Gamez J - Search Results

1

Autoimmune-like hepatitis during masitinib therapy in an amyotrophic lateral sclerosis patient.

Salvado M, Vargas V, Vidal M, Simon-Talero M, Camacho J, Gamez J. Salvado M, et al. Among authors: gamez j. World J Gastroenterol. 2015 Sep 28;21(36):10475-9. doi: 10.3748/wjg.v21.i36.10475. World J Gastroenterol. 2015. PMID: 26420975 Free PMC article.

2

Cellular transplants in amyotrophic lateral sclerosis patients: an observational study.

Gamez J, Carmona F, Raguer N, Ferrer-Sancho J, Martín-Henao GA, Martí-Beltrán S, Badia M, Gratacós M, Rodriguez-Gónzalez E, Seoane JL, Pallero-Castillo M, Burgos R, Puiggros C, Pasarin A, Bori-Fortuny I. Gamez J, et al. Cytotherapy. 2010 Sep;12(5):669-77. doi: 10.3109/14653241003774037. Cytotherapy. 2010. PMID: 20586670

3

Lithium for treatment of amyotrophic lateral sclerosis: much ado about nothing.

Gamez J, Salvado M, Martínez de la Ossa A, Badia M. Gamez J, et al. Neurologia. 2016 Oct;31(8):550-61. doi: 10.1016/j.nrl.2013.02.001. Epub 2013 Apr 10. Neurologia. 2016. PMID: 23582371 Free article. Review. English, Spanish.

4

CX3CR1 is a modifying gene of survival and progression in amyotrophic lateral sclerosis.

Lopez-Lopez A, Gamez J, Syriani E, Morales M, Salvado M, Rodríguez MJ, Mahy N, Vidal-Taboada JM. Lopez-Lopez A, et al. Among authors: gamez j. PLoS One. 2014 May 7;9(5):e96528. doi: 10.1371/journal.pone.0096528. eCollection 2014. PLoS One. 2014. PMID: 24806473 Free PMC article.

5

PFN1 mutations are also rare in the Catalan population with amyotrophic lateral sclerosis.

Syriani E, Salvans C, Salvadó M, Morales M, Lorenzo L, Cazorla S, Gamez J. Syriani E, et al. Among authors: gamez j. J Neurol. 2014 Dec;261(12):2387-92. doi: 10.1007/s00415-014-7501-x. Epub 2014 Sep 24. J Neurol. 2014. PMID: 25249294

6

UNC13A confers risk for sporadic ALS and influences survival in a Spanish cohort.

Vidal-Taboada JM, Lopez-Lopez A, Salvado M, Lorenzo L, Garcia C, Mahy N, Rodríguez MJ, Gamez J. Vidal-Taboada JM, et al. Among authors: gamez j. J Neurol. 2015 Oct;262(10):2285-92. doi: 10.1007/s00415-015-7843-z. Epub 2015 Jul 11. J Neurol. 2015. PMID: 26162714 Free article.

7

Incomplete penetrance in the Spanish family with limb-girdle muscular dystrophy type 1F.

Gamez J, Salvadó M, Gratacós M. Gamez J, et al. Muscle Nerve. 2016 Jan;53(1):156-7. doi: 10.1002/mus.24900. Epub 2015 Sep 23. Muscle Nerve. 2016. PMID: 26351998 No abstract available.

8

Study of the prevalence of familial autoimmune myasthenia gravis in a Spanish cohort.

Salvado M, Canela M, Ponseti JM, Lorenzo L, Garcia C, Cazorla S, Gili G, Raguer N, Gamez J. Salvado M, et al. Among authors: gamez j. J Neurol Sci. 2016 Jan 15;360:110-4. doi: 10.1016/j.jns.2015.11.049. Epub 2015 Nov 27. J Neurol Sci. 2016. PMID: 26723985

9

Identification and characterization of the novel point mutation m.3634A>G in the mitochondrial MT-ND1 gene associated with LHON syndrome.

Carreño-Gago L, Gamez J, Cámara Y, Alvarez de la Campa E, Aller-Alvarez JS, Moncho D, Salvado M, Galan A, de la Cruz X, Pinós T, García-Arumí E. Carreño-Gago L, et al. Among authors: gamez j. Biochim Biophys Acta Mol Basis Dis. 2017 Jan;1863(1):182-187. doi: 10.1016/j.bbadis.2016.09.002. Epub 2016 Sep 7. Biochim Biophys Acta Mol Basis Dis. 2017. PMID: 27613247 Free article.

10

SBF1 mutations associated with autosomal recessive axonal neuropathy with cranial nerve involvement.

Manole A, Horga A, Gamez J, Raguer N, Salvado M, San Millán B, Navarro C, Pittmann A, Reilly MM, Houlden H. Manole A, et al. Among authors: gamez j. Neurogenetics. 2017 Jan;18(1):63-67. doi: 10.1007/s10048-016-0505-1. Epub 2016 Dec 22. Neurogenetics. 2017. PMID: 28005197

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