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Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc
|
April 1, 1994
Detection of delta F508 cystic fibrosis mutation by polymerase chain reaction from old paraffin-embedded tissues: a retrospective autopsy study
J Palacios, B Ezquieta, C Gamallo, et al.
Human Mutation
|
January 1, 1992
Cystic fibrosis patients with mutation 1949del84 in exon 13 of the CFTR gene have a similar clinical severity as delta F508 homozygotes
V Nunes, T Casals, A Gaona, et al.
Revista Clinica Espanola
|
October 1, 1987
[Determination of beta-2-microglobulin levels in patients with systemic lupus erythematosus: correlation with clinical and biological parameters]
M E Valencia, J Molano, J J Vázquez, et al.
Human Genetics
|
August 1, 1991
The delta F508 mutation and RFLP-linked loci in Spanish cystic fibrosis families
B Peral, C Hernández-Chico, J L San Millán, et al.
Advances in Experimental Medicine and Biology
|
January 11, 2002
Mutations in the hypoxanthine-guanine phosphoribosyltransferase gene in Spanish HPRT deficient families
R J Torres, F A Mateos, J Molano, et al.
Human Mutation
|
March 29, 2000
Molecular basis of hypoxanthine-guanine phosphoribosyltransferase deficiency in thirteen Spanish families
R J Torres, F A Mateos, J Molano, et al.
Catheterization and Cardiovascular Interventions : Official Journal of the Society for Cardiac Angiography & Interventions
|
February 21, 2009
Radial compression guided by mean artery pressure versus standard compression with a pneumatic device (RACOMAP)
Jose M Cubero, Juan Lombardo, Carmela Pedrosa, et al.
Clinical Genetics
|
January 26, 2013
PLP1 gene analysis in 88 patients with leukodystrophy
P Martínez-Montero, M Muñoz-Calero, E Vallespín, et al.
Magnetic Resonance Imaging
|
May 8, 2022
Magnetic resonance imaging in patients with cardiac implantable electronic devices: A prospective study
Cristina Navarro-Valverde, Javier Ramos-Maqueda, M José Romero-Reyes, et al.
Neurologia (Barcelona, Spain)
|
March 13, 2016
Mutational spectrum of Duchenne muscular dystrophy in Spain: Study of 284 cases
I Vieitez, P Gallano, L González-Quereda, et al.
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of 4
Search research articles
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Showing results (21-30 of 33) with videos related to
Sort By:
Page
of 4
Modern Pathology : an Official Journal of the United States and Canadian Academy of Pathology, Inc
|
April 1, 1994
Detection of delta F508 cystic fibrosis mutation by polymerase chain reaction from old paraffin-embedded tissues: a retrospective autopsy study
J Palacios, B Ezquieta, C Gamallo, et al.
Human Mutation
|
January 1, 1992
Cystic fibrosis patients with mutation 1949del84 in exon 13 of the CFTR gene have a similar clinical severity as delta F508 homozygotes
V Nunes, T Casals, A Gaona, et al.
Revista Clinica Espanola
|
October 1, 1987
[Determination of beta-2-microglobulin levels in patients with systemic lupus erythematosus: correlation with clinical and biological parameters]
M E Valencia, J Molano, J J Vázquez, et al.
Human Genetics
|
August 1, 1991
The delta F508 mutation and RFLP-linked loci in Spanish cystic fibrosis families
B Peral, C Hernández-Chico, J L San Millán, et al.
Advances in Experimental Medicine and Biology
|
January 11, 2002
Mutations in the hypoxanthine-guanine phosphoribosyltransferase gene in Spanish HPRT deficient families
R J Torres, F A Mateos, J Molano, et al.
Human Mutation
|
March 29, 2000
Molecular basis of hypoxanthine-guanine phosphoribosyltransferase deficiency in thirteen Spanish families
R J Torres, F A Mateos, J Molano, et al.
Catheterization and Cardiovascular Interventions : Official Journal of the Society for Cardiac Angiography & Interventions
|
February 21, 2009
Radial compression guided by mean artery pressure versus standard compression with a pneumatic device (RACOMAP)
Jose M Cubero, Juan Lombardo, Carmela Pedrosa, et al.
Clinical Genetics
|
January 26, 2013
PLP1 gene analysis in 88 patients with leukodystrophy
P Martínez-Montero, M Muñoz-Calero, E Vallespín, et al.
Magnetic Resonance Imaging
|
May 8, 2022
Magnetic resonance imaging in patients with cardiac implantable electronic devices: A prospective study
Cristina Navarro-Valverde, Javier Ramos-Maqueda, M José Romero-Reyes, et al.
Neurologia (Barcelona, Spain)
|
March 13, 2016
Mutational spectrum of Duchenne muscular dystrophy in Spain: Study of 284 cases
I Vieitez, P Gallano, L González-Quereda, et al.
Page
of 4