Prelle A - Search Results

1

Guillain-Barré syndrome after rtPA therapy for acute stroke.

Bersano A, Santoro D, Prelle A, Lanfranconi S, Ranieri M, Tadeo CS, Bresolin N, Baron PL. Bersano A, et al. Among authors: prelle a. Neurol Sci. 2010 Dec;31(6):867-9. doi: 10.1007/s10072-010-0259-8. Epub 2010 May 8. Neurol Sci. 2010. PMID: 20454821 No abstract available.

2

Kearns-Sayre syndrome: different amounts of deleted mitochondrial DNA are present in several autoptic tissues.

Ponzetto C, Bresolin N, Bordoni A, Moggio M, Meola G, Bet L, Prelle A, Scarlato G. Ponzetto C, et al. Among authors: prelle a. J Neurol Sci. 1990 May;96(2-3):207-10. doi: 10.1016/0022-510x(90)90133-8. J Neurol Sci. 1990. PMID: 2376752

3

Chronic progressive external ophthalmoplegia: a correlative study of quantitative molecular data and histochemical and biochemical profile.

Fassati A, Bordoni A, Amboni P, Fortunato F, Fagiolari G, Bresolin N, Prelle A, Comi G, Scarlato G. Fassati A, et al. Among authors: prelle a. J Neurol Sci. 1994 May;123(1-2):140-6. doi: 10.1016/0022-510x(94)90216-x. J Neurol Sci. 1994. PMID: 8064307

4

Multiple deletions of mitochondrial DNA in sporadic and atypical cases of encephalomyopathy.

Checcarelli N, Prelle A, Moggio M, Comi G, Bresolin N, Papadimitriou A, Fagiolari G, Bordoni A, Scarlato G. Checcarelli N, et al. Among authors: prelle a. J Neurol Sci. 1994 May;123(1-2):74-9. doi: 10.1016/0022-510x(94)90206-2. J Neurol Sci. 1994. PMID: 8064325

5

Multiple deletions of mitochondrial DNA in a patient with periodic attacks of paralysis.

Prelle A, Moggio M, Checcarelli N, Comi G, Bresolin N, Battistel A, Bordoni A, Scarlato G. Prelle A, et al. J Neurol Sci. 1993 Jul;117(1-2):24-7. doi: 10.1016/0022-510x(93)90149-s. J Neurol Sci. 1993. PMID: 8410061

6

DPP6 gene variability confers increased risk of developing sporadic amyotrophic lateral sclerosis in Italian patients.

Del Bo R, Ghezzi S, Corti S, Santoro D, Prelle A, Mancuso M, Siciliano G, Briani C, Murri L, Bresolin N, Comi GP. Del Bo R, et al. Among authors: prelle a. J Neurol Neurosurg Psychiatry. 2008 Sep;79(9):1085. doi: 10.1136/jnnp.2008.149146. J Neurol Neurosurg Psychiatry. 2008. PMID: 18708572 No abstract available.

7

TARDBP (TDP-43) sequence analysis in patients with familial and sporadic ALS: identification of two novel mutations.

Del Bo R, Ghezzi S, Corti S, Pandolfo M, Ranieri M, Santoro D, Ghione I, Prelle A, Orsetti V, Mancuso M, Sorarù G, Briani C, Angelini C, Siciliano G, Bresolin N, Comi GP. Del Bo R, et al. Among authors: prelle a. Eur J Neurol. 2009 Jun;16(6):727-32. doi: 10.1111/j.1468-1331.2009.02574.x. Epub 2009 Feb 19. Eur J Neurol. 2009. PMID: 19236453

8

Aphasic and visual aura with increased vasogenic leakage: an atypical migrainosus status.

Lanfranconi S, Corti S, Bersano A, Costa A, Prelle A, Sciacco M, Bresolin N, Ghione I. Lanfranconi S, et al. Among authors: prelle a. J Neurol Sci. 2009 Oct 15;285(1-2):227-9. doi: 10.1016/j.jns.2009.06.009. Epub 2009 Jul 1. J Neurol Sci. 2009. PMID: 19573879

9

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: prelle a. 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

10

Steroid-responsive Hashimoto encephalopathy mimicking Creutzfeldt-Jakob disease.

Santoro D, Colombo I, Ghione I, Peverelli L, Bresolin N, Sciacco M, Prelle A. Santoro D, et al. Among authors: prelle a. Neurol Sci. 2011 Aug;32(4):719-22. doi: 10.1007/s10072-011-0610-8. Epub 2011 May 10. Neurol Sci. 2011. PMID: 21556866

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