Gamez J - Search Results

1

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.

2

A new mutation in the regulatory domain of the myophosphorylase gene affecting protein dimer contact.

Gamez J, Fernandez R, Bruno C, Andreu AL, Cervera C, Navarro C, Schwartz S, Dimauro S. Gamez J, et al. Muscle Nerve. 1999 Aug;22(8):1136-8. doi: 10.1002/(sici)1097-4598(199908)22:8<1136::aid-mus21>3.0.co;2-2. Muscle Nerve. 1999. PMID: 10417800

3

Autosomal dominant limb-girdle muscular dystrophy: a large kindred with evidence for anticipation.

Gamez J, Navarro C, Andreu AL, Fernandez JM, Palenzuela L, Tejeira S, Fernandez-Hojas R, Schwartz S, Karadimas C, DiMauro S, Hirano M, Cervera C. Gamez J, et al. Neurology. 2001 Feb 27;56(4):450-4. doi: 10.1212/wnl.56.4.450. Neurology. 2001. PMID: 11222786

4

A novel autosomal dominant limb-girdle muscular dystrophy (LGMD 1F) maps to 7q32.1-32.2.

Palenzuela L, Andreu AL, Gàmez J, Vilà MR, Kunimatsu T, Meseguer A, Cervera C, Fernandez Cadenas I, van der Ven PF, Nygaard TG, Bonilla E, Hirano M. Palenzuela L, et al. Among authors: gamez j. Neurology. 2003 Aug 12;61(3):404-6. doi: 10.1212/01.wnl.0000073984.46546.4f. Neurology. 2003. PMID: 12913210

5

Investigation of the role of SMN1 and SMN2 haploinsufficiency as a risk factor for Hirayama's disease: clinical, neurophysiological and genetic characteristics in a Spanish series of 13 patients.

Gamez J, Also E, Alias L, Corbera-Bellalta M, Barceló MJ, Centeno M, Raguer N, Gratacós M, Baiget M, Tizzano EF. Gamez J, et al. Clin Neurol Neurosurg. 2007 Dec;109(10):844-8. doi: 10.1016/j.clineuro.2007.07.019. Epub 2007 Sep 11. Clin Neurol Neurosurg. 2007. PMID: 17850955

6

Camptocormia associated with an expanded allele in the TATA box-binding protein gene.

Gamez J, Sierra-Marcos A, Gratacós M, Jorge L, Raguer N, Moncho-Rodriguez D, Jacas C, Conejero J, Badia M, Lorenzo-Bosquet C, Volpini V, Castell-Conesa J. Gamez J, et al. Mov Disord. 2010 Jul 15;25(9):1293-5. doi: 10.1002/mds.23057. Mov Disord. 2010. PMID: 20310027 No abstract available.

7

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

8

Limb-girdle muscular dystrophy 1F is caused by a microdeletion in the transportin 3 gene.

Melià MJ, Kubota A, Ortolano S, Vílchez JJ, Gámez J, Tanji K, Bonilla E, Palenzuela L, Fernández-Cadenas I, Pristoupilová A, García-Arumí E, Andreu AL, Navarro C, Hirano M, Martí R. Melià MJ, et al. Among authors: gamez j. Brain. 2013 May;136(Pt 5):1508-17. doi: 10.1093/brain/awt074. Epub 2013 Mar 29. Brain. 2013. PMID: 23543484 Free PMC article.

9

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.

10

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.

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