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Revista De Neurologia|July 11, 1998
[Dystrophinopathies, congenital muscular dystrophy, limb-girdle dystrophies: updated classification]S Teijeira-Bautista, D García-García, A Teijeiro-Ferreira, et al.Archives of Neurology|February 19, 2000
A novel missense mutation (W797R) in the myophosphorylase gene in Spanish patients with McArdle diseaseR Fernández, C Navarro, A L Andreu, et al.Brain : a Journal of Neurology|April 29, 2005
Autosomal dominant congenital fibre type disproportion: a clinicopathological and imaging study of a large familyM J Sobrido, J M Fernández, E Fontoira, et al.Revista De Neurologia|April 2, 1999
[Dystrophin and dystrophin-associated proteins. Their evaluation at the neuromuscular pathology laboratory]C NavarroJournal of Maxillofacial and Oral Surgery|March 2, 2016
Long-Term Follow-Up of Bimaxillary Osteomyelitis Associated with Autosomal Dominant Osteopetrosis: A Case ReportA Kulyapina, J Verdaguer Martin, C Navarro Cuellar, et al.Psychological Reports|June 11, 1998
Control of understanding in a task involving medical assistance given by telephoneB Minondo, C NavarroArchivos De Cardiologia De Mexico|September 22, 2001
[Acute pulmonary edema as a nursing emergency]M C Navarro AldanaPerceptual and Motor Skills|October 1, 1995
Dialog organization and functional communication in a medical assistance task by phoneP Marchand, C NavarroJournal of Maxillofacial Surgery|October 1, 1983
Rhomboid-to-"W" technique for excision and closure of facial skin lesionsH Izaguirre, C NavarroJournal of the Neurological Sciences|September 1, 1978
Multicystic encephalomalacia of infancy: clinico-pathological report of 7 casesI Ferrer, C NavarroPageof 73