Detalhe da pesquisa
1.
Reliability of clinical diagnosis of dystonia.
Neuroepidemiology
; 43(3-4): 213-9, 2014.
Artigo
em Inglês
| MEDLINE | ID: mdl-25402591
2.
Rare missense variants of neuronal nicotinic acetylcholine receptor altering receptor function are associated with sporadic amyotrophic lateral sclerosis.
Hum Mol Genet
; 18(20): 3997-4006, 2009 Oct 15.
Artigo
em Inglês
| MEDLINE | ID: mdl-19628475
3.
CD8(+) T cells in facioscapulohumeral muscular dystrophy patients with inflammatory features at muscle MRI.
J Clin Immunol
; 31(2): 155-66, 2011 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21063901
4.
Prevalence of small intestinal bacterial overgrowth in Parkinson's disease.
Mov Disord
; 26(5): 889-92, 2011 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-21520278
5.
Response to rehabilitation of children and adolescents with epilepsy.
Epilepsy Behav
; 20(1): 79-82, 2011 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-21130694
6.
Mixed connective tissue disease presenting as a peculiar myositis with poor muscle regeneration.
Neurol Sci
; 32(1): 171-4, 2011 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-20890626
7.
Pilot trial of simvastatin in the treatment of sporadic inclusion-body myositis.
Neurol Sci
; 32(5): 841-7, 2011 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-21695654
8.
Cephalometric findings in facioscapulohumeral muscular dystrophy patients with obstructive sleep apneas.
Sleep Breath
; 15(1): 99-106, 2011 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-20174877
9.
Substrate reduction therapy with miglustat in chronic GM2 gangliosidosis type Sandhoff: results of a 3-year follow-up.
J Inherit Metab Dis
; 33 Suppl 3: S355-61, 2010 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-20821051
10.
Analysis of MTMR1 expression and correlation with muscle pathological features in juvenile/adult onset myotonic dystrophy type 1 (DM1) and in myotonic dystrophy type 2 (DM2).
Exp Mol Pathol
; 89(2): 158-68, 2010 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-20685272
11.
Cerebellar degeneration and ocular myasthenia gravis in a patient with recurring ovarian carcinoma.
Neurol Sci
; 31(1): 79-81, 2010 Feb.
Artigo
em Inglês
| MEDLINE | ID: mdl-19806316
12.
Heart rate variability in facioscapulohumeral muscular dystrophy.
Funct Neurol
; 25(4): 211-6, 2010.
Artigo
em Inglês
| MEDLINE | ID: mdl-21388582
13.
Regulatory T cells fail to suppress CD4T+-bet+ T cells in relapsing multiple sclerosis patients.
Immunology
; 127(3): 418-28, 2009 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-19016907
14.
Prevalence of primary focal or segmental dystonia in adults in the district of foggia, southern Italy: a service-based study.
Neuroepidemiology
; 33(2): 117-23, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-19556806
15.
SOD1 G93D mutation presenting as paucisymptomatic amyotrophic lateral sclerosis.
Amyotroph Lateral Scler
; 10(5-6): 479-82, 2009.
Artigo
em Inglês
| MEDLINE | ID: mdl-19922144
16.
Glioblastoma in multiple sclerosis: a case report.
J Neurooncol
; 94(1): 141-4, 2009 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-19214706
17.
pSTAT1, pSTAT3, and T-bet as markers of disease activity in chronic inflammatory demyelinating polyradiculoneuropathy.
J Peripher Nerv Syst
; 14(2): 107-17, 2009 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-19691533
18.
Heterozygous SOD1 D90A mutation presenting as slowly progressive predominant upper motor neuron amyotrophic lateral sclerosis.
Neurol Sci
; 30(6): 517-20, 2009 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-19685200
19.
Successful treatment of acute autoimmune limbic encephalitis with negative VGKC and NMDAR antibodies.
Cogn Behav Neurol
; 22(1): 63-6, 2009 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-19372772
20.
Hyposialylation of neprilysin possibly affects its expression and enzymatic activity in hereditary inclusion-body myopathy muscle.
J Neurochem
; 105(3): 971-81, 2008 May.
Artigo
em Inglês
| MEDLINE | ID: mdl-18182043