Detalhe da pesquisa
1.
Evidence of ER stress and UPR activation in patients with Brody disease and Brody syndrome.
Neuropathol Appl Neurobiol
; 44(5): 533-536, 2018 08.
Artigo
em Inglês
| MEDLINE | ID: mdl-28801956
2.
Riboflavin-responsive multiple acyl-CoA dehydrogenase deficiency: delayed hypersensitivity reaction and efficacy of low-dose intermittent supplementation.
Eur J Neurol
; 24(7): e41-e42, 2017 07.
Artigo
em Inglês
| MEDLINE | ID: mdl-28643959
3.
Screening for Fabry disease in patients with ischaemic stroke at young age: the Italian Project on Stroke in Young Adults.
Eur J Neurol
; 24(3): e12-e14, 2017 03.
Artigo
em Inglês
| MEDLINE | ID: mdl-28211245
4.
Clinical, morphological and genetic studies in a cohort of 21 patients with myofibrillar myopathy.
Acta Myol
; 30(2): 121-6, 2011 Oct.
Artigo
em Inglês
| MEDLINE | ID: mdl-22106715
5.
Protein Expression of Canine and Feline Muscular Dystrophies.
Top Companion Anim Med
; 42: 100500, 2021 Mar.
Artigo
em Inglês
| MEDLINE | ID: mdl-33249241
6.
Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north-east Italian population sample.
Clin Genet
; 75(6): 550-5, 2009 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-19320656
7.
Facioscapulohumeral muscular dystrophy: hearing loss and other atypical features of patients with large 4q35 deletions.
Eur J Neurol
; 15(12): 1353-8, 2008 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-19049553
8.
Eyelid ptosis from sympathetic nerve dysfunction mistaken as myopathy: a simple test to identify this condition.
J Neurol Neurosurg Psychiatry
; 78(6): 632-4, 2007 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-17287241
9.
Characterization of sarcoplasmic reticulum Ca(2+) ATPase pumps in muscle of patients with myotonic dystrophy and with hypothyroid myopathy.
Neuromuscul Disord
; 26(6): 378-85, 2016 06.
Artigo
em Inglês
| MEDLINE | ID: mdl-27133661
10.
Increased expression of the normal cellular isoform of prion protein in inclusion-body myositis, inflammatory myopathies and denervation atrophy.
Brain Pathol
; 11(2): 182-9, 2001 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-11303793
11.
Implicit redundant-targets effect in visual extinction.
Neuropsychologia
; 34(1): 9-22, 1996 Jan.
Artigo
em Inglês
| MEDLINE | ID: mdl-8852689
12.
Polyglucosan body myopathy: a new case.
Neuromuscul Disord
; 2(5-6): 419-22, 1992.
Artigo
em Inglês
| MEDLINE | ID: mdl-1300190
13.
A new mutation in the mitochondrial tRNA(Ala) gene in a patient with ophthalmoplegia and dysphagia.
Neuromuscul Disord
; 11(5): 481-4, 2001 Jul.
Artigo
em Inglês
| MEDLINE | ID: mdl-11404121
14.
T-cell anti-apoptotic mechanisms in inflammatory myopathies.
J Neuroimmunol
; 111(1-2): 146-51, 2000 Nov 01.
Artigo
em Inglês
| MEDLINE | ID: mdl-11063832
15.
McArdle disease and sporadic inclusion body myositis.
Neuropathol Appl Neurobiol
; 35(4): 442-445, 2009 Aug.
Artigo
em Inglês
| MEDLINE | ID: mdl-19220759
16.
Calpain 3 deficiency presenting as fibre type disproportion.
Neuropathol Appl Neurobiol
; 35(6): 614-7, 2009 Dec.
Artigo
em Inglês
| MEDLINE | ID: mdl-19490426
17.
Chronic ophthalmoparesis in limb girdle muscular dystrophy 1C.
J Neurol Neurosurg Psychiatry
; 80(4): 448-9, 2009 Apr.
Artigo
em Inglês
| MEDLINE | ID: mdl-19289483
18.
Hypokalemic periodic paralysis. A single fiber electromyographic study.
J Neurol Sci
; 37(1-2): 107-12, 1978 Jun.
Artigo
em Inglês
| MEDLINE | ID: mdl-690662
19.
Minipolymyoclonus in congenital nemaline myopathy: a nonspecific clinical marker of neurogenic dysfunction.
Brain Dev
; 13(5): 358-62, 1991 Sep.
Artigo
em Inglês
| MEDLINE | ID: mdl-1785661
20.
Critically ill patients: immunological evidence of inflammation in muscle biopsy.
Clin Neuropathol
; 18(1): 23-30, 1999.
Artigo
em Inglês
| MEDLINE | ID: mdl-9988135