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Anales De Pediatria (Barcelona, Spain : 2003)
|
August 1, 2009
[Infection-triggered familial or recurrent acute necrotizing encephalopathy]
E López-Laso, M E Mateos-González, J L Pérez-Navero, et al.
Archivos De La Sociedad Espanola De Oftalmologia
|
March 21, 2003
[Mutation P28T in gene GK1 as the cause of a familial galactokinase deficiency]
M Girós, M D Bóveda, A Vázquez de la Cruz, et al.
Anales Espanoles De Pediatria
|
February 1, 1990
[Sudden death of a patient with 3-hydroxy-3-methylglutaryl coenzyme A lyase deficiency]
M A Vilaseca Busca, A Ribes Rubio, P Briones Godino, et al.
Brain & Development
|
July 1, 1995
An atypical French form of pyruvate carboxylase deficiency
M Pineda, J Campistol, M A Vilaseca, et al.
The Annals of Thoracic Surgery
|
December 19, 2012
True negative predictive value of endobronchial ultrasound in lung cancer: are we being conservative enough?
Bryan A Whitson, Shawn S Groth, David D Odell, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
October 9, 2001
Congenital disorders of glycosylation (CDG) may be underdiagnosed when mimicking mitochondrial disease
P Briones, M A Vilaseca, M T García-Silva, et al.
Molecular Genetics and Metabolism
|
November 16, 2001
Phenotype and genotype heterogeneity in Mediterranean citrullinemia
M A Vilaseca, K Kobayashi, P Briones, et al.
European Journal of Pediatrics
|
March 1, 1990
Methylmalonic aciduria with homocystinuria: biochemical studies, treatment, and clinical course of a Cbl-C patient
A Ribes, P Briones, M A Vilaseca, et al.
The Journal of Heart Valve Disease
|
January 27, 2010
Characterization of mitral valve anterior leaflet perfusion patterns
Julia C Swanson, Lauren R Davis, Koji Arata, et al.
Revista De Neurologia
|
September 19, 2006
[Pyruvate dehydrogenase deficit associated to the C515T mutation in exon 6 of the E1alpha gene]
O Blanco-Barca, C Gomez-Lado, E Rodrigo-Saez, et al.
Page
of 7
Search research articles
Search
Showing results (31-40 of 65) with videos related to
Sort By:
Page
of 7
Anales De Pediatria (Barcelona, Spain : 2003)
|
August 1, 2009
[Infection-triggered familial or recurrent acute necrotizing encephalopathy]
E López-Laso, M E Mateos-González, J L Pérez-Navero, et al.
Archivos De La Sociedad Espanola De Oftalmologia
|
March 21, 2003
[Mutation P28T in gene GK1 as the cause of a familial galactokinase deficiency]
M Girós, M D Bóveda, A Vázquez de la Cruz, et al.
Anales Espanoles De Pediatria
|
February 1, 1990
[Sudden death of a patient with 3-hydroxy-3-methylglutaryl coenzyme A lyase deficiency]
M A Vilaseca Busca, A Ribes Rubio, P Briones Godino, et al.
Brain & Development
|
July 1, 1995
An atypical French form of pyruvate carboxylase deficiency
M Pineda, J Campistol, M A Vilaseca, et al.
The Annals of Thoracic Surgery
|
December 19, 2012
True negative predictive value of endobronchial ultrasound in lung cancer: are we being conservative enough?
Bryan A Whitson, Shawn S Groth, David D Odell, et al.
European Journal of Paediatric Neurology : EJPN : Official Journal of the European Paediatric Neurology Society
|
October 9, 2001
Congenital disorders of glycosylation (CDG) may be underdiagnosed when mimicking mitochondrial disease
P Briones, M A Vilaseca, M T García-Silva, et al.
Molecular Genetics and Metabolism
|
November 16, 2001
Phenotype and genotype heterogeneity in Mediterranean citrullinemia
M A Vilaseca, K Kobayashi, P Briones, et al.
European Journal of Pediatrics
|
March 1, 1990
Methylmalonic aciduria with homocystinuria: biochemical studies, treatment, and clinical course of a Cbl-C patient
A Ribes, P Briones, M A Vilaseca, et al.
The Journal of Heart Valve Disease
|
January 27, 2010
Characterization of mitral valve anterior leaflet perfusion patterns
Julia C Swanson, Lauren R Davis, Koji Arata, et al.
Revista De Neurologia
|
September 19, 2006
[Pyruvate dehydrogenase deficit associated to the C515T mutation in exon 6 of the E1alpha gene]
O Blanco-Barca, C Gomez-Lado, E Rodrigo-Saez, et al.
Page
of 7