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Pete Garcia, Obispo de Barcelona (1490-1505), y dos cuestiones fundamentales: la actitud ante Fernando el Catolico, y la epoca de las reformas en Espa¤a

Paradas Pena, M. S.; Ruiz, E. M.; Grimon, V. S.

; Asociacion Espanola de Historia Moderna; Las Palmas, 1994; May, 0, 65-80 -- Las Palmas de Gran Canaria; Universidad de Las Palmas de Gran Canaria; 1994 (pages 65-80)

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Somatic mosaicism in a Duchenne/Becker muscular dystrophy patient

Juan-Mateu, J. et al.

Neuromuscular disorders : NMD.; World Muscle Society; Kumamoto, Japan, 2010; Oct, 2010, P4.06 -- Elsevier Science; 2010 Part: Part 9/10; -- 2010

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TK2 mutation presenting as indolent myopathy

Paradas, C. et al.

Neurology. VOL 80; NUMB 5, ; 2013, 504-506 -- American Academy of Neurology Part 5; (pages 504-506) -- 2013

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D.P.4.12 Phenotype and genotype study of Oculopharyngeal Muscle Dystrophy in patients from southern Spain

Paradas, c. u. et al.

Neuromuscular disorders : NMD. VOL 18; NUMBER 9-10, ; 2008, 799 -- Elsevier Science B.V., Amsterdam. -- 2008

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Prednisone can worsen ataxic neuropathy with anti-disialosyl IgM antibodies

Paradas, C. et al.

Muscle & nerve. VOL 44; NUMBER 5, ; 2011, 839-840 -- John Wiley & Sons, Ltd -- 2011

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Highly skewed inactivation of the wild-type X-chromosome in asymptomatic female carriers of spinal and bulbar muscular atrophy (Kennedy’s disease)

Paradas, C. et al.

Journal of neurology. VOL 255; NUMBER 6, ; 2008, 853-857 -- Springer Science + Business Media (pages 853-857) -- 2008

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Variable presentation of the clinical phenotype of McArdles disease in a kindred harbouring a novel compound genotype in the muscle glycogen phosphorylase gene

Paradas, C. et al.

Neuroscience letters. VOL 391; NUMBER 1-2, ; 2005, 28-31 -- Elsevier Science B.V., Amsterdam. Part: Part 1-2; (pages 28-31) -- 2005

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D.P.4.12 Phenotype and genotype study of Oculopharyngeal Muscle Dystrophy in patients from southern Spain

Paradas, c. u. et al.

Neuromuscular disorders : NMD.; World Muscle Society; Newcastle upon Tyne, 2008; Sep, 2008, 799 -- Elsevier; 2008 -- 2008

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Isolated cardiomyopathy caused by a DMD nonsense mutation in somatic mosaicism: genetic normalization in skeletal muscle

Juan-Mateu, J. et al.

Clinical genetics. VOL 82; NUMBER 6, ; 2012, 574-578 -- Blackwell Publishing Ltd Part 6; (pages 574-578) -- 2012

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Precision measurement of the structure of the CMS inner tracking system using nuclear interactions

Sirunyan, A.M. et al.

Journal of instrumentation. Volume 13:Number 10 (2018); pp P10034-P10034 -- IOP Publishing Ltd

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by this Author/Contributor:

  1. Paradas, C.
  2. Diaz-Manera, J.
  3. Stojkovic, T.
  4. Bravver, E.
  5. Pegoraro, E.

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