Pichiecchio A - Search Results

1

Congenital muscular dystrophies with cognitive impairment. A population study.

Messina S, Bruno C, Moroni I, Pegoraro E, D'Amico A, Biancheri R, Berardinelli A, Boffi P, Cassandrini D, Farina L, Minetti C, Moggio M, Mongini T, Mottarelli E, Pane M, Pantaleoni C, Pichiecchio A, Pini A, Ricci E, Saredi S, Sframeli M, Tortorella G, Toscano A, Trevisan CP, Uggetti C, Vasco G, Comi GP, Santorelli FM, Bertini E, Mercuri E. Messina S, et al. Among authors: pichiecchio a. Neurology. 2010 Sep 7;75(10):898-903. doi: 10.1212/WNL.0b013e3181f11dd5. Neurology. 2010. PMID: 20820001

2

Effectiveness of intravenous immunoglobulin treatment in adult patients with steroid-resistant monophasic or recurrent acute disseminated encephalomyelitis.

Marchioni E, Marinou-Aktipi K, Uggetti C, Bottanelli M, Pichiecchio A, Soragna D, PiccoloG, Imbesi F, Romani A, Ceroni M. Marchioni E, et al. Among authors: pichiecchio a. J Neurol. 2002 Jan;249(1):100-4. doi: 10.1007/pl00007836. J Neurol. 2002. PMID: 11954856

3

Parry-Romberg syndrome with migraine and intracranial aneurysm.

Pichiecchio A, Uggetti C, Grazia Egitto M, Zappoli F. Pichiecchio A, et al. Neurology. 2002 Aug 27;59(4):606-8; discussion 481. doi: 10.1212/wnl.59.4.606. Neurology. 2002. PMID: 12196658

4

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. Eur Radiol. 2002 Nov;12(11):2704-9. doi: 10.1007/s00330-002-1392-4. Epub 2002 May 8. Eur Radiol. 2002. PMID: 12386760

5

A short protocol for muscle MRI in children with muscular dystrophies.

Mercuri E, Pichiecchio A, Counsell S, Allsop J, Cini C, Jungbluth H, Uggetti C, Bydder G. Mercuri E, et al. Among authors: pichiecchio a. Eur J Paediatr Neurol. 2002;6(6):305-7. doi: 10.1016/s1090-3798(02)90617-3. Eur J Paediatr Neurol. 2002. PMID: 12401454

6

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: pichiecchio a. Eur J Clin Nutr. 2003 Feb;57(2):273-8. doi: 10.1038/sj.ejcn.1601524. Eur J Clin Nutr. 2003. PMID: 12571659

7

Muscle magnetic resonance imaging in patients with congenital muscular dystrophy and Ullrich phenotype.

Mercuri E, Cini C, Pichiecchio A, Allsop J, Counsell S, Zolkipli Z, Messina S, Kinali M, Brown SC, Jimenez C, Brockington M, Yuva Y, Sewry CA, Muntoni F. Mercuri E, et al. Among authors: pichiecchio a. Neuromuscul Disord. 2003 Sep;13(7-8):554-8. doi: 10.1016/s0960-8966(03)00091-9. Neuromuscul Disord. 2003. PMID: 12921792

8

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: pichiecchio a. Acta Diabetol. 2003 Oct;40 Suppl 1:S290-2. doi: 10.1007/s00592-003-0089-8. Acta Diabetol. 2003. PMID: 14618496

9

LAMA2 loss-of-function mutation in a girl with a mild congenital muscular dystrophy.

Prandini P, Berardinelli A, Fanin M, Morello F, Zardini E, Pichiecchio A, Uggetti C, Lanzi G, Angelini C, Pegoraro E. Prandini P, et al. Among authors: pichiecchio a. Neurology. 2004 Sep 28;63(6):1118-21. doi: 10.1212/01.wnl.0000138498.66940.7f. Neurology. 2004. PMID: 15452315

10

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: pichiecchio a. Arch Neurol. 2006 Feb;63(2):251-7. doi: 10.1001/archneur.63.2.251. Arch Neurol. 2006. PMID: 16476814

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