Berardinelli A - Search Results

1

Good response to the late treatment with ataluren in a boy with Duchenne muscular dystrophy: could the previous mild course of the disease have affected the outcome?

Pasca L, Gardani A, Paoletti M, Velardo D, Berardinelli A. Pasca L, et al. Among authors: berardinelli a. Acta Myol. 2022 Sep 30;41(3):121-125. doi: 10.36185/2532-1900-078. eCollection 2022. Acta Myol. 2022. PMID: 36349184 Free PMC article.

2

Muscle magnetic resonance imaging involvement in muscular dystrophies with rigidity of the spine.

Mercuri E, Clements E, Offiah A, Pichiecchio A, Vasco G, Bianco F, Berardinelli A, Manzur A, Pane M, Messina S, Gualandi F, Ricci E, Rutherford M, Muntoni F. Mercuri E, et al. Among authors: berardinelli a. Ann Neurol. 2010 Feb;67(2):201-8. doi: 10.1002/ana.21846. Ann Neurol. 2010. PMID: 20225280

3

Correction: Long Term Natural History Data in Ambulant Boys with Duchenne Muscular Dystrophy: 36-Month Changes.

Pane M, Mazzone ES, Sivo S, Sormani MP, Messina S, D'Amico A, Carlesi A, Vita G, Fanelli L, Berardinelli A, Torrente Y, Lanzillotta V, Viggiano E, D'Ambrosio P, Cavallaro F, Frosini S, Barp A, Bonfiglio S, Scalise R, De Sanctis R, Rolle E, Graziano A, Magri F, Palermo C, Rossi F, Donati MA, Sacchini M, Arnoldi MT, Baranello G, Mongini T, Pini A, Battini R, Pegoraro E, Previtali S, Bruno C, Politano L, Comi GP, Bertini E, Mercuri E. Pane M, et al. Among authors: berardinelli a. PLoS One. 2015 Dec 4;10(12):e0144079. doi: 10.1371/journal.pone.0144079. eCollection 2015. PLoS One. 2015. PMID: 26636671 Free PMC article. No abstract available.

4

Spectrum of brain changes in patients with congenital muscular dystrophy and FKRP gene mutations.

Mercuri E, Topaloglu H, Brockington M, Berardinelli A, Pichiecchio A, Santorelli F, Rutherford M, Talim B, Ricci E, Voit T, Muntoni F. Mercuri E, et al. Among authors: berardinelli a. Arch Neurol. 2006 Feb;63(2):251-7. doi: 10.1001/archneur.63.2.251. Arch Neurol. 2006. PMID: 16476814

5

Prospective study of gross motor development in children with SMA type II.

Bono R, Inverno M, Botteon G, Iotti E, Estienne M, Berardinelli A, Lanzi G, Fedrizzi E. Bono R, et al. Among authors: berardinelli a. Ital J Neurol Sci. 1995 May;16(4):223-30. doi: 10.1007/BF02282993. Ital J Neurol Sci. 1995. PMID: 7591674

6

Nonsense mutation in pseudouridylate synthase 1 (PUS1) in two brothers affected by myopathy, lactic acidosis and sideroblastic anaemia (MLASA).

Fernandez-Vizarra E, Berardinelli A, Valente L, Tiranti V, Zeviani M. Fernandez-Vizarra E, et al. Among authors: berardinelli a. BMJ Case Rep. 2009;2009:bcr05.2009.1889. doi: 10.1136/bcr.05.2009.1889. Epub 2009 Jun 9. BMJ Case Rep. 2009. PMID: 21686963 Free PMC article.

7

Effects of different ventilator settings on sleep and inspiratory effort in patients with neuromuscular disease.

Fanfulla F, Delmastro M, Berardinelli A, Lupo ND, Nava S. Fanfulla F, et al. Among authors: berardinelli a. Am J Respir Crit Care Med. 2005 Sep 1;172(5):619-24. doi: 10.1164/rccm.200406-694OC. Epub 2005 Jun 16. Am J Respir Crit Care Med. 2005. PMID: 15961699

8

Epileptic seizures, arthrogryposis, and migrational brain disorders: a syndrome?

Veggiotti P, Berardinelli A, Fazzi E, Lanzi G. Veggiotti P, et al. Among authors: berardinelli a. Acta Neurol Scand. 1995 Jun;91(6):518-9. doi: 10.1111/j.1600-0404.1995.tb00458.x. Acta Neurol Scand. 1995. PMID: 7572052 No abstract available.

9

Somatosensory and visual evoked potentials in congenital muscular dystrophy: correlation with MRI changes and muscle merosin status.

Mercuri E, Muntoni F, Berardinelli A, Pennock J, Sewry C, Philpot J, Dubowitz V. Mercuri E, et al. Among authors: berardinelli a. Neuropediatrics. 1995 Feb;26(1):3-7. doi: 10.1055/s-2007-979711. Neuropediatrics. 1995. PMID: 7791947

10

[Ehlers-Danlos syndrome. Description of 2 clinical cases].

Ottolini A, Berardinelli A, Besana D, Cetta G, Dyne KM, Lanzi G. Ottolini A, et al. Among authors: berardinelli a. Minerva Pediatr. 1992 May;44(5):231-6. Minerva Pediatr. 1992. PMID: 1620075 Italian.

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