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American Journal of Ophthalmology|August 1, 1995
Ophthalmologic findings in a patient with cerebellar ataxia, hypogonadotropic hypogonadism, and chorioretinal dystrophyF Salvador, J García-Arumí, B Corcóstegui, et al.
Neurology|February 27, 2001
Autosomal dominant limb-girdle muscular dystrophy: a large kindred with evidence for anticipationJ Gamez, C Navarro, A L Andreu, et al.
Revue D'Electroencephalographie Et De Neurophysiologie Clinique|July 1, 1977
[Developmental study of the paroxysmal tracing in the full term neonate (author's transl)]M Tallada, A Queralt, O Segura, et al.
Neurologia (Barcelona, Spain)|June 20, 2001
[Spastic paraparesias by HTLV-1: early identification of a new case. Review of the Spanish casuistics]J Gámez, L Matas, E Caballero, et al.
Acta Otorrinolaringologica Espanola|January 24, 2006
[Design and performance of a laboratory of olfactory test. Application of a new evaluation system]J I Alfonso, H Vallés, C Cervera
Journal of Food Protection|November 26, 1998
Kinetics of ascorbic acid degradation in green asparagus during heat processingM J Esteve, A Frígola, L Martorell, et al.
Human Molecular Genetics|June 1, 1997
Somatic instability of the myotonic dystrophy (CTG)n repeat during human fetal developmentL Martorell, K Johnson, C A Boucher, et al.
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