R, et al. Among authors: orcesi s. J Neurol Sci. 2011 Jan 15;300(1-2):107-13. doi: 10.1016/j.jns.2010.09.011. J Neurol Sci. 2011. PMID: 20937510

9

Body composition and energy expenditure in Duchenne muscular dystrophy.

Zanardi MC, Tagliabue A, Orcesi S, Berardinelli A, Uggetti C, Pichiecchio A. Zanardi MC, et al. Among authors: orcesi s. Eur J Clin Nutr. 2003 Feb;57(2):273-8. doi: 10.1038/sj.ejcn.1601524. Eur J Clin Nutr. 2003. PMID: 12571659

10

Measurement of skeletal muscle mass in Duchenne muscular dystrophy: use of 24-h creatinine excretion.

Franciotta D, Zanardi MC, Albertotti L, Orcesi S, Berardinelli A, Pichiecchio A, Uggetti C, Tagliabue A. Franciotta D, et al. Among authors: orcesi s. Acta Diabetol. 2003 Oct;40 Suppl 1:S290-2. doi: 10.1007/s00592-003-0089-8. Acta Diabetol. 2003. PMID: 14618496

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