Search details
1.
Variants in DTNA cause a mild, dominantly inherited muscular dystrophy.
Acta Neuropathol
; 145(4): 479-496, 2023 04.
Article
in English
| MEDLINE | ID: mdl-36799992
2.
Differential diagnosis of necrotizing myopathy.
Curr Opin Rheumatol
; 33(6): 544-553, 2021 11 01.
Article
in English
| MEDLINE | ID: mdl-34482348
3.
Circulating Cell-Free Mitochondrial DNA in Cerebrospinal Fluid as a Biomarker for Mitochondrial Diseases.
Clin Chem
; 67(8): 1113-1121, 2021 08 05.
Article
in English
| MEDLINE | ID: mdl-34352085
4.
Tumour TIF1 mutations and loss of heterozygosity related to cancer-associated myositis.
Rheumatology (Oxford)
; 57(2): 388-396, 2018 02 01.
Article
in English
| MEDLINE | ID: mdl-29149307
5.
Delayed diagnosis of late-onset Pompe disease in patients with myopathies of unknown origin and/or hyperCKemia.
Mol Genet Metab
; 114(4): 580-3, 2015 Apr.
Article
in English
| MEDLINE | ID: mdl-25752415
6.
Integrated Multi-Omics Analysis for Inferring Molecular Players in Inclusion Body Myositis.
Antioxidants (Basel)
; 12(8)2023 Aug 19.
Article
in English
| MEDLINE | ID: mdl-37627634
7.
Unravelling inclusion body myositis using a patient-derived fibroblast model.
J Cachexia Sarcopenia Muscle
; 14(2): 964-977, 2023 04.
Article
in English
| MEDLINE | ID: mdl-36860172
8.
Screening for late-onset Pompe disease in Internal Medicine departments in Spain.
Orphanet J Rare Dis
; 18(1): 256, 2023 08 31.
Article
in English
| MEDLINE | ID: mdl-37653444
9.
Malignancy and myositis: novel autoantibodies and new insights.
Curr Opin Rheumatol
; 22(6): 627-32, 2010 Nov.
Article
in English
| MEDLINE | ID: mdl-20827204
10.
The Impact of Mitochondrial Deficiencies in Neuromuscular Diseases.
Antioxidants (Basel)
; 9(10)2020 Oct 09.
Article
in English
| MEDLINE | ID: mdl-33050147
11.
Mitochondrial Dysfunction: A Common Hallmark Underlying Comorbidity between sIBM and Other Degenerative and Age-Related Diseases.
J Clin Med
; 9(5)2020 May 13.
Article
in English
| MEDLINE | ID: mdl-32413985
12.
Neutrophil dysregulation is pathogenic in idiopathic inflammatory myopathies.
JCI Insight
; 5(3)2020 02 13.
Article
in English
| MEDLINE | ID: mdl-31945019
13.
Identification of distinctive interferon gene signatures in different types of myositis.
Neurology
; 93(12): e1193-e1204, 2019 09 17.
Article
in English
| MEDLINE | ID: mdl-31434690
14.
Myositis Autoantigen Expression Correlates With Muscle Regeneration but Not Autoantibody Specificity.
Arthritis Rheumatol
; 71(8): 1371-1376, 2019 08.
Article
in English
| MEDLINE | ID: mdl-30861336
15.
[Polymyositis-dermatomyositis: incidence in Spain (1997-2004)]. / Polimiositis y dermatomiositis: incidencia en España (1997-2004).
Med Clin (Barc)
; 129(19): 721-4, 2007 Nov 24.
Article
in Spanish
| MEDLINE | ID: mdl-18053482
16.
Very Long Time Persistent HyperCKemia as the First Manifestation of McLeod Syndrome: A Case Report.
Mov Disord Clin Pract
; 9(6): 821-824, 2022 Aug.
Article
in English
| MEDLINE | ID: mdl-35937484
17.
[Hypocalcaemia: an unusual and potentially reversible cause of dilated cardiomyopathy]. / Hipocalcemia: una causa poco frecuente y potencialmente reversible de miocardiopatía dilatada.
Med Clin (Barc)
; 136(3): 133-4, 2011 Feb 12.
Article
in Spanish
| MEDLINE | ID: mdl-20044112
18.
[Transition process from paediatric to adult care in patients with inborn errors of metabolism. Consensus statement]. / Proceso de transición de la asistencia pediátrica a la adulta en pacientes con errores congénitos del metabolismo. Documento de consenso.
Med Clin (Barc)
; 147(11): 506.e1-506.e7, 2016 Dec 02.
Article
in Spanish
| MEDLINE | ID: mdl-27816186
19.
Identification of a novel myositis-associated antibody directed against cortactin.
Autoimmun Rev
; 13(10): 1008-12, 2014 Oct.
Article
in English
| MEDLINE | ID: mdl-25182205
20.
[Biologic therapy in idiopathic inflammatory myopathy]. / Terapia biológica en pacientes con miopatía inflamatoria idiopática.
Med Clin (Barc)
; 143(6): 275-80, 2014 Sep 15.
Article
in Spanish
| MEDLINE | ID: mdl-24393419