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American Journal of Ophthalmology|March 10, 2001
Bilateral optic nerve atrophy in myotonic dystrophyJ Gamez, D Montane, L Martorell, et al.
European Journal of Human Genetics : EJHG|July 6, 2000
Complex patterns of male germline instability and somatic mosaicism in myotonic dystrophy type 1L Martorell, D G Monckton, J Gamez, et al.
Human Molecular Genetics|March 21, 1998
Progression of somatic CTG repeat length heterogeneity in the blood cells of myotonic dystrophy patientsL Martorell, D G Monckton, J Gamez, et al.
Neuromuscular Disorders : NMD|June 26, 1999
A new mutation in the myophosphorylase gene (Asn684Tyr) in a Spanish patient with McArdle's diseaseA L Andreu, C Bruno, L Tamburino, et al.
Muscle & Nerve|July 27, 1999
A new mutation in the regulatory domain of the myophosphorylase gene affecting protein dimer contactJ Gamez, R Fernandez, C Bruno, et al.
Annals of Medicine|October 30, 2001
Exercise intolerance resulting from a muscle-restricted mutation in the mitochondrial tRNA(Leu (CUN)) geneC Vives-Bauza, J Gamez, M Roig, et al.
Neurology|November 13, 2002
Survival and respiratory decline are not related to homozygous SMN2 deletions in ALS patientsJ Gamez, M J Barceló, X Muñoz, et al.
Neurology|July 23, 1998
Molecular genetic analysis of McArdle's disease in Spanish patientsA L Andreu, C Bruno, J Gamez, et al.
Revista De Neurologia|May 20, 1998
[Visual evoked potentials and electroretinogram in pediatrics. Concept methodology and clinical applications]M Olesti-Marco, T Minoves-Font, M Quintillá, et al.
Neurology|August 15, 2002
Phenotypic variability in a Spanish family with MNGIEJ Gamez, C Ferreiro, M L Accarino, et al.
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