Vita G - Search Results

1

Apoptosis and apoptosis-related proteins in thyroid myopathies.

Monici MC, Rodolico C, Toscano A, Messina S, Benvenga S, Messina C, Vita G. Monici MC, et al. Among authors: vita g. Muscle Nerve. 2002 Sep;26(3):383-8. doi: 10.1002/mus.10212. Muscle Nerve. 2002. PMID: 12210368

2

A family with autosomal dominant mutilating neuropathy not linked to either Charcot-Marie-Tooth disease type 2B (CMT2B) or hereditary sensory neuropathy type I (HSN I) loci.

Bellone E, Rodolico C, Toscano A, Di Maria E, Cassandrini D, Pizzuti A, Pigullo S, Mazzeo A, Macaione V, Girlanda P, Vita G, Ajmar F, Mandich P. Bellone E, et al. Among authors: vita g. Neuromuscul Disord. 2002 Mar;12(3):286-91. doi: 10.1016/s0960-8966(01)00282-6. Neuromuscul Disord. 2002. PMID: 11801401

3

Multifocal motor neuropathy and asymptomatic Hashimoto's thyroiditis: first report of an association.

Toscano A, Rodolico C, Benvenga S, Girlanda P, Laurà M, Mazzeo A, Nobile-Orazio E, Trimarchi F, Vita G, Messina C. Toscano A, et al. Among authors: vita g. Neuromuscul Disord. 2002 Aug;12(6):566-8. doi: 10.1016/s0960-8966(01)00311-x. Neuromuscul Disord. 2002. PMID: 12117481

4

Calpain 3 deficiency in Quail Eater's disease.

Musumeci O, Aguennouz M, Cagliani R, Comi GP, Ciranni A, Rodolico C, Messina C, Vita G, Toscano A. Musumeci O, et al. Among authors: vita g. Ann Neurol. 2004 Jan;55(1):146-7. doi: 10.1002/ana.10821. Ann Neurol. 2004. PMID: 14705129 No abstract available.

5

Cardiovascular autonomic control in myotonic dystrophy type 1: a correlative study with clinical and genetic data.

Di Leo R, Rodolico C, De Gregorio C, Recupero A, Coglitore S, Annesi G, Toscano A, Messina C, Vita G. Di Leo R, et al. Among authors: vita g. Neuromuscul Disord. 2004 Feb;14(2):136-41. doi: 10.1016/j.nmd.2003.11.002. Neuromuscul Disord. 2004. PMID: 14733960

6

Axial myopathy in myasthenia: a misleading cause of dropped head.

Rodolico C, Messina S, Toscano A, Vita G, Gaeta M. Rodolico C, et al. Among authors: vita g. Muscle Nerve. 2004 Feb;29(2):329-30. doi: 10.1002/mus.10543. Muscle Nerve. 2004. PMID: 14755502 No abstract available.

7

Immunolocalization and activation of transcription factor nuclear factor kappa B in dysimmune neuropathies and familial amyloidotic polyneuropathy.

Mazzeo A, Aguennouz M, Messina C, Vita G. Mazzeo A, et al. Among authors: vita g. Arch Neurol. 2004 Jul;61(7):1097-102. doi: 10.1001/archneur.61.7.1097. Arch Neurol. 2004. PMID: 15262741

8

Autonomic function in elderly uremics studied by spectral analysis of heart rate.

Di Leo R, Vita G, Messina C, Savica V. Di Leo R, et al. Among authors: vita g. Kidney Int. 2005 Apr;67(4):1521-5. doi: 10.1111/j.1523-1755.2005.00231.x. Kidney Int. 2005. PMID: 15780106 Free article.

9

Asymptomatic hyperCKemia in a case of Danon disease due to a missense mutation in Lamp-2 gene.

Musumeci O, Rodolico C, Nishino I, Di Guardo G, Migliorato A, Aguennouz M, Mazzeo A, Messina C, Vita G, Toscano A. Musumeci O, et al. Among authors: vita g. Neuromuscul Disord. 2005 Jun;15(6):409-11. doi: 10.1016/j.nmd.2005.02.008. Epub 2005 Apr 19. Neuromuscul Disord. 2005. PMID: 15907287

10

Comparison of different techniques for detecting 17p12 duplication in CMT1A.

Patitucci A, Muglia M, Magariello A, Gabriele AL, Peluso G, Sprovieri T, Conforti FL, Mazzei R, Ungaro C, Condino F, Valentino P, Bono F, Rodolico C, Mazzeo A, Toscano A, Vita G, Quattrone A. Patitucci A, et al. Among authors: vita g. Neuromuscul Disord. 2005 Jul;15(7):488-92. doi: 10.1016/j.nmd.2005.04.006. Neuromuscul Disord. 2005. PMID: 15941660

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