Di Muzio A - Search Results

1

Facioscapulohumeral muscular dystrophy presenting isolated monomelic lower limb atrophy. Report of two patients with and without 4q35 rearrangement.

Uncini A, Galluzzi G, Di Muzio A, De Angelis MV, Ricci E, Scoppetta C, Servidei S. Uncini A, et al. Among authors: di muzio a. Neuromuscul Disord. 2002 Nov;12(9):874-7. doi: 10.1016/s0960-8966(02)00027-5. Neuromuscul Disord. 2002. PMID: 12398841 Clinical Trial.

2

Benign monomelic amyotrophy of lower limb: report of three cases.

Uncini A, Servidei S, Delli Pizzi C, Cutarella R, Di Muzio A, Gambi D, Tonali P. Uncini A, et al. Among authors: di muzio a. Acta Neurol Scand. 1992 Jun;85(6):397-400. doi: 10.1111/j.1600-0404.1992.tb06035.x. Acta Neurol Scand. 1992. PMID: 1642110

3

Identification of deletions and duplications of the DMD gene in affected males and carrier females by multiple ligation probe amplification (MLPA).

Gatta V, Scarciolla O, Gaspari AR, Palka C, De Angelis MV, Di Muzio A, Guanciali-Franchi P, Calabrese G, Uncini A, Stuppia L. Gatta V, et al. Among authors: di muzio a. Hum Genet. 2005 Jun;117(1):92-8. doi: 10.1007/s00439-005-1270-7. Epub 2005 Apr 20. Hum Genet. 2005. PMID: 15841391

4

Familial idiopathic hyper-CK-emia: an underrecognized condition.

Capasso M, De Angelis MV, Di Muzio A, Scarciolla O, Pace M, Stuppia L, Comi GP, Uncini A. Capasso M, et al. Among authors: di muzio a. Muscle Nerve. 2006 Jun;33(6):760-5. doi: 10.1002/mus.20525. Muscle Nerve. 2006. PMID: 16502425

5

Benign monomelic amyotrophy of lower limb: a rare entity with a characteristic muscular CT.

Di Muzio A, Delli Pizzi C, Lugaresi A, Ragno M, Uncini A. Di Muzio A, et al. J Neurol Sci. 1994 Nov;126(2):153-61. doi: 10.1016/0022-510x(94)90266-6. J Neurol Sci. 1994. PMID: 7853021

6

Hereditary motor and sensory neuropathy with calf hypertrophy is associated with 17p11.2 duplication.

Uncini A, Di Muzio A, Chiavaroli F, Gambi D, Sabatelli M, Archidiacono N, Antonacci R, Marzella R, Rocchi M. Uncini A, et al. Among authors: di muzio a. Ann Neurol. 1994 May;35(5):552-8. doi: 10.1002/ana.410350508. Ann Neurol. 1994. PMID: 8179301

7

Benign monomelic amyotrophies of upper and lower limb are not associated to deletions of survival motor neuron gene.

Guglielmo GD, Brahe C, Di Muzio A, Uncini A. Guglielmo GD, et al. Among authors: di muzio a. J Neurol Sci. 1996 Sep 15;141(1-2):111-3. doi: 10.1016/0022-510x(96)00154-2. J Neurol Sci. 1996. PMID: 8880702

8

A late-onset mitochondrial myopathy is associated with a novel mitochondrial DNA (mtDNA) point mutation in the tRNA(Trp) gene.

Silvestri G, Rana M, DiMuzio A, Uncini A, Tonali P, Servidei S. Silvestri G, et al. Neuromuscul Disord. 1998 Jun;8(5):291-5. doi: 10.1016/s0960-8966(98)00037-6. Neuromuscul Disord. 1998. PMID: 9673981

9

Minimal and asymptomatic chronic inflammatory demyelinating polyneuropathy.

Uncini A, Di Muzio A, De Angelis MV, Gioia S, Lugaresi A. Uncini A, et al. Among authors: di muzio a. Clin Neurophysiol. 1999 Apr;110(4):694-8. doi: 10.1016/s1388-2457(98)00070-4. Clin Neurophysiol. 1999. PMID: 10378740

10

Hepatitis C virus infection and myositis: a virus localization study.

Di Muzio A, Bonetti B, Capasso M, Panzeri L, Pizzigallo E, Rizzuto N, Uncini A. Di Muzio A, et al. Neuromuscul Disord. 2003 Jan;13(1):68-71. doi: 10.1016/s0960-8966(02)00184-0. Neuromuscul Disord. 2003. PMID: 12467735

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