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A Ruggieri

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Articles 37
Citations 462
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Recent Articles
1.
Ruggieri A, Ramachandran N, Wang P, Haan E, Kneebone C, Manavis J, et al.
Neuromuscul Disord . 2015 Feb; 25(3):207-11. PMID: 25683699
X-linked Myopathy with Excessive Autophagy (XMEA) affects proximal muscles of the lower extremities and follows a progressive course reminiscent of muscular dystrophy. It is caused by mutations in VMA21 whose...
2.
Saredi S, Ardissone A, Ruggieri A, Mottarelli E, Farina L, Rinaldi R, et al.
J Neurol Sci . 2012 May; 318(1-2):45-50. PMID: 22554691
Congenital muscular dystrophies due to defects in genes encoding proteins involved in α-dystroglycan (α-DG) glycosylation are a heterogeneous group of muscle disorders variably associated with central nervous system and eye...
3.
Scardina G, Ruggieri A, Provenzano F, Messina P
Br Dent J . 2010 Jul; 209(1):E2. PMID: 20596066
Background: Burning mouth syndrome is a chronic pathology of unknown ethiopathogenesis. The aim of this study was to evaluate whether acupuncture can produce a reduction of the burning sensation by...
4.
Scardina G, Ruggieri A, Messina P
Indian J Dent Res . 2010 Feb; 20(4):407-11. PMID: 20139561
Background: Oral lichen planus is an inflammatory chronic disease with an autimmune pathogenesis and unknown etiology that affects oral mucosa, with or without the involvement of the skin and other...
5.
Scardina G, Ruggieri A, Provenzano F, Messina P
Acupunct Med . 2009 Sep; 27(3):114-7. PMID: 19734381
Background: acupuncture is a therapeutic technique currently used in the treatment of many pathologies. The aim of this study is to evaluate the potential effect of acupuncture on "in vivo"...
6.
Mercuri E, Messina S, Bruno C, Mora M, Pegoraro E, Comi G, et al.
Neurology . 2009 Mar; 72(21):1802-9. PMID: 19299310
Background: Congenital muscular dystrophies (CMD) with reduced glycosylation of alpha-dystroglycan (alpha-DG) are a heterogeneous group of conditions associated with mutations in six genes encoding proven or putative glycosyltransferases. Objectives: The...
7.
Scardina G, Ruggieri A, Messina P
Ann Anat . 2009 Mar; 191(3):273-9. PMID: 19269146
Unlabelled: Sjögren's syndrome (SS) is a chronic autoimmune rheumatic disease characterized by a progressive lymphocytic infiltration of exocrine glands, especially salivary and lachrymal ones, leading to xerostomia, parotid gland enlargement,...
8.
Messina S, Mora M, Pegoraro E, Pini A, Mongini T, DAmico A, et al.
Neuromuscul Disord . 2008 Jun; 18(7):565-71. PMID: 18513969
Mutations in POMT1 and POMT2 genes were originally identified in Walker-Warburg syndrome (WWS) and subsequently reported in patients with milder phenotypes characterised by mental retardation with or without brain abnormalities...
9.
Inserra G, Barletta R, Santangelo L, Ruggieri A, De Crescenzo I, Carbone U
G Ital Med Lav Ergon . 2008 Apr; 29(3 Suppl):780-1. PMID: 18409958
The Implantable Cardioverter Defibrillators and the Pacemakers are devices that produce electric signals and consequently they are touchy to the electromagnetic interferences. This touchiness may cause a temporary or permanent...
10.
Zanotti S, Saredi S, Ruggieri A, Fabbri M, Blasevich F, Romaggi S, et al.
Matrix Biol . 2007 Jul; 26(8):615-24. PMID: 17662584
Extent of muscle fibrosis contributes to disease severity in muscular dystrophies. To investigate whether extracellular matrix (ECM) components contribute to the severe fibrosis observed in Duchenne muscular dystrophy (DMD) skeletal...