Vita G - Search Results

1

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

2

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

3

Clinical features and new molecular findings in muscle phosphofructokinase deficiency (GSD type VII).

Musumeci O, Bruno C, Mongini T, Rodolico C, Aguennouz M, Barca E, Amati A, Cassandrini D, Serlenga L, Vita G, Toscano A. Musumeci O, et al. Among authors: vita g. Neuromuscul Disord. 2012 Apr;22(4):325-30. doi: 10.1016/j.nmd.2011.10.022. Epub 2011 Nov 30. Neuromuscul Disord. 2012. PMID: 22133655

4

Myasthenia Gravis: Unusual Presentations and Diagnostic Pitfalls.

Rodolico C, Parisi D, Portaro S, Biasini F, Sinicropi S, Ciranni A, Toscano A, Messina S, Musumeci O, Vita G, Girlanda P. Rodolico C, et al. Among authors: vita g. J Neuromuscul Dis. 2016 Aug 30;3(3):413-418. doi: 10.3233/JND-160148. J Neuromuscul Dis. 2016. PMID: 27854225

5

Long-term treatment with subcutaneous immunoglobulin in multifocal motor neuropathy.

Gentile L, Russo M, Rodolico C, Arimatea I, Vita G, Toscano A, Mazzeo A. Gentile L, et al. Among authors: vita g. Sci Rep. 2021 Apr 28;11(1):9216. doi: 10.1038/s41598-021-88711-9. Sci Rep. 2021. PMID: 33911162 Free PMC article.

6

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

7

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

8

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

9

Recurrent syncope as persistently isolated feature of transthyretin amyloidotic polyneuropathy.

Vita G, Mazzeo A, Di Leo R, Ferlini A. Vita G, et al. Neuromuscul Disord. 2005 Mar;15(3):259-61. doi: 10.1016/j.nmd.2004.10.015. Epub 2005 Jan 28. Neuromuscul Disord. 2005. PMID: 15725588

10

Identification of the infant-type R631C mutation in patients with the benign muscular form of CPT2 deficiency.

Musumeci O, Aguennouz M, Comi GP, Rodolico C, Autunno M, Bordoni A, Baratta S, Taroni F, Vita G, Toscano A. Musumeci O, et al. Among authors: vita g. Neuromuscul Disord. 2007 Dec;17(11-12):960-3. doi: 10.1016/j.nmd.2007.05.002. Epub 2007 Jul 24. Neuromuscul Disord. 2007. PMID: 17651973

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